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Rac-大肠杆菌K12菌株携带λ rev的优先附着位点。

Rac-E. coli K12 strains carry a preferential attachment site for lambda rev.

作者信息

Diaz R, Kaiser K

出版信息

Mol Gen Genet. 1981;183(3):484-9. doi: 10.1007/BF00268769.

Abstract

Lambda rev is a hybrid lambdoid phage formed by recombination between lambda and a defective lambdoid prophage (Rac) present in most E. coli K12 derivatives. We show here that three independently derived Rac-E. coli K12 strains are specifically deleted for the entire Rac prophage consistent with loss of Rac by excisive recombination between hybrid attachment sites that flank the prophage (c.f. excision of a lambda prophage). lambda rev, in which int and PP' of lambda have been replaced by integrative recombination genes and an attachment site derived from Rac (Gottesman et al. 1974), integrates site-specifically and in the correct orientation at the preferential attachment site generated by Rac excision.

摘要

λrev是一种混合λ样噬菌体,由λ与大多数大肠杆菌K12衍生物中存在的缺陷λ样原噬菌体(Rac)之间的重组形成。我们在此表明,三个独立衍生的Rac-大肠杆菌K12菌株中,整个Rac原噬菌体被特异性删除,这与原噬菌体两侧的杂种附着位点之间通过切除性重组导致Rac丢失一致(参见λ原噬菌体的切除)。λrev中,λ的int和PP'已被整合重组基因和源自Rac的附着位点取代(戈特斯曼等人,1974年),它在Rac切除产生的优先附着位点上进行位点特异性且方向正确的整合。

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