Applsci 10 07432 v2
Applsci 10 07432 v2
sciences
Review
Oil Press-Cakes and Meals Valorization through
Circular Economy Approaches: A Review
Petraru Ancut, a and Amariei Sonia *
Faculty of Food Engineering, S, tefan cel Mare University of Suceava, 720229 Suceava, Romania;
ancuta.petraru@fia.usv.ro
* Correspondence: sonia@usm.ro; Tel.: +40-740-311-291
Received: 23 September 2020; Accepted: 20 October 2020; Published: 22 October 2020
Abstract: The food industry generates a large amount of waste every year, which opens up a research
field aimed at minimizing and efficiently managing this issue to support the concept of zero waste.
From the extraction process of oilseeds results oil cakes. These residues are a source of bioactive
compounds (protein, dietary fiber, antioxidants) with beneficial properties for health, that can be used
in foods, cosmetics, textile, and pharmaceutical industries. They can also serve as substrates for the
production of enzymes, antibiotics, biosurfactants, and mushrooms. Other applications are in animal
feedstuff and for composites, bio-fuel, and films production. This review discusses the importance of
oilseed and possible valorization methods for the residues obtained in the oil industry.
1. Introduction
In recent decades, due to the current planet issues (e.g., over-exploitation and mismanagement
of resources, the unsustainable consumption behaviors from consumers, the degradation of the
environment and equilibrium of the ecosystems, climate change), it is necessary to transition to a
circular economy model based on the development of new strategies for making the best use of our
resources and for the elimination of the concept of wastes along the supply chain. In this model,
materials are recycled (a process in which wastes are transformed into value-added products by making
them input elements for other products) and re-circulated during processing to create the concept
“waste = food” [1–3].
Any substance or object already disposed or intended to be discarded by holders is called waste.
Food wastes are edible materials (lost, discarded, or consumed by pest) collected from the food industry
in all phases, from primary agriculture up to production, processing, and direct consumption in the
households. The Food Agriculture Organization declared that annually one third of the total food
production became lost, about 1,3 billion tons (20% in oilseeds, meat and dairies, 30% in cereals, 35% in
fish and, 40–50% in fruit and vegetables). During the supply chain, a quantity of 54% of the total
waste results from cultivation and post-harvest and 46% from processing, distribution, and utilization.
Administration of these residues/wastes/by-products could be problematic due to the high disposal
costs in landfills and the creation of serious environment problems [4,5]. A solution for reducing food
wastes is extracting the maximum value from wastes and by-products. The last ones contain high
amounts of bioactive compounds (carbohydrates, lipids, organic acids, proteins, vitamins, minerals,
and antioxidants) with numerous health benefits (anti-tumoral, viral, bacterial, and mutagenic abilities)
that can be isolated and employed in foods, pharmaceutics, cosmetics, and textiles. Achieving this can
be a challenge, but at the same time could add more value to food, reducing disposal costs and risks
caused by residues [6]. Other alternatives, after the extraction are: conversion in energy, introduction
in human food, livestock and fish feedstuff, production of fertilizers and compost (generated from the
aerobic decomposition of organic matter by microorganisms and insects) [1].
This paper provides a critical review ofthe existing literature about the possible ways to re-utilized
the by-products obtained from the oil industry.
After the extraction of oil from seeds, the principal by-product obtained is oil cake/meal.
Oilcakes/meals are classified into two categories—edible and non-edible. Edible oil cake (soybean,
groundnut, rapeseed, sunflower, coconut, cottonseed, safflower, flaxseed) have a high nutritional value
and can be used in animal and human consumption as processed ingredients (protein concentrate,
isolate, hydrolysate), a substrate (in the production of bioactive compounds, surfactants, enzymes,
antibiotics, vitamins, pigments, flavors, and amino acids) and source of antioxidants. The defatted
edible cakes can be used in the diet of undernourished people by incorporating them in bakery,
infant products, and multipurpose supplements. Non-edible oilseed cake/meal (castor, neem, mauha,
karanja and linseed) are used as manure due to the presence of toxic compounds [22].
According to the U.S. Department of Agriculture (USDA), the world production of oilseeds
in 2018/2019 was 600.47 million metric tons, hence a large amount of press cakes and residues are
available. The use of these by-products and residues from the oil industries is a sustainable alternative
to reduce waste disposal and also contributes to the development at low cost, of new products rich in
nutrients [17].
Oilcakes/meals composition depends on variety, extraction method, and growing condition.
Taste and smell are characteristics to the initial raw materials without musty, mold, pro-rancid,
and foreign smells. Walnut oilcakes are yellow to light brown, and sweetish. The color of pumpkin
seeds oilcake is brown to brownish green with an insipid and a sweetish flavor. Sesame oilcake color
varies from cream to light brown and has sweetish, insipid taste. Oilcake from flaxseeds have different
shades of brown with a neutral and insipid taste [24].
As shown in Table 1, the highest content in proteins was found in groundnut cake then soybean,
almond, chia, rapeseed, sunflower, cottonseed, pumpkin, hemp, safflower, sesame, coconut, flaxseed,
and olive oilcakes. The oil content in sunflower and rapeseed is over 40%, 15–25% in soybean and
cotton, another major source is peanut (56%) [18].
Despite the fact that oilcakes are low-processed materials they are safe. Improper storage
and handling can cause rancidity (unpleasant taste and smell). During four months of storage,
Tarek-Tilistyak et al. [25] observed that the water activity remains stable inhibiting bacterial and mold
growth. The macronutrients decrease after one month and the lowest level of contamination was
detected in walnut and the highest in linseed. Further, study investigated the influence of different
packaging. More precisely, if flaxseed oilcake is packed either in paper or polypropylene and stored for
six months at room temperature it can maintain the healthy properties, nutrients, and nutraceuticals
contents typical of the raw material. Cakes stored either in paper or plastic show similar behavior—a
modest decrease of antioxidant activity, optimal omega-6/omega-3 ratio, increase in α-tocopherol
(possible from the conversion of the γ-form), decrease in crude fat (48% in paper and 51% in plastic)
and proteins (12% and 6% respectively). It was concluded that this method of preservation was
efficient and it is preferable the use of paper because is more eco-friendly [26]. It was demonstrated
that peanut oilcake, stored twelve months in vacuum packaging with low permeability, regardless of
the temperature retained its quality (good water/oil absorption and high content of unsaturated fatty
acids), antioxidant capacity, and low microorganism yeast (due to the oxygen restriction that delays
their growth and lipid oxidation) [27].
Appl. Sci. 2020, 10, 7432 4 of 30
Type Moisture % Dry Matter % Crude Protein % Crude Lipid % Ash % Crude Fiber % Carbohydrates % Reference
RAPESEED
SEC 1 3.96–10.59 88–96.04 16–45 1.1–10 6.1–15.8 8.2–17.5 21.38–47.72 [11,28–36]
CPC 2 6–10.8 86.3–94.3 14.03–40.1 5.14–23.1 5–19.7 5.5–15.46 25.1–48 [17,20,24,32,34,37–47]
HPC 3 4.7–10.1 89.9–95.3 36.1–39.1 9.2–12.2 6.9–7.1 13.1 31.5 [20,48]
M4 5.8–12 88–94.5 33.9–40.6 1.7–23 7–13.9 11–14 35.5–44 [17,40–42,49]
CANOLA
SEC 7.3–12.09 87.91–92.7 34.5–40 2.46–19.34 4.19–6.34 12.05–20.11 8.35–17 [50,51]
CPC 9.07–10 90–90.93 33.9–37.75 17.96 4.50–6.2 9.7–11.63 19.08 [52,53]
M 2.86 97.14 55.47 3.08 5.56 12.05 20.98 [53]
CHIA
SEC 10.47 89.53 41.36 0.21 7.24 27.57 23.62 [54]
CPC 6.8–10.84 89.16–93.2 28.2–35 6.52–11.39 4.58–6.27 23.81–30.46 23.53–30.24 [54,55]
SESAME
SEC 4–10 90–96 22.65–48.5 1.07–29.94 5.27–13 4–10.36 25.5–34 [21,28,56–60]
CPC 1.17– 16.8 83.2–98.83 16.96–45.9 5.10–48 3.80–12.4 3.28–22,7 22.5–46.96 [24,58,60–70]
HPC 5.05–9.3 90.7–94.95 39.1–47.1 3–13.31 3.41–10.35 3.48–9.97 20.08–42.85 [58,71]
M 0.25–10.38 89.62–99.75 30.3–59 0.40–5 6.9–11.87 3–29.37 39.9–55.4 [12,72–75]
COCONUT
SEC 5.75–9.9 90.10–94.25 17.8–19.95 3.22–9.4 2.024.9 10.3 47.7 [21,76]
CPC 6.52–11.2 88.8–93.48 17.40–25.2 15.02–15.3 4.13–8.34 10.8 53.94 [52,77–79]
OLIVE
SEC N.a 5 N.a 0.3–10.6 4 3.4–9.1 N.a N.a [80]
CPC 14.8 85.2 0.4–4.77 8.72–11.1 4.1–6.6 40–60.1 10.1–20.6 [80–82]
WALNUT
SEC 10.59 89.41 13–38.87 2,45–10 7.48 5–33 12.65 [24,25,55,83–88]
CPC 3.6–10.,5 91.8–96.4 10.30–50.4 7.95–36.80 2.79–10 6.79–18.5 17.4–49.75 [84,89]
ALMOND
CPC 5.80 94.2 51.3 19 5.30 5.6 18.80 [55]
Appl. Sci. 2020, 10, 7432 5 of 30
Table 1. Cont.
Type Moisture % Dry Matter % Crude Protein % Crude Lipid % Ash % Crude Fiber % Carbohydrates % Reference
SAFFLOWER
CPC 6.8 93.2 23.25 9.14 5.10 34.41 55.71 [55]
SOYBEAN
SEC 88.7 11.3 46–52.4 0.55–8 2–6.96 4.4–75.44 42.8–47.05 [59,90,91]
CPC 8.4–9.66 90.34–91.6 43.3–45.5 9.3–15.55 5.71–5.91 4.95–11.28 14.98–21.76 [44,92,93]
HPC 89.9 10.1 39.1 9.2 6.9 N.a. N.a [48]
M 12 88–95.79 44–49 0.5–0.65 4.21–7.5 3.5–7 35.85–47.79 [70,94]
GROUNDNUT
CPC 8.22–4.57 91.78–95.43 41.73–60 7–22.59 1.5–5.76 4.33–8.55 14.1–36.6 [55,67,95,96]
SUNFLOWER
SEC 2.56–10 90–97.44 31.9–43.38 1–23.6 6.4–7.83 13.07–28.85 25.99 [25,90,97,98]
CPC 2.5–11 89–97.5 19.93–44.9 7–16.6 4.69–8 17.4–33.4 15–28.2 [44,77,95,96,99–101]
FLAXSEED
[24–26,44,47,52,68,76,
CPC 6.89–9.27 90.73–93.1 14.4–41.97 6.11–21.4 4.7–6.27 6.29–12.9 16.26–52.45
102–105]
HPC 2.65–6.14 93.86–97.35 28.13–59.62 1.85–2.10 5.26–9.40 9.35–34.77 21.27–25.6 [53,105]
M 5.75–9.37 90.63–94.25 19.95–34.13 1.87–3.22 2.02–5.72 9.38 48.9 [103]
PUMPKIN
CPC 5–8.2 91.8–96.5 29.39–53.98 5.92–36.22 4.20–8.7 3.89–7.1 15.88–19.73 [24,47,55,77,92,106]
M 8.01 91.99 60.94 0.94 9.93 N.a. 28.19 [107]
HEMP
CPC 6.35–13.61 86.39–93.65 23.25–33.45 0.51–14.02 3.30–9.78 17.41–60.38 2.80–48.54 [47,53,55,99,106,108]
HPC 2.15 97.85 52.48 1.54 6.52 18 19.31 [52]
M 9.37 90.63 32.07 0.97 9.65 N.a. 57.31 [107]
COTTONSEED
CPC N.a N.a 24.79 8.91 6.2 7 32.2 [96]
1 2 3 4 5
SEC-solvent extracted cake; CPC- cold-pressed cake; HPC- expeller cake, M-meal; N.a- not analyzed
Appl. Sci. 2020, 10, 7432 6 of 30
4. Anti-Nutritional Factors
Anti-nutritional factors are substates of natural or synthetic origin, found in the human diet or
animal feed, which can affect the health, and growth performance of livestock. These factors can have
different effects on animals depending on their digestive process, for example, trypsin inhibitors have
a negative effect on monogastric animals, but not in ruminants because it is degraded [109]. The direct
utilization of oilseed cakes in human or animal nutrition is limited by the presence of antinutrients,
which influences the organoleptic properties, protein digestibility, and macro-/micro-elements
bioavailability [22]. The major antinutrient in oil cakes are presented in Table 2.
Canola meal contains phenolics, phytic acid, and glucosinolates, that can cause problems in food.
The main antinutritional factor (30 times higher compared to soybean) are the phenolics acid esters,
especially sinapine. This binds to protein and creates a complex that confers dark color, bitter taste,
and through oxidation, poor digestibility. Regarding glucosinolates, it was demonstrated to have a
positive effect on health in low proportion [110]. When seeds are crushed, enzymes such as myrosinase
are liberated, which are responsible for the hydrolyzation of glucosinolates in glucose and various
toxic chemicals (isothiocyanate or thiocyanate ions) [10].
Cyanogenic glycosides are the major antinutrient in flaxseed cake. In the gastrointestinal tract,
during digestion they form hydrogen cyanide, causing below 50 mg/Kg acute toxicity in adults.
Linatine, another antinutritional factor can cause pyridoxine (B6 ) deficiency [111].
The majority of oilcakes (rapeseed/canola, sesame, sunflower, soybean, groundnut, hempseed)
contain antinutrients such as phytic acid and trypsin inhibitors, which can diminish protein and
vitamin utilization. More precisely the second one (trypsin inhibitors) connects to the digestive enzyme
trypsin, thus reducing proteins adsorption and digestion. [112].
Saponins are a group of steroidal glycosides (natural foam producers) that cause hemolysis and
interference in bile acids, lipid-soluble vitamins, cholesterol, and dietary lipids [111].
Phytic acid can bind with minerals, proteins and amino acids forming phytates and insoluble
complexes, thus reducing essential nutrient bioavailability, and digestibility. They can also lower the
minerals availability and amylase activity [67].
The elimination or inactivation of these toxic substances can be achieved by various methods:
physical (dehulling, heat-cooking, autoclaving, toasting), chemical (ammoniation, the addition of
choline, methionine, ferrous sulphate, sodium carbonate), enzymatic and fermentative.
Appl. Sci. 2020, 10, 7432 7 of 30
Heat treatment can remove or reduce effectively cyanogenic glycosides, proteases, trypsin inhibitors,
glucosinolates, and phytic acid (the last one was reduced by 43%). The extraction of protein isolates is
another method useful to eliminating the anti-nutritive factors, due to the high pH used [109,111].
Extrusion, solvent extraction and biological, thermal, or microwave treatment are various methods
used to reduce or remove cyanogenic glycosides. The heat hydrolyzed the latter in hydrogen cyanide,
which is then evaporated [114].
Phytates and tannin levels in sesame oil cake can be reduced by fermentation with Lactobacillus
acidophilus, after which it can be used as feed in the diets of Labeo rohita [67]. Tannins from groundnut
oil cake can be removed through solid-state fermentation (SSF) with the help of Pichia kudriavzevii,
a process that also enhances its chemical properties [115]. The same process with Rhizopus oligosporus
DSM 1964 and ATCC 64063 was performed for flaxseed press-cake to reduce phytate by 48% and 33%
respectively, and which enhances the bioavailability of calcium, magnesium, and phosphor by 14%,
3.3% and 4% [116].
Methods for glucosinolates removal in canola are: extraction of protein based on protein micellar
mass formation with minimal loss of proteins (ultrafiltration because the toxic compounds have
low molecular weight than proteins), heat treatment (reduction of 94% and improved flavor and
palatability), use of enzyme (pectinase, protease, hemicellulase), application of organic solvent (ethanol,
methanol, and acetone). During the traditional extraction of proteins, the amount can be reduced due
to the dilution process during washing [22,110].
5. Possible Ways to Capitalize the by-Products Obtained from the Oil Industry
The most conventional practices of disposal/capitalizing oil cakes are: animal feed, landfilling,
and biofuel conversion. They can be used as animal feed due to the rich content in protein (suitable
for omnivore), cellulose, and hemicellulose (suitable for ruminants). Unfortunately, the presence
of toxic compounds (with antinutritive effects and unbalanced nutrients) can affect both animals
and humans. In landfilling, the decomposition of wastes leads to the production of methane and to
water pollution. For these reasons, governments are trying to reduce landfilling through regulations
(that impose the following measures: landfill prohibition, taxes, development of alternative solutions,
and development of infrastructures), and public awareness. Food wastes contain organic compounds
that can be converted first in energy through incineration. Increasing concerns about the high cost and
negative impact on the environment due to the emissions [4,5].
The creation of a sustainable food chain and the increasing environmental issues lead to new
valorization methods that imply the recovering/recapturing of valuable components, production of
functional ingredients, development of new products and biopolymer films [4].
The main drawbacks are high-energy consumption when using microwaves, separation issues in
ultrasonic extraction, and lack of user-friendliness in the pulsed electric field. Traditional methods
require long time extraction and large quantities of expensive, toxic, and hazardous solvents but
respect of the novel ones have better efficiency reproducibility, efficiency, and extract manipulation.
The final step implies purification with alcohol precipitation, ultrafiltration, or chromatographic
technique [118–120].
From oil press-cakes and meals can be extracted high-value components such as proteins,
antioxidants, phytochemicals, and dietary fiber [118].
with biological activity and a positive impact on human health (antioxidant, antithrombotic,
hypercholesterolemic, bile acid binding and immunomodulatory activities). These changes depend on
the type of enzyme used and the degree of hydrolysis. Peptides with antihypertensive and antioxidant
activity and high digestibility are developed by subjecting the sesame oilcake/meal hydrolysate to an
additional process of hydrolysis with alcalase, papain, and pepsin [22,124]. Protein hydrolysates from
canola can be used in enhancing cooking yield, water holding capacity, and organoleptic attributes
in meat formulation. Furthermore, enzymatic hydrolysates can be used for the formulation of a
flavor with meat characteristics [125]. Rapeseed bioactive peptides in concentrations between 30 and
50 mg/L inhibit thrombosis activity up to 90%. They also have antioxidant properties (malondialdehyde
inhibition by 50% in blood serum, inhibition of lipid peroxidation), blood pressure regulation capacity
(a peptide called rapakinin induced vasorelaxation), and bile acid-binding capacity. Peanut peptide
instead has high antithrombotic activities [125–127].
Kavitha. et al. [128] use sesame seed cake for the production of vegetable peptones. On a
media containing protein hydrolysates, yeast extract, sodium chloride, and agar were carried out
morphological and growth analysis of different organisms (Candida albicans, Bacillus subtilis, Escherichia
coli, and Saccharomyces cerevisiae). On the vegetal peptone, both prokaryotes and eukaryotes present
higher microbial growth and thus can act as a replacement for those of animal origin. Some advantages
were observed: vegetal peptone can be used for the production of amylase and the yeast produced has
a short fermentation time.
Protein concentrates from rapeseed have poor gelation ability than soybean that can be improved
by glutaminase enzyme [129]. Results also showed that presents darker color, lower purity, and yield
(due to the wide range of isoelectric points) [130]. Sensory evaluation of sausages, formulated with
canola protein concentrate in place of casein demonstrated that improves taste, texture, and aroma [125].
Sesame protein concentrate introduced in the proportion of 10% in extruded snacks lower the
carbohydrate content and enhance organoleptic properties, color, and protein content [131].
5.1.2. Antioxidants
Oil cakes/meals contains free, esterified or condensed form of phenolic acids, flavonoids and
lignans that help in reducing oxidative stress and thus preventing various types of cancer. They can be
extracted with solvent (it can be used organic solvents, alone or mixed together or non-toxic solvents
such as water, but these need to be combined with other mild extraction techniques), high pressure,
microwave, and supercritical fluid. Antioxidants extracted in this way can be used in the preparation
of foods (beverages, energy bars, bakery, and extruded products) [22,118]. The major antioxidants in
oil cakes are presented in Table 3. The antioxidative activity in soybean cake/meal is due to isoflavones
and cinnamic acid derivative and for groundnut cake/meal, phenolics, caffeic, and chlorogenic
acids. Phenolic compounds are the principal antioxidants in rapeseed, coconut, sunflower, mustard,
sesame and cotton cakes/meals [22].
Fermentation helps to improve the nutrient levels of oil cake, because during the process a
microbial synthesis of biomolecules takes place. Following this idea, Stodolak et al. [132] observed
that in flaxseed oil cake fermented for 48 h with Rhizopus oligosporus DSM 1964 and/or ATTC
6403 there was an increase of 13–85% in phenolic levels and a decrease in scavenging activity by
20–30%. The same results were obtained when peanut oil cake was fermented for 120 h with
Aspergillus awamori [133]. Another treatment useful in enhancing antioxidant capacity involves
the use of ultrasound. Maximum polyphenol content was obtained when the treatment time was
20 min and with the temperature at 70 ◦ C. The high heat is able to break the bonding between the
phenolic compounds and matrix, modifying the structure of plant membranes and causing lipoproteins
coagulation. Furthermore, prolongation of exposure means that the ultrasonic wave divided the
phenolic extract in longer periods [134].
Cold-pressed cake from walnut is a source of natural antioxidants. Bakkalbas, i [135] extracted
phenolic compound from walnut pressed cake. This extract was added in different concentrations
Appl. Sci. 2020, 10, 7432 10 of 30
(50, 100, and 200 mg/kg) to increase the oxidative stability of walnut oil. The highest result was obtained
with the addition of 200 mg/Kg. When oilcake is added directly to oil (1:100) through ultrasonic
maceration the oxidative stability decreases although the amount of total phenolic compounds increased.
This may be caused by free fatty acids (created in sonification) with a pro-oxidative effect.
The cake obtained from sesame oil contained bioactive compounds such as phytochemicals
with numerous benefits (phenolic compounds, flavonoids, tocopherols, vitamins, pigments, steroids,
carotenoids, and lignans) for health. Lignans such sesamin, sesamolin, sesamol, and sesaminol
glucosides have the following effect: anticarcinogenic, antiproliferative, antioxidant, antimicrobial,
anti-inflammatory, antidepressant, neuroprotective, and hypocholesterolemic activities [136].
Sesame meal introduced in concentrations ranging from 5 to 200 ppm acts as a stabilizer for
sunflower and soybean oil, by inhibiting double bond conjugation, thermal deterioration, and
losses of polyunsaturated fatty acids. Furthermore, in high concentrations, the efficiency is equivalent
to butylated hydroxy anisole and butylated hydroxy toluene. Products were introduced to an oven
temperature of 70 ◦ C for 72 h and subjected to oxidation in the dark, and a protective effect was
observed during the initial and final steps. This activity is attributed to the phenolic compounds
and their redox properties (extinguish singlet and triplet oxygen, decompose peroxides, adsorb,
and neutralize free radicals) [61,137]. Reshma [74] analyzed the potential of using defatted sesame cake
to inhibit two digestive enzymes (α-amylase, α-glucosidase). The result exhibits a strong inhibitory
potential for α-amylase and mild for α-glucosidase, due to the presence of phenolic compounds and
flavonoids. These modulate the enzymatic decomposition of carbohydrates by inhibiting glucosidases
and amylases.
Natural phenolic antioxidants (flavonoids, phenolic acids) from sesame and coconut oilcake and
synthetic butylated hydroxytoluene (BHT) were introduced in vanilla cake composition to compare their
potential in improve the oxidative stability and both microbial and chemical shelf-life, without changing
consumer acceptability. Both oilcakes improved chemical and microbiological stability up to 13 days,
and only up to 11 days for BHT. The sensory quality in cakes with by-products from the oil industry
was retained from the first day to day 12. Moreover, the activity of natural antioxidants is stable
thermally [137].
Sesame oilseed cake extract (lignans) at a lower amount (150 ppm) can be used as a food additive
with a role in oil stability improvement. In butter, it can reduce the lipid oxidation time much better
than BHT without changing the sensory properties [57,136].
5.2.1. Enzymes
Various enzymes have an important role in industrial application. They can be produced
by solid-state fermentation using oil cakes/ meals as substrate, because they are cheap materials
(reduce the cost production) rich in nutrients, carbon and nitrogen and are compatible for fungal
Appl. Sci. 2020, 10, 7432 12 of 30
species. Some examples are tannase, inulinase, α-amylase, glucoamylase, protease, phytase, mannase,
lipase and L-glutaminase (Table 4). Their production depends on incubation time and pH, moisture and
particle sizes of substrate. Large particles and too much content in water prevent the digestion of raw
material and microbial respiration which leads to poor growth and enzyme production [148].
Proteases are a group of enzymes with a role in the protein hydrolysis. Bacterial and fungal
species such as Bacillus horikoshii, Bacillus clausi I52, Penicillium sp., Candida utilis, Bacillus sp. 1-312,
Aspergillus oryzae (NCIM No.649, NRRL 1808), Streptomyces termovulgaris were used for protease
production with soybean (overheated), coconut, olive, palm, sesame and rapeseed oilcakes/meals
as substrates [81,148]. Gupta et al. [149] studied the ability of non-edible Mahua and Jastropha
cake to act as substrates for Aspergillus niger and Paecilomyces variotii growth and produce enzyme.
The study concluded that despite the low protease activities, solid-state fermentation is suitable in
antinutrient removal.
Lipases are hydrolytic enzymes with numerous applications in the pharmaceutical and cosmetic
industries and in dairy and bakery foods. Parihar et al. [147], Oliveira et al. [50] optimized the
production of lipase through SSF with Pseudomonas aeruginosa and Aspergillus ibericus. The highest
production was obtained when the substrate used resulted by combining two oilcakes: linseed/ olive
and sesame/ palm kernel. The obtained enzyme can be used in esterification (butyl decanoate formation
using 5% biocatalyst) and hydrolysis reactions (increase production in shorth-chain triacylglycerols).
Lipase extracted from Rhizomucos pusillus, Rhizopus rhizopodiformis and Pseudomonas sp. S1 cultivated on
olive oil cake, are suitable for oily waste water treatment and biodiesel production [150]. The enzyme
could be extracted also from Penicillium simplicissimum, Candida rugosa, Penicillium Chrysogenum S1 ,
and Candida utilis inoculated on soybean, coconut, sesame and olive oilcakes [81,147,151].
L-asparaginase is an enzyme that can be used as a drug, due to its therapeutic effect against
leukemia. A content of 90.025 IU, 310 U/gds and 5.75 U/gds was obtained in solid SSF from Aspergillus
wentii NCIM 941, Aspergillus niger C4 and Serratia marcescens, cultivated respectively on palm, sesame oil
and coconut cake [63,152,153].
α-amylase used in starch liquefaction was produced from Aspergillus oryzae, Aspergillus terreus
UF39 cultivated on two oilcakes: coconut and groundnut [79,147].
Phytase, and glucoamylase have been produced using bacterial and fungal species such as
Bacillus licheniformis, Aspergillus ficuum, and Thermomucor indicae-seudaticae respectively growing on
sunflower, rape/canola, and cotton oilcakes as substrates in solid state fermentation [10].
Xylanase, xylosidase, acetyl-xylan esterase and cellulase were produced in a SSF process with
rapeseed/canola oilcake as the substrate, on which microorganisms such as Trichoderma reesei and
Streptomyces termovulgaris were grown. Alternately, Aspergillus oryzae produced protease, phytase and
phosphatase [10,89].
L-glutaminase and phytase were produced using sesame oilcake as substrate and microorganisms
such as Zygosaccharomyces rouxii, Mucor racemosus and Rhizopus oryzae [151].
Use of coconut oilcake as a nutrient source grew a bacterial strain of Staphlococcus sp. and
fungal species such as Aspergillus ficuum, Mucor racemosus, Rhizopus oryzae, Rhizopus oligosporus and
Aspergillus niger to produce inulase, phytase, and glucoamylase [22,82,147].
Lomascolo, et al. [10] reported the production (through submerged culture medium and SSF)
of alpha-amylase and endoxylanase when using sunflower meal. The first one is obtained from
Bacillus licheniformis and the second one from Humicola lanuginose.
Appl. Sci. 2020, 10, 7432 13 of 30
Table 4. Production of enzymes through solid state fermentation using as substrates oil cakes.
5.2.2. Mushrooms
A possible valorization of agro-industrial by-products is in mushroom cultivation.
Mushrooms with good antioxidant properties were produced by SSF, using oil cakes as substrate.
Moreover, some nutrients may transfer during the growth making them, food with therapeutic
properties and high nutritional value. For example, Lentinula edodes, Ganoderma lucidum,
and Grifola frondosa are hepatoprotective, antidiabetic, anticholesterolemic, and immunologic [154,155].
Krupodorova, et al. [156] investigate the possibility of using alternative and cheap substrates
(wastes from the oil industry) for mycelial growth of 29 mushroom species. Oilcakes studied were
those obtained from walnut and soybean, rape, sunflower, linseed, pumpkin, and mustard seeds.
Soybean and walnut oilcakes were found respectively most and least suitable for mushroom growth
(24 and 2 species respectively out of 29). Low results were found also for mustard and pumpkin
(6 and 8 species). These may be due to the composition (small amount of proteins and high amount
in lipids; deficiencies in essential nutrients) and pH of the substrate. The replacement of peptone
with sunflower cake led to the growth of 12 out of 29 species of mushroom, more precisely to
Ganoderma lucidum and Laetiporus sulphureus species. Linseed/flaxseed cake supported 13 species of
mushroom growth including the Pleurotus species, results that was observed also by Jape, et al. [157].
Gregori and Pohleven [154] tested how different proportions of olive oil cake influence the
production of Ganoderma lucidum, Lentinula edodes, and Grifola frondosa. The mushroom production
decreased with the increase in proportion, they also change in color and deformed (content >40%).
The same negative effect was observed with Pleurotus ostreatus, Pleurotus eryngii, Pleurotus pulmonarius,
Appl. Sci. 2020, 10, 7432 14 of 30
Pleurotus cystidiosus and Agrocybe cylindracea species (content >60%). This was probably due to
the presence of polyphenolic compounds and low porosity, substrate aeration, and water retention
capacity [158,159].
5.2.3. Antibiotics
Antibiotics are defined as substances produced by microorganisms with the ability at low
concentration to inhibit/kill other microorganisms. Oilseeds cakes can be used as a substrate for various
antimicrobial agents and antibiotics production, doing so also reduces the cost [22,160].
Sunflower, soybean, and sesame meal were used for the production of clavulanic acid and
cephamycin C and by SSF with Bacillus licheniformis for endotoxin and bacitracin. The maximum
synthesis of the latter was found in soybean meal [22,160–162].
Neomycin is a low toxic antibiotic used in tuberculosis, wound injury, and skin diseases. It was
extracted by SSF process from Streptomyces fradiae NCIM 2418, grown on coconut cake [163].
Rifamycin is a broad-spectrum antibiotic with the ability to inhibit RNA- dependent DNA
polymerase, commercial fermentation process with industrial strain generates only rifamycin B
(modest activity) that can be chemically converted to rifamycin SV (a direct derivate product of
rifamycin, it is also more efficient). The latter was isolated in SSF from Amycolatopsis mediterranei
OVA5-E7. The maximum production was observed on the de-oiled cotton cake, followed by mustard,
sunflower, groundnut, coconut, and sesame de-oiled cake [164]. Vastrad, et al. [163,165] also extracted
rifamycin B (it is very powerful, easily biodegradable, and less toxic) from Nocardia mediterranei
MTCC14 growth on sunflower oil cake and Amycolatopsis mediterranei MTCC14 growth on coconut and
groundnut cake.
Sunflower meal can act as a substrate in the production of two antibiotics. Clavulanic acid
with broad-spectrum antibacterial activity and potent β-lactamases inhibitor could be obtained in a
solid-state fermentation process by Streptomyces clavuligerus. Cephamycin C was successfully achieved
in both submerged culture medium and solid-state fermentation (SSF), the meal served also as pH
regulator and foam controller [10]. From Bacillus subtilis grown by SSF with rapeseed meal, 5.3 g/Kg of
iturin A, and 51.3 g/Kg of poly-γ-glutamic acid were obtained in about 90 h of fermentation [166].
5.2.4. Biosurfactants
Surfactants are amphiphatic molecules (derivate from petroleum compounds) composed of a
hydrophilic and hydrophobic group that decrease interfacial and surface tension with water/hydrophobic
systems. When synthesized by different microorganisms they are called biosurfactants with numerous
advantages over the synthetic ones: low toxicity and good biodegradability, biocompatibility,
chemical diversity, and stability. Based on chemical composition they are divided into glycolipids,
lipopeptides, lipopolysaccharides, and oligosaccharides. Examples include rhamnolipids, trehalolipids,
sophorolipids, mannosylerythritol lipids. Due to these properties they can be used in the environmental
sector (bioremediation of pesticides, oil, and heavy metals, enhanced oil recovery, antimicrobial agents
and biopesticides), petrochemicals, cosmetics, food, agriculture, and pharmaceutics [167–169].
Sophorolipids, microbial biosurfactants used in detergents and cosmetics formulation,
were synthesized by Starmerella bombicola growth on residual sunflower cake through SSF.
Their effectiveness is equivalent to Triton X-100, that is a considerate environmental pollutant [170].
Thavasi et al. [171] cultivated Lactobacillus delbrueckii and Pseudomonas aeruginosa on peanut oil cake
for the production of biosurfactants (glycolipids and lipopeptides) with potential use in biodegradation
of crude oil and in bioremediation of hydrocarbon pollution environments. Another example of
biosurfactant (rhamnolipid) utilized for this purpose was synthesized from Ochrobactrum anthropi
cultivated on palm oil decanter cake [168,172].
In the pharmaceutical and food industries surfactants from Enterobacter sp. MS16 cultivated
on sunflower oil cake can be utilized as fungal inhibitor [95]. Antibacterial and antifungal activities
were shown by lipopeptide from Brevibacterium aureum MSA13 cultivated on olive/safflower oilcake.
Appl. Sci. 2020, 10, 7432 15 of 30
Glycolipids obtained from Lactobacillus delbrueckii on peanut cake also has good foaming and emulsion
capacity and for this reason, can be used in emulsion food [22].
Lipopeptides are biosurfactants isolated from Bacillus pseudomycoides OR1 cultivated on groundnut
oilcake and can be used for their antibacterial activity against foodborne, pathogens. At 50 µg/mL they
inhibit Escherichia coli, Staphylococcus aureus and Klebsiella pneumoniae. They bind to the bacterial surface,
modifying the lipid organization by changing fatty acids and thus preventing cellular processes [173].
In adult male goats, the incorporation in a concentrate mixture of walnut oilcake up to 10%
did not have negative effects on the calcium and phosphorus balance, however the high amount in
aminotransferase may cause hepatotoxic problems [180]. Similar results were concluded by Mir [86],
furthermore the level of oilcake (<10%) did not affect total gas production, efficiency biomass production,
in vitro digestibility of dry matter, microbial biomass production and true degradable organic matter.
Chipa et al. [181] evaluated the possibility of incorporation soybean press-cake, in proportions of
0–20%, as a source of proteins in the diets of beef cattle. The experiment was conducted on 20 heifers
and 20 steers for a period of 98 days. At the end of the treatment the steers were heavier that the
heifers, due to the high feed intake and conversion ratio. An increasing in growth was observed in the
diet with 6% and 13%.
5.4.1. Bread
The most consumed product is bread and can act as a vector for bioactive ingredients. For this
purpose, Pycia K., et al. [184] incorporated walnut oil and oilcake (1%, 3%, 5%) as a replacement for
wheat flour. Increasing the level of oilcake enrichment led to harder, smaller (the replacement led to a
decrease and weakening of gluten), darker and chewy bread, but with a high antioxidant potential
compared to the control. Rheological properties of the dough with different ratios (7.5%, 10% and,
12.5%) of flaxseed oil cakes were studied in the Mixolab. As the levels increased the water absorption
capacity increased, but the viscosity, amylolytic activity, and retrogradation decreased. All of these
lead to a rapid dough maturation, thus reducing by 1.5-times the total fermentation duration [185,186].
5.4.2. Biscuits
Sesame oilcake flour was incorporated in five biscuits formulation (0%, 10%, 25%, 50%, and 75%)
as a replacement for wheat flour. Products with white sesame oil cake (up to 50%) did not change
Appl. Sci. 2020, 10, 7432 17 of 30
taste and texture, but at 75% it becomes frail. Texture and taste of the first three biscuits formulation
with black sesame oil cake were good. The last two formulations were produced after taste, but only
the last one became brittle. With the previous incorporation, the diameter and weight loss (so the
microbial contamination is reduced) were reduced, but the thickness, hardness, and fracturability
increased. [71]. The same results were obtained when soybean and groundnut were used, due to the fact
that high protein flours present high water retention and the biscuits cannot develop well. Unlike the
previously analyzed products, these biscuits are considered acceptable at low-level incorporation.
Regarding the rheological properties, the first oilcake increased the water absorption more, and the
mixing characteristics of doughs. With the increasing proportion of the second oilcake (groundnut) the
farinograph bandwidth increased but became slightly irregular. This led to an increase development
of gluten protein and therefore of the dough consistency. The color of the final products become darker
with the addition of the two oilcakes, due to the brownish and yellowish color of the raw materials
used [187].
5.4.3. Snacks
On corn extrudate the addition of cold-pressed cake from sesame (0–20%) caused an imbalance
in the amino acid profile, reduced carbohydrates content and sectional expansion, and increased the
protein, fat and ash contents. Products became more darker but were organoleptically acceptable,
especially those with 20% [62].
Healthy, non-caloric, and high nutritional snacks can be achieved with the incorporation of food
industry by-products rich in antioxidants, essential fatty acids, fiber, and minerals. Cottonseed meal
was incorporated, by Jáquez, et al. [188], in corn extruded snacks at different levels (5–98%) with a 10%
optimum. With the increase in oil meal the consumer acceptance decreases, the surface becomes rougher,
lumpier, and disrupted. The same conclusions and optimum levels were found for rice/corn snacks
when defatted flaxseed meal was incorporated [96]. In accordance with the first two studies related
previously, a proportion of 5% defatted hemp oilcake can be successfully introduced in corn snacks.
The level of acceptance is lower because of the high fiber content [108]. Radočaj, et al. [106] developed
gluten-free snacks/crackers with hemp flour (from cold oilcake) and decaffeinated green tea leaves.
All formulations were qualified as healthy (high minerals, fibers, and a desirable omega-6/omega-3
ratio) and are suitable for people suffering from celiac disease. The highest appreciation was achieved
with the highest addition level.
5.4.4. Desserts
Macaron is a luxury and expensive dessert, and by adding walnut oilcake (0–50%) their quality
can be improved, and at the same time the production cost can be reduced. The improvements refer to
the decrease in carbohydrates, omega-6/omega-3 ratio, and energy which is favorable in the problems
associated with obesity, normal, and under nutrition. The addition strongly influences the amount of
linoleic and caproic acid but not the aroma of macarons. However, the sensory analysis demonstrated
that macarons with an addition of more than 10% were not appreciated, due to the increase in phenolic
and volatile compounds that affect the taste [88]. Walnut oilcake can be introduced, at different levels
0–20%, as a supplement in cake formulations. Increasing the addition, it led to a decrease in firmness,
cakes become softer due to the high-fat content of press-cake. The substitution levels increase the
total phenolic compounds and antioxidant ability but were not enough for increasing the proteins.
Sensory evaluations demonstrated that cakes supplemented with 15% were the most appreciated.
The crust color became lighter due to the addition of the skin portion of walnut [83].
grains on the substrate, the mixtures were incubated for 24 h at 25 ◦ C and then stored at 6 ◦ C for 21 days.
Acid lactic and yeast grew well on flaxseed cake without any supplementation and their viability
exceeded the recommended level for kefir products. With the increase in cake percent, the beverages
had high viscosity (due to the presence of mucilage and protein), firmness (due to the production
of polysaccharide kefiran), and antioxidant activity (due to the production of phenolic compounds
and bioactive peptides). Another advantage is in the economic field; oilcakes are cheap, safe material
available throughout the year [114].
permeability. Films produced at the same pH and temperature 50 ◦ C have total soluble protein and
matter content very high. When films are prepared at high temperature (90 ◦ C) the surface is compact
with nanoholes. At low temperature (50 ◦ C) the holes are elder and this explains the low gas barrier
ability [197].
Films obtained with pumpkin cake are not heat-sealable, so they were laminated with zein.
Bulut et al. [198] analyzed the changes in barrier, mechanical and physicochemical properties in
bilayer films made with pumpkin oil cakes and zein and their pouches during four weeks of storage.
During this time, the film loses in moisture, total soluble matter, and swelling ability. It was observed
also a good barrier for oxygen but moderate for carbon dioxide. The pouches present a high percentage
of oxygen and low in dioxide carbon due to the decrease in heat deal strength and gas transmission rate.
The addition of stabilizers as 30% glycerol and 0.5% xanthan, produced films with good mechanical
properties, poor barrier for water vapor, and very good to oxygen. With the increase in concentrations,
the transmission rate of dioxide carbon also increased. This can be advantageous for maintaining the
quality and shelf-life of foods such as cheese, vegetables, and fruits [199].
The incorporation of different essential oils (caraway, wintery savory, and basil essential oils) in the
biopolymer matrix (chitosan, Tween 20) increased the edible packaging antimicrobial and antioxidant
activity. Chitosan films with caraway are elastic, oil resistance, present low permeability to gases,
effective against Escherichia coli and Staphylococcus aureus, but only with the lowest amount of caraway
the antioxidant activity increases [194]. When increasing the concentration of Tween 20 in films with
winter savory the antioxidant activity also increases, reverse was observed in films with basil [98,200].
The ability of protein isolates to create biopolymer films with different amounts of plasticizer
and pH values was analyzed. At pH 4-8, they could not be synthesized and only moderate amount
of plasticizer produce suitable final products. Besides this, they present excellent oxygen, nitrogen,
dioxide carbon, and gas barrier properties (150–250 better than plastic) [201].
elongation at break, and water permeability. The second one improves coloration and elongation at
break, and decrease tensile strength, water permeability, and total soluble matter [202,203].
Films have antimicrobial properties when are activated with different proportion of thymol.
The latter, inhibit l. plantarum, E. Coli, S. aureus, and P. aeruginosa, at minimum concentration [127].
Comparing to the protein-based films, those create with defatted peanut flour create films, that are
more transparent and excellent water barrier [204].
Edible fiber films are difficult to make because they have poor film-forming properties. To improve
this, Wan [205] performed a dynamic high-pressure micro-fluidization treatment. The final films have
excellent solubility and mechanical properties and can be used for packaging noodles, spices, biscuits,
and candies.
7. Conclusions
This review highlights the potential application of the ample amounts of wastes and by-products
generated during the supply chain, primarily used as energy sources, landfills, and animal feedstuffs.
Moreover, we have described new green methods for their recycling and further reuse in various food
and pharmaceutical industries. This green approach also allows the protection of both the environment
and people.
Oil cake/meal are the by-products obtained after the extraction of oil from seeds. It can be used
in both animal and human diet because contain high amounts of bioactive compounds that can be
isolated and used in foods. These residues can also act as a substrate in the production of low-cost
value-added products such as fuel, surfactants, enzymes, antibiotics, vitamins, natural pigments,
flavors components, and health promoting components, such as dietary fibers, amino acids, flavonoids,
phytochemicals and proteins. All bioactive components recovered from residues can be used as
essential ingredients to produce functional ingredient, achieving thus effective waste utilization and
the successful realization of the zero waste and circular economy concepts
Appl. Sci. 2020, 10, 7432 21 of 30
Waste valorization, in the perception of the circular economy, represents a challenge but at the
same time could allow the reuse of materials into the supply chain as they add more value to foods,
reduce costs, allow economic growth and reduce risks caused by their disposal in the environment.
Author Contributions: P.A. and A.S. contributed equally to the collection of data and preparation of the paper.
All authors have read and agreed to the published version of the manuscript
Funding: This work was supported by a grant of Romanian Ministry of Education and Research, CCCDI-UEFISCDI,
project number PN-III-P2-2.1-PED-2019-3863, within PNCDI III
Conflicts of Interest: The authors declare no conflict of interest
References
1. Borrello, M.; Caracciolo, F.; Lombardi, A.; Pascucci, S.; Cembalo, L. Consumers’ Perspective on Circular
Economy Strategy for Reducing Food Waste. Sustainability 2017, 9, 141. [CrossRef]
2. Pesce, M.; Tamai, I.; Guo, D.; Critto, A.; Brombal, D.; Wang, X.; Cheng, H.; Marcomini, A. Circular Economy
in China: Translating Principles into Practice. Sustainability 2020, 12, 832. [CrossRef]
3. Esposito, B.; Sessa, M.R.; Sica, D.; Malandrino, O. Towards Circular Economy in the Agri-Food Sector.
A Systematic Literature Review. Sustainability 2020, 12, 7401. [CrossRef]
4. Otles, S.; Despoudi, S.; Bucatariu, C.; Kartal, C. Food waste management, valorization, and sustainability in
the food industry. In Food Waste Recovery, 1st ed.; Galanakis, C.M., Ed.; Elsevier Inc.: London, UK, 2015;
pp. 3–23.
5. Mateos-Aparicio, I.; Matias, A. Food industry processing by-products in foods. In The Role of Alternative
and Innovative Food Ingredients and Products in Consumer Wellness, 1st ed.; Galanakis, C., Ed.; Elsevier Inc.:
London, UK, 2019; pp. 239–281.
6. Kumar, S.; Kushwaha, R.; Verma, M.L. Recovery and utilization of bioactives from food processing waste.
In Biotechnological Production of Bioactive Compounds, 1st ed.; Verma, M.L., Chandel, A.K., Eds.; Elsevier:
Amsterdam, The Netherlands, 2020; pp. 37–68.
7. García-Rebollar, P.; Cámara, L.; Lázaro, R.; Dapoza, C.; Pérez-Maldonado, R.; Mateos, G. Influence of the
origin of the beans on the chemical composition and nutritive value of commercial soybean meals. Anim. Feed.
Sci. Technol. 2016, 221, 245–261. [CrossRef]
8. Arrutia, F.; Binner, E.; Williams, P.; Waldron, K.W. Oilseeds beyond oil: Press cakes and meals supplying
global protein requirements. Trends Food Sci. Technol. 2020, 100, 88–102. [CrossRef]
9. Wanasundara, J.; Tan, S.; Alashi, A.; Pudel, F.; Blanchard, C.L. Proteins from Canola/Rapeseed: Current Status.
In Sustainable Protein Sources; Nadathur, S.R., Wanasundara, J.P.D., Scalin, L., Eds.; Elsevier Inc.: London Wall,
UK, 2017; pp. 285–304.
10. Lomascolo, A.; Uzan-Boukhris, E.; Sigoillot, J.-C.; Fine, F. Rapeseed and sunflower meal: A review on
biotechnology status and challenges. Appl. Microbiol. Biotechnol. 2012, 95, 1105–1114. [CrossRef]
11. Ranganayaki, S.; Vidhya, R.; Jaganmohan, R. Isolation and proximate determination of protein using defatted
sesame seed oil cake. Int. J. Nutr. Metab. 2012, 4, 141–145.
12. Krimer-Malešević, V. Pumpkin Seeds: Phenolic Acids in Pumpkin Seed (Curcubita pepo L.). In Nuts and
Seeds in Health and Disease Prevention, 2nd ed.; Preedy, V., Watson, R., Eds.; Elsevier Inc.: London, UK, 2020;
pp. 533–542.
13. Özbek, Z.A.; Ergönül, P.G. Cold pressed pumpkin seed oil. In Cold Pressed Oils, 1st ed.; Ramadan, F.M., Ed.;
Elsevier Inc.: London, UK, 2020; pp. 219–229.
14. Apostol, L.; Berca, L.; Mosoiu, C.; Badea, M.; Bungau, S.; Oprea, O.B.; Cioca, G. Partially Defatted Pumpkin
(Cucurbita maxima) Seeds—A Rich Source of Nutrients for Use in Food Products. Rev. Chim. 2018,
69, 1398–1402. [CrossRef]
15. Eyres, L.; Eyres, M. Flaxseed (linseed) fibre-nutritional and culinary uses—A review. Food N. Z. 2014, 14, 26.
16. Mullen, A.M.; Alvarez, C.; Pojić, M.; Hadnadev, T.D.; Papageorgiou, M. Classification and target compounds.
In Food Waste Recovery: Processing Technologies and Industrial Techniques, 1st ed.; Galanakis, C., Ed.; Elsevier Inc.:
London, UK, 2015; pp. 25–57.
17. Sarwar, F.; Qadri, N.A.; Moghal, S. The role of oilseeds nutrition in human health: A critical review.
J. Cereals Oilseeds 2013, 4, 97–100. [CrossRef]
Appl. Sci. 2020, 10, 7432 22 of 30
18. Savoire, R.; Lanoisellé, J.-L.; Vorobiev, E. Mechanical Continuous Oil Expression from Oilseeds: A Review.
Food Bioprocess Technol. 2012, 6, 1–16. [CrossRef]
19. Ramadan, M.F. Introduction to cold pressed oils: Green technology, bioactive compounds, functionality, and
applications. In Cold Pressed Oils, 1st ed.; Ramadan, F.M., Ed.; Elsevier Inc.: London, UK, 2020; pp. 1–5.
20. Leming, R.; Lember, A. Chemical composition of expeller-extracted and cold-pressed rapeseed cake.
Agraarteadu 2005, 16, 103–109.
21. Sunil, L.; Appaiah, P.; Kumar, P.K.P.; Krishna, A.G.G. Preparation of food supplements from oilseed cakes.
J. Food Sci. Technol. 2014, 52, 2998–3005. [CrossRef] [PubMed]
22. Gupta, A.; Sharma, R.; Sharma, S.; Singh, B. Oilseed as potential functional food Ingredient. In Trends
& Prospects in Food Technology, Processing and Preservation, 1st ed.; Prodyut Kumar, P., Mahawar, M.K.,
Abobatta, W., Panja, P., Eds.; Today and Tomorrow’s Printers and Publishers: New Delhi, India, 2018;
pp. 25–58.
23. Östbring, K.; Malmqvist, E.; Nilsson, K.; Rosenlind, I.; Rayner, M. The Effects of Oil Extraction Methods on
Recovery Yield and Emulsifying Properties of Proteins from Rapeseed Meal and Press Cake. Foods 2019,
9, 19. [CrossRef] [PubMed]
24. Bochkarev, M.S.; Egorova, E.Y.; Reznichenko, I.Y.; Poznyakovskiy, V.M. Reasons for the ways of using oilcakes
in food industry. Foods Raw Mater. 2016, 4, 4–12. [CrossRef]
25. Tarek-Tilistyák, J.; Juhász-Román, M.; Jeko, J.; Mathe, E. Short-term storability of oil seed and walnut
cake—Microbiological aspect. Acta Aliment. 2014, 43, 632–639. [CrossRef]
26. Mannucci, A.; Castagna, A.; Santin, M.; Serra, A.; Mele, M.; Ranieri, A. Quality of flaxseed oil cake under
different storage conditions. LWT 2019, 104, 84–90. [CrossRef]
27. Marchetti, L.; Romero, L.; Andrés, S.C.; Califano, A. Characterization of pecan nut expeller cake and effect of
storage on its microbiological and oxidative quality. Grasas Aceites 2018, 68, 226. [CrossRef]
28. Volli, V.; Singh, R. Production of bio-oil from de-oiled cakes by thermal pyrolysis. Fuel 2012, 96, 579–585. [CrossRef]
29. Rezvani, M.; Kluth, H.; Bulang, M.; Rodehutscord, M. Variation in amino acid digestibility of rapeseed meal
studied in caecectomised laying hens and relationship with chemical constituents. Br. Poult. Sci. 2012,
53, 665–674. [CrossRef]
30. Thanaseelaan, V. Proximate Analysis, Mineral and Amino Acid Profiles of Deoiled Rapeseed Meal. Int. J.
Food Agric. Vet. Sci. 2013, 3, 66–69.
31. Sari, Y.W.; Bruins, M.E.; Sanders, J.P. Enzyme assisted protein extraction from rapeseed, soybean,
and microalgae meals. Ind. Crop. Prod. 2013, 43, 78–83. [CrossRef]
32. Maison, T. Evaluation of the Nutritional Value of Canola Meal, 00-Rapeseed Meal, and 00-Rapeseed Expellers
Fed To Pigs. Ph.D. Thesis, University of Illinois at Urbana-Champaign, Urbana-Champaign, IL, USA, 2013.
33. Thiel, A.; Muffler, K.; Tippkötter, N.; Suck, K.; Sohling, U.; Hruschka, S.M.; Ulber, R. A novel integrated
downstream processing approach to recover sinapic acid, phytic acid and proteins from rapeseed meal.
J. Chem. Technol. Biotechnol. 2015, 90, 1999–2006. [CrossRef]
34. Egorova, T.A.; Lenkova, T.H. Rapseed (Brassica napus L.) and its prospective useage (review). Agric. Biol.
2015, 50, 172–182.
35. Choi, H.B.; Jeong, J.H.; Kim, D.H.; Lee, Y.; Kwon, H.; Kim, Y.Y. Influence of Rapeseed Meal on Growth
Performance, Blood Profiles, Nutrient Digestibility and Economic Benefit of Growing-finishing Pigs.
Asian-Australasian J. Anim. Sci. 2015, 28, 1345–1353. [CrossRef] [PubMed]
36. Tofanica, B.M. Rapeseed—A Valuable Renewable Bioresource. Cellul. Chem. Technol. 2019, 53, 837–849. [CrossRef]
37. Amores, G.; Virto, M.; Nájera, A.I.; Mandaluniz, N.; Arranz, J.; Bustamante, M.Á.; Valdivielso, I.;
De Gordoa, J.R.; Garcia-Rodriguez, A.; Barron, L.J.; et al. Rapeseed and sunflower oilcake as supplements for
dairy sheep: Animal performance and milk fatty acid concentrations. J. Dairy Res. 2014, 81, 410–416. [CrossRef]
38. Jabłoński, S.J.; Biernacki, P.; Steinigeweg, S.; Łukaszewicz, M. Continuous mesophilic anaerobic digestion of
manure and rape oilcake–Experimental and modelling study. Waste Manag. 2015, 35, 105–110. [CrossRef]
39. Shi, C.; He, J.; Yu, J.; Yu, B.; Huang, Z.; Mao, X.; Zheng, P.; Chen, D. Solid state fermentation of rapeseed cake
with Aspergillus niger for degrading glucosinolates and upgrading nutritional value. J. Anim. Sci. Biotechnol.
2015, 6, 1–7. [CrossRef]
40. Kaczmarek, P.; Korniewicz, D.; Lipinski, K.; Mazur, M. Chemical composition of rapeseed products and their
use in pig nutrition. Pol. J. Nat. Sci. 2016, 31, 545–562.
Appl. Sci. 2020, 10, 7432 23 of 30
41. Salazar-Villanea, S.; Bruininx, E.M.; Gruppen, H.; Hendriks, W.H.; Carré, P.; Quinsac, A.; Van Der Poel, A.F.
Physical and chemical changes of rapeseed meal proteins during toasting and their effects on in vitro
digestibility. J. Anim. Sci. Biotechnol. 2016, 7, 1–11. [CrossRef] [PubMed]
42. Mosenthin, R.; Messerschmidt, U.; Sauer, N.; Carré, P.; Quinsac, A.; Schöne, F. Effect of the
desolventizing/toasting process on chemical composition and protein quality of rapeseed meal. J. Anim.
Sci. Biotechnol. 2016, 7, 36. [CrossRef]
43. Rommi, K.; Hakala, T.K.; Holopainen, U.; Nordlund, E.; Poutanen, K.; Lantto, R. Effect of Enzyme-Aided Cell
Wall Disintegration on Protein Extractability from Intact and Dehulled Rapeseed (Brassica rapaL. andBrassica
napusL.) Press Cakes. J. Agric. Food Chem. 2014, 62, 7989–7997. [CrossRef]
44. Tyapkova, O.; Osen, R.; Wagenstaller, M.; Baier, B.; Specht, F.; Zacherl, C. Replacing fishmeal with oilseed
cakes in fish feed—A study on the influence of processing parameters on the extrusion behavior and quality
properties of the feed pellets. J. Food Eng. 2016, 191, 28–36. [CrossRef]
45. Nega, T. Review on Nutritional Limitations and Opportunities of using Rapeseed Meal and other Rape Seed
by—Products in Animal Feeding. J. Nutr. Health Food Eng. 2018, 8, 1. [CrossRef]
46. Martin, A.; Osen, R.; Greiling, A.; Karbstein, H.P.; Emin, A. Effect of rapeseed press cake and peel on the
extruder response and physical pellet quality in extruded fish feed. Aquaculture 2019, 512, 734316. [CrossRef]
47. Cozea, A.; Ionescu, N.; Popescu, M.; Neagu, M.; Gruia, R. Comparative study concerning the composition of
certain oil cakes with phytotherapeutical potential. Rev. Chim. 2016, 67, 422–425.
48. Halmemies-Beauchet-Filleau, A.; Rinne, M.; Lamminen, M.; Mapato, C.; Ampapon, T.; Wanapat, M.;
Vanhatalo, A. Alternative and novel feeds for ruminants: Nutritive value, product quality and environmental
aspects. Animal 2018, 12, s295–s309. [CrossRef]
49. Fetzer, A.; Herfellner, T.; Stäbler, A.; Menner, M.; Eisner, P. Influence of process conditions during aqueous
protein extraction upon yield from pre-pressed and cold-pressed rapeseed press cake. Ind. Crop. Prod. 2018,
112, 236–246. [CrossRef]
50. Oliveira, F.; Souza, C.E.; Peclat, V.R.; Salgado, J.M.; Ribeiro, B.D.; Coelho, M.A.; Venâncio, A.; Belo, I.
Optimization of lipase production by Aspergillus ibericus from oil cakes and its application in esterification
reactions. Food Bioprod. Process. 2017, 102, 268–277. [CrossRef]
51. Tan, S.H.; Mailer, R.J.; Blanchard, C.L.; Agboola, S.O. Extraction and characterization of protein fractions
from Australian canola meals. Food Res. Int. 2011, 44, 1075–1082. [CrossRef]
52. Sadh, P.K.; Duhan, S.; Duhan, J.S. Agro-industrial wastes and their utilization using solid state fermentation:
A review. Bioresour. Bioprocess. 2018, 5, 1. [CrossRef]
53. Teh, S.S.; Bekhit, A.E.; Carne, A.; Birch, J. Effect of the defatting process, acid and alkali extraction on the
physicochemical and functional properties of hemp, flax and canola seed cake protein isolates. J. Food
Meas. Charact. 2013, 8, 92–104. [CrossRef]
54. Capitani, M.; Spotorno, V.; Nolasco, S.; Tomás, M. Physicochemical and functional characterization of
by-products from chia (Salvia hispanica L.) seeds of Argentina. LWT 2012, 45, 94–102. [CrossRef]
55. Montrimaitė, K.; Moščenkova, E. Food Science and Applied Biotechnology. Food Sci. Appl. Biotechnol. 2018,
1, 154–164. [CrossRef]
56. Kenari, R.E.; Mohsenzadeh, F.; Amiri, Z.R. Antioxidant activity and total phenolic compounds of Dezful
sesame cake extracts obtained by classical and ultrasound-assisted extraction methods. Food Sci. Nutr. 2014,
2, 426–435. [CrossRef]
57. Nadeem, M.; Situ, C.; Mahmud, A.; Khalique, A.; Imran, M.; Rahman, F.; Khan, S. Antioxidant Activity of
Sesame (Sesamum indicum L.) Cake Extract for the Stabilization of Olein Based Butter. J. Am. Oil Chem. Soc.
2014, 91, 967–977. [CrossRef]
58. Yasothai, R. Chemical composition of sesame oil cake—Rieview. Int. J. Sci. Environ. Technol. 2014, 3, 827–835.
59. Grasso, S. Extruded snacks from industrial by-products: A review. Trends Food Sci. Technol. 2020,
99, 284–294. [CrossRef]
60. Benítez, R.B.; Bonilla, R.A.O.; Franco, J.M. Comparison of two sesame oil extraction methods: Percolation and
pressed. Biotecnoloía Sect. Agropecu. Agroind. 2016, 14, 10. [CrossRef]
61. Mohdaly, A.A.; Smetanska, I.; Ramadan, M.F.; Sarhan, M.A.; Mahmoud, A.; Ramadan, M.F.
Antioxidant potential of sesame (Sesamum indicum) cake extract in stabilization of sunflower and soybean
oils. Ind. Crop. Prod. 2011, 34, 952–959. [CrossRef]
Appl. Sci. 2020, 10, 7432 24 of 30
62. Carvalho, C.W.; Takeiti, C.Y.; Freitas, D.D.; Ascheri, J.L. Use of sesame oil cake (Sesamum indicum L.) on corn
expanded extrudates. Food Res. Int. 2012, 45, 434–443. [CrossRef]
63. Uppuluri, K.B.; Dasari, R.K.; Sajja, V.; Jacob, A.S.; Reddy, D.S. Optimization of l-Asparaginase Production
by Isolated Aspergillus niger C4 from Sesame (black) Oil Cake under SSF using Box–Behnken Design in
Column Bioreactor. Int. J. Chem. React. Eng. 2013, 11, 103–109. [CrossRef]
64. Saleh, M.; Ghazzawi, H.; Al-Ismail, K.; Akash, M.; Al-Dabbas, M. Sesame-oil-cake (SOC) impacted consumer
liking of a traditional Jordanian dessert; a mixture response surface model approach. Int. Food Res. J. 2016,
23, 2096–2102.
65. Capellini, M.C.; Chiavoloni, L.; Giacomini, V.; Rodrigues, C.E. Alcoholic extraction of sesame seed cake
oil: Influence of the process conditions on the physicochemical characteristics of the oil and defatted meal
proteins. J. Food Eng. 2019, 240, 145–152. [CrossRef]
66. Nagendra Prasad, M.N.; Sanjay, K.R.; Prasad, D.S.; Vijay, N.; Kothari, R.; Nanjunda Swamy, S. A Review on
Nutritional and Nutraceutical Properties of Sesame. J. Nutr. Food Sci. 2012, 2, 1–6. [CrossRef]
67. Das, P.; Ghosh, K. Improvement of nutritive value of sesame oil cake in formulated diets for rohu, Labeo rohita
(Hamilton) after bio-processing through solid state fermentation by a phytase-producing fish gut bacterium.
Int. J. Aquat. Biol. 2015, 3, 89–101.
68. Elsorady, M.E. Characterization and functional properties of proteins isolated from flaxseed cake and sesame
cake. Croat. J. Food Sci. Technol. 2020, 12, 77–83. [CrossRef]
69. Hejazi, A.; Omar, J.M.A. Effect of Feeding Sesame Oil Cake on Performance, Milk and Cheese Quality of
Anglo-Nubian Goats. Hebron Univ. Res. J. 2009, 4, 81–91.
70. Omer, H.A.A.; Ahmed, S.M.; Abdel-Magid, S.S.; Bakry, B.A.; El-Karamany, M.F.; El-Sabaawy, E.H.
Nutritional impact of partial or complete replacement of soybean meal by sesame (Sesamum indicum)
meal in lambs rations. Bull. Natl. Res. Cent. 2019, 43, 98. [CrossRef]
71. Prakash, K.; Naik, S.; Vadivel, D.; Hariprasad, P.; Gandhi, D.; SaravanaDevi, S. Utilization of defatted sesame
cake in enhancing the nutritional and functional characteristics of biscuits. J. Food Process. Preserv. 2018,
42, e13751. [CrossRef]
72. Bigoniya, P.; Nishad, R.; Singh, C.S. Preventive effect of sesame seed cake on hyperglycemia and obesity
against high fructose-diet induced Type 2 diabetes in rats. Food Chem. 2012, 133, 1355–1361. [CrossRef]
73. Shu, Z.; Liu, L.; Geng, P.; Liu, J.; Shen, W.; Tu, M. Sesame cake hydrolysates improved spatial learning and
memory of mice. Food Biosci. 2019, 31, 100440. [CrossRef]
74. Reshma, M.; Namitha, L.; Sundaresan, A.; Kiran, C.R. Total Phenol Content, Antioxidant Activities and
α-Glucosidase Inhibition of Sesame Cake Extracts. J. Food Biochem. 2012, 37, 723–731. [CrossRef]
75. Achouri, A.; Nail, V.; Boye, J.I. Sesame protein isolate: Fractionation, secondary structure and functional
properties. Food Res. Int. 2012, 46, 360–369. [CrossRef]
76. Zheng, Y.; Li, Y. Physicochemical and functional properties of coconut (Cocos nucifera L) cake dietary fibres:
Effects of cellulase hydrolysis, acid treatment and particle size distribution. Food Chem. 2018, 257, 135–142.
[CrossRef] [PubMed]
77. Paweł, S.; Kazimierz, Z.; Starek, A.; Żukiewicz-Sobczak, W.; Sagan, A.; Zdybel, B.; Andrejko, D.
Compaction Process as a Concept of Press-Cake Production from Organic Waste. Sustainability 2020,
12, 1567. [CrossRef]
78. Te, K.G.; Go, A.W.; Wang, H.J.; Guevarra, R.G.; Cabatingan, L.K.; Tabañag, I.D.; Angkawijaya, A.E.; Ju, Y.-H.
Extraction of lipids from post-hydrolysis copra cake with hexane as solvent: Kinetic and equilibrium data.
Renew. Energy 2020, 158, 311–323. [CrossRef]
79. Akhter, P.; Mishra, A.; Mishra, V.; Raghav, A. Alpha amylase production from Aspergillus terreus UF39 using
oil cakes. Eurpean J. Biotechnol. Bioci. 2017, 5, 15–21.
80. Contreras, M.D.M.; Romero, I.; Moya, M.; Castro, E. Olive-derived biomass as a renewable source of
value-added products. Process Biochem. 2020, 97, 43–56. [CrossRef]
81. Moftah, O.A.S.; Grbavcic, S.; Zuza, M.; Luković, N.; Bezbradica, D.; Knežević-Jugović, Z.D. Adding Value to
the Oil Cake as a Waste from Oil Processing Industry: Production of Lipase and Protease by Candida utilis
in Solid State Fermentation. Appl. Biochem. Biotechnol. 2011, 166, 348–364. [CrossRef]
82. Ramachandran, S.; Singh, S.K.; Larroche, C.; Soccol, C.R.; Pandey, A. Oil cakes and their biotechnological
applications—A review. Bioresour. Technol. 2007, 98, 2000–2009. [CrossRef] [PubMed]
Appl. Sci. 2020, 10, 7432 25 of 30
83. Bakkalbaşi, E.; Meral, R.; Dogan, I.S. Bioactive Compounds, Physical and Sensory Properties of Cake Made
with Walnut Press-Cake. J. Food Qual. 2015, 38, 422–430. [CrossRef]
84. Grosu, C.; Boaghi, E.; Paladi, D.; Deseatnicova, O.; Vladislav, R. Prosects of using walnut oil cake in food
industry. In Proceedings of the International Conference Modern Technologies in the Food Industry, Chis, inău,
Moldova, 1–3 November 2012; pp. 362–365.
85. Jokić, S.; Moslavac, T.; Bošnjak, A.; Aladić, K.; Rajić, M.; Bilić, M. Optimization of walnut oil production.
Croat. J. Food Sci. Technol. 2014, 6, 27–35.
86. Mir, M.A.; Sharma, R.K.; Rastogi, A.; Barman, K. Effect of incorporation of walnut cake (Juglans regia) in
concentrate mixture on degradation of dry matter, organic matter and production of microbial biomass
in vitro in goat. Veter-World 2015, 8, 1172–1176. [CrossRef]
87. Bardeau, T.; Savoire, R.; Cansell, M.; Subra-Paternault, P. Recovery of oils from press cakes by CO2 -based
technology. OCL 2015, 22, D403. [CrossRef]
88. Pop, A.; Paucean, A.; Socaci, S.A.; Alexa, E.; Man, S.M.; Muresan, V.; Chis, M.S.; Salanta, L.; Popescu, I.;
Berbecea, A.; et al. Quality characteristics and volatile profile of macarons modified withwalnut oilcake
by-product. Molecules 2020, 25, 2214. [CrossRef]
89. Wang, R.; Shaarani, S.M.; Casas-Godoy, L.; Melikoğlu, M.; Vergara, C.S.; Koutinas, A.; Webb, C. Bioconversion
of rapeseed meal for the production of a generic microbial feedstock. Enzym. Microb. Technol. 2010,
47, 77–83. [CrossRef]
90. Jannathulla, R.; Dayal, J.S.; Ambasankar, K.; Muralidhar, M. Effect of Aspergillus niger fermented soybean
meal and sunflower oil cake on growth, carcass composition and haemolymph indices in Penaeus vannamei
Boone, 1931. Aquaculture 2018, 486, 1–8. [CrossRef]
91. Zamindar, N.; Bashash, M.; Khorshidi, F.; Serjouie, A.; Shirvani, M.A.; Abbasi, H.; Sedaghatdoost, A.
Antioxidant efficacy of soybean cake extracts in soy oil protection. J. Food Sci. Technol. 2017, 54, 2077–2084.
[CrossRef] [PubMed]
92. Gerliani, N.; Hammami, R.; Aïder, M. A comparative study of the functional properties and antioxidant
activity of soybean meal extracts obtained by conventional extraction and electro-activated solutions.
Food Chem. 2020, 307, 125547. [CrossRef]
93. Jahan, D.; Hussain, L.; Islam, M.; Khan, M. Comparative Study of Mustard Oil Cake and Soybean Meal
Based Artificial Diet for Rohu, Labeo rohita (Ham.) Fingerlings. Agriculturists 2013, 11, 61–66. [CrossRef]
94. Tangendjaja, B. Quality control of feed ingredients for aquaculture. In Feed and Feeding Practices in Aquaculture,
1st ed.; Davis, D.A., Ed.; Woodhead Publishing: Cambridge, UK, 2015; pp. 141–169.
95. Jadhav, M.; Kagalkar, A.; Jadhav, S.; Govindwar, S.P.; Chakankar, M. Isolation, characterization, and antifungal
application of a biosurfactant produced by Enterobacter sp. MS16. Eur. J. Lipid Sci. Technol. 2011,
113, 1347–1356. [CrossRef]
96. Grosu, C. Valorificarea S, rotului de nuci s, i Obt, inerea Produselor de Cofetărie. Ph.D. Thesis,
Technical University of Moldova, Chişinău, Moldova, 2016.
97. Bhise, S.; Kaur, A.; Manikantan, M.; Singh, B. Development of textured defatted sunflower meal by extrusion
using response surface methodology. Acta Aliment. 2015, 44, 251–258. [CrossRef]
98. Šuput, D.; Lazić, V.; Mad̄arev-Popović, S.; Hromiš, N.; Bulut, S.; Pezo, L.; Banićević, J. Effect of process parameters
on biopolymer films based on sunflower oil cake. J. Process. Energy Agric. 2018, 22, 125–128. [CrossRef]
99. Serrapica, F.; Masucci, F.; Raffrenato, E.; Sannino, M.; Vastolo, A.; Barone, C.M.A.; Di Francia, A. High Fiber
Cakes from Mediterranean Multipurpose Oilseeds as Protein Sources for Ruminants. Animal 2019, 9, 918.
[CrossRef] [PubMed]
100. Lazaro, E.; Benjamin, Y.; Robert, M. The Effects of Dehulling on Physicochemical Properties of Seed Oil and
Cake Quality of Sunflower. Tanzan. J. Agric. Sci. 2014, 13, 41–47.
101. Salgado, P.R.; Ortiz, S.E.M.; Petruccelli, S.; Mauri, A.N. Sunflower Protein Concentrates and Isolates Prepared
from Oil Cakes Have High Water Solubility and Antioxidant Capacity. J. Am. Oil Chem. Soc. 2010,
88, 351–360. [CrossRef]
102. Budžaki, S.; Strelec, I.; Krnić, M.; Alilović, K.; Tišma, M.; Zelić, B. Proximate analysis of cold-press oil
cakes after biological treatment with Trametes versicolor and Humicola grisea. Eng. Life Sci. 2018,
18, 924–931. [CrossRef]
103. Tirgar, M.; Silcock, P.; Carne, A.; Birch, E.J. Effect of extraction method on functional properties of flaxseed
protein concentrates. Food Chem. 2017, 215, 417–424. [CrossRef]
Appl. Sci. 2020, 10, 7432 26 of 30
125. Aider, M.; Barbana, C. Canola proteins: Composition, extraction, functional properties, bioactivity,
applications as a food ingredient and allergenicity—A practical and critical review. Trends Food Sci. Technol.
2011, 22, 21–39. [CrossRef]
126. Yamada, Y.; Iwasaki, M.; Usui, H.; Ohinata, K.; Marczak, E.D.; Lipkowski, A.W.; Yoshikawa, M.
Rapakinin, an anti-hypertensive peptide derived from rapeseed protein, dilates mesenteric artery of
spontaneously hypertensive rats via the prostaglandin IP receptor followed by CCK1 receptor. Peptides 2010,
31, 909–914. [CrossRef]
127. Zhang, S.B. In vitro antithrombotic activities of peanut protein hydrolysates. Food Chem. 2016, 202, 1–8.
[CrossRef] [PubMed]
128. Kavitha, N.; Selvakumar, K.; Srinivasan, G.; Madhan, R. Production and analysis of microbial growth in
enzyme hydrolysate of sesame oil seed cake. J. Biol. Inf. Sci. 2012, 1, 2–5.
129. Alashi, A.M.; Blanchard, C.L.; Mailer, R.J.; Agboola, S.O. Technological and Bioactive Functionalities of
Canola Meal Proteins and Hydrolysates. Food Rev. Int. 2013, 29, 231–260. [CrossRef]
130. Campbell, L.; Rempel, C.; Wanasundara, J.P. Canola/Rapeseed Protein: Future Opportunities and
Directions—Workshop Proceedings of IRC 2015. Plants 2016, 5, 17. [CrossRef] [PubMed]
131. Sisay, M.T.; Emire, S.A.; Ramaswamy, H.S.; Workneh, T.S. Effect of feed components on quality parameters
of wheat–tef–sesame–tomato based extruded products. J. Food Sci. Technol. 2018, 55, 2649–2660.
[CrossRef] [PubMed]
132. Stodolak, B.; Starzyńska-Janiszewska, A.; Wywrocka-Gurgul, A.; Wikiera, A. Solid-State Fermented Flaxseed
Oil Cake of Improved Antioxidant Capacity as Potential Food Additive. J. Food Process. Preserv. 2016,
41, e12855. [CrossRef]
133. Sadh, P.K.; Chawla, P.; Duhan, J.S. Fermentation approach on phenolic, antioxidants and functional properties
of peanut press cake. Food Biosci. 2018, 22, 113–120. [CrossRef]
134. Teh, S.-S.; Birch, E.J. Effect of ultrasonic treatment on the polyphenol content and antioxidant capacity of
extract from defatted hemp, flax and canola seed cakes. Ultrason. Sonochemistry 2014, 21, 346–353. [CrossRef]
135. Bakkalbaşi, E. Oxidative stability of enriched walnut oil with phenolic extracts from walnut press-cake
under accelerated oxidation conditions and the effect of ultrasound treatment. J. Food Meas. Charact. 2018,
13, 43–50. [CrossRef]
136. Şahin, S.; Elhussein, E.A.A. Assessment of sesame (Sesamum indicum L.) cake as a source of high-added value
substances: From waste to health. Phytochem. Rev. 2018, 17, 691–700. [CrossRef]
137. Mohdaly, A.A.A.; Hassanien, M.F.R.; Mahmoud, A.; Sarhan, M.A.; Smetanska, I. Phenolics Extracted from
Potato, Sugar Beet, and Sesame Processing By-Products. Int. J. Food Prop. 2013, 16, 1148–1168. [CrossRef]
138. Senanayake, C.M.; Algama, C.H.; Wimalasekara, R.L.; Weerakoon, W.N.; Jayathilaka, N.; Seneviratne, K.N.
Improvement of Oxidative Stability and Microbial Shelf Life of Vanilla Cake by Coconut Oil Meal and
Sesame Oil Meal Phenolic Extracts. J. Food Qual. 2019, 2019, 1–8. [CrossRef]
139. Teh, S.-S.; Bekhit, A.E.-D.; Birch, J. Antioxidative Polyphenols from Defatted Oilseed Cakes: Effect of Solvents.
Antioxidants 2014, 3, 67–80. [CrossRef]
140. Pickardt, C.; Eisner, P.; Kammerer, D.R.; Carle, R. Pilot plant preparation of light-coloured protein isolates
from de-oiled sunflower (Helianthus annuus L.) press cake by mild-acidic protein extraction and polyphenol
adsorption. Food Hydrocoll. 2015, 44, 208–219. [CrossRef]
141. Sarkis, J.R.; Michel, I.; Tessaro, I.C.; Marczak, L.D.F. Optimization of phenolics extraction from sesame seed
cake. Sep. Purif. Technol. 2014, 122, 506–514. [CrossRef]
142. Elleuch, M.; Bedigian, D.; Roiseux, O.; Besbes, S.; Blecker, C.; Attia, H. Dietary fibre and fibre-rich by-products
of food processing: Characterisation, technological functionality and commercial applications: A review.
Food Chem. 2011, 124, 411–421. [CrossRef]
143. Maphosa, Y.; Jideani, V.A. Dietary fiber extraction for human nutrition—A review. Food Rev. Int. 2015,
32, 98–115. [CrossRef]
144. Dhingra, D.; Michael, M.; Rajput, H.; Patil, R.T. Dietary fibre in foods: A review. J. Food Sci. Technol. 2011,
49, 255–266. [CrossRef]
145. Dungani, R.; Karina, M.; Sulaeman, A.; Hermawan, D.; Hadiyane, A. Agricultural Waste Fibers towards
Sustainability and Advanced Utilization: A Review. Asian J. Plant Sci. 2016, 15, 42–55. [CrossRef]
146. Lizardi-Jiménez, M.A.; Hernández-Martínez, R. Solid state fermentation (SSF): Diversity of applications to
valorize waste and biomass. 3 Biotech 2017, 7, 44. [CrossRef]
Appl. Sci. 2020, 10, 7432 28 of 30
147. Parihar, D.K. Production of Lipase Utilizing linseed oilcake as fermentation substrate. Int. J. Sci.
Environ. Technol. 2012, 1, 135–143.
148. Thakur, S.A.; Nemade, S.N.; Sharanappa, A. Solid State Fermentation of Overheated Soybean Meal (Waste)
For Production of Protease Using Aspergillus Oryzae. Int. J. Innov. Res. Sci. Eng. Technol. 2015,
4, 18456–18461. [CrossRef]
149. Gupta, A.; Sharma, A.; Pathak, R.; Kumar, A.; Sharma, S. Solid state fermentation of non-edible oil seed cakes
for production of proteases and cellulases and degradation of anti-nutritional factors. J. Food Biotechnol. Res.
2018, 1, 3–8.
150. Sahoo, R.; Subudhi, E.; Kumar, M. Quantitative approach to track lipase producingPseudomonassp. S1 in
nonsterilized solid state fermentation. Lett. Appl. Microbiol. 2014, 58, 610–616. [CrossRef]
151. Medhe, S.; Anand, M.; Anal, A.K. Dietary Fibers, Dietary Peptides and Dietary Essential Fatty Acids from
Food Processing By-Products. In Food Processing By-Products and Their Utilization, 1st ed.; Anil, A.K., Ed.;
John Wiley & Sons Ltd.: Hoboken, NJ, USA, 2018; pp. 111–136.
152. Satya, C.V.; Anuradha, C.; Reddy, D.S. Palm Oil Cake: A Potential Substrate for L-Asparaginase production.
Int. J. Innov. Res. Sci. Eng. Technol. 2014, 3, 14627–14632.
153. Ghosh, S.; Murthy, S.; Govindasamy, S.; Chandrasekaran, M. Optimization of L-asparaginase production by
Serratia marcescens (NCIM 2919) under solid state fermentation using coconut oil cake. Sustain. Chem. Process.
2013, 1, 9. [CrossRef]
154. Gregori, A.; Pohleven, F. Cultivation of three medicinal mushroom species on olive oil press cakes containing
substrates. Acta Agric. Slov. 2014, 103, 49–54. [CrossRef]
155. Song, B.; Ye, J.; Sossah, F.L.; Li, C.; Li, D.; Meng, L.; Xu, S.; Fu, Y.; Li, Y. Assessing the effects of different
agro-residue as substrates on growth cycle and yield of Grifola frondosa and statistical optimization of
substrate components using simplex-lattice design. AMB Express 2018, 8, 46. [CrossRef]
156. Krupodorova, T.A.; Barshteyn, V.Y. Alternative substrates for higher mushrooms mycelia cultivation.
J. BioSci. Biotechnol. 2015, 1, 339–347.
157. Jape, A.; Salunke, D.; Dighe, S.; Harsulkar, A. The Improvement of Pleuorotus Species Cultivated On Soybean
Straw Bed Supplemented with Flax Seed Meal. Int. J. Sci. Res. 2014, 3, 2012–2015.
158. Atila, F. Cultivation of Pleurotus spp., as an Alternative Solution to Dispose Olive Waste. J. Agric. Ecol.
Res. Int. 2017, 12, 1–10. [CrossRef]
159. Zervakis, G.I.; Koutrotsios, G.; Katsaris, P. Composted versus Raw Olive Mill Waste as Substrates for the
Production of Medicinal Mushrooms: An Assessment of Selected Cultivation and Quality Parameters.
BioMed Res. Int. 2013, 2013, 1–13. [CrossRef] [PubMed]
160. Farzana, K.; Shah, S.N.H.; Butt, F.B.; Awan, S.B. Biosynthesis of bacitracin in solid-state fermentation by
Bacillus licheniformis using defatted oil seed cakes as substrate. Pak. J. Pharm. Sci. 2005, 18, 55–57.
161. Zarei, I. Biosynthesis of Bacitracin in Stirred Fermenter by Bacillus Licheniformis Using Defatted Oil Seed
Cakes as Substrate. Mod. Appl. Sci. 2012, 6, 30–36. [CrossRef]
162. Ali, S.; Nelofer, R.; Andleeb, S.; Baig, S.; Shakir, H.A.; Qazi, J.I. Biosynthesis and optimization of bacitracin by
mutant Bacillus licheniformis using submerged fermentation. Indian J. Biotechnol. 2018, 17, 251–260.
163. Vastrad, B.M.; Neelagund, S.E. Optimization of Medium Composition for the Production of Neomycin
byStreptomyces fradiaeNCIM 2418 in Solid State Fermentation. Biotechnol. Res. Int. 2014, 2014, 1–11. [CrossRef]
164. Nagavalli, M.; Ponamgi, S.P.; Girijashankar, V.; Venkateswar Rao, L. Solid State Fermentation and production
of Rifamycin SV usingAmycolatopsis mediterranei. Lett. Appl. Microbiol. 2014, 60, 44–51. [CrossRef]
165. Vastrad, B.M.; Neelagund, S.E. Optimization of Process Parameters for Rifamycin B Production under Solid
State Fermentation from Amycolatopsis Mediterranean Mtcc 14. Int. J. Curr. Pharm. Res. 2012, 4, 101–108.
166. Yao, D.; Ji, Z.; Wang, C.; Qi, G.; Zhang, L.; Ma, X.; Chen, S. Co-producing iturin A and poly-γ-glutamic acid
from rapeseed meal under solid state fermentation by the newly isolated Bacillus subtilis strain 3-10. World J.
Microbiol. Biotechnol. 2011, 28, 985–991. [CrossRef]
167. Banat, I.M.; Franzetti, A.; Gandolfi, I.; Bestetti, G.; Martinotti, M.G.; Fracchia, L.; Smyth, T.J.; Marchant, R.
Microbial biosurfactants production, applications and future potential. Appl. Microbiol. Biotechnol. 2010,
87, 427–444. [CrossRef]
168. Thavasi, R. Microbial Biosurfactants: From an Environmental Application Point of View. J. Bioremediation Biodegrad.
2011, 2, 1000104. [CrossRef]
Appl. Sci. 2020, 10, 7432 29 of 30
169. Fracchia, L.; Cavallo, M.; Martinotti, G.M.; Banat, I.M. Biosurfactants and Bioemulsifiers Biomedical and
Related Applications—Present Status and Future Potentials. In Biomedical Science, Engineering and Technology;
Ghista, D.N., Ed.; InTecch Europe: Rijeka, Croatia, 2012; pp. 325–370.
170. Jiménez-Peñalver, P.; Koh, A.; Gross, R.; Gea, T.; Font, X. Biosurfactants from Waste: Structures and Interfacial
Properties of Sophorolipids Produced from a Residual Oil Cake. J. Surfactants Deterg. 2019, 23, 481–486. [CrossRef]
171. Thavasi, R.; Nambaru, V.S.; Jayalakshmi, S.; Balasubramanian, T.; Banat, I.M. Biosurfactant Production by
Pseudomonas aeruginosa from Renewable Resources. Indian J. Microbiol. 2011, 51, 30–36. [CrossRef]
172. Noparat, P.; Maneerat, S.; Saimmai, A. Utilization of palm oil decanter cake as a novel substrate for
biosurfactant production from a new and promising strain of Ochrobactrum anthropi 2/3. World J.
Microbiol. Biotechnol. 2014, 30, 865–877. [CrossRef] [PubMed]
173. Chittepu, O.R.; Reddy, C.O. Isolation and characterization of biosurfactant producing bacteria from groundnut
oil cake dumping site for the control of foodborne pathogens. Grain Oil Sci. Technol. 2019, 2, 15–20. [CrossRef]
174. Zentek, J.; Knorr, F.; Mader, A. Reducing waste in fresh produce processing and households through use
of waste as animal feed. In Global Safety of Fresh Produce: A Handbook of Best Practice, Innovative Commercial
Solutions and Case Studies, 1st ed.; Hoorfar, J., Ed.; Woodhead Publishing Limited: Cambridge, UK, 2014;
pp. 140–152.
175. Thu, T.N.; Bodin, N.; De Saeger, S.; Larondelle, Y.; Rollin, X. Substitution of fish meal by sesame oil cake
(Sesamum indicum L.) in the diet of rainbow trout (Oncorhynchus mykiss W.). Aquac. Nutr. 2010, 17, 80–89. [CrossRef]
176. Chebaibi, S.; Grandchamp, M.L.; Burgé, G.; Clément, T.; Allais, F.; Laziri, F. Improvement of protein content
and decrease of anti-nutritional factors in olive cake by solid-state fermentation: A way to valorize this
industrial by-product in animal feed. J. Biosci. Bioeng. 2019, 128, 384–390. [CrossRef]
177. Hassan, H.E.; Elhashmi, Y.H.A.; Eldar, A.A.T.; Elamin, K.M.; Elbushra, M.E. Effects of Feeding Different
Levels of Sesame Oil Cake (Sesamum indicum L.) On Performance and Carcass Characteristics of Sudan
Desert Sheep. J. Anim. Sci. Adv. 2013, 3, 91. [CrossRef]
178. Fitwi, M.; Tadesse, G. Effect of sesame cake supplementation on feed intake, body weight gain, feed conversion
efficiency and carcass parameters in the ration of sheep fed on wheat bran and teff (Eragrostis teff ) straw.
Momona Ethiop. J. Sci. 2013, 5, 89. [CrossRef]
179. Ghorbani, B.; Yansari, A.T.; Sayyadi, A.J. Effects of sesame meal on intake, digestibility, rumen characteristics,
chewing activity and growth of lambs. S. Afr. J. Anim. Sci. 2018, 48, 151. [CrossRef]
180. Mir, M.A.; Sharma, R.K.; Rastogi, A.; Haq, Z.; Ganai, I.A. Effect of dietary incorporation of walnut cake
(Juglans regia) on calcium—Phosphorus balance and blood biochemical parameters in goats. Vet. Arhiv 2018,
88, 763–771. [CrossRef]
181. Chipa, M.J.; Siebrits, F.K.; Ratsaka, M.M.; Leeuw, K.J.; Nkosi, B.D. Growth performance of feedlot weaners cattle
fed diet containing different levels of cold press soya bean oilcake. S. Afr. J. Anim. Sci. 2010, 40, 499–501.
182. Stübler, A.-S.; Heinz, V.; Aganovic, K. Development of food products. Curr. Opin. Green Sustain. Chem. 2020,
25, 100356. [CrossRef]
183. Sunil, L.; Prakruthi, A.; Prasanth Kumar, P.K.; Gopala Krishna, A.G. Development of Health Foods from
Oilseed Cakes. J. Food Process. Technol. 2016, 7, 1–6. [CrossRef]
184. Pycia, K.; Kapusta, I.; Jaworska, G. Walnut oil and oilcake affect selected the physicochemical and antioxidant
properties of wheat bread enriched with them. J. Food Process. Preserv. 2020, 44, e14573. [CrossRef]
185. Koneva, S.I.; Egorova, E.Y.; Kozubaeva, L.A.; Kuzmina, S.S.; Zakharova, A.S. Influence of Flaxseed
Flour on Dough Rheology from Wheat-Flaxseed Meal. In International Scientific and Practical Conference
“AgroSMART—Smart Solutions for Agriculture" (AgroSMART 2018); Atlantis Press: Paris, France, 2018;
pp. 370–377.
186. Behera, S.; Indumathi, K.; Mahadevamma, S.; Sudha, M.L. Oil cakes—A by-product of agriculture industry
as a fortificant in bakery products. Int. J. Food Sci. Nutr. 2013, 64, 806–814. [CrossRef]
187. Jáquez, D.R.; Casillas, F.; Flores, N.; Cooke, P.; Licon, E.D.; Soto, S.; González, I.A.; Carreón, F.O.C.;
Roldán, H.M. Effect of Glandless Cottonseed Meal Content on the Microstructure of Extruded Corn-Based
Snacks. Adv. Food Sci. 2014, 36, 125–130.
188. Bulut, S.; Lazić, V.; Mad̄arev-Popović, S.; Hromiš, N.; Šuput, D. Mono- and bilayer biopolymer films:
Synthesis and characterisation. J. Process. Energy Agric. 2017, 21, 214–218. [CrossRef]
189. Garrido, T.; Leceta, I.; Cabezudo, S.; Guerrero, P.; De La Caba, K. Tailoring soy protein film properties by
selecting casting or compression as processing methods. Eur. Polym. J. 2016, 85, 499–507. [CrossRef]
Appl. Sci. 2020, 10, 7432 30 of 30
190. Garrido, T.; Etxabide, A.; Peñalba, M.; De La Caba, K.; Guerrero, P. Preparation and characterization of soy
protein thin films: Processing–properties correlation. Mater. Lett. 2013, 105, 110–112. [CrossRef]
191. Puscaselu, R.G.; Gutt, G.; Amariei, S. Rethinking the Future of Food Packaging: Biobased Edible Films for
Powdered Food and Drinks. Molecules 2019, 24, 3136. [CrossRef] [PubMed]
192. Popović, S.; Hromiš, N.; Šuput, D.; Bulut, S.; Romanić, R.; Lazić, V. Valorization of by-products from the
production of pressed edible oils to produce biopolymer films. In Cold Pressed Oils, 1st ed.; Ramadan, F.M.,
Ed.; Elsevier Inc.: London, UK, 2020; pp. 15–30.
193. Šuput, D.; Mad̄arev-Popović, S.; Hromiš, N.; Bulut, S.; Lazić, V. Biopolymer films properties change affected
by essential oils addition. J. Process. Energy Agric. 2019, 23, 61–65. [CrossRef]
194. Salgado, P.R.; Ortiz, S.E.M.; Petruccelli, S.; Mauri, A.N. Biodegradable sunflower protein films naturally
activated with antioxidant compounds. Food Hydrocoll. 2010, 24, 525–533. [CrossRef]
195. Mad̄arev-Popović, S.; Lazic, V.; Popovic, L.; Vaštag, Ž.; Pericin, D. Effect of the addition of pumpkin oil cake
to gelatin to produce biodegradable composite films. Int. J. Food Sci. Technol. 2010, 45, 1184–1190. [CrossRef]
196. Mad̄arev-Popović, S.; Pericin, D.; Vaštag, Ž.; Popovic, L.; Lazic, V. Evaluation of edible film-forming ability
of pumpkin oil cake; effect of pH and temperature. Food Hydrocoll. 2011, 25, 470–476. [CrossRef]
197. Bulut, S.; Lazic, V.; Popovic, S.; Hromiš, N.; Šuput, D. Influence of storage period on properties of biopolymer
packaging materials and pouches. Acta Period. Technol. 2017, 48, 53–62. [CrossRef]
198. Bulut, S.; Lazic, V.; Popovic, S.; Hromis, N.; Suput, D. Influence of different concentrations of glycerol and
guar xanthan on properties of pumpkin oil cake-zein bi-layer film. Ratar. Povrt. 2017, 54, 19–24. [CrossRef]
199. Bulut, S.; Mad̄arev-Popović, S.; Hromiš, N.; Šuput, D.; Lazić, V.; Malbaša, R.; Vitas, J.S. Incorporation of
essential oils into biopolymer films based on pumpkin oil cake in order to improve their antioxidant activity.
J. Process. Energy Agric. 2019, 23, 162–166. [CrossRef]
200. Mad̄arev-Popović, S.; Peričin, D.; Vaštag, Ž.; Lazić, V.; Popović, L.M. Pumpkin oil cake protein isolate films
as potential gas barrier coating. J. Food Eng. 2012, 110, 374–379. [CrossRef]
201. Reddy, N.; Jiang, Q.; Yang, Y. Preparation and properties of peanut protein films crosslinked with citric acid.
Ind. Crop. Prod. 2012, 39, 26–30. [CrossRef]
202. Sun, Q.; Sun, C.; Xiong, L. Mechanical, barrier and morphological properties of pea starch and peanut protein
isolate blend films. Carbohydr. Polym. 2013, 98, 630–637. [CrossRef]
203. Riveros, C.G.; Martin, M.P.; Aguirre, A.; Grosso, N.R. Film preparation with high protein defatted peanut flour:
Characterisation and potential use as food packaging. Int. J. Food Sci. Technol. 2017, 53, 969–975. [CrossRef]
204. Wan, J.; Liu, C.; Liu, W.; Tu, Z.; Wu, W.; Tan, H. Optimization of instant edible films based on dietary
fiber processed with dynamic high pressure microfluidization for barrier properties and water solubility.
LWT 2015, 60, 603–608. [CrossRef]
205. Ghodrat, A.G.; Tabatabaei, M.; Aghbashlo, M.; Mussatto, S.I. Waste Management Strategies the State of the
Art. In Biogas Fundamentals, Process and Operation; Tabatabaei, M., Ghanavati, H., Eds.; Springer International
Publishing: Cham, Switzerland, 2018; Volume 6, pp. 1–33.
206. Cheng, F.; Bayat, H.; Jena, U.; Brewer, C.E. Impact of feedstock composition on pyrolysis of low-cost,
protein- and lignin-rich biomass: A review. J. Anal. Appl. Pyrolysis 2020, 147, 104780. [CrossRef]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional
affiliations.
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY) license (http://creativecommons.org/licenses/by/4.0/).