Propionate first cycle results

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Day 1 – Clomixyl 150mg –  in three divided doses.
Day 2 – Clomixyl 100mg –   in two divided doses
Following 10 days – Clomixyl 50mg  – before bed
Following 10 days – Clomixyl 50mg – before bed
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Metabolism of propanoate begins with its conversion to propionyl coenzyme A (propionyl-CoA), the usual first step in the metabolism of carboxylic acids. Since propanoic acid has three carbons, propionyl-CoA can directly enter neither beta oxidation nor the citric acid cycles. In most vertebrates, propionyl-CoA is carboxylated to D-methylmalonyl-CoA, which is isomerised to L-methylmalonyl-CoA. A vitamin B 12 -dependent enzyme catalyzes rearrangement of L-methylmalonyl-CoA to succinyl-CoA, which is an intermediate of the citric acid cycle and can be readily incorporated there.

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Because the last step leaves an unstable semiquinone at the Q i site, the reaction is not yet fully completed. A second Q cycle is necessary, with the second electron transfer from cytochrome b H reducing the semiquinone to ubiquinol. The ultimate products of the Q cycle are four protons entering the intermembrane space, two from the matrix and two from the reduction of two molecules of cytochrome c. The reduced cytochrome c is eventually reoxidized by complex IV . The process is cyclic as the ubiquinone created at the Q i site can be reused by binding to the Q o site of complex III.

Propionate first cycle results

propionate first cycle results

Because the last step leaves an unstable semiquinone at the Q i site, the reaction is not yet fully completed. A second Q cycle is necessary, with the second electron transfer from cytochrome b H reducing the semiquinone to ubiquinol. The ultimate products of the Q cycle are four protons entering the intermembrane space, two from the matrix and two from the reduction of two molecules of cytochrome c. The reduced cytochrome c is eventually reoxidized by complex IV . The process is cyclic as the ubiquinone created at the Q i site can be reused by binding to the Q o site of complex III.

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