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首页> 外文期刊>Bulletin of the Chemical Society of Japan >Resemblance of Carbocycle Formation from Carbohydrates between Archaea and Eucarya/Eubacteria.Biosynthesis of Calditol,the Characteristic Lipid-Content Molecule in Sulfolobus acidocaldarius
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Resemblance of Carbocycle Formation from Carbohydrates between Archaea and Eucarya/Eubacteria.Biosynthesis of Calditol,the Characteristic Lipid-Content Molecule in Sulfolobus acidocaldarius

机译:古细菌与真细菌/真细菌之间的碳水化合物形成的碳环化合物的相似。Calditol的生物合成,特征性脂质含量的分子在Sulfolobus acidocaldarius中

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摘要

We investigated the biosynthesis of the unique structure of calditol,a part of the characteristic lipid molecules in the major part of thermophilic archaea,Sulfolobus sp.Deuterium-labeling experiments with deuterated glucose substrates,were carried out.The results clarified that calditol was biosynthesized from glucose with C-C bond formation between C-l and C-5,and no loss of deuterium at C-6 of glucose was observed.Two reaction mechanisms were possible when these experimental findings,and conventional reports were considered.Among these,the course* that assumes C-4 oxidation as the starting point would be preferable from the resemblance to myo-inositol biosynthesis.Furthermore,the high deuterium incorporation at C-l of calditol from C-l of glucose suggests that activation,such as oxidation at C-l,is not involved in the ether C-O bonding.
机译:我们研究了嗜热古细菌Sulfolobus sp。的主要部分中部分特征性脂类分子Calditol的独特结构的生物合成。进行了氘化葡萄糖底物的氘标记实验。观察到在Cl和C-5之间形成CC键的葡萄糖,并且在C-6处的氘没有损失。考虑到这些实验结果和常规报道,可能有两种反应机理。从类似于肌醇生物合成的角度出发,以C-4氧化为起点是优选的。此外,葡萄糖中的氯从C1到Calditol的Cl的高氘掺入表明,活化(如Cl的氧化)不参与醚一氧化碳键合。

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