CLONING AND NUCLEOTIDE-SEQUENCE OF ANAEROBICALLY INDUCED PORIN PROTEIN-E1 (OPRE) OF PSEUDOMONAS-AERUGINOSA PAO1

被引:36
作者
YAMANO, Y
NISHIKAWA, T
KOMATSU, Y
机构
[1] Kanzakigawa Laboratory, Shionogi Research Laboratories, Shionogi & Co., Ltd, Toyonaka, Osaka, 561
关键词
D O I
10.1111/j.1365-2958.1993.tb01643.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The porin oprE gene of Pseudomonas aeruginosa PAO1 was isolated. Its nucleotide sequence indicated that the structural gene of 1383 nucleotide residues encodes a precursor consisting of 460 amino acid residues with a signal peptide of 29 amino acid residues, which was confirmed by the N-terminal 23-amino-acid sequence and the reaction with anti-OprE polyclonal antiserum. Anaerobiosis induced OprE production at the transcription level. The transcription start site was determined to be 40 nucleotides upstream from the ATG initiation codon. The control region contained an appropriately situated Esigma54 recognition site and the putative second half of an ANR box. The amino acid sequence of OprE had some clusters of sequence homologous with that of OprD of P. aeruginosa, which might be responsible for the outer membrane permeability of imipenem and basic amino acids.
引用
收藏
页码:993 / 1004
页数:12
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