Leow, Thean Chor and Raja Abdul Rahman, Raja Noor Zaliha and Basri, Mahiran and Salleh, Abu Bakar (2004) High Level Expression of Thermostable Lipase from Geobacillus sp. Strain T1. Bioscience, Biotechnology, and Biochemistry, 68 (1). pp. 96-103. ISSN 0916-8451
Full text not available from this repository.
Official URL: http://dx.doi.org/10.1271/bbb.68.96
A thermostable extracellular lipase of Geobacillus sp. strain T1 was cloned in a prokaryotic system. Sequence analysis revealed an open reading frame of 1,251 bp in length which codes for a polypeptide of 416 amino acid residues. The polypeptide was composed of a signal peptide (28 amino acids) and a mature protein of 388 amino acids. Instead of Gly, Ala was substituted as the first residue of the conserved pentapeptide Gly-X-Ser-X-Gly. Successful gene expression was obtained with pBAD, pRSET, pET, and pGEX as under the control of araBAD, T7, T7 lac, and tac promoters, respectively. Among them, pGEX had a specific activity of 30.19 Umg−1 which corresponds to 2927.15 Ug−1 of wet cells after optimization. The recombinant lipase had an optimum temperature and pH of 65°C and pH 9, respectively. It was stable up to 65°C at pH 7 and active over a wide pH range (pH 6–11). This study presents a rapid cloning and overexpression, aimed at improving the enzyme yield for successful industrial application.
|Keyword:||Geobacillus sp., thermostable lipase, Glutathione S-transferase (GST) fusion protein, cloning; overexpression|
|Faculty or Institute:||Faculty of Environmental Studies|
|Publisher:||Japan Society for Bioscience, Biotechnology, and Agrochemistry|
|Deposited By:||Erni Suraya Abdul Aziz|
|Deposited On:||17 May 2010 10:56|
|Last Modified:||17 May 2010 10:57|
Repository Staff Only: item control page