Biochemistry Flashcards

1
Q

Regulation of Citrate Syntase

A

Positive Regulation By Citrate

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2
Q

Regulation of Isocitrate Dehydrogenase

A

Positive by ADP and Ca2+

Negative by NADH

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3
Q

Regulation of a-ketoglutarate Dehydrogenase

A

Positive by Ca2+

Negative by NADH

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4
Q

Regulation of Malate Dehydrogenase

A

Negative by NADH

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5
Q

What are precursors of Acetyl-CoA

A
Glucose (via pyruvate)
Alanine (via Pyruvate)
Ethanol
Ketone body (Acetate)
Fatty Acid (Palmitate)
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6
Q

Why isn’t oxaloacetate a regulator?

A

The equilibrium between oxaloacetate and malate favors malate so at any time there is only a small amount of oxaloacetate available

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7
Q

How is PDH inhibited?

A

PDC Kinase phosphorylates a serine residue on E1 in response to Acetyl Coa, and NADH
PDC Phosphotase hydrolyses this phosphate to activate it in response to ADP and pyruvate and Calcium

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8
Q

What TCA cycle intermediates are used in biosynthesis

A
Citrate - Fatty Acid Synthesis
a-Ketoglutarate - AA synthesis, GABA
Succinyl CoA - Heme
Malate - Gluconeogenesis
Oxaloacetate - AA synthesis
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9
Q

What does pyruvate carboxylase do?

A

Catalyzes addition of CO2 to Pyruvate to make oxaloacetate in anapleurotic reaction

Requires biotin, activated by acetyl-coa

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10
Q

What is E1

A

Pyruvate Carboxylase
Requires TPP
Carboxylates Pyruvate to form covalent intermediate

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11
Q

What is E2

A

Transacylase
Requires Lipoic Acid (SS bond)
Grabs acyl group and transfers it onto CoASH, Subsequently reduces FAD on E3

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12
Q

What is E3

A

Dihydrolipoyl Dehydrogenase
Requires FAD and NAD
FAD is reduced to FADH2 and subsequently reduces NAD to NADH

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13
Q

What is riboflavin a precursor to?

A

Vitamin B3

Precursor to FAD and FMN

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14
Q

What is Niacin?

A

Precursor to NAD

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15
Q

What is Thiamine?

A

Vitamin B1
Necessary for TPP
Can easily become deficient in alcoholics and the malnourished

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16
Q

What is pantothenic acid?

A

Precursor to CoA

Widely distributed in foods

17
Q

What regulates Hexokinase?

A

Glucose 6 P

18
Q

What regulates PFK-1

A

F26BP, AMP are positive

H+, Citrate, and ATP are negative

19
Q

What conditions cause lactic acidosis

A
Circulatory insufficiency
Anemia
Mitochondrial enzyme defects
Poisons
Cancer
Ethanol Intoxication
Hepatic Failure
20
Q

What transporters don’t exist

A

oxaloacetate
NAD/NADH
AcCoA

21
Q

What carriers do exist?

A
Malate
Aspartate
Glutamate
Pyruvate
A-Ketoglutarate
22
Q

Where is the glycerol phosphate shuttle?

A

Most tissues

23
Q

Where is the malate aspartate shuttle?

A

Mainly liver, kidney, and heart

24
Q

What is the malate aspartate shuttle?

A

Requires transaminase reaction of aspartate to aketoglutarate and oxaloacetate to malate
Oxaloacetate reduced to malate in cytosol which is transported and reduces NAD in the IMM to NADH for the ETC
Oxaloacetate inside is transaminated to aspartate which is shuttled out and transaminated back to oxaloacetate
Transamination also converts glutamate ot akg on inside and back outside

25
Q

What cells produced lactate?

A

RBC

Working Muscle

26
Q

What cells use lactate?

A

Liver
Resting muscle
Heart

27
Q

What tissues are dependent on anaerobic glycolysis?

A
Red cells
White cells
Lens of eye
Kidney medulla
Exercising muscle
28
Q

Describe the cori cycle

A

Liver uses 2lactate and 6 ATP to create glucose which goes to the RBC and undergoes glycolysis to create 2lactate and 2 ATP which cycle back to the liver