Institute for Soil Fertility Research, P.O. Box 48, 6700 AA Wageningen, and Microbiology Department, Agricultural University of Wageningen, 6703 CT Wageningen, The Netherlands.
Appl Environ Microbiol. 1991 Dec;57(12):3482-8. doi: 10.1128/aem.57.12.3482-3488.1991.
The transfer of a genetically marked derivative of plasmid RP4, RP4p, from Pseudomonas fluorescens to members of the indigenous microflora of the wheat rhizosphere was studied by using a bacteriophage that specifically lyses the donor strain and a specific eukaryotic marker on the plasmid. Transfer of RP4p to the wheat rhizosphere microflora was observed, and the number of transconjugants detected was approximately 10 transconjugants per g of soil when 10 donor cells per g of soil were added; transfer in the corresponding bulk soil was slightly above the limit of detection. All of the indigenous transconjugants which we analyzed contained a 60-kb plasmid and were able to transfer this plasmid to a Nx RpP. fluorescens recipient strain. The indigenous transconjugants were identified as belonging to Pseudomonas spp., Enterobacter spp., Comamonas spp., and Alcaligenes spp.
我们研究了从荧光假单胞菌中转移带有遗传标记的质粒 RP4p 到小麦根际微生物区系的成员,使用了一种专门裂解供体菌株的噬菌体和质粒上的特定真核标记。当每克土壤添加 10 个供体细胞时,观察到 RP4p 向小麦根际微生物区系转移,检测到的转导子数量约为每克土壤 10 个转导子;在相应的大量土壤中的转移略高于检测限。我们分析的所有土著转导子都含有一个 60kb 的质粒,并能够将这个质粒转移到一个 Nx RpP。荧光假单胞菌受体菌株。土著转导子被鉴定为属于假单胞菌属、肠杆菌属、丛毛单胞菌属和产碱杆菌属。