Thioclava dalianensis DLFJ1-1 is an aerobe, Gram-negative, rod-shaped bacterium that was isolated from oil-degrading bacterial consortium, enriched by surface seawater.
Gram-negative rod-shaped aerobe genome sequence 16S sequence Bacteria| @ref 20215 |
|
|
| Domain Bacteria |
| Phylum Pseudomonadota |
| Class Alphaproteobacteria |
| Order Rhodobacterales |
| Family Paracoccaceae |
| Genus Thioclava |
| Species Thioclava dalianensis |
| Full scientific name Thioclava dalianensis Zhang et al. 2013 |
| @ref | Name | Growth | Medium link | Composition | |
|---|---|---|---|---|---|
| 21842 | BACTO MARINE BROTH (DIFCO 2216) (DSMZ Medium 514) | Medium recipe at MediaDive | Name: BACTO MARINE BROTH (DIFCO 2216) (DSMZ Medium 514) Composition: NaCl 19.45 g/l MgCl2 5.9 g/l Bacto peptone 5.0 g/l Na2SO4 3.24 g/l CaCl2 1.8 g/l Yeast extract 1.0 g/l KCl 0.55 g/l NaHCO3 0.16 g/l Fe(III) citrate 0.1 g/l KBr 0.08 g/l SrCl2 0.034 g/l H3BO3 0.022 g/l Na2HPO4 0.008 g/l Na-silicate 0.004 g/l NaF 0.0024 g/l (NH4)NO3 0.0016 g/l Distilled water |
| 30859 | Oxygen toleranceaerobe |
| @ref | Chebi-ID | Metabolite | Utilization activity | Kind of utilization tested | |
|---|---|---|---|---|---|
| 30859 | 30089 ChEBI | acetate | + | carbon source | |
| 30859 | 16449 ChEBI | alanine | + | carbon source | |
| 68369 | 29016 ChEBI | arginine | - | hydrolysis | from API 20NE |
| 30859 | 22653 ChEBI | asparagine | + | carbon source | |
| 30859 | 35391 ChEBI | aspartate | + | carbon source | |
| 30859 | 17057 ChEBI | cellobiose | + | carbon source | |
| 30859 | 16947 ChEBI | citrate | + | carbon source | |
| 68369 | 17634 ChEBI | D-glucose | - | fermentation | from API 20NE |
| 68369 | 16899 ChEBI | D-mannitol | + | assimilation | from API 20NE |
| 68369 | 27689 ChEBI | decanoate | - | assimilation | from API 20NE |
| 30859 | 23652 ChEBI | dextrin | + | carbon source | |
| 68369 | 4853 ChEBI | esculin | + | hydrolysis | from API 20NE |
| 30859 | 28757 ChEBI | fructose | + | carbon source | |
| 30859 | 33984 ChEBI | fucose | + | carbon source | |
| 30859 | 24148 ChEBI | galactonate | + | carbon source | |
| 68369 | 5291 ChEBI | gelatin | - | hydrolysis | from API 20NE |
| 30859 | 24265 ChEBI | gluconate | + | carbon source | |
| 68369 | 24265 ChEBI | gluconate | + | assimilation | from API 20NE |
| 30859 | 17234 ChEBI | glucose | + | carbon source | |
| 30859 | 32323 ChEBI | glucuronamide | + | carbon source | |
| 30859 | 29987 ChEBI | glutamate | + | carbon source | |
| 30859 | 17754 ChEBI | glycerol | + | carbon source | |
| 30859 | 17596 ChEBI | inosine | + | carbon source | |
| 30859 | 17240 ChEBI | itaconate | + | carbon source | |
| 30859 | 21217 ChEBI | L-alaninamide | + | carbon source | |
| 68369 | 30849 ChEBI | L-arabinose | + | assimilation | from API 20NE |
| 30859 | 24996 ChEBI | lactate | + | carbon source | |
| 30859 | 17716 ChEBI | lactose | + | carbon source | |
| 30859 | 25017 ChEBI | leucine | + | carbon source | |
| 68369 | 25115 ChEBI | malate | + | assimilation | from API 20NE |
| 30859 | 15792 ChEBI | malonate | + | carbon source | |
| 30859 | 17306 ChEBI | maltose | + | carbon source | |
| 68369 | 17306 ChEBI | maltose | + | assimilation | from API 20NE |
| 30859 | 37684 ChEBI | mannose | + | carbon source | |
| 30859 | 28053 ChEBI | melibiose | + | carbon source | |
| 30859 | 51850 ChEBI | methyl pyruvate | + | carbon source | |
| 68369 | 59640 ChEBI | N-acetylglucosamine | + | assimilation | from API 20NE |
| 68369 | 17632 ChEBI | nitrate | - | reduction | from API 20NE |
| 30859 | 28044 ChEBI | phenylalanine | + | carbon source | |
| 30859 | 26271 ChEBI | proline | + | carbon source | |
| 30859 | 26490 ChEBI | quinate | + | carbon source | |
| 30859 | 16634 ChEBI | raffinose | + | carbon source | |
| 30859 | 26546 ChEBI | rhamnose | + | carbon source | |
| 30859 | 15963 ChEBI | ribitol | + | carbon source | |
| 30859 | 17822 ChEBI | serine | + | carbon source | |
| 30859 | 30911 ChEBI | sorbitol | + | carbon source | |
| 30859 | 30031 ChEBI | succinate | + | carbon source | |
| 30859 | 26986 ChEBI | threonine | + | carbon source | |
| 30859 | 17748 ChEBI | thymidine | + | carbon source | |
| 30859 | 27082 ChEBI | trehalose | + | carbon source | |
| 68369 | 27897 ChEBI | tryptophan | - | energy source | from API 20NE |
| 68369 | 16199 ChEBI | urea | - | hydrolysis | from API 20NE |
| 30859 | 16704 ChEBI | uridine | + | carbon source |
| @ref | Value | Activity | Ec | |
|---|---|---|---|---|
| 30859 | acid phosphatase | + | 3.1.3.2 | |
| 30859 | alkaline phosphatase | + | 3.1.3.1 | |
| 68369 | arginine dihydrolase | - | 3.5.3.6 | from API 20NE |
| 68369 | beta-glucosidase | + | 3.2.1.21 | from API 20NE |
| 21842 | catalase | + | 1.11.1.6 | |
| 30859 | catalase | + | 1.11.1.6 | |
| 30859 | cytochrome oxidase | + | 1.9.3.1 | |
| 68369 | cytochrome oxidase | + | 1.9.3.1 | from API 20NE |
| 21842 | cytochrome-c oxidase | + | 1.9.3.1 | |
| 68369 | gelatinase | - | from API 20NE | |
| 30859 | urease | + | 3.5.1.5 | |
| 68369 | urease | - | 3.5.1.5 | from API 20NE |
| @ref | pathway | enzyme coverage | annotated reactions | external links | |
|---|---|---|---|---|---|
| 66794 | ppGpp biosynthesis | 100 | 4 of 4 | ||
| 66794 | coenzyme A metabolism | 100 | 4 of 4 | ||
| 66794 | formaldehyde oxidation | 100 | 3 of 3 | ||
| 66794 | adipate degradation | 100 | 2 of 2 | ||
| 66794 | phenylacetate degradation (aerobic) | 100 | 5 of 5 | ||
| 66794 | methylglyoxal degradation | 100 | 5 of 5 | ||
| 66794 | L-lactaldehyde degradation | 100 | 3 of 3 | ||
| 66794 | biotin biosynthesis | 100 | 4 of 4 | ||
| 66794 | Entner Doudoroff pathway | 100 | 10 of 10 | ||
| 66794 | cis-vaccenate biosynthesis | 100 | 2 of 2 | ||
| 66794 | threonine metabolism | 100 | 10 of 10 | ||
| 66794 | palmitate biosynthesis | 100 | 22 of 22 | ||
| 66794 | valine metabolism | 100 | 9 of 9 | ||
| 66794 | resorcinol degradation | 100 | 2 of 2 | ||
| 66794 | butanoate fermentation | 100 | 4 of 4 | ||
| 66794 | octane oxidation | 100 | 3 of 3 | ||
| 66794 | CDP-diacylglycerol biosynthesis | 100 | 2 of 2 | ||
| 66794 | C4 and CAM-carbon fixation | 100 | 8 of 8 | ||
| 66794 | UDP-GlcNAc biosynthesis | 100 | 3 of 3 | ||
| 66794 | cellulose degradation | 100 | 5 of 5 | ||
| 66794 | suberin monomers biosynthesis | 100 | 2 of 2 | ||
| 66794 | anapleurotic synthesis of oxalacetate | 100 | 1 of 1 | ||
| 66794 | folate polyglutamylation | 100 | 1 of 1 | ||
| 66794 | gluconeogenesis | 100 | 8 of 8 | ||
| 66794 | 4-hydroxyphenylacetate degradation | 90 | 9 of 10 | ||
| 66794 | lipid A biosynthesis | 88.89 | 8 of 9 | ||
| 66794 | chorismate metabolism | 88.89 | 8 of 9 | ||
| 66794 | molybdenum cofactor biosynthesis | 88.89 | 8 of 9 | ||
| 66794 | reductive acetyl coenzyme A pathway | 85.71 | 6 of 7 | ||
| 66794 | photosynthesis | 85.71 | 12 of 14 | ||
| 66794 | phenylalanine metabolism | 84.62 | 11 of 13 | ||
| 66794 | vitamin B1 metabolism | 84.62 | 11 of 13 | ||
| 66794 | NAD metabolism | 83.33 | 15 of 18 | ||
| 66794 | glutamate and glutamine metabolism | 82.14 | 23 of 28 | ||
| 66794 | pentose phosphate pathway | 81.82 | 9 of 11 | ||
| 66794 | tryptophan metabolism | 81.58 | 31 of 38 | ||
| 66794 | peptidoglycan biosynthesis | 80 | 12 of 15 | ||
| 66794 | ethylmalonyl-CoA pathway | 80 | 4 of 5 | ||
| 66794 | alanine metabolism | 79.31 | 23 of 29 | ||
| 66794 | heme metabolism | 78.57 | 11 of 14 | ||
| 66794 | citric acid cycle | 78.57 | 11 of 14 | ||
| 66794 | serine metabolism | 77.78 | 7 of 9 | ||
| 66794 | allantoin degradation | 77.78 | 7 of 9 | ||
| 66794 | 4-hydroxymandelate degradation | 77.78 | 7 of 9 | ||
| 66794 | CO2 fixation in Crenarchaeota | 77.78 | 7 of 9 | ||
| 66794 | leucine metabolism | 76.92 | 10 of 13 | ||
| 66794 | urea cycle | 76.92 | 10 of 13 | ||
| 66794 | vitamin B12 metabolism | 76.47 | 26 of 34 | ||
| 66794 | CMP-KDO biosynthesis | 75 | 3 of 4 | ||
| 66794 | dTDPLrhamnose biosynthesis | 75 | 6 of 8 | ||
| 66794 | acetate fermentation | 75 | 3 of 4 | ||
| 66794 | isoleucine metabolism | 75 | 6 of 8 | ||
| 66794 | degradation of sugar alcohols | 75 | 12 of 16 | ||
| 66794 | ketogluconate metabolism | 75 | 6 of 8 | ||
| 66794 | glycogen biosynthesis | 75 | 3 of 4 | ||
| 66794 | sulfopterin metabolism | 75 | 3 of 4 | ||
| 66794 | lactate fermentation | 75 | 3 of 4 | ||
| 66794 | pyrimidine metabolism | 73.33 | 33 of 45 | ||
| 66794 | flavin biosynthesis | 73.33 | 11 of 15 | ||
| 66794 | proline metabolism | 72.73 | 8 of 11 | ||
| 66794 | tetrahydrofolate metabolism | 71.43 | 10 of 14 | ||
| 66794 | tyrosine metabolism | 71.43 | 10 of 14 | ||
| 66794 | cardiolipin biosynthesis | 71.43 | 5 of 7 | ||
| 66794 | ubiquinone biosynthesis | 71.43 | 5 of 7 | ||
| 66794 | lipid metabolism | 70.97 | 22 of 31 | ||
| 66794 | methionine metabolism | 69.23 | 18 of 26 | ||
| 66794 | lysine metabolism | 69.05 | 29 of 42 | ||
| 66794 | purine metabolism | 68.09 | 64 of 94 | ||
| 66794 | 3-phenylpropionate degradation | 66.67 | 10 of 15 | ||
| 66794 | cyanate degradation | 66.67 | 2 of 3 | ||
| 66794 | enterobactin biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | acetyl CoA biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | aspartate and asparagine metabolism | 66.67 | 6 of 9 | ||
| 66794 | methane metabolism | 66.67 | 2 of 3 | ||
| 66794 | d-mannose degradation | 66.67 | 6 of 9 | ||
| 66794 | acetoin degradation | 66.67 | 2 of 3 | ||
| 66794 | arginine metabolism | 66.67 | 16 of 24 | ||
| 66794 | non-pathway related | 65.79 | 25 of 38 | ||
| 66794 | phenol degradation | 65 | 13 of 20 | ||
| 66794 | oxidative phosphorylation | 64.84 | 59 of 91 | ||
| 66794 | glycolysis | 64.71 | 11 of 17 | ||
| 66794 | vitamin B6 metabolism | 63.64 | 7 of 11 | ||
| 66794 | 6-hydroxymethyl-dihydropterin diphosphate biosynthesis | 62.5 | 5 of 8 | ||
| 66794 | 3-chlorocatechol degradation | 60 | 3 of 5 | ||
| 66794 | vitamin K metabolism | 60 | 3 of 5 | ||
| 66794 | gallate degradation | 60 | 3 of 5 | ||
| 66794 | glycogen metabolism | 60 | 3 of 5 | ||
| 66794 | degradation of sugar acids | 60 | 15 of 25 | ||
| 66794 | myo-inositol biosynthesis | 60 | 6 of 10 | ||
| 66794 | bile acid biosynthesis, neutral pathway | 58.82 | 10 of 17 | ||
| 66794 | degradation of aromatic, nitrogen containing compounds | 58.33 | 7 of 12 | ||
| 66794 | propanol degradation | 57.14 | 4 of 7 | ||
| 66794 | glutathione metabolism | 57.14 | 8 of 14 | ||
| 66794 | degradation of pentoses | 57.14 | 16 of 28 | ||
| 66794 | cysteine metabolism | 55.56 | 10 of 18 | ||
| 66794 | isoprenoid biosynthesis | 53.85 | 14 of 26 | ||
| 66794 | polyamine pathway | 52.17 | 12 of 23 | ||
| 66794 | histidine metabolism | 51.72 | 15 of 29 | ||
| 66794 | glycolate and glyoxylate degradation | 50 | 3 of 6 | ||
| 66794 | pantothenate biosynthesis | 50 | 3 of 6 | ||
| 66794 | cyclohexanol degradation | 50 | 2 of 4 | ||
| 66794 | aminopropanol phosphate biosynthesis | 50 | 1 of 2 | ||
| 66794 | propionate fermentation | 50 | 5 of 10 | ||
| 66794 | degradation of hexoses | 50 | 9 of 18 | ||
| 66794 | glycine metabolism | 50 | 5 of 10 | ||
| 66794 | quinate degradation | 50 | 1 of 2 | ||
| 66794 | phenylmercury acetate degradation | 50 | 1 of 2 | ||
| 66794 | ethanol fermentation | 50 | 1 of 2 | ||
| 66794 | selenocysteine biosynthesis | 50 | 3 of 6 | ||
| 66794 | sulfate reduction | 46.15 | 6 of 13 | ||
| 66794 | d-xylose degradation | 45.45 | 5 of 11 | ||
| 66794 | androgen and estrogen metabolism | 43.75 | 7 of 16 | ||
| 66794 | ascorbate metabolism | 40.91 | 9 of 22 | ||
| 66794 | factor 420 biosynthesis | 40 | 2 of 5 | ||
| 66794 | glycine betaine biosynthesis | 40 | 2 of 5 | ||
| 66794 | starch degradation | 40 | 4 of 10 | ||
| 66794 | lipoate biosynthesis | 40 | 2 of 5 | ||
| 66794 | hydrogen production | 40 | 2 of 5 | ||
| 66794 | arachidonate biosynthesis | 40 | 2 of 5 | ||
| 66794 | bacilysin biosynthesis | 40 | 2 of 5 | ||
| 66794 | metabolism of disaccharids | 36.36 | 4 of 11 | ||
| 66794 | sulfoquinovose degradation | 33.33 | 1 of 3 | ||
| 66794 | nitrate assimilation | 33.33 | 3 of 9 | ||
| 66794 | IAA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | (5R)-carbapenem carboxylate biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | sphingosine metabolism | 33.33 | 2 of 6 | ||
| 66794 | arachidonic acid metabolism | 33.33 | 6 of 18 | ||
| 66794 | chlorophyll metabolism | 33.33 | 6 of 18 | ||
| 66794 | coenzyme M biosynthesis | 30 | 3 of 10 | ||
| 66794 | benzoyl-CoA degradation | 28.57 | 2 of 7 | ||
| 66794 | dolichyl-diphosphooligosaccharide biosynthesis | 27.27 | 3 of 11 | ||
| 66794 | carnitine metabolism | 25 | 2 of 8 | ||
| 66794 | catecholamine biosynthesis | 25 | 1 of 4 | ||
| 66794 | alginate biosynthesis | 25 | 1 of 4 | ||
| 66794 | toluene degradation | 25 | 1 of 4 | ||
| 66794 | phosphatidylethanolamine bioynthesis | 23.08 | 3 of 13 |
| Cat1 | Cat2 | Cat3 | |
|---|---|---|---|
| #Engineered | #Laboratory | #Lab enrichment | |
| #Environmental | #Aquatic | #Marine | |
| #Environmental | #Aquatic | #Surface water | |
| #Host | #Microbial | #Bacteria |
| @ref | Sample type | Geographic location | Country | Country ISO 3 Code | Continent | |
|---|---|---|---|---|---|---|
| 21842 | oil-degrading bacterial consortium, enriched by surface seawater | Dalian Port | China | CHN | Asia |
Global distribution of 16S sequence JQ844756 (>99% sequence identity) for Thioclava dalianensis subclade from Microbeatlas ![]()
| @ref | Biosafety level | Biosafety level comment | |
|---|---|---|---|
| 21842 | 1 | Risk group (German classification) |
| @ref | Description | Assembly level | INSDC accession | BV-BRC accession | IMG accession | NCBI tax ID | Score | |
|---|---|---|---|---|---|---|---|---|
| 66792 | IMG-taxon 2663762756 annotated assembly for Thioclava dalianensis CGMCC 1.12325 | scaffold | 1185766 | 70.54 | ||||
| 66792 | SOAPdenovo v1.05 assembly for Thioclava dalianensis DLFJ1-1 | contig | 1185766 | 60.04 |
| 30859 | GC-content (mol%)62.5 |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125439 | spore_formation | BacteriaNetⓘ | no | 97.10 | no |
| 125439 | motility | BacteriaNetⓘ | yes | 72.20 | no |
| 125439 | gram_stain | BacteriaNetⓘ | negative | 99.30 | no |
| 125439 | oxygen_tolerance | BacteriaNetⓘ | aerobe | 81.10 | no |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125438 | gram-positive | gram-positiveⓘ | no | 98.00 | yes |
| 125438 | anaerobic | anaerobicⓘ | no | 91.88 | yes |
| 125438 | aerobic | aerobicⓘ | yes | 82.73 | no |
| 125438 | spore-forming | spore-formingⓘ | no | 90.36 | no |
| 125438 | thermophilic | thermophileⓘ | no | 97.49 | yes |
| 125438 | flagellated | motile2+ⓘ | yes | 71.83 | no |
| Topic | Title | Authors | Journal | DOI | Year | |
|---|---|---|---|---|---|---|
| Genetics | A Multilocus Sequence Analysis Scheme for Phylogeny of Thioclava Bacteria and Proposal of Two Novel Species. | Liu Y, Lai Q, Shao Z. | Front Microbiol | 10.3389/fmicb.2017.01321 | 2017 | |
| Phylogeny | Thioclava electrotropha sp. nov., a versatile electrode and sulfur-oxidizing bacterium from marine sediments. | Chang R, Bird L, Barr C, Osburn M, Wilbanks E, Nealson K, Rowe A | Int J Syst Evol Microbiol | 10.1099/ijsem.0.002723 | 2018 | |
| Phylogeny | Thioclava nitratireducens sp. nov., isolated from surface seawater. | Liu Y, Lai Q, Shao Z | Int J Syst Evol Microbiol | 10.1099/ijsem.0.001844 | 2017 | |
| Phylogeny | Thioclava indica sp. nov., isolated from surface seawater of the Indian Ocean. | Liu Y, Lai Q, Du J, Xu H, Jiang L, Shao Z | Antonie Van Leeuwenhoek | 10.1007/s10482-014-0320-3 | 2014 | |
| Phylogeny | Thioclava atlantica sp. nov., isolated from deep sea sediment of the Atlantic Ocean. | Lai Q, Li S, Xu H, Jiang L, Zhang R, Shao Z | Antonie Van Leeuwenhoek | 10.1007/s10482-014-0261-x | 2014 | |
| Phylogeny | Thioclava dalianensis sp. nov., isolated from surface seawater. | Zhang R, Lai Q, Wang W, Li S, Shao Z | Int J Syst Evol Microbiol | 10.1099/ijs.0.046094-0 | 2013 |
| #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 ) |
| #21842 | Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 29618 |
| #27189 | IJSEM 2981 2013 ( DOI 10.1099/ijs.0.046094-0 , PubMed 23378112 ) |
| #30859 | Barberan A, Caceres Velazquez H, Jones S, Fierer N.: Hiding in Plain Sight: Mining Bacterial Species Records for Phenotypic Trait Information. mSphere 2: 2017 ( DOI 10.1128/mSphere.00237-17 , PubMed 28776041 ) - originally annotated from #27189 |
| #66792 | Julia Koblitz, Joaquim Sardà, Lorenz Christian Reimer, Boyke Bunk, Jörg Overmann: Automatically annotated for the DiASPora project (Digital Approaches for the Synthesis of Poorly Accessible Biodiversity Information) . |
| #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 ) |
| #68369 | Automatically annotated from API 20NE . |
| #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 . |
| #124043 | Isabel Schober, Julia Koblitz: Data extracted from sequence databases, automatically matched based on designation and taxonomy . |
| #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 ) |
| #125439 | Philipp Münch, René Mreches, Martin Binder, Hüseyin Anil Gündüz, Xiao-Yin To, Alice McHardy: deepG: Deep Learning for Genome Sequence Data. R package version 0.3.1 . |
| #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 ) |
You found an error in BacDive? Please tell us about it!
Note that changes will be reviewed and judged. If your changes are legitimate, changes will occur within the next BacDive update. Only proposed changes supported by the according reference will be reviewed. The BacDive team reserves the right to reject proposed changes.
Successfully sent
If you want to cite this particular strain cite the following doi:
https://doi.org/10.13145/bacdive130630.20251217.10
When using BacDive for research please cite the following paper
BacDive in 2025: the core database for prokaryotic strain data