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首页> 外文期刊>Applied and Environmental Microbiology >Novel Tellurite-Amended Media and Specific Chromosomal and Ti Plasmid Probes for Direct Analysis of Soil Populations of Agrobacterium Biovars 1 and 2
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Novel Tellurite-Amended Media and Specific Chromosomal and Ti Plasmid Probes for Direct Analysis of Soil Populations of Agrobacterium Biovars 1 and 2

机译:新型亚碲酸盐改良培养基以及用于直接分析土壤杆菌农杆菌1和2的土壤染色体的特定染色体和Ti质粒探针

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Ecology and biodiversity studies of Agrobacterium spp. require tools such as selective media and DNA probes. Tellurite was tested as a selective agent and a supplement of previously described media for agrobacteria. The known biodiversity within the genus was taken into account when the selectivity of K2TeO3 was analyzed and its potential for isolating Agrobacterium spp. directly from soil was evaluated. A K2TeO3 concentration of 60 ppm was found to favor the growth of agrobacteria and restrict the development of other bacteria. Morphotypic analyses were used to define agrobacterial colony types, which were readily distinguished from other colonies. The typical agrobacterial morphotype allowed direct determination of the densities of agrobacterial populations from various environments on K2TeO3-amended medium. The bona fide agrobacterium colonies growing on media amended with K2TeO3 were confirmed to beAgrobacterium colonies by using 16S ribosomal DNA (rDNA) probes. Specific 16S rDNA probes were designed forAgrobacterium biovar 1 and related species (Agrobacterium rubi and Agrobacterium fici) and for Agrobacterium biovar 2. Specific pathogenic probes from different Ti plasmid regions were used to determine the pathogenic status of agrobacterial colonies. Various morphotype colonies from bulk soil suspensions were characterized by colony blot hybridization with 16S rDNA and pathogenic probes. All the Agrobacterium-like colonies obtained from soil suspensions on amended media were found to be bona fide agrobacteria. Direct colony counting of agrobacterial populations could be done. We found 103 to 104agrobacteria · g of dry soil?1 in a silt loam bulk soil cultivated with maize. All of the strains isolated were nonpathogenic bona fide Agrobacterium biovar 1 strains.
机译:农杆菌的生态学和生物多样性研究。需要诸如选择性培养基和DNA探针之类的工具。测试了碲酸盐作为选择剂和前述农杆菌培养基的补充。分析K2TeO3的选择性及其分离农杆菌的潜力时,应考虑该属内已知的生物多样性。直接从土壤中进行了评估。发现浓度为60 ppm的K2TeO3有利于农杆菌的生长并限制其他细菌的生长。形态分析用于确定农杆菌菌落的类型,很容易与其他菌落区分开。典型的农杆菌形态可以直接测定K2TeO3改良培养基上来自各种环境的农杆菌种群的密度。通过使用16S核糖体DNA(rDNA)探针,在用K2TeO3修饰的培养基上生长的真正农杆菌菌落被确认为农杆菌菌落。设计了针对农杆菌1和相关物种(红土壤杆菌和农杆菌)和农杆菌2的特异性16S rDNA探针。使用了来自不同Ti质粒区域的特异性致病探针来确定农杆菌菌落的致病状态。通过与16S rDNA和致病探针的菌落印迹杂交,表征了散装土壤悬浮液的各种形态型菌落。从在改良培养基上的土壤悬浮液中获得的所有农杆菌样菌落均被发现为真正的农杆菌。可以对农杆菌种群进行直接菌落计数。在用玉米栽培的粉壤土大块土壤中,我们发现了103至104的土壤杆菌·克干土壤。分离的所有菌株均为非致病性的真正农杆菌biovar 1菌株。

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