生物
毕赤酵母
多克隆站点
基因
表达式向量
基因表达
GenBank公司
计算生物学
载体(分子生物学)
遗传学
细胞生物学
分子生物学
重组DNA
作者
Irina B. Sears,J. Patrick O’Connor,Olivia W. Rossanese,Benjamin S. Glick
出处
期刊:Yeast
[Wiley]
日期:1998-06-15
卷期号:14 (8): 783-790
被引量:159
标识
DOI:10.1002/(sici)1097-0061(19980615)14:8<783::aid-yea272>3.0.co;2-y
摘要
The budding yeast Pichia pastoris is an attractive system for exploring certain questions in cell biology, but experimental use of this organism has been limited by a lack of convenient expression vectors. Here we describe a set of compact vectors that should allow for the expression of a wide range of endogenous or foreign genes in P. pastoris. A gene of interest is inserted into a modified pUC19 polylinker; targeted integration into the genome then results in stable and uniform expression of this gene. The utility of these vectors was illustrated by expressing the bacterial β-glucuronidase (GUS) gene. Constitutive GUS expression was obtained with the strong GAP promoter or the moderate YPT1 promoter. The regulatable AOX1 promoter yielded very strong GUS expression in methanol-grown cells, negligible expression in glucose-grown cells, and intermediate expression in mannitol-grown cells. GenBank Accession Numbers are: pIB1, AF027958; pIB2, AF027959; pIB3, AF027960; pIB4, AF027961. © 1998 John Wiley & Sons, Ltd.
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