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首页> 外文期刊>Journal of Hazardous Materials >Endosulfan induced alteration in bacterial protein profile and RNA yield of Klebsiella sp. M3, Achromobacter sp. M6, and Rhodococcus sp. M2
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Endosulfan induced alteration in bacterial protein profile and RNA yield of Klebsiella sp. M3, Achromobacter sp. M6, and Rhodococcus sp. M2

机译:硫丹引起的克雷伯菌属细菌蛋白质谱和RNA产量的变化。 M3,无色杆菌属。 M6和红球菌sp。 M2

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Three bacterial strains identified as Klebsiella sp. M3, Achromobacter sp. M6 and Rhodococcus sp. M2 were isolated by soil enrichment with endosulfan followed by shake flask enrichment technique. They were efficiently degrading endosulfan in the NSM (non sulfur medium) broth. Degradation of endosulfan was faster with the cell free extract of bacterial cells grown in the sulfur deficient medium (NSM) supplemented with endosulfan than that of nutrient rich medium (Luria Bertani). In the cell free extract of NSM supplemented with endosulfan as sole sulfur source, a unique band was visualized on SDS-PAGE but not with magnesium sulfate as the sole sulfur source in NSM and LB with endosulfan. Expression of a unique polypeptide band was speculated to be induced by endosulfan under sulfur starved condition. These unique polypeptide bands were identified as OmpK35 protein, sulfate binding protein and outer membrane porin protein, respectively, in Klebsiella sp. M3, Achromobacter sp. M6 and Rhodococcus sp. M2. Endosulfan showed dose dependent negative effect on total RNA yield of bacterial strains in nutrient rich medium. Absence of plasmid DNA indicated the presence of endosulfan metabolizing gene on genomic DNA.
机译:鉴定为克雷伯菌的三种细菌菌株。 M3,无色杆菌属。 M6和红球菌通过用硫丹富集土壤,然后摇瓶富集技术分离M2。他们正在NSM(无硫培养基)肉汤中有效降解硫丹。与富含营养的培养基(Luria Bertani)相比,在补充有硫丹的缺硫培养基(NSM)中生长的细菌细胞的无细胞提取物降解硫丹的速度更快。在补充有硫丹作为唯一硫源的NSM的无细胞提取物中,在SDS-PAGE上可以看到一个独特的条带,但在NSM和含硫丹的LB中,没有硫酸镁作为唯一的硫源。据推测,在硫缺乏的条件下,硫丹可以诱导独特的多肽条带的表达。这些独特的多肽条带分别在克雷伯菌中鉴定为OmpK35蛋白,硫酸盐结合蛋白和外膜孔蛋白。 M3,无色杆菌属。 M6和红球菌M2。在富营养培养基中,硫丹对细菌菌株的总RNA产量表现出剂量依赖性的负面影响。质粒DNA的缺乏表明在基因组DNA上存在硫丹代谢基因。

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