Module 1 Textbook
Module 1 Textbook
3 Cell function
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32 9780170407281
2 Cell structure and technologies
Students:
• investigate different cellular structures, including but not limited to:
INQUIRY QUESTION – examining a variety of prokaryotic and eukaryotic cells (ACSBL032, ACSBL048) ICT
What distinguishes one – describe a range of technologies that are used to determine a cell’s structure and function ICT
cell from another? • investigate a variety of prokaryotic and eukaryotic cell structures, including but not limited to:
– drawing scaled diagrams of a variety of cells (ACSBL035) ICT N
– comparing and contrasting different cell organelles and arrangements CCT
– modelling the structure and function of the fluid mosaic model of the cell membrane (ACSBL045) CCT ICT
Biology Stage 6 Syllabus © NSW Education Standards Authority for and on behalf of the Crown in right of the State of New South Wales, 2017
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9780170407281 33
When you think about it, living organisms are amazing
iStock.com/hrabar
b
to perform all functions. Other organisms contain
many different cells, each with a specific structure and
function, organised to work together to ensure effective
functioning.
Imagefolk/Minden Pictures
c
or eukaryotic cells. Prokaryotic cells are ‘primitive’ cells
and have a much simpler structure than eukaryotic
cells. There are many more prokaryotic cells on Earth
than there are eukaryotic cells. Although these two
types of cells have many differences, they share basic
similarities, with each possessing a cell membrane,
cytoplasm and ribosomes (structures that produce FIGURE 2.1 Cells are the basic structural and
proteins in the cell). functional unit of the diverse range of all living
things. a Amoeba; b roses; c animals of the Great
Barrier Reef
Prokaryotic cells
With the word derived from the Greek pro (before) and karyon (nucleus), prokaryotic cells range in
diameter from 0.1 to 5.0 μm (micrometres). The four main structures that all prokaryotic cells possess
are the cell membrane, the cytoplasm, ribosomes and genetic material. The cell (plasma) membrane
is responsible for controlling what goes into and out of the cell.
There is no membrane surrounding the genetic material and therefore no nucleus. Most of the
genetic material forms a large loop called the bacterial chromosome, with the rest in small circular
rings called plasmids. The structures inside prokaryotic cells are not surrounded by membranes – they
simply float in the fluid-like cytoplasm, as does the genetic material. Structures that are present in some
prokaryotic cells are a cell wall, pili (singular: pilus), flagella (singular: flagellum) and a capsule. Pili are
hair-like structures on the surface of some cells that allow them to adhere to nearby substances. Flagella
are whip-like tails that provide the cell with locomotion. The cell wall protects the cell and provides
structural support. The substances it is composed of differ depending on the type of cell. The capsule is a
layer composed of complex carbohydrates outside the cell wall and protects the cell.
Most organisms that are composed of prokaryotic cells are unicellular – a single cell. Some bacterial
species clump together as a colony of prokaryotic cells that work together.
Bacterial
flagellum
Cytoplasm
Capsule Chromosome: Cell Plasmid: Bacterial
DNA membrane DNA flagellum Capsule Cytoplasm Cell membrane
FIGURE 2.2 a A generalised diagram of bacteria – a prokaryotic cell; b a scientific line drawing of the cell
Prokaryotic organisms (or prokaryotes) can be divided into two main groups: bacteria and archaea.
The cells in these groups are similar in both shape and size, but differ chemically in terms of their genetic
material and proteins. Bacteria can be found in many different environments and can be either beneficial
or harmful to living organisms (Fig. 2.3a). Archaea (Fig. 2.3b) are unicellular organisms that are found in
extreme and harsh environments, such as hydrothermal vents and hot springs.
Visuals Unlimited, Inc./Woods Hole
Oceanographic Institution
a
Imagefolk/Kateryna Kon/
b
Science Photo Library
FIGURE 2.3 a Different types of bacteria; b Archaea are prokaryotes found in harsh environments such as
hydrothermal vents as shown here. Archaea are found in the water where the hot fluid is escaping.
Eukaryotic cells
The different
‘Eukaryotic’ is derived from the Greek eu (‘true’ or ‘proper’) and karyon ( ‘nucleus’). types of
These cells range in size from 10 to 100 μm and are much more complex than prokaryotic cells. organelles and
their function are
Eukaryotic cells are characterised by a membrane-bound nucleus containing the genetic material of the discussed later in
cell. All of the internal structures of these cells are membrane bound and are known as organelles. Each this chapter.
organelle has a specific function within the cell. Together these organelles carry out all of the biochemical
processes and reactions, such as respiration and photosynthesis, that are required for the successful
functioning of a living cell.
Shutterstock.com/Lebendkulturen.de
Imagefolk/Hecker/Sauer
a b c
Multicellular plants and animals are composed of a variety of different types of eukaryotic cells.
Different types
KEY CONCEPTS
INVESTIGATION 2.1
AIM
To examine and compare a variety of prokaryotic and eukaryotic cells using a light microscope
MATERIALS
• Light microscope
• Microscope slides
• Coverslips
• Onion
• Knife/scalpel
• Forceps or dissecting needles
• Eye dropper (optional)
RISK ASSESSMENT
WHAT ARE THE WHAT RISK DOES THIS HAZARD HOW CAN YOU SAFELY MANAGE THIS RISK? !
HAZARDS? POSE? RISK
ASSESSMENT
Knife/scalpel Sharp edges can cause cuts Use knife/scalpel with care, hold by the handle and
keep fingers away from sharp edge of knife.
Microscope slides/ Sharp edges can cause injury if broken Handle with care. Push gently on coverslip. Always
coverslips focus by moving objective lens away from slide.
METHOD
A Plant cell: onion
1 Remove the onion skin, cut through the onion and separate the layers.
2 Carefully lift a thin section of onion tissue from the surface of one of the layers.
3 Prepare a wet mount of this tissue using the technique outlined in the following steps.
4 Cut a piece of onion tissue about 1 cm2 in area and place this in a drop of methylene blue stain on the glass
microscope slide. Be careful not to fold the tissue over on itself.
5 Using a dissecting needle, lower the coverslip carefully to avoid the formation of air bubbles (Fig. 2.5).
6 Place a piece of paper towel over the coverslip and microscope slide to dry any excess stain.
Onion skin
Microscope slide
Drop of stain
Coverslip
RESULTS
1 Your results will include scientific diagrams including labels and total magnification of:
a an onion cell
b an Ambulia cell
c a cheek cell
d a bacterial cell
e two other cells you observed.
2 In a table, record the similarities and differences in size and structure between the cells you have observed
and drawn in the previous question:
i two plant cells: a and b
ii a plant cell and an animal cell: b and c
iii a plant cell and a bacterial cell: a and d
3 List the cells in order of size from smallest to largest.
DISCUSSION
1 Describe why methylene blue stain was used when preparing the wet mount of the onion cell.
2 Compare the size of a bacterial cell to the plant and animal cells you have seen so far.
3 Outline any cell detail seen inside the bacterial cells.
4 Identify two limitations of using a light microscope.
5 Using your observations of the cells, suggest two differences between prokaryotic and eukaryotic cells.
6 Describe how the prepared slides that you used compare to the ones that you prepared yourself.
7 Describe how using oil immersion helped you to see the internal structure of the bacterial cell.
CONCLUSION
Write a summary statement that relates to the aim of this investigation. A brief summary of what you did
(variable changed) and what you found (variables observed) is required.
Calculate the total magnification of a microscope when the magnification of the ocular lens is 103 and the
magnification of the objective lens is 103.
ANSWER LOGIC
103 203
103 403
123 4803
KEY
CONCEPTS
CHECK YOUR
1 State the two different types of cells, and list features of each. UNDERSTANDING
2 What features do the two different types of cells share?
3 Complete the following table to compare the features of prokaryotic and eukaryotic cells. 2.1
4 Draw a labelled scientific diagram of the following cells as seen through the light microscope:
• an onion cell
• a cheek cell.
5 Calculate the total magnification of a light microscope when a 123 ocular lens and a 203 objective lens
are used to view a sample. Show your working.
a
Alamy Stock Photo/Science History Images
Eyepiece
Lens to
concentrate
light source
Stage to hold
specimen
FIGURE 2.7 a Hooke’s compound microscope; b Hooke’s drawing of cork, showing the compartments he called ‘cella’
Modern microscopes
Further refinements in the structure of compound microscopes continued over the succeeding years
until we have those that are in use today.
Light microscopes
Discovering In the compound light microscope such as those you use in the school laboratory, a light source passes
the principle of through a condenser lens and then through the thin specimen. This beam of light then passes through
a compound
microscope the convex objective lens, where the image is magnified and viewed through the ocular lens (Fig. 2.8).
a
Science Source/Ted Kinsman
iStock/defun
b
FIGURE 2.9 a A fluorescence microscope; b image of cells seen through a fluorescence microscope,
showing different parts of the cell exhibiting different colours of fluorescence
Electron microscopes
Since the 1950s, studies of microscopic organisms have been revolutionised by the development of the electron
microscope. This instrument uses an electron beam instead of light, and electromagnets instead of glass
lenses. The interaction between the electrons and the object forms a viewable image on a screen (Fig. 2.10).
The use of electrons instead of light gives much greater magnification. Electron microscopes also have a much
higher resolving power than light microscopes because electrons have a much shorter wavelength than light.
The electron microscope reveals structures at not only the cellular level, but also at the subcellular
level. Materials that were formerly believed to have little or no structure have been shown to have
Electromagnetic
lenses
Virtual scanning
electron Eye
microscope
Try to get the best
possible image for
each specimen viewed
in the virtual scanning
microscope.
Final image
on screen
Information and
communication FIGURE 2.11 A transmission electron microscope (TEM)
technology FIGURE 2.10 The electron microscope currently used in biological research
capability
Getty Images/Don W Fawcett
a b
FIGURE 2.12 a TEM image of kidney cells; b SEM image of the surface of the tongue. The resolution of the microscope is
high enough to show the individual taste buds.
● Early microscopes allowed scientists to see cells for the first time.
● Magnification indicates how much an image has been increased in size.
● The resolution indicates the minimum distance objects need to be apart to be able to be seen
separately.
● Light microscopes pass light rays through thin specimens that are magnified by convex
glass lenses.
● Magnification in light microscopes can be up to 2000×, maximum resolution 200 nm.
● Living and non-living specimens can be viewed using a light microscope.
● Fluorescence microscopy targets specific structures and uses labelling of these structures with
fluorescent substances to see them.
● Electron microscopes use electron beams and electromagnets instead of light rays and lenses.
● Two types of electron microscopes are transmission electron microscopes (TEM) and scanning
electron microscopes (SEM). No living specimens can be viewed with an electron microscope.
● In a TEM, beams of electrons pass through a specimen and produce a two-dimensional image.
Very high magnification and resolution are possible (up to ten million times with some SEMs).
● In a SEM, electron beams bounce off surfaces and create a three-dimensional image.
● Confocal laser scanning microscopes use pinpoint laser beams to make images of many layers,
which are then combined into a three-dimensional model.
1m –1
10 m –2
10 m –3
10 m –4
10 m 10–5 m 10–6 m 10–7 m 10–8 m 10–9 m 10–10 m
Eye
Light microscope
Electron microscope
FIGURE 2.14 Size and comparison of images seen by the naked eye, light microscope and electron microscope
When drawing different types of cells, such as those viewed in Investigation 2.1, it is useful to draw these
cells to scale. This allows a more accurate representation of the size of these cells.
Diagrams that are drawn to scale will always contain a ‘scale bar’, which indicates the scale to which
the diagram is drawn.
The scale bar represents a specific whole number of μm and is often 1–5 cm in length. In order to
draw the scale bar:
1 Determine the actual length of the object to be drawn.
2 When the actual length of the object determined above is divided by the length of the proposed
WS
drawing, a whole number should be obtained.
For example: How to approach
length of cell 5 8 μm drawings in
biology
length of drawing 5 4 cm
Actual length 8 μm
5
Length of drawing 4 cm
2μm
Scale 5
1cm
A human cheek cell, as observed in Investigation 2.1 and shown in Figure 2.15, has a diameter of
approximately 60 μm. Its nucleus has a diameter of 6 μm. Draw a scaled diagram of the human cheek cell
and its nucleus.
Nucleus
12 mm Cheek cell
● 1 cm 5 10 mm
● 1 mm 5 1000 μm
● 1 μm 5 1000 nm
● Scaled diagrams must always contain a scale bar.
● The scale to be used can be calculated by dividing the actual size of the cell by the length of the
diagram to be drawn.
2.3
Trypanosoma
Chlamydomonas (protozoan)
(green alga) 25 μm long
5–6 μm HIV (AIDS
virus)
100 nm
T4 bacteriophage
225 nm long
Human red
blood cell Polio virus
7–8 μm 30 nm
diameter
b 0.013 mm to μm
c 4000 nm to μm
d 0.080 μm to nm.
7 Using a ruler and the scale provided, determine the actual size of the full cell shown in Figure 2.18. Show
the formula you have used and all workings.
TABLE 2.1 Comparison of the structures visible using light and electron microscopes
The arrangement of organelles also varies depending on whether the cell is a plant or animal
cell. A generalised diagram and line drawing of a eukaryotic animal cell is shown in Figure 2.19 and
a plant cell in Figure 2.20.
Plant and animal cells contain many of the same organelles. The plant cell, however, possesses a cell
wall, chloroplasts and a large vacuole that the animal cell does not.
Figure 2.21 summarises the organelles that are found in both plant and animal cells. It also shows the
organelles specific to plant cells and those that are only present in animal cells.
Protoplasm
It is in the protoplasm of cells that the functions essential to life, such as making cellular products and
respiration, are carried out. The protoplasm is the living content of a cell that is surrounded by the cell
membrane. The protoplasm is composed of the nucleus and the cytoplasm. The cytoplasm (that part of
the protoplasm outside the nucleus) consists of a liquid called the cytosol in which there are dissolved
chemical substances (for example, ions such as chloride ions), suspended organelles and insoluble
granules. Approximately 90 per cent of the cytoplasm is water – the medium in which all cell chemicals
are dissolved or suspended.
Endoplasmic
reticulum: intracellular
and intercellular
transport system
Mitochondrion:
site of cellular
respiration
Ribosomes: sites of
protein synthesis
b Endoplasmic
reticulum Cell membrane
Temporary
vacuole
Cytoplasm
Golgi
apparatus
Mitochondrion
Ribosomes
Nucleolus Nucleus
FIGURE 2.19 a A eukaryotic animal cell showing its nucleus and organelles; b a scientific line drawing of the cell
Cytoplasm: fluid
Nucleolus: involved material where
in the manufacture activities of the cell
of ribosomes within occur
the cell
Nucleus:
coordinates all
the activities of
the cell Cell wall: provides
extra support and
protection to plant
cells
b Cell membrane
Chloroplast
Cell wall
Large
permanent
vacuole
Nucleus
Nucleolus Cytoplasm
Mitochondrion
FIGURE 2.20 a A eukaryotic plant cell showing its nucleus, cell wall and other organelles; b a scientific line drawing of the cell
Cell wall
Both
a Nucleoplasm b
Nuclear pore
Nucleolus
Double nuclear
membrane Rough endoplasmic
reticulum
FIGURE 2.22 a Diagram of nucleus showing nucleolus, nuclear membrane, nucleoplasm, chromatin material and associated endoplasmic reticulum
and ribosomes; b electron micrograph image of nucleus
The nucleoplasm or nuclear sap is the liquid part of the nucleus in which the chromatin material
is found. Chromatin is made up of protein and nucleic acid. The deoxyribonucleic acid, DNA, is stored
in the nucleus. It is a very large chemical that holds, in a coded form, all the genetic information (the
‘blueprint’) necessary to control the cell’s function. This DNA contains the hereditary information of
an organism that gets passed from one generation to the next. Within one organism, the information
stored in the DNA of each cell is the same. Before a cell divides, the information on the DNA must be
copied so that it can be transmitted (passed on) to newly formed cells. The chromatin separates into
short, thick separate rod-shaped structures called chromosomes, which become visible in dividing
cells (from the Greek chromo (coloured) and soma (body), so named because chromosomes take up
stains easily when being prepared for microscopy). Each species of organism has its own particular
number of chromosomes; for example, humans have 46 chromosomes, a platypus has 52, a lettuce has
18 and a camel has 70.
a Vesicles Secretory
vesicle
Cis face
FIGURE 2.24 a Golgi body and vesicles; b diagram showing the relationship between the ER, Golgi body and the cell membrane
Lysosomes
Buzzle.com
Golgi
complex
FIGURE 2.25 a Structure of a lysosome; b electron micrograph showing lysosomes and the Golgi body (apparatus)
Inner membrane
folded into cristae Cristae
Inner membrane
Cristae Matrix space
Particles on
outer membrane Inter-membrane space
Cytosol
Lumen or cavity
FIGURE 2.26 a Simplified diagram of mitochondrion in longitudinal section; b electron micrograph of a mitochondrion
A double membrane surrounds each mitochondrion. The outer membrane gives the mitochondria
their shape and allows the passage of small substances into and out of mitochondria. The inner
membrane is folded into fine, finger-like ridges or cristae, increasing the surface area for attachment of
groups of enzymes responsible for producing energy for the cell. These appear as knob-like particles on
the inside of the cristae. The central space in a mitochondrion is filled with fluid and is termed the matrix.
It contains mitochondrial DNA and enzymes that give mitochondria the unusual feature of being able
to replicate (make copies of) themselves. The mitochondria divide by pinching off and then growing,
something that usually occurs in very active cells or cells that are about to divide.
a Endoplasmic reticulum b
Nucleus Ribosome
Mitochondria
Cell wall
Vacuole
Cytoplasm
Chloroplast
FIGURE 2.27 a Diagram of a generalised plant cell showing structures including a vacuole; b electron micrograph showing vacuole and tonoplast
Chloroplasts – photosynthesis
Chloroplasts are organelles that are green in colour, due to the presence of a pigment called
chlorophyll. Chloroplasts are responsible for photosynthesis – the manufacturing of sugar in plants,
using the energy of sunlight. Chloroplasts are not present in all plant cells; they are found only in
the green tissue of plants that can photosynthesise. Under the light microscope, they appear as
green, disc-shaped structures, smaller than the nucleus. An electron microscope is needed to see
the detailed interior.
Chloroplasts belong to a group of organelles called plastids, which are biconvex in shape. Plastids WS
contain either pigment or nutrients and vary in colour. Chloroplasts are green plastids. They are larger
Cell micrographs
than mitochondria but are similar in that they also contain their own DNA; the number of chloroplasts
per cell varies.
A double membrane surrounds chloroplasts. This allows substances to pass between the cytoplasm
and the chloroplast. Unlike mitochondria, the inner membrane of the chloroplast is not folded
(Fig. 2.28). The liquid part of the chloroplast is called the stroma and it is here that stacks of membranes
called thylakoids are found. Each stack or group of thylakoids is termed a granum (plural: grana) and the
chlorophyll is found on these membranes.
a Double b
membrane
Granum Double
(a stack of lamellae membrane
Starch grain is a granum)
in stroma
FIGURE 2.28 a Diagram of chloroplast seen in longitudinal section; b electron micrograph of a chloroplast
The layering of the membranes increases the surface area over which chlorophyll occurs, allowing
a large amount of sunlight to be absorbed for the process of photosynthesis. This captured energy of
sunlight is then used by the plant to make simple sugars. All the enzymes needed for photosynthesis
are present in the stroma, and simple sugars made during photosynthesis are stored in the stroma as
starch grains.
Chromosome Centrioles
The cellulose cell wall that surrounds plant cells differs from the cell
membrane inside it. The cell wall is not selective in terms of what substances
it does or does not allow into the cell. Its structure allows it to provide
strength and support. The strands of cellulose fibres have a little elasticity
and are somewhat flexible so they can resist pressure. Some cell walls are
thickened with additional chemicals that make the walls hard and woody (for
example, in tree trunks) or that provide waterproofing (for example, in cork
Spindle
or the waxy cuticle of leaves). Cell walls are permeable to most molecules.
FIGURE 2.29 Centrioles forming the spindles,
which hold the chromosomes in a dividing cell Centrioles – spindle production in cell division
A dense, granular structure, the centrosome, is often found near the nucleus
Science Photo Library/DR TORSTEN WITTMANN
● Organelles are membrane-bound internal structures, each with a specific function to ensure the
WS
efficient functioning of the cell.
Cell structure
● Most organelles have structures that maximise the surface area.
● Organelles and other cell structures vary in size, with only the cell membrane, cell wall, nucleus,
chloroplasts and vacuoles being big enough to be observed using a light microscope.
● The function of organelles and other cell structures is summarised in Table 2.2.
TABLE 2.2
ORGANELLE/ FUNCTION
CELL STRUCTURE
Membranes Selectively permeable boundaries, control the movement of substances into
and out of the cell/organelle
Protoplasm The living content of a cell that is surrounded by the cell membrane
Nucleus The control and information centre
Endoplasmic reticulum Transport and processing of proteins and lipids
Golgi bodies Packaging and sorting the products
Ribosomes Protein synthesis
Lysosomes Digestion and cell destruction
Mitochondria Cellular respiration – production and storage of energy (ATP)
Vacuoles Storage and support
Chloroplasts Photosynthesis
Plant cell wall Shape and support
Centrioles Spindle production in cell division
Cytoskeleton Cell shape, organelle placement and movement and cell division
Water
The lipid components of all membranes allow them to be flexible and repair themselves. This means
that the cells can change shape and grow. Cell membranes are able to break and reassemble themselves
during processes such as cell division.
This structure forms the basis of the cell membrane and all other membranes within cells, such as
those surrounding organelles. Proteins are then interspersed throughout this structure.
Membrane proteins
Protein molecules are scattered throughout, and suspended in, the lipid bilayer. Some proteins penetrate
all the way through the bilayer, forming channels that allow some materials to cross the membrane.
Other proteins may be partly embedded in the membrane. It seems that some proteins are fixed in place,
while others travel about freely. The proteins are described as ‘floating’ in the lipid bilayer ‘like icebergs in
a lipid sea’, giving a mosaic effect (Fig. 2.33).
Extracellular environment
Intracellular environment
FIGURE 2.33 A view of the fluid mosaic model of part of the cell membrane, showing embedded proteins
INVESTIGATION 2.2
AIM
To model the structure and function of the fluid mosaic model of the cell membrane
MATERIALS
Structure:
• rectangular cake or polystyrene block approximately 20 cm 3 10 cm 3 10 cm
• knife
• icing sugar, food colouring or fondant or buttercream
• marshmallows
• liquorice or modelling chocolate
• selection of lollies
• labels/toothpicks
Function:
• 2 × tea strainers
• icing sugar
• lollies, such as Smarties
• elastic band
• coloured paper
• salt
• sugar granules
• tea leaves
Knife/scalpel Sharp edges can cause cuts Use knife/scalpel with care and keep fingers away from sharp edge
of knife.
Traces of chemicals Contamination of table tops Do not eat the cake if it was prepared in a science laboratory.
METHOD
Structure
1 Trim cake to approximately the suggested size.
2 Using fondant or icing, completely coat the surface of the cake.
3 Place marshmallows to completely cover the top surface of the cake. Then place one line of marshmallows
along the top and bottom of all sides of the cake, lined up with the marshmallows on the top edge of the cake.
4 Using liquorice or modelling chocolate, make ‘tails’. Stick two of these tails per marshmallow onto the side
of the cake, leading from the marshmallow to the centre.
5 Using modelling chocolate or lollies, construct ‘proteins’ that penetrate the whole cell membrane layer, and
‘proteins’ that are only partially embedded in the membrane.
6 Attach lollies or modelling chocolate to some of these ‘proteins’ to represent the glycoproteins.
7 Use lollies or modelling chocolate to represent cholesterol and phytosterols.
8 Attach labels to all parts of the model.
Function
9 Place two teaspoons of icing sugar and two teaspoons of lollies into one of the tea strainers.
10 Tie the handles of the tea strainers together with the elastic band.
11 Shake the tea strainer over a piece of coloured paper.
12 Record in the table provided which substances pass through.
13 Repeat this process using a variety of other substances (those on the equipment list or others).
RESULTS
Structure
1 Draw a diagram or take a photo of your model.
2 Copy and complete Table 2.3 to indicate what each part of your model represents in the fluid mosaic model.
TABLE 2.3
WS
STRUCTURE IN FLUID MOSAIC MODEL REPRESENTATION IN YOUR MODEL
Function
1 Draw a diagram or take a photo of your model.
2 Complete Table 2.4 to indicate what each part of your model represents in the fluid mosaic model.
TABLE 2.4
SUBSTANCES IN MIXTURE SUBSTANCES THAT PASSED THROUGH HOLES IN TEA STRAINER
Icing sugar and lollies
CONCLUSION
Write a summary statement that relates to the aim of this investigation, including a brief summary of what you
did and what you found.
KEY CONCEPTS
● The cell membrane is selectively permeable and performs the function of controlling the
movement of substances into and out of the cell.
● The currently accepted model of the structure of the cell membrane is the fluid mosaic model.
● This model depicts a ‘fluid’ phospholipid bilayer with different types of proteins embedded in
it, creating a ‘mosaic’ effect. Proteins either penetrate from one side to the other or are only
partially embedded.
● Some membrane proteins form pores (temporary or permanent), some form active carrier
systems or channels for transport, and others (glycoproteins) have carbohydrates attached for
cell recognition.
● Cholesterol (in animals) or phytosterols (in plants) provide some flexibility to the membrane.
● Models are used in science for a number of reasons, including to simplify a concept, make a
visual representation of something that can’t be seen, or make predictions of expected results.
● Before a model is accepted, it needs to be validated – that is, certain predictions should be made
and, when tested using the model, should hold true.
● When modelling a concept in the laboratory, all parts of the model should be related to actual
parts of what is being modelled.
● The limitations of the model should also be documented.
CHECK YOUR
1 Explain the structure of a lipid bilayer. UNDERSTANDING
2 Outline the fluid mosaic model of the cell membrane.
3 List the proteins found in the cell membrane and state the function of each.
2.5
4 Explain why models are used in science and how they are validated.
5 a Sketch a two-dimensional scientific diagram of the transverse section of a cell membrane.
b Label all the different parts.
c Outline the function of each part that you have labelled.
6 Explain why the cell membrane needs to be selectively permeable for a cell to function.
Golgi apparatus:
Packaging and
sorting the products
Mitochondrion:
Cellular respiration
Ribosomes:
Protein synthesis
Bacterial
flagellum
Nucleolus: Manufacture Nucleus: The control and
ribosomes information centre
Cytoplasm
Capsule Chromosome: Cell Plasmid: COMPARISON OF ANIMAL AND PLANT CELLS
DNA membrane DNA
BIOLOGICAL DRAWING
Nucleolus
Cytoplasm Nucleus
Mitochondrion 12 mm
Cheek cell
Hydrophilic
head containing
phosphate
Hydrophobic tail
made of fatty
acid side chains
Transport Receptor Recognition Adhesion Phospholipid
protein protein protein protein bilayer
Intracellular environment
Eye
Science Source/Ted Kinsman
Eyepiece Source of
Coarse electrons
adjustment Ocular lens
Fine
adjustment Specimen
Objective lens
Electromagnetic
lenses
Specimen
Stage Eye
Condenser lens
Condenser Light source
adjustment
Base/foot
From Jekle, M., Becker, T.: Wheat dough microstructure: The relation between visual structure and mechanical behavior. Critical
reviews in food science and nutrition 55 (2015), 369–382
Review quiz
1 a Identify the features that are common to all cells. 9 Draw a scaled diagram of an animal cell that is circular and
b Outline the features that are unique to: has a diameter of 10 μm.
i prokaryotic cells 10 Copy and complete Table 2.5 to outline the structure and
ii eukaryotic cells. function of the organelles listed.
FIGURE 2.34 An unidentified cell 16 Identify the structures in the cell membrane that are
responsible for each of the following characteristics of the
cell membrane:
5 Outline how advances in technology have contributed to a flexibility
our knowledge about cells. b movement of ions into cells
6 Draw up a table to compare the following types of c ability to bind hormones.
microscopes. Headings that could be used in your table
could be: ‘Energy source’, ‘Focus’, ‘Specimen preparation’, 17 Outline the role of receptor proteins in cell membranes.
‘Magnification’, ‘Resolution’, ‘Can live specimens be viewed?’ 18 a In the model of the cell membrane, which section is
and ‘Advantages and disadvantages’. identified as the ‘fluid’ part and which is identified as
a Light microscope the ‘mosaic’ part?
b SEM b Explain why these terms are used.
c TEM 19 Using examples, describe how the structures of organelles
7 Outline the advantages of fluorescence microscopy. are related to their function.
64 11 » »CHEMISTRY
CHAPTER ONE
MODULE CELLS AS THE BASIS OF LIFE 9780170407281
3 Cell function
INQUIRY
QUESTION Students:
How do cells • investigate the way in which materials can move into and out of cells, including but not limited to:
coordinate activities – conducting a practical investigation modelling diffusion and osmosis (ACSBL046) ICT
within their internal – examining the roles of active transport, endocytosis and exocytosis (ACSBL046)
– relating the exchange of materials across membranes to the surface area to volume ratio, concentration
environment and
gradients and characteristics of the materials being exchanged (ACSBL047) ICT N
the external
• investigate cell requirements, including but not limited to:
environment?
– suitable forms of energy, including light energy and chemical energy in complex molecules (ACSBL044)
– matter, including gases, simple nutrients and ions
– removal of wastes (ACSBL044)
• investigate the biochemical processes of photosynthesis, cell respiration and the removal of cellular products
and wastes in eukaryotic cells (ACSBL049, ACSBL050, ACSBL052, ACSBL053) ICT
• conduct a practical investigation to model the action of enzymes in cells (ACSBL050)
• investigate the effects of the environment on enzyme activity through the collection of primary or secondary
data (ACSBL050, ACSBL051) ICT N
Biology Stage 6 Syllabus © NSW Education Standards Authority for and on behalf of the Crown in right of the State of New South Wales, 2017
9780170407281 65
The development of technologies to view the internal structure of cells enabled scientists to determine
the different types of cells and the structures they possess. With this knowledge our curiosity about how
cells function grew. Further development of technologies led to the study of the biochemical processes
of photosynthesis and cellular respiration, which are carried out by cells in their internal environment to
ensure the efficient and successful functioning of the organism. In order for these biochemical processes
to occur, cells must obtain the materials necessary from their external environment and must be able to
remove any wastes produced from their internal environment (Fig. 3.1) and coordinate these activities.
iStock.com/micro_photo
requirements and
waste removal
Coordination of the biochemical activities of the cell to ensure efficient cellular metabolism is the
responsibility of the nucleus. The cell membrane controls the movement of cellular requirements from
the external environment of the cell into the cell and the removal of cellular products and wastes from
the internal environment of the cell into the external environment.
Movement of materials
3.1
in and out of cells
For any cell to function effectively, it must interact with its surrounding environment and with the
cells that surround it. Substances required by cells for their functioning need to move into the internal
environment of cells and waste substances and cellular products need to pass out of cells into the external
environment. These substances move from the internal environment to the external environment by
passing through the cell membrane.
Substances needed by cells are gases (oxygen and carbon dioxide), nutrients (sugars, amino acids,
glycerol and fatty acids) and water, the main solvent in cells. Mineral salts dissolved in the water are also
required. Substances that must leave cells are wastes such as urea, uric acid and excess carbon dioxide.
They could also be products secreted by cells that may be needed to coat the outside of cells (for example,
mucus) or may pass to other cells (for example, hormones).
In both plant and animal cells, the cell membrane is in direct contact with the cytoplasm inside the
cell. The cell membrane is selectively permeable (or sometimes referred to as differentially permeable),
meaning it controls what passes across it (Fig. 3.2). The membrane controls the passage of water
and other molecules (many in a dissolved form) into or out of living cells. In contrast to the selectively
Specific
cell membrane is
non-lipid-soluble Non-lipid-soluble selectively permeable,
molecules or ions molecules allowing some
Lipid-soluble materials through but
molecules not others.
Membrane
channel
Concentration
gradient
To understand how the cell membrane controls and regulates the movement of substances, biologists
examine the structure of the cell membrane and relate this to its functioning.
Diffusion
The movement of materials into and out of cells takes place either passively or actively. Passive movement
requires no energy input and includes the processes of diffusion and osmosis.
Diffusion is the net movement of any molecules from a region of high concentration to a region of
low concentration of that substance, until equilibrium is reached (Fig. 3.3). Equilibrium is reached when
the there is no net movement of molecules in either direction – the molecules move equally in each
direction. This process does not require an energy input.
GIPhotoStock/Science Source
FIGURE 3.3 Diffusion of potassium permanganate in water from a region of high concentration until the potassium
permanganate is evenly distributed throughout the water.
For example, if someone sprays a burst of perfume in the back corner of a laboratory, the students
closest to the corner (where the perfume is the most concentrated) will smell it quickly. Students at
the front of the room (where the concentration of perfume particles is very low) will not smell it until
some time later. The perfume molecules will gradually move from the back of the room where it has
the highest concentration to the front of the room where it has the lowest concentration. This will
continue until the concentration is the same throughout the whole room (that is, it is in equilibrium).
The perfume is said to have diffused throughout the laboratory. No energy input has been required
for this process to occur.
Movement from a high concentration to a low concentration is described as movement along a
concentration gradient (a gradient is a slope). Molecules moving down a concentration gradient can be
likened to the movement of rocks rolling down a hill, needing no energy input.
The rate of diffusion changes depending on the concentration gradient. If there is a greater
difference in the concentration of substances, the concentration gradient will be steeper and diffusion
will occur faster.
Diffusion can also speed up or slow down, depending on the temperature: heat increases the rate of
diffusion because the kinetic energy of the particles increases.
FIGURE 3.4
Glass rod Investigation set-up
Starch solution
Dialysis
tubing
Water 1 iodine
potassium
iodide solution
AIM
To model the process of diffusion through the cell membrane
MATERIALS
• 2 3 800 mL beakers
• Starch solution
• Iodine potassium iodide (IKI) solution
• 2 3 20 cm section of dialysis tubing
• Filter funnel
• Fine string or cotton thread
• 50 mL measuring cylinder
• 2 3 glass rod
• Scissors
RISK ASSESSMENT
!
WHAT ARE THE HAZARDS? WHAT RISK DOES THIS HAZARD POSE? HOW CAN YOU SAFELY MANAGE THIS RISK? RISK
ASSESSMENT
Iodine potassium iodide Irritant to skin and eyes Do not ingest chemical.
solution Poisoning if ingested Do not use in confined spaces.
Irritant if inhaled Wear safety glasses.
1 Use one of the beakers to soak the dialysis tubing in water for 5 minutes.
2 Fill the other beaker three-quarters full with tap water. Add 10 drops of IKI solution and mix.
3 Remove the tubing from the water and, under running water, rub the end of the tubing between your
fingers to separate the sides.
4 Tie one end very securely with string.
5 Measure 30–40 mL of starch solution into the measuring cylinder and pour into the tubing using a filter funnel.
6 Tie off the top end of the tubing very securely with string, leaving a length of string to secure the tubing
to the glass rod.
7 Wash the outside of the tubing.
8 Tie the end of the string to the middle of the glass rod.
9 Place the rod across the top of the beaker to suspend the tube containing the starch solution in the
water 1 iodine potassium iodide solution. Ensure that the tube is fully submerged.
10 Leave undisturbed for 15–20 minutes.
11 Observe and record any colour changes that occur.
12 Use the other beaker to set up a control, leaving out the iodine potassium iodide solution.
RESULTS
Record your observations in a table like Table 3.1 for the experiment and control.
TABLE 3.1
WS
SOLUTION INITIAL COLOUR FINAL COLOUR
Investigation 3.1
Starch
Control
DISCUSSION
1 Copy and complete Table 3.2, which identifies the correlation between your model of diffusion and
diffusion across the cell membrane.
TABLE 3.2
2 Using the results obtained, copy and complete Table 3.3, which indicates the initial and final concentrations
of starch molecules and iodide ions both inside and outside the dialysis tubing. Use terms such as ‘highly
concentrated’, ‘none present’, ‘decreased concentration’, ‘increased concentration’, and ‘no change’.
Iodide ions
Starch molecules
3 Describe evidence from your investigation to support your conclusions in Table 3.3 about the change/no
change in the concentration of:
a iodide ions
b starch molecules.
4 Explain how this investigation has modelled the process of diffusion through the cell membrane. Use
the term ‘concentration gradient’ and ‘control’ and refer to the selectively permeable nature of the cell
membrane and to the size of the molecules.
5 Discuss the benefits and limitations of the model.
CONCLUSION
Write a conclusion to link your results to the aim of the investigation.
High concentration
Lipid
bilayer Concentration
of cell gradient
membrane
Low concentration
FIGURE 3.5 Simple diffusion of small molecules through the cell membrane is dependent on the concentration gradient.
Facilitated
diffusion
Facilitated diffusion Watch the
Relatively large molecules (such as glucose and amino acids) and charged particles (such as sodium and animation about
facilitated diffusion
chloride ions) do not readily pass through the phospholipid bilayer. They require certain proteins called and create a dot
point summary of
carrier proteins and channel proteins in the cell membrane to assist them in diffusing into the cell. This the process.
process is called facilitated diffusion.
High concentration
Concentration
gradient
FIGURE 3.6 Facilitated diffusion using a carrier protein in the cell membrane of a cell moves particles such as glucose along
the concentration gradient.
Small ions such as sodium ions diffuse rapidly through the cell membrane, from a high ion
concentration to a low ion concentration, via narrow passageways called channel proteins. These
channel proteins are specific for particular ions (Fig. 3.7).
Roberts, Reiss & Monger (Nelson Thornes Ltd 2000)
Adapted from Biology: Prinicples & Processes by
High concentration
Concentration
gradient
FIGURE 3.7 Facilitated diffusion through a channel protein in the cell membrane of a cell. Movement is along the
concentration gradient.
KEY CONCEPTS
● Diffusion is the movement of particles from a region of high concentration to a region of low
concentration until equilibrium is reached.
● At equilibrium, there is no net movement of particles in either direction.
● Diffusion does not require the input of energy.
● Diffusion occurs faster with a higher temperature or a steeper concentration gradient.
● Small, uncharged molecules such as oxygen and carbon dioxide will diffuse easily across the
cell membrane.
● Facilitated diffusion allows larger molecules and small electrically charged ions to diffuse
across the cell membrane aided by carrier or channel proteins.
FIGURE 3.8
a b
Solute Solutions: a a
particles Solute concentrated
particles solution (low water
concentration – high
solute concentration);
b a dilute solution
(high water
concentration – low
Solvent solute concentration)
particles Solvent
(H2O) particles
(H2O)
Water is very important to living things. It is the medium in which many of the biochemical reactions
in cells occur. Water helps keep cells in shape, it forms the fluid that bathes tissues and it also transports
materials in solution.
A solution is formed when a solute (such as salt or sugar) dissolves in a solvent. The amount of solute
dissolved in a given quantity of solvent determines the concentration of the solution.
Water is the most common solvent in a solution. A concentrated solution contains a large amount of
solute in relation to the amount of water, so the water is said to be in low concentration. A dilute solution
contains a small amount of solute in relation to the amount of water and the water is said to be in high
concentration.
Osmosis is the process by which water moves through the cell membrane. Because water is not lipid-
soluble, the movement is not directly through the lipid bilayer. Water moves through special tiny protein
channels in cell membranes called aquaporins (‘water pores’).
◗ When water is more highly concentrated outside the cell (low solute concentration) than it is inside
the cell (high solute concentration), water will move by osmosis through the selectively permeable
cell membrane into the cell and the cell may swell up.
◗ Alternatively, if the concentration of water is lower outside the cell than inside, water will move out of
the cell by osmosis and the cell may shrink.
The pressure created by water moving across a semipermeable membrane due to osmosis is called
the osmotic pressure. The more water that moves across the membrane, the higher the osmotic pressure
created (Fig. 3.9).
If the fluids inside and outside a cell are of equal solute concentration, the external solution is said
to be isotonic (‘iso’ 5 same) to the cell contents; water molecules jostle on both sides of the membrane,
moving in both directions equally (Fig. 3.10). When cells are surrounded by a solution that contains a
lower solute concentration than their cytoplasm, the external solution is said to be hypotonic (‘hypo’ 5 Osmosis
lower) to the cell contents. Net movement of water molecules will be through the membrane into the Explain the process
of osmosis. Define
cells (Fig. 3.11). The reverse applies if the cells are surrounded by a solution of higher solute concentration: the terms ‘isotonic’,
the external solution is hypertonic (‘hyper’ 5 higher) to the cells and net movement of water molecules ‘hypertonic’ and
‘hypotonic’.
will be out of the cells.
FIGURE 3.10
Isotonic solutions
separated by a
semipermeable
membrane will show
no net movement of
water molecules.
AIM
To model the process of osmosis
MATERIALS
• 3 3 600 mL beakers
• Distilled water
• Sucrose solution
• Fine string
• 2 3 glass rods
• 2 3 20 cm strips dialysis tubing
• 25 mL measuring cylinder
• 100 mL measuring cylinder
• Filter funnel
• Marking pen
• Plastic clingwrap
• Digital camera (optional)
RISK ASSESSMENT
WHAT IS THE HAZARD? WHAT RISK DOES THIS HAZARD POSE? HOW CAN YOU SAFELY MANAGE THE RISK?
!
RISK
Broken glass Injury to body Take care at all times when using glassware. ASSESSMENT
METHOD
1 Cut two pieces of dialysis tubing to 20 cm lengths and soak in a beaker of water for about 5 minutes.
2 Tie one end of each piece of tubing securely with a piece of string, leaving the other end untied.
3 Run the untied end of the tubing under water and rub it between your fingers to open it.
4 Using a filter funnel and a measuring cylinder, pour a measured volume (about 30–35 mL) of sugar solution
into the tubing so that the tubing is two-thirds full. (Record the exact volume of sugar solution used.)
5 Tie the top of the tubing with string. Attach it to a glass rod as shown in Figure 3.12. This is your
experimental apparatus.
6 Repeat the previous two steps, this time filling the tubing with distilled water instead of sugar solution. This
is your control apparatus.
7 Using a measuring cylinder, fill each beaker about half-full and record an accurate measurement of the
volume of water in each.
8 Suspend the experimental and the control apparatus each in a beaker of distilled water as shown in
Figure 3.12. Ensure that the tied ends of the dialysis tubing are just above the distilled water in the beaker
to prevent leakage. Do not have the tubing too far out of the water because evaporation may occur and
this will interfere with the accuracy of your results.
Dialysis tubing
(semipermeable Distilled
membrane) water
Sugar solution
Distilled water
Experiment Control
RESULTS
Your results will be both quantitative (measured quantities such as the volume of sucrose solution) and
qualitative (descriptive and with diagrams).
1 Draw up a suitable table to record your measurements.
2 Describe any change in water levels in both the beakers and the dialysis tubing. Diagrams are often useful
tools to aid descriptions.
DISCUSSION
TABLE 3.4
CONCLUSION
Write a conclusion to link your results to the aim of the investigation.
KEY CONCEPTS
Cytoplasm
Vacuole
containing
cell sap
Water leaves
Partially turgid vacuole by osmosis
plant cell
Vacuole shrinks,
b Cell placed in external cytoplasm moves inwards
solution whose solute
concentration is higher
than that of the cell sap
Full plasmolysis
FIGURE 3.13 The effect of immersing a partially turgid plant cell in a pure water (hypotonic solution) and b a high solute concentration (hypertonic solution)
CHECK YOUR
UNDERSTANDING 1 Draw a generalised diagram to represent a cell. On this diagram, indicate with arrows going into the cell
the substances that a cell requires. Also indicate the wastes that have to be removed from the cell, using
3.1a arrows pointing out of the cell.
2 Distinguish between a permeable membrane and a selectively permeable membrane.
3 a Identify and outline three characteristics of molecules that affect the permeability of the cell membrane
to them.
b Indicate whether each of the following substances can move easily through the cell membrane or not.
Justify each of your answers.
i Neutral molecules such as carbon dioxide and oxygen gas
ii Sodium and potassium ions
iii Water and ethanol
iv Large molecules such as proteins
4 A sugar solution is a mixture of sugar and water.
Identify the a solute and b solvent.
5 a Outline the process of diffusion.
b Identify two factors that could increase the rate of diffusion.
6 a Identify the substances that are able to move across the cell membrane by diffusion.
b Describe the process of facilitated diffusion.
c Which substances move across the cell membrane using this process?
7 a Describe the process of osmosis.
b What is the relationship between diffusion and osmosis?
c Define the terms ‘isotonic’, ‘hypotonic’ and ‘hypertonic’.
FIGURE 3.14
9 If salad greens such as celery are left on the kitchen bench for a period, they become limp. To restore their
crispness, you can soak them in cold water. Explain why this occurs.
Active transport
Active transport is the movement of molecules from a region of low concentration to a region of high
concentration, and requires the input of energy. This movement goes against the concentration gradient and
involves movement across a cell membrane that has receptors for the molecules.
Diffusion and osmosis both rely on a concentration gradient to direct the passive flow of substances from
regions of high concentration to regions of low concentration. Sometimes in living things, a chemical may need
to be moved against the concentration gradient, such as when kidney cells reabsorb glucose and amino acids
so they are not lost in urine. Active transport requires a carrier protein that spans the membrane to actively
move chemicals from a low to a high concentration, utilising cellular energy (Fig. 3.15).
Concentration
gradient
High concentration
FIGURE 3.15 Active transport via a carrier protein in the cell membrane of a cell. Energy is transferred to the carrier protein, enabling it to move the
particles against a concentration gradient.
Solute
High concentration
of solute
Diffusion: the movement of any Osmosis: the movement of water Active transport: the movement
type of molecule from a high to molecules from a high of molecules from a low
a low concentration, until concentration of water to a low concentration to a high
equilibrium is reached concentration of water, through concentration through selectively
selectively permeable membrane permeable membrane
Molecule to be transported
Carrier
proteins
Channel
Extracellular
protein Concentration
space
gradient
Lipid
bilayer
Cytoplasm
Energy
Simple Channel- Carrier-
diffusion mediated mediated
transport transport
Active transport
Passive transport
(facilitated diffusion)
FIGURE 3.16 Diffusion, osmosis and active transport across cell membranes
Comparing
processes
View the animation to
KEY
CONCEPTS
compare the processes ● Active transport is the movement of molecules from a region of low concentration to a region of
of diffusion, facilitated
diffusion and active high concentration.
transport. ● Active transport moves against the concentration gradient and requires the input of energy.
TK
either diffusion or active transport need to enter or leave a cell.
Endocytosis
When a large particle has to be moved into a cell, the cell membrane can change
its shape to surround the particle and engulf it by the process of endocytosis.
If a solid particle is engulfed, the process is termed phagocytosis (‘cell eating’).
Sometimes fluid is engulfed and the process is then called pinocytosis (‘cell
drinking’).
One example of phagocytosis occurs when a unicellular amoeba feeds on
a smaller organism. The amoeba changes shape by sending out membrane
projections filled with cytoplasm that surround the prey. When the cell
membrane of the projections meets, membrane fusion occurs. This results in FIGURE 3.17 A scanning electron micrograph
of an amoeba surrounding its prey (Tetrahymena)
the formation of a vesicle, which then stores or transports the material within for ingestion
the cytoplasm (Figs 3.17 and 3.18).
Pinocytosis occurs when the cell membrane engulfs a drop of extracellular fluid in much the same
way as phagocytosis (Fig. 3.19). Fat droplets found in the small intestine after a meal move into cells by
means of pinocytosis.
FIGURE 3.19
The process of
pinocytosis
Cytoplasm
Exocytosis
Specialised animal and plant cells produce a variety of substances, such as antibodies, neurotransmitters
and enzymes, that have important functions elsewhere in the organism. These substances are
contained within vesicles inside the cell. Cells also produce waste products that need to be moved
out of the cell. Exocytosis is the process by which these substances are transported to the external
environment of the cell.
Movement in and
out of cells
Cytoplasm
KEY CONCEPTS
● Endocytosis moves large molecules that cannot cross the cell membrane into a cell. It requires
the expenditure of energy.
● In endocytosis, the cell membrane changes shape and surrounds and engulfs the particle so
that it enters the cell.
● Phagocytosis is the process whereby solid particles are engulfed by the cell membrane.
● Pinocytosis is the engulfing of fluid substances by the cell membrane.
● Exocytosis involves a membrane-bound vesicle moving to the cell membrane, fusing with it and
then releasing its contents to the exterior of the cell.
CHECK YOUR
UNDERSTANDING 1 Define the process of active transport and provide an example of where this occurs.
2 Distinguish between the processes of active transport and simple diffusion.
3.1b 3 Describe the process of endocytosis and provide an example of where it is used.
4 Describe how the cell membrane is involved in each process listed below and provide an example of the
use of each:
a exocytosis
b endocytosis.
5 Identify three types of substances that are removed from cells.
Chemical factors
The chemical properties of a substance affect its transport across cell membranes. Many uncharged
molecules, such as ethanol, can easily penetrate the cell membrane because they can dissolve in the
Crossing the cell
membrane phospholipid bilayer. Hydrophilic, charged ions such as sodium (Na+) and potassium (K+) cannot cross
View the animation the hydrophobic centre of the membrane. Channel proteins specific for each ion allow their movement
to determine how
different substances through the cell membrane.
cross the cell Water is not lipid-soluble and therefore cannot move through the hydrophobic ‘tails’ in the cell
membrane.
membrane. Water moves through the membrane through the special aquaporins.
Concentration gradient
The relative concentration of the substance on either side of the membrane affects the rate of diffusion
of that substance. If the concentration gradient is high (that is, there is a large difference between
the concentrations on either side of the membrane), then the substance will diffuse rapidly. As the
concentration gradient decreases, the rate of diffusion will be slower. In order to maintain a rapid rate
of diffusion, cells need to maintain a high concentration gradient. When the concentration reaches
equilibrium, there will be no net movement across the cell membrane.
Plant cells carry out a process called cytoplasmic streaming, which involves organelles and cytosol
flowing around the cell in a circular movement. This enables the cell to maintain a steeper concentration
gradient as materials that diffuse into the cell are rapidly moved to another area of the cell.
Surface-area-to-volume ratio
The surface area (SA) divided by the volume (V) is called the surface-area-to-volume ratio (SA:V). This
also affects the movement of substances into and out of the cell through the cell membrane.
The surface area of a cell is the total area of the cell membrane that is around the cell. The volume of
the cell is the space taken up by the internal contents of the cell (that is, the cytoplasm and the nucleus).
A cell needs to have enough surface area to supply its volume with requirements and remove wastes.
The SA:V of a cell has a large impact on the movement of substances into and out of cells. A smaller
cell has more surface area in relation to its volume – a higher SA:V. Think of the distance from the surface
of a small cube to its centre. This distance is much less than the distance from the surface to the centre
in a large cube. Therefore, a smaller size allows a faster movement of substances between the centre and
the surface of the cell (that is, into or out of the cell). Anything that the cell needs can get to all parts of a
small cell quickly and wastes can be removed easily. This then allows the cell to perform at an optimum
level of functioning. Figure 3.21 illustrates SA:V for simplified cubic cells, but SA:V is important for the
movement of substances into and out of cells of any shape.
Nucleus
Nucleus
Nucleus
A larger cell has a smaller amount of surface area in relation to its volume – a lower SA:V (the centre
of the cell is further from the surface). This means the efficiency with which a cell obtains its nutrients
and removes its wastes is reduced as its size increases. A cell increasing in size reaches a point where the
inward movement of essential substances and the outward movement of wastes across the surface area
by diffusion are not fast enough to service the increasing volume of the cell. When a cell reaches this size,
if it is capable of dividing it will often do so. For this reason, individual cells tend to be very small.
Surface area
Area of one of cube 5 length 3 width 3 6
Area Height
side 5 length 3 width Length Volume of
cube 5 length × width 3 height Length
Width
Width
ANSWER LOGIC
Surface area of a cube 5 6 3 length of side 3 width of cell • Insert the correct formula. (Note: a cube has six sides.)
Surface area 5 6 3 1 3 1 • Extract the data from the question and insert into the formula.
5 6 cm2 • Calculate the answer.
Surface area: volume (SA:V) 5 6 4 1 • Calculate SA:V. Insert the numbers into the formula.
5 6:1 • Calculate the answer.
The shape of the cell also makes a difference to the SA:V. Spherical cells have a relatively small SA:V
compared with cells of other shapes. Long, flat cells have a higher SA:V than a spherical cell with the
same volume.
Table 3.5 shows the SA:V for three hypothetical spherical cells. It demonstrates that the smaller cell
A with a diameter of 1 mm has a higher SA:V of 6:1 than the larger diameter cells B and C. Cell B has a
SA:V of 3:1 and cell C a SA:V of 2:1. This means that for each unit of volume, cell A has 6 units of surface
area, cell B has 3 units of surface area and cell C has 2 units of surface area. It then follows that the
inward movement of essential substances and the outward movement of wastes across the surface area
by diffusion would occur much more rapidly in cell A than in cell B and be slowest in cell C.
KEY CONCEPTS
Getty Images/Science Photo
Library/Andrew Syred
● SA is calculated by finding the total area of the surface
of the shape.
● Volume is the total space that a shape takes up.
WS
● SA:V is calculated by dividing the surface area of an
object by its volume.
Surface-area-to-
● The surface-area-to-volume ratio (SA:V) of a cell will volume ratio
determine how efficiently substances move into and
out of a cell.
● A high SA:V allows the most efficient movement of
substances into and out of the cell.
FIGURE 3.23 Scanning electron ● Large cells have a low SA:V. Small cells have a large
micrograph of root hairs in oregano,
SA:V.
Origanum vulgare. The root hairs greatly
increase the surface area for absorption ● Long, flat cells have a higher SA:V than a spherical cell
of water. with the same volume.
CHECK YOUR
1 Explain how the following factors affect the movement of substances across cell membranes. Provide UNDERSTANDING
examples to support your explanation.
a Physical factors b Chemical factors 3.1c
2 Describe how the concentration gradient affects the rate of diffusion into and out of the cell.
3 a Define the following terms in relation to a cell:
i surface area ii volume iii SA:V.
b Describe the importance of SA:V in relation to the movement of substances into and out of a cell.
4 Explain how increasing the size of a cell affects the cell’s ability to obtain and remove substances by
diffusion.
5 Figure 3.24 represents two cells with the same volume: (a) a flattened cell and (b) a cube-shaped cell.
h
a Flattened cell
w
l To calculate surface area (mm2)
h SA 5 6 3 (l 3 h)
To calculate volume (mm3)
To calculate surface area (mm2) V5l3w3h
SA 5 2 3 (l 3 w) 1 2 3 (w 3 h) 1 2 × (l 3 h) Example
To calculate volume (mm3)
V5l3w3h
Example 1 mm
1 mm
1 mm
2 mm 1 mm
0.5 mm
TABLE 3.6
a Flattened cell
b Cube-shaped cell
b Which cell would be more efficient in obtaining nutrients and removing wastes? Explain your answer.
Inorganic nutrients
Some inorganic nutrients that occur in cells are listed in Table 3.7.
Carbohydrate
(e.g. starch)
Biomacromolecules
Nucleic acid
(e.g. DNA)
Protein
(e.g. enzyme)
Plants and other organisms that carry out photosynthesis absorb inorganic nutrients from the soil
and the air and use these to make their own organic nutrients. In contrast, organisms that do not carry
out photosynthesis need to ingest food to obtain organic nutrients for their cells.
Carbohydrates
Carbohydrates are a group of organic molecules made up of carbon (C), hydrogen (H) and oxygen (O)
atoms in the ratio of 1:2:1, giving the general formula for carbohydrates as (CH2O)x.
Carbohydrates are classified as monosaccharides (simple sugars), disaccharides and polysaccharides
(see Table 3.8) depending on how many monomers are linked. The product of photosynthesis, glucose, is
a monosaccharide.
Proteins
Proteins are made up of the elements carbon, hydrogen, oxygen, nitrogen, and sometimes sulfur. These
elements combine to form amino acids, which are the building blocks of proteins.
There are about 20 different amino acids; they can be put together in chains of up to 300 amino acids
to form a peptide/polypeptide chain (Fig. 3.27). Proteins are made up of one or more of these polypeptide
chains twisted together into a particular shape. The DNA in the nucleus of the cell controls the sequence
and arrangement of the amino acids, and this determines the type of protein.
FIGURE 3.28
P Nucleotide
S B monomer, made
S B S B B S
up of phosphate
Nucleotide
P (P) – sugar (S) – base
P P (B), and segments
of RNA and DNA
S B S B B S biomacromolecules.
RNA usually consists
P P P
of a single chain,
whereas DNA consists
S B S B B S of two chains in
opposite directions.
P P P
S B S B B S
S B
DNA
P
S B
P
S B
RNA
KEY CONCEPTS
● The four main groups of biomacromolecules are carbohydrates, proteins, lipids and nucleic
acids.
● These four groups of organic compounds are made up of carbon, hydrogen and oxygen atoms,
but they are in different proportions. Proteins also contain nitrogen and sometimes sulfur.
Nucleic acids also contain nitrogen and phosphorus.
● Autotrophic organisms can build their own organic compounds, whereas consumer organisms
must make their organic compounds from their food.
● Carbohydrates can be used as a source of energy, for storage of energy, and sometimes as a
structural component of the cell.
● Lipids are used for energy storage, structural parts of membranes and components of hormones.
● Proteins have a structural role in cells and tissues. Proteins such as enzymes also have a
functional role.
● The two types of nucleic acids are DNA (deoxyribonucleic acid) and RNA (ribonucleic acid).
● DNA contains chemical information that controls the cell activities and the production of
proteins. RNA assists in the manufacture of the proteins.
3.3 Enzymes
Enzymes are protein molecules that control all metabolic reactions in living cells. Without enzymes,
the reactions that occur in cells would be so slow as to hardly proceed at all. Enzymes act as biological
catalysts, controlling the rate of each step of the complex chemical reactions that take place in cells.
Catalysts are chemical substances that can accelerate (speed up) chemical reactions, are unchanged at
the end of the reaction, and can be reused many times.
Metabolism is the sum of all chemical reactions occurring within a living organism. Over 1000 different
reactions can take place in each cell. A specific enzyme catalyses each of these reactions. There are as
many enzymes in living organisms as there are types of chemical reactions.
Atoms and molecules are in constant motion and colliding. If the reactants are supplied with enough
energy, such as heat, to break their bonds, then the reaction will proceed and products will be formed.
The minimum amount of energy required to start the reaction is called the activation energy.
A1B → C1D
Reactants Products
Enzymes speed up reactions by lowering the activation energy required for the reaction. They do this
by combining with the reactants and holding them in a way that makes the reaction more likely to occur
(Fig. 3.29).
FIGURE 3.29
a b Uncatalysed Activation
Scheme of activation
Energy supplied
3 Bond binding
the substrate
breaks
Substrate–enzyme
Active sites complex fits in
lock-and-key
arrangement 5 Enzyme is free
to bind other
Enzyme substrates
b
1 Substrate is sucrose, which is Glucose Fructose
composed of glucose and
fructose bonded together
2 Substrate binds
to the enzyme 4 Products are released
Bond
3 Bond binding
the substrate
breaks
FIGURE 3.30 Sequence of steps in the ’lock-and-key’/‘induced-fit’ model of specificity of substrate–enzyme action: a lock-and-key model of enzyme
functioning; b induced-fit model of enzyme functioning. Note the change in shape of the active site in this model.
Each enzyme has its own narrow range of pH within which it functions most efficiently. Levels of
alkalinity or acidity outside the optimum pH for an enzyme have a similar effect to that of temperature
change – they alter the shape of the enzyme and slow down or stop its functioning. Extremes of pH, like
temperature, cause the enzymes to denature. Within cells, most enzymes function at or near neutral,
but enzymes in the digestive tract function in an acidic or alkaline medium. For example, the protein-
digesting enzymes pepsin and rennin, found in gastric juice in the stomach, function best in a strong
acid/low pH (Fig. 3.31b).
Optimum
temperature
Optimum pH Optimum pH
Rate of reaction
Rate of reaction
for pepsin for trypsin
30 40 50 1 2 3 4 5 6 7 8 9
Temperature of reaction (°C) pH of reaction
FIGURE 3.31 Graphs showing a the effect of temperature on the rate of enzyme action; b the pH-specificity of two digestive enzymes
INVESTIGATION 3.3
This investigation models the action of enzymes in cells (to justify the substrate–enzyme binding action
and re-usability of enzymes). It investigates the effect of substrate concentration on the activity of an enzyme.
Models make predictions to explain how things work. In this model, if enzymes bind with substrates to
AIM
1 To model the action of enzymes in cells (based on the substrate–enzyme binding action and re-usability
of enzymes)
2 To investigate the effect of substrate concentration on the activity of an enzyme
HYPOTHESIS
The activity of the enzyme will increase as the substrate concentration increases until it reaches saturation
point, after which the activity of the enzyme will remain constant.
MATERIALS
RISK ASSESSMENT
!
WHAT IS THE HAZARD? WHAT RISK DOES THE HAZARD POSE? HOW CAN YOU SAFELY MANAGE THIS RISK?
RISK
ASSESSMENT
Hydrogen peroxide Toxic if ingested, eye and skin irritant Wear safety goggles and disposable gloves.
Do not ingest.
METHOD
TABLE 3.9
TEST TUBE NO. VOLUME H2O2 (mL) VOLUME H2O (mL)
1 10 0
2 10 0
3 8 2
4 6 4
5 4 6
6 2 8
7 0 10
3 Mark the level of liquid in each test tube using the marker pen.
4 Using a cork borer, obtain six cylinders of potato of the same diameter.
5 Cut the potato cylinders so that they are of equal length (Fig. 3.33).
(AmyBrownScience.com)
Photograph provided by Amy Brown Science
cubes of potato with a small amount of water in a blender –
a few mL of this pureed potato would then be measured
into the test tubes instead of the cylinders of potato.)
6 Place a cylinder of potato into each of the test tubes
numbered 2–7 and allow the reaction to proceed for
approximately 5 minutes.
7 At the completion of this time, place another mark on
the test tube to indicate the maximum height to which
the bubbles reached.
8 Measure the difference between the level of the liquid
and the height to which the bubbles reached in each FIGURE 3.33 Preparing potato cylinders of the
same diameter and length
test tube. Record your results in a results table like
Table 3.10.
9 Compare your results with those of other groups in the class.
RESULTS
1 TABLE 3.10
HEIGHT OF BUBBLES (cm)
TEST TUBE NO. (ACTIVITY OF ENZYME) WS
1 Investigation 3.3
2
3
4
5
6
7
2 Graph the results obtained using a line graph. Remember that the independent variable goes on the x-axis
and the dependent variable is on the y-axis.
DISCUSSION
1 Identify the:
a enzyme
b substrate in this model of enzyme activity.
2 Describe how test tubes 1 and 2 model the action of enzymes in cells.
3 Was this a valid model? Justify your answer.
See p. 4 for a
4 Identify the following variables: discussion of
validity and
a independent variable reliability.
b dependent variable
c controlled variables.
5 Why was test tube 1 with no potato added used?
6 Discuss the validity of the experimental design.
7 Describe the trend obtained on your graph.
8 Is the hypothesis supported by these results?
9 Compare your results with other groups in the class and comment on the reliability of the investigation.
CONCLUSION
Write a conclusion that relates the aims of the investigation to the results of your investigation.
1 Investigate the effect of pH or the effect of temperature on enzyme activity. This can be undertaken using
the same substrate and enzyme and a similar method, or you may wish to research methods using other
readily available enzymes and substrates.
2 Define a research question and hypothesis for your investigation.
3 Follow the steps outlined in Chapter 1 to assist you with your investigation.
KEY CONCEPTS
● Cellular products and wastes must be removed from the cell to maintain efficient cell
functioning.
● Enzymes, or biological catalysts, are proteins that control cellular reactions.
● In enzyme-catalysed reactions, the substrate attaches to the shape on the surface of the
enzyme (the active site) and forms an substrate–enzyme complex.
● The reaction then occurs and the products are released. The enzyme can be re-used for the
same reaction.
● There are two models of enzyme action – the lock-and-key model and the induced-fit model.
● The activity of an enzyme increases as temperature increases until the optimal temperature
is reached. With further temperature increases the enzyme activity decreases and then stops
completely when the high temperatures destroy (denature) the structure of the enzyme.
● Each enzyme has an optimum pH at which it functions most efficiently.
● Enzyme activity is affected by the substrate concentration. As the substrate concentration
increases, the activity of the enzyme increases until all the enzymes are saturated. After this,
further increases in substrate concentration will not lead to increases in enzyme activity.
CHECK YOUR
UNDERSTANDING 1 Summarise the characteristics of enzymes.
2 Describe how an enzyme catalyses a reaction.
3.3 3 Outline how enzymes affect the activation energy required by reactants for a reaction to occur.
4 a Identify three factors that can affect the activity of an enzyme.
b Outline how each of these factors affects the activity of enzymes.
5 a Describe the lock-and-key model of enzyme activity.
b How does the induced-fit model differ from the lock-and-key model?
6 a What does the term ‘denature’ mean when applied to enzymes?
b Outline how enzymes can be denatured.
7 Discuss why enzymes are important for the maintenance of life.
8 Explain why there are thousands of different types of enzymes in the human body.
9 Explain why doctors would get worried if their patient develops a temperature in excess of 42°C.
Photosynthesis
Photosynthesis is the process by which plants utilise light energy, usually from the sun, which is
trapped by chlorophyll (contained in the chloroplast). It uses this energy to break apart water and
carbon dioxide molecules, and build them up into oxygen, energy-storing glucose molecules and
water molecules (Fig. 3.35).
● Energy in cells is transported within cells by small and mobile ATP molecules.
● ATP stores energy in a high-energy bond that attaches the third phosphate group to the ADP
molecule.
● When energy is required, the high-energy bond is broken, releasing energy, a phosphate group
and ADP.
● Photosynthesis is the process where plants use light energy, trapped by chlorophyll, to break down
water and carbon dioxide molecules, and build them up into oxygen, glucose and water molecules.
light energy
carbon dioxide 1 water ⎯⎯⎯⎯⎯⎯⎯→ glucose 1 oxygen
chlorophyll
CHECK YOUR
UNDERSTANDING 1 a Describe the relationship between ADP and ATP.
b Outline the advantages of using ATP as an energy storage molecule.
3.4a 2 a Outline the purpose of the process of photosynthesis.
b Identify the products of the light-dependent stage that are used as inputs in the light-independent
stage of photosynthesis.
3 a Write a balanced equation for photosynthesis.
b Explain why this is considered to be a summary equation.
4 Do all living plant cells carry out photosynthesis? Justify your answer.
5 Distinguish between the light-dependent and the light-independent stages of photosynthesis in terms of
location, requirements and products.
in the presence of oxygen. It is generally summarised as follows, to depict the main changes that occur Cellular respiration
during respiration.
The general equation for aerobic cellular respiration expressed as a:
◗ word equation:
many chemical reactions
glucose 1 oxygen ⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯→ carbon dioxide 1 water 1 energy (ATP)
◗ balanced equation:
many chemical reactions
C 6 H12 O6 1 6O2 1 ADP 1 P ⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯→ 6CO2 1 6H 2 O 1 36 ATP
There are at least 20 separate reactions, each catalysed by a specific enzyme that makes up this overall
pathway.
The first step in the biochemical pathway to break down glucose is the process of glycolysis. This
process occurs in the cytosol of the cell and involves the breakdown of glucose (a six-carbon molecule)
into two pyruvate molecules (each with three carbon atoms). This is accompanied by the release of energy
in the form of two molecules of ATP. This overall reaction is actually a series of 10 smaller reactions, each
catalysed by a specific enzyme.
The two molecules of pyruvate formed from one molecule of glucose then enter the mitochondria
of the cell where the rest of the series of reactions that make up aerobic cellular respiration occur.
36 ATP molecules produced for the breakdown of every glucose molecule. This
Process of glycolysis
process is summarised in Figure 3.37.
2 ATP
Photosynthesis and aerobic cellular respiration
Pyruvate
Photosynthesis and aerobic cellular respiration are related (Fig. 3.38). When you
Mitochondrion
look at the general equations for photosynthesis and aerobic cellular respiration,
Oxygen it appears that these processes may be the reverse of each other. That is not the
case because they are each made up of a series of chemical reactions that are very
34 ATP different.
Carbon Photosynthesis and aerobic cellular respiration are, however, closely related
Water
dioxide
and interdependent.
FIGURE 3.37 Glycolysis, the first stage of cellular The products of photosynthesis are used in the process of aerobic cellular
respiration, occurs in the cytoplasm and releases respiration. Similarly, the products of aerobic cellular respiration are used in the
two ATP. The second stage of aerobic cellular
respiration occurs in the mitochondria and process of photosynthesis.
releases 34 ATP. In cells that contain both chloroplasts and mitochondria, the two
processes will occur in the same cell. In cells that do not contain chloroplasts
(such as plant root cells), the products of photosynthesis (glucose and oxygen) must be supplied to
the cells for the process of aerobic cellular respiration to occur.
Respiration
(in mitochondria)
ATP
● When glucose and oxygen combine in the process of aerobic cellular respiration, energy is
produced along with water and carbon dioxide. This process is made up of many reactions.
many chemical reactions
● glucose 1 oxygen (+ ADP + P) ⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯
→ carbon dioxide 1 water 1 energy (ATP)
● The energy produced is stored in ATP molecules.
● The first step of this process occurs in the cytoplasm and is called glycolysis. In this step, one
glucose molecule is broken down into two pyruvate molecules and two ATP.
● The second step in the reaction occurs in the mitochondria where pyruvate, in the presence of
oxygen (aerobic cellular respiration), is broken down to release carbon dioxide, water and 34 ATP.
● A total of 36 ATP molecules is produced for every molecule of glucose broken down in aerobic
respiration.
● Anaerobic (without oxygen) cellular respiration produces ethanol and carbon dioxide in
bacteria, yeast and plant cells, and lactic acid in animal cells. Two ATP molecules are produced
in this process for the respiration of each molecule of glucose.
● Wastes are the products of cellular reactions that are not required.
● Many of these wastes can be removed by simple diffusion through the cell membrane.
● Other wastes can be removed by exocytosis or destroyed by the enzymes present in lysosomes.
CHECK YOUR
1 Write a balanced equation for the process of aerobic cellular respiration. UNDERSTANDING
2 Outline the role of aerobic cellular respiration in living organisms.
3 a Identify the initial reactant and the final product in the process of glycolysis. 3.4b
b Identify where in the cell glycolysis occurs.
4 Compare the products of aerobic cellular respiration with the products of anaerobic cellular respiration in
plants and animals.
5 Outline where the carbon dioxide is produced and name any other products formed in the process of
aerobic cellular respiration.
6 a Outline the conditions under which lactic acid is formed.
b Outline the fate of the lactic acid when more oxygen becomes available.
7 Summarise the ways in which wastes can be removed from the cell.
8 Outline the importance of plants coordinating the processes of photosynthesis and respiration.
CELL REQUIREMENTS AND PRODUCTS MOVEMENT OF SUBSTANCES INTO AND OUT OF CELLS
Related to:
iStock.com/micro_photo
Non-lipid-soluble
• characteristics Specific non-lipid-soluble molecules
of materials molecules or ions Lipid-soluble
• concentration molecules
gradient
Gas and
wastes Gas and nutrients
Extracellular space
The smaller the cell, the higher the SA:V and the
more efficient the exchange of substances into
Lipid bilayer
transport transport
Active transport Nucleus
Nucleus
Passive transport
(facilitated diffusion) Nucleus
Movement along a concentration gradient Movement along a concentration gradient Movement against a concentration gradient
Diffusion: the movement of any type Osmosis: the movement of water Active transport: the movement of
of molecule from a high to a low molecules from a high concentration of molecules from a low concentration to
concentration, until equilibrium is water to a low concentration of water, a high concentration through selectively
reached through selectively permeable membrane permeable membrane
• Substrate concentration
Progress of reaction Progress of reaction
BIOCHEMICAL PROCESSES
Anaerobic respiration
ATP Plants: fermentation
A P P P glucose → ethanol + carbon dioxide + adenosine triphosphate
High energy
bond C6H12O6 → 2CH3CH2OH + 2CO2 + 2ATP
Energy
P released Animals:
glucose → lactic acid + adenosine triphosphate
P
C6H12O6 → 2CH3CH2(OH)COOH + 2ATP
Free
phosphate
group Aerobic respiration
A P P Glycolysis, the first stage of cellular respiration, occurs in the cytoplasm and
ADP releases two ATP. The second stage of aerobic cellular respiration occurs in the
mitochondria and releases 34 ATP.
Photosynthesis glucose + oxygen many chemical reactions carbon dioxide + water + energy (ATP)
Photosynthesis is a series of reactions occurring C6H12O6 + 6O2 many chemical reactions 6CO2 + 6HO2 + ATP
in two stages: the light-dependent and the
light-independent stages.
Sunlight energy
light energy
2CO2 + 12H2O C6H12O6 + 6O2
chlorophyll
light energy Photosynthesis
carbon dioxide + water glucose + oxygen (in chloroplast)
chlorophyll
Light energy Water Carbon dioxide
Inside chloroplast
Glucose
Cytoplasm
Respiration
Process of glycolysis (in mitochondria)
ATP
Mitochondrion
Pyruvate 2 ATP
34 ATP
The close relationship and interdependence of the processes
Carbon dioxide Water of photosynthesis and aerobic cellular respiration.
Review quiz
1 Distinguish between the following: 8 Suggest why it is said that carbon is the element on which
a diffusion and facilitated diffusion all life depends.
b diffusion and osmosis 9 Construct a table to compare the chemical composition,
c osmosis and active transport structure and function of carbohydrates, lipids, proteins
and nucleic acids.
d exocytosis and endocytosis.
10 Identify the inorganic nutrients that are important to cells
2 Construct a table to identify and outline the different
and describe their uses in cells.
means by which substances move in and out of cells.
Include examples of substances that use each of these 11 Construct a table to identify and describe three factors
means to enter or leave the cell. that affect the activity of enzymes.
3 Draw a diagram of a unicellular freshwater organism 12 List the conditions necessary for photosynthesis.
that is placed in seawater, labelling the direction of the
13 Compare the processes of photosynthesis and aerobic
net movement of water. Justify the direction of the net
respiration, including where in the cell they occur, their
movement of the water.
requirements, their products and their purpose.
4 Outline one reason why plant cells do not burst when
14 Explain why one enzyme can catalyse only one particular
placed in a hypotonic solution.
reaction.
5 Blood cells were placed in three different solutions. After
15 Explain why cells cannot grow to a big size.
some time, cells in solution X became shrivelled. Cells in
solution Y burst and cells in solution Z remained the same. 16 Describe how the lock-and-key model explains the effect
a Which solution was hypertonic compared with the of denaturing enzymes.
blood cells? 17 Describe the inputs of photosynthesis from which oxygen
b Which cell was isotonic compared with the gas is produced.
surroundings?
18 ATP is an energy-carrier molecule. Relate its structure to its
6 a Which of the following shapes with the same volume function.
would have a higher SA:V – a flattened rectangular cell
19 A human enzyme works best at 37°C.
or a spherical cell?
a Predict what would happen to the enzyme’s activity at
b Which of these shapes would be more efficient in
very low temperatures.
ensuring the movement of substances to all areas of
the cell? Justify your answer. b Outline how this may differ from the activity of the
enzyme at very high temperatures.
7 A beaker is half-filled with water and 10 drops of food
c Describe what has happened to the active site in both
colouring are added. After half an hour, the food colouring
cases.
is evenly distributed throughout the water.
Explain the process that caused this to occur. In your 20 Your friend says she doesn’t believe the air she breathes
answer, use the terms ‘net movement’, ‘concentration out contains carbon from the food she’s eaten. Outline
gradient’, ‘diffusion’ and ‘equilibrium’. what you would say to convince her.
104 11 » »CHEMISTRY
CHAPTER ONE
MODULE CELLS AS THE BASIS OF LIFE 9780170407281
» END-OF-MODULE REVIEW
MODULE 1 : CELLS AS THE
BASIS OF LIFE
1 Use the images in Figure M1.1 to answer the following 2 a Distinguish between the processes of diffusion and
questions. osmosis.
b When a patient in a hospital is hooked up to an
i
Science Photo Library/DR KARI LOUNATMAA
c ii
i
Enzyme ii
iii
iv
FIGURE M1.2
1 mm
b Explain why the temperature of the human body has
to be maintained at approximately 37°C and why the
FIGURE M1.1 body self-regulates its temperature at 37°C, with only
small increases in temperature (a couple of degrees)
i For each of the images (a), (b) and (c), identify being tolerated.
whether they are prokaryotic, eukaryotic plant or
eukaryotic animal cells. Justify your decision in 6 Two cells have the same volume. One is spherical and the
each case. other is flat and thin. One student in class maintained that
ii Label the areas indicated on image (c). the flat and thin cell would be more efficient in obtaining
iii Use the scale provided to determine the length of nutrients and removing wastes.
the cell in image (c). Evaluate this statement.
▻ Find out about the advances in microscope technology and applications of synchrotron radiation in
biology.
▻ Study microbes in hydrothermal vents for clues as to whether life can exist on the moons of Jupiter.
▻ Find out about the discovery of water channels in cell membranes (which won a Nobel Prize in 2003).
▻ Investigate the effects of cell shape, cell size and cell structure on SA:V and rates of diffusion.
▻ Find out about quantum biology’s application to a better understanding of biological processes such
as enzyme functioning.
▻ Look into how the study of the uptake of chemicals across barriers could lead to treatment of
diseases (for example, drugs and brain infections, chemotherapy).
▻ Find out about the development of the fluid mosaic model of the cell membrane.
▻ Investigate the development by CSIRO of an enzyme-based product that can rapidly degrade
unwanted pesticide residues in agricultural soil and water.