metabolic pathways and ATP production Flashcards

glucose metabolism: explain the metabolism of glucose during glycolysis and gluconeogenesis, recall the key reactions in both pathways, and distinguish between the aerobic and anaerobic metabolism of glucose

1
Q

where does glycolysis occur

A

cytoplasm

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2
Q

is glycolysis aerobic or anaerobic

A

anaerobic

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3
Q

give the basic reaction of glycolysis, including ATP and NADH

A

1x6C glucose → 2x3C pyruvate (+2ATP, 2NADH)

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4
Q

what is the production of ATP an example of

A

substrate-level phosphorylation: ATP production by transfer of high energy PO4 3- group from intermediate substrate to ADP

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5
Q

first stage of glycolysis and significance

A

glucose → glucose-6-phosphate + H+ (irreversible; hexokinase (glucokinase in liver); ATP → ADP)

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6
Q

second stage of glycolysis

A

isomerise glucose-6-phosphate to fructose-6-phosphate

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7
Q

third stage of glycolysis and significance of product

A

fructose-6-phosphate → fructose-1,6-bisphosphate (highly symmetrical; phosphofructokinase; ATP → ADP)

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8
Q

in molecular nomenclature, what is the difference between “bi” and “di”

A

“bi” is not joined and “di”is joined

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9
Q

fourth and fifth stages of glycolysis

A

ring opens to form 2x3C; isomerisation to form 2 glyceraldehyde-3-phosphate molecules

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10
Q

sixth stage of glycolysis

A

glyceraldehyde-3-phosphate → 1,3-bisphosphoglycerate (glyceraldehyde-3-phosphate dehydrogenase; NAD+ + Pi → NADH)

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11
Q

seventh stage of glycolysis

A

1,3-bisphosphoglycerate → 3-phosphoglycerate (phosphoglycerate kinase; ADP → ATP)

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12
Q

eighth stage of glycolysis

A

isomerisation of 3-phosphoglycerate to 2-phosphoglycerate (phosphoglycerate mutase)

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13
Q

ninth stage of glycolysis

A

2-phosphoglycerate → phosphoenolpyruvate + H2O (enolase dehydration)

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14
Q

tenth stage of glycolysis

A

phosphoenolpyruvate → pyruvate (pyruvate kinase; ADP → ATP)

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15
Q

what can glucose-6-phosphate be stored as

A

glycogen or pentose phosphates used for nucleotides

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16
Q

what can glycogen be synthesised from

A

UDP-glucose

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17
Q

how are sugars stored

A

glycogen, fatty acids and cholesterol

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18
Q

when are ketone bodies used

A

when the bodt is fasting (used by brain as cannot metabolise fatty acids)

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19
Q

diagram showing generation of molecules from different glycolysis and TCA intermediates

A

diagram form metabolism 9

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20
Q

when does gluconeogenesis occur and what does it prevent

A

when the body is fasting or intense exercise to prevent low [glucose] which could lead to hypoglycaemic coma

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21
Q

short term fasting

A

break down glycogen, release fatty acids from adipose, acetyl CoA converted to ketone bodies (used in muscle to produce glucose)

22
Q

long term (12-18 hours) fasting

A

supplies exhausted

23
Q

define gluconeogenesis

A

produces glucose from non-carbohydrate sources (lactate, amino acids, glycerol)

24
Q

is gluconeogenesis the reversal of glycolysis

A

no - requires different enzymes

25
does gluconeogenesis require ATP
yes
26
where does gluconeogenesis occur
liver
27
diagram to show gluconeogenesis stages vs glycolysis
diagram from metabolism 9
28
what is the common starting point in gluconeogenesis
oxaloacetate
29
net loss of gluconeogenesis
6 ATP
30
first stage of gluconeogenesis
pyruvate → oxaloacetate (pyruvate carboxylase) in mitochondria
31
second stage of gluconeogenesis
oxaloacetate → phosphoenolpyruvate (phosphoenolpyruvate carboxykinase) in cytosol; limiting stage
32
third stage of gluconeogenesis
phosphoenolpyruvate → G3P → fructose-1,6-bisphosphate
33
fourth stage of gluconeogenesis
fructose-1,6-bisphosphate → fructose-6-phosphate (fructose-1,6-bisphosphatase) in cytosol
34
fifth stage of gluconeogenesis
fructose-6-phosphate → glucose-6-phosphate
35
sixth stage of gluconeogenesis
glucose-6-phosphate → glucose (glucose-6-phosphatase) in cytosol
36
sources of pyruvate
lactate (via LDH) and amino acids
37
source of oxaloacetate
ketogenic amino acids
38
sources of G3P
phosphoenolpyruvate, glycerol → DHAP
39
what happens to ATP and glucose demand in aerobic respiration
increase
40
pathways of aerobic metabolism
glucose secreted by liver into blood; muscle glycolysis increases (ATP production increases), gluconeogenesis increases (when ATP demand greater than supply), fatty acids increase (more available for B-oxidation)
41
what protein channels are required for cation balance in aerobic metabolism
Ca2+ATPase and Na+K+ATPase
42
aerobic pathways diagram
diagram from metabolism 9
43
when is anaerobic respiration required
when ATP demand is greater than oxidative phosphorylation supply and transport cannot keep up with glucose demand
44
pathways of anaerobic metabolism
muscle glycogen breakdown increases; glycolysis rate increases fo pyruvate accumulates and is stored as lactate in muscles; liver uses lactate to form pyruvate via LDH (gluconeogenesis) to be converted to glucose, preventing acidosis
45
anaerobic pathway diagram
diagram from metabolism 9
46
3 fates of pyruvate
alcoholic fermentation, lactate, generation of acetyl CoA
47
alcoholic fermentation
ethanal → ethanol by decarboxylases; produces NAD+ so glycolysis can continue
48
lactate production
pyruvate ⇌ lactate via lactate dehydrogenase (LDH), produces NAD+ so glycolysis can continue
49
creatine phosphate metabolism
creatine phosphate ⇌ creatine + ATP by creatine kinase
50
high levels of LDH or creatine kinase in plasma
tissue and muscle trauma, myocardial infarction