Metabolism Flashcards

1
Q

Alpha-ketoacid dehydrogenase requires ______ as a coenzyme

A

thiamine pyrophosphate (vit B1)

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2
Q

the branch-chain alpha-keto acid dehydrogenase complex is responsible for the catabolism of the branched chain amino acids _______, _______, and _______

A

leucine, valine, and isoleucine

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3
Q

Epi and NorEpi are metabolized to ________ and ________ by _______…THEN it is FURTHER broken down into ________ by _______.BOOM

A

METAnephrine and normetanephrine…catechol-O-methyltransferase (COMT)…Vanilla (Vanillylmandelic Acid) by MAO (MonoAmineOxidase)

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4
Q

What metabolic byproduct might you see in the urine of a pheochromocytoma pt?

A

Vanillylmandeic Acid

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5
Q

What breaks down a fatty acid to ACYL CoA?

A

ACYL CoA SYNTHASE

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6
Q

Remember the Carnitine Shuttle?? Which enzyme does work in the cytoplasm? Which enzyme does work in the mitochondrial matrix? WHAT ARE THESE ENZYMES CONVERTING?!?! (hint: its the SAME inside the mitochondria AND outside the mitochondira)

A

CAT I in cytoplasm…CAT II in Mitochondrial Matrix…Carnitine—–>ACYL-Carnitine

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7
Q

What is the precursor for Ketone Bodies?

A

Acetyl CoA

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8
Q

FAO: Acyl-CoA—-> (ENZYME?)—->Trans-enoyl CoA.. What is the byproduct released?

A

Acyl-CoA Dehydrogenase..FADH2

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9
Q

FAO: Tans-enoyl CoA —–>? (no enzyme given)

A

3-HydroxyAcyl CoA

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10
Q

FAO: 3-HydroxyAcyl CoA—->? (no enzyme given)…What is the BYPRODUCT?

A

3-Ketoacyl CoA…NADH

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11
Q

FAO: 3-KetoAcyl CoA—->? (no enzyme given)

A

Acetyl CoA (then to KBs!!!)

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12
Q

What are the two purely KETOGENIC amino acids? What are the 4 Glucogenic AND Ketogenic AAs?

A

Pure: 1.Leucine 2.Lysine……..Both:1.ISOleucine 2.Phenylalanine 3. 3-O-9 4.TryptoPhan

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13
Q

Which ION sees an increased extracellular concentration during TISSUE injury??

A

K+

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14
Q

______ ____-______ is responsible for the synthesis of Nor-epi from dopamine.

A

Dopamine beta-hyroxylase

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15
Q

the balance between glycolysis and gluconeogenesis is primarily regulated at the conversion between _________ and ____________

A

fructose-6-phosphate (fructose-6P) and fructose-1,6-bisphosphonate (fructose-1,6BP)

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16
Q

________ converts fructose-6P to fructose-1,6BP during GLYCOLYSIS

A

PFK-1 (phosphofructokinase-1)

17
Q

_________ catalyzes fructose-1,6BP to fructose-6P during GLUCONEOGENESIS

A

F-1,6-BPase (fructose-1,6-bisphosphonase)

18
Q

________ increases intracellular concentrations of fructose-2,6,bisphosphate, which promotes PFK-1 and fthe formation of fructose-1,6-bisphosphate…WHICH metabolic process is this?

A

INSULIN…glycolysis

19
Q

BUST OUT THE PENCIL AND PAPER: what are the 9 hydrophobic AA’s?

A

VAL-PIT-MPG: Valine, Alanine, Leucine, Phenylalanine, Isoleucine, Tryptophan, Methionine, Proline, and Glycine

20
Q

Carbamoyl phosphate synthase II is an enzyme that catalyzes the initial step in DE NOVO ______ synthesis and is located in the CYTOSOL

A

pyrimidine

21
Q

Carbamoyl phosphate synthase I of the UREA cycle is located in the ________

A

mitochondria

22
Q

Impaired ________ enzyme production RAISES the body’s glucose threshold for insulin release thus leading to diabetes

A

GLUCOKINASE

23
Q

Von-Gierke disease is a ______-__-_____ deficiency and impairs the release of free glucose generated thru glycogenolysis and gluconeogenesis

A

Glucose-6-Phosphatase