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Citric acid cycle, reactions

Aconitase catalyzes the citric acid cycle reaction citrate isocitrate... [Pg.672]

The citric acid cycle (reactions 1-8 are described in the text). [Pg.345]

See also Citric Acid Cycle Reactions, Gluconeogenesis... [Pg.137]

See also Citric Acid Cycle, Enzymes of the Citric Acid Cycle, Reaction Picture, Table 14.1,... [Pg.170]

See also / -Oxidation, Acetyl-CoA, Citric Acid Cycle Reactions, Vitamin B12... [Pg.442]

Synthesis of succinyl-CoA in mammalian cells such as the red cell and liver cell can be accomplished either from a-KG or from succinate. The formation of succinyl-CoA occurs in the mitochondria as part of the citric acid cycle reactions. The requirement for a citric acid cycle to form ALA or protoporphyrin or heme has been shown by tracer studies with acetate and succinate [39], and by inhibition studies with malonate, Ira j -aconitate, fluoracetate, and arsenite [49]. The requirement for an electron transfer system from the citric acid cycle to O2 has been shown by inhibition studies with anaerobiosis and CO. The requirement for oxidative phosphorylation has been shown by dinitrophenol inhibition of ALA synthesis dinitrophenol may also inhibit ALA-synthetase [3,49]. [Pg.89]

Since citric acid cycle intermediates are quickly labeled it is assumed that much subsequent metabolism of malate is by citric acid cycle reactions. Of course, the malate itself could enter the mitochondria, and no doubt does (Lips and Beevers, 1966 a, b MacLennan et al., 1963). Pyruvate and/or P-enolpyruvate resulting from decarboxylation probably enter the citric acid cycle via acetate. Bradbeer and Ranson (1963) found that " C-pyruvate supplied to Kalanchoe leaves in the dark was consumed by the citric acid cycle. Some was also found as free sugars. Hence, there is a slow equilibration of malate and malate degradation products with other metabolic events in the cell. Measurements of oxygen consumption during CAM metabolism can leave no doubt that the citric acid cycle is active in succulents (e.g., Szarek and Ting, 1974b Kinraide and Behan, 1975 Kaplan et al., 1976 a, b 1977). [Pg.55]

The citric acid cycle, a nine-step process, also diverts chemical energy to the production of ATP and the reduction of NAD and FAD. In each step of the citric acid cycle (also known as the Krebs cycle) a glucose metabolite is oxidized while one of the carrier molecules, NAD or FAD, is reduced. Enzymes, nature s chemical catalysts, do a remarkable job of coupling the oxidation and reduction reactions so that energy is transferred with great efficiency. [Pg.808]

Problem 5.9 Predict the products of the following polar reaction, a step in the citric acid cycle for food metabolism, by interpreting the flow of elections indicated by Uie curved arrows ... [Pg.152]

Acid-catalyzed hydration of isolated double bonds is also uncommon in biological pathways. More frequently, biological hydrations require that the double bond be adjacent to a carbonyl group for reaction to proceed. Fumarate, for instance, is hydrated to give malate as one step in the citric acid cycle of food metabolism. Note that the requirement for an adjacent carbonyl group in the addition of water is the same as that we saw in Section 7.1 for the elimination of water. We ll see the reason for the requirement in Section 19.13, but might note for now that the reaction is not an electrophilic addition but instead occurs... [Pg.221]

In contrast to laboratory reactions, enzyme-catalyzed reactions often give a single enantiomer of a chiral product, even when the substrate is achiral. One step in the citric acid cycle of food metabolism, for instance, is the aconitase-catalyzed addition of water to (Z)-aconitate (usually called ris-aconitate) to give isocitrate. [Pg.312]

A large number of biological reactions involve prochiral compounds. One of the steps in the citric acid cycle by which food is metabolized, for instance, is... [Pg.316]

Elucidating the stereochemistry of reaction at prochirality centers is a powerful method for studying detailed mechanisms in biochemical reactions. As just one example, the conversion of citrate to (ds)-aconitate in the citric acid cycle has been shown to occur with loss of a pro-R hydrogen, implying that the reaction takes place by an anti elimination mechanism. That is, the OH and H groups leave from opposite sides of the molecule. [Pg.317]

Problem 9.26 The aconitase-catalyzed addition of water to ds-aconitate in the citric acid cycle occurs with the following stereochemistry. Does the addition of the OH group occur on the Re or the Si face of the substrate What about the addition of the H Does the reaction have syn or anti stereochemistry ... [Pg.318]

The first step in the citric acid cycle is reaction of oxaloacetate with acetyl CoA to give citrate. Propose a mechanism, using acid or base catalysis as needed. [Pg.911]

Enzymes work by bringing reactant molecules together, holding them, in the orientation necessary for reaction, and providing any necessary acidic or basic sites to catalyze specific steps. As an example, let s look at citrate synthase, an enzyme that catalyzes the aldol-like addition of acetyl CoA to oxaloacetate to give citrate. The reaction is the first step in the citric acid cycle, in which acetyl groups produced by degradation of food molecules are metabolized to yield C02 and H20. We ll look at the details of the citric acid cycle in Section 29.7. [Pg.1043]

The conversion occurs through a multistep sequence of reactions catalyzed by a complex of enzymes and cofactors called the pyruvate dehydrogenase complex. The process occurs in three stages, each catalyzed by one of the enzymes in the complex, as outlined in Figure 29.11 on page 1152. Acetyl CoA, the ultimate product, then acts as fuel for the final stage of catabolism, the citric acid cycle. All the steps have laboratory analogies. [Pg.1151]

The initial stages of catabolism result in the conversion of both fats and carbohydrates into acetyl groups that are bonded through a thioester link to coenzyme A. Acetyl CoA then enters the next stage of catabolism—the citric acid cycle, also called the tricarboxylic acid (TCA) cycle, or Krebs tycle, after Hans Krebs, who unraveled its complexities in 1937. The overall result of the cycle is the conversion of an acetyl group into two molecules of C02 plus reduced coenzymes by the eight-step sequence of reactions shown in Figure 29.12. [Pg.1154]

As its name implies, the citric acid cycle is a closed loop of reactions in which the product of the hnal step (oxaloacetate) is a reactant in the first step. The intermediates are constantly regenerated and flow continuously through the cycle, which operates as long as the oxidizing coenzymes NAD+ and FAD are available. To meet this condition, the reduced coenzymes NADH and FADH2 must be reoxidized via the electron-transport chain, which in turn relies on oxygen as the ultimate electron acceptor. Thus, the cycle is dependent on the availability of oxygen and on the operation of the electron-transport chain. [Pg.1154]

Figure 29.12 MECHANISM The citric acid cycle is an eight-step series of reactions that results in the conversion of an acetyl group into two molecules of C02 plus reduced coenzymes. Individual steps are explained in the text. Figure 29.12 MECHANISM The citric acid cycle is an eight-step series of reactions that results in the conversion of an acetyl group into two molecules of C02 plus reduced coenzymes. Individual steps are explained in the text.
Step 1 of Figure 29.12 Addition to Oxaloacetate Acetyl CoA enters the citric acid cycle in step 1 by nucleophilic addition to the oxaloacetate carbonyl group, to give (S)-citryl CoA. The addition is an aldol reaction and is catalyzed by citrate synthase, as discussed in Section 26.11. (S)-Citryl CoA is then hydrolyzed to citrate by a typical nucleophilic acyl substitution reaction, catalyzed by the same citrate synthase enzyme. [Pg.1156]

Steps 7-8 of Figure 29.12 Hydration and Oxidation The final two steps in the citric acid cycle are the conjugate nucleophilic addition of water to fumarate to yield (S)-malate (L-malate) and the oxidation of (S)-malate by NAD+ to give oxaloacetate. The addition is cataiyzed by fumarase and is mechanistically similar to the addition of water to ris-aconitate in step 2. The reaction occurs through an enolate-ion intermediate, which is protonated on the side opposite the OH, leading to a net anti addition. [Pg.1158]

The final step is the oxidation of (S)-malate by NAD+ to give oxaloacetate, a reaction catalyzed by malate dehydrogenase. The citric acid cycle has now returned to its starting point, ready to revolve again. The overall result of the cycle is... [Pg.1159]


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See also in sourсe #XX -- [ Pg.672 , Pg.673 , Pg.673 , Pg.674 ]

See also in sourсe #XX -- [ Pg.672 , Pg.673 , Pg.673 , Pg.674 ]

See also in sourсe #XX -- [ Pg.396 ]

See also in sourсe #XX -- [ Pg.754 ]




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Amphibolic reactions, citric acid cycle

Citric acid cycle anaplerotic reactions

Citric acid cycle individual reactions

Citric acid cycle pyruvate dehydrogenase reaction

Citric acid cycle reaction steps

Citric acid cycle reactions fumarase

Citric acid cycle reactions isocitrate dehydrogenase

Citric acid cycle reactions stereospecificity

Citric acid cycle reactions succinate dehydrogenase

Citric acid cycle, reactions citrate formation

Citric acid cycle, reactions decarboxylation

Citric acid cycle, reactions fumarate hydration

Citric acid cycle, reactions malate oxidation

Citric acid cycle, reactions succinate oxidation

Citric cycle

Cycling reactions

Reaction cycle

Reactions of the Citric Acid Cycle

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