Molecular Components of Cells PDF
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Uploaded by HardyReasoning8940
Lebanese University - Faculty of Sciences
Reem Dakhil
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This document presents an in-depth analysis of molecular components of cells, particularly carbohydrates. It classifies carbohydrates, describes their functions, and details various modifications. The content is suitable for students studying molecular biology and biological chemistry.
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Chapter 2 Molecular Components of cells Reem Dakhil M1 Biochemistry (Lebanese University) M2 Physiology, Epigenetics, Differentiation, and Cancer (Université Grenoble Alpes) II. Carbohydrates Functions ✓ Energetic ✓ Structural ✓ Cell ident...
Chapter 2 Molecular Components of cells Reem Dakhil M1 Biochemistry (Lebanese University) M2 Physiology, Epigenetics, Differentiation, and Cancer (Université Grenoble Alpes) II. Carbohydrates Functions ✓ Energetic ✓ Structural ✓ Cell identity glycogen in animals cellulose in plant cell wall blood groups II. Carbohydrates 1. Monosaccharides Definition ✓ aka “simple oses” ✓ Most are D-stereoisomers ✓ CnH2nOn (3≤n≤6) ✓ Less diverse than proteins since: - Only a few monosaccharaides can form polymers - Different types do not combine much (max 2) D-glucose C6H12O6 II. Carbohydrates 1. Classification of Monosaccharides ✓ By functional group - Aldoses (aldehyde group) - Ketoses (ketone group) ✓ By n 3: trioses – 4: tetroses – 5: pentoses – 6: hexoses Aldose pentose: ribose Aldose hexoses: glucose, galactose, mannose Ketose hexose: fructose ribose glucose galactose mannose fructose II. Carbohydrates 2. Cyclic Oses ✓ n>4 → straight chain or cycle → cycle is more stable → or → Pyranoses (6C) & furanoses (5C) α β ✓ From intramolecular reaction between OH & aldehyde/ketone group ✓ α & β isomers: differ by orientation of OH that replaced the aldehyde/ketone - α: downward - β: upward ✓ Usually cyclic oses are switchable between α & β until polymerized. II. Carbohydrates 4. Modification ✓ Osamines addition of amine group (---NH2) eg: glucose→glucosamine. galactose→galactosamine ✓ N-acetyl osamines addition of acetyl group (---COCH3) to the amine group eg: NAG: N-acetyl galactosamine ✓ Uronic acids acidification of CH2OH into COOH eg: NANA: N-Acetyl Neuraminic Acid (from mannose) II. Carbohydrates 5. Dimers and Polymers ✓ Disaccharide: 2 oses joined by covalent bond “glycosidic bond” Its formation releases H2O - Saccharose = glucose + fructose - Lactose = glucose + galactose - Maltose = 2 glucose ✓ Oligosaccharide: short polymer of monosaccharaides can be branched / unbranched can be linked to proteins / lipids for maturation II. Carbohydrates 5. Dimers and Polymers ✓ Polysaccharide (Glycan): long chain of monosaccharides branched / unbranched simple or modified oses Functions: Structural - cellulose in plant cell wall – peptidoglycans in bacterial cell wall Energetic - glycogen in muscles – starch in plants II. Carbohydrates 5. Dimers and Polymers ✓ Homopolysaccharide: polymer of the same molecule - Starch & glycogen = branched polymers of α-D-glucose - Cellulose = unbranched polymer of β-D-glucose - Chitin = polymer of N-acetyl glucosamine, in insects shell ✓ Heteropolysaccharide: polymer of 2 diferent simple/modified oses - GAG = glucosamine + galactosamine - Hyaluronic acid = glucoronic acid + N-acetyl glucosamine - Chondroitin Sulfate = glucuronic acid + N-acetyl galactosamine - Keratan Sulfate = N-acetyl glucosamine + D-galactose FS.I Partial 2020 13)b, 14)d, 15)a, 12)c, 13)b FS.I Partial 2019