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脱硫弧菌对铀的还原作用。

Reduction of uranium by Desulfovibrio desulfuricans.

作者信息

Lovley D R, Phillips E J

机构信息

Water Resources Division, U.S. Geological Survey, Reston, Virginia 22092.

出版信息

Appl Environ Microbiol. 1992 Mar;58(3):850-6. doi: 10.1128/aem.58.3.850-856.1992.

DOI:10.1128/aem.58.3.850-856.1992
PMID:1575486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC195344/
Abstract

The possibility that sulfate-reducing microorganisms contribute to U(VI) reduction in sedimentary environments was investigated. U(VI) was reduced to U(IV) when washed cells of sulfate-grown Desulfovibrio desulfuricans were suspended in a bicarbonate buffer with lactate or H2 as the electron donor. There was no U(VI) reduction in the absence of an electron donor or when the cells were killed by heat prior to the incubation. The rates of U(VI) reduction were comparable to those in respiratory Fe(III)-reducing microorganisms. Azide or prior exposure of the cells to air did not affect the ability of D. desulfuricans to reduce U(VI). Attempts to grow D. desulfuricans with U(VI) as the electron acceptor were unsuccessful. U(VI) reduction resulted in the extracellular precipitation of the U(IV) mineral uraninite. The presence of sulfate had no effect on the rate of U(VI) reduction. Sulfate and U(VI) were reduced simultaneously. Enzymatic reduction of U(VI) by D. desulfuricans was much faster than nonenzymatic reduction of U(VI) by sulfide, even when cells of D. desulfuricans were added to provide a potential catalytic surface for the nonenzymatic reaction. The results indicate that enzymatic U(VI) reduction by sulfate-reducing microorganisms may be responsible for the accumulation of U(IV) in sulfidogenic environments. Furthermore, since the reduction of U(VI) to U(IV) precipitates uranium from solution, D. desulfuricans might be a useful organism for recovering uranium from contaminated waters and waste streams.

摘要

研究了硫酸盐还原微生物在沉积环境中促进U(VI)还原的可能性。当以乳酸盐或H2作为电子供体,将在硫酸盐中生长的脱硫脱硫弧菌的洗涤细胞悬浮于碳酸氢盐缓冲液中时,U(VI)被还原为U(IV)。在没有电子供体的情况下,或者在孵育前细胞被加热杀死时,没有U(VI)的还原。U(VI)的还原速率与呼吸性铁(III)还原微生物中的还原速率相当。叠氮化物或细胞预先暴露于空气中并不影响脱硫脱硫弧菌还原U(VI)的能力。尝试以U(VI)作为电子受体培养脱硫脱硫弧菌未成功。U(VI)的还原导致U(IV)矿物沥青铀矿在细胞外沉淀。硫酸盐的存在对U(VI)的还原速率没有影响。硫酸盐和U(VI)同时被还原。即使添加脱硫脱硫弧菌的细胞以提供非酶促反应的潜在催化表面,脱硫脱硫弧菌对U(VI)的酶促还原也比硫化物对U(VI)的非酶促还原快得多。结果表明,硫酸盐还原微生物对U(VI)的酶促还原可能是产硫化物环境中U(IV)积累的原因。此外,由于U(VI)还原为U(IV)会使铀从溶液中沉淀出来,脱硫脱硫弧菌可能是从受污染的水和废水中回收铀的有用微生物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78d0/195344/bf73365d8739/aem00044-0086-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78d0/195344/bf73365d8739/aem00044-0086-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78d0/195344/bf73365d8739/aem00044-0086-a.jpg

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