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Comparative analysis of DNA-SIP and magnetic-nanoparticle mediated isolation (MMI) on unraveling dimethoate degraders |
Luning Lian1,2,3, Yi Xing1,2,3( ), Dayi Zhang4, Longfei Jiang5, Mengke Song6, Bo Jiang1,2,3,7( ) |
1. School of Energy and Environmental Engineering, University of Science & Technology Beijing, Beijing 100083, China 2. Beijing Key Laboratory of Resource-oriented Treatment of Industrial Pollutants, University of Science & Technology Beijing, Beijing 100083, China 3. National Environmental and Energy Science and Technology International Cooperation Base, University of Science & Technology Beijing, Beijing 100083, China 4. College of New Energy and Environment, Jilin University, Changchun 130021, China 5. Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China 6. College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510642, China 7. National Engineering Laboratory for Site Remediation Technologies, Beijing 100015, China |
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Abstract ● Dimethoate degraders were identified via MMI and DNA-SIP. ● MMI identified Pseudomonas, Bacillus, Ramlibacter, Arthrobacter , and Rhodococcus. ● DNA-SIP identified Ramlibacter , Rhodococcus and Arthrobacter. ● Both oph B and oph C2 were involved in dimethoate metabolism. ● MMI shows higher resolution than DNA-SIP in identifying functional microbes. Microorganisms are crucial in the bioremediation of organophosphorus pesticides. However, most functional microorganisms (> 99%) are yet to be cultivated. This study applied two cultivation-independent approaches, DNA-SIP and magnetic-nanoparticle mediated isolation (MMI), to identify the functional microorganisms in degrading dimethoate in agricultural soils. MMI identified five dimethoate degraders: Pseudomonas, Bacillus, Ramlibacter, Arthrobacter, and Rhodococcus, whereas DNA-SIP identified three dimethoate degraders: Ramlibacter, Arthrobacter, and Rhodococcus. Also, MMI showed higher resolution than DNA-SIP in identifying functional microorganisms. Two organic phosphohydrolase (OPH) genes: ophC2 and ophB, were involved in dimethoate metabolism, as revealed by DNA-SIP and MMI. The degradation products of dimethoate include omethoate, O,O,S-trimethyl thiophosphorothioate, N-methyl-2-sulfanylacetamide, O,O-diethyl S-hydrogen phosphorodithioate, O,O,O-trimethyl thiophosphate, O,O,S-trimethyl thiophosphorodithioate, and O,O,O-trimethyl phosphoric. This study emphasizes the feasibility of using SIP and MMI to explore the functional dimethoate degraders, expanding our knowledge of microbial resources with cultivation-independent approaches.
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Keywords
Stable isotope probing (SIP)
Magnetic-nanoparticle mediated isolation (MMI)
Dimethoate
Biodegradation
Cultivation-independent approach
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Corresponding Author(s):
Yi Xing,Bo Jiang
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Issue Date: 09 August 2023
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