首页> 外文OA文献 >A lipA (yutB) Mutant, Encoding Lipoic Acid Synthase, Provides Insight into the Interplay between Branched-Chain and Unsaturated Fatty Acid Biosynthesis in Bacillus subtilis ▿ †
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A lipA (yutB) Mutant, Encoding Lipoic Acid Synthase, Provides Insight into the Interplay between Branched-Chain and Unsaturated Fatty Acid Biosynthesis in Bacillus subtilis ▿ †

机译:lipA(yutB)突变体,编码硫辛酸合酶,可深入了解枯草芽孢杆菌中支链和不饱和脂肪酸生物合成之间的相互作用play†

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摘要

Lipoic acid is an essential cofactor required for the function of key metabolic pathways in most organisms. We report the characterization of a Bacillus subtilis mutant obtained by disruption of the lipA (yutB) gene, which encodes lipoyl synthase (LipA), the enzyme that catalyzes the final step in the de novo biosynthesis of this cofactor. The function of lipA was inferred from the results of genetic and physiological experiments, and this study investigated its role in B. subtilis fatty acid metabolism. Interrupting lipoate-dependent reactions strongly inhibits growth in minimal medium, impairing the generation of branched-chain fatty acids and leading to accumulation of copious amounts of straight-chain saturated fatty acids in B. subtilis membranes. Although depletion of LipA induces the expression of the Δ5 desaturase, controlled by a two-component system that senses changes in membrane properties, the synthesis of unsaturated fatty acids is insufficient to support growth in the absence of precursors for branched-chain fatty acids. However, unsaturated fatty acids generated by deregulated overexpression of the Δ5 desaturase functionally replaces lipoic acid-dependent synthesis of branched-chain fatty acids. Furthermore, we show that the cold-sensitive phenotype of a B. subtilis strain deficient in Δ5 desaturase is suppressed by isoleucine only if LipA is present.
机译:硫辛酸是大多数生物体内关键代谢途径功能所必需的必需辅因子。我们报告了通过破坏lipA(yutB)基因获得的枯草芽孢杆菌突变体的特征,该基因编码脂酰合酶(LipA),该酶催化该辅因子从头生物合成的最后一步。 lipA的功能是从遗传和生理学实验的结果推断出来的,本研究调查了它在枯草芽孢杆菌脂肪酸代谢中的作用。中断硫辛酸酯依赖性反应强烈抑制了在基本培养基中的生长,损害了支链脂肪酸的生成,并导致枯草芽孢杆菌膜中大量直链饱和脂肪酸蓄积。尽管LipA的耗尽会诱导由感知膜特性变化的两组分系统控制的Δ5去饱和酶的表达,但在不存在支链脂肪酸前体的情况下,不饱和脂肪酸的合成不足以支持其生长。但是,由Δ5去饱和酶过表达失控产生的不饱和脂肪酸在功能上取代了硫辛酸依赖性的支链脂肪酸合成。此外,我们表明,仅当存在LipA时,异亮氨酸才能抑制Δ5去饱和酶缺乏的枯草芽孢杆菌菌株的冷敏表型。

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