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Cloning and Sequence Analysis of the hpaD Gene Responsible for Homoprotocatechuate 2,3-Dioxygenase from Pseudomonas sp. DJ-12
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Cloning and Sequence Analysis of the hpaD Gene Responsible for Homoprotocatechuate 2,3-Dioxygenase from Pseudomonas sp. DJ-12
Sang-Mahn Lee , Jong-Chan Chae 1, Youngsoo Kim 2, Chi-Kyung Kim 1
Journal of Microbiology 2001;39(4):334-337

Department of Life Science, Chongju University, Cheongju 360-764, Korea; 1 Department of Microbiology and Biotechnology, and 2 Department of Pharmacy,Department of Life Science, Chongju University, Cheongju 360-764, Korea; 1 Department of Microbiology and Biotechnology, and 2 Department of Pharmacy,
Corresponding author:  Chi-Kyung Kim , Tel: 82-43-261-2300, 
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The degradative pathway of homoprotocatechuate (HPC) is the bacterial route whereby 3,4-dihydroxyphenylacetic acid is catabolized to pyruvate and succinate by a series of sequential reactions. The HPC is catalized by homoprotocatechuate 2,3-dioxygenase (HPC-2,3O) to form 5-carboxymethyl-2-hydroxy-muco semialdehyde. In this study, the hpaD gene encoding HPC-2,3O was cloned from the chromosomal DNA of Pseudomonas sp. DJ-12 and its nucleotide sequence was analyzed. The open reding frame of hpaD gene was found to be composed of 864 nucleotide pairs and to encode a polypeptide with 287 amino acid residues. The deduced amino acid sequence of the HPC-2,3O from Pseudomonas sp. DJ-12 exhibited 60~64% homology with those of the corresponding enzymes from E. coli, Salmonella enterica, and Klebsiella pneumoniae.

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    Cloning and Sequence Analysis of the hpaD Gene Responsible for Homoprotocatechuate 2,3-Dioxygenase from Pseudomonas sp. DJ-12
    J. Microbiol. 2001;39(4):334-337.
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