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从制革厂废水灌溉土壤中分离的铬还原菌的无细胞提取物对 Cr(VI)的体外还原。

In vitro Cr(VI) reduction by cell-free extracts of chromate-reducing bacteria isolated from tannery effluent irrigated soil.

机构信息

Department of Microbial Technology and Entomology, CSIR-Central Institute of Medicinal and Aromatic Plants (CSIR-CIMAP), Lucknow, 226015, India.

出版信息

Environ Sci Pollut Res Int. 2013 Mar;20(3):1661-74. doi: 10.1007/s11356-012-1178-4. Epub 2012 Sep 15.

Abstract

Four efficient Cr(VI)-reducing bacterial strains were isolated from rhizospheric soil of plants irrigated with tannery effluent and investigated for in vitro Cr(VI) reduction. Based on 16S rRNA gene sequencing, the isolated strains SUCR44, SUCR140, SUCR186, and SUCR188 were identified as Bacillus sp. (JN674188), Microbacterium sp. (JN674183), Bacillus thuringiensis (JN674184), and Bacillus subtilis (JN674195), respectively. All four isolates could completely reduce Cr(VI) in culture media at 0.2 mM concentration within a period of 24-120 h; SUCR140 completely reduced Cr(VI) within 24 h. Assay with the permeabilized cells (treated with Triton X-100 and Tween 80) and cell-free assay demonstrated that the Cr(VI) reduction activity was mainly associated with the soluble fraction of cells. Considering the major amount of chromium being reduced within 24-48 h, these fractions could have been released extracellularly also during their growth. At the temperature optima of 28 °C and pH 7.0, the specific activity of Cr(VI) reduction was determined to be 0.32, 0.42, 0.34, and 0.28 μmol Cr(VI)min(-1)mg(-1) protein for isolates SUCR44, SUCR140, SUCR186, and SUCR188, respectively. Addition of 0.1 mM NADH enhanced the Cr(VI) reduction in the cell-free extracts of all four strains. The Cr(VI) reduction activity in cell-free extracts of all the isolates was stable in presence of different metal ions tested except Hg(2+). Beside this, urea and thiourea also reduced the activity of chromate reduction to significant levels.

摘要

从用制革废水灌溉的植物根际土壤中分离出 4 株高效 Cr(VI)还原细菌,并研究其体外 Cr(VI)还原能力。根据 16S rRNA 基因测序,分离出的菌株 SUCR44、SUCR140、SUCR186 和 SUCR188 分别鉴定为芽孢杆菌(JN674188)、微杆菌(JN674183)、苏云金芽孢杆菌(JN674184)和枯草芽孢杆菌(JN674195)。所有 4 株菌均可在 0.2mM 浓度的培养基中在 24-120 小时内完全还原 Cr(VI);SUCR140 在 24 小时内完全还原 Cr(VI)。用透性细胞(用 Triton X-100 和 Tween 80 处理)和无细胞提取物进行的测定表明,Cr(VI)还原活性主要与细胞的可溶性部分有关。考虑到在 24-48 小时内还原的大部分铬,这些细胞外的活性物质也可能在其生长过程中被释放出来。在 28°C 的最佳温度和 pH 7.0 下,Cr(VI)还原的比活性分别为 0.32、0.42、0.34 和 0.28 μmol Cr(VI)min(-1)mg(-1)蛋白质,对于 SUCR44、SUCR140、SUCR186 和 SUCR188 菌株。添加 0.1mM 的 NADH 增强了所有 4 株菌无细胞提取物中的 Cr(VI)还原。在测试的不同金属离子存在下,所有分离株的无细胞提取物中的 Cr(VI)还原活性都很稳定,除了 Hg(2+)。除此之外,尿素和硫脲也能显著降低铬酸盐还原的活性。

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