Biochemistry Flashcards

1
Q

2 parts of glycogen

A

glycogenin

multiple glucose molecules bonded together in chains

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2
Q

bonds found in glycogen molecules

A

alpha 1-4 straight

alpha 1-6 branches

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3
Q

process which produces glycogen

A

glycogenesis

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4
Q

UDP-glucose role

A

activated intermediate

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5
Q

rate limitng enzyme of glycogen production

A

hexakinase

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6
Q

gluconeogenesis produces glucose from 3 molecules

A

amino acids
lactate
glycerol

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7
Q

what is the cori cycle

A

recycles lactate formed by anaerobic respiration

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8
Q

where is the cori cycle

A

in liver

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9
Q

energy cost of cori cycle

A

6 ATP

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10
Q

break down of glycogen

A

inverse reaction of glycogenesis

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11
Q

fates of the monomer subunits of glycogen breakdown

A

glucose in blood

glycolysis in muscles

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12
Q

3 types of lipid

A

simple
compound
steroid

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13
Q

what are lipids soluble in

A

insoluble in water

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14
Q

2 components in triglycerides

A

3 fatty acids

glycerol backbone

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15
Q

products of beta oxidation

A
using triglycerides
1 acetyl CoA
1 FADH2
1 NADH +H2
1 fatty AcylCoA - 2 carbons
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16
Q

4 step synthesis of fatty acid occurs

A

condensation
reduction
dehydration
reduction and release

17
Q

lipogenesis

A

de novo synthesis of fatty acids
insulin promotes storage
glucagon signals breakdown
citrate is allosteric

18
Q

liver glycogen

A

is a storage system to maintain the blood glucose between meals

19
Q

muscles glycogen

A

provides a source of energy to muscle tissue during exercise

20
Q

what is gluconeogenesis powered by

A

oxidation of lipids

21
Q

glucose-6-phosphate in the liver

A

is converted to glucose

22
Q

glucose-6-phosphate in muscles

A

provides energy - glycolysis etc

23
Q

carnitine shuttle

A

transport fats into mitochondria

converting to acetyl CoA

24
Q

energy level of beta oxidation

A

each acetyl-CoA makes 1 FADH2, 3NADH, 1 GTP
FADH2 - 1.5 ATP
NADH - 2.5 ATP
GTP - 1 ATP

25
Q

ketones

A

are produced in the mitochondria of the liver

diffuse out to the peripheries and used in the heart and kidneys and converted back to acetyleCoA

26
Q

fatty acid synthesis

A

a starter chain is attached to ACP

acetylCoA and malonylCoA are used to add 2 C atoms per cycle, this consumed NADPH

27
Q

synthesis of triglycerides

A

glycerol-3-phosphate and 3 fatty acids form a triglyceride through esterification

28
Q

break down of amino acids

A

produce NH3 and NH4 both are toxic

29
Q

amino acid absorption

A

proteolytic enzymes in the stomach/intestine produce single amino acids
absorbed into intestinal cells and released into the blood

30
Q

amino acid protein turnover

A

tightly regulated
multiple different rates
damaged proteins have to be removed

31
Q

transamination

A

moving the amino group from an amino acid to an alpha keto acid
happens in all tissues
uses a TCA intermediate
these are transported to the liver

32
Q

deamination

A

conversion of amino groups to free ammonium ions

33
Q

synthesis of urea

A

uses water
happens in the mitochondrial matrix
way of making the toxic NH4 through less toxic products to urea that can be excreted

34
Q

2 types of amino acids

A

ketogenic - degraded to acetylCoA and can form ketone bodies
glucogenic - degraded to pyruvate