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
ketones
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
fatty acid synthesis
a starter chain is attached to ACP | acetylCoA and malonylCoA are used to add 2 C atoms per cycle, this consumed NADPH
27
synthesis of triglycerides
glycerol-3-phosphate and 3 fatty acids form a triglyceride through esterification
28
break down of amino acids
produce NH3 and NH4 both are toxic
29
amino acid absorption
proteolytic enzymes in the stomach/intestine produce single amino acids absorbed into intestinal cells and released into the blood
30
amino acid protein turnover
tightly regulated multiple different rates damaged proteins have to be removed
31
transamination
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
deamination
conversion of amino groups to free ammonium ions
33
synthesis of urea
uses water happens in the mitochondrial matrix way of making the toxic NH4 through less toxic products to urea that can be excreted
34
2 types of amino acids
ketogenic - degraded to acetylCoA and can form ketone bodies glucogenic - degraded to pyruvate