PENTOSE PHOSPHATE PATHWAY Flashcards

(34 cards)

1
Q

What is the primary function of PPP?

A

Generates NADPH and ribose from glucose-6-phosphate.

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2
Q

What are the two stages of PPP?

A

A: Oxidative phase and non-oxidative phase.

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3
Q

Key enzyme in the oxidative phase?

A

Glucose-6-phosphate dehydrogenase

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4
Q

Substrate for glucose-6-phosphate dehydrogenase?

A

Glucose-6-phosphate

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5
Q

Product of the oxidative phase?

A

NADPH

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6
Q

Byproduct of the oxidative phase?

A

CO2.

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6
Q

Function of the non-oxidative phase?

A

Interconverts sugars

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7
Q

Key enzyme in the non-oxidative phase?

A

Ribulose-5-phosphate epimerase.

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8
Q

Generation of glucose from non-carbohydrate sources.

A

gluconeogenesis

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9
Q

Alternative name for PPP

A

hexose monophosphate shunt

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10
Q

Why is NADPH important?

A

Essential for fatty acid synthesis, cholesterol synthesis, and antioxidant defenses.

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11
Q

Implication of altered PPP activity in cancer cells

A

Increased NADPH production for biosynthesis

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12
Q

How is the polyol pathway implicated in diabetes complications?

A

Converts glucose to fructose, contributing to diabetic neuropathy and cataract formation.

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13
Q

Product of glucose-6-phosphate dehydrogenase?

A

6-phosphogluconolactone

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14
Q

Enzyme that converts 6-phosphogluconolactone to 6-phosphogluconate?

A

6-phosphogluconolactonase

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15
Q

Cofactor for glucose-6-phosphate dehydrogenase?

16
Q

How is glucose-6-phosphate dehydrogenase regulated?

A

Feedback inhibition by NADPH.

17
Q

Catalyzes the conversion of glucose-6-phosphate to 6-phosphogluconolactone

A

glucose-6-phosphate dehydrogenase

18
Q

Catalyzes the conversion of 6-phosphogluconate to ribulose-5-phosphate

A

6-phosphogluconate dehydrogenase

19
Q

cofactor for 6-phosphogluconate dehydrogenase

20
Q

How is 6-phosphogluconate dehydrogenase regulated?

A

Feedback inhibition by NADPH

21
Q

Glucuronic acid is synthesized from glucose via this pathway

A

Uronic acid pathway

22
Q

Deficiency in the pathway of uronic acid leads to the condition of

A

essential pentosuria

23
Q

Deficiencies in the enzymes of fructose and galactose metabolism lead to metabolic disease such as:

A

essential fructosuria, hereditary fructose intolerance, galactosemia

24
Two phases of PPP reactions
Irreversible oxidative phase Reversible nonoxidative phase
25
A precursor of proteoglycans & conjugated glucuronides. A product of the Uronic Acid Pathway
Glucuronate
26
It is needed for the synthesis of Lactose, Glycolipids, Proteoglycans, & Glycoproteins
Galactose
27
catalyzes the phosphorylation of galactose using ATP as phosphate donor
Galactokinase
28
Precursor of Amino Sugars (Hexosamines)
Glucose
29
Major amino sugars are
glucosamine, galactosamine, mannosamine, sialic acid
30
Principal sialic acid found in human tissues
N-acetylneuraminic acid
31
Both fructose and sorbitol are found in the lens of the eye and may be involved in the pathogenesis of
Diabetic cataract
32
responsible for fructose formation from glucose
Sorbitol "polyol" pathway
33
Enzyme that catalyze the reduction of glucose to sorbitol
Aldose reductase