Characterization of three distinct extradiol dioxygenases involved in mineralization of dibenzofuran by Terrabacter sp strain DPO360

被引:46
作者
Schmid, A
Rothe, B
Altenbuchner, J
Ludwig, W
Engesser, KH
机构
[1] UNIV STUTTGART,INST MIKROBIOL,D-70569 STUTTGART,GERMANY
[2] UNIV STUTTGART,INST IND GENET,D-70569 STUTTGART,GERMANY
[3] TECH UNIV MUNICH,LEHRSTUHL MIKROBIOL,D-80290 MUNICH,GERMANY
关键词
D O I
10.1128/jb.179.1.53-62.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The dibenzofuran-degrading bacterial strain DPO360 represents a new species of the genus Terrabacter together with the previously described dibenzofuran-mineralizing bacterial strain DPO1361 (Ii.-H. Engesser, V. Strubel, Ii. Christoglou, P. Fischer, and H. G. Rast, FEMS Microbiol. Lett. 65:205-210, 1989; V. Strubel, Ph.D. thesis, University of Stuttgart, Stuttgart, Germany, 1991; V. Strubel, H. G. Rast, W. Fietz, H.-J. Knackmuss, and K.-H. Engesser, FEMS Microbiol. Lett. 58:233-238, 1989). Two 2,3-dihydroxybiphengl-1,2-dioxygenases (BphC1 and BphC2) and one catechol-2,3-dioxygenase (C23O) were shown to be expressed in Terrabacter sp. strain DPO360 growing with dibenzofuran as a sole source of carbon and energy. These enzymes exhibited strong sensitivity to oxygen. They were purified to apparent homogeneity as homodimers (BphC1 and BphC2) and as a homotetrameric catechol-2,3-dioxygenase (C23O). According to their specificity constants k(cat)/K-m, both BphC1 and BphC2 were shown to be responsible for the cleavage of 2,2',3-trihydroxybiphenyl, the first metabolite in dibenzofuran mineralization along the angular dioxygenation pathway. With this substrate, BphC2 exhibited a considerably higher k(cat)/K-m value (183 mu M/min) than BphC1 (29 mu M/min). Catechol-2,3-dioxygenase was recognized to be not involved in the ring cleavage of 2,2',3-trihydroxybiphenyl (k(cat)/K-m, 1 mu M/min). Analysis of deduced amino acid sequence data bphC1 revealed 36% sequence identity to nahC from Pseudomonas putida PpG7 (S. Harayama and M. Rekik, J. Biol. Chem. 264:15328-15333, 1989) and about 40% sequence identity to various bphC genes from different Pseudomonas and Rhodococcus strains. In addition, another 2,3-dihydroxybiphenyl-1,2-dioxygenase gene (bphC3) was cloned from the genome of Terrabacter sp. strain DPO360. Expression of this gene, however, could not be detected in Terrabacter sp. strain DPO360 after growth with dibenzofuran.
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页码:53 / 62
页数:10
相关论文
共 71 条
[1]  
ALTENBUCHNER J, 1992, METHOD ENZYMOL, V216, P457
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]   Cloning, nucleotide sequence, and characterization of the genes encoding enzymes involved in the degradation of cumene to 2-hydroxy-6-oxo-7-methylocta-2,4-dienoic acid in Pseudomonas fluorescens IP01 [J].
Aoki, H ;
Kimura, T ;
Habe, H ;
Yamane, H ;
Kodama, T ;
Omori, T .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1996, 81 (03) :187-196
[4]   3 DIFFERENT 2,3-DIHYDROXYBIPHENYL-1,2-DIOXYGENASE GENES IN THE GRAM-POSITIVE POLYCHLOROBIPHENYL-DEGRADING BACTERIUM RHODOCOCCUS-GLOBERULUS P6 [J].
ASTURIAS, JA ;
TIMMIS, KN .
JOURNAL OF BACTERIOLOGY, 1993, 175 (15) :4631-4640
[5]   SUICIDE INACTIVATION OF CATECHOL 2,3-DIOXYGENASE FROM PSEUDOMONAS-PUTIDA MT-2 BY 3-HALOCATECHOLS [J].
BARTELS, I ;
KNACKMUSS, HJ ;
REINEKE, W .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1984, 47 (03) :500-505
[6]   EVIDENCE OF HISTIDINE COORDINATION TO THE CATALYTIC FERROUS ION IN THE RING-CLEAVLNG 2,2',3-TRIHYDROXYBIPHENYL DIOXYGENASE FROM THE DIBENZOFURAN-DEGRADING BACTERIUM SPHINGOMONAS SP STRAIN RW1 [J].
BERTINI, I ;
CAPOZZI, F ;
DIKIY, A ;
HAPPE, B ;
LUCHINAT, C ;
TIMMIS, KN .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 215 (03) :855-860
[7]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]  
BUNZ P, 1993, BIODEGRADATION, V4, P1471
[9]  
BUNZ PV, 1993, J BACTERIOL, V175, P6467
[10]   BACTERIAL AND FUNGAL OXIDATION OF DIBENZOFURAN [J].
CERNIGLIA, CE ;
MORGAN, JC ;
GIBSON, DT .
BIOCHEMICAL JOURNAL, 1979, 180 (01) :175-185