Perumov D A, Machkovskiĭ V V, Iakovlev D Iu, Budovskiĭ E I
Bioorg Khim. 1984 Dec;10(12):1695-7.
The action of methoxyamine (MA) on B. subtilis transforming DNA (50 degrees C, pH 4,5 and 6,0, 1 M MA) was studied. The rate of cytosine residues modification in DNA is 250 times less than in monomer (rate constants for DNA are 1,5 X 10(-1) min-1 at pH 4,5, and 2,5 X 10(-6) min-1 in the first 300 hours of treatment at pH 6,0). At pH 4,5 the rates of cytosine (I) conversion into N4-methoxycytosine (II) and into 6-methoxyamino-5,6-dihydro-N4-methoxycytosine (III) are constant (II/III ratio is about 2,1). At pH 6,0 the II/III ratio smoothly increases from 1,0 to 1,6 (200 and 900 hours of treatment) due to a decrease in the product III accumulation rate. The frequency of MA-induced mutations shows a bell-shaped dependence on time with maxima (approximately 10%) at 80 (pH 4,5) and 500 (pH 6,0) hours of treatment. In both cases approximately 10% of cytosine residues are modified. These results suggest that either compound III is efficiently removed from the transforming DNA, or its presence does not arrest the DNA replication.
研究了甲氧基胺(MA)对枯草芽孢杆菌转化DNA(50℃,pH 4.5和6.0,1M MA)的作用。DNA中胞嘧啶残基的修饰速率比单体中的低250倍(DNA的速率常数在pH 4.5时为1.5×10⁻¹ min⁻¹,在pH 6.0处理的前300小时为2.5×10⁻⁶ min⁻¹)。在pH 4.5时,胞嘧啶(I)转化为N⁴-甲氧基胞嘧啶(II)和6-甲氧基氨基-5,6-二氢-N⁴-甲氧基胞嘧啶(III)的速率是恒定的(II/III比值约为2.1)。在pH 6.0时,由于产物III积累速率的降低,II/III比值从1.0平稳增加到1.6(处理200和900小时)。MA诱导的突变频率呈现出对时间的钟形依赖性,在pH 4.5处理80小时和pH 6.0处理500小时时达到最大值(约10%)。在两种情况下,大约10%的胞嘧啶残基被修饰。这些结果表明,要么化合物III能有效地从转化DNA中去除,要么其存在不会阻止DNA复制。