PENTOSE PHOSPHATE PATHWAY Flashcards

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?

A

NADP+.

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

A

NADP+

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
Q

Two phases of PPP reactions

A

Irreversible oxidative phase
Reversible nonoxidative phase

25
Q

A precursor of proteoglycans & conjugated glucuronides. A product of the Uronic Acid Pathway

A

Glucuronate

26
Q

It is needed for the synthesis of Lactose, Glycolipids, Proteoglycans, & Glycoproteins

A

Galactose

27
Q

catalyzes the phosphorylation of galactose using ATP as phosphate donor

A

Galactokinase

28
Q

Precursor of Amino Sugars (Hexosamines)

A

Glucose

29
Q

Major amino sugars are

A

glucosamine, galactosamine, mannosamine, sialic acid

30
Q

Principal sialic acid found in human tissues

A

N-acetylneuraminic acid

31
Q

Both fructose and sorbitol are found in the lens of the eye and may be involved in the pathogenesis of

A

Diabetic cataract

32
Q

responsible for fructose formation from glucose

A

Sorbitol “polyol” pathway

33
Q

Enzyme that catalyze the reduction of glucose to sorbitol

A

Aldose reductase