Hofer B, Ruhe G, Koch A, Köster H
Nucleic Acids Res. 1982 May 11;10(9):2763-73. doi: 10.1093/nar/10.9.2763.
The interaction of endonuclease Hinf I with single-stranded fd DNA was examined. The sizes of the cleavage products indicate that the enzyme cuts this substrate at the same sequences as double-stranded DNA (GANTC). To determine whether or not the recognition sites in single-stranded DNA have to be present in double-stranded form in order to be cleaved, DNA fragments containing complementary or non-complementary Hinf I sequences were prepared and treated as substrates. The results suggest that completely base-paired recognition sites are necessary for cleavage. Sequences surrounding the Hinf I pentanucleotides significantly modulate the reaction rates.
研究了内切核酸酶Hinf I与单链fd DNA的相互作用。切割产物的大小表明,该酶在与双链DNA相同的序列(GANTC)处切割此底物。为了确定单链DNA中的识别位点是否必须以双链形式存在才能被切割,制备了含有互补或非互补Hinf I序列的DNA片段并将其作为底物进行处理。结果表明,完全碱基配对的识别位点对于切割是必需的。Hinf I五核苷酸周围的序列显著调节反应速率。