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Physical Analysis of nahQ and tnpA Genes from Pseudomonas fluorescens
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HOME > J. Microbiol > Volume 39(4); 2001 > Article
Physical Analysis of nahQ and tnpA Genes from Pseudomonas fluorescens
Ja-Young Seol , Soon-Young Choi 1, Kyung Hee Min
Journal of Microbiology 2001;39(4):338-342

Department of Life Science, Sookmyung Women's University, Seoul 140-742, Korea; 1 Division of Molecular Biology, Ewha Women's University, Seoul 120-75Department of Life Science, Sookmyung Women's University, Seoul 140-742, Korea; 1 Division of Molecular Biology, Ewha Women's University, Seoul 120-75
Corresponding author:  Kyung Hee Min , Tel: 82-2-710-9415, 
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Pseudomonas fluorescens SM11 is a naphthalene-degrading strain whose dissimilatory genes are chromosomally encoded. We have cloned the 2.9 kb Sal I fragment harboring genes for the naphthalene-degradation upper pathway. The nucleotide sequences were determined to be nahQ, tnpA, and partial regions of nahE genes. The nahQ encodes a protein of 188 amino acid residues with a deduced molecular weight of 20.8 kDa. The high homology with other proteins suggests that NahQ may be an active and useful protein which gives a selective advantage to naphthalene degradation. Transposase(TnpA) encodes a polypeptide chain with a molecular mass of 41.8 kDa consisting of 376 amino acid residues. The deduced anino acid sequence of tnpA revealed 96% idenitity with putative transposase of P. stutzeri OX1. It was assumed that transposase plays an important role in the evolution of the catabolic-pathway in the regulation of nah expression.

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    Physical Analysis of nahQ and tnpA Genes from Pseudomonas fluorescens
    J. Microbiol. 2001;39(4):338-342.
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