ICS UNIT 2

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Last updated 7:28 PM on 6/25/26
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The Hexose Monophosphate (HMP) shunt—also known as the pentose phosphate pathway—is an alternative metabolic pathway to glycolysis.

-location: cytosol

HMP: oxidizes glucose to generate NADPH (for anabolic reactions and antioxidant) and ribose-5-phosphate “pentose phosphate pathway” (for nucleotide synthesis).

called pentose phosphate pathway it makes ribose-5-phosphate.

HMP does not oxidize glucose for ATP.

<p>The Hexose Monophosphate (HMP) shunt—also known as the pentose phosphate pathway—is an alternative metabolic pathway to glycolysis.</p><p>-location: cytosol</p><p>HMP: oxidizes glucose <strong>to generate NADPH</strong> (for anabolic reactions and antioxidant) and ribose-5-phosphate “pentose phosphate pathway” (for nucleotide synthesis).</p><p>called pentose phosphate pathway it makes ribose-5-phosphate.</p><p>HMP does not oxidize glucose for ATP.</p>
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The Hexose Monophosphate (HMP) shunt—also known as the pentose phosphate pathway—is an alternative metabolic pathway to glycolysis.

-location: cytosol

HMP: oxidizes glucose to generate NADPH (for anabolic reactions and antioxidant) and ribose-5-phosphate “pentose phosphate pathway” (for nucleotide synthesis).

called pentose phosphate pathway it makes ribose-5-phosphate.

HMP does not oxidize glucose for ATP.

The rate-limiting enzyme for the HMP (Hexose Monophosphate) shunt—also known as the Pentose Phosphate Pathway—is Glucose-6-phosphate dehydrogenase (G6PD).

The H is taken from glucose and put to NAD+, making NADH.

This enzyme catalyzes the first and irreversible step of the oxidative phase, converting glucose-6-phosphate to 6-phosphogluconolactone while generating NADPH.

Regulation of G6PD

  • stimulated by high cellular levels of NADP⁺, signaling a high demand for NADPH.

  • Allosteric Inhibition: G6PD is strongly inhibited by NADPH

  • Hormonal Control: Insulin induces the synthesis of G6PD, increasing the pathway's activity during the fed state

<p><span style="color: rgb(33, 89, 133);">The Hexose Monophosphate (HMP) shunt—also known as the pentose phosphate pathway—is an alternative metabolic pathway to glycolysis.</span></p><p><span style="color: rgb(33, 89, 133);">-location: cytosol</span></p><p><span style="color: rgb(33, 89, 133);">HMP: oxidizes glucose <strong>to generate NADPH</strong> (for anabolic reactions and antioxidant) and ribose-5-phosphate “pentose phosphate pathway” (for nucleotide synthesis).</span></p><p><span style="color: rgb(33, 89, 133);">called pentose phosphate pathway it makes ribose-5-phosphate.</span></p><p><span style="color: rgb(33, 89, 133);">HMP does not oxidize glucose for ATP.</span></p><p><span style="color: rgb(33, 89, 133);">The rate-limiting enzyme for the HMP (Hexose Monophosphate) shunt—also known as the Pentose Phosphate Pathway—is Glucose-6-phosphate dehydrogenase (G6PD).</span></p><p><span style="color: rgb(33, 89, 133);">The H is taken from glucose and put to NAD+, making NADH.</span></p><p><span style="color: rgb(33, 89, 133);">This enzyme catalyzes the first and irreversible step of the oxidative phase, converting glucose-6-phosphate to 6-phosphogluconolactone while generating NADPH.</span></p><p><strong><u>Regulation of G6PD</u></strong></p><ul><li><p><span><strong>stimulated </strong>by high cellular levels of <strong>NADP⁺</strong>, signaling a high demand for NADPH.</span></p></li><li><p><span><strong>Allosteric Inhibition:</strong> <strong>G6PD </strong>is <strong>strongly inhibited by NADPH</strong></span></p></li><li><p><span><strong>Hormonal Control:</strong> <strong>Insulin induces the synthesis of G6PD</strong>, <strong>increasing the pathway</strong>'s <strong>activity during </strong>the </span><span style="color: rgb(30, 101, 140);">fed state</span></p></li></ul><p></p>
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<p><span style="color: rgb(40, 88, 138);">This is the lactone that forms on glucose after the dehydrogenation.</span></p>

This is the lactone that forms on glucose after the dehydrogenation.

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provides a SHUNT

<p>provides a SHUNT</p>
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<p>Glut </p>

Glut

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<p>A. </p>

A.

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A)

test question

it happens in the red blood cell in the cytosol.

<p>A) </p><p>test question</p><p>it happens in the red blood cell in the cytosol. </p>
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<p>C) </p>

C)

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A)

<p>A) </p>
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C)

NADPH is the reductive agent

NADH is the electron donor

<p>C)</p><p>NADPH is the reductive agent</p><p>NADH is the electron donor</p>
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B)

you missed this question, submit this.

<p>B) </p><p>you missed this question, submit this. </p>
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<p>E) </p>

E)

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<p>C) </p>

C)

the answer is in the pathway.

<p>the answer is in the pathway. </p>
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<p>E) </p>

E)

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<p>A) </p>

A)

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<p>E) </p>

E)

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<p>B) </p>

B)

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<p>B) </p>

B)

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<p>E) </p>

E)

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<p>D) </p>

D)

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<p>B) </p>

B)

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<p>A) </p>

A)

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<p>E) </p><p>B is NOT correct. </p>

E)

B is NOT correct.

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<ol><li><p>sucrose becomes either fructose or glucose </p></li></ol><p></p>
  1. sucrose becomes either fructose or glucose

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<p>know these three enzymes</p>

know these three enzymes

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<p>people have elevate glucose in the blood, diabetes, often have eye problems, because there is glucose in their eye. </p>

people have elevate glucose in the blood, diabetes, often have eye problems, because there is glucose in their eye.

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<p>B) </p><p>we don’t want that, so we combine it to be more efficient/ </p>

B)

we don’t want that, so we combine it to be more efficient/

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<p>B) </p>

B)

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<p>A) </p><p>in the muskoloskeletal system, it’s true</p><p>in the liver, this is false. </p>

A)

in the muskoloskeletal system, it’s true

in the liver, this is false.

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<p>B) </p>

B)

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<p>A) </p>

A)

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<p>A) </p>

A)

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<p>D) </p>

D)

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<p>D) </p>

D)

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<p>1 glucose → 2 pyruvates &amp; 2 NADH. </p><p>each pyruvate has 3 carbons</p><p>this is important to keep track of so in the end we can calculate how many ATPs we could generate. </p>

1 glucose → 2 pyruvates & 2 NADH.

each pyruvate has 3 carbons

this is important to keep track of so in the end we can calculate how many ATPs we could generate.

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<p>vitamin B1 is deficient in alcoholics. </p>

vitamin B1 is deficient in alcoholics.

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regulation of pyruvate dehydrogenase complex.

<p>regulation of pyruvate dehydrogenase complex. </p>
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<p>krebs cycle: acetyl-CoA → 2NADH, 2 CO2, 1 GTP, FADH2, NADH</p><p>you cannot have over 1000ATP, once ATP count gets over 1000, you start to store it as something different (fat, etc). </p>

krebs cycle: acetyl-CoA → 2NADH, 2 CO2, 1 GTP, FADH2, NADH

you cannot have over 1000ATP, once ATP count gets over 1000, you start to store it as something different (fat, etc).

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<p>A) </p><p>we don’t form acetyl-CoA, we break it down. </p>

A)

we don’t form acetyl-CoA, we break it down.

A)

<p>A) </p>
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<p>B) </p><p>C is not the right one here (you did not get this far to explain it). </p>

B)

C is not the right one here (you did not get this far to explain it).

C)

isocitrate may be added or removed.

<p>C) </p><p>isocitrate may be added or removed. </p>
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B)

<p>B) </p>
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<p>A) </p><p>you chose C) </p>

A)

you chose C)

A)

<p>A) </p>
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<p>A) </p>

A)

<p></p>
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<p>B) </p>

B)

both A and D

<p>both A and D</p>
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<p>B) </p>

B)

A)

<p>A) </p>
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<p>A) </p>

A)

C)

<p>C) </p>
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we cannot live without oxygen for even a few minutes, because oxygen accepts the electron.

<p>we cannot live without oxygen for even a few minutes, because oxygen accepts the electron. </p>
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<p>the video goes over this. </p>

the video goes over this.

how many ATPs can you make from a glucose molecule?

1 glucose → 36-38 ATP.

<p>how many ATPs can you make from a glucose molecule?</p><p>1 glucose → 36-38 ATP. </p>
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<p>D) </p>

D)

A)

<p>A) </p>
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<p>C) </p>

C)

C)

<p>C) </p>
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<p>A) </p>

A)

C)

<p>C) </p>