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[寡脱氧核糖核苷酸的2',3'-O-[4-N-(2-氯乙基)-N-甲基氨基]亚苄基衍生物对大肠杆菌16S rRNA的互补定向烷基化作用。III. 16S rRNA与d(pACCTTGTT)rA的亚苄基衍生物相互作用的片段]

[Complementary addressed alkylation of 16s rRNA from Escherichia coli by 2',3'-0-[4-N-(2-chloroethyl)-N-methylamino]benzylidene derivatives of oligodeoxyribonucleotides. III. Segments of 16s rRNA interacting with the benzylidene derivative of d(pACCTTGTT)rA].

作者信息

Zenkova M A, Karpova G G, Levina A S

出版信息

Mol Biol (Mosk). 1989 Jul-Aug;23(4):1057-66.

PMID:2685545
Abstract

16S rRNA chain was cleaved by RNase H within covalent adduct with a 2',3'-0-[4-N-(2-chloroethyl)-N-methylamino]benzylidene derivative of d(pACCTTGTT)rA. It was shown that no less than 50% of cleavage occurs at the 1498-1506 site. The selectivity of alkylation and correspondingly the cleavage by RNase H, at this site practically does not increase when RNA was alkylated to a low extent, and also when a small excess of the reagent in respect to rRNA was used.

摘要

16S rRNA链在与d(pACCTTGTT)rA的2',3'-O-[4-N-(2-氯乙基)-N-甲基氨基]亚苄基衍生物形成的共价加合物内被RNase H切割。结果表明,至少50%的切割发生在1498-1506位点。当RNA烷基化程度较低时,以及相对于rRNA使用少量过量试剂时,该位点的烷基化选择性以及相应的RNase H切割实际上并没有增加。

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