A novel Streptomyces spp. integration vector derived from the S. venezuelae phage, SV1.

A novel Streptomyces spp. integration vector derived from the S. venezuelae phage, SV1.
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DOI:
10.1186/1472-6750-14-51
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发表时间:
2014-05-30
期刊:
影响因子:
3.5
通讯作者:
Smith MC
Smith MC
中科院分区:
工程技术3区
文献类型:
--
作者:
Fayed B;Younger E;Taylor G;Smith MC

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基于温带链霉菌int/attP基因座的整合载体是一种方便且应用广泛的载体,尤其适用于链霉菌的基因克隆。我们已经构建并测试了一种新的整合载体的基础上g27,编码整合酶,和attP网站从噬菌体,SV 1。该质粒pBF 3在S. coelicolor和S.但令人惊讶的是,在S.委内瑞拉,噬菌体SV 1的天然宿主。pBF 3有望成为一个有用的除了目前可用于链霉菌分子遗传学的整合载体的范围。
Integrating vectors based on the int/attP loci of temperate phages are convenient and used widely, particularly for cloning genes in Streptomyces spp. We have constructed and tested a novel integrating vector based on g27, encoding integrase, and attP site from the phage, SV1. This plasmid, pBF3 integrates efficiently in S. coelicolor and S. lividans but surprisingly fails to generate stable integrants in S. venezuelae, the natural host for phage SV1. pBF3 promises to be a useful addition to the range of integrating vectors currently available for Streptomyces molecular genetics.
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