Georgenia satyanarayanai JC82 is an aerobe, Gram-positive, ovoid-shaped bacterium that was isolated from soda lake.
Gram-positive ovoid-shaped aerobe genome sequence 16S sequence Bacteria| @ref 20215 |
|
|
| Domain Bacteria |
| Phylum Actinomycetota |
| Class Actinomycetes |
| Order Micrococcales |
| Family Allobogoriellaceae |
| Genus Georgenia |
| Species Georgenia satyanarayanai |
| Full scientific name Georgenia satyanarayanai Srinivas et al. 2012 |
| Synonyms (1) |
| BacDive ID | Other strains from Georgenia satyanarayanai (1) | Type strain |
|---|---|---|
| 162103 | G. satyanarayanai JCM 17755, CGMCC 1.10826 |
| @ref | Incubation period | Medium used | |
|---|---|---|---|
| 25050 | 2 days | Tryptic Soy Agar (TSA, Becton Dickinsons) |
| @ref | Name | Growth | |
|---|---|---|---|
| 25050 | Tryptic Soy Agar (TSA, Becton Dickinsons) |
| @ref | Murein short key | Type | |
|---|---|---|---|
| 20589 | A11.54 | A4alpha L-Lys-L-Glu |
| 67771 | Observationquinones: MK-8(H4) |
| @ref | Chebi-ID | Metabolite | Utilization activity | Kind of utilization tested | |
|---|---|---|---|---|---|
| 30444 | 62064 ChEBI | 2,3-butanediol | + | carbon source | |
| 25050 | 30916 ChEBI | 2-oxoglutarate | - | carbon source | |
| 30444 | 28644 ChEBI | 2-oxopentanoate | + | carbon source | |
| 25050 | 37054 ChEBI | 3-hydroxybutyrate | - | carbon source | |
| 25050 | 91122 ChEBI | 4-nitrophenyl alpha-D-glucopyranoside | + | hydrolysis | |
| 25050 | 4-nitrophenyl beta-D-galactopyranoside hydrolysate | + | hydrolysis | ||
| 25050 | 90259 ChEBI | 4-nitrophenyl beta-D-glucopyranoside | + | hydrolysis | |
| 25050 | 90146 ChEBI | 4-nitrophenyl beta-D-glucuronide | - | hydrolysis | |
| 25050 | 90148 ChEBI | 4-nitrophenyl beta-D-xylopyranoside | + | hydrolysis | |
| 30444 | 30089 ChEBI | acetate | + | carbon source | |
| 25050 | 17128 ChEBI | adipate | - | carbon source | |
| 30444 | 22599 ChEBI | arabinose | + | carbon source | |
| 30523 | 22599 ChEBI | arabinose | + | carbon source | |
| 25050 | 18305 ChEBI | arbutin | + | carbon source | |
| 25050 | 78208 ChEBI | azelaate | - | carbon source | |
| 25050 | 16958 ChEBI | beta-alanine | - | carbon source | |
| 25050 | 3122 ChEBI | bis-4-nitrophenyl phosphate | + | hydrolysis | |
| 25050 | 91050 ChEBI | bis-4-nitrophenyl-phenyl phosphonate | + | hydrolysis | |
| 25050 | 55394 ChEBI | bis-4-nitrophenyl-phosphorylcholine | - | hydrolysis | |
| 25050 | 17057 ChEBI | cellobiose | + | carbon source | |
| 30444 | 17057 ChEBI | cellobiose | + | carbon source | |
| 25050 | 16383 ChEBI | cis-aconitate | - | carbon source | |
| 25050 | 16947 ChEBI | citrate | - | carbon source | |
| 25050 | 15824 ChEBI | D-fructose | + | carbon source | |
| 25050 | 12936 ChEBI | D-galactose | + | carbon source | |
| 25050 | 17634 ChEBI | D-glucose | + | carbon source | |
| 25050 | 16899 ChEBI | D-mannitol | + | carbon source | |
| 25050 | 16024 ChEBI | D-mannose | + | carbon source | |
| 25050 | 16988 ChEBI | D-ribose | + | carbon source | |
| 25050 | 17924 ChEBI | D-sorbitol | + | carbon source | |
| 25050 | 65327 ChEBI | D-xylose | + | carbon source | |
| 30444 | 23652 ChEBI | dextrin | + | carbon source | |
| 25050 | 4853 ChEBI | esculin | + | hydrolysis | |
| 30444 | 28757 ChEBI | fructose | + | carbon source | |
| 25050 | 29806 ChEBI | fumarate | + | carbon source | |
| 30444 | 28260 ChEBI | galactose | + | carbon source | |
| 30444 | 24175 ChEBI | galacturonate | + | carbon source | |
| 25050 | 16865 ChEBI | gamma-aminobutyric acid | - | carbon source | |
| 25050 | gamma-L-glutamate-4-nitroanilide | - | hydrolysis | ||
| 25050 | 24265 ChEBI | gluconate | + | carbon source | |
| 30444 | 24265 ChEBI | gluconate | + | carbon source | |
| 30444 | 17234 ChEBI | glucose | + | carbon source | |
| 25050 | 17859 ChEBI | glutaric acid | - | carbon source | |
| 30444 | 17754 ChEBI | glycerol | + | carbon source | |
| 30444 | 28087 ChEBI | glycogen | + | carbon source | |
| 30523 | 28087 ChEBI | glycogen | + | carbon source | |
| 30444 | 17596 ChEBI | inosine | + | carbon source | |
| 25050 | 17240 ChEBI | itaconate | - | carbon source | |
| 25050 | 16977 ChEBI | L-alanine | - | carbon source | |
| 25050 | L-alanine 4-nitroanilide | + | hydrolysis | ||
| 25050 | 30849 ChEBI | L-arabinose | + | carbon source | |
| 25050 | 29991 ChEBI | L-aspartate | - | carbon source | |
| 25050 | 15971 ChEBI | L-histidine | - | carbon source | |
| 25050 | 15603 ChEBI | L-leucine | - | carbon source | |
| 25050 | 15589 ChEBI | L-malate | - | carbon source | |
| 25050 | 15729 ChEBI | L-ornithine | - | carbon source | |
| 25050 | 17295 ChEBI | L-phenylalanine | - | carbon source | |
| 25050 | 17203 ChEBI | L-proline | - | carbon source | |
| 25050 | L-proline-4-nitroanilide | - | hydrolysis | ||
| 25050 | 62345 ChEBI | L-rhamnose | - | carbon source | |
| 25050 | 17115 ChEBI | L-serine | - | carbon source | |
| 25050 | 16828 ChEBI | L-tryptophan | - | carbon source | |
| 25050 | 24996 ChEBI | lactate | - | carbon source | |
| 30444 | 25115 ChEBI | malate | + | carbon source | |
| 25050 | 68428 ChEBI | maltitol | + | carbon source | |
| 25050 | 17306 ChEBI | maltose | + | carbon source | |
| 30444 | 17306 ChEBI | maltose | + | carbon source | |
| 30523 | 29864 ChEBI | mannitol | + | carbon source | |
| 30444 | 37684 ChEBI | mannose | + | carbon source | |
| 25050 | 28053 ChEBI | melibiose | - | carbon source | |
| 25050 | 36986 ChEBI | mesaconate | - | carbon source | |
| 30444 | 51850 ChEBI | methyl pyruvate | + | carbon source | |
| 25050 | 17268 ChEBI | myo-inositol | - | carbon source | |
| 25050 | 28037 ChEBI | N-acetylgalactosamine | - | carbon source | |
| 25050 | 506227 ChEBI | N-acetylglucosamine | + | carbon source | |
| 30523 | 17632 ChEBI | nitrate | + | reduction | |
| 25050 | 17272 ChEBI | propionate | - | carbon source | |
| 25050 | 17148 ChEBI | putrescine | - | carbon source | |
| 25050 | 15361 ChEBI | pyruvate | - | carbon source | |
| 30444 | 15361 ChEBI | pyruvate | + | carbon source | |
| 25050 | 15963 ChEBI | ribitol | - | carbon source | |
| 30444 | 33942 ChEBI | ribose | + | carbon source | |
| 30523 | 33942 ChEBI | ribose | + | carbon source | |
| 25050 | 17814 ChEBI | salicin | - | carbon source | |
| 30444 | 17814 ChEBI | salicin | + | carbon source | |
| 30523 | 17814 ChEBI | salicin | + | carbon source | |
| 30444 | 30911 ChEBI | sorbitol | + | carbon source | |
| 25050 | 9300 ChEBI | suberic acid | - | carbon source | |
| 25050 | 17992 ChEBI | sucrose | + | carbon source | |
| 30444 | 17992 ChEBI | sucrose | + | carbon source | |
| 30444 | 17748 ChEBI | thymidine | + | carbon source | |
| 25050 | 15708 ChEBI | trans-aconitate | - | carbon source | |
| 25050 | 27082 ChEBI | trehalose | + | carbon source | |
| 30444 | 27082 ChEBI | trehalose | + | carbon source | |
| 30523 | 27082 ChEBI | trehalose | + | carbon source | |
| 30444 | 16704 ChEBI | uridine | + | carbon source | |
| 30444 | 18222 ChEBI | xylose | + | carbon source |
| @ref | pathway | enzyme coverage | annotated reactions | external links | |
|---|---|---|---|---|---|
| 66794 | cellulose degradation | 100 | 5 of 5 | ||
| 66794 | acetate fermentation | 100 | 4 of 4 | ||
| 66794 | vitamin K metabolism | 100 | 5 of 5 | ||
| 66794 | palmitate biosynthesis | 100 | 22 of 22 | ||
| 66794 | sulfopterin metabolism | 100 | 4 of 4 | ||
| 66794 | coenzyme A metabolism | 100 | 4 of 4 | ||
| 66794 | formaldehyde oxidation | 100 | 3 of 3 | ||
| 66794 | glycogen metabolism | 100 | 5 of 5 | ||
| 66794 | cis-vaccenate biosynthesis | 100 | 2 of 2 | ||
| 66794 | aspartate and asparagine metabolism | 100 | 9 of 9 | ||
| 66794 | adipate degradation | 100 | 2 of 2 | ||
| 66794 | denitrification | 100 | 2 of 2 | ||
| 66794 | anapleurotic synthesis of oxalacetate | 100 | 1 of 1 | ||
| 66794 | starch degradation | 100 | 10 of 10 | ||
| 66794 | folate polyglutamylation | 100 | 1 of 1 | ||
| 66794 | ceramide biosynthesis | 100 | 1 of 1 | ||
| 66794 | CDP-diacylglycerol biosynthesis | 100 | 2 of 2 | ||
| 66794 | suberin monomers biosynthesis | 100 | 2 of 2 | ||
| 66794 | methylglyoxal degradation | 100 | 5 of 5 | ||
| 66794 | ppGpp biosynthesis | 100 | 4 of 4 | ||
| 66794 | UDP-GlcNAc biosynthesis | 100 | 3 of 3 | ||
| 66794 | threonine metabolism | 100 | 10 of 10 | ||
| 66794 | Entner Doudoroff pathway | 90 | 9 of 10 | ||
| 66794 | chorismate metabolism | 88.89 | 8 of 9 | ||
| 66794 | C4 and CAM-carbon fixation | 87.5 | 7 of 8 | ||
| 66794 | ketogluconate metabolism | 87.5 | 7 of 8 | ||
| 66794 | heme metabolism | 85.71 | 12 of 14 | ||
| 66794 | reductive acetyl coenzyme A pathway | 85.71 | 6 of 7 | ||
| 66794 | photosynthesis | 85.71 | 12 of 14 | ||
| 66794 | glycolate and glyoxylate degradation | 83.33 | 5 of 6 | ||
| 66794 | glycolysis | 82.35 | 14 of 17 | ||
| 66794 | pyrimidine metabolism | 82.22 | 37 of 45 | ||
| 66794 | glutamate and glutamine metabolism | 82.14 | 23 of 28 | ||
| 66794 | metabolism of disaccharids | 81.82 | 9 of 11 | ||
| 66794 | pentose phosphate pathway | 81.82 | 9 of 11 | ||
| 66794 | lipoate biosynthesis | 80 | 4 of 5 | ||
| 66794 | metabolism of amino sugars and derivatives | 80 | 4 of 5 | ||
| 66794 | peptidoglycan biosynthesis | 80 | 12 of 15 | ||
| 66794 | flavin biosynthesis | 80 | 12 of 15 | ||
| 66794 | purine metabolism | 78.72 | 74 of 94 | ||
| 66794 | tetrahydrofolate metabolism | 78.57 | 11 of 14 | ||
| 66794 | citric acid cycle | 78.57 | 11 of 14 | ||
| 66794 | molybdenum cofactor biosynthesis | 77.78 | 7 of 9 | ||
| 66794 | serine metabolism | 77.78 | 7 of 9 | ||
| 66794 | valine metabolism | 77.78 | 7 of 9 | ||
| 66794 | phenylalanine metabolism | 76.92 | 10 of 13 | ||
| 66794 | butanoate fermentation | 75 | 3 of 4 | ||
| 66794 | glycogen biosynthesis | 75 | 3 of 4 | ||
| 66794 | isoleucine metabolism | 75 | 6 of 8 | ||
| 66794 | gluconeogenesis | 75 | 6 of 8 | ||
| 66794 | dTDPLrhamnose biosynthesis | 75 | 6 of 8 | ||
| 66794 | alanine metabolism | 72.41 | 21 of 29 | ||
| 66794 | NAD metabolism | 72.22 | 13 of 18 | ||
| 66794 | cardiolipin biosynthesis | 71.43 | 5 of 7 | ||
| 66794 | propionate fermentation | 70 | 7 of 10 | ||
| 66794 | leucine metabolism | 69.23 | 9 of 13 | ||
| 66794 | oxidative phosphorylation | 69.23 | 63 of 91 | ||
| 66794 | octane oxidation | 66.67 | 2 of 3 | ||
| 66794 | acetyl CoA biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | CO2 fixation in Crenarchaeota | 66.67 | 6 of 9 | ||
| 66794 | sulfoquinovose degradation | 66.67 | 2 of 3 | ||
| 66794 | d-mannose degradation | 66.67 | 6 of 9 | ||
| 66794 | selenocysteine biosynthesis | 66.67 | 4 of 6 | ||
| 66794 | L-lactaldehyde degradation | 66.67 | 2 of 3 | ||
| 66794 | acetoin degradation | 66.67 | 2 of 3 | ||
| 66794 | proline metabolism | 63.64 | 7 of 11 | ||
| 66794 | d-xylose degradation | 63.64 | 7 of 11 | ||
| 66794 | 6-hydroxymethyl-dihydropterin diphosphate biosynthesis | 62.5 | 5 of 8 | ||
| 66794 | degradation of sugar alcohols | 62.5 | 10 of 16 | ||
| 66794 | vitamin B1 metabolism | 61.54 | 8 of 13 | ||
| 66794 | isoprenoid biosynthesis | 61.54 | 16 of 26 | ||
| 66794 | methionine metabolism | 61.54 | 16 of 26 | ||
| 66794 | lipid metabolism | 61.29 | 19 of 31 | ||
| 66794 | cysteine metabolism | 61.11 | 11 of 18 | ||
| 66794 | degradation of pentoses | 60.71 | 17 of 28 | ||
| 66794 | non-pathway related | 60.53 | 23 of 38 | ||
| 66794 | glycine betaine biosynthesis | 60 | 3 of 5 | ||
| 66794 | factor 420 biosynthesis | 60 | 3 of 5 | ||
| 66794 | ubiquinone biosynthesis | 57.14 | 4 of 7 | ||
| 66794 | glutathione metabolism | 57.14 | 8 of 14 | ||
| 66794 | histidine metabolism | 55.17 | 16 of 29 | ||
| 66794 | arginine metabolism | 54.17 | 13 of 24 | ||
| 66794 | urea cycle | 53.85 | 7 of 13 | ||
| 66794 | tryptophan metabolism | 52.63 | 20 of 38 | ||
| 66794 | lysine metabolism | 52.38 | 22 of 42 | ||
| 66794 | degradation of sugar acids | 52 | 13 of 25 | ||
| 66794 | glycine metabolism | 50 | 5 of 10 | ||
| 66794 | kanosamine biosynthesis II | 50 | 1 of 2 | ||
| 66794 | phenylmercury acetate degradation | 50 | 1 of 2 | ||
| 66794 | myo-inositol biosynthesis | 50 | 5 of 10 | ||
| 66794 | CMP-KDO biosynthesis | 50 | 2 of 4 | ||
| 66794 | alginate biosynthesis | 50 | 2 of 4 | ||
| 66794 | mannosylglycerate biosynthesis | 50 | 1 of 2 | ||
| 66794 | ethanol fermentation | 50 | 1 of 2 | ||
| 66794 | bile acid biosynthesis, neutral pathway | 47.06 | 8 of 17 | ||
| 66794 | vitamin B6 metabolism | 45.45 | 5 of 11 | ||
| 66794 | ascorbate metabolism | 45.45 | 10 of 22 | ||
| 66794 | lipid A biosynthesis | 44.44 | 4 of 9 | ||
| 66794 | degradation of hexoses | 44.44 | 8 of 18 | ||
| 66794 | tyrosine metabolism | 42.86 | 6 of 14 | ||
| 66794 | propanol degradation | 42.86 | 3 of 7 | ||
| 66794 | degradation of aromatic, nitrogen containing compounds | 41.67 | 5 of 12 | ||
| 66794 | arachidonate biosynthesis | 40 | 2 of 5 | ||
| 66794 | chlorophyll metabolism | 38.89 | 7 of 18 | ||
| 66794 | carotenoid biosynthesis | 36.36 | 8 of 22 | ||
| 66794 | dolichyl-diphosphooligosaccharide biosynthesis | 36.36 | 4 of 11 | ||
| 66794 | cyanate degradation | 33.33 | 1 of 3 | ||
| 66794 | pantothenate biosynthesis | 33.33 | 2 of 6 | ||
| 66794 | nitrate assimilation | 33.33 | 3 of 9 | ||
| 66794 | enterobactin biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | IAA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | sphingosine metabolism | 33.33 | 2 of 6 | ||
| 66794 | (5R)-carbapenem carboxylate biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | androgen and estrogen metabolism | 31.25 | 5 of 16 | ||
| 66794 | coenzyme M biosynthesis | 30 | 3 of 10 | ||
| 66794 | benzoyl-CoA degradation | 28.57 | 2 of 7 | ||
| 66794 | mevalonate metabolism | 28.57 | 2 of 7 | ||
| 66794 | arachidonic acid metabolism | 27.78 | 5 of 18 | ||
| 66794 | cholesterol biosynthesis | 27.27 | 3 of 11 | ||
| 66794 | 3-phenylpropionate degradation | 26.67 | 4 of 15 | ||
| 66794 | carnitine metabolism | 25 | 2 of 8 | ||
| 66794 | phenol degradation | 25 | 5 of 20 | ||
| 66794 | lactate fermentation | 25 | 1 of 4 | ||
| 66794 | cyclohexanol degradation | 25 | 1 of 4 | ||
| 66794 | toluene degradation | 25 | 1 of 4 | ||
| 66794 | methanogenesis from CO2 | 25 | 3 of 12 | ||
| 66794 | phenylpropanoid biosynthesis | 23.08 | 3 of 13 | ||
| 66794 | sulfate reduction | 23.08 | 3 of 13 | ||
| 66794 | 4-hydroxymandelate degradation | 22.22 | 2 of 9 |
Global distribution of 16S sequence FN995635 (>99% sequence identity) for Georgenia satyanarayanai subclade from Microbeatlas ![]()
| @ref | Biosafety level | Biosafety level comment | |
|---|---|---|---|
| 20589 | 1 | Risk group (German classification) |
| @ref | Description | Assembly level | INSDC accession | BV-BRC accession | NCBI tax ID | Score | |
|---|---|---|---|---|---|---|---|
| 66792 | ASM919313v1 assembly for Georgenia satyanarayanai NBRC 107612 | contig | 860221 | 75.4 |
| @ref | Description | Accession | Length | Database | NCBI tax ID | |
|---|---|---|---|---|---|---|
| 20589 | Georgenia satyanarayanai partial 16S rRNA gene, type strain JC82T | FN995635 | 1437 | 860221 |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125439 | spore_formation | BacteriaNetⓘ | no | 60.20 | no |
| 125439 | motility | BacteriaNetⓘ | no | 79.50 | no |
| 125439 | gram_stain | BacteriaNetⓘ | positive | 99.40 | no |
| 125439 | oxygen_tolerance | BacteriaNetⓘ | facultative anaerobe | 88.30 | no |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125438 | gram-positive | gram-positiveⓘ | yes | 89.35 | yes |
| 125438 | anaerobic | anaerobicⓘ | no | 93.92 | yes |
| 125438 | aerobic | aerobicⓘ | yes | 76.02 | yes |
| 125438 | spore-forming | spore-formingⓘ | no | 67.99 | no |
| 125438 | thermophilic | thermophileⓘ | no | 97.50 | yes |
| 125438 | flagellated | motile2+ⓘ | no | 66.87 | no |
| Topic | Title | Authors | Journal | DOI | Year | |
|---|---|---|---|---|---|---|
| Phylogeny | Oceanitalea nanhaiensis Fu et al. 2012 is a later heterotypic synonym of Georgenia satyanarayanai Srinivas et al. 2012. | Kampfer P, Glaeser SP, Busse HJ | Int J Syst Evol Microbiol | 10.1099/ijsem.0.001550 | 2016 | |
| Phylogeny | Georgenia satyanarayanai sp. nov., an alkaliphilic and thermotolerant amylase-producing actinobacterium isolated from a soda lake. | Srinivas A, Rahul K, Sasikala C, Subhash Y, Ramaprasad EVV, Ramana CV | Int J Syst Evol Microbiol | 10.1099/ijs.0.036210-0 | 2011 | |
| Phylogeny | Georgenia faecalis sp. nov. isolated from the faeces of Tibetan antelope. | Wang X, Yang J, Huang Y, Wu X, Wang L, Han L, Li S, Li H, Fu X, Chen H, Zhu X | J Microbiol | 10.1007/s12275-020-0060-1 | 2020 |
| #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 ) |
| #20589 | Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 27632 |
| #25050 | P. G. Kämpfer, S. P.,Busse, H. J.: Oceanitalea nanhaiensis Fu et al. 2012 is a later heterotypic synonym of Georgenia satyanarayanai Srinivas et al. 2012. IJSEM 66: 5519 - 5522 2016 ( DOI 10.1099/ijsem.0.001550 , PubMed 27902219 ) |
| #26780 | IJSEM 2405 2012 ( DOI 10.1099/ijs.0.036210-0 , PubMed 22140168 ) |
| #26855 | IJSEM 2490 2012 ( DOI 10.1099/ijs.0.038018-0 , PubMed 22155759 ) |
| #30444 | 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 #26780 |
| #30523 | 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 #26855 |
| #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 ) |
| #67771 | Korean Collection for Type Cultures (KCTC) ; Curators of the KCTC; |
| #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 ) |
| #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 ) |
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