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Effects of Agronomic Treatments on Structure and Function of Ammonia-Oxidizing Communities

机译:农艺处理对氨氧化社区结构和功能的影响

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摘要

The aim of this study was to determine the effects of different agricultural treatments and plant communities on the diversity of ammonia oxidizer populations in soil. Denaturing gradient gel electrophoresis (DGGE), coupled with specific oligonucleotide probing, was used to analyze 16S rRNA genes of ammonia oxidizers belonging to the β subgroup of the division Proteobacteria by use of DNA extracted from cultivated, successional, and native deciduous forest soils. Community profiles of the different soil types were compared with nitrification rates and most-probable-number (MPN) counts. Despite significant variation in measured nitrification rates among communities, there were no differences in the DGGE banding profiles of DNAs extracted from these soils. DGGE profiles of DNA extracted from samples of MPN incubations, cultivated at a range of ammonia concentrations, showed the presence of bands not amplified from directly extracted DNA. Nitrosomonas-like bands were seen in the MPN DNA but were not detected in the DNA extracted directly from soils. These bands were detected in some samples taken from MPN incubations carried out with medium containing 1,000 μg of NH4+-N ml−1, to the exclusion of bands detected in the native DNA. Cell concentrations of ammonia oxidizers determined by MPN counts were between 10- and 100-fold lower than those determined by competitive PCR (cPCR). Although no differences were seen in ammonia oxidizer MPN counts from the different soil treatments, cPCR revealed higher numbers in fertilized soils. The use of a combination of traditional and molecular methods to investigate the activities and compositions of ammonia oxidizers in soil demonstrates differences in fine-scale compositions among treatments that may be associated with changes in population size and function.
机译:这项研究的目的是确定不同的农业处理方法和植物群落对土壤中氨氧化剂种群多样性的影响。变性梯度凝胶电泳(DGGE)结合特异性寡核苷酸探测,通过使用从人工,演替和天然落叶林土壤中提取的DNA,分析了属于变形杆菌科β亚组的氨氧化剂的16S rRNA基因。将不同土壤类型的群落概况与硝化率和最可能数(MPN)计数进行比较。尽管各社区之间测得的硝化率存在显着差异,但从这些土壤中提取的DNA的DGGE条带图谱没有差异。从MPN孵育样品中提取的DNA的DGGE图谱(在一定范围的氨浓度下培养)表明存在未从直接提取的DNA扩增的条带。在MPN DNA中可以看到类似亚硝基甲烷的条带,但在直接从土壤中提取的DNA中却没有检测到。在某些MPN孵育样品中检测到了这些条带,而MPN孵育是在含有1,000μgNH4 + -N ml-1的培养基中进行的,排除了在天然DNA中检测到的条带。通过MPN计数确定的氨氧化剂的细胞浓度比通过竞争PCR(cPCR)确定的浓度低10到100倍。尽管在不同土壤处理中氨氧化器MPN计数没有差异,但cPCR揭示施肥土壤中的数量更高。传统方法和分子方法的组合用于研究土壤中氨氧化剂的活性和组成的研究表明,处理之间精细尺度组成的差异可能与种群大小和功能的变化有关。

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