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Cloning and expression in E. coli of the HOPDA hydrolase gene from pseudomonas sp. P 20
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HOME > J. Microbiol > Volume 34(4); 1996 > Article
Cloning and expression in E. coli of the HOPDA hydrolase gene from pseudomonas sp. P 20
Lim, Jong Chul , Chae, Jong Chan , Kim, Hyong Bai 2, Kim, Chi Kyung
Journal of Microbiology 1996;34(4):349-354

Department of Microbiology; ¹Department of Pharmacy, Chungbuk National University; ²Department of Biotechnology, Korea UniversityDepartment of Microbiology; ¹Department of Pharmacy, Chungbuk National University; ²Department of Biotechnology, Korea University
Corresponding author:  Kim, Chi Kyung ,
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Pseudomonas sp. P20 is a natural isolate which is capable of degrading biphenyl and 4-chlorobiphenyl. From a clone of pCK1022 harboring pcbCD genes of Pseudomonas sp P20, a pcbD gene encoding 2-hydroxy-6-oxo-6-phenylhexa-2, 4-dienoic acid (HOPDA) hydrolase was subcloned in Escherichia coli XL-1-Blue by using pBluescript SK(+) vector. The 2.8-kb HindII fragment harboring the pcbD gene cloned in pCK 1024 had a single site for each of XhoI, SalI, BstXI, and XbaI restriction enzymes. Escherichia coli CK1024 had a single site for each of XhoI, SalI, BstXI, and XbaI restriction enzymes. Escherichia coli CK1024 carrying pCK0124 degraded HOPDA to benzoate and 2-hydroxypenta-2, 4-dienoate by HOPDA hydrolase encoded by pcbD gene as effectively as E coli CK 1022 HARBORING pcbCD genes.

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    Cloning and expression in E. coli of the HOPDA hydrolase gene from pseudomonas sp. P 20
    J. Microbiol. 1996;34(4):349-354.
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