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天蓝色链霉菌解离脂肪酸合酶的FabG和FabI的特性分析

Characterization of FabG and FabI of the Streptomyces coelicolor dissociated fatty acid synthase.

作者信息

Singh Renu, Reynolds Kevin A

机构信息

Finance and Administration, Portland State University, P. O. Box 751, Portland, OR 97207 (USA).

出版信息

Chembiochem. 2015 Mar 2;16(4):631-40. doi: 10.1002/cbic.201402670. Epub 2015 Feb 6.

Abstract

Streptomyces coelicolor produces fatty acids for both primary metabolism and for biosynthesis of the secondary metabolite undecylprodiginine. The first and last reductive steps during the chain elongation cycle of fatty acid biosynthesis are catalyzed by FabG and FabI. The S. coelicolor genome sequence has one fabI gene (SCO1814) and three likely fabG genes (SCO1815, SCO1345, and SCO1846). We report the expression, purification, and characterization of the corresponding gene products. Kinetic analyses revealed that all three FabGs and FabI are capable of utilizing both straight and branched-chain β-ketoacyl-NAC and enoyl-NAC substrates, respectively. Furthermore, only SCO1345 differentiates between ACPs from both biosynthetic pathways. The data presented provide the first experimental evidence that SCO1815, SCO1346, and SCO1814 have the catalytic capability to process intermediates in both fatty acid and undecylprodiginine biosynthesis.

摘要

天蓝色链霉菌产生脂肪酸用于初级代谢以及次级代谢产物十一烷基灵菌红素的生物合成。脂肪酸生物合成链延长循环中的第一步和最后一步还原反应分别由FabG和FabI催化。天蓝色链霉菌基因组序列有一个fabI基因(SCO1814)和三个可能的fabG基因(SCO1815、SCO1345和SCO1846)。我们报道了相应基因产物的表达、纯化及特性。动力学分析表明,所有三种FabG和FabI分别能够利用直链和支链的β-酮酰基-NAC和烯酰基-NAC底物。此外,只有SCO1345能区分来自两种生物合成途径的酰基载体蛋白(ACP)。所呈现的数据提供了首个实验证据,即SCO1815、SCO1346和SCO1814具有处理脂肪酸和十一烷基灵菌红素生物合成中中间体的催化能力。

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