Mizuno S, Whiteley H R
J Bacteriol. 1968 Apr;95(4):1221-37. doi: 10.1128/jb.95.4.1221-1237.1968.
A "nuclear fraction" prepared from Bacillus subtilis was a more efficient template than purified deoxyribonucleic acid for the synthesis of ribonucleic acid by exogenously added ribonucleic acid polymerase isolated from B. subtilis. The initial rate of synthesis with the nuclear fraction was higher and synthesis continued for several hours, yielding an amount of ribonucleic acid greater than the amount of deoxyribonucleic acid used as the template. The product was heterogenous in size, with a large portion exceeding 23S. When purified deoxyribonucleic acid was the template, a more limited synthesis was observed with a predominantly 7S product. However, the ribonucleic acids produced in vitro from these templates were very similar to each other and to in vivo synthesized ribonucleic acid as determined by the competition of ribonucleic acid from whole cells in the annealing of in vitro synthesized ribonucleic acids to deoxyribonucleic acid. Treatment of the nuclear fraction with heat (60 C for 15 min) or trypsin reduced the capacity of the nuclear fraction to synthesize ribonucleic acid to the level observed with purified deoxyribonucleic acid.
从枯草芽孢杆菌制备的“核组分”,作为合成核糖核酸的模板,比纯化的脱氧核糖核酸更高效,用于由从枯草芽孢杆菌分离的外源添加的核糖核酸聚合酶合成核糖核酸。使用核组分时的初始合成速率更高,合成持续数小时,产生的核糖核酸量大于用作模板的脱氧核糖核酸量。产物大小不均一,大部分超过23S。当纯化的脱氧核糖核酸作为模板时,观察到合成更有限,主要产物为7S。然而,通过体外合成的核糖核酸与脱氧核糖核酸退火时全细胞核糖核酸的竞争测定,这些模板体外产生的核糖核酸彼此非常相似,并且与体内合成的核糖核酸相似。用热(60℃处理15分钟)或胰蛋白酶处理核组分,会使核组分合成核糖核酸的能力降低到用纯化的脱氧核糖核酸时观察到的水平。