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
glycogenesis is activated by blank
insulin
26
glycogenolysis requires these enzymes
debrancher (4,4 transferase) , glycogen phosphorylase, glucose 6 phosphatase, glut 2
27
glycogenesis uses these enzymes
udp glucose pyrophosphorylase, brancher enzyme (4,6 transferase), glycogen synthase
28
glycogenolysis product
many glucose 1 phosphates
29
pka inhibits glycolysis because pka phosphorylates blank which makes it less active
pfk 2
30
pfk 2 makes blank less active which leads to less blank
pfk 1, glycolysis
31
what enzymes are affected in an error of gluconeogenesis
pyruvate carboxylase, PEPCK, fructose 1,6 diphosphatase, glucose 6 phosphatase
32
acetyl coA carboxylase (ACC) is inhibited by blank and blank
pka, ampk
33
ACC is allosterically controlled by blank and blank
citrate (more active), malonyl CoA (less active(
34
ACC is activated by blank
insulin
35
ACC is inactivated by blank
glucagon/epinephrine