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人体中木糖醇代谢生成草酸盐的模型:果糖激酶和醛缩酶的作用

Models for the metabolic production of oxalate from xylitol in humans: a role for fructokinase and aldolase.

作者信息

James H M, Bais R, Edwards J B, Rofe A M, Conyers A J

出版信息

Aust J Exp Biol Med Sci. 1982 Feb;60(Pt 1):117-22. doi: 10.1038/icb.1982.11.

Abstract

It has been proposed previously that oxalate precursors may be formed in the transketolase reaction during the metabolism of xylitol. It is shown in this paper that fructokinase and aldolase, purified from human liver, provide an alternative model in that, in coupled sequence, they produce glycolaldehyde, an oxalate precursor, from D-xylulose via D-xylulose 1-phosphate; D-fructose does not give rise to glycolaldehyde. It is concluded that metabolic pathways based on a combination of the transketolase, fructokinase and aldolase reactions can account for the production of glucose, lactate, tetronates (C-threonic and D-erythronic acids) and oxalate (precursors) during the metabolism of xylitol administered parenterally.

摘要

先前有人提出,木糖醇代谢过程中,转酮醇酶反应可能会形成草酸盐前体。本文表明,从人肝脏中纯化得到的果糖激酶和醛缩酶提供了另一种模型,即它们依次作用,通过D-木酮糖-1-磷酸从D-木酮糖生成乙醇醛,一种草酸盐前体;D-果糖不会产生乙醇醛。得出的结论是,基于转酮醇酶、果糖激酶和醛缩酶反应组合的代谢途径可以解释经肠胃外给予木糖醇后代谢过程中葡萄糖、乳酸、四羟酸(C-苏糖酸和D-赤藓糖酸)和草酸盐(前体)的产生。

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