National High Technology Research and Development Program of China (863 Program)?(No. 2008AA10Z309), Natural Foundation of Jiangsu (No. BK2007160), High Technology Program of Jiangsu (No. BE2008308).
Lipases are important biocatalysts that are widely used in food processing and bio-diesel production. However, organic solvents could inactivate some lipases during applications. Therefore, the efficient cloning and expression of the organic solvent-tolerant lipase is important to its application. In this work, we first found out an organic solvent-tolerant lipase from Staphylococcus saprophyticus M36 and amplified the 741 bp Lipase gene lip3 (GenBank Accession No. FJ979867), by PCR, which encoded a 31.6 kD polypeptide of 247 amino acid residues. But the lipase shared 83% identity with tentative lip3 gene of Staphylococcus saprophyticus (GenBank Accession No. AP008934). We connected the gene with expression vector pET-DsbA, transformed it into Escherichia coli BL21 (DE3), and obtained the recombinant pET-DsbA-lip3. With the induction by 0.4 mmol/L of isopropyl beta-D-thiogalactopyranoside at pH 8.0, OD600 1.0, 25oC for 12 h, the lipase activity reached up to 25.8 U/mL. The lipase expressed was stable in the presence of methanol, n-hexane, and isooctane, n-heptane.
汤彦翀,卢亚萍,吕凤霞,别小妹,郭瑶,陆兆新. 腐生葡萄球菌M36耐有机溶剂脂肪酶基因的克隆与原核表达[J]. Chinese Journal of Biotechnology, 2009, 25(12): 1989-1995
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