毕赤酵母
生物化学
共转运蛋白
生物
磷酸盐
分子生物学
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脂肪酶
基因
化学
重组DNA
酶
肽序列
运输机
作者
Jungoh Ahn,Jiyeon Hong,Myongsoo Park,Hyeokweon Lee,Eungyo Lee,Chun-Suk Kim,Joo-Hwan Lee,Eui‐Sung Choi,Joon‐Ki Jung,Hongweon Lee
摘要
To develop a functional phosphate-regulated promoter in Pichia pastoris, a phosphate-responsive gene, PHO89, 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 1alpha 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.
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