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在盘基网柄菌中,肌醇逐步磷酸化生成肌醇六磷酸。

Stepwise phosphorylation of myo-inositol leading to myo-inositol hexakisphosphate in Dictyostelium.

作者信息

Stephens L R, Irvine R F

机构信息

Biochemistry Department, AFRC Institute of Animal Physiology & Genetics Research, Cambridge Research Station, UK.

出版信息

Nature. 1990 Aug 9;346(6284):580-3. doi: 10.1038/346580a0.

Abstract

Although myo-inositol hexakisphosphate (InsP6; phytate) is the most abundant inositol phosphate in nature and probably has a wide variety of functions, neither the route of its synthesis from myo-inositol nor its metabolic relationships with other inositol-containing compounds (such as the second messenger inositol 1,4,5-trisphosphate, Ins(1,4,5)P3) are known. Here we report that the pathway by which InsP6 is synthesized in the cellular slime mould Dictyostelium, and in cell-free preparations derived from them, is catalysed by a series of soluble ATP-dependent kinases independently of the metabolism of both phosphatidylinositol and Ins(1,4,5)P3. The intermediates between myo-inositol and InsP6 are Ins3P, Ins(3,6)P2, Ins(3,4,6)P3, Ins(1,3,4,6)P4 and Ins(1,3,4,5,6)P5. The 3- and 5-phosphates of InsP6 take part in futile cycles in which Ins(1,2,4,5,6)P5 and Ins(1,2,3,4,6)P5 are rapidly formed by dephosphorylation of InsP6, only to be rephosphorylated to yield their precursor.

摘要

尽管肌醇六磷酸(InsP6;植酸)是自然界中最丰富的肌醇磷酸,可能具有多种功能,但其从肌醇合成的途径以及与其他含肌醇化合物(如第二信使肌醇1,4,5-三磷酸,Ins(1,4,5)P3)的代谢关系均不为人所知。在此,我们报告在细胞黏菌盘基网柄菌及其衍生的无细胞制剂中,InsP6的合成途径是由一系列可溶性ATP依赖性激酶催化的,这一过程独立于磷脂酰肌醇和Ins(1,4,5)P3的代谢。肌醇和InsP6之间的中间产物是Ins3P、Ins(3,6)P2、Ins(3,4,6)P3、Ins(1,3,4,6)P4和Ins(1,3,4,5,6)P5。InsP6的3-磷酸和5-磷酸参与无效循环,其中Ins(1,2,4,5,6)P5和Ins(1,2,3,4,6)P5通过InsP6的去磷酸化迅速形成,随后又重新磷酸化以产生其前体。

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