Glucose Oxidation & Shuttles Flashcards

1
Q

Mention the three principal phases of cellular respiration

A
  1. Oxidation of fuels
  2. Conversion of energy from fuel oxidation into high energy phosphate bond
  3. Utilization of high phosphate bond energy
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2
Q

The convergent product of oxidation of most fuels

A

Acetyl CoA

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3
Q

Complete oxidation of acetyl CoA occurs in …… and produces ….&….

A

Tricarboxylic acid cycle

NADH & FADH2

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4
Q

Define the electron transport chain

A

A process in which electrons are transferred from NADH and FADH2 to O2.

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5
Q

Enumerate processes requiring ATP

A

Muscle contraction, maintaing intracellular Na concentration, anabolic pathways & detoxification.

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6
Q

The ETC occurs in ….., while …..&….. occur in mitochondrial matrix.

A

Inner mitochondrial membrane

TCA & oxidation of fatty acids

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7
Q

Compare aerobic & anaerobic glycolysis fate of NADH & pyruvate

A

A: NADH reoxidized in ETC, pyruvate completely oxidized in TCA cycle.
An: NADH reoxidised by conversion of pyruvate to lactate.

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8
Q

Examples of anaerobic glycolysis

A

In RBCs , kidney medulla & exercising muscle

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9
Q

NADH is indirectly transferred to inside the mitochondria by …..

A

Shuttle mechanism (malatae aspartate shuttle & glycerophosphate shuttle)

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10
Q

Describe the steps of malate shuttle

A

Electrons from NADH convert oxaloacetate to malate by cytosolic malate dehydrogenase.
Malate crosses the inner mitochondrial membrane by special translocase.
Electrons of malate reform NADH, and oxaloacetate is reformed (by mitochondrial malate dehydrogenase) which is converted by AST to aspartate which is transported out by aspartate/glutamate exchange translocase.

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11
Q

The major shuttle is

A

Glycerol phosphate shuttle

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12
Q

Describe the mechanism of glycerol phosphate shuttle

A

Cytoplasmic Glycerol 3-phosphate dehydrogenase uses electrons from NADH to convert DHAP to GAP which diffuses to mitochondria then its electrons are donated to give FADH2 (gives 2 ATP in ETC)

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13
Q

PDC reaction is one of

A

Oxidative decarboxylation

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14
Q

Mention the 3 enzymes of PDC

A

Pyruvate dehydrogenase, dihydrolipoyl transacetylase & dihdrolipoyl dehydrogenase

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15
Q

Mention the coenzymes of PDC

A

Thiamin pyrophosphate, lipoic acid, CoASH, FAD and NAD+.

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16
Q

…….. inhibits pyruvate dehydrogenase while ….. activates it. (Covalent modification)

A

Phosphorylation

Dephosphorylation

17
Q

PDC kinase is inhibited by ….&…., while it is activated by ….&…… .

A

ADP & pyruvate

Acetyl CoA & NADH

18
Q

Mention the regulation of PDC phosphatase in the heart

A

Calcium is required for its activity
Increased mitochondrial Ca++ during rapid contraction activates the phosphatase, thereby increasing the amount of active PDC.

19
Q

Describe the hormonal regulation of PDC

A

Insulin favor the active, dephosphorylated form, while glucagon favors the phosphorylated, inactive form.

20
Q

Mention the fates of pyruvate

A

Converted to: alanine, lactate, acetyl CoA, oxaloacetate.

21
Q

…..&…. Are irreversible enzyme acting on pyruvate, while ….&…. Are reversible

A

Pyruvate carboxylase, PDC

LDH, transamination

22
Q

Dietary deficiency of thiamin pyrophosphate results in the following diseases:

A

Beriberi

Wernicke-Korsakoff syndrome

23
Q

Alcohol addiction result in deficiency of ….

A

Thiamin pyrophosphate

24
Q

…. Inhibits lipoic acid containing enzymes such as …..&….. .

A

Arsenite

PDC & alpha-ketoglutarate dehydrogenase complex

25
Q

Abnormalities in the PDC lead to accumulation of ….

A

Lactate