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Ct-Ketoglutarate

Most amino acids lose their nitrogen atom by a transamination reaction in which the -NH2 group of the amino acid changes places with the keto group of ct-ketoglutarate. The products are a new a-keto acid plus glutamate. The overall process occurs in two parts, is catalyzed by aminotransferase enzymes, and involves participation of the coenzyme pyridoxal phosphate (PLP), a derivative of pyridoxine (vitamin UJ. Different aminotransferases differ in their specificity for amino acids, but the mechanism remains the same. [Pg.1165]

These also are direct capture agents for CN. The CN ion reacts with carbonyl groups to form cyanohydrins, resulting in a sequestering action. Among cyanohydrin formers, ct-ketoglutaric acid has shown some promise experimentally as a CN antidote (Hume et al, 1995 Moore et al., 1986), and there is a possible additional antidotal activity by causing a decrease in convulsions (Yamamoto, 1990). [Pg.523]

See also Glyoxylate Cycle, Aconitase, Citrate, Isocitrate Dehydrogenase, ct-Ketoglutarate, Fluorocitrate, Citric Acid Cycle Intermediates, Figure 14.3, Table 14.1... [Pg.139]

Vaillancourt FH, Yin J, Walsh CT (2005) SyrB2 in Syringomycin E Biosynthesis is a Nonheme Fen a-Ketoglutarate- and 02-Dependent Halogenase. Proc Natl Acad Sci USA 102 10111... [Pg.432]

Figure 2.4. The provision of acetyl-CoA and NADPH for lipogenesis. PPP, pentose phosphate pathway T, tricarboxylate transporter K, a-ketoglutarate transporter. In ruminants, pyruvate dehydrogenase, ATP-citrate lyase and malic enzyme activities are low and perhaps non-functional. (From Murray et al., 1988. Harper s Biochemistry, 21st edn, p. 207, Appleton and Lange, Norwalk, CT reproduced with permission of The McGraw-Hill Companies). Figure 2.4. The provision of acetyl-CoA and NADPH for lipogenesis. PPP, pentose phosphate pathway T, tricarboxylate transporter K, a-ketoglutarate transporter. In ruminants, pyruvate dehydrogenase, ATP-citrate lyase and malic enzyme activities are low and perhaps non-functional. (From Murray et al., 1988. Harper s Biochemistry, 21st edn, p. 207, Appleton and Lange, Norwalk, CT reproduced with permission of The McGraw-Hill Companies).
M7. Marshall, L. M., and Drew, F. D., Determination of fumaric, cts-aconitic and a-ketoglutaric acids in rabbit kidney and liver by partition chromatography. Federation Proc. 9, 199 (1950). [Pg.112]

Isotopic C marked with asterisk. All the isotope appears in the a-carboxyl of o-ketoglutaric acid if the side reaction between citric and m-aconitic acids is neglected. The side reaction, as shown in Scheme 4, would produce a second isotopic form of cts-aconitic acid but its quantities would be small if the side reaction is slow.)... [Pg.118]

Vaillancourt FH, Yin J, Walsh CT. SyrB2 in syringomycin E biosynthesis is a nonheme Fe-11 alpha-ketoglutarate- and 02-dependent halogenase. Proc. Nat. Acad. Sci. USA 2005 102 10111-10116. [Pg.1396]


See other pages where Ct-Ketoglutarate is mentioned: [Pg.280]    [Pg.228]    [Pg.328]    [Pg.842]    [Pg.25]    [Pg.342]    [Pg.791]    [Pg.280]    [Pg.228]    [Pg.328]    [Pg.842]    [Pg.25]    [Pg.342]    [Pg.791]    [Pg.149]    [Pg.615]    [Pg.670]    [Pg.675]    [Pg.183]    [Pg.184]    [Pg.262]    [Pg.89]   
See also in sourсe #XX -- [ Pg.131 ]




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