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1 University of Bergen, Centre for Integrated Petroleum Research (CIPR), Allégaten 41, N-5007 Bergen, Norway
2 University of Bergen, Department of Biology, Jahnebakken 5, N-5020 Bergen, Norway
Correspondence
Terje Torsvik
terje.torsvik{at}bio.uib.no
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ABSTRACT |
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7c and C17 : 0 cyclo, and the cells also contained dimethylacetals. Cloning and sequencing of a 1505 bp long fragment of the 16S rRNA gene showed that strain H3T is a member of the Deltaproteobacteria and is related closely to Desulfotignum balticum DSM 7044T. The G+C content of the DNA was 52.0 mol% and the DNA–DNA similarity to D. balticum DSM 7044T was 56.1 %. Based on differences in DNA sequence and the unique property of toluene degradation, it is proposed that strain H3T should be designated a member of a novel species within the genus Desulfotignum, for which the name Desulfotignum toluenicum sp. nov. is proposed. The type strain is H3T (=DSM 18732T=ATCC BAA-1460T).
A supplementary table showing the varying bases in the analysed Desulfotignum sp. 16S rRNA gene sequences, and supplementary figures showing a transmission electron micrograph of unstained cells of Desulfotignum toluenicum H3T and rep-PCR profiles for the analysed strains of Desulfotignum, are available with the online version of this paper.
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MAIN TEXT |
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TOPABSTRACTMAIN TEXTREFERENCES |
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) was described as Desulfotignum balticum (Kuever et al., 2001). The type strain, Desulfotignum balticum DSM 7044T, has the ability to oxidize aromatic compounds such as benzoic acid and 4-hydroxybenzoate, but does not oxidize toluene. The genus also contains the sulphate-reducing bacterium Desulfotignum phosphitoxidans, which grows lithoautotrophically with phosphite as electron donor and sulphate as electron acceptor (Schink et al., 2002).
Strain H3T was isolated from an anaerobic enrichment culture inoculated with bacteria from an oil-reservoir model column (Myhr et al., 2002), supplied with 0.8 % (v/v) crude oil as the only carbon source. The enrichment culture was diluted serially with crude oil as carbon source in reduced bicarbonate-buffered seawater medium (Widdel & Pfennig, 1981) modified to 1.2 g KH2PO4 l–1 and 0.25 g NH4Cl l–1 (W20). The 10–7 dilution was submitted to an anoxic agar dilution series (Widdel & Bak, 1992) with 10 mM sodium caproate. After four consecutive agar dilution series of bacteria originating from the 10–7 dilution described above, three beige-coloured colonies (strains H1, H2 and H3T) were picked and propagated in W20 with caproate (10 mM). Strain H3T was characterized fully. Desulfotignum balticum DSM 7044T was purchased from the Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSMZ; Braunschweig, Germany).
Growth was monitored by light microscopy in a Zeiss phase-contrast microscope and by hydrogen sulphide measurements (Cord-Ruwisch, 1985). Cells were counted in a Thoma chamber, but cell counts were difficult in cultures supplied with crude oil, due to disturbances from oil in the preparations. Transmission electron microscopy (TEM) of unstained preparations of strain H3T was done at the electron microscope facilities at the University of Bergen, Norway. TEM images with size bars were used to determine the cell size. Salt requirement for growth was tested in DSMZ medium 383a (http://www.dsmz.de/media/med383a.htm) in triplicate with 0–60 g NaCl l–1 in intervals of 5.0 g l–1 (pH 7.0, 30 °C). The pH range for growth was tested in triplicate as described by Knoblauch et al. (1999) in medium 383a adjusted to a pH value between 4.94 and 9.06 (30 °C) and the temperature optimum was tested in duplicate in medium 383a in a temperature-gradient block with temperatures between 9.9 and 48.2 °C (pH 7.0).
Gram typing was determined by thorough mixing of cells of strain H3T in a drop of 3 % (w/v) KOH on a glass slide, followed by incubation at room temperature for 1 min. Catalase activity was tested in 3 % (v/v) hydrogen peroxide.
The fatty acid composition, DNA base composition and DNA–DNA hybridization value to Desulfotignum balticum DSM 7044T were determined at the DSMZ by standard protocols.
Cells of strain H3T were 0.6–1.0 µm in diameter and 1.4–2.5 µm in length. The cell shape varied from short blunt rods, almost cigar-shaped in the early growth phase, to long and slightly curved rods in late exponential phase. The cells were covered with an extracellular layer that appeared like a halo around the cells. Turbid, well-grown cultures had a strong tendency to attach to the inner walls of the growth tubes. A TEM image of strain H3T is available as Supplementary Fig. S1 in IJSEM Online. Growth occurred between 0.5 and 5.5 % (w/v) NaCl (optimum, 1.5 %), between pH 6.5 and 9.0 (optimum, 7.2) and between 16 and 35 °C (optimum, 34 °C). Strain H3T was Gram-negative and catalase-positive.
The predominant fatty acids were 16 : 0 (20.3 %), 16 : 17c (14.0 %) and 17 : 0 cyclo (13.4 %) and, in addition, four different dimethylacetals were found that were unique to strain H3T (Table 1). The DNA G+C content was determined as 52.0 mol% and the DNA–DNA hybridization value to Desulfotignum balticum DSM 7044T was 56.1 %.
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) before 0.5 ml sterile and anoxic hydrocarbon solution was added per 16 ml culture. The culture tubes were incubated in a near-horizontal position with the orifices below the liquid surface (Widdel et al., 2006). In addition to strain H3T, Desulfotignum balticum DSM 7044T was tested with toluene and crude oil as carbon sources. Strain H3T grew with toluene and crude oil (Fig. 1a, b), whereas Desulfotignum balticum DSM 7044T did not, and whole-oil GC (Skaare, 2007) showed that 4.4 mM of the toluene naturally present in crude oil was depleted from the oil when 8.1 mM H2S was produced after 50 days incubation (Fig. 1b). Strain H3T is the first member of the genus Desulfotignum with the ability to grow solely on a monoaromatic hydrocarbon, i.e. toluene. Intermediate products from incomplete hydrocarbon oxidation were not detected by GC, which indicated complete oxidation of toluene to CO2. The H2S : toluene molar ratio during growth on toluene was approximately 2, which was lower than the 4.12 ratio shown for Desulfobacula toluolica DSM 7467T (Rabus et al., 1993). The results from the complete substrate analysis for strain H3T are listed in Table 2.
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) did not have a complementary sequence in the 16S rRNA gene of the reference strain Desulfotignum balticum DSM 7044T. Combined with the primer A8f (Edwards et al., 1989), a 1505 bp long DNA fragment was PCR-amplified by standard protocols, cloned into the pCR4-TOPO vector (Invitrogen) and sequenced by using the primers T3, T7 (Invitrogen) and 338f (Lane, 1991). The partial sequences were assembled to a consensus sequence by using the Institut Pasteur CAP alignment tool (http://www.pasteur.fr/english.html). Cloning and sequencing of the 16S rRNA gene resulted in seven distinct sequences, with reciprocal sequence similarity between 98.6 and 99.9 %. Three clone sequences, 1, 4 and 7, were chosen to represent strain H3T in GenBank and submitted under the accession numbers EF207157 (clone 1), EF207158 (clone 4) and EF207159 (clone 7), as demonstrated previously for novel Clostridium species (Spring et al., 2003). All variable nucleotides are presented in Supplementary Table S1 in IJSEM Online.
CAP-assembled clone sequences were aligned in CLUSTAL_X (Thompson et al., 1997) to 16S rRNA gene sequences of members of the Deltaproteobacteria available in GenBank (Benson et al., 2004), obtained by BLAST search (Wheeler et al., 2003). Similarity values between sequences were calculated by using the Matrix Global Alignment Tool (MatGAT; Campanella et al., 2003). The phylogenetic relationships were presented graphically in a neighbour-joining tree (Saitou & Nei, 1987) based on the CLUSTAL_X alignment of the 16S rRNA gene sequences, with Escherichia coli as outgroup (Fig. 2). The tree was bootstrapped by 1000 recalculations and evaluated by the maximum-parsimony and maximum-likelihood algorithms (PHYLIP software package; Felsenstein, 2001). The 16S rRNA gene sequences of clones of strain H3T were 98.7–99.9 % similar to that of Desulfotignum balticum DSM 7044T, and placed strain H3T within the genus Desulfotignum. Still, the DNA–DNA hybridization value of 56.1 % to Desulfotignum balticum DSM 7044T showed that the novel strain H3T did not belong to the species Desulfotignum balticum (Wayne et al., 1987) and defined strain H3T as a member of a novel species within the genus Desulfotignum. Strain H3T was also related to Desulfobacula toluolica DSM 7467T (Rabus et al., 1993) and Desulfobacula phenolica DSM 3384T (Kuever et al., 2001), which have been shown to degrade toluene. Sulphate-reducing bacteria able to degrade aliphatic hydrocarbons, Desulfoglaeba alkanexedens ALDCT (Davidova et al., 2006), strain Hxd3 (Aeckersberg et al., 1991), Desulfatibacillum aliphaticivorans CV2803T (Cravo-Laureau et al., 2004), strain Pnd3 (Aeckersberg et al., 1998) and strain AK-01 (So & Young, 1999), were affiliated to remote clusters.
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; Versalovic et al., 1991) were performed with whole cells; extracted DNA was obtained by using a FastDNA SPIN kit for soil (Qbiogene). Strains H3T and Desulfotignum balticum DSM 7044T had very similar genomic fingerprints, but differed by the lack of bands of approximately 450 and 900 bp in the fingerprint of Desulfotignum balticum DSM 7044T. A picture showing the rep-PCR patterns for the analysed Desulfotignum species is available as Supplementary Fig. S2 in IJSEM Online. Based on the DNA–DNA hybridization value of 56.1 % to Desulfotignum balticum DSM 7044T, the fatty acid composition and the ability to degrade toluene, we conclude that strain H3T should be assigned to a novel species within the genus Desulfotignum, for which the name Desulfotignum toluenicum sp. nov. is proposed.
Description of Desulfotignum toluenicum sp. nov.
Desulfotignum toluenicum (tol.u.en'i.cum. N.L. n. toluenum toluene; L. suff. -icus -a -um suffix used with the sense of belonging to; N.L. neut. adj. toluenicum pertaining to toluene).
Rod-shaped, mesophilic, Gram-negative and sulphate-reducing. Cells are 0.6–1.0 µm in diameter and 1.4–2.5 µm in length, and have a tendency to curve with ageing. Motility is not observed and there are no flagella. Growth occurs at NaCl concentrations between 0.5 and 5.5 % (v/w), with optimum growth at 1.5 % NaCl, at temperatures between 16 and 35 °C (optimum, 34 °C) and at pH values between 6.5 and 9.0 (optimum, 7.2). The predominant fatty acids are C16 : 0, C16 : 17c and C17 : 0 cyclo and the cells also contain dimethylacetals. Catalase-positive. The following are used as substrates for growth: toluene, crude oil, formate, benzoate, 4-hydroxybenzoate, acetate, butyrate, caproate, heptanoate, nonate, decanoate, tetradecanonate, hexadecanoate, pyruvate, fumarate, succinate and H2/CO2. Vitamins are required for growth. n-Alkanes (nC7–nC9 and nC12), ethylbenzene, m-, p-, or o-xylene, lactate, valerate, undecanoate, dodecanoate, octadecanoate, ethanol and malate are not used as substrates. Electron acceptors are sulphate and sulphite. No growth was observed with thiosulphate or elemental sulphur as electron acceptor or with caproate as electron donor. The DNA G+C content is 52.0 mol%.
The type strain, H3T (=DSM 18732T=ATCC BAA-1460T), was isolated from an oil-reservoir model column at the University of Bergen, Norway.
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ACKNOWLEDGEMENTS |
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) and cell counts (
) are shown. (b) H2S concentrations produced with crude oil (
) as carbon sources.