Description of Proteiniphilum saccharofermentans sp. nov., Petrimonas mucosa sp. nov. and Fermentimonas caenicola gen. nov., sp. nov., isolated from mesophilic laboratory-scale biogas reactors, and emended description of the genus Proteiniphilum.

Three novel, facultatively anaerobic bacteria of the family Porphyromonadaceae (phylum Bacteroidetes) were isolated from mesophilic laboratory-scale biogas reactors. The strains were Gram-negative rods. Optimal growth occurred between 35 and 45 °C and at pH 7.1-7.8. The main fermentation products were acetic and propionic acids. The predominant fatty acid in all strains was anteiso-C15 : 0, and the only respiratory quinone detected was menaquinone MK-8. 16S rRNA gene sequence comparison indicated that strains M3/6T and ING2-E5BT were most closely related to the type strain of Proteiniphilum acetatigenes, with sequence similarities of 97.3 and 94.5 %. Strain ING2-E5AT showed the closest affiliation to the type strain of Petrimonas sulfuriphila, with 97 % sequence identity. DNA-DNA hybridization of strain M3/6T and ING2-E5AT with the most closely related type strains showed 43.3-45.6 and 23.8-25.7 % relatedness, respectively, which supports the conclusion that both isolates represent novel species. Phylogenetic analysis and comparison of cellular fatty acid patterns indicated that strain ING2-E5BT cannot be classified as a member of any previously described genus. Therefore, because of the physiological, genotypic and chemotaxonomic differences, it is proposed to designate novel species within the genera Proteiniphilum and Petrimonas, Proteiniphilum saccharofermentans sp. nov. (type strain M3/6T = DSM 28694T = CECT 8610T = LMG 28299T) and Petrimonas mucosa sp. nov. (type strain ING2-E5AT = DSM 28695T = CECT 8611T), and a novel species of a new genus, Fermentimonas caenicola gen. nov., sp. nov. (type strain of Fermentimonas caenicola is ING2-E5BT = DSM 28696T = CECT 8609T = LMG 28429T). In addition, an emended description of the genus Proteiniphilum is provided.

[1]  Noel R. Krieg,et al.  Bacteroidetes phyl. nov. , 2015 .

[2]  A. Pühler,et al.  Community shifts in a well-operating agricultural biogas plant: how process variations are handled by the microbiome , 2015, Applied Microbiology and Biotechnology.

[3]  U. Szewzyk,et al.  Dynamic variation of the microbial community structure during the long-time mono-fermentation of maize and sugar beet silage , 2015, Microbial biotechnology.

[4]  M. Sakamoto,et al.  Dysgonomonas termitidis sp. nov., isolated from the gut of the subterranean termite Reticulitermes speratus. , 2015, International journal of systematic and evolutionary microbiology.

[5]  A. Pühler,et al.  Complete genome sequence of the novel Porphyromonadaceae bacterium strain ING2-E5B isolated from a mesophilic lab-scale biogas reactor. , 2015, Journal of biotechnology.

[6]  Michael Schmidt,et al.  Changes of the microbial population structure in an overloaded fed-batch biogas reactor digesting maize silage. , 2014, Bioresource technology.

[7]  A. Stams,et al.  Microbacter margulisiae gen. nov., sp. nov., a propionigenic bacterium isolated from sediments of an acid rock drainage pond. , 2014, International journal of systematic and evolutionary microbiology.

[8]  Kun Zhang,et al.  Dysgonomonas macrotermitis sp. nov., isolated from the hindgut of a fungus-growing termite. , 2014, International journal of systematic and evolutionary microbiology.

[9]  M. Klocke,et al.  Clostridium bornimense sp. nov., isolated from a mesophilic, two-phase, laboratory-scale biogas reactor. , 2014, International journal of systematic and evolutionary microbiology.

[10]  V. Zverlov,et al.  Comparative genotyping of Clostridium thermocellum strains isolated from biogas plants: genetic markers and characterization of cellulolytic potential. , 2014, Systematic and applied microbiology.

[11]  M. Drillich,et al.  Falsiporphyromonas endometrii gen. nov., sp. nov., isolated from the post-partum bovine uterus, and emended description of the genus Porphyromonas Shah and Collins 1988. , 2014, International journal of systematic and evolutionary microbiology.

[12]  A. Wright,et al.  Comparative metagenomic analysis of bacterial populations in three full-scale mesophilic anaerobic manure digesters , 2013, Applied Microbiology and Biotechnology.

[13]  R. Heyer,et al.  Metagenome and metaproteome analyses of microbial communities in mesophilic biogas-producing anaerobic batch fermentations indicate concerted plant carbohydrate degradation. , 2013, Systematic and applied microbiology.

[14]  S. Kleinsteuber,et al.  Microbial community structure and dynamics during anaerobic digestion of various agricultural waste materials , 2013, Applied Microbiology and Biotechnology.

[15]  Kazuya Watanabe,et al.  Dysgonomonas oryzarvi sp. nov., isolated from a microbial fuel cell. , 2012, International journal of systematic and evolutionary microbiology.

[16]  S. Sørensen,et al.  Profiling of the metabolically active community from a production-scale biogas plant by means of high-throughput metatranscriptome sequencing. , 2012, Journal of biotechnology.

[17]  A. Goesmann,et al.  Characterization of microbial biofilms in a thermophilic biogas system by high-throughput metagenome sequencing. , 2012, FEMS microbiology ecology.

[18]  S. Ratering,et al.  Unexpected Stability of Bacteroidetes and Firmicutes Communities in Laboratory Biogas Reactors Fed with Different Defined Substrates , 2012, Applied and Environmental Microbiology.

[19]  Noel R. Krieg,et al.  Phylum XIV. Bacteroidetes phyl. nov. , 2010 .

[20]  B. Linke,et al.  Novel upflow anaerobic solid-state (UASS) reactor. , 2010, Bioresource technology.

[21]  W. Ludwig,et al.  Notes on the characterization of prokaryote strains for taxonomic purposes. , 2010, International journal of systematic and evolutionary microbiology.

[22]  Naryttza N. Diaz,et al.  Phylogenetic characterization of a biogas plant microbial community integrating clone library 16S-rDNA sequences and metagenome sequence data obtained by 454-pyrosequencing. , 2009, Journal of biotechnology.

[23]  Tianlun Li,et al.  Insights into networks of functional microbes catalysing methanization of cellulose under mesophilic conditions. , 2009, Environmental microbiology.

[24]  Zhihua Zhou,et al.  The structure of the bacterial and archaeal community in a biogas digester as revealed by denaturing gradient gel electrophoresis and 16S rDNA sequencing analysis , 2009, Journal of applied microbiology.

[25]  K. Schleifer,et al.  The All-Species Living Tree project: a 16S rRNA-based phylogenetic tree of all sequenced type strains. , 2008, Systematic and applied microbiology.

[26]  Naryttza N. Diaz,et al.  The metagenome of a biogas-producing microbial community of a production-scale biogas plant fermenter analysed by the 454-pyrosequencing technology. , 2008, Journal of biotechnology.

[27]  Andreas Tauch,et al.  Taxonomic composition and gene content of a methane-producing microbial community isolated from a biogas reactor. , 2008, Journal of biotechnology.

[28]  J. Wiegel,et al.  Clostridium aciditolerans sp. nov., an acid-tolerant spore-forming anaerobic bacterium from constructed wetland sediment. , 2007, International journal of systematic and evolutionary microbiology.

[29]  H. Akasaka,et al.  Paludibacter propionicigenes gen. nov., sp. nov., a novel strictly anaerobic, Gram-negative, propionate-producing bacterium isolated from plant residue in irrigated rice-field soil in Japan. , 2006, International journal of systematic and evolutionary microbiology.

[30]  Xiuzhu Dong,et al.  Proteiniphilum acetatigenes gen. nov., sp. nov., from a UASB reactor treating brewery wastewater. , 2005, International journal of systematic and evolutionary microbiology.

[31]  B. Tindall,et al.  Petrimonas sulfuriphila gen. nov., sp. nov., a mesophilic fermentative bacterium isolated from a biodegraded oil reservoir. , 2005, International journal of systematic and evolutionary microbiology.

[32]  H. Kishino,et al.  Dating of the human-ape splitting by a molecular clock of mitochondrial DNA , 2005, Journal of Molecular Evolution.

[33]  K. Schleifer,et al.  ARB: a software environment for sequence data. , 2004, Nucleic acids research.

[34]  M. Sakamoto,et al.  Reclassification of Bacteroides forsythus (Tanner et al. 1986) as Tannerella forsythensis corrig., gen. nov., comb. nov. , 2002, International journal of systematic and evolutionary microbiology.

[35]  D. Claus,et al.  A standardized Gram staining procedure , 1992, World journal of microbiology & biotechnology.

[36]  W. Whitman,et al.  Precise Measurement of the G+C Content of Deoxyribonucleic Acid by High-Performance Liquid Chromatography , 1989 .

[37]  T. Devine,et al.  Fatty Acids, Antibiotic Resistance, and Deoxyribonucleic Acid Homology Groups of Bradyrhizobium japonicum , 1988 .

[38]  Lawrence G. Wayne,et al.  International Committee on Systematic Bacteriology: Announcement of the Report of the Ad Hoc Committee on Reconciliation of Approaches to Bacterial Systematics , 1988 .

[39]  T. Wood Preparation of crystalline, amorphous, and dyed cellulase substrates , 1988 .

[40]  K. Komagata,et al.  Determination of DNA base composition by reversed-phase high-performance liquid chromatography , 1984 .

[41]  K. Schleifer,et al.  Studies on the spectrophotometric determination of DNA hybridization from renaturation rates. , 1983, Systematic and applied microbiology.

[42]  L. Miller Single derivatization method for routine analysis of bacterial whole-cell fatty acid methyl esters, including hydroxy acids , 1982, Journal of clinical microbiology.

[43]  P. Cashion,et al.  A rapid method for the base ratio determination of bacterial DNA. , 1977, Analytical biochemistry.

[44]  J. Ley,et al.  The quantitative measurement of DNA hybridization from renaturation rates. , 1970, European journal of biochemistry.

[45]  G. L. Miller Use of Dinitrosalicylic Acid Reagent for Determination of Reducing Sugar , 1959 .