FA Degradation & Ketone Body Synthesis Flashcards

1
Q

Beta Oxidation Energy Math

Acetyl-CoA’s
Rounds of B-Oxidation
NADH, FADH =

A

Beta Oxidation Energy Math
Acetyl-CoA’s = #/2
Rounds of B-Oxidation = Acetyl-CoA-1 (4 carbon broke in 2)
NADH, FADH = [1, 1] per round.

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2
Q

Name the two Lipases involed in FA degredation, thier location and their function

A

Lipoprotein (on endothelial cells of BV/tissue cells) - hydrolyzes TG in VLDL’s and Chylomicrons

Hormone Sensitive Lipase (cytosol of adipose tissue) - controls mobilization of FA from TG stored in adipose tissue.

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3
Q

What happens to FA and Glycerol produced by ADIPOSE tissue lipase? (HSL)

A

Released to Circulating blood.
FA binds to albumen
glycerol no binging - goes to liver (gluconeogenesis/glucose)

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4
Q

Hormonal Regulation of both Lipases

A

Lipoprotein Lipase (+) Insulin, Apolipoprotien C2

Hormone Sensitive Lipase (+) Glucagon, Epinephrine
(-) insulin, prostoglandin

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5
Q

B-Oxidation occurs in the _____ yielding _______, The 4 step process is _________; _____ ATP are generated per C16’s; The _____ goes to the TCA cycle, the ______ go to Terminal oxidation

A

????, 1 Acetyl-CoA, 1 FADH2, 1 NADH + H per cycle.
Dehydrogenation (FADH2), hydroxylation, oxidation (NADH), thiolysis (Acetyl-CoA); 129
Acetyl-CoA, NADH/FADH2

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6
Q

Explain the three general steps of FA degradation

A

1) Fatty Acid Activation: Acetyl CoA –> Fatty Acyl-CoA by FAC - Synthase
2) CPT1 binds acyl group (FA - no CoA) joins it with carnitine (1 ATP); Carnitine carries Acyl Group to innermembrane (middle). Translocase moves (Carnitine+Acyl) to Matrix.

CPTII relieves carnitine and Acyl group is transferred back to CoA by (1 ATP)

3) 4 Step B-Oxidation (beginning with acyl-CoA dehydrogenase) DHDT

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7
Q

There a 4 types of Acyl-CoA dehydrogenases (use FAD+)

A

VLCAD: 20-24 (peroxisomes)
LCAD: 12-18
MCAD: 6-10 carbons
SCAD: 4-6 carbons

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8
Q

Small and medium carbon FA ______ need carnitine to cross the mitochondrial membrane. They _____ need toe be be activated first.

A

dont, do

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9
Q

What occurs when a acyl-CoA dehydration are in defect: What do you expect to see?

A

Fat accumulation (no lysis)
Accumulation of acyl bound carnitine in blood (cant enter matrix)
Jaundice

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10
Q

Regulation of Carnitine shuttle is the ________: (-) in presence of _____ inhibits CPT-1; Carnitine can come from ____ or is made by the liver

A

Rate limiting, Malonyl Co A (product of FA synthesis), Diet.

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11
Q

What is the final product of B-Oxidation of Odd chain fatty acid? What are the called? Where do they go? What are cofactors of this reaction

A

AcCoA + Propionyl-CoA (C3)
propionyl-CoA converted to Succinyl-CoA –> glucose (only FA that can produce glucose)
need biotin B7, B12

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12
Q

What is the final product of B-Oxidation of un-saturated chain fatty acid? Why the stop? What enzymes are needed to fix? what about polyunsaturated?

A

Enzymes stop at Cis configuration. Ditto,

S: isomerase
P: NADPH dependent reductase

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13
Q

What happens to very long FA/Branched, when degraded?
How is FAD use different?
Name the enzyme that causes reduction to water
What are the products of one round of this digestion

A

Digested in the Peroxisomes,
FADH not used for energy
Catalyse
NADH and 1 Acetyl-CoA

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14
Q

What are the products of Omega/Alpha oxidation respectively? Where do they occur Respectively?

A

O: (dicarboxilic acids) ER
A: (hydroxylated FA) ER and Mitochondria

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15
Q

Ketone Body Synthesis: What Enzyme cleaves HMG-CoA (used in cholesterol synthesis too) ? What are the products

A

HMG-CoA Lyase, Acetyl CoA & Acetoacetic Acid (interchanged with 3- Hydroxybutyrate)

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