Carbs II Flashcards

1
Q

In the absence of oxygen, what substrate serves as an electron acceptor to regenerate NAD? What product is formed?

A

Pyruvate. Lactic acid.

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2
Q

What cells rely exclusively on glycolysis?

A

red blood cells

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3
Q

What is the first reaction of glycolysis?

A

hexokinase converts glucose into glucose-6-phosphate

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4
Q

What is the second reaction of glycolysis?

A

glucose phosphate isomerase converts glucose-6-phosphate into Fructose-6-phosphate

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5
Q

What is the third reaction of glycolysis?

A

phosphofructokinase converts F6P into F16bP

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6
Q

What is the fourth step of glycolysis?

A

F16bP is split into DHAP and GAP by fructose bisphosphate aldolase

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7
Q

What enzyme converts DHAP to GAP?

A

triose phosphate isomerase

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8
Q

What enzyme converts GA3P into 13bPG?

A

GAPDH

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9
Q

What enzyme of glycolysis produces a reducing equivalent?

A

GAPDH

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10
Q

What reaction does phosphoglycerate kinase catalyze?

A

1,3bPG to 3-phosphoglycerate kinase

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11
Q

What reaction to phosphoglyceromutase catalyze?

A

3-phosphoglycerate to 2-phosphoglycerate

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12
Q

What reaction does enolase catalyze?

A

2-phosphoglycerate to phosphoenolpyruvate

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13
Q

What reaction does pyruvate kinase catalyze?

A

phosphenolpyruvate into pyruvate

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14
Q

What two reactions of glycolysis yield ATP?

A

pyruvate kinase and phosphoglycerate kinase

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15
Q

What is the function of fructokinase?

A

to phosphoryplate fructose into F1P

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16
Q

What is the fate of F1P?

A

Conversion to DHAP and glyceraldehyde

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17
Q

What is the fate of fructose in muscle?

A

Fructose will be slowly converted to F6P by hexokinase

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18
Q

What hormone’s activity is independent of insulin? What are the implications of this?

A

Fructokinase. Diabetics can tolerate fructose as well as non-diabetics.

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19
Q

What tissue does hexokinase convert fructose into fructose-6-phosphate?

20
Q

What tissue does fructokinase convert fructose into F1P?

21
Q

What does essential frustosuria is caused by a deficiency in what enzyme?

A

liver fructokinase

22
Q

What is hereditary fructose intolerance?

A

a defective Aldolase B

23
Q

What is the function of Aldolase B?

A

to convert fructose-1-phosphate into glyceraldehyde and DHAP

24
Q

During aldolase B deficiency, what product accumulates in the liver?

A

fructose-1-phosphate

25
What is galactosemia?
failure to utilize galactose in glycolysis
26
What are the three regulated enzymes of glycolysis?
hexokinase, phosphofructokinase, pyruvate kinase
27
What two enzymes of glycolysis are regulated by insulin?
hexokinase and pyruvate kinase
28
What is the function of F26bP?
F26bP acts as an accelerator of glycolysis and an inhibitor of gluconeogenesis
29
What does high [cAMP] signal?
fasting state
30
What is the function of cAMP in relation to its effects on metabolism?
cAMP functions to reduce glucose consumption by glycolysis
31
What does insulin do to cAMP levels?
Insulin inhibits cAMP formation
32
How does glucagon affect cAMP levels?
glucagon acts to raise cAMP levels
33
What second messenger inhibits PFK II?
PKA
34
What are the two functions of F26bP?
to activate PFK I and to inhibit fructose bisphosphotase
35
What two shuttle systems can the cell use to ensure NAD availability for glycolysis?
malate-asparate shuttle and the glycerol phosphate shuttle
36
What tissues use the malate-aspartate shuttle?
liver and heart
37
What tissues use the glycerol phosphate shuttle?
muscle and brain
38
What molecule is transported to the liver during Cori cycle?
lactic acid is transported
39
What happens to lactic acid in the liver during the Cori cycle?
lactic acid is converted to pyruvate
40
What is the fate of pyruvate in the liver?
pyruvate is used to manufacture glucose
41
What requires an NADH, pyruvate to lactate or lactate to pyruvate?
pyruvate to lactate requires an NADH
42
Can liver failure highlight the effects of the Cori cycle?
yes. lactic acidosis can occur without a functioning liver.
43
How are hemolytic anemia and glycolysis connected?
defects in glycolysis and highlighted in hemolytic anemia
44
What is the most common hereditary enzymatic deficiency in glycolysis?
pyruvate kinase deficiency
45
What do defects of any glycolytic enzyme do to the RBC?
lysis of the cells due to inability to maintain memrbane potential
46
What glycolytic enzyme is affected by arsenate?
GAPDH