Carbohydrates Flashcards

1
Q

What are five functions of carbohydrates?

A

Energy source and storage

Structural components of cell walls

Lubricant

Protection

Communication in cell-cell signaling

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2
Q

What is an aldehyde/aldose?

A

Carbonyl group is located at the end of a carbon chain

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3
Q

What is a ketone/ketose?

A

Carbonyl group is located in any other position

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4
Q

What are stereoisomers?

A

Compounds with the same composition and the same order of atomic connections but different molecular arrangements in space

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5
Q

What is an enantiomer?

A

Pairs of stereoisomers that are mirror images of one another but cannot be superimposed on each other

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6
Q

What type of isomer of monosaccharides exists in living organisms?

A

D isomers

E.g. Dextrose (D-glucose)

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7
Q

What are diastereomers?

A

Pairs of stereoisomers that are not mirror images of each other

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8
Q

What are epimers?

A

Two sugars that differ only in configuration around one carbon atom

E.g. Galactose is an epimer of glucose at C-4
Mannose is an epimer of glucose at C-2

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9
Q

What is a pyranose?

A

6-sided ring structure of a monosaccharide

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10
Q

What is a furanose?

A

5-sided ring structure of a monosaccharide

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11
Q

How is a hemiacetal formed?

A

Through the addition of an -OH group to the aldehyde in a monosaccharide

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12
Q

How is a hemiketal formed?

A

Through the addition of an -OH group to the ketone of a monosaccharide

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13
Q

What is an anomer?

A

Isomeric forms of monosaccharide that differ in configuration about the C1 carbon

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14
Q

What is the anomeric carbon?

A

The former carbonyl carbon (C1) in the chain form of the monosaccharide that becomes the new chiral carbon in the ring structure

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15
Q

What is configuration a of a monosaccharide ring?

A

If the -OH group on opposite side of the ring as CH2OH

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16
Q

What is configuration B of a monosaccharide ring?

A

If the -OH group ends up on the same side of the ring

17
Q

What ring configuration is most often found in nature?

18
Q

What is a glycosidic bond?

A

Bond formed through the addition of an alcohol group to and aldehyde or ketone (C-O)

19
Q

What can hydrolyze glycosidic bonds?

20
Q

What are glycosidic bonds resistant to?

A

Cleavage by base

21
Q

What is a reducing sugar?

A

Sugar that has a free anomeric carbon and can be reduced

E.g. all monosaccharides, Lactose and Maltose

22
Q

What are polysaccharides?

A

Natural carbohydrates usually occur as polymers

Can be homo-, hetero-, linear or branched

Do not have a defined molecular wight

Synthesis intrinsic to enzymes that catalyze polymerization of monomeric units

23
Q

What is starch?

A

Storage polysaccharide in plants

polymers of glucose

24
Q

What is amylose?

A

Unbranched starch polymer

a1-4 linkages

25
What is amylopectin?
Similar to amylose but has a1-6 branches every 24-30 residues
26
What is glycogen?
Storage polysaccharide in animals D-glucose polymer with a1-6 branches every 8-12 residues Can store a higher concentration of glucose as glycogen
27
What is inulin?
Polysaccharide of fructose Soluble in water, but can't be digested Used to determine GFR
28
What are Dextrans?
Polysaccharide of a1-6 D-glucose with a1-2,3 and 4 branches made by yeast and bacteria found in dental plaque
29
What is cellulose?
linear, unbranched glucose polymer in the B configuration
30
What are glycosaminoglycans?
Contain amino sugars and uronic acids Attached to proteins to form proteoglycans
31
What are glycoproteins?
Proteins containing branched or unbranched oligosaccharide chains Attached via anomeric carbons
32
What does hypoglycemia lead to?
lethargy, coma, permanent brain damage, death
33
What does hyperglycemia lead to?
impaired blood flow changes in osmolality of body fluids intracellular acidosis increased superoxide radical production