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Phylogenetic assessment of culture collection strains of Thiobacillus thioparus, and definitive 16S rRNA gene sequences for T. thioparus, T. denitrificans, and Halothiobacillus neapolitanus
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Boden, Rich, Cleland, David, Green, Peter N., Katayama, Yoko, Uchino, Yoshihito, Murrell, J. C. (J. Colin) and Kelly, Donovan P., 1940-. (2011) Phylogenetic assessment of culture collection strains of Thiobacillus thioparus, and definitive 16S rRNA gene sequences for T. thioparus, T. denitrificans, and Halothiobacillus neapolitanus. Archives of Microbiology, Vol.194 (No.3). pp. 187-195. ISSN 0302-8933
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Official URL: http://dx.doi.org/10.1007/s00203-011-0747-0
Abstract
The 16S rRNA gene sequences of 12 strains of Thiobacillus thioparus held by different culture collections have been compared. A definitive sequence for the reference type strain (Starkey; ATCC 8158T) was obtained. The sequences for four examples of the Starkey type strain were essentially identical, confirming their sustained identity after passage through different laboratories. One strain (NCIMB 8454) was reassigned as a strain of Halothiobacillus neapolitanus, and a second (NCIMB 8349) was a species of Thermithiobacillus. These two strains have been renamed in their catalog by the National Collection of Industrial and Marine Bacteria. The 16S rRNA gene sequence of the type strain of Halothiobacillus neapolitanus (NCIMB 8539T) was determined and used to confirm the identity of other culture collection strains of this species. The reference sequences for the type strains of Thiobacillus thioparus and Halothiobacillus neapolitanus have been added to the online List of Prokaryotic Names with Standing in Nomenclature. Comparison of the 16S rRNA gene sequences available for strains of Thiobacillus denitrificans indicated that the sequence for the type strain (NCIMB 9548T) should always be used as the reference sequence for new and existing isolates.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QR Microbiology |
| Divisions: | Faculty of Science > Life Sciences (2010- ) |
| Library of Congress Subject Headings (LCSH): | Phylogeny, Bacteriology -- Cultures and culture media, Thiobacillus |
| Journal or Publication Title: | Archives of Microbiology |
| Publisher: | Springer |
| ISSN: | 0302-8933 |
| Date: | 2011 |
| Volume: | Vol.194 |
| Number: | No.3 |
| Number of Pages: | 9 |
| Page Range: | pp. 187-195 |
| Identification Number: | 10.1007/s00203-011-0747-0 |
| Status: | Peer Reviewed |
| Publication Status: | Published |
| Access rights to Published version: | Restricted or Subscription Access |
| References: | Amouric A, Brochier-Armanet, Johnson DB, Bonnefoy V, Hallberg KB (2011) Phylogenetic and genetic variation among Fe(II)-oxidizing acidithiobacilli supports the view that these comprise multiple species with different ferrous iron oxidation pathways. Microbiol (UK) 157:111-122 Aroca G, Urrutia H, Núñez D, Oyarzan P, Aranciba A, Guerrero K (2007) Comparison of the removal of hydrogen sulfide in biotrickling filters inoculated with Thiobacillus thioparus and Acidithiobacillus thiooxidans. Electron J Biotechnol [on-line] 10:514-520 Baldensperger J, Garcia JL (1975) Reduction of oxidized inorganic nitrogen compounds by a new strain of Thiobacillus denitrificans. Arch Microbiol 103:31-36 Battaglia-Brunet F, El Achbouni H, Quemeneur M, Hallberg KB, Kelly DP, Joulian C (2011) Proposal that the arsenite-oxidizing organisms Thiomonas cuprina and “Thiomonas arsenivorans” be reclassified as strains of Thiomonas delicata. Int J Syst Evol Microbiol doi:101099/ijs0023408-0 (January 7 2011) Beijerinck MW (1904) Ueber die Bakterien, welche sich im Dunkeln mit Kohlensäure als Kohlenstoffquelle ernähren können. Centralbl Bakteriol Parasitenkd Infektionskr Hyg Abt II 11:592-599 Beller HR, Chain PSG, Letain TE, Chakicherla A, Larimer FW, Richardson PM, Coleman MA, Wood AP, Kelly DP (2006) The genome sequence of the obligately chemolithotrophic, facultatively anaerobic bacterium Thiobacillus denitrificans. J Bacteriol 188:1473-1488 Boden R, Thomas E, Savani P, Kelly DP, Wood AP (2008) Novel methylotrophic bacteria isolated from the River Thames (London, UK). Environ Microbiol 10:3225-3236 Brandl H (2008) Microbial leaching of metals. In: Rehm H-J, Reed G. (eds) Biotechnology: Special Processes, 2nd edn, vol 10. Wiley-VCH Verlag GmbH, Weinheim, pp 192-217 Chen S, Qiu, G-Z, Qin W-Q, Lan Z-Y (2008) Bioleaching of sphalerite by Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans cultured in 9K medium modified with pyrrhotite. J Cent South Univ Technol 15:503-507 Chen Y, Wu Liqin, Boden R, Hillebrand A, Kumarasan D, Moussard H, Baciu M, Lu Y, Murrell JC (2009) Life without light: microbial diversity and evidence of sulfur- and ammonium-based chemolithotrophy in Movile Cave. ISME J 3:1093-1104 Ehrlich HL, Brierley CL (eds) (1990). Microbial Mineral Recovery. New York, McGraw-Hill, Inc., 454 pp Evangelou VP, Zhang YL (1995) A review: pyrite oxidation mechanisms and acid mine drainage prevention. Crit Revs Environ Sci Technol 25:141-199 Harrison AP (1982) Genomic and physiological diversity amongst strains of Thiobacillus ferroxidans, and genomic comparison with Thiobacillus thiooxidans. Arch Microbiol 131:68-76 Hiraishi A, Imhoff JF (2005) Genus II. Acidiphilium Harrison 1981. In: Brenner DJ, Krieg NR, Staley JT, Garrity GM (eds) Bergey’s Manual of Systematic Bacteriology, 2nd edn, vol 2 part C. Springer, New York, pp 54-62 Hutchinson M, Johnstone KI, White D (1965) The taxonomy of certain thiobacilli. J Gen Microbiol 41:357-366 Hutchinson M, Johnstone KI, White D (1966) Taxonomy of the acidophilic thiobacilli. J Gen Microbiol 44:373-381 Hutchinson M, Johnstone KI, White D (1967) Taxonomy of anaerobic thiobacilli. J Gen Microbiol 47:17-23 Hutchinson M, Johnstone KI, White D (1969) Taxonomy of the genus Thiobacillus: outcome of numerical taxonomy applied to the group as a whole. J Gen Microbiol 57:397-410 Justin P, Kelly DP (1978) Growth kinetics of Thiobacillus denitrificans accompanying the transition from aerobic and anaerobic growth. J Gen Microbiol 107:123-130 Kanagawa T, Kelly DP (1986) Breakdown of dimethyl sulphide by mixed cultures and by Thiobacillus thioparus. FEMS Microbiol Lett 34:13–19 Kanagawa T, Mikami E (1989) Removal of methanethiol, dimethyl sulphide, dimethyl disulphide, and hydrogen sulphide from contaminated air by Thiobacillus thioparus Tk-m. Appl Environ Microbiol 55:555-558 Karavaiko GI, Turova TP, Kondrateva TF, Lysenko AM, Kolganova TV, Ageeva SN, Luntyan LM, Pivovarova TA (2003) Phylogenetic heterogeneity of the species Acidithiobacillus ferrooxidans. Int J Syst Evol Microbiol 53:113-119 Katayama Y, Kuraishi H (1978) Characteristics of Thiobacillus thioparus and its thiocyanate assimilation. Can J Microbiol 24:804-810 Katayama-Fujimura Y, Tsuzaki N, Kuraishi, N (1982) Ubiquinone, fatty acid and DNA base composition determination as a guide to the taxonomy of the genus Thiobacillus. J Gen Microbiol 128:1599-1611 Katayama Y, Uchino Y, Wood AP, Kelly DP (2006) Confirmation of Thiomonas delicata (formerly Thiobacillus delicatus) as a distinct species of the genus Thiomonas Moreira and Amils 1997 with comments on some species currently assigned to the genus. Int J Syst Evol Microbiol 56:2553-2557 Katayama Y, Narahara Y, Inoue Y, Amano F, Kanagawa T, Kuraishi H (1992) A thiocyanate hydrolase of Thiobacillus thioparus. J Biol Chem 267:9170-9175 Katayama Y, Matsushita Y, Kaneko M, Kondo M, Mizuno T, Nyunoya H (1998) Cloning of genes coding for the three subunits of thiocyanate hydrolase of Thiobacillus thioparus THI 115 and their evolutionary relationships to nitrile hydratase. J Bacteriol 180:2583-2589 Kelly, D.P. (1982) Biochemistry of the chemolithotrophic oxidation of inorganic sulphur. Phil. Trans. R. Soc. Lond. B 298, 499-528 Kelly DP (1985) Metallgewinnung aus Erzen durch bakterielles Auslagen: gegenwärtiger Stand und zukünftige Aufgaben. In: Küster E (ed) Mikrobiologie und Umweltschutz, Wissenschaftliche Buchgesellschaft, Darmstadt, pp. 161-182 Kelly DP (2008) Stable isotope fractionation and discrimination between the sulfur atoms of thiosulfate during oxidation by Halothiobacillus neapolitanus. FEMS Microbiol Lett 282:299-308 Kelly DP (2010) Global consequences of the microbial production and consumption of inorganic and organic sulfur compounds. In: Timmis KN (ed) Microbiology of Hydrocarbons, Oils, Lipids. Springer, Heidelberg, chapter 53, pp 3087-3095 Kelly DP, Harrison AP (1989) Genus Thiobacillus Beijerinck 1904. In: Staley JT, Bryant MP, Pfennig N, Garrity GM (eds) Bergey’s Manual of Systematic Bacteriology, 1st edn, vol 3. Williams & Wilkins, Baltimore, pp 1842-1858 Kelly DP, Wood AP (1998) Microbes of the sulfur cycle. In: Burlage RS, Atlas R, Stahl D, Geese G, Sayler G. (eds) Techniques in Microbial Ecology. Oxford University Press, New York, pp 31-57 Kelly DP, Wood AP (2000a) Reclassification of some species of Thiobacillus to the newly designated genera Acidithiobacillus gen. nov., Halothiobacillus gen. nov. and Thermithiobacillus gen. nov. Int J Syst Evol Microbiol 50:511-516 Kelly DP, Wood AP (2000b) Confirmation of Thiobacillus denitrificans as a species of the genus Thiobacillus, in the -subclass of the Proteobacteria, with strain NCIMB 9548 as the type strain. Int J Syst Evol Microbiol 50:547-550 Kelly DP, McDonald IR, Wood AP (2000) Proposal for the reclassification of Thiobacillus novellus as Starkeya novella gen. nov., comb. nov., in the -subclass of the Proteobacteria. Int J Syst Evol Microbiol 50:1797-1802 Kelly DP, Wood AP, Stackebrandt E (2005) Genus II Thiobacillus Beijerinck 1904. In: Brenner DJ, Krieg NR, Staley JT, Garrity GM (eds) Bergey’s Manual of Systematic Bacteriology, 2nd edn, vol 2 part C. Springer, New York, pp 764-769 Kelly DP, Euzéby JP, Goodhew CF, Wood AP (2006) Redefining Paracoccus denitrificans and Paracoccus pantotrophus and the case for a reassessment of the strains held by international culture collections. Int J Syst Evol Microbiol 56:2495-2500 Kelly DP, Uchino Y, Huber H, Amils R, Wood AP (2007) Reassessment of the phylogenetic relationships of Thiomonas cuprina. Int J Syst Evol Microbiol. 56:2720-2724 Lane DJ, Stahl DA, Olsen GJ, Heller DJ, Pace NR (1985) Phylogenetic analysis of the genera Thiobacillus and Thiomicrospira by 5S rRNA sequences. J Bacteriol 163:75-81 Lane DJ, Harrison AP, Stahl D, Pace B, Giovannoni SJ, Olsen GJ, Pace NR (1992) Evolutionary relationships among sulfur- and iron-oxidizing eubacteria. J Bacteriol 174:269-278 Mudd GM, Patterson J (2010) Continuing pollution from the Rum Jungle U-Cu project: a critical evaluation of environmental monitoring and rehabilitation. Environ Pollution 158: 1252-1260 Pankhurst ES (1964) Polarographic evidence for the production of polythionates during the bacterial oxidation of thiosulphate. J Gen Microbiol 34:427-439 Parker CD (1945) The isolation of a species of bacterium associated with the corrosion of concrete exposed to atmospheres containing hydrogen sulfide. Aust J Exp Biol Med Sci 23, 81-90 Parker CD (1947) Species of sulphur bacteria associated with the corrosion of concrete. Nature 159:439-440 Parker CD (1957) Genus V. Thiobacillus Beijerinck 1904. In: Breed RS, Murray RGE, Smith PH (Eds) Bergey’s Manual of Determinative Bacteriology, 7th edn. Williams & Wilkins, Baltimore, pp 83-88 Parker CD, Prisk J (1953) The oxidation of inorganic compounds of sulphur by various sulphur bacteria. J Gen Microbiol 8:344-364 Parker CD, Jackson D (1965) The microbial flora of concrete surfaces. In: Hydrogen Sulfide Corrosion of Concrete Sewers, Melbourne and Metropolitan Board of Works, Melbourne, Australia, Technical Paper No. A8, part 6, pp.1-29 Rainey FA, Kelly DP, Stackebrandt E, Burghardt J, Hiraishi A, Katayama Y, Wood AP (1999) A re-evaluation of the taxonomy of Paracoccus denitrificans and a proposal for the combination Paracoccus pantotrophus comb. nov. Int J Syst Bacteriol 49:645–651 Ramirez M, Gomez JM, Aroca G, Cantero D (2009) Removal of hydrogen sulfide by immobilized Thiobacillus thioparus in a biotrickling filter packed with polyurethane foam. Bioresour Technol 100:4989-4895 Rawlings DE (2002) Heavy metal mining using microbes. Ann Rev Microbiol 56:65-91 Smith NA, Kelly DP (1988) Isolation and physiological characterization of autotrophic sulphur bacteria oxidizing dimethyl disulphide as sole source of energy. J Gen Microbiol 134:1407-1417 Staley JT (2006) The bacterial species dilemma and the genomic–phylogenetic species concept. Phil Trans R Soc B 361:1899-1909 Staley JT (2009) The phylogenomic species concept. Microbiology Today (SGM), May 2009, pp. 80-83 Starkey RL (1934) Cultivation of organisms concerned in the oxidation of thiosulfate. J Bacteriol 28:365-386 Sublette KL, Sylvester ND (1987) Oxidation of hydrogen sulfide by Thiobacillus denitrificans: desulfurization of natural gas. Biotechnol Bioeng 29:49-257 Taylor, BF, Hoare DS, Hoare SL (1971) Thiobacillus denitrificans as an obligate chemolithotroph. Arch Microbiol 78:193-204 Trautwein K (1921) Zur Physiologie und Morphologie der Thionsäurebakterien. Zentralbl Bakteriol Parasitenkd Infektionskr Hyg, Abt II, 53:513-548 Trudinger PA (1959) Initial products of thiosulphate oxidation by Thiobacillus X. Biochim Biophys Acta 31:270-272 Trudinger PA (1961) Thiosulphate oxidation and cytochromes in Thiobacillus X. 2. Thiosulphate-oxidizing enzyme. Biochem J 78:680-686 Trudinger PA (1964) Oxidation of thiosulphate by intact cells of Thiobacillus X: effects of some experimental conditions. Aust J Biol Sci 17:738-751 Vishniac WV (1974) Genus I. Thiobacillus Beijerinck 1904. In: Buchanan RE, Gibbons NE (eds) Bergey’s Manual of Determinative Bacteriology, 8th edn. Williams & Wilkins, Baltimore, pp 456-461 Vlasceanu L, Popa R, Kinkle BK (1997) Characterization of Thiobacillus thioparus LV43 and its distribution in a chemoautotrophically based groundwater ecosystem. Appl Environ Microbiol 63:3123-3127 Waltenbury, DR, Leduc LG, Ferroni GD (2005) The use of RAPD genomic fingerprinting to study relatedness in strains of Acidithiobacillus ferrooxidans. J Microbiol Meth 62:103-112 Williams KP, Gillespie JJ, Sobral BWS, Nordberg EK, Snyder EE, Shallom JM, Dickerman AW (2010) Phylogeny of Gammaproteobaceria. J Bacteriol 192:2305-2314 Wood AP, Kelly DP (1985) Physiological characteristics of a new thermophilic obligately chemolithotrophic Thiobacillus species, Thiobacillus tepidarius. Int J Syst Bacteriol 35:434-437 Wood AP, Kelly DP (1986) Chemolithotrophic metabolism of the newly-isolated moderately thermophilic, obligately autotrophic Thiobacillus tepidarius. Arch Microbiol 144:71-77 Wood AP, Kelly DP (1991) Isolation and characterisation of Thiobacillus halophilus sp. nov., a sulphur-oxidising autotrophic eubacterium from a Western Australian hypersaline lake. Arch Microbiol 156:277-280 Zhang Z, Lei Z, He X, Zhang Z, Yang Y, Sugiura N (2009) Nitrate removal by Thiobacillus denitrificans immobilized on poly(vinyl alcohol) carriers. J Hazardous Materials 163:1090-1095 |
| URI: | http://wrap.warwick.ac.uk/id/eprint/39102 |
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