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  2. Oxidative decarboxylation - Wikipedia

    en.wikipedia.org/wiki/Oxidative_decarboxylation

    Oxidative decarboxylation is a decarboxylation reaction caused by oxidation. ... The hydroxyethyl group is electron-rich, and in its reaction with lipoamide it is in ...

  3. Pyruvate decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_decarboxylase

    Pyruvate decarboxylase is an enzyme (EC 4.1.1.1) that catalyses the decarboxylation of pyruvic acid to acetaldehyde.It is also called 2-oxo-acid carboxylase, alpha-ketoacid carboxylase, and pyruvic decarboxylase. [1]

  4. Dihydrolipoyl transacetylase - Wikipedia

    en.wikipedia.org/wiki/Dihydrolipoyl_transacetylase

    Pyruvate decarboxylation requires a few cofactors in addition to the enzymes that make up the complex. The first is thiamine pyrophosphate (TPP), which is used by pyruvate dehydrogenase to oxidize pyruvate and to form a hydroxyethyl-TPP intermediate. This intermediate is taken up by dihydrolipoyl transacetylase and reacted with a second ...

  5. Pyruvate dehydrogenase complex - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase_complex

    Pyruvate dehydrogenase complex (PDC) is a complex of three enzymes that converts pyruvate into acetyl-CoA by a process called pyruvate decarboxylation. [1] Acetyl-CoA may then be used in the citric acid cycle to carry out cellular respiration, and this complex links the glycolysis metabolic pathway to the citric acid cycle. Pyruvate ...

  6. Hydroxylation - Wikipedia

    en.wikipedia.org/wiki/Hydroxylation

    The hydroxylation of proteins occurs as a post-translational modification and is catalyzed by 2-oxoglutarate-dependent dioxygenases. [5] Hydroxylation improves water‐solubility, as well as affecting their structure and function.

  7. Pyruvate dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase

    Pyruvate dehydrogenase is an enzyme that catalyzes the reaction of pyruvate and a lipoamide to give the acetylated dihydrolipoamide and carbon dioxide.The conversion requires the coenzyme thiamine pyrophosphate.

  8. Decarboxylative cross-coupling - Wikipedia

    en.wikipedia.org/wiki/Decarboxylative_cross-coupling

    The first reported decarboxylative cross coupling reaction was an Ullmann reaction, in 1966 by Nilsson et al. Thermal decarboxylation of copper benzoates, in the presence of an aryl halide, was found to produce (both symmetric and unsymmetric) biaryls through aryl-Cu intermediates. [2] First reported decarboxylative Ullmann coupling (Nilsson, 2005)

  9. MHETase - Wikipedia

    en.wikipedia.org/wiki/MHETase

    The native enzyme is incapable of working on BHET, mono(2-hydroxyethyl)-isophthalate (MHEI), or mono(2-hydroxyethyl)-furanoate (MHEF). MHEI is a likely industrial PET degradation product due to the use of isophthalate comonomer. MHEF is a product of PEF degradation by PETase. Protein engineering research aims to overcome these barriers. [2]