Nikol'skaia I I, Tediashvili M G, Vasil'eva M B, Chanishvili T G, Debov S S
Vopr Virusol. 1978 Nov-Dec(6):724-31.
In Shigella sonnei cells there is a host DNA specificity system responsible for modification and restriction of DDII phage. DNA methylase from Shigella stutzeri cells is specific for adenine and catalyses the appearance of 6-'-methylaminopurine in the acceptory DNA. Methylases from Shigella sonnei cells are specific for adenine and cytosine and provide for the presence of 6'-methylaminopurine and 5'-methylcytosine in DNA. The modifying activity of these cells may be equally likely associated with both the enzymes. A simplified version of the additional methylation test has been developed for the study of enzyme specificity. The results of additional and cross methylation suggest that several adenine methylases are present in the cells of these Shigella, one of these enzymes being shared by Shigella stutzeri and Shigella sonnei. The DNA's isolated from Shigella sonnei and Shigella stutzeri cells are undermethylated and in vitro undergo additional methylation upon incubation with the appropriate enzyme.
在宋内志贺氏菌细胞中,存在一种负责对DDII噬菌体进行修饰和限制的宿主DNA特异性系统。斯氏志贺氏菌细胞的DNA甲基化酶对腺嘌呤具有特异性,并催化受体DNA中6'-甲基氨基嘌呤的出现。宋内志贺氏菌细胞的甲基化酶对腺嘌呤和胞嘧啶具有特异性,并使DNA中存在6'-甲基氨基嘌呤和5'-甲基胞嘧啶。这些细胞的修饰活性可能同样与这两种酶有关。为了研究酶的特异性,已经开发了一种简化版的额外甲基化测试。额外甲基化和交叉甲基化的结果表明,这些志贺氏菌细胞中存在几种腺嘌呤甲基化酶,其中一种酶为斯氏志贺氏菌和宋内志贺氏菌所共有。从宋内志贺氏菌和斯氏志贺氏菌细胞中分离出的DNA甲基化不足,并且在与适当的酶一起孵育时在体外会发生额外的甲基化。