Lee S B, Bailey J E
Department of Chemical Engineering, California Institute of Technology, Pasadena, California 91125.
Biotechnol Bioeng. 1984 Nov;26(11):1383-9. doi: 10.1002/bit.260261116.
A mathematical model based on molecular mechanisms for regulation of the lactose (lac) operon in Escherichia coli has been extended and applied to investigate the lac promoter function in the chromosome and in multicopy plasmids. The model simulates the influence of certain host cell mutations and also mutations in the lac promoter sequence in the chromosome in reasonable agreement with previous experimental measurements. The effect of the plasmid copy number and the cloning vector size on the promoter function of a cloned lac regulatory sequence in multicopy plasmids has also been examined. Model results indicate that the efficiency of the cloned lac promoter function is significantly decreased as the number of promoters per cloning vector and size of the vector are increased. The simulation results predict a maximum in the cloned gene transcription rate with respect to the plasmid copy number.
一个基于大肠杆菌乳糖(lac)操纵子调控分子机制的数学模型已得到扩展,并应用于研究染色体和多拷贝质粒中的lac启动子功能。该模型模拟了某些宿主细胞突变以及染色体中lac启动子序列突变的影响,与先前的实验测量结果合理吻合。还研究了质粒拷贝数和克隆载体大小对多拷贝质粒中克隆的lac调控序列启动子功能的影响。模型结果表明,随着每个克隆载体中启动子数量和载体大小的增加,克隆的lac启动子功能效率显著降低。模拟结果预测了克隆基因转录速率相对于质粒拷贝数存在一个最大值。