Trisaccharides are oligosaccharides composed of three monosaccharides with two glycosidic bonds connecting them. Similar to the disaccharides, each glycosidic bond can be formed between any hydroxyl group on the component monosaccharides. Even if all three component sugars are the same (e.g., glucose), different bond combinations (regiochemistry) and stereochemistry (alpha- or beta-) result in trisaccharides that are diastereoisomers with different chemical and physical properties.[1][2]
Examples
edit| Trisaccharide | Unit 1 | Bond | Unit 2 | Bond | Unit 3 |
|---|---|---|---|---|---|
| Nigerotriose | glucose | α(1→3) | glucose | α(1→3) | glucose |
| Maltotriose | glucose | α(1→4) | glucose | α(1→4) | glucose |
| Melezitose | glucose | α(1→2) | fructose | α(1→3) | glucose |
| Maltotriulose | glucose | α(1→4) | glucose | α(1→4) | fructose |
| Raffinose | galactose | α(1→6) | glucose | β(1→2) | fructose |
| Kestose | glucose | α(1↔2) | fructose | β(1←2) | fructose |
References
edit- ^ Nelson, David L. (2021). Lehninger principles of biochemistry. Michael M. Cox, Aaron A. Hoskins (8th ed.). New York, NY. ISBN 978-1-319-22800-2. OCLC 1243000176.
{{cite book}}: CS1 maint: location missing publisher (link) - ^ Berg, Jeremy M. (2019). Biochemistry. John L. Tymoczko, Gregory J., Jr. Gatto, Lubert Stryer (9th ed.). New York. ISBN 978-1-319-11467-1. OCLC 1037810557.
{{cite book}}: CS1 maint: location missing publisher (link)
External links
edit- Trisaccharides at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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