甲基化
脱氧核糖核酸酶
化学
酶
生物化学
脱氧核糖核酸酶ⅰ
水解
DNA
DNA甲基化
磷酸盐
转移RNA
孵化
分子生物学
生物
核糖核酸
基因表达
基因
基序列
作者
Rachkus IuA,Kanopkaĭte Si
出处
期刊:PubMed
日期:1988-02-01
卷期号:53 (2): 278-82
摘要
The effects of NaCl, EDTA and tRNA on methylation and enzymatic properties of deoxyribonuclease I (DNase I) were investigated. The methylation was carried out by S-methylmethionine (vitamin U) in the phosphate-citric buffer pH 4.0. It was found that 0.5 M NaCl decreases by about 30% the incorporation of CH3-groups into the DNase, whereas 1.5 M NaCl-by 47%. A similar, although a less pronounced effect, was exerted by tRNA within the concentration range of 1.36-34.7 microM. On the contrast, EDTA (0.01-0.05 M) stimulated the incorporation of CH3-groups by 15 and 30%, respectively. The functional properties of methylated DNase I in the presence of EDTA remained unaffected. The enzyme methylation in the presence of NaCl or tRNA caused deceleration of the 3H-DNA hydrolysis (by 15-30%) only within the first 20 min of the reaction.
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