Department of Plant Pathology, University of California at Berkeley, Berkeley, California 94720.
Appl Environ Microbiol. 1993 Jul;59(7):2071-6. doi: 10.1128/aem.59.7.2071-2076.1993.
Plasmid NAH7 was transferred from Pseudomonas putida PpG7 to P. putida R20 [R20(NAH7)], an antagonist of Pythium ultimum. The plasmid did not affect growth or survival of R20(NAH7) and was stably maintained under nonselective conditions in broth and soil and on sugar beet seeds. Plasmid NAH7 conferred to R20(NAH7) the ability to utilize salicylate in culture, agricultural field soil, and on sugar beet seeds. The metabolic activity of R20(NAH7), but not the wild-type R20, was greatly increased in soil by amendment with salicylate (250 mug/g) as measured by induced respiration. Population densities of R20(NAH7) were also enhanced in salicylate-amended soil, increasing from approximately 1 x 10 CFU/g to approximately 3 x 10 CFU/g after 35 h of incubation. In contrast, population densities of R20(NAH7) in nonamended soil were approximately 3 x 10 CFU/g of soil after 35 h of incubation. The concentration of salicylate in soil affected the rate and extent of population increase by R20(NAH7). At 50 to 250 mug of salicylate per g of soil, population densities of R20(NAH7) increased to approximately 10 CFU/g of soil by 48 h of incubation, with the fastest increase at 100 mug/g. A lag phase of approximately 24 h occurred before the population density increased in the presence of salicylate at 500 mug/g; at 1,000 mug/g, population densities of R20(NAH7) declined over the time period of the experiment. Population densities of R20(NAH7) on sugar beet seeds in soils amended with 100 mug of salicylate per g were not increased while ample carbon was present in the spermosphere. However, after carbon from the seed had been utilized, population densities of R20(NAH7) decreased significantly less (P = 0.005) on sugar beet seeds in soil amended with salicylate than in nonamended soil.
质粒 NAH7 从恶臭假单胞菌 PpG7 转移到 P. putida R20[R20(NAH7)],后者是腐霉的拮抗剂。该质粒不影响 R20(NAH7)的生长或存活,并在非选择性条件下在肉汤、土壤和甜甜菜种子中稳定维持。质粒 NAH7 赋予 R20(NAH7)在培养物、农业田间土壤和甜甜菜种子中利用水杨酸的能力。与野生型 R20 相比,通过用水杨酸(250 微克/克)改良,R20(NAH7)的代谢活性在土壤中大大增加,如诱导呼吸所测量的。用水杨酸(250 微克/克)改良土壤后,R20(NAH7)的种群密度也增加,在 35 小时的孵育后从约 1 x 10 CFU/g 增加到约 3 x 10 CFU/g。相比之下,在未改良的土壤中,R20(NAH7)的种群密度在 35 小时的孵育后约为 3 x 10 CFU/g 的土壤。土壤中水杨酸的浓度影响 R20(NAH7)种群增加的速度和程度。在 50 至 250 微克水杨酸/克土壤的浓度下,R20(NAH7)的种群密度在 48 小时的孵育后增加到约 10 CFU/g 的土壤,在 100 微克/g 时增加最快。在 500 微克/g 存在水杨酸的情况下,种群密度在出现之前出现约 24 小时的滞后期;在 1000 微克/g 时,R20(NAH7)的种群密度在实验期间下降。在土壤中添加 100 微克水杨酸/克时,甜甜菜种子上的 R20(NAH7)的种群密度没有增加,而在精子体中存在充足的碳。然而,在用种子中的碳进行利用后,在添加水杨酸的土壤中,R20(NAH7)的种群密度显著减少(P = 0.005),而在未添加土壤中的种群密度则显著减少。