Biogas production from protein-rich biomass: fed-batch anaerobic fermentation of casein and of pig blood and associated changes in microbial community composition

PLoS One. 2013 Oct 16;8(10):e77265. doi: 10.1371/journal.pone.0077265. eCollection 2013.

Abstract

It is generally accepted as a fact in the biogas technology that protein-rich biomass substrates should be avoided due to inevitable process inhibition. Substrate compositions with a low C/N ratio are considered difficult to handle and may lead to process failure, though protein-rich industrial waste products have outstanding biogas generation potential. This common belief has been challenged by using protein-rich substrates, i.e. casein and precipitated pig blood protein in laboratory scale continuously stirred mesophilic fed-batch biogas fermenters. Both substrates proved suitable for sustained biogas production (0.447 L CH4/g protein oDM, i.e. organic total solids) in high yield without any additives, following a period of adaptation of the microbial community. The apparent key limiting factors in the anaerobic degradation of these proteinaceous materials were the accumulation of ammonia and hydrogen sulfide. Changes in time in the composition of the microbiological community were determined by next-generation sequencing-based metagenomic analyses. Characteristic rearrangements of the biogas-producing community upon protein feeding and specific differences due to the individual protein substrates were recognized. The results clearly demonstrate that sustained biogas production is readily achievable, provided the system is well-characterized, understood and controlled. Biogas yields (0.45 L CH4/g oDM) significantly exceeding those of the commonly used agricultural substrates (0.25-0.28 L CH4/g oDM) were routinely obtained. The results amply reveal that these high-energy-content waste products can be converted to biogas, a renewable energy carrier with flexible uses that can replace fossil natural gas in its applications. Process control, with appropriate acclimation of the microbial community to the unusual substrate, is necessary. Metagenomic analysis of the microbial community by next-generation sequencing allows a precise determination of the alterations in the community composition in the course of the process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / chemistry
  • Ammonium Compounds / chemistry
  • Animals
  • Biofuels*
  • Biomass*
  • Bioreactors
  • Biotransformation
  • Blood / metabolism
  • Blood / microbiology
  • Caseins / chemistry
  • Caseins / metabolism
  • Enzyme Activation
  • Fatty Acids / chemistry
  • Fermentation
  • Industrial Waste*
  • Microbiota
  • Peptide Hydrolases / chemistry
  • Peptide Hydrolases / metabolism
  • Substrate Specificity
  • Swine
  • Time Factors

Substances

  • Acetates
  • Ammonium Compounds
  • Biofuels
  • Caseins
  • Fatty Acids
  • Industrial Waste
  • Peptide Hydrolases

Grants and funding

This work was supported by EU projects HUSRB/1002/214/041 IPA, HURO/1001/193/2.2.2. CBC, and IEE/10/235 SI2.591589 GreenGasGrids. Funding from Baross_ALGOLABH OMFB-00356/2010, TÁMOP 4.2.4.A/2-11-1-2012-0001 and TÁMOP-4.2.2/B-10/1-2010-0012 is gratefully acknowledged. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.