Degradation of substituted phenylurea herbicides by Arthrobacter globiformis strain D47 and characterization of a plasmid-associated hydrolase gene, puhA

被引:89
作者
Turnbull, GA
Ousley, M
Walker, A
Shaw, E
Morgan, JAW [1 ]
机构
[1] Hort Res Int, Dept Microbiol & Plant Pathol, Wellesbourne CV35 9EF, Warwick, England
[2] Hort Res Int, Dept Soil & Environm Sci, Wellesbourne CV35 9EF, Warwick, England
关键词
D O I
10.1128/AEM.67.5.2270-2275.2001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Arthrobacter globiformis D47 was shown to degrade a range of substituted phenylurea herbicides in soil. This strain contained two plasmids of approximately 47 kb (pHRIM620) and 34 kb (pHRIM621). Plasmid-curing experiments produced plasmid-free strains as well as strains containing either the 47- or the 34-kb plasmid. The strains were tested for their ability to degrade diuron, which demonstrated that the degradative genes were located on the 47-kb plasmid, Studies on the growth of these strains indicated that the ability to degrade diuron did not offer a selective advantage to A. globiformis D47 on minimal medium designed to contain the herbicide as a sole carbon source. The location of the genes on a plasmid and a lack of selection would explain why the degradative phenotype, as with many other pesticide-degrading bacteria, ran be lost on subculture. A 22-kb EcoRI Fragment of plasmid pHRIM620 was expressed in Escherichia coli and enabled cells to degrade diuron, Transposon mutagenesis of this fragment identified one open reading frame that was essential for enzyme activity. A smaller subclone of this gene (2.5 kb) expressed in E. coli coded for the protein that degraded diuron, This gene and its predicted protein sequence showed only a low level of protein identity (25% over ca, 440 amino acids) to other database sequences and was named after the enzyme it encoded, phenylurea hydrolase (puhA gene).
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页码:2270 / 2275
页数:6
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共 37 条
[1]   A REVIEW OF BACTERIAL-DEGRADATION OF PESTICIDES [J].
AISLABIE, J ;
LLOYDJONES, G .
AUSTRALIAN JOURNAL OF SOIL RESEARCH, 1995, 33 (06) :925-942
[2]   INTERACTION OF THE REGULATORY PROTEIN NICR1 WITH THE PROMOTER REGION OF THE PAO1-ENCODED 6-HYDROXY-D-NICOTINE OXIDASE GENE OF ARTHROBACTER-OXIDANS [J].
BERNAUER, H ;
MAUCH, L ;
BRANDSCH, R .
MOLECULAR MICROBIOLOGY, 1992, 6 (13) :1809-1820
[3]   The atzB gene of Pseudomonas sp strain ADP encodes the second enzyme of a novel atrazine degradation pathway [J].
BoundyMills, KL ;
deSouza, ML ;
Mandelbaum, RT ;
Wackett, LP ;
Sadowsky, MJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (03) :916-923
[4]   6-HYDROXY-D-NICOTINE OXIDASE OF ARTHROBACTER-OXIDANS - GENE STRUCTURE OF THE FLAVOENZYME AND ITS RELATIONSHIP TO 6-HYDROXY-L-NICOTINE OXIDASE [J].
BRANDSCH, R ;
HINKKANEN, AE ;
MAUCH, L ;
NAGURSKY, H ;
DECKER, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1987, 167 (02) :315-320
[5]   PLASMID PAO1 OF ARTHROBACTER-OXIDANS ENCODES 6-HYDROXY-D-NICOTINE OXIDASE - CLONING AND EXPRESSION OF THE GENE IN ESCHERICHIA-COLI [J].
BRANDSCH, R ;
FALLER, W ;
SCHNEIDER, K .
MOLECULAR AND GENERAL GENETICS, 1986, 202 (01) :96-101
[6]   Invariance of plastic strains with respect to imposed rate at boundary [J].
Chung, K ;
Wagoner, RH .
METALS AND MATERIALS-KOREA, 1998, 4 (01) :25-31
[7]   Rapid biodegradation of diuron and other phenylurea herbicides by a soil bacterium [J].
Cullington, JE ;
Walker, A .
SOIL BIOLOGY & BIOCHEMISTRY, 1999, 31 (05) :677-686
[8]   The atrazine catabolism genes atzABC are widespread and highly conserved [J].
de Souza, ML ;
Seffernick, J ;
Martinez, B ;
Sadowsky, MJ ;
Wackett, LP .
JOURNAL OF BACTERIOLOGY, 1998, 180 (07) :1951-1954
[9]   TRANSPOSON MUTAGENESIS AND CLONING ANALYSIS OF THE PATHWAYS FOR DEGRADATION OF 2,4-DICHLOROPHENOXYACETIC ACID AND 3-CHLOROBENZOATE IN ALCALIGENES-EUTROPHUS JMP134(PJP4) [J].
DON, RH ;
WEIGHTMAN, AJ ;
KNACKMUSS, HJ ;
TIMMIS, KN .
JOURNAL OF BACTERIOLOGY, 1985, 161 (01) :85-90
[10]   Cloning of inulin fructotransferase (DFA III-producing) gene from Arthrobacter globiformis C11-1 [J].
Haraguchi, K ;
Mori, S ;
Hayashi, K .
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2000, 89 (06) :590-595