Nicolas Haroune, Bruno Combourieu, Pascale Besse, Martine Sancelme, Anne-Marie Delort
{"title":"1H NMR:一种研究环境中污染物命运的工具","authors":"Nicolas Haroune, Bruno Combourieu, Pascale Besse, Martine Sancelme, Anne-Marie Delort","doi":"10.1016/S1387-1609(01)01322-6","DOIUrl":null,"url":null,"abstract":"<div><p>In situ <sup>1</sup>H NMR, directly performed on biological fluids is a very powerful tool to study the fate of pollutants in the environment. The biodegradation of 2-aminobenzothiazole by <em>Rhodococcus rhodochrous</em> was monitored by reverse phase HPLC and by in situ <sup>1</sup>H NMR, methods performed directly on culture media without purification. The xenobiotic was biotransformed into a hydroxylated derivative. The chemical structure of this metabolite was determined by a long-range <sup>1</sup>H–<sup>15</sup>N heteronuclear shift correlation without any previous <sup>15</sup>N enrichment of the compound. This approach allowed the assignment of the metabolite structure to 2-amino-6-hydroxybenzothiazole.</p></div>","PeriodicalId":100305,"journal":{"name":"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry","volume":"4 10","pages":"Pages 759-763"},"PeriodicalIF":0.0000,"publicationDate":"2001-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1387-1609(01)01322-6","citationCount":"10","resultStr":"{\"title\":\"1H NMR: a tool to study the fate of pollutants in the environment\",\"authors\":\"Nicolas Haroune, Bruno Combourieu, Pascale Besse, Martine Sancelme, Anne-Marie Delort\",\"doi\":\"10.1016/S1387-1609(01)01322-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In situ <sup>1</sup>H NMR, directly performed on biological fluids is a very powerful tool to study the fate of pollutants in the environment. The biodegradation of 2-aminobenzothiazole by <em>Rhodococcus rhodochrous</em> was monitored by reverse phase HPLC and by in situ <sup>1</sup>H NMR, methods performed directly on culture media without purification. The xenobiotic was biotransformed into a hydroxylated derivative. The chemical structure of this metabolite was determined by a long-range <sup>1</sup>H–<sup>15</sup>N heteronuclear shift correlation without any previous <sup>15</sup>N enrichment of the compound. This approach allowed the assignment of the metabolite structure to 2-amino-6-hydroxybenzothiazole.</p></div>\",\"PeriodicalId\":100305,\"journal\":{\"name\":\"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry\",\"volume\":\"4 10\",\"pages\":\"Pages 759-763\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1387-1609(01)01322-6\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1387160901013226\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1387160901013226","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
1H NMR: a tool to study the fate of pollutants in the environment
In situ 1H NMR, directly performed on biological fluids is a very powerful tool to study the fate of pollutants in the environment. The biodegradation of 2-aminobenzothiazole by Rhodococcus rhodochrous was monitored by reverse phase HPLC and by in situ 1H NMR, methods performed directly on culture media without purification. The xenobiotic was biotransformed into a hydroxylated derivative. The chemical structure of this metabolite was determined by a long-range 1H–15N heteronuclear shift correlation without any previous 15N enrichment of the compound. This approach allowed the assignment of the metabolite structure to 2-amino-6-hydroxybenzothiazole.