| Title | Cloning, Expression in Escherichia coli, and Enzymatic Properties of a Lipase from Pseudomonas sp. SW-3 |
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| Author | Sun-Young An 1 , Sang-Wan Kim 1 , Yong-Lark Choi 1 , Young-Su Cho 1 , Woo-Hong Joo 2 and oung-Choon Lee 1, * |
| Address | 1 Faculty of Biotechnology, College of Natural Resources and Life Science, Dong-A University, Busan 604-714, Korea; 2Department of Biology, Changwon National University, Gyeongnam 641-773, Korea |
| Bibliography | Journal of Microbiology, 41(2),95-101, 2003, |
| DOI | |
| Key Words | DNA cloning, expression, lipase, Pseudomonas, refolding |
| Abstract | The lipase gene (lipA) and its activator gene (lipB) of Pseudomonas sp. SW-3 were cloned and sequenced. The lipB was found to be present immediately downstream of lipA. The deduced amino acid sequences of lipA and lipB showed a high level of homology to those of other lipases belonging to the family I.1 of bacterial lipases. When lipA was expressed in Escherichia coli using T7 promoter, an active lipase was produced in cells carrying both lipA and lipB, but not in cells harboring only lipA. Recombinant lipase (rPSL) overproduced in an insoluble form was solubilized in the presence of 8 M urea, purified in a ureadenatured form and refolded by removing urea in the presence of the Ca^2+ ion. RPLS had maximum activity at pH 8.0 and 50℃, was stable at pHs from 7.0 to 9.0 and below 50 ℃, and showed the highest activity toward the p-nitrophenyl ester of palmitate (C16). |
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