Glycolysis Flashcards

1
Q

When the B cells of the pancrease cannot respond to high blood glucose levels, what has been mutated and inherited?

A

glucokinase

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2
Q

when does glucokinase become very active?

A

when there is a higher than normal concentration of glucose

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3
Q

if the mitochondria is absent in red blood cells, how do they get there energy supply?

A

from glycolysis

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4
Q

what is the most important regulated step?

A

PFK1

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5
Q

why are the regulated steps irreversible?

A

they are irreversible because energy is being added in the form of ATP

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6
Q

what is the first rate limiting step?

A

hexokinase and glucokinase

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7
Q

why does glucokinase need to be phophorylated?

A

it needs to be phosphorylated, so that it can stay in the liver

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8
Q

after glucose is phosphorylated what is the next step?

A

it is changed from a aldose to a ketose..by phosphoglucose isomerase

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9
Q

why is the second rate limiting step important?

A

because it is the committed step

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10
Q

what happens in the 3rd step of glycolysis?

A

phosphofructokinase adds another phosphate to fructose to create fructose 1,6 bisphosphate

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11
Q

what is PFK-1 inhibited by?

A

ATP, citrate, Fructose bisphosphotASE-2, glucagon

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12
Q

what activates PFK-1?

A

Fructose 2,6 bisphosphate, AMP, ADP,PFK-2, insulin

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13
Q

what makes fructose 2,6 bisphosphate?

A

PFK-2

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14
Q

when insulin come into the cell how does it activate PFK2?

A

it activates it by dephosphorylating it

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15
Q

what are the bidirectional enzymes?

A

pfk2(gets dephosphorylated) and fructose bisphosphotase 2 (phosphorylated)

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16
Q

when glucagon is present what happens to PFK2?

A

PFK2 in phosphorylated and becomes inactive to prevent glycolysis, while fructose 2 bisphosphotase becomes active for gluconeogenesis

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17
Q

what does aldose do to fructose 1, 6 bisphosphate?

A

it cleaved it into 2 trioses( dihydroxyacetone phosphate and glyceralaldehyde 3 phosphate

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18
Q

where is aldose A present?

A

in the muscle

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19
Q

where is aldose B present?

A

in the liver

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20
Q

what does glyceraldehyde 3 phosphate dehydrogenase result in in the energy producing phase?

A

NADH

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21
Q

since dihydroxyacetone phosphate cannot fed into glycolysis what does it have to form into by triosephosphateisomerase?

A

glyceraldehyde 3 phosphate

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22
Q

what does phosphoglycerate kinase result in the formation of?

A

1,3-bisphophosglycerate and ATP (substarte level phosphorylation)

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23
Q

when 1,3 bisphosphoglycerate is formed, why is it important?

A

it is important because it is a high energy intermediate that results in in the formation of ATP without involving the electron transport chain-

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24
Q

What type of reaction is involved with 1,3-BPG?

A

it is a substrate level phosphorylation reaction which is important during periods of low oxygen.. hypoxia- this make ATP in its own- it can add a phosphate group directly to ADP to form ATP- without involvment of electron transport chain

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25
Q

what does phosphoglycerate kinase form?

A

3-phosphoglycerate

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26
Q

what does phosphoglycerate mutase produce?

A

2- phosphoglycerate

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27
Q

what does arsenate inhibit?

A

stops the formation of 1,3 bisphosphate by inhibiting glyceraladehyde phosphate dehydrogenase
Arsenic disrupts ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis.

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28
Q

why is phosphoenolpyruvate a high energy compound?

A

Its a high yield energy compound that results in the formation of ATP, without the involvment of the ETC in mitochndria(substrate level phosphorylation)

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29
Q

why are substrate level phosphorylation reactions important during periods of low oxygen(hypoxia)?

A

because they can produce ther own ATP without the involvment of the ETC in mitochondria

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30
Q

which enzyme results in the formation of the 2nd ATP in glycolysis?

A

pyruvate kinase

31
Q

what is the result at the end of glycolysis?

A

2 molecules of pyruvate

32
Q

what type of reaction is pyruvate kinase?

A

irreversible

33
Q

what does fluoride inhibit?

A

enolase which makes phosphoenolpyruvate(PEP)

34
Q

which step is the regulated step that is associated with disorders?

A

the step when phosphoenlpyruvate is converted to pyruvate by pyruvate kinase

35
Q

where does the cycle began to make two of everything?

A

at glyceraldehyde-3-phosphate

36
Q

what are the two conditions that pyruvate can sustain?

A

aerobic(abundance of O2 and mitochondria), anaerobic(no mitochondria or no oxygen)

37
Q

what is the function of pyruvate dehydrogenase?

A

it helps convert pyruvate to AcetylCoA in aerobic respiration

38
Q

what is the function of lactate dehydrogenase?

A

it transfers pyruvate to lactate in anaerobic coditions

39
Q

what cycle does acetyl CoA enter?

A

TCA Cycle( Citric acid cycle, kreb cycle)

40
Q

what cycle does lactate enter into?

A

the liver via the cori cycle

41
Q

in gluconeogenesis in the liver what does pyruvate carboxylase form?

A

oxaloacetate

42
Q

when is lactate produced?

A

( by the process of fermentation) during normal metabolism and exercise.

43
Q

when lactate accumulates in the muscle what happens to the Ph?

A

the pH will drop and may manifest as cramps during intense exercise

44
Q

where does lactate in the muscle and red blood cells go?

A

it diffuses out of the cell and is taken to the liver where it is used for gluconeogenesis (cori cycle)

45
Q

what is special about heart muscles when dealing with pyruvate?

A

the heart muscles convert lactate to pyruvate and later to acetyl CoA, to enable it to enter the TCA cycle.

46
Q

what may happen with cardiac muscle hypoxia?

A

results in lactate formation( myocardial infarction)

47
Q

what type of pathway is glycolysis?

A

it is a catabolic pathway

48
Q

what are the three irreversible regulatory steps?

A

glucokinase/hexokinase, phosphofructokinase-1, pyruvate kinase

49
Q

how many ATP’s have been produced from glyceraldehyde 3 phosphate dehydrogenase in glycolysis ?

A

2x3=6, 2 NADH from glyceraldehyde 3 phosphate dehydrogenase

50
Q

NADH formed from the cytosol is transported into the mitochondria by ?

A

malate-aspartate or glycerol-phosphate shuttle

51
Q

how many ATP are used in glycolysis?

A

2 ATP

52
Q

what is the total amount of ATP in aerobic glycolysis?

A

8 ATP

53
Q

what happens to NADH when lactate is formed?

A

it is reoxidized to be avialiable for glyceraldehyde 3 phosphate dehydrogenase

54
Q

how many NADH + H+ are formed in anaerobic glycolysis?

A

2 (formed in glyceraldehyde 3 phosphate dehydrogenase reaction)

55
Q

how many ATP’s are used in anaerobic glycolysis?

A

2

56
Q

what is the total of ATP in anaerobic glycolysis?

A

2ATP

57
Q

in adipose tissues, what is used to provide glycerol components that is used for triacylgylecerol formation?

A

glyceraldehyde

58
Q

in red blood cell, where do they get there major energy source?

A

glycolysis

59
Q

what does anaerobic glycolysis help produce that will help with unloading for hemeglobin?

A

2,3 bisphosphoglycerate(2,3-BPG)

60
Q

what type of deifiency occurs in hemolytic anemia?

A

erythorcyte pyruvate kinase deificiency

61
Q

defects in glycolysis would result in blank and blank due to decreased blank?

A

hemolysis, hemolytic anemia and ATP generation

62
Q

what is compromised in hemolysis in pyruvate kinase/ hexokinase?

A

the Na+/K+ ATPase=RBC lysis

63
Q

what are the factors that tell you that lactic acidosis isa metabolic acidosis?

A

pH is low, HCO3- is decreased, PCO2 is decreased

64
Q

when lactic acidosis occurs what can we observe about lactate acidosis?

A

there is an increased conversion of pyruvate to lactate

65
Q

what can cause lactate acidosis?

A

strenuous activity, inherited deficiency of pyruvate dehydrigenase, thiamine deficiency, defect in gluconeogenessis, decreased blood supply resulting in the anaerobic metabolism

66
Q

WHat is the second most common form of hemolytic anemia due to RBC enzyme deficiency( G6PD)?

A

pyruvate kinase dificency

67
Q

what is “warburg effect?”

A

when most cancer cells use glycolysis as the main source of ATP

68
Q

patients with pyruvate kinase deficency wil have what affect on 23BPG?

A

increase unloading and vice versa for hexokinase

69
Q

what is “flurodeoxyglucose(FDG)”?

A

used for positrion emission for tumor cells

70
Q

When PFK2 is inactive what happens to FBP2?

A

it is activated

71
Q

what is the role of fuctose 2,6- bisphosphate?

A

regulation in liver

72
Q

what is the purpose of glycolysis?

A

the breaking down of glucose( high energy molecule) to produce energy

73
Q

what is the cori cycle?

A

lactate produced by anaerobic glycolysis in the muscles moves to the liver and is converted to glucose, which then returns to the muscles and is metabolized back to lactate.