Improvement of biogas production by bioaugmentation.

Biogas production technologies commonly involve the use of natural anaerobic consortia of microbes. The objective of this study was to elucidate the importance of hydrogen in this complex microbial food chain. Novel laboratory biogas reactor prototypes were designed and constructed. The fates of pure hydrogen-producing cultures of Caldicellulosiruptor saccharolyticus and Enterobacter cloacae were followed in time in thermophilic and mesophilic natural biogas-producing communities, respectively. Molecular biological techniques were applied to study the altered ecosystems. A systematic study in 5-litre CSTR digesters revealed that a key fermentation parameter in the maintenance of an altered population balance is the loading rate of total organic solids. Intensification of the biogas production was observed and the results corroborate that the enhanced biogas productivity is associated with the increased abundance of the hydrogen producers. Fermentation parameters did not indicate signs of failure in the biogas production process. Rational construction of more efficient and sustainable biogas-producing microbial consortia is proposed.

Changes in the Archaea microbial community when the biogas fermenters are fed with protein-rich substrates.

Terminal restriction fragment length polymorphism (T-RFLP) was applied to study the changes in the composition of the methanogens of biogas-producing microbial communities on adaptation to protein-rich monosubstrates such as casein and blood. Specially developed laboratory scale (5-L) continuously stirred tank reactors have been developed and used in these experiments. Sequencing of the appropriate T-RF fragments selected from a methanogen-specific (mcrA gene-based) library revealed that the methanogens responded to the unconventional substrates by changing the community structure. T-RFLP of the 16S rDNA gene confirmed the findings.

Exploitation of the extremely thermophilic Caldicellulosiruptor saccharolyticus in hydrogen and biogas production from biomasses.

Caldicellulosiruptor saccharolyticus has attracted considerable attention by virtue of its ability to degrade various polysaccharide, oligosaccharide and monosaccharide substrates at temperatures above 70 degrees C, while its ability to convert various sugars to hydrogen has led to C. saccharolyticus being selected for the fermentative production of hydrogen. In this study, the utilization of a pure cellulosic substrate and mixed biomasses of plant origin was investigated. Cellulase biosynthesis can be triggered by growing cells on various monomeric carbohydrates, e.g. glucose or fructose. Pretreatment with cellulase-producing Bacilli improves the hydrogen yield, indicating that C. saccharolyticus alone can only partially decompose cellulosic substrates. The hydrogen-producing activity of C. saccharolyticus can be exploited in biogas technologies. With appropriate induction of the polymer-degrading enzymes, C. saccharolyticus may become a prime candidate with which to improve the yield and efficacy of practical hydrogen- and biogas-producing processes.