- Home
- Publications
- International Journal of Systematic and Evolutionary Microbiology
- Volume 65, Issue 11
- Article

f Halobellus ramosii sp. nov., an extremely halophilic archaeon isolated from a saline-wetland wildfowl reserve
- Authors: Azahara Pérez-Davó1 , Margarita Aguilera1 , Ana González-Paredes1 , María Luján Jiménez-Pranteda1 , Mercedes Monteoliva-Sánchez1
-
- VIEW AFFILIATIONS
-
1 Department of Microbiology, Faculty of Pharmacy, University of Granada, Campus Universitario de Cartuja s/n 18071, Granada, Spain
- Correspondence Mercedes Monteoliva-Sánchez [email protected]
- First Published Online: 01 November 2015, International Journal of Systematic and Evolutionary Microbiology 65: 3847-3852, doi: 10.1099/ijsem.0.000503
- Subject: NEW TAXA - Archaea
- Cover date:




Halobellus ramosii sp. nov., an extremely halophilic archaeon isolated from a saline-wetland wildfowl reserve, Page 1 of 1
< Previous page | Next page > /docserver/preview/fulltext/ijsem/65/11/3847_ijsem000503-1.gif
-
An extremely halophilic archaeon, strain S2FP14T, was isolated from a brine sample from the inland hypersaline lake Fuente de Piedra, a saline-wetland wildfowl reserve located in the province of Málaga in southern Spain. Colonies were red-pigmented and the cells were Gram-staining-negative, motile and pleomorphic. S2FP14T was able to grow in media containing 12.5–30 % (w/v) total salts (optimum 20 %) at pH 7–8.5 (optimum 7.5) and at 25–50 °C (optimum 37 °C). The 16S rRNA gene sequence analysis indicated that this strain represented a member of the genus Halobellus. S2FP14T showed a similarity of 99.5 % to Halobellus inordinatus YC20T, 96.1 % to Halobellus litoreus GX31T, 95.9 % to Halobellus limi TBN53T, 95.5 % to Halobellus rarus YC21T, 95.2 % to Halobellus rufus CBA1103T, 94.6 % to Halobellus salinus CSW2.24.4T and 94.6 % to Halobellus clavatus TNN18T. The rpoB′ gene sequence similarity of strain S2FP14T was 97.4 % to 87.6 % with members of genus Halobellus. The major phospholipids of strain S2FP14T were phosphatidylglycerol phosphate methyl ester and phosphatidylglycerosulfate, plus a very small amount of phosphatidylglycerol and an archaeal analogue of bisphosphatidylglycerol. With regard to glycolipid composition, the most abundant glycolipids were the sulfated diglycosyl diphytanilglyceroldiether and a glycosyl-cardiolipin. The G+C content of strain S2FP14T genomic DNA was 61.4 mol%. The DNA–DNA hybridization between strain S2FP14T and Halobellus inordinatus JCM 18361T was 51 %. Based on the phylogenetic, phenotypic and chemotaxonomic features, a novel species, Halobellus ramosii sp. nov. is proposed. The type strain is S2FP14T ( = CECT 8167T = DSM 26177T).
-
The GenBank/EMBL/DDBJ accession numbers for the 16S rRNA and rpoB′ gene sequences of strain S2FP14T are JQ910929 and KP659190, respectively.
© 2015 IUMS | Published by the Microbiology Society
-
Berd D.. ( 1973;). Laboratory identification of clinically important aerobic actinomycetes. Appl Microbiol 25: 665––681 [PubMed].
-
Cha I. T., Yim K. J., Song H. S., Lee H. W., Hyun D. W., Kim K. N., Seo M. J., Kim D., Choi J. S., other authors. ( 2014;). Halobellus rufus sp. nov., an extremely halophilic archaeon isolated from non-purified solar salt. Antonie van Leeuwenhoek 105: 925––932 [CrossRef] [PubMed].
-
Chenna R., Sugawara H., Koike T., Lopez R., Gibson T. J., Higgins D. G., Thompson J. D.. ( 2003;). Multiple sequence alignment with the clustal series of programs. Nucleic Acids Res 31: 3497––3500 [CrossRef] [PubMed].
-
Cui H. L., Yang X., Gao X., Xu X. W.. ( 2011;). Halobellus clavatus gen. nov.,sp. nov. and Halorientalis regularis gen. nov., sp. nov., two new members of the family Halobacteriaceae. Int J Syst Evol Microbiol 61: 2682––2689 [CrossRef] [PubMed].
-
Cui H. L., Yang X., Zhou Y. G., Liu H. C., Zhou P. J., Dyall-Smith M. L.. ( 2012;). Halobellus limi sp. nov. and Halobellus salinus sp. nov., isolated from two marine solar salterns. Int J Syst Evol Microbiol 62: 1307––1313 [CrossRef] [PubMed].
-
Dussault H. P.. ( 1955;). An improved technique for staining red halophilic bacteria. J Bacteriol 70: 484––485 [PubMed].
-
Ferragut C., Leclerc H.. ( 1976;). Etude comparative des méthodes de détermination du T m de l'ADN bactérien. Ann Microbiol 127: 223––235.
-
Kates M.. ( 1993;). Membrane lipids of Archaea. . In The Biochemistry of Archaea (Archaeobacteria), pp. 261––296. Edited by Kates M., Kushner D. J., Matheson A. T.. Amsterdam: Elsevier; [CrossRef].
-
Kharroub K., Lizama C., Aguilera M., Boulahrouf A., Campos V., Ramos-Cormenzana A., Monteoliva-Sánchez M.. ( 2008;). Halomicrobium katesii sp. nov., an extremely halophilic archaeon. Int J Syst Evol Microbiol 58: 2354––2358 [CrossRef] [PubMed].
-
Lind E., Ursing J.. ( 1986;). Clinical strains of Enterobacter agglomerans (synonyms: Erwinia herbicola, Erwinia milletiae) identified by DNA–DNA-hybridization. Acta Pathol Microbiol Immunol Scand [B] 94: 205––213 [PubMed].
-
Lobasso S., Pérez-Davó A., Vitale R., Sánchez M. M., Corcelli A.. ( 2015;). Deciphering archaeal glycolipids of an extremely halophilic archaeon of the genus Halobellus by MALDI-TOF/MS. Chem Phys Lipids 186: 1––8 [CrossRef] [PubMed].
-
Marmur J., Doty P.. ( 1962;). Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature. J Mol Biol 5: 109––118 [CrossRef] [PubMed].
-
Minegishi H., Kamekura M., Itoh T., Echigo A., Usami R., Hashimoto T.. ( 2010;). Further refinement of the phylogeny of the Halobacteriaceae based on the full-length RNA polymerase subunit B′ (rpoB′) gene. Int J Syst Evol Microbiol 60: 2398––2408 [CrossRef] [PubMed].
-
Oren A.. ( 2002;). Halophilic Microorganisms and Their Environments Dordrecht: Kluwer Academic Publishers; [CrossRef].
-
Oren A., Ventosa A., Grant W. D.. ( 1997;). Proposed minimal standards for description of new taxa in the order Halobacteriales. Int J Syst Bacteriol 47: 233––238 [CrossRef].
-
Owen R. J., Hill L. R.. ( 1979;). The estimation of base compositions, base pairing and genome size of bacterial deoxyribonucleic acids. . In Identification Methods for Microbiologists, pp. 277––296. Edited by Skinner F. A., Lovelock D. W.. London: Academic Press;.
-
Park S.-J., Cha I.-T., Kim S.-J., Shin K.-S., Hong Y., Roh D.-H., Rhee S.-K.. ( 2012;). Salinisphaera orenii sp. nov., isolated from a solar saltern. Int J Syst Evol Microbiol 62: 1877––1883 [CrossRef] [PubMed].
-
Qiu X.-X., Mou Y.-Z., Zhao M.-L., Zhang W. J., Han D., Ren M., Cui H.-L.. ( 2013;). Halobellus inordinatus sp. nov., from a marine solar saltern and an inland salt lake of China. Int J Syst Evol Microbiol 63: 3975––3980 [CrossRef] [PubMed].
-
Smibert R. M., Krieg N. R.. ( 1981;). General characterization. . In Manual of Methods for General Bacteriology, pp. 409––443. Edited by Gerhardt P., Murray R. G. E., Costilow R. N., Nester E. D., Wood W. A., Krieg N. R., Phillips G. B.. Washington, DC: American Society for Microbiology;.
-
Smibert R. M., Krieg N. R.. ( 1994;). Phenotypic characterization. . In Methods for General and Molecular Bacteriology, pp. 607––654. Edited by Gerhardt P., Murray R. G. E., Wood W. A., Krieg N. R.. Washington, DC: American Society for Microbiology;.
-
Stackebrandt E., Goebel B. M.. ( 1994;). Taxonomic note: a place for DNA-DNA reassociation and 16S rRNA sequence analysis in the present species definition in bacteriology. Int J Syst Bacteriol 44: 846––849 [CrossRef].
-
Subov N. N.. ( 1931;). Oceanographical Tables Moscow: USSR Oceanographic Institute Hydrometeorological Commission;.
-
Tamura K., Stecher G., Peterson D., Filipski A., Kumar S.. ( 2013;). mega6: molecular evolutionary genetics analysis version 6.0. Mol Biol Evol 30: 2725––2729 [CrossRef] [PubMed].
-
Ventosa A., Quesada E., Rodríguez-Valera R., Ruiz-Berraquero F., Ramos-Cormenzana A.. ( 1982;). Numerical taxonomy of moderately Gram-negative rods. J Gen Microbiol 128: 1959––1968.
-
Zhang W.-J., Han D., Qiu X.-X., Zhao M.-L., Mou Y.-Z., Cui H.-L., Li Z.-R.. ( 2013;). Halobellus rarus sp. nov., a halophilic archaeon from an inland salt lake of China. Antonie van Leeuwenhoek 104: 377––384 [CrossRef] [PubMed].
-
Ziemke F., Höfle M. G., Lalucat J., Rosselló-Mora R.. ( 1998;). Reclassification of Shewanella putrefaciens Owen's genomic group II as Shewanella baltica sp. nov. Int J Syst Bacteriol 48: 179––186 [CrossRef] [PubMed].

Supplementary Data
Data loading....

Article metrics loading...

Full text loading...
Author and Article Information
-
This Journal
/content/journal/ijsem/10.1099/ijsem.0.000503dcterms_title,dcterms_subject,pub_serialTitlepub_serialIdent:journal/ijsem AND -contentType:BlogPost104 -
Other Society Journals
/content/journal/ijsem/10.1099/ijsem.0.000503dcterms_title,dcterms_subject-pub_serialIdent:journal/ijsem AND -contentType:BlogPost104 -
PubMed
-
Google Scholar
Figure data loading....