Koh B T, Tan R B, Yap M G
Department of Chemical Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore.
Biotechnol Bioeng. 1998 Jun 5;58(5):502-9. doi: 10.1002/(sici)1097-0290(19980605)58:5<502::aid-bit6>3.0.co;2-h.
A genetically structured mathematical model of the trp attenuator in Escherichia coli based on known coupling mechanisms of the transcription of the trp leader region and translation of the trp leader peptide region is proposed. The model simulates, both qualitatively and quantitatively, the effects of tryptophan on the repression of cloned gene products. It shows that repression by attenuation mechanism alone operates over a narrow trp concentration range of 1 to 5 microM compared with 1 to 100 microM for trp repressor mechanism. This implies that attenuation by transcription termination is not relaxed until tryptophan starvation is severe. Simulation results show that the attenuator starts to derepress when the repressor is about 40% repressed, and becomes significantly derepressed only when the repressor repression decreased to about 20%. Unlike the case of repressor-operator interaction, the operating range of tryptophan concentration in the attenuator mechanism is not sensitive to plasmid copy number.
基于已知的大肠杆菌色氨酸操纵子前导区转录与色氨酸前导肽区翻译的偶联机制,提出了一种基因结构数学模型。该模型定性和定量地模拟了色氨酸对克隆基因产物抑制的影响。结果表明,与色氨酸阻遏机制在1至100微摩尔的浓度范围相比,仅衰减机制的抑制作用在1至5微摩尔的狭窄色氨酸浓度范围内起作用。这意味着直到色氨酸严重缺乏时,转录终止引起的衰减才会减弱。模拟结果表明,当阻遏蛋白约40%被抑制时,衰减子开始去抑制,只有当阻遏蛋白抑制降至约20%时,衰减子才会显著去抑制。与阻遏蛋白-操纵基因相互作用的情况不同,衰减机制中色氨酸浓度的作用范围对质粒拷贝数不敏感。