Gaziev A I, Fomenko L A, Zakrzhevskaia D T, Sigaeva V A
Biokhimiia. 1985 May;50(5):814-9.
The nucleoid isolated from E. coli cells was subjected to further deletion by treatment with 2 M NaCl. After disintegration of this nucleoid by ultrasonication, two fractions were obtained, i. e., a rapidly (RS) and slowly sedimenting (SS) ones. The protein, RNA and DNA patterns in the RS fraction are similar to that of the eukaryotic cell nuclear matrix. Electrophoretic analysis of total non-dissociating by 2 M NaCl proteins revealed that the RS and SS fractions predominantly contain proteins with Mr 31,27 and 23 kD. The protein with Mr = 31 kD is firmly bound to DNA, does not dissociate in the guanidine hydrochloride (4 M)-urea (5 M) mixture as well as in solution of 1% sodium-dodecyl sulphate and may be responsible for the chromosome binding to the E. coli membrane.
从大肠杆菌细胞中分离出的类核体用2M氯化钠处理后进一步缺失。通过超声处理使该类核体解体后,得到了两个组分,即快速沉降(RS)组分和慢速沉降(SS)组分。RS组分中的蛋白质、RNA和DNA模式与真核细胞核基质的相似。对2M氯化钠处理后不解离的总蛋白质进行电泳分析表明,RS和SS组分主要含有分子量为31、27和23kD的蛋白质。分子量为31kD的蛋白质与DNA紧密结合,在盐酸胍(4M)-尿素(5M)混合物以及1%十二烷基硫酸钠溶液中均不解离,可能负责染色体与大肠杆菌膜的结合。