Abstract
The heterotrophic, aerobic, facultatively anaerobic under denitrifying conditions, catalase- and oxidase-positive, non-motile strain MT-CBb6A5T, which was isolated from an acidic lake located in Wisconsin (USA), was characterized. The strain grew on NSY medium over a temperature range of 15–30 °C and a NaCl range of 0.0–0.3 % (w/v). The predominant fatty acids were C16 : 0,C18 : 1ω7c, 11-methyl C18 : 1ω7c, feature 3 (including C16 : 1ω7c), and feature 2 (including C14 : 0 3-OH). The DNA G+C content of the strain was 40.3 mol%. Phylogenetic analysis as well as strong similarities in phenotypic and chemotaxonomic traits indicated the affiliation with the genus Polynucleobacter. 16S rRNA gene sequence similarity values with the two described species of the genus Polynucleobacter ranged from 95.6 to 96.0 %. The strain differs from the two described species of the genus Polynucleobacter in the ability to assimilate oxalic and glycolic acids, and in the presence of the fatty acids C15 : 1ω8c and C16 : 0 3-OH as well as in quantitative differences in fatty acid composition. It has to be assumed that the strain shares with other free-living bacteria of the genus Polynucleobacter a planktonic lifestyle in the water column of freshwater habitats. Based on the phylogeny revealed and the chemotaxonomic and phenotypic differences from Polynucleobacter necessarius and Polynucleobacter cosmopolitanus, we propose to establish the novel species Polynucleobacter rarus sp. nov. with the type strain MT-CBb6A5T (=DSM 21648T =CIP 109928T).
K. Heckmann and H.-J. Schmidt described the genus Polynucleobacter to accommodate bacteria living as obligate endosymbionts in cells of freshwater ciliates affiliated with the genus Euplotes, and the species Polynucleobacter necessarius for obligate endosymbionts of Euplotes aediculatus (Heckmann & Schmidt, 1987). Recently, a close phylogenetic relationship between such obligate endosymbionts and obligately free-living strains was demonstrated (Vannini et al., 2007). Consequently, the description of the genus Polynucleobacter and the species P. necessarius was emended by adding descriptions of free-living strains (Hahn et al., 2009). Due to the very pronounced differences in lifestyle of the closely related obligately endosymbiotic and obligately free-living strains, the placement of these organisms in the two subspecies P. necessarius subsp. necessarius (for endosymbionts of E. aediculatus and Euplotes harpa) and P. necessarius subsp. asymbioticus (for obligately free-living strains) was proposed (Hahn et al., 2009). Furthermore, the species Polynucleobacter cosmopolitanus representing the second species within the genus Polynucleobacter was described recently (Hahn et al., 2010). This species accommodates, so far, exclusively free-living strains. The obligately free-living bacteria affiliated with these two species represent aerobic, chemo-organotrophic, non-motile bacteria. Investigations employing fluorescent in situ hybridization (FISH) probes specific for P. necessarius or P. cosmopolitanus demonstrated that the free-living strains representing these two taxa possess a planktonic lifestyle and contribute significantly to bacterioplankton in freshwater habitats (Hahn et al., 2005; Wu & Hahn, 2006; Salcher et al., 2008). The highest contributions of P. necessarius and P. cosmopolitanus reported so far were about 60 % and 8 %, respectively, of total bacterial cell numbers (Hahn et al., 2005, 2010). Numerous studies employing cultivation-independent methods for the exploration of bacterial diversity in freshwater, marine and terrestrial habitats revealed that bacteria of the genus Polynucleobacter are present in a broad variety of freshwater habitats (e.g. Hiorns et al., 1997; Crump et al., 1999; Crump & Hobbie, 2005; Zwart et al., 2002; Burkert et al., 2003; Hahn et al., 2005; Grossart et al., 2008) but reports on their presence at off-shore marine and terrestrial sites are lacking.
In previous studies, a monophyletic cluster of strains (minimal 16S rRNA gene sequence similarity of 95.7 %, Hahn, 2003) including a sequence of an endosymbiotic P. necessarius strain (Springer et al., 1996) was described as ‘Polynucleobacter necessarius cluster’ (Zwart et al., 2002), which was later subdivided in four monophyletic subclusters designated A to D (Hahn, 2003). The previously emended species P. necessarius is equivalent to subcluster C (also known as subcluster PnecC), and the recently described species P. cosmopolitanus is equivalent to subcluster D (PnecD). Here we describe a strain affiliated with subcluster A (PnecA) and propose to establish for this strain the species Polynucleobacter rarus sp. nov. Note that this new species represents only a fraction of the highly diverse subcluster A of the ‘Polynucleobacter necessarius cluster’.
Isolation and characterization
Strain MT-CBb6A5T was isolated from Crystal Bog Lake (Newton et al., 2006) by using the filtration-acclimatization method (Hahn, 2003; Hahn et al., 2004). This isolation method includes a step of filtration through 0.2 μm filters, which seems to contradict the cell dimensions of the cultivated strain presented below. However, variations of pore sizes of the filter or much smaller in situ cell sizes of the strain may be responsible for the passing of the ancestor cell through the filter. At the time of writing, only a single strain affiliated with subcluster A of the ‘P. necessarius cluster’ has been isolated, while >150 and >50 strains of subcluster C (P. necessarius) and subcluster D (P. cosmopolitanus), respectively, have been isolated (Hahn, 2003; Hahn et al., 2005, 2010; Watanabe et al., 2009). The isolation method for bacteria of the genus Polynucleobacter developed by Watanabe et al. (2009) uses a 0.8 μm filtration step, whereas, in several isolation experiments, Hahn et al. (2005, 2009) replaced the filtration step by a dilution step (dilution-acclimatization method); thus, the singular isolation of a Polynucleobacter strain affiliated with subcluster A cannot exclusively be explained by the utilization of 0.2 μm filters.
Initially, pure cultures of the strain in liquid NSY medium (Hahn et al., 2004) showed formation of flocks; however, this trait disappeared after some subcultivation steps. The investigated strain was routinely grown on NSY and R2A (Remel) medium with concentrations of 3 g l−1; however, similar to previously investigated Polynucleobacter strains, the biomass yield of strain MT-CBb6A5T on these media was much lower than that observed for other members of the family Burkholderiaceae. Growth at different temperatures and growth under anoxic conditions in an anaerobic chamber were examined on NSY agar or on NSY medium supplemented with nitrate (0.8 mM). NaCl tolerance was determined using NSY agar supplemented with different NaCl concentrations (0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 1.0, 1.25, 1.5, 1.75 and 2.0 %, w/v). The temperature range supporting growth was tested on NSY agar plates exposed to different temperatures (5, 15, 20, 25, 30 and 35 °C). Utilization of various substrates was investigated in the same way as for previously described species of the genus Polynucleobacter (Hahn et al., 2009, 2010). Briefly, growth enabled by utilization of a specific substrate was determined by comparison of optical density (OD) established in liquid one-tenth-strength NSY medium (0.3 g l−1) with and without 0.5 g test substance l−1. OD differences of <10 %, of 10–50 % and of >50 % of the OD established on the medium without test substance were scored after 10 days of growth as no utilization (−), weak utilization (W) and good utilization (+), respectively.
Sequencing and phylogenetic analyses of 16S rRNA genes were performed as described previously (Hahn, 2003; Hahn et al., 2005). Neighbour-joining trees were calculated by using the software MEGA4 (Tamura et al., 2007) and maximum-likelihood trees were generated by using the RaxML web server (Stamatakis et al., 2008). The G+C content of DNA was determined as described by Tóth et al. (2008). Fatty acid methyl esters (FAMEs) were obtained as described by Kämpfer & Kroppenstedt (1996) and separated by a gas chromatograph (model 6890, Hewlett Packard). Peaks were automatically computed using the Microbial Identification standard software package (Sasser, 1990).
The results of the phenotypic and chemotaxonomic characterization of strain MT-CBb6A5T are presented in Tables 1 and 2. The strain differs from strains of P. necessarius subsp. asymbioticus and P. cosmopolitanus in the relatively large cell widths, and in the frequently observable presence of multiple nucleoid structures (Fig. 1). Such structures were reported for endosymbiotic strains recently assigned to the subspecies P. necessarius subsp. necessarius and the genus name refers to them (Heckmann & Schmidt, 1987); however, this feature was only rarely observed in other free-living Polynucleobacter strains (Hahn, 2003; Hahn et al., 2009, 2010). Furthermore, the investigated strain differed from both previously described taxa in the ability to utilize oxalic and glycolic acids (Table 3). Strain MT-CBb6A5T showed visible growth under anoxic conditions only on NSY medium supplemented with increased concentrations of nitrate and not on standard NSY medium. This observation could result from nitrate respiration.
Table 1. Traits characterizing strain MT-CBb6A5T and strains of the previously described taxa P. necessarius subsp. asymbioticus and P. cosmopolitanus.
Taxa: 1, Polynucleobacter rarus sp. nov. MT-CBb6A5T; 2, P. necessarius subsp. asymbioticus (n=4; data from Hahn et al., 2009); 3, P. cosmopolitanus (n=5; Hahn et al., 2010). Note that the subspecies P. necessarius subsp. necessarius lacks a sufficient phenotypic and chemotaxonomic description due to the lack of pure cultures. All taxa are non-motile, positive for catalase and oxidase activities, grow anaerobically on NSY medium + 0.8 mM nitrate, assimilate pyruvic acid and do not assimilate l-serine. −, Negative; +, positive; W, weakly positive; +/−, some strains positive and some strains negative; +/W, some strains positive and some strains weakly positive; W/−, some strains weakly positive and some strains negative.
| Characteristic | 1 | 2 | 3 |
|---|---|---|---|
| Cell morphology | Straight rods | Straight or curved rods | Curved rods |
| Nucleoids visible (DAPI) | Frequently | Rarely | Rarely |
| Cell length (μm) | 0.8–1.8 | 0.5–2.9 | 0.4–1.4 |
| Cell width (μm) | 0.6–0.8 | 0.3–0.5 | 0.3–0.5 |
| Growth at 5 °C | − | + | +/− |
| Growth at 35 °C | − | +/− | + |
| NaCl tolerance (%, w/v) | 0.3(W) | 0.3–0.5 | 0.3–0.5 |
| Anaerobic growth on NSY medium | − | +/− | + |
| Growth in mineral medium with acetic acid and B12 | W | W/− | W/− |
| Assimilation of: | |||
| Urea | − | +/− | +/− |
| Thiosulfate | − | +/− | +/− |
| Formic acid | − | W/− | − |
| Glyoxylic acid | + | W/− | W/− |
| Glycolic acid | W | − | − |
| Acetic acid | + | + | + |
| Oxalic acid | W | − | − |
| Propionic acid | − | +/− | +/W |
| Malonic acid | − | +/− | +/− |
| Oxaloacetic acid | − | +/− | + |
| Malic acid | + | +/W | + |
| Succinic acid | + | + | + |
| Fumaric acid | + | +/W | + |
| Levulinic acid | + | W/− | W/− |
| Citric acid | − | − | +/− |
| d-Mannose | W | W/− | W/− |
| d-Glucose | − | W/− | W/− |
| d-Galacturonic acid | + | W | +/W |
| d-Galactose | − | W/− | W |
| d-Lyxose | W | W/− | − |
| d-Fructose | W | W/− | − |
| d-Fucose | W | W/− | − |
| d-Sorbitol | − | W/− | − |
| l-Glutamate | − | +/− | W/− |
| l-Aspartate | − | +/− | − |
| l-Cysteine | W | +/W | + |
| l-Alanine | − | W/− | +/W |
| l-Asparagine | − | W/− | − |
| Betaine | − | W/− | − |
| DNA G+C content (mol%) | 40.3 | 44–46 | 44.9 |
Table 2. Whole-cell fatty acid composition of strain MT-CBb6A5T as compared with strains of P. necessarius subsp. asymbioticus and P. cosmopolitanus.
Taxa: 1, Polynucleobacter rarus MT-CBb6A5T; 2, P. necessarius subsp. asymbioticus QLW-P1DMWA-1T (data from Hahn et al., 2009); 3, P. necessarius (n=3; Hahn et al., 2009); 4, P. cosmopolitanus MWH-MoIso2T (Hahn et al., 2010); 5, P. cosmopolitanus (n=5; Hahn et al., 2010). Values are percentages of the summed fatty acids named in the peak library of the MIDI system (contents ≥0.1%). Strains were grown on R2A agar plates for 3–5 days at 28 °C. tr, Trace, may be detected or not in independent experiments.
| Fatty acid | 1 | 2 | 3 | 4 | 5 |
|---|---|---|---|---|---|
| Saturated | |||||
| C12 : 0 | 3.0 | 3.4 | 3.4–5.5 | − | − |
| C14 : 0 | 0.4 | 0.9 | 0.3–1.2 | 0.7 | 0.6–2.3 |
| C15 : 0 | tr | 0.3 | tr | 0.2 | tr |
| C16 : 0 | 19.8 | 22.2 | 15.5–33.5 | 15.4 | 11.0–15.4 |
| C17 : 0 | 0.3 | − | tr | − | tr |
| C18 : 0 | 0.5 | 1.2 | 0.5–2.6 | 0.8 | 0.5–1.1 |
| Unsaturated | |||||
| C14 : 1ω5c | 0.2 | − | 0–0.6 | 0.6 | 0–0.6 |
| C15 : 1ω8c | 0.2 | − | − | − | − |
| C15 : 1ω6c | 0.3 | − | 0–0.6 | − | − |
| C16 : 1ω5c | 0.5 | 0.9 | 0–0.9 | 0.3 | 0.3–1.1 |
| C17 : 1ω6c | tr | − | − | 0.5 | 0–0.7 |
| C18 : 1ω9c | tr | − | 0–0.4 | 0.3 | 0–2.0 |
| C18 : 1ω7c | 21.8 | 12.9 | 0.25–20.4 | 28.7 | 28.7–38.1 |
| C18 : 1ω5c | − | − | − | 0.2 | tr |
| 11-Methyl C18 : 1ω7c | 7.5 | 3.1 | 0.2–8.1 | 3.7 | 0.4–3.7 |
| 10-Methyl C19 : 0 | 0.4 | − | − | 0.7 | 0–0.7 |
| Hydroxylated | |||||
| C12 : 0 2-OH | − | 2.5 | 1.3–2.5 | − | − |
| C12 : 0 3-OH | − | − | − | 11.1 | 7.1–11.2 |
| C16 : 0 3-OH | 0.3 | − | − | − | – |
| Summed features | |||||
| 1 (C12 : 0 ALDE?) | 1.8 | 0.4 | 0.4–2.1 | 0.1 | tr |
| 2 (including C14 : 0 3-OH) | 6.9 | 9.6 | 8.4–9.9 | 0.6 | 0.6–3.9 |
| 3 (including C16 : 1ω7c) | 35.9 | 41.3 | 35.6–45.0 | 34.7 | 31.5–36.5 |
| 7 (including C19 : 1ω6c) | − | 0.4 | 0.2–2.0 | 1.5 | 0–1.5 |
Fig. 1.
Epifluorescence microscopic images of cells of strain MT-CBb6A5T stained with the nucleic acid dye 4′,6-diamidino-2-phenylindole (DAPI). Note that the image shows a collection of cells showing multiple nucleoids, which is a trait not shared by all cells present in cultures of the strain. The fraction of cells showing this trait is variable and seems to be influenced by the age of the culture. Bar, 2 μm.
Table 3. Discriminative characteristics separating strain MT-CBb6A5T from P. necessarius subsp. asymbioticus and P. cosmopolitanus.
Taxa: 1, Polynucleobacter rarus sp. nov. MT-CBb6A5T; 2, P. necessarius subsp. asymbioticus [n=3 (fatty acids) or 4 (phenotypic features); data from Hahn et al., 2009]; 3, P. cosmopolitanus [n=3 (phenotypic features) or 5 (fatty acids); Hahn et al., 2010]. P. rarus sp. nov. differs from the obligately endosymbiotic P. necessarius subsp. necessarius in its free-living lifestyle. Note that only an incomplete phenotypic and chemotaxonomic description of P. necessarius subsp. necessarius is available because of the lack of pure cultures. −, Negative; +, positive.
| Characteristic | 1 | 2 | 3 |
|---|---|---|---|
| Nucleoids visible (DAPI)* | Frequently | Rarely | Rarely |
| Cell width (μm) | 0.6–0.8 | 0.3–0.5 | 0.3–0.5 |
| Utilization of glycolic acid | + | − | − |
| Utilization of oxalic acid | + | − | − |
| C12 : 0 | + | + | − |
| C15 : 1ω8c | + | − | − |
| C12 : 0 2-OH | − | + | − |
| C16 : 0 3-OH | + | − | − |
| DNA G+C content (mol%) | 40.3 | 44–46 | 44.9 |
Staining with a fluorescent nucleic acid dye (e.g. DAPI) and epifluorescence microscopic observation.
The G+C content of the DNA of strain MT-CBb6A5T was 40.3 mol%, which is substantially lower than those of P. necessarius strains (44–46 mol%) and the P. cosmopolitanus type strain (44.9 mol%). Whole-cell fatty acids of strain MT-CBb6A5T were dominated by the unsaturated components C16 : 1ω7c (feature 3), C18 : 1ω7c and 11-methyl C18 : 1ω7c and straight chain C16 : 0. Relatively high amounts of feature 2, including C14 : 0 3-OH, were also detected. The pattern, consisting of these major components and a high number of minor compounds, resembled those of the two other species of the genus Polynucleobacter, confirming the membership of the strain in this genus. The novel strain contained C12 : 0, a feature differentiating it from P. necessarius subsp. asymbioticus. Furthermore, strain MT-CBb6A5T was characterized by the presence of low amounts of C16 : 0 3-OH and C15 : 1ω8c, which were lacking in the other Polynucleobacter strains. Instead, strain MT-CBb6A5T was devoid of C12 : 0 2-OH and C12 : 0 3-OH, which are present in P. necessarius subsp. asymbioticus and P. cosmopolitanus, respectively.
Phylogeny
The phylogenetic analysis of the almost complete 16S rRNA gene sequence of strain MT-CBb6A5T demonstrated a close relationship with the two previously described species of the genus Polynucleobacter but also demonstrated a clustering separate from those two taxa (Fig. 2). Note that a more detailed phylogenetic analysis including the 16S rRNA gene and the 16S–23S ITS sequences of strain MT-CBb6A5T was published previously (Hahn et al., 2010). The sequence similarities between 16S rRNA genes of strain MT-CBb6A5T and the type strain of P. necessarius subsp. asymbioticus, a sequence representing P. necessarius subsp. necessarius ‘E24’, and the type strain of P. cosmopolitanus were 96.0 %, 95.6 % and 96.0 %, respectively.
Fig. 2.
Neighbour-joining tree based on almost complete 16S rRNA gene sequences, reconstructing the phylogenetic position of strain MT-CBb6A5T. Bar, 0.01 substitutions per nucleotide position. Note that previous analysis of the phylogeny of the genus Polynucleobacter, which analysed 16S rRNA gene sequences and 16S–23S ITS sequences by the neighbour-joining and maximum-likelihood method (Hahn et al., 2010), confirmed the phylogenetic position of strain MT-CBb6A5T in the Polynucleobacter clade.
Ecology of Polynucleobacter rarus sp. nov.
Despite the lack of both quantitative in situ data and systematic surveys on the distribution of P. rarus sp. nov., it seems that this taxon represents, in contrast to P. necessarius subsp. asymbioticus and P. cosmopolitanus, a rare species. A blast search with the almost complete 16S rRNA gene sequence of strain MT-CBb6A5T as a query resulted in only nine hits (all affiliated with subcluster A of the ‘Polynucleobacter cluster’) with sequence similarities >97 %. Most of these hits represent environmental sequences of uncultured bacteria. The closest hit (accession number FR667321), representing a bacterium from a high mountain lake located in the Pyrenees, Spain (M. Bartrons, unpublished data), shares with P. rarus sp. nov. a sequence similarity of only 99.5%. The other eight sequences originate from the Adirondack lakes, New York (accession number EF520438, Percent et al., 2008), the estuaries Chesapeake Bay and Delaware Bay (accession numbers EU801586 and EU800645, Shaw et al., 2008), from Arctic Toolik Lake (accession number AF534432, Crump et al., 2003), from Lake Shirakoma, Japan (accession numbers AB599841 and AB599847, K. Watanabe, Y. Ishii, N. Komatsu, T. Honma, R. Miyata, N. Noda, Y. Sekiguchi, S. Hayashi and A. Imai, unpublished data) and from Crystal Bog Lake (two identical sequences with accession numbers AY792238 and AY792240, Newton et al., 2006). The latter two sequences share with strain MT-CBb6A5T the same origin but only sequence similarities of 97.7 %. Similar blast searches with the type strains of of P. cosmopolitanus and P. necessarius subsp. asymbioticus resulted in >100 hits representing environmental sequences and cultivated strains with sequence similarities ranging from 98.5 % to 100 %, respectively. Thus, the under representation of strains affiliated to subcluster A relative to members of other subclusters in Polynucleobacter culture collections seems to result mainly from a relative rareness of the taxon in the environment.
The origin of strain MT-CBb6A5T and the closest related taxa from the water column of freshwater lakes or from rivers and estuaries receiving water from freshwater lakes seems to indicate that strains affiliated with P. rarus sp. nov. dwell in the water column of freshwater systems as free-living planktonic bacteria. Such a lifestyle was demonstrated for P. necessarius subsp. asymbioticus and P. cosmopolitanus previously (Hahn et al., 2005; Wu & Hahn, 2006). On the other hand, the initial observation of flock formation in liquid cultures could hint at an attached lifestyle of the strain. Dystrophic Crystal Bog Lake, from which the type strain of P. rarus sp. nov. was isolated, is a shallow, acidic lake strongly influenced by the surrounding bog, which results in a relatively high concentration of allochtonous humic substances in the water of the lake (Newton et al., 2006). A preference of P. rarus sp. nov. for acidic habitats is likely; however, the small dataset available for this taxon enables only preliminary conclusions.
Results from the phylogenetic analysis and chemotaxonomic investigations demonstrated the affiliation of strain MT-CBb6A5T to the genus Polynucleobacter (Tables 1 and 2, Fig. 2) but also revealed pronounced differences between this strain and strains affiliated with previously described species of the genus Polynucleobacter (Table 3). The 16S rRNA gene sequence similarities determined between strain MT-CBb6A5T and strains representing the two P. necessarius subspecies as well as P. cosmopolitanus of <97 % clearly indicate that the investigated strain represents a new species of the genus Polynucleobacter. Therefore, we propose to establish the species Polynucleobacter rarus sp. nov. with strain MT-CBb6A5T as the type strain. Note that we do not propose to tentatively include all strains of the so-called subcluster A (PnecA) in this new species. This subcluster represents, in contrast to subclusters PnecC (P. necessarius) and PnecD (P. cosmopolitanus), a phylogenetically more diverse subcluster, which makes it more likely than the other two subclusters to consist of more than one species.
Description of Polynucleobacter rarus sp. nov.
Polynucleobacter rarus (ra’rus. L. masc. adj. rarus rare, referring to the observation that this species represents a rare species, in contrast to the previously described species of the genus Polynucleobacter).
Straight, non-motile rods, 0.8–1.8 μm in length and 0.6–0.8 μm in width. Staining with nucleic acid dyes results in the microscopical visibility of multiple nucleoids in a significant fraction of cells. Chemo-organotrophic and aerobic; anaerobic growth in the presence of nitrate. Can be cultivated on NSY and R2A medium. Colonies grown on NSY agar are unpigmented, circular and convex with smooth surface. Mesophilic; no growth at 5 °C or 35 °C. Grows without NaCl. Maximum NaCl concentration tolerated is 0.3 % (w/v). Oxidase- and catalase-positive. Utilizes glyoxylate, glycolate, acetate, oxalate, pyruvate, malate, succinate, fumarate, levulinate, d-mannose, d-galacturonic acid, d-lyxose, d-fructose, d-fucose and l-cysteine when these substrates are provided in a medium containing low amounts of NSY. Does not utilize formate, propionate, malonate, oxaloacetate, citrate, d-glucose, d-galactose, d-sorbitol, l-glutamate, l-aspartate, l-alanine, l-serine, l-asparagine or betaine. Major cellular fatty acids are C16 : 0, C18 : 1ω7c, 11-methyl C18 : 1ω7c, feature 3 (including C16 : 1ω7c), and feature 2 (including C14 : 03-OH). The DNA G+C content of the type strain is 40.3 mol%. The sole cultivated strain currently representing this species is a free-living strain.
The type strain is MT-CBb6A5T (=DSM 21648T =CIP 109928T), isolated from the water column (pelagic zone) of Crystal Bog Lake in Wisconsin, USA.
Acknowledgements
We thank K. McMahon for providing a water sample from Crystal Bog Lake. We appreciate the determination of the G+C content by P. Schumann, DSMZ, and of the fatty acids by R.M. Kroppenstedt, DSMZ. This study was supported by the Austrian Science Fund (Project P19853 granted to M. W. H.).
Abbreviation
- OD
optical density
Footnotes
The GenBank/EMBL/DDBJ accession number for the 16S rRNA gene sequence of strain MT-CBb6A5T is FM208182.
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