Germaine G R, Anderson D L
J Bacteriol. 1966 Sep;92(3):662-7. doi: 10.1128/jb.92.3.662-667.1966.
Germaine, G. R. (University of Minnesota, Minneapolis), and D. L. Anderson. Binding of homologous polymerized deoxyribonucleic acid by Streptomyces griseus. J. Bacteriol. 92:662-667. 1966-An irreversible P(32) deoxyribonucleic acid (DNA) binding system is described for Streptomyces griseus S104. The 69% guanine plus cytosine (GC) S. griseus DNA was bound by late exponential -early stationary phase cultures. Simultaneous addition of deoxyribonuclease with the P(32)-DNA to maximally receptive cultures reduced the uptake by 98%. Saturation of the binding ability occurred after 20-min incubation of cells with P(32)-DNA. Preparative cesium chloride density gradient centrifugation of the P(32)-DNA revealed that 98% of the label banded in the position expected for S. griseus DNA. Sedimentation of the P(32)-DNA at both 23 and 37 mug/ml indicated a molecular weight of 10.8 million. Attempts to transform S. griseus S104 auxotrophs to prototrophy by use of immediate and delayed selective procedures were unsuccessful.
杰曼,G.R.(明尼苏达大学,明尼阿波利斯),以及D.L.安德森。灰色链霉菌对同源聚合脱氧核糖核酸的结合。《细菌学杂志》92:662 - 667。1966年——描述了一种用于灰色链霉菌S104的不可逆的P(32)脱氧核糖核酸(DNA)结合系统。69%鸟嘌呤加胞嘧啶(GC)含量的灰色链霉菌DNA被指数后期 - 稳定期早期的培养物结合。在向最大感受态培养物中同时添加脱氧核糖核酸酶和P(32)-DNA,使摄取量降低了98%。细胞与P(32)-DNA孵育20分钟后,结合能力达到饱和。对P(32)-DNA进行制备性氯化铯密度梯度离心显示,98%的放射性标记条带位于灰色链霉菌DNA预期的位置。P(32)-DNA在23和37微克/毫升浓度下的沉降表明其分子量为1080万。尝试通过即时和延迟选择性程序将灰色链霉菌S104营养缺陷型转化为原养型未成功。