Metabolism Flashcards

1
Q

acetyl CoA made available by…

A

oxidation of fatty acids, ketone bodies, monosaccharides, amino acids, ethanol

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2
Q

cofactors of PDC

A
  1. TPP (B1)
  2. Lipoate
  3. Coenzyme A (B5)
  4. FAD (B2)
  5. NAD (B3)
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3
Q

PDC regulated by

A

increased ATP/AMP, NADH/NAD, acetyl CoA/CoA, PDK (-) and PDP (+), CO2

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4
Q

starvation effect on PDC

A

increases transcription of PDK which inhibits PDC preventing glycolysis and promotes fat utilization so glucose can be used for brain

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5
Q

AA that make a ketoglutarate

A

glutamate, histidine, proline, arginine

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6
Q

AA that make fumarate

A

phenylalanine, tyrosine, aspartate

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7
Q

AA that make succinyl CoA

A

methionine, SAM, valine, isoleucine, threonine

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8
Q

AA that make acetyl CoA

A

leucine, isoleucine, lysine, tryptophan

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9
Q

disorders of TCA due to problems in

A

a ketoglutarate dehydrogenase, succinate dehydrogenase, fumarase

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10
Q

AA that make pyruvate

A

threonine, tryptophan, glycine, alanine, serine, cysteine

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11
Q

3 ways to transport OAA to cytoplasm for gluconeogenesis

A

OAA –> PEP by PEPCK and transported by anion transporter
OAA –> malate by malate dehydrogenase –> cytoplasm
OAA –> aspartate –> cytoplasm –> back to OAA

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12
Q

gluconeogenesis precursors

A

amino acids from proteins (mainly alanine)
lactate from RBC/muscle
glycerol from triacylglycerols

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13
Q

short and medium chain FA enter mitochondrial matrix via..

A

monocarboxylate transporter

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14
Q

B-oxidation inhibited by

A

malonyl-CoA and ATP/NADH

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15
Q

w-oxidation

A

ER, uses cytochrome pf450, O2 and NADPH

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16
Q

what converts acetoacetate to acetoacetyl-CoA?

A

succinyl-CoA

17
Q

adipose tissue can only make triacylglycerols when…

A

the cell is in the fed state and glycolysis is working to give DHAP

18
Q

sources of one carbon groups

A

serine, glycine, formaldehyde, histidine, formate

19
Q

2 rxns of B12

A
  1. homocysteine to methionine

2. methylmalonyl CoA to succinyl CoA (no donation just rearrangement)

20
Q

SAM rxn

A

methionine + ATP –> SAM

21
Q

what’s needed to absorb B12

A

intrinsic factor

22
Q

what reactions need vitamin B6 (PLP)

A

making cysteine from homocysteine

ALT/AST

23
Q

routes for amine removal from amino acid

A

ALT/AST

oxidative deamination of glutamate via glutamate dehydrogenase

24
Q

urea cycle regulation

A
  1. substrate availability (arginine) in feed-forward mechanism
  2. allosteric activation of carbamoyl phosphate synthetase I (CPSI) by NAG
  3. induction/repression of enzyme synthesis during high protein diet/starvation
25
purine salvage pathway enzymes
adenine phosphoribosyltransferase | HGPRT
26
what contributes nitrogen to urea
aspartate and ammonia
27
what controls CPSTI
Arginine
28
what inhibits complex 4 of ETC
CN, CO, H2S, sodium azide bind iron in heme of cytochrome aa of cytochrome oxidase
29
what inhibits complex 3 of ETC
antimycin A and dimercaprol bind cytochrome c reductase in complex III
30
barbituates and rotenone
inhibit transfer of electrons from iron-sulfur centers in Complex I to CoQ
31
sources of primary ROS in cell
CoQ, oxidases peroxidases and oxygenases, ionizing radiation