Chapter 10: Carbohydrates Flashcards

1
Q

Carbohydrates

A

Carbon based molecules that are rich in hydroxyl (C - OH)

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2
Q

What is linkage of carbohydrates?

A

Glycosidic

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3
Q

Polysaccharides

A

Polymers of covalently linked monosaccharides

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4
Q

Monosaccharrides

A

Simplest carbohydrates
Cn(H20)n
Lowest n=3

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5
Q

Function of carbohydrates

A
  • major energy sources: carbohydrate oxidation
  • essential structural/ protective componets
  • cell to cell recognition signals
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6
Q

Examples of monosaccharides

A

Dihydroxyacetone
D and L glyceraldehyde

Have 3 carbons

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7
Q

D Configuration

A

OH on right of highest numbered steric carbon

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7
Q

Mostly highly oxidized carbon is

A

C-1

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8
Q

L Configuration

A

OH on left of highest numbered steric carbon

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9
Q

In Haworth projection, D sugar CH2OH on C5

A

will be up

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10
Q

In Haworth projection, L sugar CH2OH on C5

A

will be down

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11
Q

Enantiomer

A

Nonsuperimposable mirror images

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12
Q

How to calculate streoisomer

A

of steroisomers = 2^n
n= # of chiral centers

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13
Q

Diasteroisomers

A

Isomers that are not mirror images

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14
Q

Epimers

A

Differ at only ONE carbon atom

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15
Q

Anomers

A

Isomers that differ at new asymmetric carbon after cyclization
Formation of a cyclic hemiacetal creates another
diastereoisomeric form

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16
Q

Anomeric carbon

A

Only carbon bonded to 2 oxygen atoms

17
Q

Alpha form of anomers

A

Hydroxyl of C1 (anomeric carbon) is below the plane of ring
C5 of CH2OH and C1 of OH are opposite

18
Q

Beta form of anomers

A

Hydroxyl of C1 (anomeric carbon) is above the plane of ring
C5 of CH2OH of C1 of Oh are on same side

19
Q

Cyclization

A

OH attack C=O to form ring

20
Q

Sugar alcohols (alditols)

A

carbonyl group of sugar is reduced to an alcohol (OH) group

21
Q

Deoxy sugars

A

Reduced sugars where hydrogen atom is substitued for one of hydroxyl groups

22
Q

Reducing sugars

A

Sugars that react with oxidizing agent

23
Q

Tollens reagant test

A

Used to detect presence of reducing agent
Ag(NH3)2+ used as oxidizing agent

24
Nonreducing sugars
Sugars that do not react with oxidizing agnet
25
O glycosidic bond
Bond formed between anomeric carbon atom of sugar and a hydroxyl group of another molecule
26
N glycosidic bond
Bond formed between anomeric carbon of sugar and amine
27
Phosphate esters
Intermediates in breakdown of carbohydrates to provide energy Formed by transfer of a phosphate group from ATP to give ADP and phosphorylated sugar
28
Oligosaccharides
Contain 2 or more monosaccharides linked by O glycosidic bonds
29
Glycosyltransferases
Catalyze formation of glycosidic bonds
30
Sucrose
Disaccharide Glucose + fructose
31
Lactose
Disaccharide Glucose + galactose
32
Maltose
Disaccharide Gluocse + Glucose
33
What are storage forms of glucose?
Glycogen and Starch
34
Glycogen
Most units linked by alpha 1,4 glycosidic bonds with branches formed by alpha 1,6 glycosidic bonds every 12 glucose units
35
Starch
In plants, glucose is stored as starch 2 Forms: Amylose and Amylopectin
36
Amylose
Fornm of starch Linear polymer of glucose units linked by alpha 1,4 glycosidic bonds
37
Amylopectin
Form of starch Branched polymer with alpha 1,6 glycosidic bond for every 30 alpha 1,4 glycosidic bonds
38
Cellulose
Structural componet of plants made of chains of glucose Homopolymer of glucose units linked by beta 1,4 glycosidic bonds
39
Glycoproteins
Proteins linked to oligosaccharides
40
O linked glycoproteins
Joined to serine or threonine in protein Golgi apparatus
41
N linked glycoproteins
Joined to asparagine in protein E.R. and golgi apparatus