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Genomic and Functional Characterization of Environmental Strains of SDS-Degrading Pseudomonas spp. Providing a Source of New Sulfatases

机译:SDS降解假单胞菌属物种的环境菌株的基因组和功能表征提供了新的硫酸酯酶的来源

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摘要

Biochemical, physiological and genomic comparisons of two Pseudomonas strains, assigned previously to the Pseudomonas jessenii subgroup, which are efficient SDS-degraders were carried out. A GO enrichment analysis showed that the genomes of SDS-degraders encode more genes connected with bacterial cell wall biosynthesis and alkanesulfonate monooxygenase activity than their closest relatives from the P. jessenii subgroup. A transcriptomic analysis of the most promising strain exposed to detergent suggests that although SDS can be later utilized as a carbon source, in early stages it influences cell envelope integrity, causing a global stress response followed by cell wall modification and induction of repair mechanisms. Genomes of the analyzed strains from P. jessenii group encode multiple putative sulfatases and their enzymatic activity was experimentally verified, which led to the identification of three novel enzymes exhibiting activity toward SDS. Two of the novel alkylsulfatases showed their highest activity at pH 8.0 and the temperature of 60°C or 70°C. One of the enzymes retained its activity even after 1 h of incubation at 60°C. Ions like K+ and Mg2+ enhanced enzymatic activity of both proteins, whereas Cu2+ or EDTA had inhibitory effects.
机译:进行了两个以前被归类为假单胞菌亚种的假单胞菌菌株的生化,生理和基因组比较,它们是有效的SDS降解剂。 GO富集分析表明,SDS降解基因组编码的细菌基因比细菌近亲更接近于与细菌细胞壁生物合成和链烷磺酸单加氧酶活性相关的基因。对暴露于去污剂中最有希望的菌株的转录组学分析表明,尽管SDS以后可以用作碳源,但在早期阶段它会影响细胞包膜的完整性,引起整体应激反应,随后引起细胞壁修饰和诱导修复机制。被分析的来自耶氏疟原虫组的菌株的基因组编码多个推定的硫酸酯酶,并通过实验验证了它们的酶活性,从而鉴定了三种对SDS表现出活性的新型酶。两种新型烷基硫酸酯酶在pH 8.0和60°C或70°C的温度下显示出最高的活性。即使在60°C孵育1小时后,其中一种酶仍保持其活性。诸如K + 和Mg 2 + 的离子增强了这两种蛋白质的酶活性,而Cu 2 + 或EDTA则具有抑制作用。

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