Noviherbaspirillum denitrificans JCM 17722 is a facultative anaerobe, mesophilic, Gram-negative prokaryote that forms circular colonies and was isolated from rice paddy soil under denitrification-inducing conditions.
Gram-negative motile rod-shaped colony-forming facultative anaerobe mesophilic genome sequence 16S sequence| @ref 20215 |
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| Domain Pseudomonadati |
| Phylum Pseudomonadota |
| Class Betaproteobacteria |
| Order Burkholderiales |
| Family Oxalobacteraceae |
| Genus Noviherbaspirillum |
| Species Noviherbaspirillum denitrificans |
| Full scientific name Noviherbaspirillum denitrificans corrig. Ishii et al. 2017 |
| Synonyms (1) |
| @ref: | 68999 |
| multimedia content: | DSM_113107.jpg |
| multimedia.multimedia content: | https://www.dsmz.de/microorganisms/photos/DSM_113107.jpg |
| caption: | Micrograph of DSM 113107. Scale bar represents 2 um. |
| intellectual property rights: | Leibniz-Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH |
| manual_annotation: | 1 |
| @ref | Name | Growth | Medium link | Composition | |
|---|---|---|---|---|---|
| 68999 | R2A MEDIUM (DSMZ Medium 830) | Medium recipe at MediaDive | Name: R2A MEDIUM (DSMZ Medium 830) Composition: Agar 15.0 g/l Casamino acids 0.5 g/l Starch 0.5 g/l Glucose 0.5 g/l Proteose peptone 0.5 g/l Yeast extract 0.5 g/l K2HPO4 0.3 g/l Na-pyruvate 0.3 g/l MgSO4 x 7 H2O 0.05 g/l Distilled water | ||
| 43245 | Reasoner's 2A agar (R2A) | ||||
| 43245 | DNBNS medium | 100-fold diluted nutrient broth (DNB; Difco) supplemented with 3 mM nitrate and 4.4 mM succinate | |||
| 43245 | nutritient agar | ||||
| 43245 | trypticase soy broth (TSB) |
| @ref | Ability | Type | PH | PH range | |
|---|---|---|---|---|---|
| 43245 | positive | growth | 5.5-9.0 | alkaliphile |
| 43245 | Oxygen tolerancefacultative anaerobe |
| @ref | Salt | Growth | Tested relation | Concentration | |
|---|---|---|---|---|---|
| 43245 | NaCl | growth | 1 %(w/v) |
| @ref | Chebi-ID | Metabolite | Utilization activity | Kind of utilization tested | |
|---|---|---|---|---|---|
| 43245 | 52682 ChEBI | 1,2-butandiol | - | growth | |
| 43245 | 30089 ChEBI | acetate | + | electron donor | |
| 43245 | 17968 ChEBI | butyrate | + | electron donor | |
| 43245 | 62968 ChEBI | cellulose | - | growth | |
| 43245 | 17045 ChEBI | dinitrogen oxide | + | electron acceptor | |
| 43245 | 16236 ChEBI | ethanol | - | growth | |
| 43245 | 28757 ChEBI | fructose | - | growth | |
| 43245 | 28260 ChEBI | galactose | - | growth | |
| 43245 | 24265 ChEBI | gluconate | - | growth | |
| 43245 | 17234 ChEBI | glucose | - | growth | |
| 43245 | 17754 ChEBI | glycerol | + | electron donor | |
| 43245 | 24996 ChEBI | lactate | + | electron donor | |
| 43245 | 17716 ChEBI | lactose | - | growth | |
| 43245 | 17306 ChEBI | maltose | - | growth | |
| 43245 | 37684 ChEBI | mannose | - | growth | |
| 43245 | 17632 ChEBI | nitrate | + | electron donor | |
| 43245 | 16301 ChEBI | nitrite | + | electron acceptor | |
| 43245 | 15361 ChEBI | pyruvate | + | electron donor | |
| 43245 | 30911 ChEBI | sorbitol | - | growth | |
| 43245 | 28017 ChEBI | starch | - | growth | |
| 43245 | 30031 ChEBI | succinate | + | electron donor | |
| 43245 | 53423 ChEBI | tween 40 | + | growth | |
| 43245 | 53426 ChEBI | tween 80 | + | growth | |
| 43245 | 31011 ChEBI | valerate | + | electron donor | |
| 43245 | 18222 ChEBI | xylose | - | growth |
| @ref | pathway | enzyme coverage | annotated reactions | external links | |
|---|---|---|---|---|---|
| 66794 | butanoate fermentation | 100 | 4 of 4 | ||
| 66794 | Entner Doudoroff pathway | 100 | 10 of 10 | ||
| 66794 | adipate degradation | 100 | 2 of 2 | ||
| 66794 | threonine metabolism | 100 | 10 of 10 | ||
| 66794 | ethanol fermentation | 100 | 2 of 2 | ||
| 66794 | citric acid cycle | 100 | 14 of 14 | ||
| 66794 | molybdenum cofactor biosynthesis | 100 | 9 of 9 | ||
| 66794 | propanol degradation | 100 | 7 of 7 | ||
| 66794 | aspartate and asparagine metabolism | 100 | 9 of 9 | ||
| 66794 | L-lactaldehyde degradation | 100 | 3 of 3 | ||
| 66794 | biotin biosynthesis | 100 | 4 of 4 | ||
| 66794 | methylglyoxal degradation | 100 | 5 of 5 | ||
| 66794 | palmitate biosynthesis | 100 | 22 of 22 | ||
| 66794 | ppGpp biosynthesis | 100 | 4 of 4 | ||
| 66794 | valine metabolism | 100 | 9 of 9 | ||
| 66794 | resorcinol degradation | 100 | 2 of 2 | ||
| 66794 | hydrogen production | 100 | 5 of 5 | ||
| 66794 | cyanate degradation | 100 | 3 of 3 | ||
| 66794 | UDP-GlcNAc biosynthesis | 100 | 3 of 3 | ||
| 66794 | coenzyme A metabolism | 100 | 4 of 4 | ||
| 66794 | formaldehyde oxidation | 100 | 3 of 3 | ||
| 66794 | CDP-diacylglycerol biosynthesis | 100 | 2 of 2 | ||
| 66794 | folate polyglutamylation | 100 | 1 of 1 | ||
| 66794 | ubiquinone biosynthesis | 100 | 7 of 7 | ||
| 66794 | denitrification | 100 | 2 of 2 | ||
| 66794 | anapleurotic synthesis of oxalacetate | 100 | 1 of 1 | ||
| 66794 | cis-vaccenate biosynthesis | 100 | 2 of 2 | ||
| 66794 | reductive acetyl coenzyme A pathway | 100 | 7 of 7 | ||
| 66794 | suberin monomers biosynthesis | 100 | 2 of 2 | ||
| 66794 | tetrahydrofolate metabolism | 92.86 | 13 of 14 | ||
| 66794 | phenylalanine metabolism | 92.31 | 12 of 13 | ||
| 66794 | starch degradation | 90 | 9 of 10 | ||
| 66794 | serine metabolism | 88.89 | 8 of 9 | ||
| 66794 | lipid A biosynthesis | 88.89 | 8 of 9 | ||
| 66794 | isoleucine metabolism | 87.5 | 7 of 8 | ||
| 66794 | gluconeogenesis | 87.5 | 7 of 8 | ||
| 66794 | photosynthesis | 85.71 | 12 of 14 | ||
| 66794 | heme metabolism | 85.71 | 12 of 14 | ||
| 66794 | phenol degradation | 85 | 17 of 20 | ||
| 66794 | vitamin B1 metabolism | 84.62 | 11 of 13 | ||
| 66794 | leucine metabolism | 84.62 | 11 of 13 | ||
| 66794 | glycolate and glyoxylate degradation | 83.33 | 5 of 6 | ||
| 66794 | purine metabolism | 82.98 | 78 of 94 | ||
| 66794 | glycolysis | 82.35 | 14 of 17 | ||
| 66794 | glutamate and glutamine metabolism | 82.14 | 23 of 28 | ||
| 66794 | vitamin B6 metabolism | 81.82 | 9 of 11 | ||
| 66794 | proline metabolism | 81.82 | 9 of 11 | ||
| 66794 | lysine metabolism | 80.95 | 34 of 42 | ||
| 66794 | phenylacetate degradation (aerobic) | 80 | 4 of 5 | ||
| 66794 | ethylmalonyl-CoA pathway | 80 | 4 of 5 | ||
| 66794 | propionate fermentation | 80 | 8 of 10 | ||
| 66794 | 3-chlorocatechol degradation | 80 | 4 of 5 | ||
| 66794 | peptidoglycan biosynthesis | 80 | 12 of 15 | ||
| 66794 | alanine metabolism | 79.31 | 23 of 29 | ||
| 66794 | tryptophan metabolism | 78.95 | 30 of 38 | ||
| 66794 | 4-hydroxymandelate degradation | 77.78 | 7 of 9 | ||
| 66794 | chorismate metabolism | 77.78 | 7 of 9 | ||
| 66794 | NAD metabolism | 77.78 | 14 of 18 | ||
| 66794 | CO2 fixation in Crenarchaeota | 77.78 | 7 of 9 | ||
| 66794 | allantoin degradation | 77.78 | 7 of 9 | ||
| 66794 | d-mannose degradation | 77.78 | 7 of 9 | ||
| 66794 | cysteine metabolism | 77.78 | 14 of 18 | ||
| 66794 | CMP-KDO biosynthesis | 75 | 3 of 4 | ||
| 66794 | sulfopterin metabolism | 75 | 3 of 4 | ||
| 66794 | acetate fermentation | 75 | 3 of 4 | ||
| 66794 | 6-hydroxymethyl-dihydropterin diphosphate biosynthesis | 75 | 6 of 8 | ||
| 66794 | glycogen biosynthesis | 75 | 3 of 4 | ||
| 66794 | C4 and CAM-carbon fixation | 75 | 6 of 8 | ||
| 66794 | ketogluconate metabolism | 75 | 6 of 8 | ||
| 66794 | androgen and estrogen metabolism | 75 | 12 of 16 | ||
| 66794 | flavin biosynthesis | 73.33 | 11 of 15 | ||
| 66794 | pentose phosphate pathway | 72.73 | 8 of 11 | ||
| 66794 | histidine metabolism | 72.41 | 21 of 29 | ||
| 66794 | cardiolipin biosynthesis | 71.43 | 5 of 7 | ||
| 66794 | tyrosine metabolism | 71.43 | 10 of 14 | ||
| 66794 | glutathione metabolism | 71.43 | 10 of 14 | ||
| 66794 | lipid metabolism | 70.97 | 22 of 31 | ||
| 66794 | methionine metabolism | 69.23 | 18 of 26 | ||
| 66794 | urea cycle | 69.23 | 9 of 13 | ||
| 66794 | pyrimidine metabolism | 68.89 | 31 of 45 | ||
| 66794 | degradation of sugar alcohols | 68.75 | 11 of 16 | ||
| 66794 | non-pathway related | 68.42 | 26 of 38 | ||
| 66794 | enterobactin biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | octane oxidation | 66.67 | 2 of 3 | ||
| 66794 | nitrate assimilation | 66.67 | 6 of 9 | ||
| 66794 | degradation of aromatic, nitrogen containing compounds | 66.67 | 8 of 12 | ||
| 66794 | 3-phenylpropionate degradation | 66.67 | 10 of 15 | ||
| 66794 | acetyl CoA biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | acetoin degradation | 66.67 | 2 of 3 | ||
| 66794 | methane metabolism | 66.67 | 2 of 3 | ||
| 66794 | oxidative phosphorylation | 65.93 | 60 of 91 | ||
| 66794 | metabolism of disaccharids | 63.64 | 7 of 11 | ||
| 66794 | arginine metabolism | 62.5 | 15 of 24 | ||
| 66794 | sulfate reduction | 61.54 | 8 of 13 | ||
| 66794 | isoprenoid biosynthesis | 61.54 | 16 of 26 | ||
| 66794 | glycogen metabolism | 60 | 3 of 5 | ||
| 66794 | cellulose degradation | 60 | 3 of 5 | ||
| 66794 | lipoate biosynthesis | 60 | 3 of 5 | ||
| 66794 | gallate degradation | 60 | 3 of 5 | ||
| 66794 | vitamin K metabolism | 60 | 3 of 5 | ||
| 66794 | bile acid biosynthesis, neutral pathway | 58.82 | 10 of 17 | ||
| 66794 | aminopropanol phosphate biosynthesis | 50 | 1 of 2 | ||
| 66794 | cyclohexanol degradation | 50 | 2 of 4 | ||
| 66794 | mannosylglycerate biosynthesis | 50 | 1 of 2 | ||
| 66794 | ribulose monophosphate pathway | 50 | 1 of 2 | ||
| 66794 | quinate degradation | 50 | 1 of 2 | ||
| 66794 | toluene degradation | 50 | 2 of 4 | ||
| 66794 | pantothenate biosynthesis | 50 | 3 of 6 | ||
| 66794 | catecholamine biosynthesis | 50 | 2 of 4 | ||
| 66794 | phenylmercury acetate degradation | 50 | 1 of 2 | ||
| 66794 | dTDPLrhamnose biosynthesis | 50 | 4 of 8 | ||
| 66794 | glycine metabolism | 50 | 5 of 10 | ||
| 66794 | selenocysteine biosynthesis | 50 | 3 of 6 | ||
| 66794 | 4-hydroxyphenylacetate degradation | 50 | 5 of 10 | ||
| 66794 | phosphatidylethanolamine bioynthesis | 46.15 | 6 of 13 | ||
| 66794 | degradation of sugar acids | 44 | 11 of 25 | ||
| 66794 | benzoyl-CoA degradation | 42.86 | 3 of 7 | ||
| 66794 | vitamin B12 metabolism | 41.18 | 14 of 34 | ||
| 66794 | arachidonate biosynthesis | 40 | 2 of 5 | ||
| 66794 | factor 420 biosynthesis | 40 | 2 of 5 | ||
| 66794 | creatinine degradation | 40 | 2 of 5 | ||
| 66794 | glycine betaine biosynthesis | 40 | 2 of 5 | ||
| 66794 | degradation of hexoses | 38.89 | 7 of 18 | ||
| 66794 | phenylpropanoid biosynthesis | 38.46 | 5 of 13 | ||
| 66794 | cholesterol biosynthesis | 36.36 | 4 of 11 | ||
| 66794 | ascorbate metabolism | 36.36 | 8 of 22 | ||
| 66794 | degradation of pentoses | 35.71 | 10 of 28 | ||
| 66794 | polyamine pathway | 34.78 | 8 of 23 | ||
| 66794 | IAA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | (5R)-carbapenem carboxylate biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | arachidonic acid metabolism | 33.33 | 6 of 18 | ||
| 66794 | sphingosine metabolism | 33.33 | 2 of 6 | ||
| 66794 | coenzyme M biosynthesis | 30 | 3 of 10 | ||
| 66794 | aclacinomycin biosynthesis | 28.57 | 2 of 7 | ||
| 66794 | carotenoid biosynthesis | 27.27 | 6 of 22 | ||
| 66794 | lactate fermentation | 25 | 1 of 4 | ||
| 66794 | alginate biosynthesis | 25 | 1 of 4 | ||
| 66794 | carnitine metabolism | 25 | 2 of 8 | ||
| 66794 | methanogenesis from CO2 | 25 | 3 of 12 |
| Cat1 | Cat2 | Cat3 | |
|---|---|---|---|
| #Engineered | #Agriculture | #Field | |
| #Environmental | #Terrestrial | #Soil | |
| #Host | #Plants | #Herbaceous plants (Grass,Crops) |
| @ref | Sample type | Geographic location | Country | Country ISO 3 Code | Continent | Isolation procedure | |
|---|---|---|---|---|---|---|---|
| 43245 | rice paddy soil under denitrification-inducing conditions | Tokyo | Japan | JPN | Asia | functional single cell isolation method | |
| 67770 | Rice paddy soil under denitrification-inducing conditions | Tokyo | Japan | JPN | Asia | ||
| 68999 | Rice Paddy Soil | Field Production Science Center, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Nishi-Tokyo, Tokyo | Japan | JPN | Asia |
Global distribution of 16S sequence AB542397 (>99% sequence identity) for Noviherbaspirillum denitrificans from Microbeatlas ![]()
| @ref | Biosafety level | Biosafety level comment | |
|---|---|---|---|
| 68999 | 1 | Risk group (German classification) |
| @ref | Description | Assembly level | INSDC accession | BV-BRC accession | IMG accession | NCBI tax ID | |
|---|---|---|---|---|---|---|---|
| 67770 | ASM221144v1 assembly for Noviherbaspirillum denitrificans TSA40 | scaffold | 1968433 |
| @ref | Description | Accession | Length | Database | NCBI tax ID | |
|---|---|---|---|---|---|---|
| 43245 | Herbaspirillum sp. TSA40 gene for 16S ribosomal RNA, partial sequence, strain: TSA40 | AB542397 | 1458 | 1968433 |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125438 | gram-positive | gram-positiveⓘ | no | 96.00 | no |
| 125438 | anaerobic | anaerobicⓘ | no | 92.91 | yes |
| 125438 | aerobic | aerobicⓘ | yes | 72.03 | yes |
| 125438 | spore-forming | spore-formingⓘ | no | 88.79 | no |
| 125438 | thermophilic | thermophileⓘ | no | 96.82 | yes |
| 125438 | flagellated | motile2+ⓘ | yes | 87.77 | yes |
| Topic | Title | Authors | Journal | DOI | Year | |
|---|---|---|---|---|---|---|
| Genetics | A small step to discover candidate biological control agents from preexisting bioresources by using novel nonribosomal peptide synthetases hidden in activated sludge metagenomes. | Tomita S, Kuroda K, Narihiro T. | PLoS One | 10.1371/journal.pone.0294843 | 2023 | |
| Phylogeny | Massilia horti sp. nov. and Noviherbaspirillum arenae sp. nov., two novel soil bacteria of the Oxalobacteraceae. | Peta V, Raths R, Bucking H | Int J Syst Evol Microbiol | 10.1099/ijsem.0.004765 | 2021 | |
| Phylogeny | Noviherbaspirillum denitrificans sp. nov., a denitrifying bacterium isolated from rice paddy soil and Noviherbaspirillum autotrophicum sp. nov., a denitrifying, facultatively autotrophic bacterium isolated from rice paddy soil and proposal to reclassify Herbaspirillum massiliense as Noviherbaspirillum massiliense comb. nov. | Ishii S, Ashida N, Ohno H, Segawa T, Yabe S, Otsuka S, Yokota A, Senoo K | Int J Syst Evol Microbiol | 10.1099/ijsem.0.001875 | 2017 |
| #20215 | Parte, A.C., Sardà Carbasse, J., Meier-Kolthoff, J.P., Reimer, L.C. and Göker, M.: List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ. IJSEM ( DOI 10.1099/ijsem.0.004332 ) |
| #43245 | Satoshi Ishii, Naoaki Ashida, Hiroki Ohno, Takahiro Segawa, Shuhei Yabe, Shigeto Otsuka, Akira Yokota, Keishi Senoo: Noviherbaspirillum denitrificans sp. nov., a denitrifying bacterium isolated from rice paddy soil and Noviherbaspirillum autotrophicum sp. nov., a denitrifying, facultatively autotrophic bacterium isolated from rice paddy soil and proposal to reclassify Herbaspirillum massiliense as Noviherbaspirillum massiliense comb. nov.. IJSEM 67: 1841 - 1848 2017 ( DOI 10.1099/ijsem.0.001875 , PubMed 28629495 ) |
| #66794 | Antje Chang, Lisa Jeske, Sandra Ulbrich, Julia Hofmann, Julia Koblitz, Ida Schomburg, Meina Neumann-Schaal, Dieter Jahn, Dietmar Schomburg: BRENDA, the ELIXIR core data resource in 2021: new developments and updates. Nucleic Acids Res. 49: D498 - D508 2020 ( DOI 10.1093/nar/gkaa1025 , PubMed 33211880 ) |
| #67770 | Japan Collection of Microorganism (JCM) ; Curators of the JCM; |
| #68999 | Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 113107 |
| #69479 | João F Matias Rodrigues, Janko Tackmann,Gregor Rot, Thomas SB Schmidt, Lukas Malfertheiner, Mihai Danaila,Marija Dmitrijeva, Daniela Gaio, Nicolas Näpflin and Christian von Mering. University of Zurich.: MicrobeAtlas 1.0 beta . |
| #125438 | Julia Koblitz, Lorenz Christian Reimer, Rüdiger Pukall, Jörg Overmann: Predicting bacterial phenotypic traits through improved machine learning using high-quality, curated datasets. 2024 ( DOI 10.1101/2024.08.12.607695 ) |
| #126262 | A. Lissin, I. Schober, J. F. Witte, H. Lüken, A. Podstawka, J. Koblitz, B. Bunk, P. Dawyndt, P. Vandamme, P. de Vos, J. Overmann, L. C. Reimer: StrainInfo—the central database for linked microbial strain identifiers. ( DOI 10.1093/database/baaf059 ) |
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