Enolase is the enzyme responsible for catalyzing the conversion of 2-phosphoglycerate into phosphoenolpyruvate. This reaction takes place during glycolysis. All other enzymes are involved in the sequence of reactions known as the citric acid cycle.

This is the correct sequence of intermediates in the citric acid cycle. Note that both citrate and cis-aconitase are substrates for the same enzyme, aconitase. The net yield of one turn of the citric acid cycle is: , and . The electron carriers then participate in the electron transport system along the inner mitochondrial membrane.

The citric acid cycle starts with the combination of a four-carbon molecule (oxaloacetate) and a two-carbon molecule (acetyl-CoA) to form a six-carbon molecule (citrate). Since the citric acid cycle is indeed a cycle, oxaloacetate must be regenerated. Thus, two molecules of carbon dioxide are produced throughout the citric acid cycle. The first molecule of carbon dioxide is produced during the conversion of isocitrate into alpha-ketoglutarate. This reaction is catalyzed by isocitrate dehydrogenase. Alpha-ketoglutarate, a five-carbon molecule, is then converted into the four-carbon molecule succinyl-CoA via alpha-ketoglutarate dehydrogenase, yielding another molecule of carbon dioxide. The remaining steps of the citric acid cycle do not involve any more production of carbon dioxide since both succinyl-CoA and oxaloacetate are both four-carbon molecules.

The enzyme alpha-ketoglutarate dehydrogenase catalyzes the conversion of alpha-ketoglutarate (5 carbons) to succinyl-CoA (4 carbons). During this step, one carbon is lost as carbon dioxide and one molecule of  is produced. This step is the second, and last step in the Krebs cycle in which carbon dioxide is formed. Recall that the starting material, oxaloacetate, is also 4 carbons long.

During the step in which one of the carbons of isocitrate is lost as carbon dioxide, one molecule  is also produced. This reaction is catalyzed by isocitrate dehydrogenase. This leaves a five-carbon molecule known as alpha-ketoglutarate. In the next step, alpha ketoglutarate dehydrogenase acts upon alpha-ketoglutarate and a carbon is lost as carbon dioxide and another molecule of  is produced. Later in the cycle, succinate dehydrogenase catalyzes the conversion of succinate to fumarate. This reaction produces one molecule of . The enzyme fumarase then converts fumarate to malate. The final step in the citric acid cycle is the regeneration of oxaloacetate from malate. Malate dehydrogenase catalyzes this reaction, which produces the third molecule of . Note that this is for one turn of the citric acid cycle i.e., for one molecule of acetyl-CoA. Each molecule of glucose yields two molecules of acetyl-CoA via glycolysis and pyruvate dehydrogenase complex.

Some catabolic pathways do indeed make citric acid cycle intermediates; for example, plants and bacteria use phospoenolpyruvate carboxylase to create oxaloacetate from phosphoenolypyruvate. Anaplerotic reactions refill the citric acid cycle with intermediates, rather than remove them. Some archaea have a complete citric acid cycle; it is the bacteria that mostly do not have a complete cycle. In eukaryotes, citrate cleavage does indeed take place in the cytosol; that citrate is transported to the cytosol from mitochondria, and the acetyl-CoA can be used for fatty acid synthesis.

The citric acid cycle is a series of reactions that occur within the matrix of the mitochondria. With every turn of the cycle, one acetyl-CoA molecule enters, and a variety of molecules leave. These leaving molecules include , , , and ATP. The acetyl-CoA that enters the cycle is derived from other cellular pathways, such as beta-oxidation and glycolysis. In this way, the citric acid cycle serves as a conduit by which metabolites from other pathways can be broken down to ultimately provide energy for the cell.

Since the citric acid cycle occurs in mitochondria, only eukaryotes are capable of performing this process. Also, the citric acid cycle is not responsible for the production of urea from ammonia. Rather, it is the urea cycle that performs this role. It is worth noting, however, that the citric acid cycle and the urea cycle are energetically linked by the aspartate-argininosuccinate shunt. This is because these two cycle share a few common intermediates, and the citric acid cycle can help to offset the demanding energy requirements of the urea cycle.

When glycogen phosphorylase reaches a branching point in glycogen, the bonds switch from being alpha-1,4-glycosidic bonds to alpha-1,6-glycosidic bonds.  It is unable to cleave these bonds, and so other enzymes (a transferase and a glucosidase) must come into play.

Glycogen is first debranched and broken down from its non-reducing end by glycogen phosphorylase to give the product G1P, which is then converted into G6P by phosphoglutomutase. Glycogen synthase, glycogen branching enzyme, and UDP-glucose pyrophosphorylase are required for glycogen synthesis.

Glycogen phosphorylase, the rate-limiting enzyme of glycogenolysis  does not breaks alpha 1,6 glycosidic bonds. It releases glucose from glycogen by hydrolyzing alpha 1,4 glycosidic bonds until it reaches a branch point in the glycogen molecule. At this time, another enzyme, a debranching alpha 1,6 glycosidase hydrolyzes the alpha 1,6 glycosidic bonds. Glycogen phosphorylase is under regulation by many hormones, including insulin and glucagon, as well as epinephrine.