High-level expression of Candida parapsilosis lipase/acyltransferase in Pichia pastoris

被引:72
作者
Brunel, L
Neugnot, V
Landucci, L
Boze, WN
Moulin, G
Bigey, F [1 ]
Dubreucq, E
机构
[1] Univ Montpellier 2, ENSAM, INRA, UMR Ingn React Biol Bioprod IR2B, F-34095 Montpellier 5, France
[2] ENSAM, INRA, F-34060 Montpellier 1, France
关键词
Candida parapsilosis lipase/acyltransferase; Pichia pastoris; heterologous protein production; high-cell density fed-batch culture;
D O I
10.1016/j.jbiotec.2004.03.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Candida parapsilosis has been previously shown to produce a lipase/acyltransferase (EC 3.1.1.3) that preferentially catalyses transfer reactions such as alcoholysis over hydrolysis in the presence of suitable nucleophiles other than water, even in aqueous media (a(w) > 0.9). This enzyme has been shown to belong to a new family of lipases. The present work describes the cloning of the gene coding for this lipase/acyltransferase in the yeast Pichia pastoris and the heterologous high-level expression of the recombinant enzyme. The lipase/acyltransferase gene, in which the sequence encoding the signal peptide was replaced by that of the alpha-factor of Saccharomyces cerevisiae, was placed under the control of the methanol inducible promoter of the alcohol oxidase 1 gene (AOX1). A transformed P. pastoris clone, containing five copies of the lipase/acyltransferase gene, was selected for the production of recombinant enzyme. The fed-batch culture supernatant contained 5.8 g l(-1) (weighted) of almost pure recombinant lipase/acyltransferase displaying the same catalytic behavior as the original enzyme. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 50
页数:10
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