Dowling D N, Pipke R, Dwyer D F
Federal Institute for Biotechnology, Microbiology Department, Braunschweig, FRG.
FEMS Microbiol Lett. 1993 Oct 15;113(2):149-54. doi: 10.1111/j.1574-6968.1993.tb06506.x.
In this report we describe the development and construction of a DNA module which encodes bph genes for the metabolism of PCBs and which is capable of stable integration into the chromosome of Gram negative bacteria. Introduction of the bph-module into Pseudomonas putida KT2442, Pseudomonas sp. strain B13 and its genetically engineered derivative B13FR1 expanded the biodegradative ability of these strains to include biphenyl and 4-chlorobiphenyl. The bph operon was stably inherited under laboratory conditions. Behavior of the genetically engineered strains was evaluated under simulated natural habitat conditions in lake sediment microcosms with respect to survival and removal of 4-chlorobiphenyl. The genetically engineered strains persisted under these conditions and were effective in degrading 4-chlorobiphenyl over a five day incubation period.
在本报告中,我们描述了一个DNA模块的开发与构建,该模块编码用于多氯联苯代谢的bph基因,并且能够稳定整合到革兰氏阴性细菌的染色体中。将bph模块导入恶臭假单胞菌KT2442、假单胞菌属菌株B13及其基因工程衍生物B13FR1,扩大了这些菌株的生物降解能力,使其能够降解联苯和4-氯联苯。bph操纵子在实验室条件下能够稳定遗传。在湖泊沉积物微观世界模拟自然栖息地条件下,对基因工程菌株在4-氯联苯存活和去除方面的行为进行了评估。这些基因工程菌株在这些条件下能够持续存在,并在五天的培养期内有效降解4-氯联苯。