Heeb S, Itoh Y, Nishijyo T, Schnider U, Keel C, Wade J, Walsh U, O'Gara F, Haas D
Laboratoire de Biologie Microbienne, Université de Lausanne, Switzerland.
Mol Plant Microbe Interact. 2000 Feb;13(2):232-7. doi: 10.1094/MPMI.2000.13.2.232.
The minimal replicon of the Pseudomonas plasmid pVS1 was genetically defined and combined with the Escherichia coli p15A replicon, to provide a series of new, oligocopy cloning vectors (5.3 to 8.3 kb). Recombinant plasmids derived from these vectors were stable in growing and nongrowing cells of root-colonizing P. fluorescens strains incubated under different environmental conditions for more than 1 month.
对假单胞菌质粒pVS1的最小复制子进行了遗传学定义,并将其与大肠杆菌p15A复制子相结合,以提供一系列新的低拷贝克隆载体(5.3至8.3 kb)。源自这些载体的重组质粒在不同环境条件下培养超过1个月的根定殖荧光假单胞菌菌株的生长细胞和非生长细胞中均稳定存在。