High-level production and secretion of recombinant proteins by the dimorphic, yeast Arxula adeninivorans

被引:23
|
作者
Wartmann, T
Böer, E
Pico, AH
Sieber, H
Bartelsen, O
Gellissen, G
Kunze, G
机构
[1] Inst Pflanzengenet & Kulturpflanzenforsch, D-06466 Gatersleben, Germany
[2] Rhein Biotech GmbH, D-40595 Dusseldorf, Germany
关键词
Arxula adeninivorans; heterologous gene expression; dimorphism; secretion; transformation;
D O I
10.1111/j.1567-1364.2002.tb00105.x
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
The non-conventional dimorphic thermo- and salt-resistant yeast Arxula adeninivorans has been developed as a host for heterologous gene expression. For assessment of the system two model genes have been selected: the GFP gene encoding the intracellular green fluorescent protein, and the HSA gene encoding the secreted human serum albumin. The expression system includes two host strains, namely A. adeninivorans LS3, which forms budding cells at 30degreesC and mycelia at >42degreesC, and the strain A. adeninivorans 135, which forms mycelia at temperatures as low as 30degreesC. For expression control the constitutive A. adeninivorans-derived TEF1-promoter and S. cerevisiae-derived PHO5-terminator were selected. The basic A. adeninivorans transformation/expression vector pAL-HPH1 is further equipped with the Escherichia coli-derived hph gene conferring hygromycin B resistance and the 25S rDNA from A. adeninivorans for rDNA targeting. Transformants were obtained for both budding cells and mycelia. In both cell types similar expression levels were achieved and the GFP was localised in the cytoplasm while more than 95% of the HSA accumulated in the culture medium. In initial fermentation trials on a 200-ml shake flask scale maximal HSA product levels were observed after 96 h of cultivation. 0 2002 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:363 / 369
页数:7
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