winter midterm Flashcards

1
Q

glycosidic bond and composition of:

  • maltose
  • lactose
  • sucrose
A
  • alpha 1-4, 2 glucose
  • beta 1-4, galactose + glucose
  • alpha1-beta2, fructose + glucose
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2
Q

which of the enzymes is incorrectly paired with its location of function?

A

isocitrate dehydrogenase and glyoxosome

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3
Q

what does glucagon upregulate?

A

glycogen phosphorylase A

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4
Q

which steps of glycolosis generate ATP? (2)

A

1,3 bisphosphate –> 3 phosphoglycerate

phosphoenolpyruvate –> pyruvate

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5
Q

glycogen synthase:

A

requires glucose-1-P to be activated by UDP

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6
Q

what is correct about the citric acid cycle?

A

directly generates 2 water molecules/acyl-CoA

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7
Q

the structure shown below is:

A

fructose-2,6-bisphosphate

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8
Q

triglyceride levels of the 4 lipoproteins

A

chylomicrons: 85
VLDL: 50
LDL: 10
HDL: 4

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9
Q

which enzyme is mismatched with is function?

A

lipoamine - deamination

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10
Q

which of the following is true about ketogenesis?

A

ketogenesis is absent in people with systemic carnitine deficiency

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11
Q

omega oxidation of fatty acids:

A

involves sequentially alcohol, aldehyde and acid intermediates

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12
Q

identify the ketone bodies (structure)

A

CH3 - C(=O) - CH2 - C (=O,O-) and

CH3 - C(H,OH) - CH2 - C (=O, O-)

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13
Q

what is thiolase involved in? (4)

A
  • ketogenesis pathway
  • works in mitochondria
  • converts acetoacetyl-CoA back into Acetyl-CoA in the peripheral tissues
  • aka ACAT
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14
Q

what phospho/sphingolipids are found primarily in the outer leaflet of the plasma membrane?

A

phosphotidylcholine and sphingomyelin

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15
Q

peroxisomal B-oxidation of fatty acids involves:

A
  • export of NADH and H+ to the mitochondria for reoxidation to NAD
  • export of acetyl CoA to mitochondria to enter the CAC
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16
Q

lioprotein lipase action involves:

A

activation of the enzyme by alipoprotein CII

17
Q

pyruvate kinase remains active in muscle during glycogenolysis because:

A
  • muscle need glycolysis to generate energy
  • muscle lacks glycogen receptors
  • muscle lacks glucose-6-phosphatase
18
Q

PFK-1 is downregulated by:

A

ATP and citrate

19
Q

which of the following enzymes/pathways is correctly listed with its regualtor?

A

all of the above

20
Q

Fehlings solution?

A
  • reducing sugars (glucose, galactose, fructose) interact with the solution to produce a red colour (specifically interact with the Cu ions)
  • non-reducing sugars dont interact (sucrose) so theres no color change
21
Q

steps of mitochondrial B-oxidation of fatty acids to acetyl CoA:

A

occur while fatty acids are attached to coenzyme A

22
Q

pyruvate dehydrogenase:

A
  • occurs in mitochondrial matrix
  • converts pyruvate to acetyl CoA
  • eliminates Co2/generates NADH (coupled)
  • has 3 subunits and 5 coenzymes (TPP, lipoic acid, coenzyme A, FAD, NAD+)
23
Q

human G6PD deficiency results in:

A
  • compromised NADPH production for antioxidant defences
  • little biosynthesis of ribose-5-phosphate
  • increased sensitivity to chemotherpeutic drugs
24
Q

which of the following statements about the synthesis of DHA from an essential acid in mamals is (are) correct?

A

all of the above

25
Q

during later stages of fasting, the brain becomes dependent on which of the following enzymes to efficiently generate energy?

A

thiolase, pep carboxykinase, 3B-ketoacyl CoA transferase

everything but citrate