Understanding the Kreb Cycle and ATP

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SUMMARY

The Krebs cycle is an exergonic process that releases GTP, which is chemically equivalent to ATP, and reduces NAD+ to NADH for ATP production in the electron transport chain. The overall reaction is exergonic due to a decrease in Gibbs free energy (ΔG < 0), achieved by lowering potential energy through the formation of stable carbon-oxygen bonds and increasing disorder by breaking down larger molecules into smaller ones. The cycle utilizes acetyl-CoA, releasing carbon dioxide and regenerating coenzyme A, contributing to the overall energy yield of cellular respiration.

PREREQUISITES
  • Understanding of Gibbs free energy and its equation (ΔG = ΔH - TΔS)
  • Knowledge of metabolic pathways, specifically glycolysis and the Krebs cycle
  • Familiarity with electron carriers like NAD+ and NADH
  • Basic concepts of chemical bonding, particularly carbon-oxygen and carbon-hydrogen bonds
NEXT STEPS
  • Study the detailed mechanisms of the Krebs cycle and its role in cellular respiration
  • Learn about the electron transport chain and its connection to ATP synthesis
  • Explore the concept of exergonic vs. endergonic reactions in biochemical processes
  • Investigate the role of acetyl-CoA in metabolism and its sources
USEFUL FOR

Students of biochemistry, molecular biology researchers, and educators seeking to deepen their understanding of metabolic pathways and energy production in cells.

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Having some trouble understanding if the Kreb cycle is exergonic or endergonic?
I know it has to be exergonic because it's releasing ATP?
 
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tica86 said:
Having some trouble understanding if the Kreb cycle is exergonic or endergonic?
I know it has to be exergonic because it's releasing ATP?

GTP is actually is released, which from a potential chemical energy perspective, is equivalent to ATP. The Krebs cycle reduces the electron carrier NAD+ to NADH, which is used in the electron transport chain after the Krebs cycle to create ATP. The overall process must be exergonic, or else we would not have made far past being protoplasm. Individual endergonic reactions in the overall process are generally overcome through the use of highly energetic phophate-containing compounds; glycolysis is the best example of this, where 2 ATPs are consumed but 4 are gained, with a net of two ATP out.
 
What makes a process exergonic? Well, it is helpful to consider the equation for Gibbs free energy: ΔG = ΔH - TΔS. Since exergonic processes bring your system to a state of lower free energy (i.e. ΔG < 0), processes that lower the potential energy of your system (ΔH < 0) or increase its disorder (ΔS > 0) will help a process be more exergonic.

How does one lower the potential energy of the system? Well, for carbon-based compounds, the answer is basically by increasing the number of bonds carbon has to oxygen. This is true because carbon-oxygen bonds are much more stable (i.e. have a lower potential energy) than carbon-hydrogen or carbon-carbon bonds.

What about the disorder of the system? One easy way to increase the disorder of a system is to break large molecules into smaller molecules.

Now, consider the Krebs cycle. The cell feeds acetyl-CoA into the Krebs cycle and it releases two molecules of carbon dioxide and regenerates free coenzyme A (CoA). Does this process create products that have a lower potential energy than the reactants? Does the process increase the entropy of the system?
 

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