Sayadi S, Nasri M, Berry F, Barbotin J N, Thomas D
Laboratoire de Technologie Enzymatique, UA no. 523 du CNRS, Université de Technologie de Compiègne, France.
J Gen Microbiol. 1987 Jul;133(7):1901-8. doi: 10.1099/00221287-133-7-1901.
The effect of temperature on the stability of pTG201, a plasmid carrying the xylE gene (which encodes catechol 2,3-dioxygenase from Pseudomonas putida), and the production of catechol 2,3-dioxygenase in free and immobilized Escherichia coli during continuous culture have been studied at various temperatures. Immobilization of cells increased the stability of pTG201 considerably, even under conditions when expression of the xylE product was enhanced. Since xylE transcription was controlled by the lambda PR promoter and cI857 repressor, increasing derepression temperatures increased catechol 2,3-dioxygenase productivity and decreased pTG201 stability. A two-stage continuous culture system to overcome the impact of the high-level expression of the xylE gene on the stability of pTG201 is described. In the first stage, immobilized cells were grown in the repressed state in order to prevent loss of pTG201, whereas in the second stage, cultures were maintained in the derepressed state.
研究了温度对携带xylE基因(编码恶臭假单胞菌的儿茶酚2,3-双加氧酶)的质粒pTG201稳定性的影响,以及在连续培养过程中游离和固定化大肠杆菌中儿茶酚2,3-双加氧酶的产生情况。在不同温度下进行了研究。细胞固定化显著提高了pTG201的稳定性,即使在xylE产物表达增强的条件下也是如此。由于xylE转录受λPR启动子和cI857阻遏物控制,提高去阻遏温度会提高儿茶酚2,3-双加氧酶的生产力并降低pTG201的稳定性。描述了一种两阶段连续培养系统,以克服xylE基因高表达对pTG201稳定性的影响。在第一阶段,固定化细胞在阻遏状态下生长,以防止pTG201丢失,而在第二阶段,培养物保持在去阻遏状态。