Biochemistry Flashcards

1
Q

what are the 3 main glycogen metabolic pathways

A

glycogenesis: synthesis of glycogen from glucose
glycogenolysis: breakdown from glycogen to from glucose
gluconeogenesis: de novo synthesis pf glucose from metabolic precursors (AAs, lactate)

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2
Q

what is glycogen?

A

a polymer of glucose

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3
Q

what 2 substances are needed for glycogenesis?

A

UDP & Glycogen synthase

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4
Q

what is UDP?

A

activated form of glucose

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5
Q

what is glycogen synthase?

A

key enzyme that synthesises glycogen from UDP-glucose.

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6
Q

True/False…

glycogen synthase is rate limiting

A

True…

it can only add 1 glucose molecule to glycogen at a time

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7
Q

what is the key enzyme for glycogenolysis?

A

glycogen phosphorylase

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8
Q

what does glycogen phosphorylase do?

A

cleaves off 1 glucose from glycogen at a time.

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9
Q

which organ can dephosphorylate glucose-6-phosphate to form glucose?

A

the liver, muscle can’t do this

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10
Q

when does gluconeogenesis usually kick in?

A

during prolonged starvation

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11
Q

what are the precursors, energy supply and location of gluconeogenesis?

A

precursors: AAs, lactate, glycerol
energy: oxidation of fatty acids from adipose tissue
location: liver

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12
Q

what determines glycolysis or gluconeogenesis?

A

hormones, high AMP/ADP, high ATP, acetyl-coA etc

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13
Q

what is the Cori Cycle?

A

lactate formation

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14
Q

describe the Cori Cycle…

A

lactate formed in fast twitch muscles > lactate transported to liver by blood > liver converts lactate to glucose

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15
Q

what are the 3 classes of lipids

A

simple (fatty acids, triglycerides)
compound (phosphorylase, glycol, lipo)
steroids (cholesterol, steroid hormones)

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16
Q

True/False…

fatty acids are a straight chain

A

True

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17
Q

True/False…

fatty acids have an odd number of C atoms

A

False…

even number

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18
Q

what does saturated, unsaturated and polyunsaturated in terms of bonds mean?

A

saturated- single bond
unsaturated- double bond
polyunsaturated- several double bonds

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19
Q

what are fats broken down to?

A

monoglycerides

20
Q

short and medium FAs absorbed by…

A

mucosal cells

21
Q

long FAs and monoglycerides are…

A

resynthesised into triglycerides

22
Q

what are chylomicrons?

A

triglycerides coated with protein, cholesterol, phospholipid

23
Q

what happens to chylomicrons

A

cleaved by lipases to form free fatty acids which can be resynthesised or oxidised

24
Q

triglycerides are composed of…

A

1 glycerol & 3 FAs, have a high energy yield

25
what happens during lipolysis
1. initial cleavage of triglycerides by hormone sensitive lipases 2. FAs are then converted o acetyl-CoA (in cytoplasm- req 2 ATP) 3. FAs undergo oxidation to provide energy (matrix of mitochondria)
26
what is the carnitine shuttle
allows acetyl CoA to travel to matrix for B-oxidation
27
what does b-oxidation produce?
produces 1 acetyl-coA, 1 FADH, 1 NADH + H+, 1 fatty acyl-CoA
28
how are ketone bodies formed?
formed in mitochondria of liver and eventually converted back to acetyl CoA
29
what does fatty acid oxidation usually yield if carb and fat degradation is balanced?
acetyl co-A which enter Citric Acid Cycle
30
what happens in fatty acid oxidation if in starvation or a diabetic?
oxaloacetate is used for gluconeogenesis, fatty acids are oxidised to provide energy so acetyl-CoA converted to ketone bodies
31
what is dangerous about ketosis
ketoacidosis may occur
32
where does de novo synthesis of fatty acids occur?
in the liver, kidney, mammary glands, adipose tissue and brain
33
why does denovo synthesis of FAs occur?
during excess energy intake
34
where does lipogenesis occur
cytoplasm
35
what is citrate's role in acetyl co A transport?
carries acetyl co-A from mitochondria to cytoplasm for lipogenesis
36
once in cytoplasm, what happens to the acetyl co-A?
activated to malonyl-CoA which donates carbon atoms to new lipid
37
what is the cycle of lipogenesis?
1. condensation 2. reduction 3. dehydration 4. reduction & release
38
once what no of carbon atoms is reached, does the FA release itself?
C16
39
what enzyme is needed for the synthesis of FAs from acetyl-coA
fatty acid synthase
40
what enzyme controls lipogenesis?
acetyl-coA Carboxylase - activates acetyl-CoA to malonyl-CoA
41
what is acetyl-coA Carboxylase activated and inhibited by?
activated: insulin, glucagon, epinephrine, citrate inhibited: palmitoyl-CoA
42
what does triglyceride synthesis require?
glucose-3-phosphate
43
where does amino acid metabolism occur?
liver
44
what happens if AAs can't be degraded?
are absorbed into intestinal cells and released into blood
45
what are AA produced ammonium ions excreted by and why?
they are toxic so excreted by urea, uric acid, creatinine
46
how is urea synthesised?
AA > glutamic acid > NADH + NH4+ + aspartic acid > urea
47
after removal of an amino group in transmission stage of urea synthesis, what are remaining carbon skeletons converted to?
either glucose or oxidised to join TCA cycle