Catabolic Pathways and Metabolism - Biochemistry

A catabolic reaction is defined as a reaction used to break down a large molecule into smaller subunits. Of the following options, glycogenolysis is the only option where a larger molecule (glycogen) is broken down into smaller subunits (individual glucose molecules).

Hexokinase and glucokinase are two enzymes that serve similar roles but have different characteristics. Hexokinase is found in all tissues, is inhibited by glucose 6 phosphate, and is not induced by insulin. It has a physiologic role of providing cells with a basal level of glucose 6 phosphate necessary for energy production.

In the glycolytic pathway, 2 molecules of ATP must be used. The purpose of these molecules is to phosphorylate 2 intermediates in the pathway:

1. Glucose must be phosphorylated to glucose-6-phosphate.

2. Fructose-6-phosphate must be phosphorylated to fructose-1,6-bisphosphate.

The first step in glycolysis is the conversion of glucose to glucose-6-phosphate through the consumption on one ATP molecule. Glucose is reacted upon by the enzyme hexokinase to carry out this step. Kinases are a group of enzymes that add phosphate groups by removing them from an ATP. All of these other enzymes catalyze subsequent reactions in glycolysis.

Hydroxyacyl-CoA dehydrogenase oxidizes the beta hydroxyl group, forming a carbonyl.

Thiolase catalyzes the cleavage of the beta-ketoacyl-CoA.

NAD is required for the oxidation of beta-hydroxyacyl-CoA to beta-Ketoacyl-CoA by hydroxyacyl-CoA dehydrogenase.

The two major products of the thiolase-catalyzed reaction are acetyl-CoA and a fatty acyl-CoA shortened by two carbons.

To answer this question, we'll need to keep in mind some of the highlights of beta oxidation. When a fatty acid is broken down by this method, the hydrocarbon chain is broken down two carbons at a time through a series of repeating reactions. These two carbons come off in the form of acetyl-CoA, with an additional generation of one molecule each of NADH and . Since we know the original chain we're starting with contains twelve carbons, we know that there will be six molecules of acetyl-CoA produced. Furthermore, in order to generate these six molecules, beta-oxidation must proceed five times. Thus, we are going to have five molecules of NADH and five molecules of . The acetyl-CoA generated from beta oxidation is able to enter the citric acid cycle. For each molecule of acetyl-CoA that goes through the cycle, 1 molecule of ATP, 1 molecule of , and 3 molecules of NADH are generated. Therefore, since six molecules will be sent into the citric acid cycle, there will be a total generation of six molecules of ATP, six molecules of , and eighteen molecules of NADH. Now, we need to add everything up. So far, we have six molecules of ATP. We also have five molecules of NADH from beta-oxidation, and eighteen from the citric acid cycle, for a total of twenty-three. We've also obtained five molecules of from beta-oxidation, and another six from the citric acid cycle for a total of eleven. All of the NADH and that was generated from these reactions can donate their electrons into the electron transport chain to generate ATP. The rule of thumb is that for every NADH, molecules of ATP are produced. And for every molecules of , molecules of ATP is made. So, we have:

And if we add to this the six ATP that was generated directly by substrate-level phosphorylation in the citric acid cycle, that gives us a total of:

Palmitate is a sixteen-carbon chain and its beta-oxidation will produce 8 acetyl-CoA molecules, since each acetyl-CoA is two-carbons long. Glucose, on the other hand, will be broken down to form 2 acetyl-CoA molecules. Therefore, palmitate forms 4 times as many acetyl-CoA molecules.

This first step of beta oxidation is catalyzed by acyl-CoA dehydrogenase. One way to remember is that the enzyme is named for exactly what it does: remove a hydrogen (dehydrogenate) from acyl-CoA, which is the reactant. In order to be acetyl-CoA the R-group must specifically be a methyl group.

This second step of beta oxidation is catalyzed by enoyl-CoA hydratase. One way to remember is that the enzyme is named for exactly what it does: adding water (hydrate) across the double bond of enoyl-CoA, which is the reactant.

This third step in beta oxidation is catalyzed by L-hydroxacyl-CoA dehydrogenase. One way to remember is that the enzyme is named for exactly what it does: remove a hydrogen (dehydrogenate) L-hydroxyacyl-CoA (the reactant).

This fourth step in beta oxidation is catalyzed by thiolase. The reduced form of coenzyme-A is used as a cofactor to cleave the bond between the alpha and the beta carbon.

removes two hydrogens to form . These two electrons will be donated to the electron transport chain.

Enoyl-CoA hydratase catalyzes the the addition of water across the carbon-carbon double bond.

Three enzymes are ultimately involved in activating fatty acids as fatty acyl-CoA and transferring this molecule into the inner mitochondrial matrix to be broken down via the beta-oxidation pathway. The first enzyme is acyl-CoA synthetase. This enzyme is a type of ATPase, and it uses the thermodynamically favorable dephosphorylation of ATP to drive the synthesis of fatty acyl-CoA from a fatty acid and CoASH. Fatty acids alone cannot cross mitochondrial membranes, but fatty acyl-CoA can cross the outer membrane.

Carnitine palmitoyl transferase II also synthesizes fatty acyl-CoA but acyl-CoA synthetase is the first enzyme to do so, and its dephosphorylation of ATP is what initially activates a fatty acid.

The carnitine transport protein, known as the carnitine-acylcarnitine translocase, allows the facilitated diffusion of a fatty acid into the mitochondrial matrix. Fatty acids cannot be transported into the mitochondrial matrix alone.

Following this step, carnitine palmitoyl transferase II catalyzes the reaction that reforms fatty acyl-CoA from CoASH and the fatty acylcarnitine.

Acyl-CoA dehydrogenase converts fatty acyl-CoA to trans-Δ2-enoyl-CoA forming the high energy redox cofactor from .