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首页> 外文期刊>Biological chemistry >Does BcgI, a Unique Restriction Endonuclease, Require Two Recognition Sites for Cleavage?
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Does BcgI, a Unique Restriction Endonuclease, Require Two Recognition Sites for Cleavage?

机译:BcgI(唯一的限制性内切核酸酶)是否需要两个识别位点才能进行切割?

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BcgI is a multi-subunit restriction-modification (R-M) complex. BcgI prefers pBR322 DNA over pUC19 in a DNA cleavage reaction. Linearized pBR322 contains two BcgI recognition sites and pUC19 has only one site. To test whether two target sites are required for BcgI cleavage, one of the two sites in pBR322 was deleted, and as a result pBR322-1 became a poor substrate for BcgI. Conversely, adding a BcgI site to pUC19 makes it a much better substrate for BcgI cleavage. In addition, the BcgI (R-M) complex forms a heterohexamer in solution that is capable of interacting with two recognition sites. Our results suggest that BcgI requires two recognition sites for cleavage.
机译:BcgI是一个多亚基限制修饰(R-M)复合物。在DNA裂解反应中,BcgI比pUC19更喜欢pBR322 DNA。线性化的pBR322包含两个BcgI识别位点,而pUC19仅具有一个位点。为了测试BcgI切割是否需要两个靶位点,pBR322中的两个位点之一被删除,结果pBR322-1成为BcgI的较差底物。相反,在pUC19中添加BcgI位点使其成为BcgI切割的更好的底物。另外,BcgI(R-M)复合物在溶液中形成能够与两个识别位点相互作用的异六聚体。我们的结果表明,BcgI需要两个识别位点进行切割。

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