穿梭机载体
多克隆站点
生物
克隆载体
质粒
安培电阻
遗传学
限制酶
枯草芽孢杆菌
多克隆位点
大肠杆菌
克隆(编程)
分子生物学
载体(分子生物学)
重组DNA
基因
细菌
计算机科学
程序设计语言
作者
Hiromi Ishiwa,Harue Shibahara
出处
期刊:The Japanese Journal of Genetics
[The Genetics Society of Japan]
日期:1985-01-01
卷期号:60 (3): 235-243
被引量:56
摘要
In vivo and in vitro recombination techniques were used to construct a new cloning vector, pHY300PLK (4.7 kb) from the shuttle vector pHY460 (7kb). The newly derived shuttle vector can replicate and express the tetracycline resistance gene (TcR) in both Escherichia coli and Bacillus subtilis. pHY300PLK contains the TcR gene, the ampicillin resistance gene (ApR), two replication origins for E. coli and B. subtilis and a polylinker derived from πAN7. The unique cloning sites are BalI, BamHI, BanI, BglI, BglII, BstEII, EcoRI, EcoRV, HindIII, HpaI, SalI, SmaI, PvuI and XbaI, pHY300 PLK is characterized as a copy-number mutant in E. coli. (Key words: shuttle vector; B, subtilis; tetracycline; ampicillin; copy-number mutant; incompatibility)
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