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大肠杆菌和噬菌体λ宿主修饰的脱氧核糖核酸中的甲基化碱基。

Methylated bases in the host-modified deoxyribonucleic acid of Escherichia coli and bacteriophage lambda.

作者信息

Gough M, Lederberg S

出版信息

J Bacteriol. 1966 Apr;91(4):1460-8. doi: 10.1128/jb.91.4.1460-1468.1966.

Abstract

Gough, Michael (Brown University, Providence, R.I.), and Seymour Lederberg. Methylated bases in the host-modified deoxyribonucleic acid of Escherichia coli and bacteriophage lambda. J. Bacteriol. 91:1460-1468. 1966.-The deoxyribonucleic acid (DNA) from strains of Escherichia coli and phage lambda was examined to determine whether the types or amounts of methionine-derived methylated bases present correlated with the host-specific modification of that DNA. The DNA of strain C600 (which has K-12 modification specificity) and of a modificationless mutant of C600 are similar in their content of 5-methylcytosine and 6-methylaminopurine. Strains Bc251 and its P1-lysogen differ in P1-controlled specificity, but they have the same content of 6-methylaminopurine, and both lack 5-methylcytosine in their DNA. Phage lambda contains the same methylated bases as its host of origin, but in reduced amounts and in different proportions. Although minor amounts of these methylated bases may have importance as a result of their location, the presence of the majority of these methylated bases is irrelevant to the specificity of host modification of DNA.

摘要

戈夫,迈克尔(布朗大学,罗德岛州普罗维登斯),以及西摩·莱德伯格。大肠杆菌和噬菌体λ宿主修饰的脱氧核糖核酸中的甲基化碱基。《细菌学杂志》91:1460 - 1468。1966年。——对来自大肠杆菌菌株和噬菌体λ的脱氧核糖核酸(DNA)进行检测,以确定所存在的甲硫氨酸衍生的甲基化碱基的类型或数量是否与该DNA的宿主特异性修饰相关。C600菌株(具有K - 12修饰特异性)及其无修饰突变体的DNA在5 - 甲基胞嘧啶和6 - 甲基腺嘌呤的含量上相似。Bc251菌株及其P1溶原菌在P1控制的特异性上有所不同,但它们6 - 甲基腺嘌呤的含量相同,并且它们的DNA中都缺乏5 - 甲基胞嘧啶。噬菌体λ所含的甲基化碱基与其原始宿主相同,但含量减少且比例不同。尽管这些甲基化碱基中的少量可能因其位置而具有重要性,但这些甲基化碱基中的大多数的存在与DNA宿主修饰的特异性无关。

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Methylation pattern of lambda deoxyribonucleic acid.λ 脱氧核糖核酸的甲基化模式
J Virol. 1972 Nov;10(5):937-42. doi: 10.1128/JVI.10.5.937-942.1972.

本文引用的文献

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ROLE OF METHYLATION IN HOST CONTROLLED MODIFICATION OF PHAGE T1.甲基化在宿主控制的噬菌体T1修饰中的作用
Biochem Biophys Res Commun. 1965 Feb 3;18:440-5. doi: 10.1016/0006-291x(65)90728-x.

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