Phosphate-Responsive Promoter of a Pichia pastoris Sodium Phosphate Symporter

被引:46
作者
Ahn, Jungoh [1 ]
Hong, Jiyeon [1 ]
Park, Myongsoo [1 ]
Lee, Hyeokweon [1 ]
Lee, Eungyo [1 ]
Kim, Chunsuk [1 ]
Lee, Joohwan [1 ]
Choi, Eui-sung [2 ]
Jung, Joon-ki [1 ]
Lee, Hongweon [1 ]
机构
[1] KRIBB, Ctr Biotechnol Proc Engn, Taejon 305806, South Korea
[2] KRIBB, Syst Microbiol Res Ctr, Taejon 305806, South Korea
关键词
HETEROLOGOUS-PROTEIN-PRODUCTION; SACCHAROMYCES-CEREVISIAE; ESCHERICHIA-COLI; ALKALINE-PHOSPHATASE; REGULATED PROMOTER; EXPRESSION; GENE; NITROGEN; SEQUENCE; SYSTEM;
D O I
10.1128/AEM.02913-08
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 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
To develop a functional phosphate-regulated promoter in Pichia pastoris, a phosphate-responsive gene, P-HO89, which encodes a putative sodium (Na+)-coupled phosphate symporter, was isolated. Sequencing analyses revealed a 1,731-bp open reading frame encoding a 576-amino-acid polypeptide with 12 putative transmembrane domains. The properties of the PHO89 promoter (P-PHO89) were investigated using a bacterial lipase gene as a reporter in 5-liter jar fermentation experiments. P-PHO89 was tightly regulated by phosphate and was highly activated when the cells were grown in a phosphate-limited external environment. Compared to translation elongation factor 1 alpha and the glyceraldehyde-3-phosphate dehydrogenase promoter, P-PHO89 exhibited strong transcriptional activity with higher specific productivity (amount of lipase produced/cell/h). Furthermore, a cost-effective and simple P-PHO89-based fermentation process was developed for industrial application. These results demonstrate the potential for efficient use of P-PHO89 for controlled production of recombinant proteins in P. pastoris.
引用
收藏
页码:3528 / 3534
页数:7
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