Cloning and heterologous expression of two cold-active lipases from the Antarctic bacterium Psychrobacter sp. G

• Published in: Polar research Vol. 29; no. 3; pp. 421 - 429
• Main Authors: Xuezheng, Lin, Shuoshuo, Cui, Guoying, Xu, Shuai, Wang, Ning, Du, Jihong, Shen
• Format: Journal Article
• Language: English
• Published: Oxford Routledge 01.01.2010; Wiley-Blackwell
• Subjects: Animal, plant and microbial ecology; Antarctic; Bacteriology; Biological and medical sciences; cold-active lipase; Fundamental and applied biological sciences. Psychology; gene cloning; gene expression; Metabolism. Enzymes; Microbial ecology; Microbiology; Psychrobacter; Various environments (extraatmospheric space, air, water); Antarctica; Temperature; gene cloning; Cold; Enzyme; cold-active lipase; Environmental factor; Ecology; Gene expression; Antarctic; Climatic zone; Genetic transfer; Psychrobacter; Bacteria; Polar region; Lipolytic enzyme
• ISSN: 0800-0395; 1751-8369; 1751-8369
• DOI: 10.3402/polar.v29i3.6087

Antarctic bacteria producing extracellular lipolytic enzymes with activity at low temperature were isolated, and the most promising strain, named G, was identified as a Psychrobacter species based on 16S rDNA sequence alignment. The genomic DNA of this bacterium was used to construct its plasmid genomic library into pUC118 plasmid vectors, and to screen the cold-active lipolytic enzyme genes. Two genes encoding for cold-active lipolytic enzymes, Lip-1452 (with an open reading frame of 1452 bp in length) and Lip-948 (with an open reading frame of 948 bp in length), were screened. The primary structure of the two lipases deduced from the nucleotide sequence showed a consensus pentapeptide containing the active serine (Lip-1452, GDSAG, and Lip-948, GNSMG) and a conserved His-Gly dipeptide in the N-terminal part of the enzyme. Protein sequence alignment and conserved regions analysis indicated that the two lipases probably belonged to family IV and family V of the bacterial lipolytic enzymes, respectively. The upstream and downstream sequences of the two lipolytic lipases were also obtained. The two lipase genes were cloned into the expression vector pCold III and integrated into Escherichia coli BL21 (DE3). The functional expression of both lipase genes by E. coli BL21 (DE3) cells was observed as the formation of clear haloes around colonies on a 1% (vol/vol) tributyrin plate upon induction with isopropyl-b-Dthiogalactopyranoside at 5°C. A lipase activity assay showed that the specific activity of the pCold III+Lip-948 expression system was up to 3.7 U ml, -1 , whereas that of pCold III+Lip-1452 was very low.