Chapter 8 Flashcards
What is the general formula for carbohydrates?
(CH2O)n
What is a monosaccharide?
Simple sugar (one residue)
What is an oligosaccharide?
2-10 simple sugar residues
What is a polysaccharide?
Polymer of simple sugars
What is an aldose?
monosaccharide with a carbonyl group on the endmost Carbon
What is a ketose?
monosaccharide with a ketose group on the endmost carbon (COCH2OH)
How many carbons are needed for each monosaccharide to be considered chiral?
Aldose: 3C or more
Ketose: 4C or more
What carbon is stereochemistry of a monosaccharide determined with?
Highest numbered or lowest chiral carbon – one closest to CH2OH group
What are the two sterochemistry designations of monosaccharides?
D (OH is on the right)
L (OH is on the left)
What sterochemical designation of sugars predominates in nature?
D sugars
What is a stereoisomer?
Compounds that only differ in spatial arrangement of atoms – same chemical formula
What is an enantiomer?
Nonsuperimposeable mirror images (D vs L)
What is a diastereomer?
Stereoisomers (same chemical formula, different arrangement) that aren’t mirror images
What is an epimer?
Diastereomer (different arrangements of same chemical formula that aren’t mirror images) that only differ at a single stereocenter
What is the difference between a hemiacetal and hemiketal?
Hemiacetal - H
Hemiketal - R group
How do you form a hemiacetal? Hemiketal?
Alcohol + Aldehyde = Hemiacetal
Alcohol + Ketone = Hemiketal
What is a reducing sugar?
Sugar with a free aldehyde group
What is the function of acetals and ketals in sugars?
Links multiple monosaccharides together (two R group connections)
What is the reaction that forms glycosidic bonds?
Condensation Reaction
What type of glycosidic bond is hard for the body to break?
Beta
What is the difference between homopolysaccharides and heteropolysaccharides?
Homopolysaccharides consist of repeating single sugar
Heteropolysaccharide consist of multiple sugars
Starch and glycogen are _____ molecules
Storage
Chitin and Cellulose are _____ molecules
Structural
What is starch?
Glucose storage in plants
What is amylose?
Form of starch that is glucose with alpha-1,4 links and one reducing end (one long chain)
What is amylopectin?
Form of starch that has alpha-1,6 branches every 12-30 molecules
What is glycogen?
Glucose storage in animals
What is the structure of glycogen?
Glucose linearly bound alpha-1,4 but has Alpha-1,6 branches every 8-12 residues
Is amylopectin or glycogen more tightly packed?
Glycogen; every 8-12 residues compared to 12-30 for amylopectin
What is the worlds most abundant natural polymer?
Cellulose
What is cellulose?
Structural polysaccharide of plants
What makes up cellulose?
Glucose bonded by Beta-1,4 linkages
What is chitin?
Structural polysaccharide of crustaceans, insects, spiders, and fungal cell wells
What is the structural difference of chitin compared to cellulose?
Carbon 2 has N-acetyl group (NHC(O)CH3)
What are glycosaminglycans?
Linear chains of repeating disaccharides
What is heparin?
Natural anticoagulent
What is hyaluronates?
Vitreous human and synovial fluid
What are chondroitins and keratin sulate?
Make up tendons, cartilage, and other connective tissues
What is dermatan sulfate?
Extracellular matrix of skin
What are glycoproteins?
Sugars attached to proteins
What are O-linked saccharides?
Attached to the hydroxyl group of serine or threonine
What are N-linked saccharides?
Attached via amide nitrogen of asparagine residues
What is a lipopolysaccharide?
Lipid group joined to a polysaccharide
What coats the other membrane of gram-negative bacteria?
Lipopolysaccharide
What are proteoglycans?
Glycoproteins whose carbohydrates are mostly glycosaminoglycans O-linked to serine residues
What makes up bacterial cell walls?
Peptidoglycan
Describe D-Ribose:
H-C=O
H-C-OH
H-C-OH
H-C-OH
CH2OH
Right, Right, Right
Describe D-Glyceraldehyde:
H-C=O
H-C-OH
CH2OH
Right
Describe D-Glucose:
H-C=O
H-C-OH
HO-C-H
H-C-OH
H-C-OH
CH2OH
Right, Left, Right, Right
Describe D-Mannose:
H-C=O
HO-C-H
HO-C-H
H-C-OH
H-C-OH
CH2OH
Left, Left, Right, Right
Describe D-Galactose:
H-C=O
H-C-OH
HO-C-H
HO-C-H
H-C-OH
CH2OH
Right, Left, Left, Right
Describe Dihydroxyacetone:
CH2OH
C=O
CH2OH
Describe D-Ribulose:
CH2OH
C=O
H-C-OH
H-C-OH
CH2OH
Describe D-Fructose:
CH2OH
C=O
HO-C-H
H-C-OH
H-C-OH
CH2OH