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Thiocyanate Degradation by a Highly Enriched Culture of the Neutrophilic Halophile Thiohalobacter sp. Strain FOKN1 from Activated Sludge and Genomic Insights into Thiocyanate Metabolism

机译:硫氰酸盐通过富集的嗜中性嗜嗜辣嗜盐硫杆菌SP的培养物降解。 从活性污泥和基因组洞察硫氰酸酯代谢的菌株Fokn1

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摘要

Thiocyanate (SCN-) is harmful to a wide range of organisms, and its removal is essential for environmental protection. A neutrophilic halophile capable of thiocyanate degradation, Thiohalobacter sp. strain FOKN1, was highly enriched (relative abundance; 98.4%) from activated sludge collected from a bioreactor receiving thiocyanate-rich wastewater. The enrichment culture degraded 3.38 mM thiocyanate within 140 h, with maximum activity at pH 8.8, 37 degrees C, and 0.18 M sodium chloride. Thiocyanate degradation was inhibited by 30 mg L-1 phenol, but not by thiosulfate. Microbial thiocyanate degradation is catalyzed by thiocyanate dehydrogenase, while limited information is currently available on the molecular mechanisms underlying thiocyanate degradation by the thiocyanate dehydrogenase of neutrophilic halophiles. Therefore, (meta)genomic and proteomic analyses of enrichment cultures were performed to elucidate the whole genome sequence and proteome of Thiohalobacter sp. strain FOKN1. The 3.23-Mb circular Thiohalobacter sp. strain FOKN1 genome was elucidated using a PacBio RSII sequencer, and the expression of 914 proteins was identified by tandem mass spectrometry. The Thiohalobacter sp. strain FOKN1 genome had a gene encoding thiocyanate dehydrogenase, which was abundant in the proteome, suggesting that thiocyanate is degraded by thiocyanate dehydrogenase to sulfur and cyanate. The sulfur formed may be oxidized to sulfate by the sequential oxidation reactions of dissimilatory sulfite reductasc, adenosine-5'-phosphosulfate reductase, and dissimilatory ATP sulfurylasc. Although the Thiohalobacter sp. strain FOKN1 genome carried a gene encoding cyanate lyase, its protein expression was not detectable. The present study advances the understanding of the molecular mechanisms underlying thiocyanate degradation by the thiocyanate dehydrogenase of neutrophilic halophiles.
机译:硫氰酸酯(SCN-)对广泛的生物有害,其去除对于环保是必不可少的。一种能够硫氰酸酯降解的中性嗜嗜嗜中性嗜嗜盐嗜睡症。菌株Fokn1从接受富含硫氰酸酯的废水的生物反应器收集的活性污泥的高度富集(相对丰度; 98.4%)。富集培养物在140小时内降解3.38mm硫氰酸酯,最大活性在pH 8.8,37℃和0.18米氯化钠。将硫氰酸酯降解抑制30mg L-1苯酚,但不是通过硫代硫酸盐。微生物硫代氰酸酯降解由硫氰酸酯脱氢酶催化,而硫氰酸噻唑酯脱氢酶的硫氰酸酯脱氢酶的分子机制目前可以获得有限的信息。因此,进行(Meta)富集培养物的基因组和蛋白质组学分析,以阐明硫代杆菌SP的全基因组序列和蛋白质组。菌株Fokn1。 3.23mb圆形硫代菌杆菌sp。使用PACBIO RSII测序仪阐明菌株FOKN1基因组,通过串联质谱法鉴定914蛋白的表达。硫代骨杆菌sp。菌株Fokn1基因组具有编码硫氰酸酯脱氢酶的基因,该基因在蛋白质组中丰富,表明硫氰酸酯脱氢酶降解到硫和氰酸酯。形成的硫可以通过散发亚硫酸盐雷丁,腺苷-5'-磷酸硫酸盐还原酶和含量异化ATP巯基脲的顺序氧化反应氧化成硫酸盐。虽然硫代骨杆菌sp。菌株Fokn1基因组携带编码氰酸酯裂解酶的基因,其蛋白质表达是不可检测的。本研究进展了硫氰酸噻唑盐脱氢酶对硫氰酸噻唑酯脱氢酶的分子机制的理解。

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