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

24
Q

how is PFK acting in muscle cells during activity?

A

AMP high, ATP low so glycolysis is promoted

25
After a meal, insulin is high. what happens with PFK1, FBPase-2, and PFK2?
PFK2 is active generating F2,6BP which activates PFK1. glycolysis is stimulated
26
In a fasting state. what happens with PFK1, FBPase-2, and PFK2?
FBPase-2 is active causing F2,6BP levels to fall which inactivates PFK1. glycolysis is inhibited
27
pyruvate kinase allosteric activators and inhibitors
``` - = ATP + = F1,6BP ```
28
pyruvate kinase activation by F1,6BP is example of ____
feed forward activation
29
When glucose is low, glucagon is ___, PKA is (active or inactive), liver PK gets phosphorylated, and is turned off. This is the switch to _____
high. active | gluconeogenesis
30
reduced pyruvate kinase: glycolysis is inhibited, PEP enters _____
gluconeogenesis
31
Fate of pyruvate: aerobic, fed conditions:
pyruvate to acetyl CoA or alanine
32
Fate of pyruvate: anaerobic, fed condition:
pyruvate to lactate
33
Fate of pyruvate: aerobic, fasting:
pyruvate to oxaloacetate
34
what inhibits Glyceraldehyde 3-P dehydrogenase?
mercury and arsenate
35
how does mercury inhibit Glyceraldehyde 3-P dehydrogenase?
inactivates the enzyme
36
how does arsenate inhibit Glyceraldehyde 3-P dehydrogenase?
substitutes with inorganic P in the reaction and forms 1-arseno-3 phosphoglycerate which is an unstable molecule
37
Pyruvate kinase adds phosphate to what molecule
ADP
38
Partial lack of ____ or _____ activity depletes cells of ATP
pyruvate kinase | phosphoglycerate kinase
39
Cells need ATP to
export electrolytes and to maintain proper osmotic balance between cytosol and extracellular compartment.
40
No ATP leads to
swelling and destruction of RBCs which leads to hemolytic anemia
41
Hereditary fructose intolerance is a defect in what enzyme
aldolase B
42
Hereditary fructose intolerance causes
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