Sphingomonas sanxanigenens NX02 is a mesophilic, Gram-negative, rod-shaped prokaryote that was isolated from cornfield soil.
Gram-negative rod-shaped mesophilic genome sequence 16S sequence| @ref 20215 |
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| Domain Pseudomonadati |
| Phylum Pseudomonadota |
| Class Alphaproteobacteria |
| Order Sphingomonadales |
| Family Sphingomonadaceae |
| Genus Sphingomonas |
| Species Sphingomonas sanxanigenens |
| Full scientific name Sphingomonas sanxanigenens Huang et al. 2009 |
| Synonyms (1) |
| @ref | Name | Growth | Medium link | Composition | |
|---|---|---|---|---|---|
| 8232 | REACTIVATION WITH LIQUID MEDIUM (DSMZ Medium 535b) | Medium recipe at MediaDive | Name: REACTIVATION WITH LIQUID MEDIUM (DSMZ Medium 535b) Composition: Trypticase soy broth 30.0 g/l Casein peptone 17.0 g/l Agar 15.0 g/l NaCl 5.0 g/l Soy peptone 3.0 g/l K2HPO4 2.5 g/l D(+)-Glucose 2.5 g/l Distilled water | ||
| 39797 | MEDIUM 72- for trypto casein soja agar | Distilled water make up to (1000.000 ml);Trypto casein soy agar (40.000 g) | |||
| 122484 | CIP Medium 72 | Medium recipe at CIP | |||
| 8232 | TRYPTICASE SOY BROTH AGAR (DSMZ Medium 535) | Medium recipe at MediaDive | Name: TRYPTICASE SOY BROTH AGAR (DSMZ Medium 535) Composition: Trypticase soy broth 30.0 g/l Agar 15.0 g/l Distilled water |
| @ref | Ability | Type | PH | |
|---|---|---|---|---|
| 28879 | positive | optimum | 7.25 |
| @ref | Oxygen tolerance | Confidence | |
|---|---|---|---|
| 125439 | obligate aerobe | 99.5 |
| 28879 | Spore formationno |
| @ref | Salt | Growth | Tested relation | Concentration | |
|---|---|---|---|---|---|
| 28879 | NaCl | positive | optimum | 0.025 % |
| 28879 | Observationaggregates in clumps |
| @ref | Chebi-ID | Metabolite | Utilization activity | Kind of utilization tested | |
|---|---|---|---|---|---|
| 68369 | 17128 ChEBI | adipate | - | assimilation | from API 20NE |
| 28879 | 22599 ChEBI | arabinose | + | carbon source | |
| 68369 | 29016 ChEBI | arginine | - | hydrolysis | from API 20NE |
| 28879 | 17057 ChEBI | cellobiose | + | carbon source | |
| 68369 | 17634 ChEBI | D-glucose | + | assimilation | from API 20NE |
| 68369 | 17634 ChEBI | D-glucose | - | fermentation | from API 20NE |
| 68369 | 16899 ChEBI | D-mannitol | - | assimilation | from API 20NE |
| 68369 | 16024 ChEBI | D-mannose | + | assimilation | from API 20NE |
| 68369 | 27689 ChEBI | decanoate | - | assimilation | from API 20NE |
| 28879 | 23652 ChEBI | dextrin | + | carbon source | |
| 28879 | 4853 ChEBI | esculin | + | hydrolysis | |
| 28879 | 28260 ChEBI | galactose | + | carbon source | |
| 28879 | 5291 ChEBI | gelatin | + | carbon source | |
| 68369 | 5291 ChEBI | gelatin | - | hydrolysis | from API 20NE |
| 68369 | 24265 ChEBI | gluconate | + | assimilation | from API 20NE |
| 28879 | 17234 ChEBI | glucose | + | carbon source | |
| 68369 | 30849 ChEBI | L-arabinose | + | assimilation | from API 20NE |
| 68369 | 25115 ChEBI | malate | + | assimilation | from API 20NE |
| 68369 | 17306 ChEBI | maltose | + | assimilation | from API 20NE |
| 28879 | 37684 ChEBI | mannose | + | carbon source | |
| 28879 | 28053 ChEBI | melibiose | + | carbon source | |
| 28879 | 51850 ChEBI | methyl pyruvate | + | carbon source | |
| 68369 | 59640 ChEBI | N-acetylglucosamine | - | assimilation | from API 20NE |
| 28879 | 17632 ChEBI | nitrate | + | reduction | |
| 68369 | 17632 ChEBI | nitrate | - | reduction | from API 20NE |
| 28879 | 16634 ChEBI | raffinose | + | carbon source | |
| 28879 | 17992 ChEBI | sucrose | + | carbon source | |
| 28879 | 27082 ChEBI | trehalose | + | carbon source | |
| 68369 | 27897 ChEBI | tryptophan | - | energy source | from API 20NE |
| 68369 | 16199 ChEBI | urea | - | hydrolysis | from API 20NE |
| 28879 | 27248 ChEBI | urocanic acid | + | carbon source |
| @ref | pathway | enzyme coverage | annotated reactions | external links | |
|---|---|---|---|---|---|
| 66794 | palmitate biosynthesis | 100 | 22 of 22 | ||
| 66794 | CDP-diacylglycerol biosynthesis | 100 | 2 of 2 | ||
| 66794 | sulfopterin metabolism | 100 | 4 of 4 | ||
| 66794 | coenzyme A metabolism | 100 | 4 of 4 | ||
| 66794 | adipate degradation | 100 | 2 of 2 | ||
| 66794 | formaldehyde oxidation | 100 | 3 of 3 | ||
| 66794 | acetate fermentation | 100 | 4 of 4 | ||
| 66794 | biotin biosynthesis | 100 | 4 of 4 | ||
| 66794 | starch degradation | 100 | 10 of 10 | ||
| 66794 | cis-vaccenate biosynthesis | 100 | 2 of 2 | ||
| 66794 | Entner Doudoroff pathway | 100 | 10 of 10 | ||
| 66794 | valine metabolism | 100 | 9 of 9 | ||
| 66794 | butanoate fermentation | 100 | 4 of 4 | ||
| 66794 | methylglyoxal degradation | 100 | 5 of 5 | ||
| 66794 | threonine metabolism | 100 | 10 of 10 | ||
| 66794 | ppGpp biosynthesis | 100 | 4 of 4 | ||
| 66794 | UDP-GlcNAc biosynthesis | 100 | 3 of 3 | ||
| 66794 | folate polyglutamylation | 100 | 1 of 1 | ||
| 66794 | anapleurotic synthesis of oxalacetate | 100 | 1 of 1 | ||
| 66794 | tetrahydrofolate metabolism | 100 | 14 of 14 | ||
| 66794 | suberin monomers biosynthesis | 100 | 2 of 2 | ||
| 66794 | cellulose degradation | 100 | 5 of 5 | ||
| 66794 | creatinine degradation | 100 | 5 of 5 | ||
| 66794 | lactate fermentation | 100 | 4 of 4 | ||
| 66794 | gluconeogenesis | 100 | 8 of 8 | ||
| 66794 | C4 and CAM-carbon fixation | 100 | 8 of 8 | ||
| 66794 | taurine degradation | 100 | 1 of 1 | ||
| 66794 | NAD metabolism | 94.44 | 17 of 18 | ||
| 66794 | citric acid cycle | 92.86 | 13 of 14 | ||
| 66794 | phenylalanine metabolism | 92.31 | 12 of 13 | ||
| 66794 | proline metabolism | 90.91 | 10 of 11 | ||
| 66794 | pentose phosphate pathway | 90.91 | 10 of 11 | ||
| 66794 | propionate fermentation | 90 | 9 of 10 | ||
| 66794 | chorismate metabolism | 88.89 | 8 of 9 | ||
| 66794 | CO2 fixation in Crenarchaeota | 88.89 | 8 of 9 | ||
| 66794 | aspartate and asparagine metabolism | 88.89 | 8 of 9 | ||
| 66794 | serine metabolism | 88.89 | 8 of 9 | ||
| 66794 | molybdenum cofactor biosynthesis | 88.89 | 8 of 9 | ||
| 66794 | degradation of sugar acids | 88 | 22 of 25 | ||
| 66794 | isoleucine metabolism | 87.5 | 7 of 8 | ||
| 66794 | reductive acetyl coenzyme A pathway | 85.71 | 6 of 7 | ||
| 66794 | ubiquinone biosynthesis | 85.71 | 6 of 7 | ||
| 66794 | propanol degradation | 85.71 | 6 of 7 | ||
| 66794 | photosynthesis | 85.71 | 12 of 14 | ||
| 66794 | glutamate and glutamine metabolism | 85.71 | 24 of 28 | ||
| 66794 | purine metabolism | 85.11 | 80 of 94 | ||
| 66794 | leucine metabolism | 84.62 | 11 of 13 | ||
| 66794 | d-xylose degradation | 81.82 | 9 of 11 | ||
| 66794 | methionine metabolism | 80.77 | 21 of 26 | ||
| 66794 | glycogen metabolism | 80 | 4 of 5 | ||
| 66794 | peptidoglycan biosynthesis | 80 | 12 of 15 | ||
| 66794 | ethylmalonyl-CoA pathway | 80 | 4 of 5 | ||
| 66794 | phenylacetate degradation (aerobic) | 80 | 4 of 5 | ||
| 66794 | gallate degradation | 80 | 4 of 5 | ||
| 66794 | pyrimidine metabolism | 80 | 36 of 45 | ||
| 66794 | heme metabolism | 78.57 | 11 of 14 | ||
| 66794 | allantoin degradation | 77.78 | 7 of 9 | ||
| 66794 | alanine metabolism | 75.86 | 22 of 29 | ||
| 66794 | histidine metabolism | 75.86 | 22 of 29 | ||
| 66794 | arginine metabolism | 75 | 18 of 24 | ||
| 66794 | 6-hydroxymethyl-dihydropterin diphosphate biosynthesis | 75 | 6 of 8 | ||
| 66794 | dTDPLrhamnose biosynthesis | 75 | 6 of 8 | ||
| 66794 | CMP-KDO biosynthesis | 75 | 3 of 4 | ||
| 66794 | glycogen biosynthesis | 75 | 3 of 4 | ||
| 66794 | tryptophan metabolism | 73.68 | 28 of 38 | ||
| 66794 | 3-phenylpropionate degradation | 73.33 | 11 of 15 | ||
| 66794 | flavin biosynthesis | 73.33 | 11 of 15 | ||
| 66794 | metabolism of disaccharids | 72.73 | 8 of 11 | ||
| 66794 | chlorophyll metabolism | 72.22 | 13 of 18 | ||
| 66794 | glutathione metabolism | 71.43 | 10 of 14 | ||
| 66794 | tyrosine metabolism | 71.43 | 10 of 14 | ||
| 66794 | cardiolipin biosynthesis | 71.43 | 5 of 7 | ||
| 66794 | lipid metabolism | 70.97 | 22 of 31 | ||
| 66794 | glycolysis | 70.59 | 12 of 17 | ||
| 66794 | isoprenoid biosynthesis | 69.23 | 18 of 26 | ||
| 66794 | vitamin B1 metabolism | 69.23 | 9 of 13 | ||
| 66794 | androgen and estrogen metabolism | 68.75 | 11 of 16 | ||
| 66794 | degradation of sugar alcohols | 68.75 | 11 of 16 | ||
| 66794 | non-pathway related | 68.42 | 26 of 38 | ||
| 66794 | 4-hydroxymandelate degradation | 66.67 | 6 of 9 | ||
| 66794 | acetyl CoA biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | cyanate degradation | 66.67 | 2 of 3 | ||
| 66794 | sulfoquinovose degradation | 66.67 | 2 of 3 | ||
| 66794 | octane oxidation | 66.67 | 2 of 3 | ||
| 66794 | degradation of hexoses | 66.67 | 12 of 18 | ||
| 66794 | acetoin degradation | 66.67 | 2 of 3 | ||
| 66794 | L-lactaldehyde degradation | 66.67 | 2 of 3 | ||
| 66794 | enterobactin biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | phenol degradation | 65 | 13 of 20 | ||
| 66794 | vitamin B6 metabolism | 63.64 | 7 of 11 | ||
| 66794 | ketogluconate metabolism | 62.5 | 5 of 8 | ||
| 66794 | phosphatidylethanolamine bioynthesis | 61.54 | 8 of 13 | ||
| 66794 | cysteine metabolism | 61.11 | 11 of 18 | ||
| 66794 | degradation of pentoses | 60.71 | 17 of 28 | ||
| 66794 | myo-inositol biosynthesis | 60 | 6 of 10 | ||
| 66794 | 3-chlorocatechol degradation | 60 | 3 of 5 | ||
| 66794 | factor 420 biosynthesis | 60 | 3 of 5 | ||
| 66794 | lipoate biosynthesis | 60 | 3 of 5 | ||
| 66794 | degradation of aromatic, nitrogen containing compounds | 58.33 | 7 of 12 | ||
| 66794 | d-mannose degradation | 55.56 | 5 of 9 | ||
| 66794 | lipid A biosynthesis | 55.56 | 5 of 9 | ||
| 66794 | nitrate assimilation | 55.56 | 5 of 9 | ||
| 66794 | sulfate reduction | 53.85 | 7 of 13 | ||
| 66794 | urea cycle | 53.85 | 7 of 13 | ||
| 66794 | oxidative phosphorylation | 52.75 | 48 of 91 | ||
| 66794 | lysine metabolism | 52.38 | 22 of 42 | ||
| 66794 | kanosamine biosynthesis II | 50 | 1 of 2 | ||
| 66794 | glycolate and glyoxylate degradation | 50 | 3 of 6 | ||
| 66794 | vitamin E metabolism | 50 | 2 of 4 | ||
| 66794 | ribulose monophosphate pathway | 50 | 1 of 2 | ||
| 66794 | cyclohexanol degradation | 50 | 2 of 4 | ||
| 66794 | 4-hydroxyphenylacetate degradation | 50 | 5 of 10 | ||
| 66794 | coenzyme M biosynthesis | 50 | 5 of 10 | ||
| 66794 | toluene degradation | 50 | 2 of 4 | ||
| 66794 | aminopropanol phosphate biosynthesis | 50 | 1 of 2 | ||
| 66794 | arachidonic acid metabolism | 50 | 9 of 18 | ||
| 66794 | pantothenate biosynthesis | 50 | 3 of 6 | ||
| 66794 | alginate biosynthesis | 50 | 2 of 4 | ||
| 66794 | phenylmercury acetate degradation | 50 | 1 of 2 | ||
| 66794 | quinate degradation | 50 | 1 of 2 | ||
| 66794 | glycine metabolism | 50 | 5 of 10 | ||
| 66794 | ethanol fermentation | 50 | 1 of 2 | ||
| 66794 | vitamin B12 metabolism | 47.06 | 16 of 34 | ||
| 66794 | bile acid biosynthesis, neutral pathway | 47.06 | 8 of 17 | ||
| 66794 | arachidonate biosynthesis | 40 | 2 of 5 | ||
| 66794 | glycine betaine biosynthesis | 40 | 2 of 5 | ||
| 66794 | carnitine metabolism | 37.5 | 3 of 8 | ||
| 66794 | carotenoid biosynthesis | 36.36 | 8 of 22 | ||
| 66794 | ascorbate metabolism | 36.36 | 8 of 22 | ||
| 66794 | polyamine pathway | 34.78 | 8 of 23 | ||
| 66794 | (5R)-carbapenem carboxylate biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | selenocysteine biosynthesis | 33.33 | 2 of 6 | ||
| 66794 | sphingosine metabolism | 33.33 | 2 of 6 | ||
| 66794 | IAA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | methane metabolism | 33.33 | 1 of 3 | ||
| 66794 | aclacinomycin biosynthesis | 28.57 | 2 of 7 | ||
| 66794 | benzoyl-CoA degradation | 28.57 | 2 of 7 | ||
| 66794 | methanogenesis from CO2 | 25 | 3 of 12 | ||
| 66794 | catecholamine biosynthesis | 25 | 1 of 4 |
| Cat1 | Cat2 | Cat3 | |
|---|---|---|---|
| #Engineered | #Agriculture | #Field | |
| #Environmental | #Terrestrial | #Soil | |
| #Host | #Plants | #Herbaceous plants (Grass,Crops) |
Global distribution of 16S sequence DQ789172 (>99% sequence identity) for Sphingomonas sanxanigenens from Microbeatlas ![]()
| @ref | Description | Assembly level | INSDC accession | BV-BRC accession | IMG accession | NCBI tax ID | Score | |
|---|---|---|---|---|---|---|---|---|
| 66792 | ASM51220v2 assembly for Sphingomonas sanxanigenens DSM 19645 = NX02 | complete | 1123269 | 96.51 | ||||
| 66792 | Sphingomonas sanxanigenens DSM 19645 | complete | 1123269 | 73.92 |
| 8232 | GC-content (mol%)66.4 |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125439 | oxygen_tolerance | BacteriaNetⓘ | obligate aerobe | 99.50 | no |
| 125439 | gram_stain | BacteriaNetⓘ | negative | 95.80 | no |
| 125439 | motility | BacteriaNetⓘ | yes | 61.80 | no |
| 125439 | spore_formation | BacteriaNetⓘ | no | 89.20 | no |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125438 | gram-positive | gram-positiveⓘ | no | 91.07 | yes |
| 125438 | anaerobic | anaerobicⓘ | no | 93.05 | no |
| 125438 | aerobic | aerobicⓘ | yes | 89.92 | no |
| 125438 | spore-forming | spore-formingⓘ | no | 84.79 | yes |
| 125438 | thermophilic | thermophileⓘ | no | 96.97 | yes |
| 125438 | flagellated | motile2+ⓘ | yes | 71.04 | no |
| Topic | Title | Authors | Journal | DOI | Year | |
|---|---|---|---|---|---|---|
| Identification and characterization of two CRISPR/Cas systems associated with the mosquito microbiome. | Hegde S, Rauch HE, Hughes GL, Shariat N. | Access Microbiol | 10.1099/acmi.0.000599.v4 | 2023 | ||
| The evolutionary life cycle of the polysaccharide biosynthetic gene cluster based on the Sphingomonadaceae. | Wu M, Huang H, Li G, Ren Y, Shi Z, Li X, Dai X, Gao G, Ren M, Ma T. | Sci Rep | 10.1038/srep46484 | 2017 | ||
| Genome Sequence and Characterization of a Xanthorhodopsin-Containing, Aerobic Anoxygenic Phototrophic Rhodobacter Species, Isolated from Mesophilic Conditions at Yellowstone National Park. | Kyndt JA, Robertson S, Shoffstall IB, Ramaley RF, Meyer TE. | Microorganisms | 10.3390/microorganisms10061169 | 2022 | ||
| Metabolism | Genomewide characterisation of the genetic diversity of carotenogenesis in bacteria of the order Sphingomonadales. | Siddaramappa S, Viswanathan V, Thiyagarajan S, Narjala A. | Microb Genom | 10.1099/mgen.0.000172 | 2018 | |
| Evolutionary Genomics of an Ancient Prophage of the Order Sphingomonadales. | Viswanathan V, Narjala A, Ravichandran A, Jayaprasad S, Siddaramappa S. | Genome Biol Evol | 10.1093/gbe/evx024 | 2017 | ||
| Diversity of Phototrophic Genes Suggests Multiple Bacteria May Be Able to Exploit Sunlight in Exposed Soils from the Sør Rondane Mountains, East Antarctica. | Tahon G, Tytgat B, Willems A. | Front Microbiol | 10.3389/fmicb.2016.02026 | 2016 | ||
| Genetics | Analysis of 1,000+ Type-Strain Genomes Substantially Improves Taxonomic Classification of Alphaproteobacteria. | Hordt A, Lopez MG, Meier-Kolthoff JP, Schleuning M, Weinhold LM, Tindall BJ, Gronow S, Kyrpides NC, Woyke T, Goker M. | Front Microbiol | 10.3389/fmicb.2020.00468 | 2020 | |
| Phylogeny | Sphingomonas gilva sp. nov., isolated from mountain soil. | Zhu D, Niu Y, Liu D, Wang G, Zheng S | Int J Syst Evol Microbiol | 10.1099/ijsem.0.003645 | 2019 | |
| Phylogeny | Sphingomonaszeicaulis sp. nov., an endophytic bacterium isolated from maize root. | Gao JL, Sun P, Wang XM, Cheng S, Lv F, Qiu TL, Yuan M, Sun JG | Int J Syst Evol Microbiol | 10.1099/ijsem.0.001262 | 2016 | |
| Phylogeny | Hephaestia caeni gen. nov., sp. nov., a novel member of the family Sphingomonadaceae isolated from activated sludge. | Felfoldi T, Vengring A, Marialigeti K, Andras J, Schumann P, Toth EM | Int J Syst Evol Microbiol | 10.1099/ijs.0.053736-0 | 2013 | |
| Phylogeny | Sphingomonas sanxanigenens sp. nov., isolated from soil. | Huang HD, Wang W, Ma T, Li GQ, Liang FL, Liu RL | Int J Syst Evol Microbiol | 10.1099/ijs.0.000257-0 | 2009 |
| #8232 | Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 19645 |
| #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 ) |
| #25319 | IJSEM 719 2009 ( DOI 10.1099/ijs.0.000257-0 , PubMed 19329595 ) |
| #28879 | 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 #25319 |
| #39797 | ; Curators of the CIP; |
| #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 . |
| #122484 | Collection of Institut Pasteur ; Curators of the CIP; CIP 110406 |
| #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 ) |
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