Carbohydrates Lecture Notes PDF

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Document Details

FondGodel

Uploaded by FondGodel

Notre Dame of Midsayap College

2011

Jane B. Reece, Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Robert B. Jackson ,Erin Barley, Kathleen Fitzpatrick

Tags

carbohydrates biology macromolecules biochemistry

Summary

This document provides lecture notes on carbohydrates for a Campbell Biology course. It covers the structure and function of large biological molecules, the synthesis and breakdown of polymers, and different types of carbohydrates. The course materials seem to be from a 2011 edition.

Full Transcript

LECTURE PRESENTATIONS For CAMPBELL BIOLOGY, NINTH EDITION Jane B. Reece, Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Robert B. Jackson Chapter 5 The Structure and Function of Large Biological Molecules...

LECTURE PRESENTATIONS For CAMPBELL BIOLOGY, NINTH EDITION Jane B. Reece, Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Robert B. Jackson Chapter 5 The Structure and Function of Large Biological Molecules Lectures by Erin Barley Kathleen Fitzpatrick © 2011 Pearson Education, Inc. Overview: The Molecules of Life All living things are made up of four classes of large biological molecules: carbohydrates, lipids, proteins, and nucleic acids Macromolecules are large molecules composed of thousands of covalently connected atoms Molecular structure and function are inseparable © 2011 Pearson Education, Inc. Figure 5.1 Concept 5.1: Macromolecules are polymers, built from monomers A polymer is a long molecule consisting of many similar building blocks These small building-block molecules are called monomers Three of the four classes of life’s organic molecules are polymers – Carbohydrates – Proteins – Nucleic acids © 2011 Pearson Education, Inc. The Synthesis and Breakdown of Polymers A dehydration reaction occurs when two monomers bond together through the loss of a water molecule Polymers are disassembled to monomers by hydrolysis, a reaction that is essentially the reverse of the dehydration reaction © 2011 Pearson Education, Inc. Animation: Polymers Right-click slide / select “Play” © 2011 Pearson Education, Inc. Figure 5.2 (a) Dehydration reaction: synthesizing a polymer 1 2 3 Short polymer Unlinked monomer Dehydration removes a water molecule, forming a new bond. 1 2 3 4 Longer polymer (b) Hydrolysis: breaking down a polymer 1 2 3 4 Hydrolysis adds a water molecule, breaking a bond. 1 2 3 Figure 5.2a (a) Dehydration reaction: synthesizing a polymer 1 2 3 Short polymer Unlinked monomer Dehydration removes a water molecule, forming a new bond. 1 2 3 4 Longer polymer Figure 5.2b (b) Hydrolysis: breaking down a polymer 1 2 3 4 Hydrolysis adds a water molecule, breaking a bond. 1 2 3 The Diversity of Polymers Each cell has thousands of different HO macromolecules Macromolecules vary among cells of an organism, vary more within a species, and vary even more between species An immense variety of polymers can be built from a small set of monomers © 2011 Pearson Education, Inc. Concept 5.2: Carbohydrates serve as fuel and building material Carbohydrates include sugars and the polymers of sugars The simplest carbohydrates are monosaccharides, or single sugars Carbohydrate macromolecules are polysaccharides, polymers composed of many sugar building blocks © 2011 Pearson Education, Inc. Sugars Monosaccharides have molecular formulas that are usually multiples of CH2O Glucose (C6H12O6) is the most common monosaccharide Monosaccharides are classified by – The location of the carbonyl group (as aldose or ketose) – The number of carbons in the carbon skeleton © 2011 Pearson Education, Inc. Figure 5.3 Aldoses (Aldehyde Sugars) Ketoses (Ketone Sugars) Trioses: 3-carbon sugars (C3H6O3) Glyceraldehyde Dihydroxyacetone Pentoses: 5-carbon sugars (C5H10O5) Ribose Ribulose Hexoses: 6-carbon sugars (C6H12O6) Glucose Galactose Fructose Figure 5.3a Aldose (Aldehyde Sugar) Ketose (Ketone Sugar) Trioses: 3-carbon sugars (C3H6O3) Glyceraldehyde Dihydroxyacetone Figure 5.3b Aldose (Aldehyde Sugar) Ketose (Ketone Sugar) Pentoses: 5-carbon sugars (C5H10O5) Ribose Ribulose Figure 5.3c Aldose (Aldehyde Sugar) Ketose (Ketone Sugar) Hexoses: 6-carbon sugars (C6H12O6) Glucose Galactose Fructose Though often drawn as linear skeletons, in aqueous solutions many sugars form rings Monosaccharides serve as a major fuel for cells and as raw material for building molecules © 2011 Pearson Education, Inc. Figure 5.4 1 6 6 2 5 5 3 4 1 4 1 4 2 2 5 3 3 6 (a) Linear and ring forms 6 5 4 1 3 2 (b) Abbreviated ring structure A disaccharide is formed when a dehydration reaction joins two monosaccharides This covalent bond is called a glycosidic linkage © 2011 Pearson Education, Inc. Animation: Disaccharide Right-click slide / select “Play” © 2011 Pearson Education, Inc. Figure 5.5 1–4 glycosidic 1 linkage 4 Glucose Glucose Maltose (a) Dehydration reaction in the synthesis of maltose 1–2 glycosidic 1 linkage 2 Glucose Fructose Sucrose (b) Dehydration reaction in the synthesis of sucrose Polysaccharides Polysaccharides, the polymers of sugars, have storage and structural roles The structure and function of a polysaccharide are determined by its sugar monomers and the positions of glycosidic linkages © 2011 Pearson Education, Inc. Storage Polysaccharides Starch, a storage polysaccharide of plants, consists entirely of glucose monomers Plants store surplus starch as granules within chloroplasts and other plastids The simplest form of starch is amylose © 2011 Pearson Education, Inc. Figure 5.6 Chloroplast Starch granules Amylopectin Amylose (a) Starch: 1 m a plant polysaccharide Mitochondria Glycogen granules Glycogen (b) Glycogen: 0.5 m an animal polysaccharide Figure 5.6a Chloroplast Starch granules 1 m Glycogen is a storage polysaccharide in animals Humans and other vertebrates store glycogen mainly in liver and muscle cells © 2011 Pearson Education, Inc. Figure 5.6b Mitochondria Glycogen granules 0.5 m Structural Polysaccharides The polysaccharide cellulose is a major component of the tough wall of plant cells Like starch, cellulose is a polymer of glucose, but the glycosidic linkages differ The difference is based on two ring forms for glucose: alpha () and beta () © 2011 Pearson Education, Inc. Animation: Polysaccharides Right-click slide / select “Play” © 2011 Pearson Education, Inc. Figure 5.7 (a)  and  glucose ring structures 4 1 4 1  Glucose  Glucose 1 4 1 4 (b) Starch: 1–4 linkage of  glucose monomers (c) Cellulose: 1–4 linkage of  glucose monomers Figure 5.7a 4 1 4 1  Glucose  Glucose (a)  and  glucose ring structures Figure 5.7b 1 4 (b) Starch: 1–4 linkage of  glucose monomers 1 4 (c) Cellulose: 1–4 linkage of  glucose monomers Polymers with  glucose are helical Polymers with  glucose are straight In straight structures, H atoms on one strand can bond with OH groups on other strands Parallel cellulose molecules held together this way are grouped into microfibrils, which form strong building materials for plants © 2011 Pearson Education, Inc. Figure 5.8 Cell wall Cellulose microfibrils in a plant cell wall Microfibril 10 m 0.5 m Cellulose molecules  Glucose monomer Figure 5.8a Figure 5.8b Cell wall 10 m Figure 5.8c Cellulose microfibrils in a plant cell wall 0.5 m Enzymes that digest starch by hydrolyzing  linkages can’t hydrolyze  linkages in cellulose Cellulose in human food passes through the digestive tract as insoluble fiber Some microbes use enzymes to digest cellulose Many herbivores, from cows to termites, have symbiotic relationships with these microbes © 2011 Pearson Education, Inc. Chitin, another structural polysaccharide, is found in the exoskeleton of arthropods Chitin also provides structural support for the cell walls of many fungi © 2011 Pearson Education, Inc. Figure 5.9 The structure of the chitin monomer Chitin forms the exoskeleton of arthropods. Chitin is used to make a strong and flexible surgical thread that decomposes after the wound or incision heals. Figure 5.9a Chitin forms the exoskeleton of arthropods. Figure 5.9b Chitin is used to make a strong and flexible surgical thread that decomposes after the wound or incision heals.

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