week 15 Flashcards
(218 cards)
How many ATP molecules can be produced from a single glucose molecule through these processes?
The processes can produce a total of 32 ATP molecules.
Can the number of ATP molecules produced vary? If so, why?
Yes, the number of ATP molecules produced can vary. It may be 30 ATP instead of 32 ATP. The variation is due to shuttle systems that move NADH between different parts of the cell.
What is the role of the shuttle systems in the variation of ATP production?
The shuttle systems help transfer NADH from the cytosol to the mitochondria. The way NADH transfers its energy to a hydrogen ion can affect the total ATP produced.
How does the transfer of energy impact the total ATP produced?
The transfer of energy between NADH and the hydrogen ion can affect the efficiency of ATP production, resulting in either 32 ATP or 30 ATP.
What is the summary of the variation in ATP production from glucose?
The variation in the total ATP amount produced from glucose is due to shuttle systems that move NADH between different parts of the cell, impacting the transfer of energy and resulting in either 32 ATP or 30 ATP.
Where is NADH+H+ recharged or “reoxidized” in cellular respiration?
NADH+H+ is recharged or “reoxidized” in the Electron Transport Chain (ETC).
What molecules can easily pass through the inner membrane of the mitochondria?
Molecules like CO2, water, and oxygen can easily pass through the inner membrane of the mitochondria.
Where is NADH+H+ located in the cytosol or the matrix of the mitochondria?
NADH+H+ produced during glycolysis is located in the cytosol, while NADH+H+ produced in processes like pyruvate oxidation and the citric acid cycle is located in the matrix of the mitochondria.
How are the NADH+H+ molecules produced in the matrix of the mitochondria reoxidized?
The NADH+H+ molecules produced in the matrix of the mitochondria are reoxidized in a specific complex of the Electron Transport Chain called Complex 1.
What is the challenge in reoxidizing the NADH+H+ located in the cytosol?
The challenge is that NADH+H+ in the cytosol cannot directly cross the inner mitochondrial membrane as there is no specific transport system for it.
Can the NADH+H+ generated in the mitochondria easily reach the Electron Transport Chain?
Yes, the NADH+H+ molecules generated in the mitochondria can easily reach the Electron Transport Chain and be reoxidized.
What is the main difference between NADH+H+ in the mitochondria and the cytosol in terms of crossing the inner mitochondrial membrane?
NADH+H+ molecules in the mitochondria can directly cross the inner mitochondrial membrane, while those in the cytosol face a challenge because they cannot directly cross the inner mitochondrial membrane.
What are the two shuttles involved in the transport of electrons from the cytosol into the mitochondria?
The two shuttles involved are the malate-aspartate shuttle and the glycerol-3-phosphate shuttle.
Where does NAD exist in the cell?
NAD exists in both the cytosol and the matrix of the mitochondria.
Do the pools of NAD in the cytosol and the matrix mix together?
No, the pools of NAD in the cytosol and the matrix do not mix together.
What role do the cofactors of NAD play in cellular processes?
The presence and ratio of cofactors in the cytosol and the matrix of NAD play a significant role in determining metabolic processes inside the cells.
Why can’t NADH+H+ from the cytosol directly enter Complex 1 of the electron transport chain?
NADH+H+ from the cytosol cannot directly enter Complex 1 of the electron transport chain because NAD+ (the oxidized form of NAD) cannot cross the inner membrane of the mitochondria directly.
How are electrons from NADH in the cytosol transported into the mitochondria?
The electrons from NADH in the cytosol are transported into the mitochondria through the malate-aspartate shuttle and the glycerol-3-phosphate shuttle.
What is the function of the malate-aspartate shuttle and the glycerol-3-phosphate shuttle?
The malate-aspartate shuttle and the glycerol-3-phosphate shuttle help move electrons across the mitochondrial inner membrane, allowing their participation in the electron transport chain.
What is the mitochondria carrier family?
The mitochondria carrier family is a group of proteins located in the inner membrane of mitochondria, consisting of 53 carriers.
How many carriers in the mitochondria carrier family have unknown functions?
About one-third of the carriers in the mitochondria carrier family have unknown functions.
What is the main purpose of the carriers in the mitochondria carrier family?
The main purpose of these carriers is to transport various substances across the impermeable inner membrane of mitochondria to support important cellular processes like oxidative phosphorylation.
What are some examples of substances transported by the carriers in the mitochondria?
Some examples of transported substances include amino acids, nucleotides (such as ADP and ATP), cofactors like thiamine pyrophosphate, inorganic ions, phosphate, protons, and fatty acids and di- and tri-carboxylates.
What are the different mechanisms used by these carriers?
The carriers can work through different mechanisms. Antiporters transport one molecule in while another molecule is transported out. Symporters transport two molecules in the same direction, often accompanied by a hydrogen ion. Uniporters transport a single molecule from one side of the membrane to the other.