citric acid cycle

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citric acid cycle:

see Krebs cycleKrebs cycle,
series of chemical reactions carried out in the living cell; in most higher animals, including humans, it is essential for the oxidative metabolism of glucose and other simple sugars.
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Citric acid cycle

In aerobic cells of animals and certain other species, the major pathway for the complete oxidation of acetyl coenzyme A (the thioester of acetic acid with coenzyme A); also known as the Krebs cycle or tricarboxylic acid cycle. Reduced electron carriers generated in the cycle are reoxidized by oxygen via the electron transport system; water is formed, and the energy liberated is conserved by the phosphorylation of adenosine diphosphate (ADP) to adenosine triphosphate (ATP). Reactions of the cycle also function in metabolic processes other than energy generation. The role of the cycle in mammalian tissues will be emphasized in this article. See Adenosine diphosphate (ADP), Coenzyme, Enzyme

The first step in the cycle involves the condensation of the acetyl portion of acetyl coenzyme A (CoA) with the four-carbon compound oxaloacetate to form citrate, a tricarboxylate containing six carbons (see illustration). A shift of the hydroxyl group of citrate to an adjacent carbon results in the formation of d -threo-isocitrate, which in turn is oxidized to the five-carbon compound α-ketoglutarate and carbon dioxide (CO2). In a second oxidative decarboxylation reaction, α-ketoglutarate, in the presence of CoA, is converted to succinyl CoA and another molecule of CO2. In the subsequent formation of the four-carbon compound succinate and CoA, the energy in the thioester bond of succinyl CoA is conserved by the formation of guanosine triphosphate (GTP) from guanosine diphosphate (GDP) and inorganic phosphate. Fumarate is formed from succinate by the removal of two atoms of hydrogen, and the unsaturated compound is then hydrated to l -malate. The dehydrogenation of malate forms oxaloacetate, the starting four-carbon compound of the metabolic cycle. Thus, beginning with the two-carbon acetyl group, one completion of the cycle results in the formation of two molecules of carbon dioxide.

Citric acid cycleenlarge picture
Citric acid cycle

The oxidation of acetyl CoA to CO2 in the cycle occurs without direct reaction with molecular oxygen. The oxidations occur at dehydrogenation reactions in which hydrogen atoms and electrons are transferred from intermediates of the cycle to the electron carriers nicotinamide adenine dinucleotide (NAD+) and flavin adenine dinucleotide (FAD). The electrons from NADH and FADH2 are transferred to molecular oxygen via a series of electron transport carriers, with regeneration of NAD+ and FAD. The energy liberated in the electron transport chain is partially conserved by the formation of ATP from ADP and inorganic phosphate, by a process called oxidative phosphorylation. The energy generated as oxygen accepts electrons from the reduced coenzymes generated in one turn of the cycle results in the maximal formation of 11 molecules of ATP. Because GTP obtained by phosphorylation of GDP at the succinyl CoA to succinate step of the cycle is readily converted to ATP by nucleotide diphosphokinase, the yield is 12 molecules of ATP per molecule of acetyl CoA metabolized. See Nicotinamide adenine dinucleotide (NAD)

The electron transport and oxidative phosphorylation systems and the enzymes required for the citric acid cycle are located in the mitochondria of cells, which are the major source of ATP for energy-consuming reactions in most tissues. The citric acid cycle does not occur in all cells. For example, mature human red blood cells do not contain mitochondria and the cycle is absent. In these cells, ATP is formed by the anaerobic conversion of glucose to lactate (anaerobic glycolysis). See Mitochondria

Acetyl CoA is formed from carbohydrates, fats, and the carbon skeleton of amino acids. The origin of a precursor and the extent of its utilization depend on the metabolic capability of a specific tissue and on the physiological state of the organism. For example, most mammalian tissues have the capacity to convert glucose to pyruvate in a reaction called glycolysis. Pyruvate is then taken up from cellular cytosol by mitochondria and oxidatively decarboxylated to acetyl CoA and carbon dioxide by pyruvate dehydrogenase. Acetyl CoA is also the end product of fatty acid oxidation in mitochondria. However, the fatty acid oxidation pathway occurs in fewer tissues than does glycolysis or the citric acid cycle. The amino acids follow varied pathways for forming compounds that can enter the citric acid cycle. See Amino acids

In addition to the cycle's role in yielding catabolic energy, portions of it can supply intermediates for synthetic processes, such as the synthesis of the fatty acid moiety of triglycerides from glucose (lipogenesis), and formation of glucose from the carbon skeletons of certain amino acids, lactate, or glycerol (gluconeogenesis). See Carbohydrate metabolism, Cell (biology), Glucose, Glycogen, Lipid metabolism, Metabolism

citric acid cycle

[′si‚trik ′as·əd ′sī·kəl]
(biochemistry)
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Most relevant to competitively grown crops is the theory that it serves to waste protons and e-when ATP is already in abundance, allowing the TCA cycle and glycolysis to proceed in production of carbon intermediates needed in biosyntheses.
The TCA cycle is also a factory for intermediates with oxoglutarate serving as precursor to porphyrins (chlorophyll, cytochrome) and amino acids (and thus protein).
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This appreciably simplifies the metabolic maps of reductive autotrophs and allows for the next generalization: that all carbon fixation pathways, oxidative and reductive, yield outputs that are routed through gluconeogenesis and glycolysis (catabolic pathways that occur only in the oxidative heterotrophs), and oxidative or reductive TCA cycles, or parts of these cycles.
The glycolytic pathway consists of a sequence of biochemical transformations in which sugar (typically glucose or fructose) is converted to a compound known as acetyl coenzyme A, or acetyl CoA, that enters the TCA cycle, resulting in the formation of a large amount of ATP.
Under progressively oxygen-limiting growth conditions, the reactions that convert 2-oxoglutarate to oxaloacetate are used more heavily by first reversing some of the steps of the TCA cycle to generate citrate, which is split into acetate and oxaloacetate by citrate lyase (Fig.
2] (Haapanen et al, 1959), the reductive TCA cycle, with its remarkable ability to fix carbon solely from C[O.
The observation that the antimicrobial activity evident in nutrient-limited medium is amplified when supplemented with a TCA cycle intermediate seems to support our experimental model; the bioactive compound may be an intermediate drawn off the TCA cycle.
Low molecular weight carboxylic acids are produced and consumed during the TCA cycle and glycolysis, so these compounds are ubiquitous in marine organisms.