4.8 Article

Identification of Antimonate Reducing Bacteria and Their Potential Metabolic Traits by the Combination of Stable Isotope Probing and Metagenomic-Pangenomic Analysis

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 20, Pages 13902-13912

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c03967

Keywords

antimony; DNA-SIP; metagenomic-binning; metal-reducing bacteria

Funding

  1. National Natural Science Foundation of China [41771301, 41907212]
  2. Science and Technology Planning Project of Guangzhou [201904010366, 202002020072]
  3. GDAS' Project of Science and Technology Development [2020GDASYL-20200102018, 2019GDASYL-0301002]
  4. Guangdong Basic and Applied Basic Research Foundation [2019A1515011559, 2021A1515011461, 2021A1515011374]
  5. Guangdong Introducing Innovative and Enterpreneurial Talants [2017GC010570]
  6. Science and Technology Planning Project of Guangdong Province [2019B110210003]
  7. Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01Z176]

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Microorganisms play an important role in altering the speciation, mobility, and bioavailability of antimony (Sb), particularly in the reduction of Sb(V). By using DNA-stable isotope probing and metagenomics analysis, this study identified Pseudomonas and Geobacter as potential Sb(V)-reducing bacteria in Sb-contaminated sites, with Geobacter potentially playing a key role in Sb(V) reduction based on the presence of specific genes. This work provides valuable insights into the microbial community responsible for Sb(V) reduction.
Microorganisms play an important role in altering antimony (Sb) speciation, mobility, and bioavailability, but the understanding of the microorganisms responsible for Sb(V) reduction has been limited. In this study, DNA-stable isotope probing (DNA-SIP) and metagenomics analysis were combined to identify potential Sb(V)-reducing bacteria (SbRB) and predict their metabolic pathways for Sb(V) reduction. Soil slurry cultures inoculated with Sb-contaminated paddy soils from two Sb-contaminated sites demonstrated the capability to reduce Sb(V). DNA-SIP identified bacteria belonging to the genera Pseudomonas and Geobacter as putative SbRB in these two Sb-contaminated sites. In addition, bacteria such as Lysinibacillus and Dechloromonas may potentially participate in Sb(V) reduction. Nearly complete draft genomes of putative SbRB (i.e., Pseudomonas and Geobacter) were obtained, and the genes potentially responsible for arsenic (As) and Sb reduction (i.e., respiratory arsenate reductase (arrA) and antimonate reductase (anrA)) were examined. Notably, bins affiliated with Geobacter contained arrA and anrA genes, supporting our hypothesis that they are putative SbRB. Further, pangenomic analysis indicated that various Geobacter-associated genomes obtained from diverse habitats also contained arrA and anrA genes. In contrast, Pseudomonas may use a predicted DMSO reductase closely related to sbrA (Sb(V) reductase gene) clade II to reduce Sb(V), which may need further experiments to verify. This current work represents a demonstration of using DNA-SIP and metagenomic-binning to identify SbRB and their key genes involved in Sb(V) reduction and provides valuable data sets to link bacterial identities with Sb(V) reduction.

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