Belimov A A, Dodd I C, Safronova V I, Hontzeas N, Davies W J
All-Russia Research Institute for Agricultural Microbiology (ARRIAM), Podbelskogo Sh., 3, Pushkin-8, 196608, St-Petersburg, Russian Federation.
J Exp Bot. 2007;58(6):1485-95. doi: 10.1093/jxb/erm010. Epub 2007 Feb 24.
The role of bacterial 1-aminocyclopropane-1-carboxylate (ACC) deaminase activity in the interaction between tomato (Lycopersicon esculentum=Solanum lycopersicum) and Pseudomonas brassicacearum was studied in different strains. The phytopathogenic strain 520-1 possesses ACC deaminase activity, an important trait of plant growth-promoting rhizobacteria (PGPR) that stimulates root growth. The ACC-utilizing PGPR strain Am3 increased in vitro root elongation and root biomass of soil-grown tomato cv. Ailsa Craig at low bacterial concentrations (10(6) cells ml-1 in vitro and 10(6) cells g-1 soil) but had negative effects on in vitro root elongation at higher bacterial concentrations. A mutant strain of Am3 (designated T8-1) that was engineered to be ACC deaminase deficient failed to promote tomato root growth in vitro and in soil. Although strains T8-1 and 520-1 inhibited root growth in vitro at higher bacterial concentrations (>10(6) cells ml-1), they did not cause disease symptoms in vitro after seed inoculation, or in soil supplemented with bacteria. All the P. brassicacearum strains studied caused pith necrosis when stems or fruits were inoculated with a bacterial suspension, as did the causal organism of this disease (P. corrugata 176), but the non-pathogenic strain Pseudomonas sp. Dp2 did not. Strains Am3 and T8-1 were marked with antibiotic resistance and fluorescence to show that bacteria introduced to the nutrient solution or on seeds in vitro, or in soil were capable of colonizing the root surface, but were not detected inside root tissues. Both strains showed similar colonization ability either on root surfaces or in wounded stems. The results suggest that bacterial ACC deaminase of P. brassicacearum Am3 can promote growth in tomato by masking the phytopathogenic properties of this bacterium.
研究了不同菌株中细菌1-氨基环丙烷-1-羧酸(ACC)脱氨酶活性在番茄(Lycopersicon esculentum = Solanum lycopersicum)与油菜黄单胞菌相互作用中的作用。植物病原菌株520-1具有ACC脱氨酶活性,这是促进植物生长的根际细菌(PGPR)的一个重要特性,可刺激根生长。利用ACC的PGPR菌株Am3在低细菌浓度(体外10⁶个细胞/毫升和土壤中10⁶个细胞/克)下增加了土壤种植的番茄品种艾尔莎·克雷格的体外根伸长和根生物量,但在较高细菌浓度下对体外根伸长有负面影响。一株经基因工程改造为ACC脱氨酶缺陷型的Am3突变株(命名为T8-1)在体外和土壤中均未能促进番茄根生长。尽管菌株T8-1和520-1在较高细菌浓度(>10⁶个细胞/毫升)下抑制体外根生长,但种子接种后在体外或添加细菌的土壤中均未引起病害症状。当用细菌悬浮液接种茎或果实时,所有研究的油菜黄单胞菌菌株都会导致髓部坏死,该病的致病生物(皱纹假单胞菌176)也是如此,但非致病菌株假单胞菌属Dp2不会。菌株Am3和T8-1用抗生素抗性和荧光标记,以表明引入营养液或体外种子上或土壤中的细菌能够定殖在根表面,但在根组织内部未检测到。两种菌株在根表面或受伤茎中均表现出相似的定殖能力。结果表明,油菜黄单胞菌Am3的细菌ACC脱氨酶可通过掩盖该细菌的植物致病特性来促进番茄生长。