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质粒DNA从大肠杆菌到巴弗洛霉素B1产生菌浅黄链霉菌的属间接合转移

Intergeneric conjugal transfer of plasmid DNA from Escherichia coli to Kitasatospora setae, a bafilomycin B1 producer.

作者信息

Choi Sun-Uk, Lee Chang-Kwon, Hwang Yong-Il, Kinoshita Hiroshi, Nihira Takuya

机构信息

International Center for Biotechnology, Osaka University, 2-1 Yamadaoka, 565-0871 Suita, Osaka, Japan.

出版信息

Arch Microbiol. 2004 Apr;181(4):294-8. doi: 10.1007/s00203-004-0654-8. Epub 2004 Feb 7.

Abstract

An effective transformation procedure for Kitasatospora setae was established based on transconjugation from Escherichia coli ET12567 (pUZ8002) using a phi C31-derived integration vector, pSET152, containing oriT and attP fragments. While no transconjugation was observed under the standard transconjugation conditions for Streptomyces species, sufficient transconjugation (>1 x 10(-6)) was achieved on ISP4 medium containing 30 mM MgCl(2) using a 25- to 125-fold excess of E. coli donor cells. In addition, the sequence and location of the chromosomal integration site attB of K. setae was identified for the first time in genera of non- Streptomyces actinomycetes. K. setae contains a single phi C31 attB site. Similar to the case of Streptomyces species, the attB site of K. setae is present within an ORF encoding a pirin-homolog, but the K. setae-attB sequence deviates slightly from the consensus sequence of Streptomyces attB sequences.

摘要

基于从大肠杆菌ET12567(pUZ8002)进行的接合转移,使用含有oriT和attP片段的phi C31衍生整合载体pSET152,建立了一种有效的刺孢北里孢菌转化程序。虽然在链霉菌属的标准接合转移条件下未观察到接合转移,但使用过量25至125倍的大肠杆菌供体细胞,在含有30 mM MgCl₂的ISP4培养基上实现了足够的接合转移(>1×10⁻⁶)。此外,在非链霉菌放线菌属中首次鉴定了刺孢北里孢菌染色体整合位点attB的序列和位置。刺孢北里孢菌含有单个phi C31 attB位点。与链霉菌属的情况类似,刺孢北里孢菌的attB位点存在于编码pirin同源物的开放阅读框内,但刺孢北里孢菌-attB序列与链霉菌attB序列的共有序列略有偏差。

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