Ronchel M C, Molina L, Witte A, Lutbiz W, Molin S, Ramos J L, Ramos C
Department of Biochemistry and Molecular and Cellular Biology of Plants, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, Granada, Spain.
Appl Environ Microbiol. 1998 Dec;64(12):4904-11. doi: 10.1128/AEM.64.12.4904-4911.1998.
Active biological containment systems are based on the controlled expression of killing genes. These systems are of interest for the Pseudomonadaceae because of the potential applications of these microbes as bioremediation agents and biopesticides. The physiological effects that lead to cell death upon the induction of expression of two different heterologous killing genes in nonpathogenic Pseudomonas putida KT2440 derivatives have been analyzed. P. putida CMC4 and CMC12 carry in their chromosomes a fusion of the PA1-04/03 promoter to the Escherichia coli gef gene and the phiX174 lysis gene E, respectively. Expression of the killing genes is controlled by the LacI protein, whose expression is initiated from the XylS-dependent Pm promoter. Under induced conditions, killing of P. putida CMC12 cells mediated by phiX174 lysis protein E was faster than that observed for P. putida CMC4, for which the Gef protein was the killing agent. In both cases, cell death occurred as a result of impaired respiration, altered membrane permeability, and the release of some cytoplasmic contents to the extracellular medium.
主动生物遏制系统基于杀伤基因的可控表达。由于这些微生物作为生物修复剂和生物杀虫剂的潜在应用,这些系统对假单胞菌科具有重要意义。我们分析了在非致病性恶臭假单胞菌KT2440衍生物中诱导表达两种不同的异源杀伤基因后导致细胞死亡的生理效应。恶臭假单胞菌CMC4和CMC12在其染色体中分别携带PA1 - 04/03启动子与大肠杆菌gef基因以及phiX174裂解基因E的融合体。杀伤基因的表达由LacI蛋白控制,其表达从依赖XylS的Pm启动子开始。在诱导条件下,由phiX174裂解蛋白E介导的恶臭假单胞菌CMC12细胞的杀伤速度比恶臭假单胞菌CMC4快,后者的杀伤剂是Gef蛋白。在这两种情况下,细胞死亡都是由于呼吸受损、膜通透性改变以及一些细胞质内容物释放到细胞外培养基中所致。