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  • 1
    Online Resource
    Online Resource
    Informa UK Limited ; 2010
    In:  Bioscience, Biotechnology, and Biochemistry Vol. 74, No. 2 ( 2010-02-23), p. 433-436
    In: Bioscience, Biotechnology, and Biochemistry, Informa UK Limited, Vol. 74, No. 2 ( 2010-02-23), p. 433-436
    Type of Medium: Online Resource
    ISSN: 0916-8451 , 1347-6947
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2010
    detail.hit.zdb_id: 2110940-0
    SSG: 12
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  • 2
    In: International Journal of Systematic and Evolutionary Microbiology, Microbiology Society, Vol. 64, No. Pt_4 ( 2014-04-01), p. 1296-1303
    Abstract: An obligately anaerobic bacterial strain designated T-1-35 T was isolated as a dominant cultivable cellulose-degrading bacterium from soil of a Japanese rice field as an anaerobic filter-paper degrader. Cells of strain T-1-35 T stained Gram-positive and were non-spore-forming rods with rounded ends, 0.8–1.0×3.5–15.0 µm, and motile by means of two to four polar flagella. Cells of strain T-1-35 T exhibited pleomorphism: in aged cultures (over 90 days of incubation), almost all cells were irregularly shaped. Although no spore formation was observed, cells tolerated high temperatures, up to 90 °C for 10 min. The temperature range for growth was 15–40 °C, with an optimum at 35 °C. The pH range for growth was 5.5–9.0, with an optimum at pH 8.0–8.5 (slightly alkaliphilic). Strain T-1-35 T fermented some carbohydrates to produce ethanol and lactate as the major products. Major cellular fatty acids were iso-C 16 : 0 and iso-C 13 : 0 3-OH. Phylogenetic analysis based on the 16S rRNA gene sequence revealed that strain T-1-35 T belonged to Clostridium rRNA cluster III. The closest relative of strain T-1-35 T was Bacteroides cellulosolvens WM2 T , with 16S rRNA gene sequence similarity of 93.4 %. Phenotypic, physiological and molecular genetic methods demonstrated that strain T-1-35 T was distinct from its phylogenetic relatives (members of Clostridium rRNA cluster III) because it predominantly produced ethanol, iso-C 13 : 0 3-OH was a major cellular fatty acid and it always exhibited pleomorphism. On the basis of the results of a polyphasic taxonomic study, strain T-1-35 T is considered to represent a novel genus and species, Anaerobacterium chartisolvens gen. nov., sp. nov. The type strain of Anaerobacterium chartisolvens is T-1-35 T ( = DSM 27016 T  = NBRC 109520 T ). In addition, from the results of our phylogenetic analysis and its phenotypic features, the species Bacteroides cellulosolvens Murray et al. 1984 is proposed to be reclassified in the new genus Pseudobacteroides as Pseudobacteroides cellulosolvens gen. nov., comb. nov., with the type strain WM2 T ( = ATCC 35603 T  = DSM 2933 T  = NRCC 2944 T ).
    Type of Medium: Online Resource
    ISSN: 1466-5026 , 1466-5034
    Language: English
    Publisher: Microbiology Society
    Publication Date: 2014
    detail.hit.zdb_id: 215062-1
    detail.hit.zdb_id: 2056611-6
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    Microbiology Society ; 2015
    In:  International Journal of Systematic and Evolutionary Microbiology Vol. 65, No. Pt_3 ( 2015-03-01), p. 943-951
    In: International Journal of Systematic and Evolutionary Microbiology, Microbiology Society, Vol. 65, No. Pt_3 ( 2015-03-01), p. 943-951
    Abstract: An obligately anaerobic bacterial strain designated KC3 T was isolated from a rice straw-degrading culture, for which soil of a Japanese rice field was used as the inoculum. Cells of strain KC3 T were determined to be non-cellulolytic, Gram-stain-positive, non-motile, ellipsoidal, spore-forming rods, 0.8–1×4–25 µm. Endospores were formed at a terminal position in elongated cells (12–25 µm, mean 15 µm). The temperature range for growth was 20–50 °C, with an optimum at 37 °C. The pH range for growth was 5.0–7.5, with an optimum at pH 6.0 (slightly acidophilic). Strain KC3 T fermented cellobiose to lactate, butyrate, acetate, formate, hydrogen and carbon dioxide. The major cellular fatty acids ( 〉 10 %) were C 14 : 0 , C 16 : 0 and C 19 : 0 cyclo 11,12 dimethylacetal. The DNA G+C content of strain KC3 T was 37.5 mol%. 16S rRNA gene sequence analysis revealed that strain KC3 T shared low sequence similarity ( 〈 93 %) with type strains of the genus Clostridium sensu stricto ( Clostridium rRNA cluster I). Analyses of the DNA gyrase A and ATP synthase beta subunit sequences supported the affiliation of strain KC3 T to the genus Clostridium sensu stricto. The evidence presented here indicates that strain KC3 T represents a novel species of the genus Clostridium , for which the name Clostridium oryzae sp. nov. is proposed. The type strain of Clostridium oryzae is KC3 T ( = DSM 28571 T  = NBRC 110163 T ).
    Type of Medium: Online Resource
    ISSN: 1466-5026 , 1466-5034
    Language: English
    Publisher: Microbiology Society
    Publication Date: 2015
    detail.hit.zdb_id: 215062-1
    detail.hit.zdb_id: 2056611-6
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Microbiology Society ; 2019
    In:  International Journal of Systematic and Evolutionary Microbiology Vol. 69, No. 1 ( 2019-01-01), p. 220-226
    In: International Journal of Systematic and Evolutionary Microbiology, Microbiology Society, Vol. 69, No. 1 ( 2019-01-01), p. 220-226
    Type of Medium: Online Resource
    ISSN: 1466-5026 , 1466-5034
    Language: English
    Publisher: Microbiology Society
    Publication Date: 2019
    detail.hit.zdb_id: 215062-1
    detail.hit.zdb_id: 2056611-6
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    Microbiology Society ; 2019
    In:  International Journal of Systematic and Evolutionary Microbiology Vol. 71, No. 3 ( 2019-06-06)
    In: International Journal of Systematic and Evolutionary Microbiology, Microbiology Society, Vol. 71, No. 3 ( 2019-06-06)
    Abstract: Biological soil disinfestation (BSD) or reductive soil disinfestation (RSD) is a bioremediation method used to suppress or eliminate soil-borne plant pathogens by stimulating activities of indigenous anaerobic bacteria of the soil. An anaerobic bacterial strain (TW1 T ) was isolated from an anoxic soil sample subjected to the BSD treatment and comprehensively characterized. Cells of the strain were Gram-stain-positive, slightly curved and motile rods producing terminal spores. The strain was aerotolerant. Strain TW1 T was saccharolytic and produced acetate, butyrate, H 2 and CO 2 as fermentation end products. Strain TW1 T decomposed β-1,3-glucan (curdlan and laminarin) and degraded mycelial cells of an ascomycete Fusarium plant pathogen. Major cellular fatty acids of strain TW1 T were C 14 : 0 , C 14 : 0 dimethylacetal (DMA), C 16 : 0 aldehyde and C 16 : 0 DMA. Strain TW1 T made a group on the phylogenetic tree constructed based on 16S rRNA gene sequences with species such as Clostridium fallax (96.3 %) and Clostridium polyendosporum (96.0 %). Whole genome analysis of strain TW1 T showed that the total length of the genome was 5.28 Mb with the DNA G+C content of 31.3 mol%. The average nucleotide identity (ANIb) between strain TW1 T and C. fallax was 71.2 %. Presence of the genes encoding laminarinase or GH16 β-glucosidase was confirmed from the genome analysis of strain TW1 T . Based on the genomic, phylogenetic and phenotypic properties obtained, we propose strain TW1 T should be assigned in the genus Clostridium in the family Clostridiaceae as Clostridium fungisolvens sp. nov. The type strain TW1 T (=NBRC 112097 T =DSM 110791 T ).
    Type of Medium: Online Resource
    ISSN: 1466-5026 , 1466-5034
    Language: English
    Publisher: Microbiology Society
    Publication Date: 2019
    detail.hit.zdb_id: 215062-1
    detail.hit.zdb_id: 2056611-6
    SSG: 12
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  • 6
    In: International Journal of Systematic and Evolutionary Microbiology, Microbiology Society, Vol. 73, No. 1 ( 2023-01-27)
    Abstract: An obligately anaerobic bacterial strain (TB5 T ) was isolated from a soil sample subjected to reductive or biological soil disinfestation. Cells of the strain were Gram-stain-positive, spore-forming and motile rods. The strain grew at 15–40 °C (optimum, 37 °C) and pH 5.4–7.5 (optimum, pH 7.3). Strain TB5 T utilized a wide variety of carbohydrates including polysaccharides (cellulose, xylan, starch, inulin, glucomannan and laminarin) and organic acids. Acetate, ethanol, H 2 and CO 2 were products from the substrates utilized. The major components of the cellular fatty acids were C 16 : 1  ω 7 c DMA, C 16 : 0 DMA and C 18 : 1  ω 7 c DMA. The diagnostic amino acid of the cell-wall peptidoglycan was meso -diaminopimelic acid. The closest related species to strain TB5 T based on 16S rRNA gene sequences was Clostridium populeti 743A T (95.4 % sequence similarity). The genome size of strain TB5 T was 5.09 Mb and the genomic DNA G+C content was 32.7 mol%. Strain TB5 T had genes encoding polysaccharide-decomposing enzymes such as cellulase, xylanase, β-glucosidase and β-mannosidase in the genome. Based on the phylogenetic, genomic and phenotypic data, a novel species of a novel genus in the family Lachnospiraceae , Anaeromicropila herbilytica gen. nov., sp. nov., is proposed to accommodate the strain. The type species is Anaeromicropila herbilytica with strain TB5 T (=NBRC 112093 T =DSM 110037 T ) as the type strain. For the closest related species C. populeti , Anaeromicropila populeti comb. nov. is proposed with an emended description of the species.
    Type of Medium: Online Resource
    ISSN: 1466-5026 , 1466-5034
    Language: English
    Publisher: Microbiology Society
    Publication Date: 2023
    detail.hit.zdb_id: 215062-1
    detail.hit.zdb_id: 2056611-6
    SSG: 12
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  • 7
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 1999
    In:  Proceedings of the National Academy of Sciences Vol. 96, No. 15 ( 1999-07-20), p. 8522-8527
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 96, No. 15 ( 1999-07-20), p. 8522-8527
    Abstract: In the budding yeast, Saccharomyces cerevisiae , protein kinases Ste20p (p21 Cdc42p/Rac -activated kinase), Ste11p [mitogen-activated protein kinase (MAPK) kinase kinase], Ste7p (MAPK kinase), Fus3p, and Kss1p (MAPKs) are utilized for haploid mating, invasive growth, and diploid filamentous growth. Members of the highly conserved Ste20p/p65 PAK protein kinase family regulate MAPK signal transduction pathways from yeast to man. We describe here a potent negative regulator of Ste20p in the yeast filamentous growth-signaling pathway. We identified a mutant, hsl7 , that exhibits filamentous growth on rich medium. Hsl7p belongs to a highly conserved protein family in eukaryotes. Hsl7p associates with the noncatalytic region within the amino-terminal half of Ste20p as well as Cdc42p. Deletions of HSL7 in haploid and diploid strains led to cell elongation and enhancement of both haploid invasive growth and diploid pseudohyphal growth. However, deletions of STE20 in haploid and diploid greatly diminished these hsl7 -associated phenotypes. In addition, overexpression of HSL7 inhibited pseudohyphal growth. Thus, Hsl7p may inhibit the activity of Ste20p in the S. cerevisiae filamentous growth-signaling pathway. Our genetic analyses suggest the possibility that Cdc42p and Hsl7p compete for binding to Ste20p for pseudohyphal development when starved for nitrogen.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 1999
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 8
    Online Resource
    Online Resource
    Microbiology Society ; 2011
    In:  International Journal of Systematic and Evolutionary Microbiology Vol. 61, No. 6 ( 2011-06-01), p. 1246-1252
    In: International Journal of Systematic and Evolutionary Microbiology, Microbiology Society, Vol. 61, No. 6 ( 2011-06-01), p. 1246-1252
    Abstract: A pure culture of an obligately anaerobic, hydrogenotrophic, methanogenic archaeon, designated strain 169 T , which grows with hydrogen and carbon dioxide as the sole energy and carbon sources, was isolated from an anaerobic propionate-oxidizing enrichment culture originally obtained as an inoculant from rice-field soil in Japan. Cells of strain 169 T were non-motile, Gram-reaction-variable and rod-shaped or slightly curved rods with rounded ends (1.6–5.0×0.35–0.5 µm). Strain 169 T had fimbriae at both ends of the cell (up to ~10 per cell) but did not possess flagella. Ultrathin sections showed a single-layered, electron-dense cell wall about 6 nm thick, which is typical of Gram-positive bacteria. Growth was observed at 15 °C–45 °C (optimum 40 °C), at pH  6.5–9.6 (optimum pH 7.5–8.5) and in 0–70 g NaCl l −1 (0–1.2 M) (optimum 5 g NaCl l −1 ; 0.086 M). Strain 169 T utilized only hydrogen and carbon dioxide as energy and carbon sources. The DNA G+C content was 39.3 mol%. The results of 16S rRNA gene sequence analysis indicated that strain 169 T was most closely related to Methanobacterium subterraneum DSM 11074 T (96.8 % sequence similarity) and Methanobacterium formicicum DSM 1535 T (96.4 %). On the basis of its morphological, physiological and phylogenetic characteristics, strain 169 T ( = DSM 22026 T  = JCM 15797 T ) represents a novel species of the genus Methanobacterium , for which the name Methanobacterium kanagiense sp. nov. is proposed.
    Type of Medium: Online Resource
    ISSN: 1466-5026 , 1466-5034
    Language: English
    Publisher: Microbiology Society
    Publication Date: 2011
    detail.hit.zdb_id: 215062-1
    detail.hit.zdb_id: 2056611-6
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    Hindawi Limited ; 2010
    In:  International Journal of Microbiology Vol. 2010 ( 2010), p. 1-1
    In: International Journal of Microbiology, Hindawi Limited, Vol. 2010 ( 2010), p. 1-1
    Type of Medium: Online Resource
    ISSN: 1687-918X , 1687-9198
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2010
    detail.hit.zdb_id: 2467270-1
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  • 10
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1994
    In:  The Journal of Biochemistry Vol. 115, No. 4 ( 1994-4), p. 683-688
    In: The Journal of Biochemistry, Oxford University Press (OUP), Vol. 115, No. 4 ( 1994-4), p. 683-688
    Type of Medium: Online Resource
    ISSN: 1756-2651 , 0021-924X
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 1994
    detail.hit.zdb_id: 2009977-0
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