Important importants for Test 2 Flashcards

1
Q

glycosidic bond in raffinose

A

galactose alpha 1,6 glucose

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2
Q

raffinose requires blank for digestion

A

galactosidase

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3
Q

functions of HDL

A

donate apoC2 and apoE, extract cholesterol, converte cholesterol to cholesterol ester

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4
Q

inadequate tissue oxygenation, myocardial infarction, pulmonary embolism, severe hemorrhage, and inborn errors in metabolism can cause blank

A

lactic acidosis

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5
Q

galactose 1 phosphate uridylyl transferase facilitates blank metabolism by converting blank to blank utilizing blank as a cosubstrate

A

galactose metabolism, galactose 1P, glucose 1P, UDP

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6
Q

which cofactor is required for pyruvate decarboxylase

A

thiamine pyrophosphate

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7
Q

cofactor required for alcohol dehydrogenase

A

nadh

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8
Q

E1 is rate limiting, blank, and involves the blank of pyruvate in pdc mediated pyruvate metabolism

A

irreversible, decarboxylation

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9
Q

E2 is when TPP is oxidized to produce blank

A

acetyl CoA

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10
Q

E3 has FADH2 oxidized by NAD+ to form blank

A

nadh

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11
Q

role of glycerol 3P dehydrogenase in electron shuttling is to take electrons from blank and reduce blank to glycerol 3P

A

nadh, DHAP

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12
Q

glycerol 3P is reoxidezed back to blank by flavoprotein dehydrogenase

A

FADH2

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13
Q

electron shuttle wastes energy because it converts blank to blank

A

NADH (3 atp), FADH2 (2 atp)

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14
Q

enzymes involved in fatty acid oxidation

A

fatty acyl coA synthetase, pyrophosphatase

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15
Q

symptoms of mcad deficiency

A

hypoglycemia, lactic acidosis, etc

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16
Q

cause of methylmalonic acidosis

A

lack of vitamin b12 which causes yield of succinyl coA to decrease

17
Q

defective alpha oxidation leads to blank

A

refsum’s disease (neurological)

18
Q

role of peroxisomal fatty acid beta oxidation

A

convert very long/long chain FA to 8 carbon chain

19
Q

defective peroxisomal oxidation leads to blank

A

zellweger syndrome (neurological)

20
Q

in ketone body activation for oxidation, acetoacetate is activated in the blank by blank

A

mitochondria, 3 ketoacyl coA transferase

21
Q

ketoacidosis can be caused by these

A

low insulin, alcoholism, low carb diet

22
Q

driving forces of glycogenolysis

A

high intracellular ratio of phosphate to glucose 1P

23
Q

glycogenesis driving forces

A

utp hydrolysis

24
Q

glycogenolysis is activated by blank

A

glucagon/epinephrine

25
Q

glycogenesis is activated by blank

A

insulin

26
Q

glycogenolysis requires these enzymes

A

debrancher (4,4 transferase) , glycogen phosphorylase, glucose 6 phosphatase, glut 2

27
Q

glycogenesis uses these enzymes

A

udp glucose pyrophosphorylase, brancher enzyme (4,6 transferase), glycogen synthase

28
Q

glycogenolysis product

A

many glucose 1 phosphates

29
Q

pka inhibits glycolysis because pka phosphorylates blank which makes it less active

A

pfk 2

30
Q

pfk 2 makes blank less active which leads to less blank

A

pfk 1, glycolysis

31
Q

what enzymes are affected in an error of gluconeogenesis

A

pyruvate carboxylase, PEPCK, fructose 1,6 diphosphatase, glucose 6 phosphatase

32
Q

acetyl coA carboxylase (ACC) is inhibited by blank and blank

A

pka, ampk

33
Q

ACC is allosterically controlled by blank and blank

A

citrate (more active), malonyl CoA (less active(

34
Q

ACC is activated by blank

A

insulin

35
Q

ACC is inactivated by blank

A

glucagon/epinephrine