乌拉3
质粒
生物
穿梭机载体
低拷贝数
酿酒酵母
酵母
遗传学
自主复制序列
可选择标记
分子生物学
复制的起源
载体(分子生物学)
基因
重组DNA
作者
Thomas Christianson,Robert Sikorski,Michael Dante,James H. Shero,Philip Hieter
出处
期刊:Gene
[Elsevier BV]
日期:1992-01-01
卷期号:110 (1): 119-122
被引量:1469
标识
DOI:10.1016/0378-1119(92)90454-w
摘要
A set of four yeast shuttle vectors that incorporate sequences from the Saccharomyces cerevisiae 2 mu endogenous plasmid has been constructed. These yeast episomal plasmid (YEp)-type vectors (pRS420 series) differ only in their yeast selectable markers, HIS3, TRP1, LEU2 or URA3. The pRS420 plasmids are based on the backbone of a multifunctional phagemid, pBluescript II SK+, and share its useful properties for growth in Escherichia coli and manipulation in vitro. The pRS420 plasmids have a copy number of about 20 per cell, equivalent to that of YEp24. During non-selective yeast growth, pRS420 plasmids are lost through mitotic segregation at rates similar to other YEp vectors and yeast centromeric plasmid (YCp) vectors, in the range of 1.5-5% of progeny per doubling. The pRS420 series provides high-copy-number counterparts to the current pRS vectors [Sikorski and Hieter, Genetics 122 (1989) 19-27].
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