SEQUENCE OF THE PLASMID-ENCODED CATECHOL 1,2-DIOXYGENASE-EXPRESSING GENE, PHEB, OF PHENOL-DEGRADING PSEUDOMONAS-SP STRAIN EST1001

被引:47
|
作者
KIVISAAR, M
KASAK, L
NURK, A
机构
[1] Laboratory of Plasmid Biology, Estonian Biocenter 202400 Tartu,
关键词
RECOMBINANT DNA; PROMOTER; TRANSPOSON TN4652; EXPRESSION IN ESCHERICHIA-COLI AND PSEUDOMONAS-PUTIDA; PYROCATECHASES;
D O I
10.1016/0378-1119(91)90098-V
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Phenol monooxygenase (PMO) and catechol 1,2-dioxygenase (C120), the two first enzymes of the phenol-degradation pathways, are encoded by a 3.4-kb DNA fragment cloned from Pseudomonas sp. EST1001 plasmid DNA. We have previously shown that activation of the cloned genes in Pseudomonas putida PaW85 is controlled by insertion of the 17-kb transposon, Tn4652, from the host chromosome into the plasmid carrying these genes [Kivisaar et al. Plasmid 24 (1990) 25-36]. Transcription of the DNA encoding PMO (pheA) and C120 (pheB) is activated by a promoter located on a 0.2-kb SacI-ClaI fragment from Tn4652. We have determined the nucleotide sequence of pheB. The 906-bp gene encodes a protein product with a deduced M(r) of 33 362. The relationship between the pheB gene and other C12O-encoding genes has been shown: comparison of the pheB sequence with sequences of catA of Alcaligenes calcoaceticus, tfdC of A. eutrophus and clcA of P. putida demonstrated that there are conserved residues in all the four protein products of these genes.
引用
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页码:15 / 20
页数:6
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