Glycolysis Flashcards

1
Q

Major pathway for glucose metabolism that converts glucose into 3 carbon compounds to provide energy

A

Glycolysis

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2
Q

Site of glycolysis

A

CYTOSOL

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3
Q

Substrate of glycolysis

A

GLUCOSE

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4
Q

End products of glycolysis

A

2 molecules of either pyruvate or lactate

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5
Q

Step that is Rate Limiting

A

Fructose 6 phosphate –> Fructose 1,6-bisphosphate

PHOSPHOFRUCTOKINASE

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6
Q

3 Important Steps in Glycolysis

A

Step 1: Phosphorylation of glucose

Step 2: Phosphorylation of fructose 6-phosphate

Step 3: Formation of Pyruvate

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7
Q

Found in most tissues

Inhibited by glucose 6-phosphate

LOW Km, HIGH affinity
LOW Vmax

A

Hexokinase

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8
Q

Found in LIVER and ISLET cells of PANCREAS

Inhibited by fructose 6-phosphate

HIGH Km, LOW affinity
HIGH Vmax

Liver activity induced by insulin

A

Glucokinase

acts only when glucose is very high >100 mg/dL

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9
Q

Most POTENT activator of PFK-1

A

Fructose 2,6 BP

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10
Q

2 steps in glycolysis that produce ATP via substrate level phosphorylation

A

1,3 bisphosphoglycerate –> 3 phosphoglycerate
PHOSPHOGLYCRTAE KINASE

Phosphoenolpyruvate –> pyruvate
PYRUVATE KINASE

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11
Q

Oxidation reaction that passes electrons to NAD+ to make NADH

A

Glyceraldehyde-3-phosphate –> 1,3 bisphosphoglycerate

GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE

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12
Q

Major fate of pyruvate in lens, cornea, kidney (medulla), testes, RBCs, WBCs

A

Anaerobic glycolysis

pyruvate –> LACTATE
lactate dehydrogenase

NADH - used to REDUCE pyruvate to lactate

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13
Q

No. of ATPs from Aerobic glycolysis

A

7 ATPs

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14
Q

No. of ATPs from anaerobic glycolysis

A

2 ATPs

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15
Q

Cells w/ mitochondria

Cells w/ adequate O2 supply

A

Aerobic Glycolysis

END PRODUCT: Pyruvate

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16
Q

Cells w/o mitochondria

Cells w/o adequate O2 supply

A

Anaerobic Glycolysis

END PRODUCT: Lactate

17
Q

Number of ATPs generated

A

From Aerobic Glycolysis - 7 ATP

From Pyruvate Dehydrogenase - 2 NADH = 5 ATP

From TCA cycle (2 acetyl CoA from 1 mol of glucose) - 2x10 = 20 ATP

NET ATP = 7+5+20 = 32 ATP

18
Q

Found in RBCs where the reaction catalyzed by phosphoglycerate kinase is bypassed

A

RAPAPORT LUEBERING SHUNT PATHWAY

1,3 BPG –> 2,3 BPG
BIPHOSPHOGLYCERATE MUTASE

19
Q

Fates of Pyruvate

A

To Glucose (Gluconeogenesis)

To Lactate (Lactate dehydrogenase)

To Oxaloacetate (Pyruvate Carboxylase)

To Acetyl CoA (Pyruvate Dehydrogenase)

To Alanine (Alanine Amino Transferase)

20
Q

Coenzymes of PYRUVATE DEHYDROGENASE COMPLEX

Pyruvate –> Acetyl CoA

A

Tender Loving Care For Nancy

Thiamine pyrophosphate
Lipomide
Coenzyme A (Pantothenic acid)
FAD
NAD+
21
Q

MC enzyme defect in glycolysis

A

Pyruvate kinase

HEMOLYTIC ANEMIA

22
Q

MCC of congenital LACTIC ACIDOSIS

A

Pyruvate dehydrogenase deficiency

x-linked dominant
increased lactate + decreased acetyl CoA –> psychomotor retardation and death

TREATMENT: ketogenic diet

23
Q

Fate of Acetyl CoA

A

FA Synthesis
Ketone Body Synthesis
Cholesterol Synthesis
TCA cycle

CANNOT BE CONVERTED TO GLUCOSE

24
Q

Coenzyme Prosthetic Groups

A

Thiamine diphosphate of E1 (pyruvate decarboxylase)

Lipoic acid of E2 (dihydrolipoyl transacetylase)

FAD of E3 (dihydrolipoyl dehydrogenase)

25
Q

Coenzyme Cosubstrates Groups

A

CoA

NAD+

26
Q

The MC form of PDHC deficiency is caused by mutations to

A

Thiamine diphosphate of E1 (pyruvate decarboxylase)

27
Q

End products that INHIBIT PDH COMPLEX

A

Acetyl CoA

NADH

28
Q

Covalent modification of PDH Complex

A

ACTIVE in DEphosphorylated state

INACTIVE in PHOsphorylated state

29
Q

PDH is PHOSPHORYLATED (inactivated) by

A
PDH KINASE
-activated in increase in
ATP/ADP
Acetyl CoA/CoA
NADH/NAD
30
Q

PDH is DEPHOSPHORYLATED (activated) by

A

PDH PHOSPHATASE

-activated by INSULIN