首页> 美国卫生研究院文献>Journal of Bacteriology >New Pathway for Long-Chain n-Alkane Synthesis via 1-Alcohol in Vibrio furnissii M1
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New Pathway for Long-Chain n-Alkane Synthesis via 1-Alcohol in Vibrio furnissii M1

机译:在糠醛弧菌M1中通过1-醇合成长链正构烷烃的新途径

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摘要

Alkane biosynthesis in the bacterium Vibrio furnissii M1 involves the synthesis of long-chain alkanes via 1-alcohol. Evidence for this novel pathway are the following. (i) Both even- and odd-carbon-number n-alkanes were produced from glucose, while only even-carbon-number fatty acids were produced in V. furnissii M1. This result cannot be explained by the decarbonylation pathway. (ii) Pentadecane and hexadecane were produced from 1-hexadecanoic acid by membrane fractions of V. furnissii M1, and radioisotope precursor-tracer experiments, in which 1-[1-14C]hexadecanoic acid was fed, identified the corresponding alcohol, aldehyde, and alkane derivatives. Since all metabolites maintained the radioisotope label at 1-C, they were produced by a pathway in which the carbon structure was retained, i.e., a reduction pathway. (iii) n-Hexadecane was produced when 1-hexadecanol was fed to membrane preparations.
机译:弗氏弧菌M1细菌中的烷烃生物合成涉及通过1-醇合成长链烷烃。这种新颖途径的证据如下。 (i)弗氏弧菌M1均由葡萄糖产生偶数碳原子数和奇数碳原子数的正构烷烃。该结果不能通过脱羰途径来解释。 (ii)通过V. furnissii M1的膜级分和放射性同位素前体-示踪剂实验,由1-十六烷酸生成十五烷和十六烷,其中加入了1- [1- <1-upup14 C]十六烷酸,确定了相应的醇,醛和烷烃衍生物。由于所有代谢物都将放射性同位素标记保持在1-C,因此它们是通过保留碳结构的途径(即还原途径)产生的。 (iii)当将十六烷醇加入到膜制剂中时产生正十六烷。

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