Biotransformation of the triketone herbicide mesotrione by a Bacillus strain.: Metabolite profiling using liquid chromatography/electrospray ionization quadrupole time-of-flight mass spectrometry

被引:42
作者
Durand, Stephanie [1 ]
Legeret, Bertrand [1 ]
Martin, Anne-Sophie [1 ]
Sancelme, Martine [1 ]
Delort, Anne-Marie [1 ]
Besse-Hoggan, Pascale [1 ]
Combourieu, Bruno [1 ]
机构
[1] Univ Blaise Pascal, CNRS, UMR 6504, Lab Synth & Etude Syst Interet Biol, F-63177 Aubiere, France
关键词
D O I
10.1002/rcm.2627
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The metabolic pathway involved in the biotransformation of the herbicide mesotrione by the bacterial strain Bacillus sp. 3B6 was investigated by a reliable liquid chromatography/electrospray ionization quadrupole time-of-flight mass spectrometry (LC/ESI-QTOF-MS) method. The LC/ESI-MS method, both in positive and negative mode, with the assistance of MS2 fragments and isotopic pattern analyses, allowed us to identify five metabolites. This work constitutes the first complete monitoring of mesotrione degradation kinetics. Among the transformation products found by both techniques, one was formed by intramolecular cyclization between a hydroxylamine and a keto function, which is quite a rare biological reactivity process. For each identified metabolite, a fragmentation pathway is proposed for negative and positive mode. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:2603 / 2613
页数:11
相关论文
共 42 条
[1]   Determination of mesotrione residues and metabolites in crops, soil, and water by liquid chromatography with fluorescence detection [J].
Alferness, P ;
Wiebe, L .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (14) :3926-3934
[2]   Time-resolved infrared spectroscopy of intermediates and products from photolysis of 1-(2-nitrophenyl)ethyl phosphates: Reaction of the 2-nitrosoacetophenone byproduct with thiols [J].
Barth, A ;
Corrie, JET ;
Gradwell, MJ ;
Maeda, Y ;
Mantele, W ;
Meier, T ;
Trentham, DR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (18) :4149-4159
[3]   SELECTIVE REDUCTION OF AROMATIC NITRO-COMPOUNDS WITH STANNOUS CHLORIDE IN NON-ACIDIC AND NON-AQUEOUS MEDIUM [J].
BELLAMY, FD ;
OU, K .
TETRAHEDRON LETTERS, 1984, 25 (08) :839-842
[4]   Quantitative structure-activity relationships of mutagenic and carcinogenic aromatic amines [J].
Benigni, R ;
Giuliani, A ;
Franke, R ;
Gruska, A .
CHEMICAL REVIEWS, 2000, 100 (10) :3697-3714
[5]   Controlled protein precipitation in combination with chip-based nanospray infusion mass spectrometry. An approach for metabolomics profiling of plasma [J].
Boernsen, KO ;
Gatzek, S ;
Imbert, G .
ANALYTICAL CHEMISTRY, 2005, 77 (22) :7255-7264
[6]   Quantitative determination of chlortetracycline content in animal plasma at controlled keto-enol tautomerism by liquid chromatography-electrospray ionization-tandem mass spectrometry [J].
Cherlet, M ;
Croubels, S ;
De Backer, P .
JOURNAL OF CHROMATOGRAPHY A, 2006, 1102 (1-2) :116-124
[7]   First isolation and characterization of a bacterial strain that biotransforms the herbicide mesotrione [J].
Durand, S. ;
Amato, P. ;
Sancelme, M. ;
Delort, A. -M. ;
Combourieu, B. ;
Besse-Hogan, P. .
LETTERS IN APPLIED MICROBIOLOGY, 2006, 43 (02) :222-228
[8]   Adsorption and degradation of the weak acid mesotrione in soil and environmental fate implications [J].
Dyson, JS ;
Beulke, S ;
Brown, CD ;
Lane, MCG .
JOURNAL OF ENVIRONMENTAL QUALITY, 2002, 31 (02) :613-618
[9]   Application of positive and negative electrospray ionization, collision-induced dissociation and tandem mass spectrometry to a study of the fragmentation of 6-hydroxyluteolin 7-O-glucoside and 7-O-glucosyl-(l → 3)-glucoside [J].
Es-Safi, NE ;
Kerhoas, L ;
Ducrot, PH .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2005, 19 (19) :2734-2742
[10]  
Fabian WMF, 1999, J PHYS ORG CHEM, V12, P635, DOI 10.1002/(SICI)1099-1395(199908)12:8<635::AID-POC166>3.3.CO