008 TCA Cycle and Organ Specific Shuttles Flashcards

1
Q

other names for TCA

A

Tricarboxylic acid cycle (TCA)
citric acid cycle
krebs cycle

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2
Q

this cycle is amphibolic

A

meaning it has both catabolism and anabolism in the pathway

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3
Q

function of TCA cycle

A

oxidizing carbon fuels for harvesting high energy electrons
source of precursors for biosynthesis
takes place in the mitochondria

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4
Q

precursors of acetyl CoA

A
fats/LIPIDS  (fatty acids and glycerol)
polysaccharides/CARBS (glucose, other sugars) --> pyruvate
PROTEINS (AA) essential amino acids
ethanol
acetic acid
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5
Q

three energy equivalent substances

A

NADH
FADH2
GTP

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6
Q

acetyl CoA

A

activated form of acetate
high energy bond embedded in thirster group
delta G= -7.5 kcal/mole

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7
Q

this catalyzes the decarboxylation of pyruvate into Acetyl CoA

A

pyruvate dehydrogenase complex (PDC)

this happens in the mitochondria using the pyruvate mitochondrial carrier (PMC)

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8
Q

steps 1 and 2

A

condensation and isomerization to generate isocitrate

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9
Q

step 3 and 4

A

irreversible oxidation and decarboxylations (NADH, CO2, and Succinyl CoA)

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10
Q

step 5

A

formation of succinate and GTP

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11
Q

steps 6-8

A

produce FADH2, NADH, and regenerate oxaloacetate

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12
Q

which steps are regulated and irreversible

A

steps 1,3, and 4

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13
Q

in a phosphate deficiency, PDC is always in

A

phosphorylated form (inactive)
glucose—>lactate rather than acetyl coA
results in lactic acidosis (high levels in blood of lactic acid)
central nervous system affected the most

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14
Q

when cellular ATP levels are low, activity of TCA is

A

increased

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15
Q

high cellular levels of ATP triggers the

A

inhibition mechanism of TCA cycle (mitochondrial ETC inhibition)

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16
Q

reactions that provides intermediates for pathways

A

anaplerotic reactions

17
Q

two major anaplerotic reactions

A
  1. degradation of amino acids

2. carboxylation of pyruvate

18
Q

molecules used in metabolic processes takes place in the mitochondria. they can penetrate the outer membrane but

A

cannot penetrate the inner membrane, require a shuttle system to cross. this is more regulated

19
Q

reduced NADH cannot cross the mitochondrial membrane, so there are two shuttle systems

A
  1. malate-aspartate shuttle

2. glycerophosphate shuttle

20
Q

malate-aspartate shuttle

A

operates in heart, liver and kidneys (energy consuming organs that work really hard)
generates reduced NADH in mito-matrix
reduced NADH enters ETC at Complex-1

21
Q

glycerophosphate shuttle

A

operates in skeletal muscle and brain (instant energy, need it now!)
Generates reduced FADH2 in the inner mito membrane
reduced FADH2 joins to ETC at CoQ