biochem lipids

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53 Terms

1
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what regulates lipolysis

hormonal mechanisms: insulin, gluacagon, epinephrine, cortisol , coordination of CH, lipid and protein metabolism

2
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biosynthesis in liver first step

acetyl coa → malonyl coa

-happen in cytosol

-use enzyme acetyl coa carboxylase

-use biotin vitB7 as cofactor

3
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what is the commitment enzyme for biosynthesis in liver

acetyl coa carboxylase

4
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biosynthesis in liver second step

malonyl coa→ fatty acid

-happen in cytosol

-use enzyme fatty acid synthase

-use NADPH as cofactor

5
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carnitine shuttle

transports long fatty acid chains into mitochondria for catabolism

6
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what inhibits the carnitine shuttle and prevents synthesis and breakdown simultaneously

malonyl coa

7
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where does ketogenesis happen during fasting and starvation

liver

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what can the liver make but cant use

ketone bodies

9
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what is the main ketone body exported during catabolism

beta-hydroxybutyrate

10
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if there are excess nutrients in the body

-high malonyl coa

-carnitine shuttle inhibited

-fatty acid stay in cytosol and synthesis happens

11
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if there is fasting or starvation occuring

-low malonyl coa

-carnitine shuttle activated

-fatty acid enter mitochondria and beta oxidation happens

12
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long fatty acid chain would go to

carnitine shuttle

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short/medium fatty acid chain would go

and diffuse

14
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very long fatty acid chains would go to

peroxisome

15
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beta oxidation occurs ___________ and is entirely _________

mitochondria, oxidative

16
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what do odd chain fatty acids produce and what vitamin is needed

produce propionyl coa and needs vitamin b12

17
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excess of acetyl coa in liver leads to

ketogenesis

18
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methylmalonyl coa aciduria caused by deficiency in _______, accumulates _________

vitamin b12, propionyl coa

19
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fat malabsorption is missing ________, accumulates _________

bile salts/lipases, unabsorbed fats

20
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diabetic ketoacidosis missing __________, accumulates ________

insulin deficiency, excess ketone bodies

21
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zellweger syndrome

peroxisome biogenesis disorder that leads to multiorgan disorder and early death

22
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acetyl coa carboxylase requires presence of ________ for polymerization to its active form

citrate

23
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acetyl coa carboxylase is regulated by

phosphorylation-dephosphorylation mechanism and hormonally

24
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first stage of biosynthesis and storage of fatty acids

precursor malonyl coa

25
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second stage of biosynthesis and storage of fatty acids

elongation of fatty acid

26
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elongation of fatty acid takes place in

cytosol

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what enzyme contribute to elongation of fatty acid

fatty acid synthase

28
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starting material for fatty acid synthesis and elongation

fatty acid synthesis staring point = acetyl coa + malonyl coa

elongation starting point = existing fatty acid + malonyl coa

29
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end product for fatty acid synthesis and elongation

fatty acid synthesis staring point = palmitate (16C)

elongation starting point = longer fatty acids (18-24C)

30
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elongation of fatty acids also called

macrolipogenesis

31
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how does elongation of fatty acids occur

  1. Elongation adds 2 carbons at a time using Malonyl-CoA

  2. Done by Fatty Acid Synthase — a dimer with 7 enzymes in 3 domains

  3. Has a flexible arm that moves the chain between enzyme domains

  4. Can produce fatty acids up to 22-24 carbons lons


32
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step 1 of elongation of fatty acids

acetyl coa→ malonyl coa, product is malonyl coa (commitment step)

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step 2 of elongation of fatty acids

malonyl coa → palmitate, product is palmitate (16C, the first product made)

34
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step 3 of elongation of fatty acids

palmitate → longer fatty acid, 18-24 carbon fatty acids (second product made, final)

35
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lipases hydrolyze ____, by releasing 1 fatty acids at a time, yielding ____ and _____

TAG, DAG, glycerol

36
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glycerol is converted to dihydroxyacetone phosphate by catalyzed

glycerol kinase (1st) and glycerol phosphate dehydrogenase (2nd)

37
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process of glycerol converted to dihydroxyacetone phosphate

glycerol kinase glycerol phosphate dehydrogenase

glycerol —→ glycerol 3p -—→ dihydroxyacetone phosphate

38
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first step of catabolism is

activation of fatty acid to their coa derivative by using ATP as energy source (using fatty acyl coa synthase also known as fatty acid thiokinase)

39
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once fatty acid reaches acyl coa form its

fully activated

40
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fatty acids are never free roaming without being binded to

albumin in the plasma (direct to tissues needing energy) or lipoproteins (to adipose for storage or tissue for energy)

41
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liver uses fatty acids as source of energy for

gluconeogenesis

42
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excess acetyl coa accumulates during

fasting/starvation

43
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during starvation brain converts to using __________ for more than 50% of its energy metabolism

ketone bodies

44
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during starvation the brain uses ketone bodies sparing ______ thus reducing degradation of muscle protein for ___________

glucose, gluconeogenesis

45
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fatty acids are stored as

TAGs

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TAGs are produced from

glycerol 3P

47
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fatty acids are an immediate

source of energy

48
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2 carbons at a time released from carboxyl end of fatty acid result in

acetyl coa, fadh2, nadh

49
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synthesis of fatty acids and TAG called ______ and happens in ________

lipogenesis, cytosol

50
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degradation of triglycerides is called _______ and catabolism of fatty acids happens by ______ and are entirely _______

lipolysis, b-oxidation, oxidative

51
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end product of acetyl coenzyme a in muscle

metabolized by TCA and oxidative phosphorylation → produces ATP

52
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end product of acetyl coenzyme a in liver

used to synthesize keton bodies (ketogenesis) then exported to other tissues

53
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regulation of fat metabolism by

-involvement of insulin, glucagon, epinephrine, cortisol

-rate of lipolysis in adipose tissue