Ishii Nobuyoshi, Matsui Kazuaki, Fuma Shoichi, Takeda Hiroshi, Kawabata Zen'ichiro
Environmental and Toxicological Sciences Research Group, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555, Japan.
FEMS Microbiol Lett. 2004 Nov 15;240(2):151-4. doi: 10.1016/j.femsle.2004.09.024.
We studied the transforming ability of the extracellular plasmid DNA released from a genetically engineered Escherichia coli pEGFP and the culturing conditions for the release of transforming DNA. The transforming ability was evaluated by transformation of competent cells with filtrates of E. coli pEGFP cultures. The number of transformants increased with time when E. coli pEGFP cells grew exponentially in rich medium, but not in stationary phase or when inoculated in freshwater. These results suggested that crude extracellular plasmid DNA had transforming ability and this transforming DNA was mainly released by actively growing bacteria.
我们研究了从基因工程大肠杆菌pEGFP释放的细胞外质粒DNA的转化能力以及转化DNA释放的培养条件。通过用大肠杆菌pEGFP培养物的滤液转化感受态细胞来评估转化能力。当大肠杆菌pEGFP细胞在丰富培养基中指数生长时,转化子数量随时间增加,但在稳定期或接种于淡水中时则不然。这些结果表明,粗制的细胞外质粒DNA具有转化能力,且这种转化DNA主要由活跃生长的细菌释放。