Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac.

Quinclorac is a widely used herbicide in rice filed. Unfortunately, quinclorac residues are phytotoxic to many crops/vegetables. The degradation of quinclorac in nature is very slow. On the other hand, degradation of quinclorac using bacteria can be an effective and efficient method to reduce its co...

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Main Authors: Yingying Li, Wu Chen, Yunsheng Wang, Kun Luo, Yue Li, Lianyang Bai, Feng Luo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5624592?pdf=render
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spelling doaj-39a3bc2a7f574d459ae46a5a72de7d372020-11-25T02:42:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011210e018572110.1371/journal.pone.0185721Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac.Yingying LiWu ChenYunsheng WangKun LuoYue LiLianyang BaiFeng LuoQuinclorac is a widely used herbicide in rice filed. Unfortunately, quinclorac residues are phytotoxic to many crops/vegetables. The degradation of quinclorac in nature is very slow. On the other hand, degradation of quinclorac using bacteria can be an effective and efficient method to reduce its contamination. In this study, we isolated a quinclorac bioremediation bacterium strain F4 from quinclorac contaminated soils. Based on morphological characteristics and 16S rRNA gene sequence analysis, we identified strain F4 as Mycobacterium sp. We investigated the effects of temperature, pH, inoculation size and initial quinclorac concentration on growth and degrading efficiency of F4 and determined the optimal quinclorac degrading condition of F4. Under optimal degrading conditions, F4 degraded 97.38% of quinclorac from an initial concentration of 50 mg/L in seven days. Our indoor pot experiment demonstrated that the degradation products were non-phytotoxic to tobacco. After analyzing the quinclorac degradation products of F4, we proposed that F4 could employ two pathways to degrade quinclorac: one is through methylation, the other is through dechlorination. Furthermore, we reconstructed the whole genome of F4 through single molecular sequencing and de novo assembly. We identified 77 methyltransferases and eight dehalogenases in the F4 genome to support our hypothesized degradation path.http://europepmc.org/articles/PMC5624592?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yingying Li
Wu Chen
Yunsheng Wang
Kun Luo
Yue Li
Lianyang Bai
Feng Luo
spellingShingle Yingying Li
Wu Chen
Yunsheng Wang
Kun Luo
Yue Li
Lianyang Bai
Feng Luo
Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac.
PLoS ONE
author_facet Yingying Li
Wu Chen
Yunsheng Wang
Kun Luo
Yue Li
Lianyang Bai
Feng Luo
author_sort Yingying Li
title Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac.
title_short Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac.
title_full Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac.
title_fullStr Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac.
title_full_unstemmed Identifying and sequencing a Mycobacterium sp. strain F4 as a potential bioremediation agent for quinclorac.
title_sort identifying and sequencing a mycobacterium sp. strain f4 as a potential bioremediation agent for quinclorac.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Quinclorac is a widely used herbicide in rice filed. Unfortunately, quinclorac residues are phytotoxic to many crops/vegetables. The degradation of quinclorac in nature is very slow. On the other hand, degradation of quinclorac using bacteria can be an effective and efficient method to reduce its contamination. In this study, we isolated a quinclorac bioremediation bacterium strain F4 from quinclorac contaminated soils. Based on morphological characteristics and 16S rRNA gene sequence analysis, we identified strain F4 as Mycobacterium sp. We investigated the effects of temperature, pH, inoculation size and initial quinclorac concentration on growth and degrading efficiency of F4 and determined the optimal quinclorac degrading condition of F4. Under optimal degrading conditions, F4 degraded 97.38% of quinclorac from an initial concentration of 50 mg/L in seven days. Our indoor pot experiment demonstrated that the degradation products were non-phytotoxic to tobacco. After analyzing the quinclorac degradation products of F4, we proposed that F4 could employ two pathways to degrade quinclorac: one is through methylation, the other is through dechlorination. Furthermore, we reconstructed the whole genome of F4 through single molecular sequencing and de novo assembly. We identified 77 methyltransferases and eight dehalogenases in the F4 genome to support our hypothesized degradation path.
url http://europepmc.org/articles/PMC5624592?pdf=render
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