Characterization and solvent stable features of Strep-tagged purified recombinant lipase from thermostable and solvent tolerant Bacillus sp. strain 42

• Main Authors: Tengku Abdul Hamid, Tengku Haziyamin, Eltaweel, Mohamed Abdallah, Raja Abdul Rahman, Raja Noor Zaliha, Basri, Mahiran, Salleh, Abu Bakar
• 格式: Article
• 语言: English
• 出版: Springer 2009
• 在线阅读: http://psasir.upm.edu.my/id/eprint/13533/1/Characterization%20and%20solvent%20stable%20features%20of%20strep.pdf; http://psasir.upm.edu.my/id/eprint/13533/; http://link.springer.com/article/10.1007%2FBF03175607

A 1.2 kb lipase gene (AY 78735) from solvent stable and thermostableBacillus sp. strain 42 was overexpressed in a heterologous system that allowed for an extensive characterization of its solvent stability and thermostability. An overexpression was achieved using pET51b vector withEscherichia coli host strain BL21(DE3)pLysS, in which optimum expression was at 22–24 h incubation at 37°C, with lipase activity reached at 80.0 U mL−1 (specific activity 160.0 U mg−1), after induction by 0.5 mM IPTG. This expression was 11.5 fold higher and superseded the pQE-30UA/M15 (pREP4) host-vector system, which only achieved at 17.0 U mL−1 (34.0 U mg−1). The fusion lipase contains N-terminal Strep-tag II affinity tag that in one step of purification, the lipase was purified to homogeneity using Strep-tag II agarose column. The lipase was purified at 1.3 fold and 70% recovery with the elution fraction gave a band of 43 kDa in SDS-PAGE. The purified fusion lipase was most active at 70°C and pH 8.0, and was stable in a broad pH range of 7–10. It showed hydrolysis preference towards olive, sunflower and corn oils. Based on solvent stability studies in 30 min pre-incubation in 25% v/v solvents with a shaking rate at 150 strokes per min, the purified Lip 42 showed a different residual activity profiles depending on solvents and temperatures. Lip 42 was found be stable in polar organic solvents such as DMSO, DMF, acetone, methanol, heptanol and octanol, which could make it as a potential biocatalyst for the use in industrial biodiesel production.