Stevens R H, Goncharoff P, Furgang D, Fine D H, Schreiner H C, Figurski D H
Divisions of Oral Infectious Disease and Endodontics, Columbia University, New York, NY.
Oral Microbiol Immunol. 1993 Apr;8(2):100-4. doi: 10.1111/j.1399-302x.1993.tb00553.x.
The size, configuration and restriction map of Actinobacillus actinomycetemcomitans bacteriophage phi Aa DNA was determined by means of restriction endonuclease analysis. Digestion of the phi Aa DNA with restriction enzymes Hind III, Eco RI and Sal I produced 6, 5, and 4 fragments, respectively. Based upon the sum of the sizes of the restriction fragments of these enzymes, the DNA was estimated to be 47.2 kilobase pairs in length. A restriction map was constructed using Hind III and Sal I. Incubation with exonuclease Bal 31 for increasing lengths of time resulted in progressive hydrolysis of the DNA, as expected for a linear molecule. No sub-molar fragments or diffuse bands were observed in the agarose gels of the restriction endonuclease digests of the phi Aa DNA. Attempts at ligating the ends of the DNA were consistently unsuccessful. Therefore, we found no evidence for cohesive ends, a circular permutation of the genome or for headful packaging mechanism from a concatameric DNA precursor.
通过限制性内切酶分析确定了伴放线放线杆菌噬菌体φAa DNA的大小、构型和限制酶切图谱。用限制性内切酶Hind III、Eco RI和Sal I消化φAa DNA分别产生了6、5和4个片段。根据这些酶的限制片段大小总和,估计该DNA长度为47.2千碱基对。使用Hind III和Sal I构建了限制酶切图谱。用核酸外切酶Bal 31孵育不同时间导致DNA逐渐水解,这符合线性分子的预期情况。在φAa DNA的限制性内切酶消化产物的琼脂糖凝胶中未观察到亚摩尔片段或弥散条带。连接DNA末端的尝试一直未成功。因此,我们没有发现粘性末端、基因组的环状排列或来自串联DNA前体的头部充满包装机制的证据。