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耻垢分枝杆菌中不饱和脂肪酸的完全营养缺陷型需要删除两组基因。

Complete auxotrophy for unsaturated fatty acids requires deletion of two sets of genes in Mycobacterium smegmatis.

作者信息

Di Capua Cecilia B, Doprado Mariana, Belardinelli Juan Manuel, Morbidoni Héctor R

机构信息

Laboratorio de Microbiología Molecular, Facultad de Ciencias Médicas, Universidad Nacional de Rosario, Rosario, Argentina.

出版信息

Mol Microbiol. 2017 Oct;106(1):93-108. doi: 10.1111/mmi.13753. Epub 2017 Aug 11.

Abstract

The synthesis of unsaturated fatty acids in Mycobacterium smegmatis is poorly characterized. Bioinformatic analysis revealed four putative fatty acid desaturases in its genome, one of which, MSMEG_1886, is highly homologous to desA3, the only palmitoyl/stearoyl desaturase present in the Mycobacterium tuberculosis genome. A MSMEG_1886 deletion mutant was partially auxotrophic for oleic acid and viable at 37°C and 25°C, although with a long lag phase in liquid medium. Fatty acid analysis suggested that MSMEG_1886 is a palmitoyl/stearoyl desaturase, as the synthesis of palmitoleic acid was abrogated, while oleic acid contents dropped by half in the mutant. Deletion of the operon MSMEG_1741-1743 (highly homologous to a Pseudomonas aeruginosa acyl-CoA desaturase) had little effect on growth of the parental strain; however the double mutant MSMEG_1886-MSMEG_1741-1743 strictly required oleic acid for growth. The ΔMSMEG_1886-ΔMSMEG_1741 double mutant was able to grow (poorly but better than the ΔMSMEG_1886 single mutant) in solid and liquid media devoid of oleic acid, suggesting a repressor role for ΔMSMEG_1741. Fatty acid analysis of the described mutants suggested that MSMEG_1742-43 desaturates C18:0 and C24:0 fatty acids. Thus, although the M. smegmatis desA3 homologue is the major player in unsaturated fatty acid synthesis, a second set of genes is also involved.

摘要

耻垢分枝杆菌中不饱和脂肪酸的合成特征尚不明确。生物信息学分析表明,其基因组中有4个推定的脂肪酸去饱和酶,其中一个名为MSMEG_1886,与结核分枝杆菌基因组中唯一的棕榈酰/硬脂酰去饱和酶desA3高度同源。MSMEG_1886缺失突变体对油酸部分营养缺陷,在37℃和25℃下可存活,不过在液体培养基中会有较长的延迟期。脂肪酸分析表明,MSMEG_1886是一种棕榈酰/硬脂酰去饱和酶,因为突变体中棕榈油酸的合成被消除,而油酸含量下降了一半。操纵子MSMEG_1741 - 1743(与铜绿假单胞菌酰基辅酶A去饱和酶高度同源)的缺失对亲本菌株的生长影响不大;然而,双突变体MSMEG_1886 - MSMEG_1741 - 1743的生长严格需要油酸。ΔMSMEG_1886 - ΔMSMEG_1741双突变体能够在不含油酸的固体和液体培养基中生长(生长较差,但比ΔMSMEG_1886单突变体好),这表明ΔMSMEG_1741具有阻遏作用。对上述突变体的脂肪酸分析表明,MSMEG_1742 - 43使C18:0和C24:0脂肪酸去饱和。因此,尽管耻垢分枝杆菌desA3同源物是不饱和脂肪酸合成的主要参与者,但第二组基因也参与其中。

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