Description of Sporanaerobium hydrogeniformans gen. nov., sp. nov., an obligately anaerobic, hydrogen-producing bacterium isolated from Aravali hot spring in India

An obligately anaerobic bacterium XHS1971 T , capable of degrading cellulose and xylan, was isolated from a sediment sample of Aravali hot spring, Ratnagiri, India. Cells of strain XHS1971 T were Gram-stain-negative, spore-forming, motile, long-rods. Growth was observed at temperatures 30–50 °C (opt...

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Veröffentlicht in:Archives of microbiology 2023-09, Vol.205 (9), p.305-305, Article 305
Hauptverfasser: Hivarkar, Sai Suresh, Vasudevan, Gowdaman, Dhakephalkar, Prashant K., Dagar, Sumit Singh
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creator Hivarkar, Sai Suresh
Vasudevan, Gowdaman
Dhakephalkar, Prashant K.
Dagar, Sumit Singh
description An obligately anaerobic bacterium XHS1971 T , capable of degrading cellulose and xylan, was isolated from a sediment sample of Aravali hot spring, Ratnagiri, India. Cells of strain XHS1971 T were Gram-stain-negative, spore-forming, motile, long-rods. Growth was observed at temperatures 30–50 °C (optimum 40–45 °C), pH 5.0–10.0 (optimum pH 8.0) and NaCl concentrations 0–0.5% (optimum 0%). Generation time of strain XHS1971 T was 5 h under optimised growth conditions. Strain XHS1971 T showed the ability to metabolise different complex and simple sugars constituting lignocellulosic biomass. Glucose was fermented majorly into hydrogen, formic acid, acetic acid, and ethanol, whereas carbon dioxide, butyric acid, lactic acid and succinic acid were produced in traces. 16S rRNA gene analysis of strain XHS1971 T revealed  5%) were C 14:0 , C 16:0 , C 18:0 , and C 16:1 ω7 c . The genome size of the strain was 3.74 Mb with 35.3 mol% G + C content, and genes were annotated to carbohydrate metabolism, including genes involved in the degradation of cellulose and xylan and the production of hydrogen, ethanol and acetate. The uniqueness of strain was further validated by digital DNA-DNA hybridisation (dDDH), Average Nucleotide Identity (ANI), and Average Amino Acid Identity (AAI) values of 22%, 80%, and 63%, respectively, with nearest phylogenetic affiliates. Based on the detailed analyses, we propose a new genus and species, Sporanaerobium hydrogeniformans gen. nov., sp. nov., for strain XHS1971 T (= MCC3498 T  = KCTC15729 T  = JCM32657 T ) within family Lachnospiraceae .
doi_str_mv 10.1007/s00203-023-03641-6
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Cells of strain XHS1971 T were Gram-stain-negative, spore-forming, motile, long-rods. Growth was observed at temperatures 30–50 °C (optimum 40–45 °C), pH 5.0–10.0 (optimum pH 8.0) and NaCl concentrations 0–0.5% (optimum 0%). Generation time of strain XHS1971 T was 5 h under optimised growth conditions. Strain XHS1971 T showed the ability to metabolise different complex and simple sugars constituting lignocellulosic biomass. Glucose was fermented majorly into hydrogen, formic acid, acetic acid, and ethanol, whereas carbon dioxide, butyric acid, lactic acid and succinic acid were produced in traces. 16S rRNA gene analysis of strain XHS1971 T revealed &lt; 94.5% homology with Cellulosilyticum lentocellum DSM5427 T followed by Cellulosilyticum ruminicola JCM14822 T , identifying strain as a distinct member of family Lachnospiraceae . The major cellular fatty acids (&gt; 5%) were C 14:0 , C 16:0 , C 18:0 , and C 16:1 ω7 c . The genome size of the strain was 3.74 Mb with 35.3 mol% G + C content, and genes were annotated to carbohydrate metabolism, including genes involved in the degradation of cellulose and xylan and the production of hydrogen, ethanol and acetate. The uniqueness of strain was further validated by digital DNA-DNA hybridisation (dDDH), Average Nucleotide Identity (ANI), and Average Amino Acid Identity (AAI) values of 22%, 80%, and 63%, respectively, with nearest phylogenetic affiliates. 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Cells of strain XHS1971 T were Gram-stain-negative, spore-forming, motile, long-rods. Growth was observed at temperatures 30–50 °C (optimum 40–45 °C), pH 5.0–10.0 (optimum pH 8.0) and NaCl concentrations 0–0.5% (optimum 0%). Generation time of strain XHS1971 T was 5 h under optimised growth conditions. Strain XHS1971 T showed the ability to metabolise different complex and simple sugars constituting lignocellulosic biomass. Glucose was fermented majorly into hydrogen, formic acid, acetic acid, and ethanol, whereas carbon dioxide, butyric acid, lactic acid and succinic acid were produced in traces. 16S rRNA gene analysis of strain XHS1971 T revealed &lt; 94.5% homology with Cellulosilyticum lentocellum DSM5427 T followed by Cellulosilyticum ruminicola JCM14822 T , identifying strain as a distinct member of family Lachnospiraceae . The major cellular fatty acids (&gt; 5%) were C 14:0 , C 16:0 , C 18:0 , and C 16:1 ω7 c . The genome size of the strain was 3.74 Mb with 35.3 mol% G + C content, and genes were annotated to carbohydrate metabolism, including genes involved in the degradation of cellulose and xylan and the production of hydrogen, ethanol and acetate. The uniqueness of strain was further validated by digital DNA-DNA hybridisation (dDDH), Average Nucleotide Identity (ANI), and Average Amino Acid Identity (AAI) values of 22%, 80%, and 63%, respectively, with nearest phylogenetic affiliates. 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Vasudevan, Gowdaman ; Dhakephalkar, Prashant K. ; Dagar, Sumit Singh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-7efca0d995968feecacd4d2a522398bf9ee0e117911b3fcc754bed16ad9f615c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>acetates</topic><topic>Acetic acid</topic><topic>Amino acids</topic><topic>Anaerobiosis</topic><topic>Bacteria</topic><topic>Bacteria, Anaerobic - genetics</topic><topic>Bacterial Typing Techniques</topic><topic>Base Composition</topic><topic>Biochemistry</topic><topic>biomass</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Butyric acid</topic><topic>Carbohydrate metabolism</topic><topic>Carbohydrates</topic><topic>Carbon dioxide</topic><topic>Cell Biology</topic><topic>Cellulose</topic><topic>Cellulose - metabolism</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>Ecology</topic><topic>Ethanol</topic><topic>family</topic><topic>Fatty acids</topic><topic>Fatty Acids - analysis</topic><topic>Formic acid</topic><topic>Genes</topic><topic>Genomes</topic><topic>glucose</topic><topic>Growth conditions</topic><topic>Homology</topic><topic>Hot springs</topic><topic>Hot Springs - microbiology</topic><topic>Hybridization</topic><topic>Hydrogen</topic><topic>Hydrogen - metabolism</topic><topic>Hydrogen production</topic><topic>India</topic><topic>Lachnospiraceae</topic><topic>Lactic acid</topic><topic>Life Sciences</topic><topic>Lignocellulose</topic><topic>Microbial Ecology</topic><topic>Microbiology</topic><topic>New genera</topic><topic>new genus</topic><topic>New species</topic><topic>Nucleotides</topic><topic>Original Paper</topic><topic>Phylogeny</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>rRNA 16S</topic><topic>Sediment samplers</topic><topic>sediments</topic><topic>Sequence Analysis, DNA</topic><topic>Sodium chloride</topic><topic>species</topic><topic>Strain analysis</topic><topic>Succinic acid</topic><topic>Xylan</topic><topic>Xylans</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hivarkar, Sai Suresh</creatorcontrib><creatorcontrib>Vasudevan, Gowdaman</creatorcontrib><creatorcontrib>Dhakephalkar, Prashant K.</creatorcontrib><creatorcontrib>Dagar, Sumit Singh</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; 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Cells of strain XHS1971 T were Gram-stain-negative, spore-forming, motile, long-rods. Growth was observed at temperatures 30–50 °C (optimum 40–45 °C), pH 5.0–10.0 (optimum pH 8.0) and NaCl concentrations 0–0.5% (optimum 0%). Generation time of strain XHS1971 T was 5 h under optimised growth conditions. Strain XHS1971 T showed the ability to metabolise different complex and simple sugars constituting lignocellulosic biomass. Glucose was fermented majorly into hydrogen, formic acid, acetic acid, and ethanol, whereas carbon dioxide, butyric acid, lactic acid and succinic acid were produced in traces. 16S rRNA gene analysis of strain XHS1971 T revealed &lt; 94.5% homology with Cellulosilyticum lentocellum DSM5427 T followed by Cellulosilyticum ruminicola JCM14822 T , identifying strain as a distinct member of family Lachnospiraceae . The major cellular fatty acids (&gt; 5%) were C 14:0 , C 16:0 , C 18:0 , and C 16:1 ω7 c . The genome size of the strain was 3.74 Mb with 35.3 mol% G + C content, and genes were annotated to carbohydrate metabolism, including genes involved in the degradation of cellulose and xylan and the production of hydrogen, ethanol and acetate. The uniqueness of strain was further validated by digital DNA-DNA hybridisation (dDDH), Average Nucleotide Identity (ANI), and Average Amino Acid Identity (AAI) values of 22%, 80%, and 63%, respectively, with nearest phylogenetic affiliates. Based on the detailed analyses, we propose a new genus and species, Sporanaerobium hydrogeniformans gen. nov., sp. nov., for strain XHS1971 T (= MCC3498 T  = KCTC15729 T  = JCM32657 T ) within family Lachnospiraceae .</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37572166</pmid><doi>10.1007/s00203-023-03641-6</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; SpringerLink Journals - AutoHoldings
subjects acetates
Acetic acid
Amino acids
Anaerobiosis
Bacteria
Bacteria, Anaerobic - genetics
Bacterial Typing Techniques
Base Composition
Biochemistry
biomass
Biomedical and Life Sciences
Biotechnology
Butyric acid
Carbohydrate metabolism
Carbohydrates
Carbon dioxide
Cell Biology
Cellulose
Cellulose - metabolism
Deoxyribonucleic acid
DNA
DNA, Bacterial - chemistry
DNA, Bacterial - genetics
Ecology
Ethanol
family
Fatty acids
Fatty Acids - analysis
Formic acid
Genes
Genomes
glucose
Growth conditions
Homology
Hot springs
Hot Springs - microbiology
Hybridization
Hydrogen
Hydrogen - metabolism
Hydrogen production
India
Lachnospiraceae
Lactic acid
Life Sciences
Lignocellulose
Microbial Ecology
Microbiology
New genera
new genus
New species
Nucleotides
Original Paper
Phylogeny
RNA, Ribosomal, 16S - genetics
rRNA 16S
Sediment samplers
sediments
Sequence Analysis, DNA
Sodium chloride
species
Strain analysis
Succinic acid
Xylan
Xylans
title Description of Sporanaerobium hydrogeniformans gen. nov., sp. nov., an obligately anaerobic, hydrogen-producing bacterium isolated from Aravali hot spring in India
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