chp 7 Flashcards

(105 cards)

1
Q

glucose and fructose are an example of wt carbohydrates

A

monosacchrides

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

wt do we call OH group

A

hydroxyls

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

aldeyde group

A

CHO

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

ketone gorup

A

C=O

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

glucose is an example of which monosachrides

A

aldehyde

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

fructose is which type of monosachrides ?

A

ketone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

how many carbons does glucose has ?

A

6 carbons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

wdym by ismoers

A

Compounds with the same formula but different structures.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Glucose, fructose, mannose, and galactose are examples of wt ?

A

ismoers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

D-glucose vs D-galactose are an example of which isomer ?

A

Epimers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

D-glucose vs L-glucose are an example of which ismoer ?

A

Enantiomers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

D-glucose vs D-mannose are an example of which

A

Diastereomers , epimers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

when do sugars form rings

A

Sugars with 4 or more carbons mostly exist in cyclic form in water

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

why do they form ring sometimes
?

A

Because the aldehyde or ketone group on one end
reacts with a hydroxyl group (–OH) on another carbon

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

if the OH is down wts it called

A

alpha (α)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

if the OH is up wts it called

A

beta (β)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What’s the difference between furanose and pyranose?

A

Furanose = 5-membered ring

Pyranose = 6-membered ring

Fructose often forms furanose, glucose often forms pyranose.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Mutarotation

A

When you put a sugar like glucose in water, it can change between 3 forms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Aldehyde group (–CHO) after oxidation becomes wt ?

A

Aldonic acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

The carbonyl and hydroxyl groups can undergo
several chemical reactions

A

oxidation, reduction,
isomerization, esterification, glycoside formation, and
glycosylation reactions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

If the top of the sugar (the –CHO group) is oxidized it becomes wt ?

A

aldonic acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

If the bottom –CH₂OH is oxidized it becomes wt?

A

uronic acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

If you add hydrogen to the sugar’s –CHO or =O group becomes wt ?

A

it becomes a sugar alcohol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

if we add a hydrogen to the glucose , it becomes wt?

A

Sorbitol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Isomerization
This is when the sugar changes form but keeps the same formula.
26
Esterification
The –OH groups of sugar react with acids forming esters
27
Esterification is important in wt
Important in joint tissues and cell membranes
28
Glycoside formation
Normally, the sugar ring has an anomeric carbon that is reactive (hemiacetal or hemiketal). If you react it with an alcohol, you get a glycosidic bond and a glycoside.
29
Mannose is reduced , it becomes wt?
mannitol
30
where can we find sorbitol or mannitol ?
used in food and medicines (to keep moisture, sweeten products, etc.)
31
example of a lactone
vitamin C
32
lactone formation
the new acid (aldonic or uronic) can react with its own –OH group
33
what connect sugars in disaccharides (like sucrose) and polysaccharides (like starch or cellulose).
glycosidic bonds
34
vitamin C lactone is an example of which reaction ?
oxidation
35
sorbitol is an example of which reaction ?
reduction
36
Sulfate/carboxyl esters is formed in which reaction ?
esterfications
37
glycosylation is controlled by wt ?
enzymes
38
Glycosylation
A sugar is added to a protein or lipid
39
A sugar sticks randomly to a protein wts this
Glycation
40
where can we find glycation
in diabetes
41
Glycosylationis essential for wt ?
proper protein folding and function.
42
wt do we call the enzyme that helps the attach of sugar to a proteein in glycosylation ?
glycosyltransferases help attach sugars using: O-glycosidic bonds (to oxygen atoms) N-glycosidic bonds (to nitrogen atoms)
43
When a sugar is added to a protein in your body during hormone or enzyme production — that’s?
glycosylation
44
Glycation can further form wt ?
AGEs (Advanced Glycation End-products)
45
Glycation Starts by forming a
Schiff base, which rearranges into a stable structure called an Amadori product.
46
Known as dextrose
Glucose (D-Glucose)
47
Called fruit sugarsed as a sweetener in food. Sperm use it as an energy source.
Fructose (D-Fructose)
48
Needed to make lactose, glycoproteins, glycolipids,
Galactose
49
A genetic disorder called galactosemia results from the inability to metabolize it.
galactose
50
D-glucuronic acid an example of who ?
Uronic Acids
51
function of D-glucuronic acid
helps the liver remove toxins by making them more water-soluble.
52
Glucosamine & Galactosamine an example of wt ?
Amino Sugars
53
2-deoxy-D-ribose and fucose are examples of wt ?
deoxy sugars
54
Deoxy Sugars wdwm
Monosaccharides that have an –OH replaced by an –H or –CH3
55
Amino Sugars is replaced with wt ?
in amino sugars, a hydroxyl group (usually on carbon 2) is replaced with an amine group
56
Disaccharides wdwm
Two monosaccharides linked by a glycosidic bond
57
lactose is considered disaccharides or mono ?
dis
58
Maltose is considered disaccharides or mono ?
disacchrides
59
a(1,4) is found where
Maltose Starch Glycogen
60
a(1,4) enzymes can break this bond for ?
energy
61
lactase function
breaks this bond in our intestines
62
is lactose considered a reducing sugar >?
yes
63
maltose
is an intermediate product of starch hydrolysis
64
Cellobiose found in ?
From cellulose 🪵
65
Enzyme that digests cellobiose
β-glucosidase
66
Glucose + Glucose β(1→4) who r we talking abt ?
Cellobiose
67
Galactose + Glucose β(1→4) who r we talking abt ?
Lactose
68
sucrose made of ?
Glucose + Fructose
69
Linkage: α,β(1→2) for who ?
Sucrose
70
sucrose is a non-reducing sugar true of false
very true
71
which disacchrides can u find in cane sugar ?
sucrose
72
wdym by both anomeric carbons ?
It’s the carbon that used to be the carbonyl group (C=O) before the sugar closed into a ring. In glucose, that’s carbon number 1. In fructose, it’s carbon number 2.
73
Polysaccharides
These are large chains of sugar units (monosaccharides) linked together by glycosidic bonds.
74
Glycans
These are large chains of sugar units (monosaccharides) linked together by glycosidic bonds.
75
Oligosaccharides
are short chains made of 10 to 15 monosaccharides (simple sugar units) linked together.
76
polysacchrides
If there are hundreds or thousands, it's a polysaccharide.
77
O-linked in the oxygen comes from which amino acid
serine or threonine
78
two classes of Polysaccharides
Homoglycans – only one type of sugar Heteroglycans – more than one type of sugar
79
found in fungi cell walls and insects’ shells.
Chitin
80
main part of plant cell walls.
Cellulose
81
plants’ energy storage, major carb in human food.
Starch
82
Amylose linked by ?
α(1→4)
83
Amylopectin linked by ?
α(1→4) and α(1→6)
84
wt energy source is found in liver an muscles ?
glycogen
85
who is more branched glycogen or amylopectin
glycogen
86
Structural polysaccharide in plants Made of D-glucose linked by β(1→4) bonds who ?
Cellulose
87
Unbranched, forms microfibrils (strong sheets) who ?
cellulose
88
Used in fiber, wood, paper, textiles Humans can’t digest who ?
cellulose
89
Heteroglycans types
Glycosaminoglycans (GAGs) Glycolipids GPI anchors
90
Important in connective tissues and cell membranes
poly hetero
91
GAGS
These are long linear chains of repeating sugar units:
92
5 common types: of gags
Hyaluronic acid Chondroitin sulfate Dermatan sulfate Heparin/heparan sulfate Keratan sulfate
93
great for cushioning and structure (like in cartilage). who ?
Gags because they hold lots of water
94
🧬 Glycoconjugates
These are sugar + protein or lipid combinations.
95
Glycoconjugates. Two main types:
Proteoglycans andGlycoproteins
96
Contain mostly carbohydrate (up to 95%). Made of core proteins + many GAGs (via N or O linkages). who ?
Proteoglycans
97
which Glycoconjugates Found in: Cartilage Extracellular matrix
Proteoglycans
98
example of proteoglycans ?
Aggrecan
99
Roles of proteoglycans
tructure Cell signaling Disorders like Hurler’s syndrome (enzyme deficiency leads to GAG buildup).
100
Glycoproteins
Protein + smaller carbohydrate chains
101
how is sugar attched in Glycoproteins
Sugar attached via N- or O-linkages
102
where is glycoproteins made in ?
Made in endoplasmic reticulum and Golgi apparatus.
103
O-glycan synthesis mainly happens
golgi
104
roles of glycoproteins
Hormones Receptors Enzymes Cell adhesion Found in blood, membranes, and secretions
105