The true statements are:
- Substrate level phosphorylation ocvurs during Pyruvate oxidation
- 32 ATP molecules can be made by cellular respiration but only 2 ATP molecules when oxygen is lacking
- Electrons move from protein to protein due to increasing electronegativity in the electron transport chain
- ADP is phosphorylated in the matrix of the mitochondria during oxidative phosphorylation
- ATP inhibits pyruvate dehydrogenase by feedback inhibition
<h3>What is glucose oxidation?</h3>
Glucose oxidation refers to the process in the cells in which glucose molecules are oxidized to form ATP and carbon dioxide in the presence of oxygen.
The first stage of glucose oxidation is the conversion to pyruvate.
Pyruvate is oxidized to acetylCoA.
AcetylCoA enters the citric acid cycle to produce reducing equivalents, NADH for the electron transport chain.
- The true statements about pyruvate oxidation is that there is substrate level phosphorylation during the process
- When there is sufficient oxygen, 36 ATP molecules can be made (theoretically) by cellular respiration. However, when oxygen is lacking, only 2 ATP molecules are made.
- In the electron transport chain of cellular respiration, electrons move from protein to protein due to increasing electronegativity
- During oxidative phosphorylation, ADP is phosphorylated in the matrix of the mitochondria
- Aerobic respiration can be regulated by feedback inhibition of pyruvate dehydrogenase by ATP.
Learn more about pyruvate oxidation at: brainly.com/question/22565849
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Answer:
Volume
Explanation:
This is a Physics question, and that means we can definitely do some experiment with this.
See Archimedes' law of buoyancy.
The nucleus and the ribosomes to synthesize protein synthesis.
Answer:
e. None of the above
Explanation:
For me as a Researcher, the reason could be increased Concentration of your DNA sample which you are using as your template. Try to decrease the concentration of DNA (up to 100 ng per reaction is enough and can increase up to 200 ng). so the reason for getting non specific bands is increase concentration of DNA which results in non specific amplification and also degradation of DNA in the reaction which you can see in your gel electrophoresis results.
i always corrected my results using the same technique that is lowering the concentration of DNA between 100 and 200 ng per single reaction of PCR.
