Paludifilum halophilum SMBg3 is an aerobe, chemoorganotroph, spore-forming prokaryote that forms filamentous colonies and was isolated from superficial sediment of a solar saltern.
spore-forming Gram-positive filament-shaped colony-forming aerobe chemoorganotroph thermophilic genome sequence 16S sequence| @ref 20215 |
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| Domain Bacillati |
| Phylum Bacillota |
| Class Bacilli |
| Order Caryophanales |
| Family Thermoactinomycetaceae |
| Genus Paludifilum |
| Species Paludifilum halophilum |
| Full scientific name Paludifilum halophilum Frikha-Dammak et al. 2016 |
| @ref | Gram stain | Cell shape | |
|---|---|---|---|
| 25075 | positive | filament-shaped |
| @ref | Colony size | Colony color | Colony shape | Incubation period | Medium used | |
|---|---|---|---|---|---|---|
| 25075 | 4.0-8.0 mm | pale yellow | filamentous | 7 days | Bennett ’ s medium |
| @ref | Name | Growth | Medium link | Composition | |
|---|---|---|---|---|---|
| 25075 | Bennett ’ s medium | ||||
| 23824 | GYM STREPTOMYCES MEDIUM 10% NACL (DSMZ Medium 1159) | Medium recipe at MediaDive | Name: GYM STREPTOMYCES MEDIUM 10% NACL (DSMZ Medium 1159) Composition: NaCl 100.0 g/l Agar 15.0 g/l Malt extract 10.0 g/l Yeast extract 4.0 g/l Glucose 4.0 g/l CaCO3 2.0 g/l Distilled water | ||
| 23824 | 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 |
| 25075 | Oxygen toleranceaerobe |
| 25075 | Typechemoorganotroph |
| @ref | Chebi-ID | Metabolite | Utilization activity | Kind of utilization tested | |
|---|---|---|---|---|---|
| 25075 | 22599 ChEBI | arabinose | + | carbon source | |
| 25075 | 29016 ChEBI | arginine | - | nitrogen source | |
| 25075 | casein | + | hydrolysis | ||
| 25075 | 62968 ChEBI | cellulose | - | hydrolysis | |
| 25075 | 16947 ChEBI | citrate | - | carbon source | |
| 25075 | 16991 ChEBI | dna | - | hydrolysis | |
| 25075 | 4853 ChEBI | esculin | + | hydrolysis | |
| 25075 | 28757 ChEBI | fructose | + | carbon source | |
| 25075 | 5291 ChEBI | gelatin | + | hydrolysis | |
| 25075 | 17234 ChEBI | glucose | - | fermentation | |
| 25075 | 17234 ChEBI | glucose | + | carbon source | |
| 25075 | 28300 ChEBI | glutamine | - | nitrogen source | |
| 25075 | 15428 ChEBI | glycine | + | nitrogen source | |
| 25075 | 17368 ChEBI | hypoxanthine | - | hydrolysis | |
| 25075 | 25017 ChEBI | leucine | - | nitrogen source | |
| 25075 | 18059 ChEBI | lipid | - | hydrolysis | |
| 25075 | 25094 ChEBI | lysine | + | nitrogen source | |
| 25075 | 17306 ChEBI | maltose | + | carbon source | |
| 25075 | 29864 ChEBI | mannitol | - | carbon source | |
| 25075 | 37684 ChEBI | mannose | + | carbon source | |
| 25075 | 17268 ChEBI | myo-inositol | + | carbon source | |
| 25075 | 17632 ChEBI | nitrate | - | reduction | |
| 25075 | 16301 ChEBI | nitrite | - | reduction | |
| 25075 | 18257 ChEBI | ornithine | + | nitrogen source | |
| 25075 | 28044 ChEBI | phenylalanine | - | nitrogen source | |
| 25075 | 26271 ChEBI | proline | + | nitrogen source | |
| 25075 | 30911 ChEBI | sorbitol | + | carbon source | |
| 25075 | 28017 ChEBI | starch | + | carbon source | |
| 25075 | 28017 ChEBI | starch | + | hydrolysis | |
| 25075 | 17992 ChEBI | sucrose | + | carbon source | |
| 25075 | 27897 ChEBI | tryptophan | - | energy source | |
| 25075 | 27897 ChEBI | tryptophan | - | nitrogen source | |
| 25075 | 18186 ChEBI | tyrosine | - | hydrolysis | |
| 25075 | 16199 ChEBI | urea | - | hydrolysis | |
| 25075 | 15318 ChEBI | xanthine | - | hydrolysis | |
| 25075 | 18222 ChEBI | xylose | + | carbon source |
| @ref | pathway | enzyme coverage | annotated reactions | external links | |
|---|---|---|---|---|---|
| 66794 | anapleurotic synthesis of oxalacetate | 100 | 1 of 1 | ||
| 66794 | aspartate and asparagine metabolism | 100 | 9 of 9 | ||
| 66794 | acetate fermentation | 100 | 4 of 4 | ||
| 66794 | palmitate biosynthesis | 100 | 22 of 22 | ||
| 66794 | ppGpp biosynthesis | 100 | 4 of 4 | ||
| 66794 | methylglyoxal degradation | 100 | 5 of 5 | ||
| 66794 | vitamin K metabolism | 100 | 5 of 5 | ||
| 66794 | lipoate biosynthesis | 100 | 5 of 5 | ||
| 66794 | biotin biosynthesis | 100 | 4 of 4 | ||
| 66794 | L-lactaldehyde degradation | 100 | 3 of 3 | ||
| 66794 | threonine metabolism | 100 | 10 of 10 | ||
| 66794 | cis-vaccenate biosynthesis | 100 | 2 of 2 | ||
| 66794 | cardiolipin biosynthesis | 100 | 7 of 7 | ||
| 66794 | aerobactin biosynthesis | 100 | 1 of 1 | ||
| 66794 | suberin monomers biosynthesis | 100 | 2 of 2 | ||
| 66794 | UDP-GlcNAc biosynthesis | 100 | 3 of 3 | ||
| 66794 | CDP-diacylglycerol biosynthesis | 100 | 2 of 2 | ||
| 66794 | sulfopterin metabolism | 100 | 4 of 4 | ||
| 66794 | coenzyme A metabolism | 100 | 4 of 4 | ||
| 66794 | formaldehyde oxidation | 100 | 3 of 3 | ||
| 66794 | aminopropanol phosphate biosynthesis | 100 | 2 of 2 | ||
| 66794 | kanosamine biosynthesis II | 100 | 2 of 2 | ||
| 66794 | adipate degradation | 100 | 2 of 2 | ||
| 66794 | cellulose degradation | 100 | 5 of 5 | ||
| 66794 | folate polyglutamylation | 100 | 1 of 1 | ||
| 66794 | C4 and CAM-carbon fixation | 100 | 8 of 8 | ||
| 66794 | gluconeogenesis | 100 | 8 of 8 | ||
| 66794 | degradation of sugar alcohols | 93.75 | 15 of 16 | ||
| 66794 | tetrahydrofolate metabolism | 92.86 | 13 of 14 | ||
| 66794 | phenylalanine metabolism | 92.31 | 12 of 13 | ||
| 66794 | vitamin B1 metabolism | 92.31 | 12 of 13 | ||
| 66794 | starch degradation | 90 | 9 of 10 | ||
| 66794 | valine metabolism | 88.89 | 8 of 9 | ||
| 66794 | chorismate metabolism | 88.89 | 8 of 9 | ||
| 66794 | isoleucine metabolism | 87.5 | 7 of 8 | ||
| 66794 | heme metabolism | 85.71 | 12 of 14 | ||
| 66794 | photosynthesis | 85.71 | 12 of 14 | ||
| 66794 | reductive acetyl coenzyme A pathway | 85.71 | 6 of 7 | ||
| 66794 | leucine metabolism | 84.62 | 11 of 13 | ||
| 66794 | glycolate and glyoxylate degradation | 83.33 | 5 of 6 | ||
| 66794 | selenocysteine biosynthesis | 83.33 | 5 of 6 | ||
| 66794 | vitamin B12 metabolism | 82.35 | 28 of 34 | ||
| 66794 | glutamate and glutamine metabolism | 82.14 | 23 of 28 | ||
| 66794 | propionate fermentation | 80 | 8 of 10 | ||
| 66794 | metabolism of amino sugars and derivatives | 80 | 4 of 5 | ||
| 66794 | glycogen metabolism | 80 | 4 of 5 | ||
| 66794 | glycine betaine biosynthesis | 80 | 4 of 5 | ||
| 66794 | myo-inositol biosynthesis | 80 | 8 of 10 | ||
| 66794 | Entner Doudoroff pathway | 80 | 8 of 10 | ||
| 66794 | peptidoglycan biosynthesis | 80 | 12 of 15 | ||
| 66794 | serine metabolism | 77.78 | 7 of 9 | ||
| 66794 | molybdenum cofactor biosynthesis | 77.78 | 7 of 9 | ||
| 66794 | urea cycle | 76.92 | 10 of 13 | ||
| 66794 | purine metabolism | 75.53 | 71 of 94 | ||
| 66794 | flavin biosynthesis | 73.33 | 11 of 15 | ||
| 66794 | pyrimidine metabolism | 73.33 | 33 of 45 | ||
| 66794 | methionine metabolism | 73.08 | 19 of 26 | ||
| 66794 | proline metabolism | 72.73 | 8 of 11 | ||
| 66794 | pentose phosphate pathway | 72.73 | 8 of 11 | ||
| 66794 | NAD metabolism | 72.22 | 13 of 18 | ||
| 66794 | ubiquinone biosynthesis | 71.43 | 5 of 7 | ||
| 66794 | glutathione metabolism | 71.43 | 10 of 14 | ||
| 66794 | arginine metabolism | 70.83 | 17 of 24 | ||
| 66794 | glycolysis | 70.59 | 12 of 17 | ||
| 66794 | histidine metabolism | 68.97 | 20 of 29 | ||
| 66794 | tryptophan metabolism | 68.42 | 26 of 38 | ||
| 66794 | octane oxidation | 66.67 | 2 of 3 | ||
| 66794 | cyanate degradation | 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 | acetoin degradation | 66.67 | 2 of 3 | ||
| 66794 | alanine metabolism | 65.52 | 19 of 29 | ||
| 66794 | lipid metabolism | 64.52 | 20 of 31 | ||
| 66794 | degradation of pentoses | 64.29 | 18 of 28 | ||
| 66794 | citric acid cycle | 64.29 | 9 of 14 | ||
| 66794 | d-xylose degradation | 63.64 | 7 of 11 | ||
| 66794 | non-pathway related | 63.16 | 24 of 38 | ||
| 66794 | oxidative phosphorylation | 62.64 | 57 of 91 | ||
| 66794 | 6-hydroxymethyl-dihydropterin diphosphate biosynthesis | 62.5 | 5 of 8 | ||
| 66794 | ketogluconate metabolism | 62.5 | 5 of 8 | ||
| 66794 | factor 420 biosynthesis | 60 | 3 of 5 | ||
| 66794 | coenzyme M biosynthesis | 60 | 6 of 10 | ||
| 66794 | phenylacetate degradation (aerobic) | 60 | 3 of 5 | ||
| 66794 | lysine metabolism | 59.52 | 25 of 42 | ||
| 66794 | isoprenoid biosynthesis | 57.69 | 15 of 26 | ||
| 66794 | propanol degradation | 57.14 | 4 of 7 | ||
| 66794 | tyrosine metabolism | 57.14 | 8 of 14 | ||
| 66794 | cysteine metabolism | 55.56 | 10 of 18 | ||
| 66794 | nitrate assimilation | 55.56 | 5 of 9 | ||
| 66794 | degradation of sugar acids | 52 | 13 of 25 | ||
| 66794 | degradation of hexoses | 50 | 9 of 18 | ||
| 66794 | butanoate fermentation | 50 | 2 of 4 | ||
| 66794 | quinate degradation | 50 | 1 of 2 | ||
| 66794 | pantothenate biosynthesis | 50 | 3 of 6 | ||
| 66794 | toluene degradation | 50 | 2 of 4 | ||
| 66794 | CMP-KDO biosynthesis | 50 | 2 of 4 | ||
| 66794 | dTDPLrhamnose biosynthesis | 50 | 4 of 8 | ||
| 66794 | phenylmercury acetate degradation | 50 | 1 of 2 | ||
| 66794 | glycogen biosynthesis | 50 | 2 of 4 | ||
| 66794 | lactate fermentation | 50 | 2 of 4 | ||
| 66794 | glycine metabolism | 50 | 5 of 10 | ||
| 66794 | ethanol fermentation | 50 | 1 of 2 | ||
| 66794 | mannosylglycerate biosynthesis | 50 | 1 of 2 | ||
| 66794 | polyamine pathway | 47.83 | 11 of 23 | ||
| 66794 | sulfate reduction | 46.15 | 6 of 13 | ||
| 66794 | phenylpropanoid biosynthesis | 46.15 | 6 of 13 | ||
| 66794 | phosphatidylethanolamine bioynthesis | 46.15 | 6 of 13 | ||
| 66794 | cholesterol biosynthesis | 45.45 | 5 of 11 | ||
| 66794 | metabolism of disaccharids | 45.45 | 5 of 11 | ||
| 66794 | d-mannose degradation | 44.44 | 4 of 9 | ||
| 66794 | 4-hydroxymandelate degradation | 44.44 | 4 of 9 | ||
| 66794 | degradation of aromatic, nitrogen containing compounds | 41.67 | 5 of 12 | ||
| 66794 | gallate degradation | 40 | 2 of 5 | ||
| 66794 | arachidonate biosynthesis | 40 | 2 of 5 | ||
| 66794 | bacilysin biosynthesis | 40 | 2 of 5 | ||
| 66794 | hydrogen production | 40 | 2 of 5 | ||
| 66794 | arachidonic acid metabolism | 38.89 | 7 of 18 | ||
| 66794 | androgen and estrogen metabolism | 37.5 | 6 of 16 | ||
| 66794 | vitamin B6 metabolism | 36.36 | 4 of 11 | ||
| 66794 | phenol degradation | 35 | 7 of 20 | ||
| 66794 | (5R)-carbapenem carboxylate biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | enterobactin biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | lipid A biosynthesis | 33.33 | 3 of 9 | ||
| 66794 | IAA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | bile acid biosynthesis, neutral pathway | 29.41 | 5 of 17 | ||
| 66794 | ascorbate metabolism | 27.27 | 6 of 22 | ||
| 66794 | 3-phenylpropionate degradation | 26.67 | 4 of 15 | ||
| 66794 | carnitine metabolism | 25 | 2 of 8 | ||
| 66794 | vitamin E metabolism | 25 | 1 of 4 | ||
| 66794 | cyclohexanol degradation | 25 | 1 of 4 | ||
| 66794 | carotenoid biosynthesis | 22.73 | 5 of 22 |
| Cat1 | Cat2 | Cat3 | |
|---|---|---|---|
| #Environmental | #Aquatic | #Pond (small) | |
| #Environmental | #Terrestrial | #Sediment |
| @ref | Sample type | Geographic location | Country | Country ISO 3 Code | Continent | Latitude | Longitude | Enrichment culture | Enrichment culture composition | Enrichment culture duration | Enrichment culture temperature | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 23824 | superficial sediment of a solar saltern | Sfax (thalossohaline natural ecosystem in the central eastern coast, about 34° 39' N 10° 42' E) | Tunisia | TUN | Africa | 34.65 | 10.7 34.65/10.7 | |||||
| 25075 | superficial sediment of non-crystallizer M1 pond | Streptomyces isolation agar medium | containing l-1: 5 g glucose, 4 g sodium propionate, 2 g casein, 0.5 g K2HPO4 , 0.5 g MgSO4 .7H2O, 200 ml sterile soil extract, 150 g NaCl and 20 g agar, pH = 7.2, ampicillin (5 µg ml-1) and cycloheximide (50 µg ml-1) | 21 days | 37 |
Global distribution of 16S sequence KP229518 (>99% sequence identity) for Paludifilum halophilum subclade from Microbeatlas ![]()
| @ref | Biosafety level | Biosafety level comment | |
|---|---|---|---|
| 23824 | 1 | Risk group (German classification) |
| @ref | Description | Assembly level | INSDC accession | BV-BRC accession | IMG accession | NCBI tax ID | Score | |
|---|---|---|---|---|---|---|---|---|
| 66792 | Paludifilum halophilum DSM 102817 | complete | 1642702 | 91.91 | ||||
| 66792 | ASM224535v1 assembly for Paludifilum halophilum DSM 102817 | contig | 1642702 | 23.91 |
| @ref | Description | Accession | Length | Database | NCBI tax ID | |
|---|---|---|---|---|---|---|
| 23824 | Paludifilum halophilum strain SMBg3 16S ribosomal RNA gene, partial sequence | KP229518 | 1362 | 1642702 |
| @ref | GC-content (mol%) | Method | |
|---|---|---|---|
| 23824 | 51.2 | high performance liquid chromatography (HPLC) |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125439 | spore_formation | BacteriaNetⓘ | yes | 91.10 | no |
| 125439 | motility | BacteriaNetⓘ | yes | 74.30 | no |
| 125439 | gram_stain | BacteriaNetⓘ | variable | 66.40 | no |
| 125439 | oxygen_tolerance | BacteriaNetⓘ | facultative anaerobe | 87.10 | no |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125438 | gram-positive | gram-positiveⓘ | yes | 79.02 | yes |
| 125438 | anaerobic | anaerobicⓘ | no | 86.33 | yes |
| 125438 | spore-forming | spore-formingⓘ | yes | 93.96 | yes |
| 125438 | aerobic | aerobicⓘ | yes | 76.06 | no |
| 125438 | thermophilic | thermophileⓘ | no | 63.17 | no |
| 125438 | flagellated | motile2+ⓘ | no | 72.43 | no |
| Topic | Title | Authors | Journal | DOI | Year | |
|---|---|---|---|---|---|---|
| Metabolism | Enhancement of Antibacterial Activity of Paludifilum halophilum and Identification of N-(1-Carboxy-ethyl)-phthalamic Acid as the Main Bioactive Compound. | Frikha-Dammak D, Fakhfakh J, Belhaj D, Bouattour E, Ayadi H, Chaabouni M, Ayadi H, Maalej S | Biomed Res Int | 10.1155/2020/4805706 | 2020 | |
| Pathogenicity | Antagonistic Properties of Some Halophilic Thermoactinomycetes Isolated from Superficial Sediment of a Solar Saltern and Production of Cyclic Antimicrobial Peptides by the Novel Isolate Paludifilum halophilum. | Frikha Dammak D, Zarai Z, Najah S, Abdennabi R, Belbahri L, Rateb ME, Mejdoub H, Maalej S | Biomed Res Int | 10.1155/2017/1205258 | 2017 | |
| Metabolism | Genome analysis of the salt-resistant Paludifilum halophilum DSM 102817(T) reveals genes involved in flux-tuning of ectoines and unexplored bioactive secondary metabolites. | Frikha-Dammak D, Ayadi H, Hakim-Rekik I, Belbahri L, Maalej S | World J Microbiol Biotechnol | 10.1007/s11274-021-03147-7 | 2021 | |
| Stress | The saltern-derived Paludifilum halophilum DSM 102817(T) is a new high-yield ectoines producer in minimal medium and under salt stress conditions. | Ayadi H, Frikha-Dammak D, Fakhfakh J, Chamkha M, Hassairi I, Allouche N, Sayadi S, Maalej S | 3 Biotech | 10.1007/s13205-020-02512-x | 2020 | |
| Phylogeny | Paludifilum halophilum gen. nov., sp. nov., a thermoactinomycete isolated from superficial sediment of a solar saltern. | Frikha-Dammak D, Fardeau ML, Cayol JL, Ben Fguira-Fourati L, Najeh S, Ollivier B, Maalej S | Int J Syst Evol Microbiol | 10.1099/ijsem.0.001523 | 2016 |
| #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 ) |
| #23824 | Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 102817 |
| #25075 | D. F. Frikha-Dammak, M. L.,Cayol, J. L.,Ben Fguira-Fourati, L.,Najeh, S.,Ollivier, B.,Maalej, S.: Paludifilum halophilum gen. nov., sp. nov., a thermoactinomycete isolated from superficial sediment of a solar saltern. IJSEM 66: 5371 - 5378 2016 ( DOI 10.1099/ijsem.0.001523 , PubMed 27671055 ) |
| #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 ) |
| #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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