Regulation of Cellular Respiration (Article) - Khan Academy
Regulation of Cellular Respiration (Article) - Khan Academy
Regulation of Cellular Respiration (Article) - Khan Academy
Regulation of cellularrespiration
How cellular respiration can be sped up or slowed down. Key
enzymes and feedback inhibition.
Introduction
You can sometimes have too much of a good thing. For instance, consider
ice cream sandwiches. Maybe you really like ice cream sandwiches and buy
a bunch of them at the store. If youre very hungry, that might be a good
choice: you can eat them all quickly, before they melt. If youre only a little
hungry, though, that might be a bad choice: most of the sandwiches will melt
uneaten, at which point you will have wasted some money.
Cells face a related problem when they break down fuels, such as glucose, to
produce ATP. If the cells supply of ATP is low, it would do well to break down
glucose as quickly as possible, replenishing the ATP it needs to keep the
lights on. If the supply of ATP is high, on the other hand, it might not be such
a good idea to oxidize glucose at top speed. ATP is an unstable molecule,
and if it sits around in the cell too long, its likely to spontaneously hydrolyze
back to ADP. This is like the case of the melted ice cream sandwich: the cell
has spent glucose to make ATP, and that ATP ends up going to waste.
Its important for a cell to carefully match the activity of its fuel breakdown
(pathways to its energy needs at a given moment. Here, we'll see how cells
turn cellular respiration pathways up or down in response to ATP levels
and other metabolic signals.
The primary target for regulation a biochemical pathway is often the enzyme
that catalyzes the pathways firstcommitted step(that is, the first step that is
not readily reversible). The concept of a committed step can get a little
complicated when there are many intersecting metabolic pathways, as in
cellular respiration, but this is still a useful idea to keep in mind.
How are the enzymes that control metabolic pathways regulated? A number
cellular respiration enzymes are controlled by the binding of regulatory
molecules at one or more allosteric sites. (Anallosteric siteis just a
regulatory site other than the active site.) Binding of a regulator to the
allosteric site of an enzyme changes its structure, making it more or less
active.
The molecules that bind cellular respiration enzymes act as signals, giving
the enzyme information about the cell's energy state. ATP, ADP, and NADH
are examples of molecules that regulate cellular respiration enzymes. ATP,
for instance, is a "stop" signal: high levels mean that the cell has enough ATP
and does not need to make more through cellular respiration. This is a case
offeedback inhibition, in which a product "feeds back" to shut down its
pathway.
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Regulation of glycolysis
Several steps in glycolysis are regulated, but the most important control point
is the third step of the pathway, which is catalyzed by an enzyme
calledphosphofructokinase(PFK). This reaction is the first committed step,
making PFK a central target for regulation of the glycolysis pathway as a
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whole .
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PFK is regulated by ATP, an ADP derivative called AMP, and citrate, as well
as some other molecules we won't discuss here.
Citrate.Citrate, the first product of the citric acid cycle, can also inhibit
PFK. If citrate builds up, this is a sign that glycolysis can slow down,
because the citric acid cycle is backed up and doesnt need more fuel.
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Pyruvate oxidation
The next key control point comes after glycolysis, when pyruvate is converted
to acetyl CoA. This conversion step is irreversible in many organisms and
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controls how much acetyl CoA fuel enters the citric acid cycle . The enzyme
that catalyzes the conversion reaction is called pyruvate dehydrogenase.
ATP and NADH make this enzyme less active, while ADP makes it more
active. So, more acetyl CoA is made when energy stores are low.
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At each stage, we can see similar elements. For instance, we see feedback
inhibition at many stages, at the level of pathways and of individual reactions.
Monitoring of the cell's energy state through levels of molecules like ATP,
ADP, AMP, and NADH is another common feature.
The diagram below summarizes the key enzymes weve discussed, along
with some of their most important regulators.
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Ask a question...
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In all the steps involved in Krebs cycle which are regulated and
which are not and why?
2votes Comment Flag 3 months agoby Ann Laubstein
I thought ADP was too stable to lose another phosphate group. So,
does the cell mistakenly use ADP in place of ATP when it's low on
the latter?
1vote Comment Flag 9 months agoby jrtf2001
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ATP is the most common energy carrier for the cell. Each
phosphate that you remove conveys energy but less each
level. ATP has more energy than ADP for example. The cell
sometimes doesn't need all the energy from ATP -> ADP and
thus, ADP -> AMP can be used to drive a reaction. This is why
the cell might use ADP. Our enzymes are pretty good at
choosing the right energy carrier that leads to the best
efficiencies. ADP usually doesn't carry enough energy to
power a reaction requiring ATP.
2votes 1 comment Flag 7 months agoby Don Zhu
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