Chapter 20: The Pentose Phosphate Pathway Flashcards

1
Q

Two stages of the PPP

A
  • Oxidative

- Non-oxidative

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2
Q

Shunts of the PPP

A
  • Pentose shunt

- Monophosphate shunt

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3
Q

PPP is a mostly

A
  • Anabolic cytoplasmic pathway

- Connection with glycolysis

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4
Q

PPP is significant in organs/tissues

A
  • Liver
  • Kidney
  • Adipose tissue
  • Adrenal cortex
  • Neurones
  • RBCs (along with glycolysis)
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5
Q

PPP is significant in cells

A
  • Neutrophils

- Macrophages

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6
Q

Neutrophils and macrophages kill

A
  • Microorganisms

- Minimal importance in muscle

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7
Q

PPP is responsible for synthesis and degradation of

A
  • Pentoses
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8
Q

PPP is central to formation of

A
  • NADPH
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9
Q

There is no direct consumption or production of

A
  • ATP in the pentose phosphate pathway
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10
Q

Non-oxidative phase of the PPP involves

A
  • Isomerization/epimerization phase

- Rearrangement phase

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11
Q

Overall, the PPP produces

A
  • NADPH upon oxidation of glucose-6-phosphate to ribulose-5-phosphate
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12
Q

Glucose-6-phosphate dehydrogenase is

A
  • The rate limiting enzyme
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13
Q

G-6-P DH is highly specific for

A
  • NADP+

- Primary regulation point

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14
Q

G-6-P DH is strongly inhibited by

A
  • NADPH
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15
Q

The most common of all human enzymopathies (G-6-P DH)

A
  • Favism (consumption of fava beans) and hemolytic anemia

- Leads to reduced formation of NADPH

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16
Q

Mutant enzyme (G-6-P DH) is rapidly degraded

A
  • And RBCs (lacking a nucleus) cannot re-synthesize it
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17
Q

Individuals with G-6-P DH enzymopathy react to

A
  • Antimalarial drugs (primaquine)
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18
Q

Mutations of G-6-P DH protect against

A
  • Malaria (just like sickle cell)
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19
Q

6-phosphogluconate dehydrogenase catalyzes

A
  • Oxidative decarboxylation of 6-phosphogluconate to ribulose 5-phosphate
  • Produces NADPH
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20
Q

Overall reaction of the oxidative phase of PPP

A
  • Glucose-6-phosphate + 2NADP+ + H2O –> Ribulose-5-phosphate + 2NADPH + 2H+ + CO2
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21
Q

Interconversion of ribulose-5-phosphate with ribose-5-phosphate or xylulose-5-phosphate produces

A
  • 5 C sugars
22
Q

Ribose-5-phosphate can be rearranged to regenerate

A
  • Glycolytic intermediates
23
Q

The rearrangement of ribose-5-phosphate is brought about through the action of

A
  • Transketolase

- Transaldolase

24
Q

Transketolase is a family of enzymes with

A
  • Broad substrate specificity
25
Transketolase transfers a
- 2 carbon unit --> ketose to aldose
26
Transketolase requires
- TPP cofactor (thus defective in alcoholics)
27
Transketolase appears in assay of
- RBC diagnostic of thiamine deficiency
28
Transaldolase is a family of enzymes with
- Broad substrate specificity
29
Transaldolase transfers a
- 3 carbon unit --> ketose to aldose
30
The PPP is closely linked with
- The glycolytic pathway
31
Degradation of pentoses occurs via
- Transketolase (2C) activity | - Transaldolase (3C) activity
32
Functions of the PPP is to provide
- NADPH - Pentoses - Pathway for synthesis/degradation
33
PPP provides NADPH for biosynthesis of
- Fatty acids - Steroids - Neurotransmitters - Reduced glutathione
34
PPP provides pentoses for
- Nucleic acid synthesis
35
PPP provides a pathway for the synthesis and degradation of
- Pentoses (to glycolytic intermediates)
36
Cellular NADPH from PPP is utilized by
- Fatty acid synthesis | - Regeneration of tripeptide GSH
37
Regenration of tripeptide GSH is important in
- Protection from cancer - Protection from hemolysis & hemolytic anemia - Detoxification - Activation of sulfhydryl enzymes
38
Protection of RBCs from hemolysis and hemolytic anemia maintains
- RBC integrity
39
Reduced glutathione is regenerated by
- NADPH-dependent glutathione reductase
40
GSH reacts with reactive oxygen metabolites including peroxides (H2S2) in a reaction catalyzed by
- Glutathione peroxidase
41
H2S2 can irreversibly damage
- Hb
42
Glucose-6-phopshate is used in both
- Glycolysis | - Pentose phosphate pathway
43
Excess ribose-5-phopshate (R5P) can be converted to
- Glycolytic intermediates
44
Flux of G6P through the PPP is governed by
- The situation that prevails within the given cell | - Relative requirements for ribose-5-phosphate and NADPH
45
The PPP is entirely
- Cytoplasmic | - Neither consumes nor produces ATP
46
PPP activity is high in
- Adrenal glands - Site of steroid hormone biosynthesis - Liver - Site of cholesterol - Fatty acid synthesis - Testes - Adipose tissue - Mammary glands
47
Glucose-6-phopshate dehydrogenase catalyzes the irreversible, rate limiting oxidation of
- Glucose-6-phosphate to 6-phosphogluconolactone | - Primary control point of the PPP
48
Defects in the G6P enzyme represent a common enzymopathy and affected individuals suffer from
- Hemolytic anemia, but are resistant to malaria
49
The PPP produces NADPH for
- Reductive biosynthesis | - Reduction of oxidized glutathione
50
The PPP produces pentoses for
- Nucleic acid biosynthesis