4.7 Article

Bacteria responsible for nitrate-dependent antimonite oxidation in antimony-contaminated paddy soil revealed by the combination of DNA-SIP and metagenomics

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SOIL BIOLOGY & BIOCHEMISTRY
卷 156, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.soilbio.2021.108194

关键词

Nitrate-dependent antimonite oxidation; Nitrate-dependent antimonite-oxidizing bacteria; Paddy soil; DNA-SIP

资金

  1. National Natural Science Foundation of China [41907285, 41771301]
  2. GDAS' Project of Science and Technology Development [2019GDASYL-0103053, 2019GDASYL-0301002, 2019GDASYL-0103047, 2019GDASYL-0103046, 2020GDASYL-20200103086]
  3. Science and Technology Planning Project of Guangzhou [202002020072]
  4. Guangdong Foundation for Program of Science and Technology Research [2019B121205006]
  5. Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01Z176]
  6. High-level Leading Talent Introduction Program of GDAS [2016GDASRC-0103]
  7. Guangdong Introducing Innovative and Entrepreneurial Talents [2017GC010570]

向作者/读者索取更多资源

The oxidation of antimonite (Sb(III)) can reduce the toxicity of antimony (Sb) and its uptake in rice fields, with nitrate playing a key role. This study investigated the potential of nitrate-dependent antimonite oxidation in Sb-contaminated rice paddies and identified bacteria responsible for this process. These findings enhance our understanding of the diversity of nitrate-dependent antimonite oxidizing bacteria.
Antimonite (Sb(III)) oxidation (SbO) can decrease the toxicity of antimony (Sb) and its uptake into rice, thus serving an ecological role in bioremediation of Sb contamination in rice paddies and decreasing the translocation and accumulation of Sb in rice. Nitrate as the electron acceptor can be coupled to SbO in anoxic environments, which, however, has not been reported in paddy soils. Here we investigate the potential for nitrate-dependent SbO in Sb-contaminated rice paddies and identify nitrate-dependent Sb(III)-oxidizing bacteria (SbOB) using stable isotope probing (SIP) coupled with amplicon and shotgun metagenomic sequencing. Anaerobic SbO was exclusively observed in the paddy soil amended with both Sb(III) and NO3-, whereas no apparent SbO was detected in the soil amended with Sb(III) only. The increasing abundance of the arsenite oxidase gene (aioA) suggests that nitrate-dependent SbO was catalysed by microorganisms harbouring the aioA gene. After 60-day DNA-SIP incubation, an obvious shift in the relative abundance of aioA gene to heavy DNA fractions occurred only in the treatment amended with C-13-NaHCO3, Sb(III) and NO3-, suggesting the incorporation of C-13 by nitrate-dependent SbOB. Accordingly, a number of putative nitrate-dependent SbOB were identified in the paddy soil, including Azoarcus, Azospira and Chelativorans. Metagenomic analysis further revealed that they contained aioA genes and genes involved in denitrification and carbon fixation, supporting their capability for nitrate-dependent SbO. These observations suggested the occurrence of nitrate-dependent SbO in paddy soils. A number of putative nitrate-dependent SbOB (i.e., Azoarcus, Azospira and Chelativorans) were reported here, which expands our current knowledge regarding the diversity of nitrate-dependent SbOB. In addition, this study provides a proof of concept using DNA-SIP to identify nitrate-dependent SbOB.

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