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Analysis of endophytic bacterial communities of potato by plating and denaturing gradient gel electrophoresis (DGGE) of 16S rDNA based PCR fragments

机译:通过基于16S rDNA的PCR片段的铺板和变性梯度凝胶电泳(DGGE)分析马铃薯的内生细菌群落

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The diversity of endophytic bacterial populations of potato (Solanum tuberosum cv Desirée) was assessed using a combination of dilution plating of plant macerates followed by isolation and characterization of isolates, and direct PCR-DGGE on the basis of DNA extracted from plants. The culturable endophytic bacterial communities detected in potato stem bases as well as in roots were in most cases on the order 103 to 105 CFU g−1 of fresh plant tissue. Dilution plating revealed that a range of bacterial types dominated these populations. Dominant isolates fell into the α and γ subgroups of the Proteobacteria, as well as in the Flavobacterium/Cytophaga group. Different representatives of the Firmicutes were also found. The most frequently isolated strains (>5% of the total) were characterized as different Pseudomonas spp. (including P. aureofaciens, P. corrugata, and P. putida), Agrobacterium radiobacter, Stenotrophomonas maltophilia, and Flavobacterium resinovorans, using fatty acid methyl ester (FAME) analysis and/or sequencing of their partial 16S ribosomal RNA genes. Other Proteobacteria or Firmicutes were also found, albeit infrequently, and mainly in potato stem tissue. The fate of three putative potato endophytes, Stenotrophomonas maltophilia, Bacillus sp., and Sphingomonas paucimobilis, was monitored following their release into potato plants via injection, via root dipping, or via the soil. Following stem injection, the S. maltophilia and Bacillus inoculants could be tracked over time periods of, respectively, 22 and 1 day(s) by dilution plating as well as via PCR-DGGE. However, only S. maltophilia was able to colonize, and persist in, plant tissue from soil or dipped roots. S. paucimobilis was never recovered from the plant irrespective of the mode of introduction. The diversity of the indigenous bacterial flora associated with potato was then monitored via PCR-DGGE. The patterns obtained revealed the existence of bacterial communities of limited complexity, with communities from potato stems typically differing from those from stem peel and roots. Evidence was obtained for the endophytic occurrence of a range of organisms falling into the α, β, and γ subgroups of the Proteobacteria as well as in the Firmicutes. Several of the sequences found matched those from isolates, suggesting that the molecular evidence reported culturable organisms. However, a number of sequences did not have matching sequences from isolates, suggesting that non-culturable or as-yet-uncultured endophytic organisms were being detected.
机译:马铃薯的内生细菌种群多样性(Solanum tuberosum cvDesirée)通过对植物浸软质进行稀释平板接种,然后对分离物进行分离和表征,并基于从植物中提取的DNA直接进行PCR-DGGE进行评估。在马铃薯茎基部和根中发现的可培养的内生细菌群落在大多数情况下为新鲜植物组织的103 至105 CFU g-1 。稀释平板显示这些种群主要是细菌类型。优势分离株分为Proteobacteria的α和γ亚组,以及黄杆菌/噬菌体组。还找到了Firmicutes的不同代表。最常分离的菌株(>总数的5%)被表征为不同的假单胞菌。 (包括金黄色葡萄球菌,皱纹假单胞菌和恶臭假单胞菌),放射线农杆菌,嗜麦芽单胞菌和嗜热黄杆菌,使用脂肪酸甲酯(FAME)分析和/或对其16S部分核糖体RNA基因进行测序。虽然很少见,但也发现了其他变形杆菌或Firmicutes,主要存在于马铃薯茎组织中。通过注射,浸根或通过土壤将三种假定的马铃薯内生菌,嗜麦芽窄食单胞菌,芽孢杆菌和短鞘氨醇单胞菌的命运监测。茎注射后,可以分别通过稀释平板和PCR-DGGE在22天和1天的时间段内跟踪嗜麦芽孢杆菌和接种芽孢杆菌。但是,只有嗜麦芽孢杆菌能够从土壤或浸根中定植并保留在植物组织中。不论引入方式如何,都从未从植物中回收到古菌。然后通过PCR-DGGE监测与马铃薯有关的本地细菌菌群的多样性。所获得的模式揭示了复杂程度有限的细菌群落的存在,马铃薯茎的群落通常不同于茎皮和根。有证据表明,内生菌属于变形杆菌的α,β和γ亚组,以及属于Firmicutes。发现的几个序列与分离株的序列匹配,表明分子证据报道了可培养的生物。然而,许多序列没有来自分离株的匹配序列,这表明正在检测到不可培养的或尚未培养的内生生物。

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