Pyruvate dehydrogenase complex is a mechanism that occurs between glycolysis and the citric acid cycle. This is because pyruvate cannot enter the citric acid cycle right after glycolysis. The purpose of pyruvate dehydrogenase complex is to modify (or convert) pyruvate, the end product of glycolysis, to the acetyl CoA, which enters the citric acid cycle.
The enzymes involved are:
- E1: Pyruvate dehydrogenase (the TPP, or thiamine pyrophosphate is attached to it)
- E 2: Dihydrolipoyl transacetylase (the lipoic acid is attached to it)
- E 3: Dihydrolipoyl dehydrogenase (the FAD is attached to it)
Let's now look at what happens in details (please, look at the picture below while you read):
E1:
First of all, pyruvate comes in and interacts with TPP, which is attached to E1 (pyruvate dehydrogenase). TPP has a ring that interacts directly with pyruvate. As a result, a CO2 is released, and the rest of the pyruvate (the hydroxyethyl group) is attached to the TPP, forming hydroxyethyl TPP.
E2:
Next, the hydroxyethyl group is transferred to the disulfide bond in the lipoic acid. Remember, the lipoic acid is attached to the second enzyme (E2) of the pyruvate dehydrogenase complex, the dihydrolipoyl transacetylase. That leads to the reduction of one of the sulfurs, because it gains hydrogen (this hydrogen comes from the hydroxyethyl group). The hydroxyethyl group without one of this hydrogens, which was given off to this sulfur is now forming acetyl group. An acetyl group attached to a sulfur forms a thioester bond, which is a high energy bond. The CoA-SH comes in and takes the acetyl group from this sulfur on the lipoic acid. CoA-SH also gives of its hydrogen to the sulfur, so now, we have made the acetyl CoA.
(Both of the sulfurs that before formed the disulfide bond are now reduced, because each of them has a hydrogen)
E3:
Furthermore, the lipoic acid cannot react with the hydroxyethyl TPP, because it doesn't have the disulfide bond. The FAD, which is attached to the third enzyme, dihydrolipoyl dehydrogenase, picks up these hydrogens, regegenerating the disulfide bond. As a result, FADH2 is formed. However, it cannot flow right to the ETC (electron transport chain), because it is attached to the dihydrolipoyl dehydrogenase. The NAD+ then comes in and becomes reduced to NADH + H+.
In addition:
The TPP is regenerated when hydroxyethyl group is removed from hydroxyethyl TPP.
The lipoic acid is regenerated when the disulfide bond is regenerated.
The FAD is regenerated when NAD+ comes in and picks up the hydrogen (a hydrogen ion is also released as a result of that) from FADH2.
This is going to be much easier to understand if you watch my video about this :).
Please, check out my video about enzymes :)
What are enzymes?
Enzymes refer to proteins that catalyze chemical reactions in our body. They are also called catalytic proteins. Enzymes speed up (or catalyze) chemical reactions by lowering the energy of activation (EA), which is the amount of energy needed to start a reaction. Enzymes exhibit tertiary structure.
How do enzymes work?
An enzyme binds to a substrate, forming enzyme-substrate complex. Thus, enzymes bind to the substrates when they are ''in action'', or when they catalyze a reaction. When an enzyme binds to a substrate, the shape of the enzymes alters as the substrate enters the active site, which is the place on the enzyme where the substrate can bind. Enzymes are substrate specific, which means that for instance enzyme A binds only to the substrate A etc.
However, enzymes often require assistance from substances called coenzymes and cofactors. These are substances that help enzymes in reaction catalysis, but cannot catalyze a reaction on their own. Coenzymes are organic substances, while cofactors are inorganic.
Competitive and noncompetitive (allosteric) inhibition
The enzymatic activity is highly controlled and regulated. This can be done in a number of ways. For instance, genes that code for a specific enzymes can be switched on and off. The enzymes that have already been produced are regulated by competitive and noncompetitive inhibition.
Competitive inhibition means that the substrate and a substrate-like substance (an inhibitor) ''competete'' for the active site of the enzyme. If the inhibitor binds to the enzyme, the enzyme won't work.
Noncompetitive inhibition, also known as allosteric inhibition, means that the inhibitor binds to another site of the enzyme (not to the active site). That causes the whole enzyme to undergo a change in its conformation, and the active site is changed. Thus, it's impossible for the substrate to bind to the enzyme.
PLEASE WATCH THIS VIDEO THAT I'VE MADE ABOUT GLYCOLYSIS :)
Step 1:
A phosphate is attached to the glucose molecule. The phosphate comes from ATP, which becomes ADP after donating the phosphate. The enzyme that facilitates this reaction is called hexokinase. When the first step is finished, we have
glucose-6-phosphate.
Step 2:
An isomer of glucose-6-phosphate is created by the enzyme phosphoglucose isomerase. The isomer created is called fructose-6-phosphate.
Step 3:
The enzyme called phosphofructokinase attaches a phosphate from ATP to fructose-6-phosphate. The phosphate is attached on the first carbon of
fructose-6-phosphate, so the product that is formed is fructose1,6-bisphosphate. Of course, ATP donated a phosphate, so it left off as ADP.
Steps 4 and 5:
In the fourth step, the enzyme aldolase splits fructose 1,6-bisphosphate to two three-carbon molecules, which are isomers of each other. These are dihydroxyacetone phosphate and glyceraldehyde 3-phosphate.
In step 5, the enzyme triphosphate isomerase converts dihydroxyacetone phosphate into glyceraldehyde 3-phosphate.
(Remember, since we have now 2 three-carbon molecules, so there is double amount of each product from now. For instance, if one ATP is produced from one three-carbon molecule, there are two ATP molecules produced in total.)
Step 6:
Glyceraldehyde 3-phosphate is converted to 1,3-bisphosphoglycerate. The enzyme that catalyzes this reaction is called glyceraldehyde phosphate dehydrogenase. Hydogen ion is released, and NAD + Pi come in. Pi is donated to the glyceraldehyde 3-phosphate, and it is attached to the 1st carbon. NAD picks up the hydrogen ions. What we get is 1,3-bisphosphoglycerate.
Step 7:
The phosphate is removed from 1,3-bisphosphoglycerate, and 3-bisphosphoglycerate is formed. The phosphate that has been removed is attached to the ADP that comes in, so it becomes ATP. The enzyme that catalyzes this reaction is phosphoglycerate kinase.
Step 8:
The enzyme phosphoglyceromutase removes the phosphate from the third carbon of the 3-phosphoglycerate, and attaches it on the 2nd carbon. Thus, 3-phosphoglycerate becomes 2-phosphoglycerate.
Step 9:
2-phosphoglycerate is converted to phosphoenolpyruvate by enolase. During this reaction, water is released.
Step 10:
Phosphoenolpyruvate (PEP) looses its phosphate. This phosphate is donated to ADP, so it becomes ATP. The enzyme that catalyzes this reaction is called pyruvate kinase. The end product of glycolysis is pyruvate, which is used later in cellular respiration.
What is glycolysis and why is it important?
Our cells obtain their energy from glucose. However, they cannot use it directly. First, they need to transform the energy from glucose to the form of energy that they can use. Cells use energy in the form of ATP. Thus, a cell transforms the energy in glucose to ATP, the form of energy that they can utilize. The process in which this occurs is cellular respiration. Glycolysis is the initial step of cellular respiration. The end products of glycolysis are used further during cellular respiration. Therefore, glycolysis is very important.
What is made and what is used during glycolysis?
Glycolysis uses 2 ATP molecules, but it makes 4 ATP molecules. Thus, our net gain will be: 4 ATP - 2 ATP = 2 ATP. During glycolysis, the cell also produces two NADH molecules. Water is also released.
Where does glycolysis occur?
Glycolysis occurs in the cytoplasm of the cell:
PLEASE, CHECK OUT MY VIDEO ABOUT THE BIG PICTURE OF GLYCOLYSIS
The structure of ATP
ATP stands for Adenosine triphosphate (as you can see from the title :)). What does that mean? Adenosine refers to the nucleotide adenine (the same type of adenine that is present in our DNA!) bond to ribose (the same type of sugar that is present in RNA!)
There are three (tri = three) phosphate groups attached to adenosine. All of them are negatively charged, which makes ATP an unstable molecule.
What do we need ATP for?
ATP is an energy carrier. It provides energy for all cells activities. For instance, if we want to contract a muscle, proteins in the muscle cells need ATP. Active transport into and out of the cell, such as phagocytosis or pinocytosis, also requires energy. This energy is provided by ATP.
How? Well, it transfers a phosphate group. This occurs during ATP hydrolysis. When the molecule of ATP is hydrolyzed, a phosphate is transferred and energy is released. The picture below shows how that looks like.
Please click here to watch my video about ATP
