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Anaerobium acetethylicum gen. nov., sp. nov., a strictly anaerobic, gluconate-fermenting bacterium isolated from a methanogenic bioreactor

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2015

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International Journal of Systematic and Evolutionary Microbiology. 2015, 65(10), pp. 3289-3296. ISSN 1466-5026. eISSN 1466-5034. Available under: doi: 10.1099/ijsem.0.000410

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A novel strictly anaerobic, mesophilic bacterium was enriched and isolated with gluconate as sole substrate from a methanogenic sludge collected from a biogas reactor. Cells of strain GluBS11T stained Gram-positive and were non-motile, straight rods, measuring 3.0-4.5 × 0.8-1.2 μm. The temperature range for growth was 15-37 °C, with optimal growth at 30 °C, the pH range was 6.5-8.5, with optimal growth at pH 7, and the generation time under optimal conditions was 60 min. API Rapid 32A reactions were positive for α-galactosidase, α-glucosidase and β-glucosidase and negative for catalase and oxidase. A broad variety of substrates was utilized, including gluconate, glucose, fructose, maltose, sucrose, lactose, galactose, melezitose, melibiose, mannitol, erythritol, glycerol and aesculin. Products of gluconate fermentation were ethanol, acetate, formate, H2 and CO2. Neither sulfate nor nitrate served as an electron acceptor. Predominant cellular fatty acids (>10 %) were C14 : 0, C16 : 0, C16 : 1ω7c/iso-C15 : 0 2-OH and C18 : 1ω7c. The DNA G+C content of strain GluBS11T was 44.1 mol%. Phylogenetic analysis based on 16S rRNA gene sequence data revealed that strain GluBS11T is a member of subcluster XIVa within the order Clostridiales. The closest cultured relatives are Clostridium herbivorans (93.1 % similarity to the type strain), Clostridium populeti (93.3 %), Eubacterium uniforme (92.4 %) and Clostridium polysaccharolyticum (91.5 %). Based on this 16S rRNA gene sequence divergence (>6.5 %) as well as on chemotaxonomic and phenotypic differences from these taxa, strain GluBS11T is considered to represent a novel genus and species, for which the name Anaerobium acetethylicum gen. nov., sp. nov. is proposed. The type strain of Anaerobium acetethylicum is GluBS11T ( = LMG 28619T = KCTC 15450T = DSM 29698T).

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570 Biowissenschaften, Biologie

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ISO 690PATIL, Yogita, Madan JUNGHARE, Michael PESTER, Nicolai MÜLLER, Bernhard SCHINK, 2015. Anaerobium acetethylicum gen. nov., sp. nov., a strictly anaerobic, gluconate-fermenting bacterium isolated from a methanogenic bioreactor. In: International Journal of Systematic and Evolutionary Microbiology. 2015, 65(10), pp. 3289-3296. ISSN 1466-5026. eISSN 1466-5034. Available under: doi: 10.1099/ijsem.0.000410
BibTex
@article{Patil2015-10-01Anaer-32344,
  year={2015},
  doi={10.1099/ijsem.0.000410},
  title={Anaerobium acetethylicum gen. nov., sp. nov., a strictly anaerobic, gluconate-fermenting bacterium isolated from a methanogenic bioreactor},
  number={10},
  volume={65},
  issn={1466-5026},
  journal={International Journal of Systematic and Evolutionary Microbiology},
  pages={3289--3296},
  author={Patil, Yogita and Junghare, Madan and Pester, Michael and Müller, Nicolai and Schink, Bernhard}
}
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    <dcterms:abstract xml:lang="eng">A novel strictly anaerobic, mesophilic bacterium was enriched and isolated with gluconate as sole substrate from a methanogenic sludge collected from a biogas reactor. Cells of strain GluBS11&lt;sup&gt;T&lt;/sup&gt; stained Gram-positive and were non-motile, straight rods, measuring 3.0-4.5 × 0.8-1.2 μm. The temperature range for growth was 15-37 °C, with optimal growth at 30 °C, the pH range was 6.5-8.5, with optimal growth at pH 7, and the generation time under optimal conditions was 60 min. API Rapid 32A reactions were positive for α-galactosidase, α-glucosidase and β-glucosidase and negative for catalase and oxidase. A broad variety of substrates was utilized, including gluconate, glucose, fructose, maltose, sucrose, lactose, galactose, melezitose, melibiose, mannitol, erythritol, glycerol and aesculin. Products of gluconate fermentation were ethanol, acetate, formate, H&lt;sub&gt;2&lt;/sub&gt; and CO&lt;sub&gt;2&lt;/sub&gt;. Neither sulfate nor nitrate served as an electron acceptor. Predominant cellular fatty acids (&gt;10 %) were C&lt;sub&gt;14 : 0&lt;/sub&gt;, C&lt;sub&gt;16 : 0&lt;/sub&gt;, C&lt;sub&gt;16 : 1&lt;/sub&gt;ω7c/iso-C&lt;sub&gt;15 : 0&lt;/sub&gt; 2-OH and C&lt;sub&gt;18 : 1&lt;/sub&gt;ω7c. The DNA G+C content of strain GluBS11&lt;sup&gt;T&lt;/sup&gt; was 44.1 mol%. Phylogenetic analysis based on 16S rRNA gene sequence data revealed that strain GluBS11&lt;sup&gt;T&lt;/sup&gt; is a member of subcluster XIVa within the order Clostridiales. The closest cultured relatives are Clostridium herbivorans (93.1 % similarity to the type strain), Clostridium populeti (93.3 %), Eubacterium uniforme (92.4 %) and Clostridium polysaccharolyticum (91.5 %). Based on this 16S rRNA gene sequence divergence (&gt;6.5 %) as well as on chemotaxonomic and phenotypic differences from these taxa, strain GluBS11&lt;sup&gt;T&lt;/sup&gt; is considered to represent a novel genus and species, for which the name Anaerobium acetethylicum gen. nov., sp. nov. is proposed. The type strain of Anaerobium acetethylicum is GluBS11&lt;sup&gt;T&lt;/sup&gt; ( = LMG 28619&lt;sup&gt;T&lt;/sup&gt; = KCTC 15450&lt;sup&gt;T&lt;/sup&gt; = DSM 29698&lt;sup&gt;T&lt;/sup&gt;).</dcterms:abstract>
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