质粒
酿酒酵母
穿梭机载体
生物
同源重组
多克隆站点
表达式向量
绿色荧光蛋白
基因
FLP-FRT重组
大肠杆菌
克隆载体
异源的
遗传学
异源表达
分子生物学
基因表达
载体(分子生物学)
分子克隆
遗传重组
重组DNA
重组
出处
期刊:Methods in molecular biology
日期:2012-01-01
卷期号:: 41-46
被引量:3
标识
DOI:10.1007/978-1-61779-770-5_4
摘要
Expression plasmids for Saccharomyces cerevisiae offer a wide choice of vector copy number, promoters of varying strength and selection markers. These expression plasmids are usually shuttle vectors that can be propagated both in yeast and bacteria, making them useful in gene cloning. For heterologous production of membrane proteins, we used the green fluorescent protein (GFP) fusion technology which was previously developed in the Escherichia coli system. We designed an expression plasmid carrying an inducible GAL1 promoter, a gene encoding a membrane protein of interest and the GFP-octa-histidine sequence. Here we describe construction of multi-copy yeast expression plasmids by homologous recombination in S. cerevisiae.
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