Halanaeroarchaeum sulfurireducens HSR2 is an obligate anaerobe, Gram-negative, coccus-shaped archaeon that was isolated from anaerobic sediments of chloride-sulfate hypersaline lakes.
Gram-negative coccus-shaped obligate anaerobe genome sequence 16S sequence Archaea| @ref 20215 |
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| Domain Archaea |
| Phylum Methanobacteriota |
| Class Halobacteria |
| Order Halobacteriales |
| Family Halobacteriaceae |
| Genus Halanaeroarchaeum |
| Species Halanaeroarchaeum sulfurireducens |
| Full scientific name Halanaeroarchaeum sulfurireducens Sorokin et al. 2016 |
| @ref | Gram stain | Cell length | Cell width | Cell shape | Motility | |
|---|---|---|---|---|---|---|
| 43637 | negative | 1-2 µm | 0.5-1.5 µm | coccus-shaped |
| 43637 | Oxygen toleranceobligate anaerobe |
| @ref | Spore formation | Confidence | |
|---|---|---|---|
| 125438 | 93.337 |
| @ref | pathway | enzyme coverage | annotated reactions | external links | |
|---|---|---|---|---|---|
| 66794 | vitamin K metabolism | 100 | 5 of 5 | ||
| 66794 | ethanol fermentation | 100 | 2 of 2 | ||
| 66794 | methylglyoxal degradation | 100 | 5 of 5 | ||
| 66794 | factor 420 biosynthesis | 100 | 5 of 5 | ||
| 66794 | formaldehyde oxidation | 100 | 3 of 3 | ||
| 66794 | coenzyme A metabolism | 100 | 4 of 4 | ||
| 66794 | UDP-GlcNAc biosynthesis | 100 | 3 of 3 | ||
| 66794 | suberin monomers biosynthesis | 100 | 2 of 2 | ||
| 66794 | folate polyglutamylation | 100 | 1 of 1 | ||
| 66794 | anapleurotic synthesis of oxalacetate | 100 | 1 of 1 | ||
| 66794 | 6-hydroxymethyl-dihydropterin diphosphate biosynthesis | 100 | 8 of 8 | ||
| 66794 | chorismate metabolism | 88.89 | 8 of 9 | ||
| 66794 | gluconeogenesis | 87.5 | 7 of 8 | ||
| 66794 | C4 and CAM-carbon fixation | 87.5 | 7 of 8 | ||
| 66794 | isoleucine metabolism | 87.5 | 7 of 8 | ||
| 66794 | flavin biosynthesis | 86.67 | 13 of 15 | ||
| 66794 | citric acid cycle | 85.71 | 12 of 14 | ||
| 66794 | phenylalanine metabolism | 84.62 | 11 of 13 | ||
| 66794 | pantothenate biosynthesis | 83.33 | 5 of 6 | ||
| 66794 | ethylmalonyl-CoA pathway | 80 | 4 of 5 | ||
| 66794 | threonine metabolism | 80 | 8 of 10 | ||
| 66794 | glutamate and glutamine metabolism | 78.57 | 22 of 28 | ||
| 66794 | molybdenum cofactor biosynthesis | 77.78 | 7 of 9 | ||
| 66794 | d-mannose degradation | 77.78 | 7 of 9 | ||
| 66794 | valine metabolism | 77.78 | 7 of 9 | ||
| 66794 | palmitate biosynthesis | 77.27 | 17 of 22 | ||
| 66794 | vitamin B1 metabolism | 76.92 | 10 of 13 | ||
| 66794 | acetate fermentation | 75 | 3 of 4 | ||
| 66794 | proline metabolism | 72.73 | 8 of 11 | ||
| 66794 | NAD metabolism | 72.22 | 13 of 18 | ||
| 66794 | reductive acetyl coenzyme A pathway | 71.43 | 5 of 7 | ||
| 66794 | propanol degradation | 71.43 | 5 of 7 | ||
| 66794 | photosynthesis | 71.43 | 10 of 14 | ||
| 66794 | cardiolipin biosynthesis | 71.43 | 5 of 7 | ||
| 66794 | Entner Doudoroff pathway | 70 | 7 of 10 | ||
| 66794 | purine metabolism | 67.02 | 63 of 94 | ||
| 66794 | acetoin degradation | 66.67 | 2 of 3 | ||
| 66794 | aspartate and asparagine metabolism | 66.67 | 6 of 9 | ||
| 66794 | glycolate and glyoxylate degradation | 66.67 | 4 of 6 | ||
| 66794 | serine metabolism | 66.67 | 6 of 9 | ||
| 66794 | L-lactaldehyde degradation | 66.67 | 2 of 3 | ||
| 66794 | cyanate degradation | 66.67 | 2 of 3 | ||
| 66794 | CO2 fixation in Crenarchaeota | 66.67 | 6 of 9 | ||
| 66794 | octane oxidation | 66.67 | 2 of 3 | ||
| 66794 | methionine metabolism | 65.38 | 17 of 26 | ||
| 66794 | glycolysis | 64.71 | 11 of 17 | ||
| 66794 | pyrimidine metabolism | 64.44 | 29 of 45 | ||
| 66794 | alanine metabolism | 62.07 | 18 of 29 | ||
| 66794 | leucine metabolism | 61.54 | 8 of 13 | ||
| 66794 | lipoate biosynthesis | 60 | 3 of 5 | ||
| 66794 | propionate fermentation | 60 | 6 of 10 | ||
| 66794 | 3-chlorocatechol degradation | 60 | 3 of 5 | ||
| 66794 | phenylacetate degradation (aerobic) | 60 | 3 of 5 | ||
| 66794 | histidine metabolism | 58.62 | 17 of 29 | ||
| 66794 | arginine metabolism | 58.33 | 14 of 24 | ||
| 66794 | ubiquinone biosynthesis | 57.14 | 4 of 7 | ||
| 66794 | cysteine metabolism | 55.56 | 10 of 18 | ||
| 66794 | non-pathway related | 55.26 | 21 of 38 | ||
| 66794 | pentose phosphate pathway | 54.55 | 6 of 11 | ||
| 66794 | oxidative phosphorylation | 53.85 | 49 of 91 | ||
| 66794 | urea cycle | 53.85 | 7 of 13 | ||
| 66794 | lysine metabolism | 52.38 | 22 of 42 | ||
| 66794 | lipid metabolism | 51.61 | 16 of 31 | ||
| 66794 | phenylmercury acetate degradation | 50 | 1 of 2 | ||
| 66794 | butanoate fermentation | 50 | 2 of 4 | ||
| 66794 | glutathione metabolism | 50 | 7 of 14 | ||
| 66794 | carotenoid biosynthesis | 50 | 11 of 22 | ||
| 66794 | ketogluconate metabolism | 50 | 4 of 8 | ||
| 66794 | aminopropanol phosphate biosynthesis | 50 | 1 of 2 | ||
| 66794 | selenocysteine biosynthesis | 50 | 3 of 6 | ||
| 66794 | glycine metabolism | 50 | 5 of 10 | ||
| 66794 | cis-vaccenate biosynthesis | 50 | 1 of 2 | ||
| 66794 | tyrosine metabolism | 50 | 7 of 14 | ||
| 66794 | CDP-diacylglycerol biosynthesis | 50 | 1 of 2 | ||
| 66794 | glycogen biosynthesis | 50 | 2 of 4 | ||
| 66794 | 4-hydroxyphenylacetate degradation | 50 | 5 of 10 | ||
| 66794 | tryptophan metabolism | 47.37 | 18 of 38 | ||
| 66794 | sulfate reduction | 46.15 | 6 of 13 | ||
| 66794 | mevalonate metabolism | 42.86 | 3 of 7 | ||
| 66794 | heme metabolism | 42.86 | 6 of 14 | ||
| 66794 | degradation of aromatic, nitrogen containing compounds | 41.67 | 5 of 12 | ||
| 66794 | vitamin B12 metabolism | 41.18 | 14 of 34 | ||
| 66794 | gallate degradation | 40 | 2 of 5 | ||
| 66794 | bacilysin biosynthesis | 40 | 2 of 5 | ||
| 66794 | coenzyme M biosynthesis | 40 | 4 of 10 | ||
| 66794 | isoprenoid biosynthesis | 38.46 | 10 of 26 | ||
| 66794 | carnitine metabolism | 37.5 | 3 of 8 | ||
| 66794 | cholesterol biosynthesis | 36.36 | 4 of 11 | ||
| 66794 | degradation of pentoses | 35.71 | 10 of 28 | ||
| 66794 | tetrahydrofolate metabolism | 35.71 | 5 of 14 | ||
| 66794 | enterobactin biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | sphingosine metabolism | 33.33 | 2 of 6 | ||
| 66794 | acetyl CoA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | IAA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | nitrate assimilation | 33.33 | 3 of 9 | ||
| 66794 | 4-hydroxymandelate degradation | 33.33 | 3 of 9 | ||
| 66794 | (5R)-carbapenem carboxylate biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | methanogenesis from CO2 | 33.33 | 4 of 12 | ||
| 66794 | phenol degradation | 30 | 6 of 20 | ||
| 66794 | degradation of sugar acids | 28 | 7 of 25 | ||
| 66794 | degradation of hexoses | 27.78 | 5 of 18 | ||
| 66794 | vitamin B6 metabolism | 27.27 | 3 of 11 | ||
| 66794 | dolichyl-diphosphooligosaccharide biosynthesis | 27.27 | 3 of 11 | ||
| 66794 | 3-phenylpropionate degradation | 26.67 | 4 of 15 | ||
| 66794 | polyamine pathway | 26.09 | 6 of 23 | ||
| 66794 | dTDPLrhamnose biosynthesis | 25 | 2 of 8 | ||
| 66794 | lactate fermentation | 25 | 1 of 4 | ||
| 66794 | cyclohexanol degradation | 25 | 1 of 4 | ||
| 66794 | toluene degradation | 25 | 1 of 4 | ||
| 66794 | CMP-KDO biosynthesis | 25 | 1 of 4 | ||
| 66794 | catecholamine biosynthesis | 25 | 1 of 4 | ||
| 66794 | biotin biosynthesis | 25 | 1 of 4 | ||
| 66794 | phosphatidylethanolamine bioynthesis | 23.08 | 3 of 13 | ||
| 66794 | lipid A biosynthesis | 22.22 | 2 of 9 |
| @ref | Description | Assembly level | INSDC accession | IMG accession | NCBI tax ID | Score | |
|---|---|---|---|---|---|---|---|
| 66792 | ASM101111v1 assembly for Halanaeroarchaeum sulfurireducens HSR2 | complete | 1604004 | 97.06 |
| @ref | Description | Accession | Database | |
|---|---|---|---|---|
| 43637 | Halanaeroarchaeum sulfurireducens strain HSR2 16S ribosomal RNA gene, partial sequence | KM875608 |
| @ref | GC-content (mol%) | Method | |
|---|---|---|---|
| 43637 | 62.8 | genome sequence analysis |
| @ref | Trait | Model | Prediction | Confidence in % | In training data |
|---|---|---|---|---|---|
| 125438 | gram-positive | gram-positiveⓘ | no | 76.18 | yes |
| 125438 | anaerobic | anaerobicⓘ | no | 69.20 | no |
| 125438 | aerobic | aerobicⓘ | no | 59.47 | yes |
| 125438 | spore-forming | spore-formingⓘ | no | 93.34 | no |
| 125438 | thermophilic | thermophileⓘ | no | 80.85 | yes |
| 125438 | flagellated | motile2+ⓘ | no | 89.00 | no |
| Topic | Title | Authors | Journal | DOI | Year | |
|---|---|---|---|---|---|---|
| International Committee on Systematics of Prokaryotes Subcommittee on the taxonomy of Halobacteria and Subcommittee on the taxonomy of Halomonadaceae. Minutes of the joint open meeting, 11 July 2017, Valencia, Spain. | Arahal DR, Oren A, Ventosa A. | Int J Syst Evol Microbiol | 10.1099/ijsem.0.002296 | 2017 | ||
| Halo(natrono)archaea from hypersaline lakes can utilize sulfoxides other than DMSO as electron acceptors for anaerobic respiration. | Sorokin DY, Roman P, Kolganova TV. | Extremophiles | 10.1007/s00792-021-01219-y | 2021 | ||
| Complete genome sequence of 'Halanaeroarchaeum sulfurireducens' M27-SA2, a sulfur-reducing and acetate-oxidizing haloarchaeon from the deep-sea hypersaline anoxic lake Medee. | Messina E, Sorokin DY, Kublanov IV, Toshchakov S, Lopatina A, Arcadi E, Smedile F, La Spada G, La Cono V, Yakimov MM. | Stand Genomic Sci | 10.1186/s40793-016-0155-9 | 2016 | ||
| Phylogeny | Proposed minimal standards for description of new taxa of the class Halobacteria. | Cui HL, Hou J, Amoozegar MA, Dyall-Smith ML, de la Haba RR, Minegishi H, Montalvo-Rodriguez R, Oren A, Sanchez-Porro C, Ventosa A, Vreeland RH. | Int J Syst Evol Microbiol | 10.1099/ijsem.0.006290 | 2024 | |
| Pyridoxal 5'-phosphate synthesis and salvage in Bacteria and Archaea: predicting pathway variant distributions and holes. | Denise R, Babor J, Gerlt JA, de Crecy-Lagard V. | Microb Genom | 10.1099/mgen.0.000926 | 2023 | ||
| Anaerobic carboxydotrophy in sulfur-respiring haloarchaea from hypersaline lakes. | Sorokin DY, Merkel AY, Messina E, Tugui C, Pabst M, Golyshin PN, Yakimov MM. | ISME J | 10.1038/s41396-022-01206-x | 2022 | ||
| Metabolism | Sucrose Metabolism in Haloarchaea: Reassessment Using Genomics, Proteomics, and Metagenomics. | Williams TJ, Allen MA, Liao Y, Raftery MJ, Cavicchioli R. | Appl Environ Microbiol | 10.1128/aem.02935-18 | 2019 | |
| Enzymology | Sulfur Respiration in a Group of Facultatively Anaerobic Natronoarchaea Ubiquitous in Hypersaline Soda Lakes. | Sorokin DY, Messina E, La Cono V, Ferrer M, Ciordia S, Mena MC, Toshchakov SV, Golyshin PN, Yakimov MM. | Front Microbiol | 10.3389/fmicb.2018.02359 | 2018 | |
| Metabolism | Depthwise microbiome and isotopic profiling of a moderately saline microbial mat in a solar saltern. | Paul V, Banerjee Y, Ghosh P, Busi SB. | Sci Rep | 10.1038/s41598-020-77622-w | 2020 | |
| Phylogeny | Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats. | Sorokin DY, Messina E, Smedile F, Roman P, Damste JSS, Ciordia S, Mena MC, Ferrer M, Golyshin PN, Kublanov IV, Samarov NI, Toshchakov SV, La Cono V, Yakimov MM. | ISME J | 10.1038/ismej.2016.203 | 2017 | |
| Metabolism | Elemental sulfur and acetate can support life of a novel strictly anaerobic haloarchaeon. | Sorokin DY, Kublanov IV, Gavrilov SN, Rojo D, Roman P, Golyshin PN, Slepak VZ, Smedile F, Ferrer M, Messina E, La Cono V, Yakimov MM. | ISME J | 10.1038/ismej.2015.79 | 2016 | |
| Scientific novelty beyond the experiment. | Hallsworth JE, Udaondo Z, Pedros-Alio C, Hofer J, Benison KC, Lloyd KG, Cordero RJB, de Campos CBL, Yakimov MM, Amils R. | Microb Biotechnol | 10.1111/1751-7915.14222 | 2023 | ||
| Phylogeny | Halanaeroarchaeum sulfurireducens gen. nov., sp. nov., the first obligately anaerobic sulfur-respiring haloarchaeon, isolated from a hypersaline lake. | Sorokin DY, Kublanov IV, Yakimov MM, Rijpstra WIC, Sinninghe Damste JS | Int J Syst Evol Microbiol | 10.1099/ijsem.0.001041 | 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 ) |
| #43637 | Dimitry Y. Sorokin, Ilya V. Kublanov, Mikhail M. Yakimov, W. Irene C. Rijpstra, Jaap S. Sinninghe Damsté: Halanaeroarchaeum sulfurireducens gen. nov., sp. nov., the first obligately anaerobic sulfur-respiring haloarchaeon, isolated from a hypersaline lake. IJSEM 66: 2377 - 2381 2016 ( DOI 10.1099/ijsem.0.001041 , PubMed 27031647 ) |
| #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 ) |
| #67770 | Japan Collection of Microorganism (JCM) ; Curators of the JCM; |
| #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 ) |
| #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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