Marrs B
J Bacteriol. 1981 Jun;146(3):1003-12. doi: 10.1128/jb.146.3.1003-1012.1981.
Plasmid pBLM2, a derivative of RP1 with enhanced chromosome mobilization activity in Rhodopseudomonas capsulata, was isolated by screening rare exconjugant clones for sex factor activity. pBLM2 mobilized all known genes affecting photosynthesis as well as chromosomal genes for streptomycin and rifampin resistance and tryptophan and cytochrome biosynthesis. Tight linkage was exhibited among the genes affecting photosynthesis. The frequency of successful transfer of chromosomal markers reached 6 X 10(-4) per donor cell. R-primes were occasionally formed during conjugation, and a number of R-primes bearing the genes for photosynthesis were isolated by screening R. capsulata exconjugants with complementation phenotypes for the ability to transmit plasmid-borne R. capsulata genes to Escherichia coli cells. These R-primes were unstable in R. capsulata, but stable in E. coli or Pseudomonas fluorescens. Complementation and recombination events that occurred upon introduction of R-primes into R. capsulata mutants with altered photosynthetic apparatuses could be visualized as variations in colony pigmentation. Each R-prime studied complemented all known types of mutation affecting the differentiation of the photosynthetic apparatus, and no other R. capsulata gene was identified on those plasmids. The R. capsulata genes borne on the R-primes were not functional in E. coli or P. fluorescens.
质粒pBLM2是RP1的衍生物,在荚膜红假单胞菌中具有增强的染色体转移活性,通过筛选罕见的接合后克隆的性别因子活性而分离得到。pBLM2转移了所有影响光合作用的已知基因以及链霉素、利福平抗性、色氨酸和细胞色素生物合成的染色体基因。影响光合作用的基因之间表现出紧密连锁。染色体标记成功转移的频率达到每个供体细胞6×10⁻⁴。在接合过程中偶尔会形成R-prime,通过筛选具有互补表型的荚膜红假单胞菌接合后体将质粒携带的荚膜红假单胞菌基因传递给大肠杆菌细胞的能力,分离出了许多携带光合作用基因的R-prime。这些R-prime在荚膜红假单胞菌中不稳定,但在大肠杆菌或荧光假单胞菌中稳定。将R-prime引入具有改变的光合装置的荚膜红假单胞菌突变体时发生的互补和重组事件可以通过菌落色素沉着的变化来观察。研究的每个R-prime都互补了所有已知类型的影响光合装置分化的突变,并且在那些质粒上没有鉴定出其他荚膜红假单胞菌基因。R-prime携带的荚膜红假单胞菌基因在大肠杆菌或荧光假单胞菌中无功能。