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两组编码具有新启动子特异性的RNA聚合酶的荚膜特异性大肠杆菌噬菌体。

Two groups of capsule-specific coliphages coding for RNA polymerases with new promoter specificities.

作者信息

Dietz A, Andrejauskas E, Messerschmid M, Hausmann R

出版信息

J Gen Virol. 1986 May;67 ( Pt 5):831-8. doi: 10.1099/0022-1317-67-5-831.

Abstract

Four bacteriophages (A16, CK235, phi 1.2 and K31) which specifically attack different encapsulated strains of Escherichia coli have been shown to be related to bacteriophage T7 (which is unable to grow on encapsulated hosts). The conclusion that phages A16 and CK235 are related to T7 is based on similarities in the pattern of expression of intracellular phage proteins, early appearance, in infected host cells, of a phage DNA-specific RNA polymerase and hybridization (albeit to a low extent) of A16 DNA and of CK235 DNA to T7 DNA. The first two criteria also apply to phages phi 1.2 and K31 but hybridization of their DNAs with T7 DNA could not be detected. The RNA polymerases of CK235 and A16 have similar template specificities and the same applies to the RNA polymerases of phi 1.2 and K31. None of the new RNA polymerases can use T7 DNA as template.

摘要

四种专门攻击不同荚膜化大肠杆菌菌株的噬菌体(A16、CK235、phi 1.2和K31)已被证明与噬菌体T7(无法在荚膜化宿主上生长)有关。噬菌体A16和CK235与T7相关这一结论基于细胞内噬菌体蛋白质表达模式的相似性、感染宿主细胞中噬菌体DNA特异性RNA聚合酶的早期出现以及A16 DNA和CK235 DNA与T7 DNA的杂交(尽管程度较低)。前两个标准也适用于噬菌体phi 1.2和K31,但未检测到它们的DNA与T7 DNA的杂交。CK235和A16的RNA聚合酶具有相似的模板特异性,phi 1.2和K31的RNA聚合酶也是如此。新的RNA聚合酶均不能将T7 DNA用作模板。

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