Biogeographic Patterns of Microbial Communities Associated with Syntrophic Butyrate Degradation in Paddy Soils in Eastern China

被引:0
|
作者
Fei Y. [1 ]
Jiao S. [1 ]
Lu Y. [1 ]
机构
[1] College of Urban and Environmental Sciences, Peking University, Beijing
关键词
Butyrate degradation; Methanogenic production; Microbial biogeography; Relative abundance of Syntrophomonas;
D O I
10.13209/j.0479-8023.2020.109
中图分类号
学科分类号
摘要
The authors collected 34 paddy soil samples along the latitude from eastern China. Enrichment experiment was conducted under anaerobic conditions with sodium butyrate as the sole substrate. The authors investigated the microbial community characteristics and the functional activity of syntrophic butyrate degradation and the biogeographic patterns of relative abundance of Syntrophomonas in these soils by Illumina sequencing of 16S rRNA genes. The lag phase of CH4 production (3-14 days) increased towards higher latitudes, whereas the maximum rate of CH4 production did not. The correlation analysis on influencing factors revealed that Syntropho-monas was the key syntrophic bacterial taxon associated with butyrate degradation and its relative abundance was significantly influenced by mean annual temperature (MAT). The sampling sites with a relatively high abundance of Syntrophomonas had a shorter time for the complete degradation of butyrate. Distance-decay patterns cha-racterized by a steeper slope were found in microbial communities associated with syntrophic butyrate degradation (p<0.05), indicating that the construction of microbial communities was driven by both spatial distance and envi-ronmental factors. © 2021 Peking University.
引用
收藏
页码:143 / 152
页数:9
相关论文
共 27 条
  • [1] Bouwman A F, Boumans L J M, Batjes N H., Emissions of N<sub>2</sub>O and NO from fertilized fields: Summary of available measurement data, Global Biogeochemi-cal Cycles, 16, 4, pp. 774-787, (2002)
  • [2] Schink B., Energetics of syntrophic cooperation in methanogenic degradation, Microbiology and Molecular Biology Reviews, 61, 2, pp. 262-280, (1997)
  • [3] Schink B, Stams A J M., Syntrophism among prokar-yotes, (2006)
  • [4] Roderick I., Metabolic activity of fatty acid-oxidizing bacteria and the contribution of acetate, propionate, butyrate, and CO<sub>2</sub> to Methanogenesis in cattle waste at 40 and 60℃, Applied and Environmental Micro-biology, 41, 6, pp. 1363-1373, (1981)
  • [5] Zou B Z, Takeda K, Tonouchi A, Et al., Characteristics of an anaerobic, syntrophic, butyrate-degrading bacterium in paddy field soil, Bioscience Biotechnology and Biochemistry, 67, 10, pp. 2059-2067, (2003)
  • [6] Wei Z, Jianchao Z, Yahai L., Stimulation of carbon nanomaterials on syntrophic oxidation of butyrate in sediment enrichments and a defined coculture, Scien-tific Reports, 8, 1, (2018)
  • [7] Li H, Chang J, Liu P, Et al., Direct interspecies electron transfer accelerates syntrophic oxidation of but-yrate in paddy soil enrichments, Environmental Mic-robiology, 17, 5, pp. 1533-1547, (2015)
  • [8] Li F, Tianze S, Wei Z, Et al., Stimulatory effect of magnetite nanoparticles on a highly enriched butyrate-oxidizing consortium, Frontiers in microbiology, 9, (2018)
  • [9] Zhang J, Lu Y., Conductive Fe<sub>3</sub>O<sub>4</sub> nanoparticles accelerate syntrophic methane production from butyrate oxidation in two different lake sediments, Frontiers in Microbiology, 7, (2016)
  • [10] Martiny J B H, Bohannan B J M, Brown J H, Et al., Microbial biogeography: putting microorganisms on the map, Nature Reviews Microbiology, 4, 2, pp. 102-112, (2006)