Carbohydrates Flashcards

(56 cards)

1
Q

carbohydrates stored as ……….. in human

A

glycogen

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2
Q

monosaccharide’s

A

glucose galactose fructose

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3
Q

disaccharides

A

monomers linked with glycosidic bonds

hydroxyl + carbon group

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4
Q

important disaccharides

A

maltose
lactose
sucrose

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5
Q

Maltose is a breakdown product of

A

starch

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6
Q

maltose can be ………. (so is a reducing sugar)

A

oxidised

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7
Q

Lactose is formed from a glycosidic bond between

reducing sugar

A

galactose and glucose

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8
Q

Sucrose is NOT a

A

reducing sugar

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9
Q

two types of glucose polymer in starch

A

amylose

amylopectin

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10
Q

Starch has lots of ………….. and very few ………….

A

non-reducing ends

reducing ends

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11
Q

90% of glycogen is kept in the

A

liver and skeletal muscle

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12
Q

Glycoproteins

A

proteins that have carbohydrates covalently attaches

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13
Q

Glycosaminoglycans (GAGS)

A

polymers made from repeated units of hexuronic acid and an amino sigar

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14
Q

Proteoglycan

A

made from GAGs covalently attaching to proteins

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15
Q

Mucopolysaccharidoses

A

disorders caused by the absence or malfunction of enzymes that are required to breakdown GAGs

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16
Q

Mucopolysaccharidoses example

A

hurler syndrome

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17
Q

Glucose is absorbed through an

A

ATP powered process

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18
Q

ATP driven Na+ pump maintain a low cellular Na+

A

so glucose can be continually moved in to the epithelial cells

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19
Q

cellulose and hemicellulose cannot be

A

digested by the gut

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20
Q

lack of oligosaccharides leads to

A

poor health

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21
Q

Most common disaccharide deficiency

A

lactose intolerance

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22
Q

Glucose diffuses through the intestinal epithelium into the

A

portal blood and on to the liver

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23
Q

Glucose is immediately phosphorylated into

A

glucose 6 phosphate by the hepatocytes

24
Q

Synthesis of glycogen

glycogenin begins the process by covalently binding glucose from

A

UDP-glucose

forms 8 glucose residues

25
Synthesis of glycogen glycogen synthase takes over to...
extend the glucose chains
26
Synthesis of glycogen the chains formed by glycogen synthase are broken by...
glycogen-branching enzymes then reattached by alpha 1 to 6 bonds to give BRANCH POINTS
27
von gierke's disease
liver glucose-6-phosphatase deficiency high liver glycogen low blood glucose high blood lacatate
28
McArdle's disease
skeletal muscle phosphorylase deficiency high MUSCLE glycogen
29
Glycolysis
saves some potential energy from glucose/glucose-6-phosphate by forming ATP through substrate level phosphorylation
30
Glycolysis gives a net gain of ....ATP (and NADH) per glucose molecule
2
31
only G3p can participate in glycolysis so....
the other 3 C sugar produced must convert into G3P so theres 2 G3Ps per glucose molecules
32
Glycolysis first step
glucose to G6P
33
glycolysis G6P -->
F6P
34
Glycolysis F6P -->
F 1,6 p bisp
35
F16 bisp then gets cleaved to give
splitting of glycolysis 2 different 3C triose sugars
36
after 2 G3P's are formed...
oxidation of G3P to 1,3 bisPG
37
1,2 bis pG to
ADP 2 ATP are produced
38
3-PG to
2 - PG
39
2 PG to
PEP
40
PEP to
ADP 2 ATPs produced final step that produces pyruvate
41
No NAD+ mean no
glycolysis
42
What happens to pyruvate? can turn into......
ethanol lactate co2
43
pyruvate goes to lactate in cells lacking
oxygen via fermentation
44
Cori Cycle
ATP is make via substrate level phosphorylation - producing lactate
45
in the cori cycle - lactate is converted to glucose in the liver by...
gluconeogenesis
46
bypass reactions
4 reactions that sidestep the 3 irreversible reactions of glycolysis
47
..... and ......... can enter glycolysis at various points
fructose and galactose
48
pentose pathway produces
NADPH for all organisms
49
pentose pathway has 2 phases
irreversible oxidative part reversible, non-oxidative part
50
NAD+ is used in
metabolism of dietary sugars in the redox reactions of glycolysis
51
NADP+ is used in
anabolism to convert simple precursors into FAs
52
alcohol inhibits
gluconeogenesis
53
black water fever
G6P dehydrogenase deficiency
54
TCA cycle occurs in the
mitochondrial matrix
55
TCA cycle removes e-'s and passes them on to form
NADH and FADH2
56
TCA pyruvate from glycolysis and FAs are oxidised to
acetyl CoA in the mitochondrial matrix via the help of pyruvate dehydrogenase