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Biochemical dehydrogenations examples

The second function, and the one pertinent to this section, is the decarboxylation of oxalosuccinic acid to 2-oxoglutaric acid. This is simply a biochemical example of the ready decarboxylation of a P-ketoacid, involving an intramolecular hydrogen-bonded system. This reaction could occur chemically without an enzyme, but it is known that isocitric acid, the product of the dehydrogenation, is still bound to the enzyme isocitrate dehydrogenase when decarboxylation occurs. [Pg.389]

Few examples of photochemical dehydrogenation reactions accompanied by cyclization are reported in the literature. 2,3,5-Triphenyl-tetrazolium chloride (CV), which is used biochemically as reduction indicator, on irradiation in ethanol with ultraviolet light, undergoes dehydrogenation accompanied by cyclization to yield 2,3 (2,2 -bi-phenylene)-5-phenyltetrazolium chloride (CVI).106 167 Light-induced cyclization of substituted derivatives of CV to the corresponding bi-phenylene derivatives has been reported recently. sl 33... [Pg.93]


See other pages where Biochemical dehydrogenations examples is mentioned: [Pg.407]    [Pg.276]    [Pg.189]    [Pg.44]    [Pg.173]    [Pg.164]    [Pg.140]    [Pg.130]   
See also in sourсe #XX -- [ Pg.48 ]




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