Edelmann P L, Edlin G
J Bacteriol. 1974 Nov;120(2):657-65. doi: 10.1128/jb.120.2.657-665.1974.
Measurements of the lactose repressor over a tenfold range of cell growth rates were made on protein extracts from Escherichia coli cultures grown in media with various carbon energy sources. The concentration of lactose repressor varied with the number of genome equivalents per cell over this range in growth rates, suggesting that the number of lactose molecules within the cell is determined by the number of I gene copies present. The timing of repressor synthesis during the cell division cycle and its correlation with deoxyribonucleic acid synthesis was examined by synchronizing the cell division cycle of E. coli ED1039, in which the Lac region has been transposed from 10 to 36 min on the genetic map. Measurements of lactose repressor in the synchronized culture revealed a burst of repressor synthesis at the time of I gene duplication. The concentration of lactose repressor was found to decrease as a function of total cell protein during the division cycle until an increase in synthesis occurred, suggesting that repressor synthesis probably does not occur throughout the division cycle. A model for I gene regulation is proposed.
在以各种碳能源为培养基生长的大肠杆菌培养物的蛋白质提取物中,对乳糖阻遏物在十倍细胞生长速率范围内进行了测量。在这个生长速率范围内,乳糖阻遏物的浓度随每个细胞基因组当量数的变化而变化,这表明细胞内乳糖分子的数量由存在的I基因拷贝数决定。通过同步大肠杆菌ED1039的细胞分裂周期,研究了细胞分裂周期中阻遏物合成的时间及其与脱氧核糖核酸合成的相关性,在该菌株中,Lac区域已从遗传图谱上的10分钟处转座到36分钟处。在同步培养物中对乳糖阻遏物的测量显示,在I基因复制时阻遏物合成出现爆发。发现乳糖阻遏物的浓度在分裂周期中作为总细胞蛋白的函数而降低,直到合成增加,这表明阻遏物合成可能并非在整个分裂周期中都发生。提出了一个I基因调控模型。