FOUNDATION-metabolism Flashcards

1
Q

what is glycogenesis?

A

glucose——->glycogen

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2
Q

what is glycogenolysis?

A

glycogen——->glucose

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3
Q

what is glycolysis?

A

glucose——–>pyruvate

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4
Q

what is gluconeogenesis?

A

amino acids and fatty acids——>glucose

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5
Q

what is the process that converts fatty acids to acteyl CoA and what does this then enter?

A

BETA OXIDATION

-goes on to enter krebs cycle

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6
Q

which process is the only one that can occur anaerobically as well as aerobically?

A

glycolysis

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7
Q

which pathway comes off from Glucose-6-phosphate, and what does it convert?

A

pentose phosphate

-converts NADP+ into NADPH

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8
Q

where is glucose stored?

A

liver and muscles as glycogen

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9
Q

where is glucose released from in a state of hypoglycaemia?

A

only the liver

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10
Q

where are triglycerides stored?

A

liver and adipose tissue

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11
Q

where does glycolysis take place?

A

cytoplasm

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12
Q

how many ATP molecules are gained in glycolysis?

A

2ATP

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13
Q

what are the products of glycolysis?

A

pyruvate

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14
Q

where does the krebs cycle take place?

A

inner mitochondrial matrix

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15
Q

what is the beginning reaction of the krebs cycle?

A

oxaloacetate + acetyl group=citrate (6c)

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16
Q

how is ATP made in the krebs cycle?

A

substrate phosphorylation

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17
Q

where does oxidative phosphorylation take place?

A

-inner mitochondrial membrane

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18
Q

what is oxygens role in oxidative phosphorylation?

A

final electron transporter

19
Q

which step in the respiration chain generates the most ATP?

A

oxidative phosphorylation

-34 atp molecules

20
Q

what is catabolism?

A

breakdown of molecules
-mostly oxidative=release energy
eg oxidative phosphorylation

21
Q

what is anabolism?

A

requires energy to reduce substances and build them into larger molecules
eg protein synthesis

22
Q

what is energy coupling?

A

one system provides energy to power another system

23
Q

what are exergonic reactions?

A

release energy into the surrounding environment

24
Q

what are endogenic reactions?

A

takes energy from the surrounding environment

25
how does fatty acid chain length affect what can happen in lipolysis?
- short and medium fatty acids can enter mitochondria directly - long chain fatty acids are shuttled into mitochondria a using a carnitive carrier-proteins
26
what is the molecule that amino acids, fatty acids, glucose and glycerol metabolised into after digestion?
Acetyl CoA
27
what is an amphibolic reaction? Give an example.
both anabolic and catabolic | eg Krebs cycle
28
what are the products of the krebs cycle?
- 2atp | - FADH2/ NADH-for ETC
29
what is the role of FADH2/ NADH in oxidative phosphorylation?
- oxidation (FADH2--->FAD and NADH--->NAD) drive movement of e- down etc - drives H+ across membrane - H+ leave intermembrane space via ATPsynthase - ADP +Pi----->ATP
30
what are the steps of glucose in carbohydrate metabolism?
GLUCOSE---->PYRUVATELACTATE (anaerobic) OR GLUCOSE----->PYRUVATE---->ACETYL COA---->TCA---->ETC
31
what are the other products of carbohydrate metabolism?
glucose into... - glycogen (glucose-1-phosphate pathway) - nucleic acid (pentose-phosphate pathway) - amino acid synthesis (via pyruvate and TCA) - glycerol of FAs - cholesterol-acetyl coA
32
which process breaks down triglycerides into glycerol and fatty acids?
lipolysis
33
what occurs after lipolysis?
- fatty acids enter mitochondria (depending on size if too long then using carnitive proteins) as acyl CoA - acyl CoA is oxidised in beta oxidation - -->each cycle of beta oxidation reduced FA chain by 2 carbons-producing 2c acetyl CoA - --->also produces reduced products to enter ETC - --->continues until only 2c acetyl coa is left - acetyl coa either converts into ketone bodies or enters TCA
34
outline the 2 types of amino acids
- glucogenic - ketogenic some can be both
35
what is the role of glucogenic aas?
convert to glucose via pyruvate
36
what is the role of ketogenic aas?
convert to acetyl CoA or ketone bodies-depending on body's need
37
where are essential amino acids obtained?
diet
38
where are non-essential aas derived?
diet | transamination
39
what happens to excess amino acids?
catabolised to urea after deamination
40
what happens to the carbon skeleton of amino acids after transamination?
``` oxidised to co2 via TCA (glucogenic--->pyruvate--->acetyl coa) or forms glucose or forms ketone bodies ```
41
what is transamination?
process by which amino groups are removed from amino acids and transferred to acceptor keto-acids to generate the amino acid version of the keto-acid and the keto-acid version of the original amino acid.
42
describe features of metabolism in a fed state
- glycogenesis (more glucose stored as glycogen) - glycolysis (glucose broken down into ATP) - lipogenesis (triglyceride synthesis from FFAs) - AA synthesis
43
which hormone promotes metabolism?
insulin
44
describe the features of metabolism in a starving state
- glycogenolysis-more glucose - gluconeogenesis-more glucose - lipolysis in adipose release FFAs and glycerol - glycerol--->glucose - moreoxidation of FFAs and ketone bodies for more energy - protein/ aas--->glucose