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首页> 外文期刊>Soil Science and Plant Nutrition >Carbon flow into ammonia-oxidizing bacteria and archaea during decomposition of 13C-labeled plant residues in soil.
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Carbon flow into ammonia-oxidizing bacteria and archaea during decomposition of 13C-labeled plant residues in soil.

机译:碳在土壤中 13 C标记的植物残体的分解过程中流入氨氧化细菌和古细菌。

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Incorporation of plant residues into soil brings about nitrification when ammonification of organic nitrogen derived from plant residues proceeds. In the present study, we traced carbon flow into ammonia-oxidizing bacteria (AOB) and ammonia-oxidizing archaea (AOA) during decomposition of plant residues in a soil, by isotope 13 carbon (13C)-DNA stable isotope probing and denaturing gradient gel electrophoresis (DGGE) analysis of amoA genes encoding ammonia monooxygenase subunit A. Unlabeled (12C) and 13C-labeled dried rice (Oryza sativa) callus (Oryza sativa L. cv. Yukihikari) was used as a model plant residue. The soil with or without the dried rice callus was aerobically incubated with 55% of maximum water holding capacity for 56 days. DGGE analysis of AOB and AOA communities showed that the band patterns of the callus-treated soil gradually changed during incubation and was distinctly different from the no-callus treatment (control) after 28 and 42 days of incubation, respectively. Subsequent analysis after isopycnic centrifugation of the soil DNA showed that 13C-enriched AOB clones were obtained at 14 and 28 days, whereas 13C-enriched AOA clones were found at 28 days of incubation. The AOB community consisted of members of clusters 1, 9 and 11 and other members of Nitrosospira spp., of which most of the 13C-enriched clones were affiliated with clusters 1 and 9. The AOA community mostly belonged to the clusters consisting of clones obtained mainly from terrestrial environments. The 13C-enriched AOA clones were all closely related to "Nitrososphaera viennensis" and Candidatus Nitrososphaera gargensis. Our study showed that carbon derived from the dried rice callus flowed into both the AOB and AOA communities in the aerobically incubated soil during decomposition.
机译:当源自植物残留物的有机氮被氨化时,将植物残留物掺入土壤会引起硝化作用。在本研究中,我们通过同位素13碳( 13 C)-追踪了土壤中植物残留物分解过程中流入氨氧化细菌(AOB)和氨氧化古细菌(AOA)的碳流, DNA稳定同位素探测和变性梯度凝胶电泳(DGGE)分析编码氨单加氧酶亚基A的 amoA 基因。未标记( 12 C)和 13 使用C标记的稻米愈伤组织(Oryza sativa L. cv。Yukihikari)的残渣作为模型植物残渣。将有或没有干稻call的土壤与最大持水量的55%进行有氧培养56天。 DGGE对AOB和AOA群落的分析表明,在孵化28天和42天后,愈伤组织处理过的土壤的带型在孵化过程中逐渐改变,并且与非愈伤组织处理(对照)明显不同。等速离心土壤DNA后的分析表明,富集 13 C的AOB克隆在第14和28天获得,而富集 13 C的AOA克隆在28和28天获得孵化的天数。 AOB社区由群集1、9和11的成员以及亚硝基螺旋藻 spp。的其他成员组成,其中大多数 13 C富集的克隆都与群集1相关联。 9. AOA社区主要属于由主要从陆地环境获得的克隆组成的集群。富含 13 C的AOA克隆均与“ Nitrososphaera viennensis ”和 Candidatus Nitrososphaera gargensis密切相关。我们的研究表明,分解过程中,干稻愈伤组织产生的碳流入需氧培养土壤中的AOB和AOA群落。

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