Sulfate-reducing bacteria mediate thionation of diphenylarsinic acid under anaerobic conditions

被引:8
|
作者
Guan, Ling [1 ,2 ,3 ]
Shiiya, Ayaka [2 ]
Hisatomi, Shihoko [2 ]
Fujii, Kunihiko [4 ]
Nonaka, Masanori [3 ]
Harada, Naoki [3 ]
机构
[1] Niigata Univ, Ctr Fostering Innovat Leadership, Nishi Ku, Niigata 9502181, Japan
[2] Niigata Univ, Grad Sch Sci & Technol, Nishi Ku, Niigata 9502181, Japan
[3] Niigata Univ, Inst Sci & Technol, Nishi Ku, Niigata 9502181, Japan
[4] Niigata Univ, Off Environm & Safety, Nishi Ku, Niigata 9502181, Japan
基金
日本学术振兴会;
关键词
Anaerobic transformation; Desulfotomaculum acetoxidans; Diphenylarsinic acid; Diphenylthioarsinic acid; Sulfate-reducing bacteria; Thionation; CHEMICAL WARFARE AGENTS; SOIL; TRANSFORMATION; DESULFOVIBRIO; SPECIATION; NOV;
D O I
10.1007/s10532-014-9713-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Diphenylarsinic acid (DPAA) is often found as a toxic intermediate metabolite of diphenylchloroarsine or diphenylcyanoarsine that were produced as chemical warfare agents and were buried in soil after the World Wars. In our previous study Guan et al. (J Hazard Mater 241-242:355-362, 2012), after application of sulfate and carbon sources, anaerobic transformation of DPAA in soil was enhanced with the production of diphenylthioarsinic acid (DPTAA) as a main metabolite. This study aimed to isolate and characterize anaerobic soil microorganisms responsible for the metabolism of DPAA. First, we obtained four microbial consortia capable of transforming DPAA to DPTAA at a high transformation rate of more than 80 % after 4 weeks of incubation. Sequencing for the bacterial 16S rRNA gene clone libraries constructed from the consortia revealed that all the positive consortia contained Desulfotomaculum acetoxidans species. In contrast, the absence of dissimilatory sulfite reductase gene (dsrAB) which is unique to sulfate-reducing bacteria was confirmed in the negative consortia showing no DPAA reduction. Finally, strain DEA14 showing transformation of DPAA to DPTAA was isolated from one of the positive consortia. The isolate was assigned to D. acetoxidans based on the partial 16S rDNA sequence analysis. Thionation of DPAA was also carried out in a pure culture of a known sulfate-reducing bacterial strain, Desulfovibrio aerotolerans JCM 12613(T). These facts indicate that sulfate-reducing bacteria are microorganisms responsible for the transformation of DPAA to DPTAA under anaerobic conditions.
引用
收藏
页码:29 / 38
页数:10
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