Cloning and expression of organic solvent tolerant lipase gene from Staphylococcus saprophyticus M36 / 生物工程学报
Chinese Journal of Biotechnology
; (12): 1989-1995, 2009.
Article
de Zh
| WPRIM
| ID: wpr-336277
Bibliothèque responsable:
WPRO
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, 25 degrees C 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.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Composés chimiques organiques
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Solvants
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Stabilité enzymatique
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Protéines recombinantes
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Données de séquences moléculaires
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Séquence nucléotidique
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Chimie
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Séquence d'acides aminés
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Clonage moléculaire
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Escherichia coli
langue:
Zh
Texte intégral:
Chinese Journal of Biotechnology
Année:
2009
Type:
Article