{"title":"荧光假单胞菌降解和转化克百威杀虫剂产生的新型衍生物化合物","authors":"","doi":"10.1016/j.aac.2023.11.008","DOIUrl":null,"url":null,"abstract":"<div><p>Carbofuran insecticide is one of the insecticides most often used by Indonesian farmers. The United Nations Environment Program (UNEP) 2011 in the decision of UNEP/FAO/RC/CRC.11/6, agreed that the active ingredient Carbofuran is dangerous to human health and the environment. <em>P. fluorescens</em> bacteria are known to be able to remediate carbofuran-contaminated soil. This study examines more deeply the biodegradation and biotransformation processes of Carbofuran in <em>P. fluorescens</em> bacteria. The research was carried out at the Laboratory of Plant Diseases, Faculty of Agriculture, Brawijaya University; Analytical Chemistry Laboratory, State Polytechnic of Malang; and Analytical Chemistry Laboratory, Udayana University from February to August 2020. The results showed that <em>P. fluorescens</em> was able to degrade the insecticide Carbofuran in liquid media up to 82 % and the growth of <em>P. fluorescens</em> bacteria reached 2.9 x 10<sup>12</sup> CFU/mL, bacteria <em>P. fluorescens</em> is able to degrade the insecticide Carbofuran in a mixture of soil and compost up to 85 % and the growth of <em>P. fluorescens</em> bacteria reaches 7.5 x 10<sup>13</sup> CFU/mL, resulting in Carbofuran insecticide derivatives from the biotransformation process, there are 3-hydroxy-7-phenol; 2,3-dihydro-1-benzofuran-2,2,7-triol; (2Z)-2-[(2Z)-pent-2-en-1-ylidene]butane-1,4,4-trio; 7-phenol; 2,2,3-trihydroxy-2,3-dihydro-1-benzofuran-7-yl hydrogen carbonate; 2,2-dimethyl-2,3-dihydro-1-benzofuran-7-yl acetate; 7-(hydroxymethoxy)-2,3-dihydro-1-benzofuran-2,2,3,5-tetrol; 3-hidroksi-2-fenilpropil Carbamat; 2-(3-hydroperoxy-2-hydroxyphenyl)ethane-1,1-diol, 3-keto-7-fenol; 4-hydroxy-2,2-dimethyl-2,3-dihydro-1H-inden-1-one; 3-hydroxy-carbofuran; and 7-methoxy-2,2-dimethyl-2,3-dihydro-1-benzofuran-3,5-diol. Carbofuran derivative compounds from the biodegradation of <em>P. fluorescens</em> bacteria are less toxic than the active ingredient Carbofuran.</p></div>","PeriodicalId":100027,"journal":{"name":"Advanced Agrochem","volume":"3 3","pages":"Pages 237-245"},"PeriodicalIF":0.0000,"publicationDate":"2023-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2773237123001016/pdfft?md5=fb120571ba89a79c5d8c1f5bffc0102b&pid=1-s2.0-S2773237123001016-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Novel derivative compound produced from carbofuran insecticide degradation and transformation promoted by Pseudomonas fluorescens\",\"authors\":\"\",\"doi\":\"10.1016/j.aac.2023.11.008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Carbofuran insecticide is one of the insecticides most often used by Indonesian farmers. The United Nations Environment Program (UNEP) 2011 in the decision of UNEP/FAO/RC/CRC.11/6, agreed that the active ingredient Carbofuran is dangerous to human health and the environment. <em>P. fluorescens</em> bacteria are known to be able to remediate carbofuran-contaminated soil. This study examines more deeply the biodegradation and biotransformation processes of Carbofuran in <em>P. fluorescens</em> bacteria. The research was carried out at the Laboratory of Plant Diseases, Faculty of Agriculture, Brawijaya University; Analytical Chemistry Laboratory, State Polytechnic of Malang; and Analytical Chemistry Laboratory, Udayana University from February to August 2020. The results showed that <em>P. fluorescens</em> was able to degrade the insecticide Carbofuran in liquid media up to 82 % and the growth of <em>P. fluorescens</em> bacteria reached 2.9 x 10<sup>12</sup> CFU/mL, bacteria <em>P. fluorescens</em> is able to degrade the insecticide Carbofuran in a mixture of soil and compost up to 85 % and the growth of <em>P. fluorescens</em> bacteria reaches 7.5 x 10<sup>13</sup> CFU/mL, resulting in Carbofuran insecticide derivatives from the biotransformation process, there are 3-hydroxy-7-phenol; 2,3-dihydro-1-benzofuran-2,2,7-triol; (2Z)-2-[(2Z)-pent-2-en-1-ylidene]butane-1,4,4-trio; 7-phenol; 2,2,3-trihydroxy-2,3-dihydro-1-benzofuran-7-yl hydrogen carbonate; 2,2-dimethyl-2,3-dihydro-1-benzofuran-7-yl acetate; 7-(hydroxymethoxy)-2,3-dihydro-1-benzofuran-2,2,3,5-tetrol; 3-hidroksi-2-fenilpropil Carbamat; 2-(3-hydroperoxy-2-hydroxyphenyl)ethane-1,1-diol, 3-keto-7-fenol; 4-hydroxy-2,2-dimethyl-2,3-dihydro-1H-inden-1-one; 3-hydroxy-carbofuran; and 7-methoxy-2,2-dimethyl-2,3-dihydro-1-benzofuran-3,5-diol. Carbofuran derivative compounds from the biodegradation of <em>P. fluorescens</em> bacteria are less toxic than the active ingredient Carbofuran.</p></div>\",\"PeriodicalId\":100027,\"journal\":{\"name\":\"Advanced Agrochem\",\"volume\":\"3 3\",\"pages\":\"Pages 237-245\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2773237123001016/pdfft?md5=fb120571ba89a79c5d8c1f5bffc0102b&pid=1-s2.0-S2773237123001016-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Agrochem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2773237123001016\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Agrochem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2773237123001016","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
克百威杀虫剂是印度尼西亚农民最常用的杀虫剂之一。联合国环境规划署(UNEP)2011 年在 UNEP/FAO/RC/CRC.11/6 号决定中同意,活性成分克百威对人类健康和环境有害。众所周知,荧光屏杆菌能够修复受克隆呋喃污染的土壤。本研究更深入地探讨了克百威在荧光团细菌中的生物降解和生物转化过程。该研究于 2020 年 2 月至 8 月在 Brawijaya 大学农学院植物病害实验室、Malang 州立理工学院分析化学实验室和 Udayana 大学分析化学实验室进行。结果表明,荧光茯苓菌在液体培养基中对杀虫剂克百威的降解率高达 82%,荧光茯苓菌的生长量达到 2.9 x 1012 CFU/mL;荧光茯苓菌在土壤和堆肥混合物中对杀虫剂克百威的降解率高达 85%,荧光茯苓菌的生长量达到 7.5 x 1013 CFU/mL,从生物转化过程中产生的克百威杀虫剂衍生物有 3-羟基-7-苯酚;2,3-二氢-1-苯并呋喃-2,2,7-三醇;(2Z)-2-[(2Z)-戊-2-烯-1-亚基]丁烷-1,4,4-三酮;7-苯酚;2,2,3-三羟基-2,3-二氢-1-苯并呋喃-7-基碳酸氢盐;2,2-二甲基-2,3-二氢-1-苯并呋喃-7-基乙酸酯;7-(羟基甲氧基)-2,3-二氢-1-苯并呋喃-2,2,3,5-四醇;3-hidroksi-2-fenilpropil Carbamat;2-(3-hydroperoxy-2-hydroxyphenyl)ethane-1,1-diol, 3-keto-7-fenol; 4-hydroxy-2,2-dimethyl-2,3-dihydro-1H-inden-1-one; 3-hydroxy-carbofuran; and 7-methoxy-2,2-dimethyl-2,3-dihydro-1-benzofuran-3,5-diol.由 P. fluorescens 细菌生物降解产生的克百威衍生物的毒性低于活性成分克百威。
Novel derivative compound produced from carbofuran insecticide degradation and transformation promoted by Pseudomonas fluorescens
Carbofuran insecticide is one of the insecticides most often used by Indonesian farmers. The United Nations Environment Program (UNEP) 2011 in the decision of UNEP/FAO/RC/CRC.11/6, agreed that the active ingredient Carbofuran is dangerous to human health and the environment. P. fluorescens bacteria are known to be able to remediate carbofuran-contaminated soil. This study examines more deeply the biodegradation and biotransformation processes of Carbofuran in P. fluorescens bacteria. The research was carried out at the Laboratory of Plant Diseases, Faculty of Agriculture, Brawijaya University; Analytical Chemistry Laboratory, State Polytechnic of Malang; and Analytical Chemistry Laboratory, Udayana University from February to August 2020. The results showed that P. fluorescens was able to degrade the insecticide Carbofuran in liquid media up to 82 % and the growth of P. fluorescens bacteria reached 2.9 x 1012 CFU/mL, bacteria P. fluorescens is able to degrade the insecticide Carbofuran in a mixture of soil and compost up to 85 % and the growth of P. fluorescens bacteria reaches 7.5 x 1013 CFU/mL, resulting in Carbofuran insecticide derivatives from the biotransformation process, there are 3-hydroxy-7-phenol; 2,3-dihydro-1-benzofuran-2,2,7-triol; (2Z)-2-[(2Z)-pent-2-en-1-ylidene]butane-1,4,4-trio; 7-phenol; 2,2,3-trihydroxy-2,3-dihydro-1-benzofuran-7-yl hydrogen carbonate; 2,2-dimethyl-2,3-dihydro-1-benzofuran-7-yl acetate; 7-(hydroxymethoxy)-2,3-dihydro-1-benzofuran-2,2,3,5-tetrol; 3-hidroksi-2-fenilpropil Carbamat; 2-(3-hydroperoxy-2-hydroxyphenyl)ethane-1,1-diol, 3-keto-7-fenol; 4-hydroxy-2,2-dimethyl-2,3-dihydro-1H-inden-1-one; 3-hydroxy-carbofuran; and 7-methoxy-2,2-dimethyl-2,3-dihydro-1-benzofuran-3,5-diol. Carbofuran derivative compounds from the biodegradation of P. fluorescens bacteria are less toxic than the active ingredient Carbofuran.