Pseudohalioglobus lutimaris HF004 is an aerobe, Gram-negative, rod-shaped prokaryote that forms circular colonies and was isolated from marine sediment sample.
Gram-negative rod-shaped colony-forming aerobe genome sequence 16S sequence| @ref 20215 |
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| Domain Pseudomonadati |
| Phylum Pseudomonadota |
| Class Gammaproteobacteria |
| Order Cellvibrionales |
| Family Halieaceae |
| Genus Pseudohalioglobus |
| Species Pseudohalioglobus lutimaris |
| Full scientific name Pseudohalioglobus lutimaris (Shi et al. 2018) Kang et al. 2020 |
| Synonyms (1) |
| @ref | Colony size | Colony color | Colony shape | Incubation period | Medium used | |
|---|---|---|---|---|---|---|
| 65359 | 0.5-0.8 mm | beige | circular | 3 days | marine agar 2216 |
| @ref | Chebi-ID | Metabolite | Utilization activity | Kind of utilization tested | |
|---|---|---|---|---|---|
| 65359 | 30916 ChEBI | 2-oxoglutarate | + | oxidation | |
| 65359 | 30089 ChEBI | acetate | + | oxidation | |
| 65359 | 13705 ChEBI | acetoacetate | + | oxidation | |
| 65359 | 2509 ChEBI | agar | - | hydrolysis | |
| 65359 | 58187 ChEBI | alginate | - | hydrolysis | |
| 65359 | 62968 ChEBI | cellulose | - | hydrolysis | |
| 65359 | 16947 ChEBI | citrate | + | assimilation | |
| 65359 | 16988 ChEBI | D-ribose | + | builds acid from | |
| 65359 | 16443 ChEBI | D-tagatose | + | builds acid from | |
| 65359 | 28066 ChEBI | gentiobiose | + | oxidation | |
| 65359 | 32323 ChEBI | glucuronamide | + | oxidation | |
| 65359 | 15589 ChEBI | L-malate | + | oxidation | |
| 65359 | 17632 ChEBI | nitrate | + | reduction | |
| 65359 | potassium 5-dehydro-D-gluconate | + | builds acid from | ||
| 65359 | 28017 ChEBI | starch | - | hydrolysis | |
| 65359 | 17992 ChEBI | sucrose | + | oxidation | |
| 65359 | 32528 ChEBI | turanose | + | oxidation | |
| 65359 | 53424 ChEBI | tween 20 | + | hydrolysis | |
| 65359 | 53423 ChEBI | tween 40 | + | hydrolysis | |
| 65359 | 53425 ChEBI | tween 60 | + | hydrolysis | |
| 65359 | 53426 ChEBI | tween 80 | + | hydrolysis |
| @ref | ChEBI | Metabolite | Is antibiotic | Is sensitive | Sensitivity conc. | |
|---|---|---|---|---|---|---|
| 65359 | 31168 | acetylspiramycin | 30 µg (disc) | |||
| 65359 | 204928 | cefotaxime | 30 µg (disc) | |||
| 65359 | 29007 | ceftriaxone | 30 µg (disc) | |||
| 65359 | 3745 | clindamycin | ||||
| 65359 | 48923 | erythromycin | 15 µg (disc) | |||
| 65359 | 17833 | gentamicin | 10 µg (disc) | |||
| 65359 | 6472 | lincomycin | ||||
| 65359 | 100246 | norfloxacin | 10 µg (disc) | |||
| 65359 | 7731 | ofloxacin | 5 µg (disc) | |||
| 65359 | 18208 | penicillin g | 10 µg (disc) | |||
| 65359 | 17076 | streptomycin | 10 µg (disc) | |||
| 65359 | 53727 | sulfamethoxydiazine | 5 µg (disc) | |||
| 65359 | 27902 | tetracycline | ||||
| 65359 | 28001 | vancomycin |
| @ref | Value | Activity | Ec | |
|---|---|---|---|---|
| 65359 | acid phosphatase | + | 3.1.3.2 | |
| 65359 | alkaline phosphatase | + | 3.1.3.1 | |
| 65359 | alpha-chymotrypsin | - | 3.4.21.1 | |
| 65359 | alpha-galactosidase | - | 3.2.1.22 | |
| 65359 | alpha-glucosidase | - | 3.2.1.20 | |
| 65359 | alpha-mannosidase | - | 3.2.1.24 | |
| 65359 | beta-D-fucosidase | - | 3.2.1.38 | |
| 65359 | beta-galactosidase | - | 3.2.1.23 | |
| 65359 | beta-glucosidase | - | 3.2.1.21 | |
| 65359 | beta-glucuronidase | - | 3.2.1.31 | |
| 65359 | catalase | + | 1.11.1.6 | |
| 65359 | cystine arylamidase | + | 3.4.11.3 | |
| 65359 | cytochrome oxidase | - | 1.9.3.1 | |
| 65359 | esterase (C 4) | + | ||
| 65359 | esterase Lipase (C 8) | + | ||
| 65359 | leucine arylamidase | + | 3.4.11.1 | |
| 65359 | lipase (C 14) | - | ||
| 65359 | N-acetyl-beta-glucosaminidase | - | 3.2.1.52 | |
| 65359 | naphthol-AS-BI-phosphohydrolase | + | ||
| 65359 | trypsin | - | 3.4.21.4 | |
| 65359 | valine arylamidase | + |
| @ref | pathway | enzyme coverage | annotated reactions | external links | |
|---|---|---|---|---|---|
| 66794 | quinate degradation | 100 | 2 of 2 | ||
| 66794 | ppGpp biosynthesis | 100 | 4 of 4 | ||
| 66794 | UDP-GlcNAc biosynthesis | 100 | 3 of 3 | ||
| 66794 | CDP-diacylglycerol biosynthesis | 100 | 2 of 2 | ||
| 66794 | cis-vaccenate biosynthesis | 100 | 2 of 2 | ||
| 66794 | methylglyoxal degradation | 100 | 5 of 5 | ||
| 66794 | denitrification | 100 | 2 of 2 | ||
| 66794 | adipate degradation | 100 | 2 of 2 | ||
| 66794 | sulfopterin metabolism | 100 | 4 of 4 | ||
| 66794 | formaldehyde oxidation | 100 | 3 of 3 | ||
| 66794 | cardiolipin biosynthesis | 100 | 7 of 7 | ||
| 66794 | L-lactaldehyde degradation | 100 | 3 of 3 | ||
| 66794 | biotin biosynthesis | 100 | 4 of 4 | ||
| 66794 | ethanol fermentation | 100 | 2 of 2 | ||
| 66794 | gluconeogenesis | 100 | 8 of 8 | ||
| 66794 | taurine degradation | 100 | 1 of 1 | ||
| 66794 | aspartate and asparagine metabolism | 100 | 9 of 9 | ||
| 66794 | palmitate biosynthesis | 100 | 22 of 22 | ||
| 66794 | folate polyglutamylation | 100 | 1 of 1 | ||
| 66794 | ceramide biosynthesis | 100 | 1 of 1 | ||
| 66794 | ubiquinone biosynthesis | 100 | 7 of 7 | ||
| 66794 | toluene degradation | 100 | 4 of 4 | ||
| 66794 | anapleurotic synthesis of oxalacetate | 100 | 1 of 1 | ||
| 66794 | suberin monomers biosynthesis | 100 | 2 of 2 | ||
| 66794 | tetrahydrofolate metabolism | 92.86 | 13 of 14 | ||
| 66794 | citric acid cycle | 92.86 | 13 of 14 | ||
| 66794 | leucine metabolism | 92.31 | 12 of 13 | ||
| 66794 | phenylalanine metabolism | 92.31 | 12 of 13 | ||
| 66794 | Entner Doudoroff pathway | 90 | 9 of 10 | ||
| 66794 | glutamate and glutamine metabolism | 89.29 | 25 of 28 | ||
| 66794 | serine metabolism | 88.89 | 8 of 9 | ||
| 66794 | valine metabolism | 88.89 | 8 of 9 | ||
| 66794 | lipid A biosynthesis | 88.89 | 8 of 9 | ||
| 66794 | C4 and CAM-carbon fixation | 87.5 | 7 of 8 | ||
| 66794 | reductive acetyl coenzyme A pathway | 85.71 | 6 of 7 | ||
| 66794 | glycolate and glyoxylate degradation | 83.33 | 5 of 6 | ||
| 66794 | phenylacetate degradation (aerobic) | 80 | 4 of 5 | ||
| 66794 | cellulose degradation | 80 | 4 of 5 | ||
| 66794 | propionate fermentation | 80 | 8 of 10 | ||
| 66794 | alanine metabolism | 79.31 | 23 of 29 | ||
| 66794 | heme metabolism | 78.57 | 11 of 14 | ||
| 66794 | molybdenum cofactor biosynthesis | 77.78 | 7 of 9 | ||
| 66794 | CO2 fixation in Crenarchaeota | 77.78 | 7 of 9 | ||
| 66794 | chorismate metabolism | 77.78 | 7 of 9 | ||
| 66794 | lipid metabolism | 77.42 | 24 of 31 | ||
| 66794 | purine metabolism | 76.6 | 72 of 94 | ||
| 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 | dTDPLrhamnose biosynthesis | 75 | 6 of 8 | ||
| 66794 | isoleucine metabolism | 75 | 6 of 8 | ||
| 66794 | CMP-KDO biosynthesis | 75 | 3 of 4 | ||
| 66794 | butanoate fermentation | 75 | 3 of 4 | ||
| 66794 | flavin biosynthesis | 73.33 | 11 of 15 | ||
| 66794 | NAD metabolism | 72.22 | 13 of 18 | ||
| 66794 | propanol degradation | 71.43 | 5 of 7 | ||
| 66794 | histidine metabolism | 68.97 | 20 of 29 | ||
| 66794 | androgen and estrogen metabolism | 68.75 | 11 of 16 | ||
| 66794 | octane oxidation | 66.67 | 2 of 3 | ||
| 66794 | acetyl CoA biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | pyrimidine metabolism | 66.67 | 30 of 45 | ||
| 66794 | acetoin degradation | 66.67 | 2 of 3 | ||
| 66794 | methane metabolism | 66.67 | 2 of 3 | ||
| 66794 | enterobactin biosynthesis | 66.67 | 2 of 3 | ||
| 66794 | peptidoglycan biosynthesis | 66.67 | 10 of 15 | ||
| 66794 | tryptophan metabolism | 65.79 | 25 of 38 | ||
| 66794 | glutathione metabolism | 64.29 | 9 of 14 | ||
| 66794 | photosynthesis | 64.29 | 9 of 14 | ||
| 66794 | degradation of sugar acids | 64 | 16 of 25 | ||
| 66794 | vitamin B6 metabolism | 63.64 | 7 of 11 | ||
| 66794 | proline metabolism | 63.64 | 7 of 11 | ||
| 66794 | arginine metabolism | 62.5 | 15 of 24 | ||
| 66794 | urea cycle | 61.54 | 8 of 13 | ||
| 66794 | cysteine metabolism | 61.11 | 11 of 18 | ||
| 66794 | non-pathway related | 60.53 | 23 of 38 | ||
| 66794 | phenol degradation | 60 | 12 of 20 | ||
| 66794 | starch degradation | 60 | 6 of 10 | ||
| 66794 | factor 420 biosynthesis | 60 | 3 of 5 | ||
| 66794 | gallate degradation | 60 | 3 of 5 | ||
| 66794 | threonine metabolism | 60 | 6 of 10 | ||
| 66794 | glycogen metabolism | 60 | 3 of 5 | ||
| 66794 | hydrogen production | 60 | 3 of 5 | ||
| 66794 | 4-hydroxyphenylacetate degradation | 60 | 6 of 10 | ||
| 66794 | bile acid biosynthesis, neutral pathway | 58.82 | 10 of 17 | ||
| 66794 | glycolysis | 58.82 | 10 of 17 | ||
| 66794 | isoprenoid biosynthesis | 57.69 | 15 of 26 | ||
| 66794 | tyrosine metabolism | 57.14 | 8 of 14 | ||
| 66794 | polyamine pathway | 56.52 | 13 of 23 | ||
| 66794 | d-mannose degradation | 55.56 | 5 of 9 | ||
| 66794 | nitrate assimilation | 55.56 | 5 of 9 | ||
| 66794 | lysine metabolism | 54.76 | 23 of 42 | ||
| 66794 | pentose phosphate pathway | 54.55 | 6 of 11 | ||
| 66794 | sulfate reduction | 53.85 | 7 of 13 | ||
| 66794 | methionine metabolism | 53.85 | 14 of 26 | ||
| 66794 | 3-phenylpropionate degradation | 53.33 | 8 of 15 | ||
| 66794 | glycine metabolism | 50 | 5 of 10 | ||
| 66794 | phenylmercury acetate degradation | 50 | 1 of 2 | ||
| 66794 | aminopropanol phosphate biosynthesis | 50 | 1 of 2 | ||
| 66794 | ketogluconate metabolism | 50 | 4 of 8 | ||
| 66794 | coenzyme A metabolism | 50 | 2 of 4 | ||
| 66794 | alginate biosynthesis | 50 | 2 of 4 | ||
| 66794 | degradation of sugar alcohols | 50 | 8 of 16 | ||
| 66794 | cyclohexanol degradation | 50 | 2 of 4 | ||
| 66794 | pantothenate biosynthesis | 50 | 3 of 6 | ||
| 66794 | mannosylglycerate biosynthesis | 50 | 1 of 2 | ||
| 66794 | degradation of pentoses | 46.43 | 13 of 28 | ||
| 66794 | ascorbate metabolism | 45.45 | 10 of 22 | ||
| 66794 | arachidonic acid metabolism | 44.44 | 8 of 18 | ||
| 66794 | 4-hydroxymandelate degradation | 44.44 | 4 of 9 | ||
| 66794 | benzoyl-CoA degradation | 42.86 | 3 of 7 | ||
| 66794 | vitamin K metabolism | 40 | 2 of 5 | ||
| 66794 | 3-chlorocatechol degradation | 40 | 2 of 5 | ||
| 66794 | lipoate biosynthesis | 40 | 2 of 5 | ||
| 66794 | glycine betaine biosynthesis | 40 | 2 of 5 | ||
| 66794 | arachidonate biosynthesis | 40 | 2 of 5 | ||
| 66794 | metabolism of amino sugars and derivatives | 40 | 2 of 5 | ||
| 66794 | ethylmalonyl-CoA pathway | 40 | 2 of 5 | ||
| 66794 | degradation of hexoses | 38.89 | 7 of 18 | ||
| 66794 | phosphatidylethanolamine bioynthesis | 38.46 | 5 of 13 | ||
| 66794 | cholesterol biosynthesis | 36.36 | 4 of 11 | ||
| 66794 | metabolism of disaccharids | 36.36 | 4 of 11 | ||
| 66794 | oxidative phosphorylation | 36.26 | 33 of 91 | ||
| 66794 | selenocysteine biosynthesis | 33.33 | 2 of 6 | ||
| 66794 | (5R)-carbapenem carboxylate biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | IAA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | sphingosine metabolism | 33.33 | 2 of 6 | ||
| 66794 | cyanate degradation | 33.33 | 1 of 3 | ||
| 66794 | degradation of aromatic, nitrogen containing compounds | 33.33 | 4 of 12 | ||
| 66794 | vitamin B1 metabolism | 30.77 | 4 of 13 | ||
| 66794 | coenzyme M biosynthesis | 30 | 3 of 10 | ||
| 66794 | aclacinomycin biosynthesis | 28.57 | 2 of 7 | ||
| 66794 | dolichyl-diphosphooligosaccharide biosynthesis | 27.27 | 3 of 11 | ||
| 66794 | catecholamine biosynthesis | 25 | 1 of 4 | ||
| 66794 | vitamin E metabolism | 25 | 1 of 4 | ||
| 66794 | lactate fermentation | 25 | 1 of 4 | ||
| 66794 | carnitine metabolism | 25 | 2 of 8 | ||
| 66794 | phenylpropanoid biosynthesis | 23.08 | 3 of 13 | ||
| 66794 | carotenoid biosynthesis | 22.73 | 5 of 22 |
| @ref | Sample type | Sampling date | Geographic location | Country | Country ISO 3 Code | Continent | Latitude | Longitude | Enrichment culture | Isolation procedure | |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 65359 | marine sediment sample | 2013-09 | coast of Weihai | China | CHN | Asia | 37.533 | 122.063 37.533/122.063 | marine agar 2216 | The marine sediment sample was serially diluted to 10-5 with sterilized seawater, and 0.1 ml aliquots of each dilution were spread onto marine agar 2216 | |
| 67771 | From the coastal area of Weihai marine sediment | China | CHN | Asia |
Global distribution of 16S sequence KR528479 (>99% sequence identity) for Halioglobus from Microbeatlas ![]()
| @ref | Description | Assembly level | INSDC accession | BV-BRC accession | IMG accession | NCBI tax ID | Score | |
|---|---|---|---|---|---|---|---|---|
| 66792 | ASM286682v1 assembly for Pseudohalioglobus lutimaris HF004 | contig | 1737061 | 63.43 |
| @ref | Description | Accession | Database | |
|---|---|---|---|---|
| 65359 | Pseudohalioglobus lutimaris strain HF004 16S ribosomal RNA gene, partial sequence | KR528479 |
| @ref | GC-content (mol%) | Method | |
|---|---|---|---|
| 65359 | 57.2 | genome sequence analysis |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125439 | spore_formation | BacteriaNetⓘ | no | 99.80 | no |
| 125439 | motility | BacteriaNetⓘ | yes | 87.60 | no |
| 125439 | gram_stain | BacteriaNetⓘ | negative | 99.80 | no |
| 125439 | oxygen_tolerance | BacteriaNetⓘ | facultative aerobe | 66.00 | no |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125438 | gram-positive | gram-positiveⓘ | no | 97.89 | no |
| 125438 | anaerobic | anaerobicⓘ | no | 96.28 | yes |
| 125438 | aerobic | aerobicⓘ | yes | 75.96 | yes |
| 125438 | spore-forming | spore-formingⓘ | no | 92.11 | no |
| 125438 | thermophilic | thermophileⓘ | no | 97.41 | yes |
| 125438 | flagellated | motile2+ⓘ | yes | 64.60 | no |
| #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 ) |
| #65359 | Ming-Jing Shi, Chong Wang, Xu-Ting Wang, Zong-Jun Du: Halioglobus lutimaris sp. nov., isolated from coastal sediment. IJSEM 68: 876 - 880 2018 ( DOI 10.1099/ijsem.0.002601 , PubMed 29458490 ) |
| #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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