DS/ Reducing vs non-reducing α ( D) glucopyranosyl 1 2 fructofuranoside β ( D) galactopyranosyl 1 4 glucopyranose SucroseLactose.

Slides:



Advertisements
Similar presentations
The stereochemical relationships, shown in Fischer projection, among the D-aldoses with three to six carbon atoms.
Advertisements

Carbohydrates: Oligosaccahrdes and Polysaccharides.
Chapter 7 Carbohydrates and Glycobiology. Chapter 7: Carbohydrates Learning Goals 1.Structures of “boxed” sugars: open chain and ring. 2.Amino-, deoxy-,
Biochemistry Sixth Edition
(Chapter 7). - Overview - Classification and Structure of Carbohydrates : A) Isomers and epimers B) Enantiomers 1 st Lecture: Pages :
Structure, properties and function of saccharides Vladimíra Kvasnicová.
Biochemistry 2/e - Garrett & Grisham Copyright © 1999 by Harcourt Brace & Company Chapter 7 Carbohydrates to accompany Biochemistry, 2/e by Reginald Garrett.
Prentice Hall c2002Chapter 81 Chapter 8 - Carbohydrates Carbohydrates (“hydrate of carbon”) have empirical formulas of (CH 2 O) n, where n ≥ 3 Monosaccharides.
Biology 107 Macromolecules I September 2, Macromolecules I Student Objectives:As a result of this lecture and the assigned reading, you should understand.
1 Chapter 16 Carbohydrates 16.7 Disaccharides 16.8 Polysaccharides.
Disaccharides. Disaccharides - Maltose Glucose + glucose; alpha acetal linkage.
Polysaccharides are polymers of hundreds to thousands of monosaccharides joined by glycosidic linkages. One function of polysaccharides is as an energy.
© SSER Ltd..
Carbohydrates: Structure and Function
BIOMOLECULES Carbohydrates.
1 Chapter 12 Outline 12.1 Monosaccharides - Aldose and ketose -Glyceraldehyde, Stereoisomers (Mirror image = enantiomer), D and L isomers of Glyceraldehyde.
UNIT 4. CARBOHYDRATES Introduction Classification Monosaccharides. Classification. Stereoisomers. Cyclic structures. Reducing sugars.
Chapter 5- The Structure and Function of Macromolecules Carbohydrates

Chapter 7 Carbohydrates and the Glycoconjugates of Cell Surfaces
AP Biology Macromolecules. AP Biology Macromolecules  Smaller organic molecules join together to form larger molecules Macromolecules  4 major classes.
Carbohydrates General molecular formula: C n H 2n O n 1 : 2 : 1 When we say macromolecules what does that mean? It means huge molecular mass (hundreds.
Phosphate Ester Formation
Carbohydrates and the Glycoconjugates of Cell Surfaces
Dr. Saidunnisa Professor of Biochemistry Carbohydrates-II.
7P2-1 Monosaccharides Monosaccharide stereoisomers Cyclic structures Reactions Examples and derivatives Di and oligosaccharides (We are here.) Polysaccharides.
Biochemistry Unit.  Composed of carbon, hydrogen, and oxygen in a 1:2:1 ratio.  The basic unit is called a monosaccharide and includes glucose, fructose,
Carbohydrates. Structure and Function How do we define a carbohydrate? aldehydes or ketones with multiple hydroxyl groups “hydrate” of carbon – C-H 2.
DR AMINA TARIQ BIOCHEMISTRY
Chapter 7 Carbohydrates and Glycobiology. Carbohydrates are everywhere
Carbohydrates. Introduction: Carbohydrates are the most abundant organic compounds in the plant world They are storehouses of chemical energy (glucose,
Carbohydrates. Most abundant class of biological molecules on Earth Originally produced through CO 2 fixation during photosynthesis.
Prentice Hall c2002Chapter 81 Chapter 8 - Carbohydrates Carbohydrates (“hydrate of carbon”) have empirical formulas of (CH 2 O) n, where n ≥ 3 Monosaccharides.
Saccharides Vladimíra Kvasnicová. SACCHARIDES (carbohydrates, glycides) = polyhydroxyaldehydes or polyhydroxyketones D-glucose D-fructose.
Chapter 10 – Carbohydrates
Chapter 8 (part2) Carbohydrates: oligo- and polysaccharides.
MACROMOLECULES. Four Types of Macromolecules 1. Carbohydrates 2. Lipids 3. Proteins 4. Nucleic Acids.
CARBOHYDRATE CHEMISTRY DR AMINA TARIQ BIOCHEMISTRY.
Review Question 1 How many molecules of water are needed to completely hydrolyze a polymer that is 10 monomers long? 9.
17.5 Properties of Monosaccharides
Carbohydrates. Structure of Carbohydrates Properties of Carbohydrates Most abundant class of organic molecules Source: Photosynthesis Classification.
DISACCHARIDES Disaccharides are two monosaccharide units linked together by acetal or ketal glycosidic linkages. A glycosidic linkage is identified by:
Carbohydrates.
Carbo (carbon) hydrate (water) Sugar = saccharide Single = monosaccharide Pair = disaccharide Many = polysaccharide Glucose = a monosaccharide Outcomes.
Biological Macromolecules Large molecules that perform many important biological functions  Carbohydrates  Lipids  Proteins  Nucleic Acids Many are.
CARBOHYDRATES PART 2 ECDA Aug DISACCHARIDES.
Carbohydrates and Glycobiology. Monosaccharides – consist of a simple polyhydroxy aldehyde or ketone unit Disaccharide – two monosaccharide units Oligosaccharides.
Carbohydrates serve a variety of functions Energy storage and food Structure and support Lubrication Protection Recognition and signaling Component of.
Carbohydrates -IV-. Polysaccharides 3 Polysaccharides Polysaccharides are polymers of 10 or more monosaccharide units Homopolysaccharides: Homopolysaccharides:
Carbohydrates What are they? Formula = (CH 2 O) n where n > 3 Also called sugar Major biomolecule in body What do cells do with carbs? Oxidize them for.
CARBOHYDRATE CHEMISTRY SUURBAAR JENNIFER. I NTRODUCTION Carbohydrates are one of the three major classes of biological molecules. Carbohydrates are also.
CARBOHYDRATE CHEMISTRY UNIT-1 CHAPTER-2. I NTRODUCTION Carbohydrates are one of the three major classes of biological molecules. Carbohydrates are also.
CHAPTER 7 Carbohydrates and Glycobiology
Chapter 5 The Structure and Function of Macromolecules Intro & Carbohydrates.
© SSER Ltd..
Carbohydrates, Proteins and Lipids
Part I – Introduction; Carbohydrates; Lipids
CARBOHYDARTE II Done By :Nisreen Moh’d
Carbohydrate.
POLYSACCHARIDES.
© SSER Ltd..
Carbohydrates Dr. Gamal Gabr.
CARBOHYDRATES UNIT #2 BIOMOLECULES.
Carbohydrates Section 3.2.
Carbohydrates Disaccharides Polysaccharides.
Macromolecules & Carbohydrates
Part II: Carbohydrates
Polysaccharides Cellulose: the major structural component of plants, especially wood and plant fibers a linear polymer of approximately 2800 D-glucose.
Chapter 8 (part 1) Carbohydrates.
Sugars 10/29/09.
Presentation transcript:

DS/ Reducing vs non-reducing α ( D) glucopyranosyl 1 2 fructofuranoside β ( D) galactopyranosyl 1 4 glucopyranose SucroseLactose

Amylose amylopectin glycogen cellulose

DS that are formed by the linkage of sugars derivatives

Definition and properties: Definition and properties: *They are composed of many sugar residues. *They are composed of many sugar residues. *All are nonreducing. *All are nonreducing. Polysaccharides

PS/Different classification. 1- Branched vs linear polysaccharides. 1- Branched vs linear polysaccharides. Example: amylose, inulin, and amylopectin, glycogen 2- Sturctural vs storage polysaccharides. 2- Sturctural vs storage polysaccharides. Example: Cellulose, pectin and glycogen, inulin. Example: Cellulose, pectin and glycogen, inulin. 3- Homo vs hetero polysaccharides. 3- Homo vs hetero polysaccharides. Example: Amylon, cellulose and glycosaminoglycanes. Example: Amylon, cellulose and glycosaminoglycanes.

PS/ linear vs Branched AmyloseAmylopectin / Glycogen Branched linear

Structural vs storage

Other Structural Polysaccharides Alginates - Ca-binding polymers in algae Alginates - Ca-binding polymers in algae and agaropectin - Agarose and agaropectin - galactose polymers Glycosaminoglycans - repeating disaccharides with amino sugars and negative charges Glycosaminoglycans - repeating disaccharides with amino sugars and negative charges

Dextrans If you change the main linkages between glucose from alpha(1,4) to alpha(1,6), you get a new family of polysaccharides - dextrans If you change the main linkages between glucose from alpha(1,4) to alpha(1,6), you get a new family of polysaccharides - dextrans Branches can be (1,2), (1,3), or (1,4) Branches can be (1,2), (1,3), or (1,4) Dextrans formed by bacteria are components of dental plaque Cross-linked are used as "" gels in column chromatography Cross-linked dextrans are used as "Sephadex" gels in column chromatography These gels are up to 98% water! These gels are up to 98% water!

PS/Homo vs Heteropolysaccharide Amylose, inulin, and amylopectin, glycogen, Cellulose Amylose, inulin, and amylopectin, glycogen, Cellulose Chitin - exoskeletons of crustaceans, insects and spiders, and cell walls of fungi Chitin - exoskeletons of crustaceans, insects and spiders, and cell walls of fungi Similar to cellulose, but Similar to cellulose, but C-2s are N- acetyl Cellulose strands are parallel, chitins can be parallel or antiparallel Cellulose strands are parallel, chitins can be parallel or antiparallel

Hetero PS (Glycosaminoglucans)

(GAG+ peptide) Glycoproteins vs Proteoglycans

Two main classes of ECM molecules: a) Glycosaminoglycans mostly proteoglycans polysaccharide chains - glycosaminoglycans, GAGs, covalently bound to proteins highly hydrated, porous, gels b) fibrous proteins (embedded in the above gel) structural (collagen, elastin) strengthen the ECM adhesive (fibronectin, laminin) attach cells to the appropriate part of ECM

Polysaccharides/ Peptidoglycanes Gram positive bacteria Gram Negative bacteria

Glycoproteins

Glycolipids (Crebroside, Ganglioside) Glycolipids Vs Lipopolysaccharides

Relative swetness & Artificial sweetners Relative sweetness of sugar Sucrose: 100 Sucrose: 100 Glc: 70 Glc: 70 Fru:170 Fru:170 Mal: 30 Mal: 30 Lac: 16 Lac: 16 Relative sweetness of Artificial sweetners Cyclamate: 3, 000 Cyclamate: 3, 000 Aspartam: 20, 000 Aspartam: 20, 000 Saccarin: 40, 000 Saccarin: 40, 000 Monilin: 400, 000 Monilin: 400, 000

Different ways for qualitative and quantitative identification of sugars Crystal formation(Osazones) Furfral and hydroxy furfural reaction with cyclic alcohol. Furfral and hydroxy furfural reaction with cyclic alcohol. Iodine Iodine Enzymatic Enzymatic Glucokinase Glucokinase Hexokinase Hexokinase Oxidative and reductive reactions: Benedict Oxidative and reductive reactions: Benedict

Benedict: An assay for sugars Cu + Cu 2+