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[Cloning, expression and characterization of a novel lipase gene lipB from Aspergillus niger F044] Wei sheng wu xue bao = Acta microbiologica Sinica [Wei Sheng Wu Xue Bao] Journal article

 
Yang J, Zhang Z, Liu L, Yan Y 
[Cloning, expression and characterization of a novel lipase gene lipB from Aspergillus niger F044] [English Abstract, Journal Article, Research Support, Non-U.S. Gov't]
Wei Sheng Wu Xue Bao 2009 Aug 4; 49(8):1095-101.


OBJECTIVE: We cloned, expressed and characterized a novel lipase gene lipB from Aspergillus niger F044, to facilitate the large scale production and application of that enzyme.
METHOD: We cloned lipB gene and the cDNA sequence by PCR and RT-PCR, and then cloned the open reading frame of lipB into pET28a vector and expressed by isopropyl beta-D-1-thiogalactopyranoside (IPTG) induction. After Ni-agarose purification, the characteristics were determined and the conformation change was checked by circular dichroism methods.
RESULTS: The novel lipase genes cDNA of lipB were cloned from Aspergillus niger F044 (GenBank: FJ536287, FJ536288) and expressed in Escherichia coli. The molecular weight of LipB was about 43 kDa. The optimal substrate of this enzyme is 4-nitrophenyl octanoate (pNPC-C8) with Km = 5.98 mmol/L. The optimal temperature and pH was 50 degrees C and pH 6.0. The enzyme was stable below 40 degrees C. After incubated at 60 degrees C for 1 h, only 18.8% activity remained. After treated by 2 mmol/L Ca2+ for 1 h, the activity improved 2.6-fold.
CONCLUSION: Enzymatic characteristics of LipB determined showed this enzyme might have potential in industrial applications.



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