glycolysis and regulation Flashcards

1
Q

completely reliant on glycolysis

A

red blood cells

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2
Q

what cells oxidize glucose to pyruvate to generate ATP

A

all cells

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3
Q

products of anaerobic glycolysis vs aerobic

A

lactate as opposed to TCA cycle participation

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4
Q

LDH does what to produce lactate

A

NADH is oxidized to NAD+ in the cytosol which is used in a step to convert 1-glyceraldehyde-3P to 1,3BPG

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5
Q

how is lactate removed from RBCs and exercising tissue?

A

Cori Cycle

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6
Q

Cori cycle links

A

liver and muscle

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7
Q

Describe the Cori Cycle

A
  1. in RBC glucose goes through glycolysis to yield 2 lactate
  2. 2 lactates are transferred to liver through blood
  3. 2 lactate in liver reconverted to pyruvate by LDH then to glucose by gluconeogenesis
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8
Q

what happens when you produce too much lactate?

A

lactic acidosis

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9
Q

how do you get lactic acidosis and what are some causes

A

increased NADH/NAD+ ratio which prevents pyruvate from getting into TCA cycle and directs to lactate.
causes: excess alcohol, hypoxia, and TCA/ETC cycle issues

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10
Q

glycolysis is a major pathway for oxidizing glucose and

A

metabolizing other dietary sugars, fructose and galactose

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11
Q

ATP/ADP ratio is high are we going through glycolysis?

A

no

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12
Q

ATP/ADP ration is low but concentration of AMP and ADP are. glycolysis rate will ___

A

increase

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13
Q

hexokinase inhibited by ___

A

Glucose 6-phosphate

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14
Q

PFK1 inhibited by ____ and activated by ___

A
- = ATP and citrate
\+ = AMP and F2,6-bisphosphate
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15
Q

pyruvate kinase inhibited by ___ and activated by ____

A
- = ATP
\+ = F1,6-Bisphosphate
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16
Q

Hexokinase vs Glucokinase Km

A

glucokinase high

hexokinase low

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17
Q

Hexokinase vs Glucokinase affinity for glucose

A

glucokinase low

hexokinase high

18
Q

Glucokinase found in ____ while hexokinase found in ____

A

glucokinase: liver and pancreatic beta cells
hexokinase: all other cells

19
Q

Hexokinase vs Glucokinase Vmax

A

glucokinase higher

hexokinase lower

20
Q

Hexokinase vs Glucokinase induced by insulin?

A

glucokinase yes

hexokinase no

21
Q

Hexokinase vs Glucokinase feedback inhibited by glucose-6-P?

A

glucokinase no

hexokinase yes

22
Q

PFK1 is a tetramer and has 6 binding sites that are:

A

2 substrates: ATP and Fructose 6-P

4 allosteric modulators: inhibitors are ATP and citrate while activators are AMP and Fructose 2,6 bisphosphate

23
Q

what enzyme senses hormonal signaling by insulin and glucagon

A

PFK1

24
Q

how is PFK acting in muscle cells during activity?

A

AMP high, ATP low so glycolysis is promoted

25
Q

After a meal, insulin is high. what happens with PFK1, FBPase-2, and PFK2?

A

PFK2 is active generating F2,6BP which activates PFK1. glycolysis is stimulated

26
Q

In a fasting state. what happens with PFK1, FBPase-2, and PFK2?

A

FBPase-2 is active causing F2,6BP levels to fall which inactivates PFK1. glycolysis is inhibited

27
Q

pyruvate kinase allosteric activators and inhibitors

A
- = ATP
\+ = F1,6BP
28
Q

pyruvate kinase activation by F1,6BP is example of ____

A

feed forward activation

29
Q

When glucose is low, glucagon is ___, PKA is (active or inactive), liver PK gets phosphorylated, and is turned off. This is the switch to _____

A

high. active

gluconeogenesis

30
Q

reduced pyruvate kinase: glycolysis is inhibited, PEP enters _____

A

gluconeogenesis

31
Q

Fate of pyruvate: aerobic, fed conditions:

A

pyruvate to acetyl CoA or alanine

32
Q

Fate of pyruvate: anaerobic, fed condition:

A

pyruvate to lactate

33
Q

Fate of pyruvate: aerobic, fasting:

A

pyruvate to oxaloacetate

34
Q

what inhibits Glyceraldehyde 3-P dehydrogenase?

A

mercury and arsenate

35
Q

how does mercury inhibit Glyceraldehyde 3-P dehydrogenase?

A

inactivates the enzyme

36
Q

how does arsenate inhibit Glyceraldehyde 3-P dehydrogenase?

A

substitutes with inorganic P in the reaction and forms 1-arseno-3 phosphoglycerate which is an unstable molecule

37
Q

Pyruvate kinase adds phosphate to what molecule

A

ADP

38
Q

Partial lack of ____ or _____ activity depletes cells of ATP

A

pyruvate kinase

phosphoglycerate kinase

39
Q

Cells need ATP to

A

export electrolytes and to maintain proper osmotic balance between cytosol and extracellular compartment.

40
Q

No ATP leads to

A

swelling and destruction of RBCs which leads to hemolytic anemia

41
Q

Hereditary fructose intolerance is a defect in what enzyme

A

aldolase B

42
Q

Hereditary fructose intolerance causes

A

cellular phosphate to accumulate in Fructose 1-P form which depletes cell of inorganic P. inorganic P becomes too low for glyceraldehyde 3P dehydrogenase to function. ultimately, lack of aldolase B activity prevents liver cell from making ATP