Nosikov V V, Braga E A, Polianovskiĭ O L
Mol Biol (Mosk). 1977 Sep-Oct;11(5):1079-89.
It is shown that distamycin A and actinomycin D protect the recognition sites of certain restriction endonucleases from the attack by these nucleases due to specific interaction of these antibiotics with double-stranded DNA. Distamycin A protects A-T containing sites and actinomycin G-C rich sites. Among Hind II recognition sites which have alternative structure (GTPyPuAC) distamycin A protects only Hpa I similar sites (GTTAAC). It is shown with several restriction endonucleases that antibiotic action depends on the nucleotide sequences in the recognition sites and in their closest environment. Proper concentrations of antibiotic give rise to larger fragments. Use of both distamycin A and actinomycin D allows to obtain a set of overlapping fragments. The data obtained with various DNAs and restriction endonucleases allow to conclude that these antibiotics may be useful for DNA mapping and for preparation of large functional fragments of DNA.
研究表明,由于双氢链霉素A和放线菌素D与双链DNA的特异性相互作用,它们可保护某些限制性内切核酸酶的识别位点免受这些核酸酶的攻击。双氢链霉素A保护含A-T的位点,而放线菌素保护富含G-C的位点。在具有替代结构(GTPyPuAC)的Hind II识别位点中,双氢链霉素A仅保护与Hpa I相似的位点(GTTAAC)。用几种限制性内切核酸酶研究表明,抗生素的作用取决于识别位点及其最邻近区域的核苷酸序列。适当浓度的抗生素会产生更大的片段。同时使用双氢链霉素A和放线菌素D可获得一组重叠片段。用各种DNA和限制性内切核酸酶获得的数据表明,这些抗生素可能有助于DNA图谱分析以及制备大的功能性DNA片段。