Answer:
The cytosolic and mitochondrial pools of CoA are kept separate, and no radioactive CoA from the cytosolic pool enters the mitochondrion.
Explanation:
- Fatty acyl group condensed with CoA in the cytosol are first transferred to carnitine and in this process, CoA is released.
- After this, it is transported into the mitochondrion, where it is again condensed with CoA.
- In this way, the cytosolic and mitochondrial pools of CoA are kept separate, and due to this reason, no radioactive CoA from the cytosolic pool enters the mitochondrion.
- Therefore, according to the given question, the C14 CoA that is added into the liver homogenate along with palmitate shows cytosolic radioactive fraction but not mitochondrial as in the mitochondria a different CoA joins palmitate and not the one containing C14.
Each time a new ATP is created, ATP synthase must process 5 protons.
<h3>Where is ATP synthase found and what does it do?</h3>
- ADP and phosphate are converted into ATP by the mitochondrial enzyme ATP synthase, which is located in the inner membrane.
- Protons are transported over a gradient created by electron transfer from the chemically positive to the negative side of the proton, which drives the flux of protons.
<h3>How does photosynthesis's ATP synthase function?</h3>
- The light-driven production of ATP is catalyzed by the chloroplast ATP synthase, which is activated in the light and deactivated in the dark by redox-modulation via the thioredoxin system.
- This down-regulation is thought to be crucial for minimizing wasted ATP hydrolysis at night.
<h3>What makes ATP synthase so crucial?</h3>
All cellular functions are powered by ATP, which is constantly used by cells and required for production. About 100 ATP molecules can be produced by each ATP synthase every second.
learn more about ATP synthase here
<u>brainly.com/question/893601</u>
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