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Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

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Figure Regulatory Mechanisms in Pyruvate Dehydrogenase and the TCA Cycle covalent modification of enzymes ex: phosphorylation of pyruvate dehydrogenase (non-covalent) product and feedback inhibition (e.g. by NADH, ATP, citrate) allosteric effectors (ADP/ATP, Ca++)

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Page 1: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Page 584

Glycolysis and TCA cycle: final accounting

• based on ~2.5 ATP/NADH and 1.5 ATP/FADH2• ~32 ATP/(glucose oxidized to 6CO2)

Text – Figures, pg. 584

Page 2: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Free Energies for TCA Reactions

• note necessity of low (i.e. large negative) G for citrate synthase to drive preceding malate dehydrogenase reaction. This results in low oxaloacetate concentration.

• large negative G steps are points of regulation.*

***

Page 3: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Figure 17-15

Regulatory Mechanisms in Pyruvate Dehydrogenase and the TCA Cycle

• covalent modification of enzymes ex: phosphorylation of pyruvate dehydrogenase

• (non-covalent) product and feedback inhibition (e.g. by NADH, ATP, citrate)

• allosteric effectors (ADP/ATP, Ca++)

Page 4: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Figure 17-16

Points of Regulation in the TCA Cycle

inhibition

activationText – Figure 17-16

Page 5: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Figure 17-17

TCA Cycle intermediates are a major source of molecules for other metabolic pathways

• note that several of the molecules look like amino acids, except for the absence of an -amino group

Text – Figure 17-17

Page 6: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Page 589

TCA Cycle intermediates are a major source of molecules for other metabolic pathways

ex: production of glutamate from -ketoglutarate

Page 7: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Production of some other amino acids by transamination reactions

ex: production of alanine and -ketoglutarate from glutamate and pyruvate

Page 8: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Page 589

Production of some other amino acids by transamination reactions

ex: production of aspartate and pyruvate from oxaloacetate and alanine

Page 9: Page 584 Glycolysis and TCA cycle: final accounting based on ~2.5 ATP/NADH and 1.5 ATP/FADH2 ~32 ATP/(glucose oxidized to 6CO2) Text – Figures, pg. 584

Page 590

The depletion of TCA cycle intermediates for use in other pathways must be offset by replenishing (anaplerotic) reactions, including pyruvate carboxylase.

Text – Figure, pg. 590