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原生质球制剂中大肠杆菌素E2诱导的脱氧核糖核酸降解的重建

Reconstitution of colicin E2-induced deoxyribonucleic acid degradation in spheroplast preparations.

作者信息

Almendinger R, Hager L P

出版信息

Antimicrob Agents Chemother. 1973 Aug;4(2):167-77. doi: 10.1128/AAC.4.2.167.

Abstract

Spheroplasts are insensitive to colicin E(2) and do not show deoxyribonucleic acid (DNA) degradation even in the presence of massive amounts of E(2). However, when both endonuclease I and E(2) were present, spheroplast DNA was degraded by an endonucleolytic activity which gave rise primarily to double-strand DNA cleavages, producing fragments having an average molecular weight of 9 x 10(6). Pancreatic ribonuclease could substitute for colicin E(2) in the reconstitution system, but pancreatic deoxyribonuclease could not replace endonuclease I. However, colicin E(2) could not activate transfer ribonucleic acid-inhibited endonuclease I in an in vitro system where pancreatic ribonuclease caused full stimulation.

摘要

原生质球对大肠杆菌素E(2)不敏感,即使存在大量的E(2),也不会出现脱氧核糖核酸(DNA)降解。然而,当核酸内切酶I和E(2)同时存在时,原生质球DNA会被一种核酸内切活性降解,这种活性主要导致双链DNA断裂,产生平均分子量为9×10(6)的片段。胰腺核糖核酸酶可以在重组系统中替代大肠杆菌素E(2),但胰腺脱氧核糖核酸酶不能替代核酸内切酶I。然而,在胰腺核糖核酸酶能完全刺激的体外系统中,大肠杆菌素E(2)不能激活被转移核糖核酸抑制的核酸内切酶I。

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