Abstract
Three sulfate-reducing bacterial strains designated SM40T, SM41, and SM43 were isolated from marine sediment in the region of Skhira located in the Gulf of Gabes (Tunisia). These strains grew in anaerobic media with phosphogypsum as a sulfate source and sodium lactate as an electron and carbon source. One of them, strain SM40T, was characterized by phenotypic and phylogenetic methods. Cells were ovoid, Gram-stain-negative and non-motile. The temperature limits for growth were 10 and 55 °C with an optimum at 35 °C and the pH range was 6.5–8.1 with an optimum at pH 7.5. Growth was observed at salinities ranging from 10 to 80 g NaCl l−1 with an optimum at 30 g NaCl l−1. Strain SM40T was able to utilize butanol, ethanol, formate, l-glucose, glycerol, lactate, propanol, propionate, and pyruvate as electron donors for the reduction of sulfate, sulfite, or thiosulfate to H2S. Without electron acceptors, strain SM40T fermented butanol and pyruvate. The DNA G+C content of strain SM40T was 52.6 mol %. Phylogenetic analysis based on the 16S rRNA gene sequence of the isolate revealed that strain SM40T was closely related to the species in the genus Desulfobulbus of the family Desulfobulbaceae. The sequence similarity between strain SM40 and Desulfobulbus marinus was 95.4%. The phylogenetic analysis, DNA G+C content, and differences in substrate utilization suggested that strain SM40 represents a new species of the genus Desulfobulbus, D. aggregans sp. nov. The type strain is strain SM40T (=DSM 28693T = JCM 19994T).


Similar content being viewed by others
Explore related subjects
Discover the latest articles and news from researchers in related subjects, suggested using machine learning.References
Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25:3389–3402
Cole JR, Wang Q, Cardenas E, Fish J, Chai B, Farris RJ, Kulam-Syed-Mohideen AS, McGarrell DM, Marsh T, Garrity GM, Tiedje JM (2009) The Ribosomal Database Project: improved alignments and new tools for rRNA analysis. Nucleic Acids Res 37:141–145
Cord-Ruwisch R (1985) A quick method for the determination of dissolved and precipitated sulfides in cultures of sulfate reducing bacteria. J Microbiol Methods 4:33–36
Devereux R, Delaney M, Widdel F, Stahl DA (1989) Natural relationships among sulfate-reducing eubacteria. J Bacteriol 171:6689–6695
Edgar RC (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32:1792–1797
Fardeau ML, Ollivier B, Patel B K C, Magot M, Thomas P, Rimbault A, Rocchiccioli F, Garcia JL (1997) Thermotoga hypogea sp. nov., a xylanolytic, thermophilic bacterium from an oil-producing well. Int J Syst Bacteriol 47:1013–1019
Felsenstein J (1981) Evolutionary trees from DNA sequences: a maximum likehood approach. J Mol Evol 17:368–376
Felsenstein J (1985) Confidence limits of phylogenesis. Evol Int J org Evol 39:783–791
Fitch WM (1971) Toward defining the course of evolution: minimum change for a specific tree topology. Syst Zool 20:406–416
Hungate RE (1969) A roll tube method for the cultivation of strict anaerobes. Method Microbiol 3B:117–132
Jørgensen BB (1982) Mineralization of organic matter in the seabed: the role of sulphate reduction. Nature 296:643–645
Kuever J, Rainey FA, Widdel F (2005) Class IV Deltaproteobacteria class nov. In: Brenner DJ, Krieg NR, Staley JT, Garrity GM (eds.) Bergey’s manual of systematic bacteriology, vol. 2, 2nd edn. Springer, New York, pp 922–1144
Kumar S, Stecher G, Tamura K (2016) MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 33:1870–1874
Lien T, Madsen M, Steen IH, Gjerdevik K (1998) Desulfobulbus rhabdoformis sp. nov., a sulfate reducer from a water-oil separation system. Int J Syst Bact 48:469–474
Louati A, Elleuch B, Kallel M, Saliot A, Dagaut J (2001) Hydrocarbon contamination of coastal sediments from the Sfax area (Tunisia), Mediterranean Sea. Mar Pollut Bull 42:445–452
Mesbah M, Premachandran U, Whitman W (1989) Precise measurement of the G+C content of deoxyribonucleic acid by high performance liquid chromatography. Int J Syst Bact 39:159–167
Saitou N, Nei M (1987) The neighbour-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:405–425
Samain E, Dubourguier HC, Albagnac G (1984) Isolation and characterization of Desulfobulbus elongatus sp. nov. from a mesophilic industrial digester. Syst Appl Microbiol 5:391–401
Sass A, Rutters H, Cypionka H, Sass H (2002) Desulfobulbus mediterraneus sp. nov., a sulfate-reducing bacterium growing on mono- and disaccharides. Arch Microbiol 177:468–474
Sorokin DY, Tourova TP, Panteleeva AN, Muyzer G (2012) Desulfonatronobacter acidivorans gen. nov., sp. nov. and Desulfobulbus alkaliphilus sp. nov., haloalkaliphilic heterotrophic sulfate-reducing bacteria from soda lakes. Int J Syst Evol Microbiol 62:2107–2113
Soussi N, Ennet P, Koponen J, Sarkkula J, Ben Mustapha S (1995) Impact of the phosphogypsum waste in the Gulf of Gabes (Tunisia). In: Proceedings of the second international conference on the mediterranean coastal environment, Tarragona, Spain, pp 24–27
Suzuki D, Ueki A, Amaishi A, Ueki K (2007) Diversity of substrate utilization and growth characteristics of sulfate-reducing bacteria isolated from estuarine sediment in Japan. J Gen Appl Microbiol 53:119–132
Weisburg W, Barns S, Pelletier D, Lane D (1991) 16 S ribosomal DNA amplification for phylogenetic study. J Bact 173:697–703
Widdel F, Pfennig N (1981) Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. I. Isolation of new sulfate-reducing bacteria enriched with acetate from saline environments. Description of Desulfobacter postgatei gen. nov., sp. nov. Arch Microbiol 129:395–400
Widdel F, Pfennig N (1982) Studies on dissimilatory sulfate reducing bacteria that decompose fatty acids. II. Incomplete oxidation of propionate by Desulfobulbus propionicus gen. nov., sp. nov. Arch Microbiol 131:360–365
Zaghden H, Kallel M, Louati A, Elleuch B, Oudot J (2005) Hydrocarbons in surface sediments from the Sfax coastal zone (Tunisia), Mediterranean Sea. Mar Pollut Bull 50:1287–1294
Acknowledgements
HK was supported by the Tunisian Chemical Group fellowship.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
There are no conflicts of interest.
Additional information
The GenBank Accession Number for Strain 28693T is KU180234.
Rights and permissions
About this article
Cite this article
Kharrat, H., Karray, F., Bartoli, M. et al. Desulfobulbus aggregans sp. nov., a Novel Sulfate Reducing Bacterium Isolated from Marine Sediment from the Gulf of Gabes. Curr Microbiol 74, 449–454 (2017). https://doi.org/10.1007/s00284-017-1211-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00284-017-1211-4


