Research article Special Issues

Syntrophic microbial communities on straw as biofilm carrier increase the methane yield of a biowaste-digesting biogas reactor

  • Received: 19 April 2015 Accepted: 06 August 2015 Published: 21 August 2015
  • Biogas from biowaste can be an important source of renewable energy, but the fermentation process of low-structure waste is often unstable. The present study uses a full-scale biogas reactor to test the hypothesis that straw as an additional biofilm carrier will increase methane yield; and this effect is mirrored in a specific microbial community attached to the straw. Better reactor performance after addition of straw, at simultaneously higher organic loading rate and specific methane yield confirmed the hypothesis. The microbial communities on straw as a biofilm carrier and of the liquid reactor content were investigated using 16S rDNA amplicon sequencing by means of 454 pyrosequencing technology. The results revealed high diversity of the bacterial communities in the liquid reactor content as well as the biofilms on the straw. The most abundant archaea in all samples belonged to the genera Methanoculleus and Methanosarcina. Addition of straw resulted in a significantly different microbial community attached to the biofilm carrier. The bacterium Candidatus Cloacamonas acidaminovorans and methanogenic archaea of the genus Methanoculleus dominated the biofilm on straw. Syntrophic interactions between the hydrogenotrophic Methanoculleus sp. and members of the hydrogen-producing bacterial community within biofilms may explain the improved methane yield. Thus, straw addition can be used to improve and to stabilize the anaerobic process in substrates lacking biofilm-supporting structures.

    Citation: Frank R. Bengelsdorf, Christina Gabris, Lisa Michel, Manuel Zak, Marian Kazda. Syntrophic microbial communities on straw as biofilm carrier increase the methane yield of a biowaste-digesting biogas reactor[J]. AIMS Bioengineering, 2015, 2(3): 264-276. doi: 10.3934/bioeng.2015.3.264

    Related Papers:

  • Biogas from biowaste can be an important source of renewable energy, but the fermentation process of low-structure waste is often unstable. The present study uses a full-scale biogas reactor to test the hypothesis that straw as an additional biofilm carrier will increase methane yield; and this effect is mirrored in a specific microbial community attached to the straw. Better reactor performance after addition of straw, at simultaneously higher organic loading rate and specific methane yield confirmed the hypothesis. The microbial communities on straw as a biofilm carrier and of the liquid reactor content were investigated using 16S rDNA amplicon sequencing by means of 454 pyrosequencing technology. The results revealed high diversity of the bacterial communities in the liquid reactor content as well as the biofilms on the straw. The most abundant archaea in all samples belonged to the genera Methanoculleus and Methanosarcina. Addition of straw resulted in a significantly different microbial community attached to the biofilm carrier. The bacterium Candidatus Cloacamonas acidaminovorans and methanogenic archaea of the genus Methanoculleus dominated the biofilm on straw. Syntrophic interactions between the hydrogenotrophic Methanoculleus sp. and members of the hydrogen-producing bacterial community within biofilms may explain the improved methane yield. Thus, straw addition can be used to improve and to stabilize the anaerobic process in substrates lacking biofilm-supporting structures.


    加载中
    [1] Mshandete AM, Björnsson L, Kivaisi AK, et al. (2008) Performance of biofilm carriers in anaerobic digestion of sisal leaf waste leachate. EJB 11: 93-100.
    [2] Andersson J, Björnsson L (2002) Evaluation of straw as a biofilm carrier in the methanogenic stage of two-stage anaerobic digestion of crop residues. Bioresour Technol 85: 51-56. doi: 10.1016/S0960-8524(02)00071-8
    [3] Flemming H, Wingender J (2010) The biofilm matrix. Nat Rev Micro 8: 623-633.
    [4] Schink B, Stams AM (2013) Syntrophism among prokaryotes. In Rosenberg E, DeLong E, Lory S, Stackebrandt E, Thompson F (eds.), The Prokaryotes. Springer Berlin Heidelberg; 471-493.
    [5] Sutherland IW (2001) Biofilm exopolysaccharides: a strong and sticky framework. Microbiology 147: 3-9.
    [6] Langer S, Schropp D, Bengelsdorf FR, et al. (2013) Dynamics of biofilm formation during anaerobic digestion of organic waste. Anaerobe 29: 44-51.
    [7] Westerholm M, Levén L, Schnürer A (2012) Bioaugmentation of syntrophic acetate-oxidizing culture in biogas reactors exposed to increasing levels of ammonia. Appl Environ Microbiol 78: 7619-7625. doi: 10.1128/AEM.01637-12
    [8] Fotidis IA, Karakashev D, Angelidaki I (2013) The dominant acetate degradation pathway/methanogenic composition in full-scale anaerobic digesters operating under different ammonia levels. Int J Environ Sci Technol E-pub: 1-8.
    [9] Bengelsdorf FR, Gerischer U, Langer S, et al. (2013) Stability of a biogas-producing bacterial, archaeal and fungal community degrading food residues. FEMS Microbiol Ecol 84: 201-212. doi: 10.1111/1574-6941.12055
    [10] Fernández N, Díaz E, Amils R, et al. (2008) Analysis of microbial community during biofilm development in an anaerobic wastewater treatment reactor. Microb Ecol 56: 121-132. doi: 10.1007/s00248-007-9330-2
    [11] Nettmann E, Bergmann I, Pramschufer S, et al. (2010) Polyphasic analyses of methanogenic archaea communities in agricultural biogas plants. Appl Environ Microbiol 76: 2540-2548. doi: 10.1128/AEM.01423-09
    [12] Bengelsdorf FR. 2011. Characterization of the microbial community in a biogas reactor supplied with organic residues. Ph. D. thesis. Ulm University, Ulm.
    [13] McKenna P, Hoffmann C, Minkah N, et al. 2008. The macaque gut microbiome in health, lentiviral infection, and chronic enterocolitis. PLoS Pathog; e20.
    [14] Nicol GW, Glover LA, Prosser JI. (2003) The impact of grassland management on archaeal community structure in upland pasture rhizosphere soil. Environ Microbiol 5: 152-162. doi: 10.1046/j.1462-2920.2003.00399.x
    [15] Cole JR, Wang Q, Cardenas E, et al. (2009) The ribosomal database project: improved alignments and new tools for rRNA analysis. Nucleic Acids Res 37: D141-D145. doi: 10.1093/nar/gkn879
    [16] Angelidaki I, Ahring BK (1993) Thermophilic anaerobic digestion of livestock waste: the effect of ammonia. Appl Microbiol Biotechnol 38: 560-564.
    [17] Koster IW, Lettinga G (1988) Anaerobic digestion at extreme ammonia concentrations. Biological Wastes 25: 51-59. doi: 10.1016/0269-7483(88)90127-9
    [18] Li A, Chu Y, Wang X, et al. (2013) A pyrosequencing-based metagenomic study of methane-producing microbial community in solid-state biogas reactor. Biotechnol Biofuels 6: 3. doi: 10.1186/1754-6834-6-3
    [19] Martínez MA, Romero H, Perotti NI (2014) Two amplicon sequencing strategies revealed different facets of the prokaryotic community associated with the anaerobic treatment of vinasses from ethanol distilleries. Bioresour Technol 153: 388-392. doi: 10.1016/j.biortech.2013.12.030
    [20] Wirth R, Kovacs E, Maroti G, et al. (2012) Characterization of a biogas-producing microbial community by short-read next generation DNA sequencing. Biotechnol Biofuels 5: 41-56.
    [21] Kröber M, Bekel T, Diaz NN, et al. (2009) Phylogenetic characterization of a biogas plant microbial community integrating clone library 16S-rDNA sequences and metagenome sequence data obtained by 454-pyrosequencing. J Biotechnol 142: 38-49. doi: 10.1016/j.jbiotec.2009.02.010
    [22] Freundt EA, Whitcomb RF, Barile MF, et al. (1984) Proposal for elevation of the family Acholeplasmataceae to ordinal rank: Acholeplasmatales. Int J Syst Bacteriol 34: 346-349. doi: 10.1099/00207713-34-3-346
    [23] Razin S (2006) The genus Mycoplasma and related genera (Class Mollicutes). In Dworkin M, Falkow S, Rosenberg E, Schleifer K, Stackebrandt E (eds.), The Prokaryotes. Springer New York; 836-904.
    [24] Pelletier E, Kreimeyer A, Bocs S, et al. (2008) “Candidatus Cloacamonas acidaminovorans”: genome sequence reconstruction provides a first glimpse of a new bacterial division. J Bacteriol 190: 2572-2579. doi: 10.1128/JB.01248-07
    [25] Whitman W, Bowen T, Boone D (2006) The Methanogenic Bacteria, In Dworkin M, Falkow S, Rosenberg E, Schleifer K, Stackebrandt E (eds.), The Prokaryotes, 3rd ed., Springer, New York. 3: 165-207.
    [26] Lykidis A, Chen C, Tringe SG, et al. (2011) Multiple syntrophic interactions in a terephthalate-degrading methanogenic consortium. ISME J 5: 122-130. doi: 10.1038/ismej.2010.125
    [27] Sun L, Müller B, Westerholm M, et al. (2014) Syntrophic acetate oxidation in industrial CSTR biogas digesters. J Biotechnol 171: 39-44. doi: 10.1016/j.jbiotec.2013.11.016
    [28] Kazda M, Zak M, Kern M, et al. (2013) Treatment of liquid and solidmunicipal waste in anaerobic digestion optimized for biogas production. Fresenius Environ Bull 22: 2048-2052.
  • Reader Comments
  • © 2015 the Author(s), licensee AIMS Press. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0)
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Metrics

Article views(6364) PDF downloads(1231) Cited by(11)

Article outline

Figures and Tables

Figures(3)  /  Tables(2)

/

DownLoad:  Full-Size Img  PowerPoint
Return
Return

Catalog