Butch Christopher, Cope Elizabeth D, Pollet Pamela, Gelbaum Leslie, Krishnamurthy Ramanarayanan, Liotta Charles L
School of Chemical and Biological Engineering and ‡School of Chemistry and Biochemistry, Georgia Institute of Technology , Atlanta, Georgia 30332, United States.
J Am Chem Soc. 2013 Sep 11;135(36):13440-5. doi: 10.1021/ja405103r. Epub 2013 Aug 30.
An abiotic formation of meso- and DL-tartrates in 80% yield via the cyanide-catalyzed dimerization of glyoxylate under alkaline conditions is demonstrated. A detailed mechanism for this conversion is proposed, supported by NMR evidence and (13)C-labeled reactions. Simple dehydration of tartrates to oxaloacetate and an ensuing decarboxylation to form pyruvate are known processes that provide a ready feedstock for entry into the citric acid cycle. While glyoxylate and high hydroxide concentration are atypical in the prebiotic literature, there is evidence for natural, abiotic availability of each. It is proposed that this availability, coupled with the remarkable efficiency of tartrate production from glyoxylate, merits consideration of an alternative prebiotic pathway for providing constituents of the citric acid cycle.
结果表明,在碱性条件下,通过氰化物催化乙醛酸二聚反应可非生物合成中酒石酸和DL - 酒石酸,产率达80%。通过核磁共振(NMR)证据和(13)C标记反应,提出了这种转化的详细机制。酒石酸简单脱水生成草酰乙酸,随后脱羧形成丙酮酸,这些都是已知的过程,可为进入柠檬酸循环提供现成的原料。虽然乙醛酸和高浓度氢氧化物在益生元文献中并不常见,但有证据表明它们在自然界中可非生物获得。有人提出,这种可得性,再加上从乙醛酸生产酒石酸的显著效率,值得考虑一种替代的益生元途径来提供柠檬酸循环的成分。