Cloning and expression of organic solvent tolerant lipase gene from Staphylococcus saprophyticus M36
DOI:
CSTR:
Author:
Affiliation:

Clc Number:

Fund Project:

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).

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    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.

    Reference
    Related
    Cited by
Get Citation

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

Copy
Share
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:September 16,2009
  • Revised:
  • Adopted:
  • Online:
  • Published:
Article QR Code