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1 Departamento de Producción Vegetal, Instituto de Recursos Naturales y Agrobiología, IRNA-CSIC, Spain
2 Departamento de Microbiología y Genética, Lab. 209, Edificio Departamental, Campus Miguel de Unamuno, Universidad de Salamanca, 37007 Salamanca, Spain
3 Laboratory of Microbiology, Dept Biochemistry, Physiology and Microbiology, Faculty of Sciences, Ghent University, Ghent, Belgium
Correspondence
Encarna Velázquez
evp{at}gugu.usal.es
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7c. The G+C content of the DNA was 53·1 mol%. Strain LMG 128 grew at 4 °C but not at 40 °C, and tolerated up to 5 % NaCl. The pH range for growth was 6–8. It produced urease and 
-galactosidase, and hydrolysed aesculin. Denitrification was negative. Growth was observed with many carbohydrates as the only carbon source. The data from this polyphasic study indicate that this strain belongs to a new genus of the family ‘Phyllobacteriaceae’, and therefore it is proposed that strain LMG 128T should be reclassified as representing a novel species within the new genus Hoeflea gen. nov., for which the name Hoeflea marina sp. nov. is proposed.
The GenBank/EMBL/DDBJ accession number for the 16S rRNA gene sequence of strain LMG 128T is AY598817.
A neighbour-joining tree based on nearly complete 16S rRNA gene sequences of Hoeflea marina LMG 128T and related organisms of the family ‘Phyllobacteriaceae’ is available as supplementary material in IJSEM Online.
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; Ahrens & Rheinheimer, 1967) for star-shaped Agrobacterium-like organisms. In the 8th edition of Bergey's Manual of Determinative Bacteriology, Ahrens withdrew her proposal of classifying these organisms as Agrobacterium ferrugineum (Allen & Holding, 1974) and the species was not included in the Approved Lists (Skerman et al., 1980). However, Rüger & Höfle (1992) revived the name Agrobacterium ferrugineum when they described marine, star-shaped, aggregate-forming bacteria. The type strain (=Ahrens A7T=ATCC 25652T) of this species has been recently reclassified as belonging to the new genus Pseudorhodobacter (Uchino et al., 2002). Strain LMG 128 (=Ahrens A43=ATCC 25654) was initially included in the species Agrobacterium ferrugineum (Ahrens, 1968), but this strain was not studied by Rüger & Höfle (1992), who only took into consideration the type strain in their study (=Ahrens A7T=ATCC 25652T). The nearly complete sequence of the 16S rRNA-encoding gene of LMG 128 indicates that it does not belong to the genus Agrobacterium, or to the genus Pseudorhodobacter, but to a new genus within the family ‘Phyllobacteriaceae’. In the present study we describe the phylogenetic, morphological, chemotaxonomic and physiological characteristics of this organism. On the basis of these data, we propose to place strain LMG 128T within a new genus, Hoeflea, as Hoeflea marina gen. nov., sp. nov.
DNA extraction, PCR of the 16S rRNA gene and sequencing of the PCR products were performed as previously described (Rivas et al., 2002). A nearly complete 16S rRNA gene sequence (1477 nucleotides) was obtained and was compared with those deposited in the databases. Sequences were aligned using the CLUSTAL_X software (Thompson et al., 1997). Distances were calculated according to Kimura's two-parameter method (Kimura, 1980). Phylogenetic trees were inferred by using the neighbour-joining method (Saitou & Nei, 1987). The bootstrap analysis was based on 1000 resamplings. The MEGA 2 package (Kumar et al., 2001) was used for all analyses. Based on the 16S rRNA gene sequence analysis, strain LMG 128T formed a new branch within the family ‘Phyllobacteriaceae’ (Fig. 1), and its closest relatives were Aquamicrobium defluvii (Bambauer et al., 1998) and Defluvibacter lusatiensis (Fritsche et al., 1999), with 16S rRNA gene sequence similarities of 95·5 and 95·1 %, respectively (a more complete phylogenetic tree is available as supplementary material in IJSEM Online).
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. The morphological characteristics of strain LMG 128T are presented in the species description.
For fatty acid methyl ester (FAME) analysis, strain LMG 128T was cultivated for 24 h at 28 °C on TSBA plates containing 30 g trypticase soy broth (BBL), supplemented with 15 g Bacto agar (l distilled water)–1 (Difco). The cells were saponified, and the fatty acids were methylated to FAMEs and extracted following the Sherlock Microbial Identification System version 3.0 (MIDI, 1999). FAMEs were separated on an Agilent 6890A series gas chromatograph, with 7683 autoinjector and autosampler tray module (Agilent Technologies). Separation of FAMEs was achieved with a fused-silica capillary column (25 mx0·2 mm), with cross-linked 5 % phenylmethyl silicone (film thickness, 0·33 µm; HP Ultra2). Hydrogen served as the carrier gas. Peak integration and identification were performed using the Hewlett Packard Chemstation software and Sherlock software. The results of the analysis are shown in Table 1. For comparison, the type strains of Aquamicrobium defluvii and Pseudorhodobacter ferrugineus were also included. As P. ferrugineus could not be grown on TSBA, it was grown on marine agar (Medium 12; BCCM/LMG catalogue of strains, http://www.belspo.be/bccm/db/media.htm). All three strains contained as a major component the mono-unsaturated straight-chain 18 : 17c (60–80 %). Minor fatty acids were the saturated straight-chain components 16 : 0 and 18 : 0. No significant hydroxy fatty acids were detected in LMG 128T (summed feature 3, comprising 14 : 0 3-OH and 16 : 1 iso, which could not be separated, was present at less than 1 %), whereas Aquamicrobium defluvii and P. ferrugineus contained 12 : 0 3-OH and 10 : 0 3-OH, respectively. For D. lusatiensis, Fritsche et al. (1999) reported that the main component was octadecanoic acid (18 : 1) and that 12 : 0 3-OH was present as a diagnostic component in small amounts. Strain LMG 128T contained a significant amount (7·5 %) of 18 : 17c 11Me, whereas no methylated fatty acids were detected in the other strains. To exclude the possibility that the original strain LMG 128T, deposited by R. Ahrens in 1969, had been contaminated or mislabelled during strain maintenance at the culture collection, we included lyophilized cultures from different batches, from 1973 and 1992. Both had identical FAME patterns.
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, b). Similar to other related genera from the order ‘Rhizobiales’ (Fritsche et al., 1999), the major respiratory lipoquinone in strain LMG128T was ubiquinone Q-10. The polar lipid pattern of strain LMG 128T was composed of phosphatidylglycerol, phosphatidylethanolamine, phosphatidylmonomethylethanolamine and sulphoquinovosyldiacylglyceride. Small amounts of diphosphatidylglycerol, an unidentified phospholipid and an unidentified phosphoglycolipid were also detected.
DNA from strain LMG 128T was prepared according to Chun & Goodfellow (1995). The mol% G+C content was determined by using the thermal denaturation method (Mandel & Marmur, 1968). The G+C content of strain LMG 128T was 53·1 mol%.
Catalase and oxidase activities were determined as described previously (Rivas et al., 2003). Other physiological and biochemical tests were done by using API 20NE (bioMérieux), according to the manufacturer's instructions. P. ferrugineus LMG 22047T and Aquamicrobium defluvii LMG 22048T were also included for comparison. The temperature range for growth was determined by incubating cultures on Yeast Mannitol agar (YMA) medium (Vincent, 1970) at 4–45 °C. The pH range was determined on YMA medium, with a final pH between 4·0 and 9·0. Salt tolerance was studied on YMA medium containing 0–8 % (w/v) NaCl. Differentiating physiological characteristics are listed in Table 2. They clearly demonstrate that strain LMG 128T is different from strains of neighbouring genera.
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Description of Hoeflea gen. nov.
Hoeflea (Hoef.le.a'. N.L. fem. n. Hoeflea honouring Manfred Höfle, German microbiologist, in recognition of his contribution to the taxonomy of marine bacteria).
Gram-negative, non-spore-forming, short, regular and motile rod-shaped cells. Strictly aerobic and chemo-organotrophic. Oxidase- and catalase-positive. Grow in the presence of NaCl concentrations up to 5 % (w/v), although salt is not essential for growth. Temperature range for growth is 4–37 °C and the pH range for growth is 6–8. Do not reduce nitrate to nitrite or nitrogen. The major respiratory lipoquinone is ubiquinone Q-10. The polar lipids are phosphatidylglycerol, phosphatidylethanolamine, phosphatidylmonomethylethanolamine and sulphoquinovosyldiacylglyceride. Diphosphatidylglycerol, an unidentified phospholipid and an unidentified phosphoglycolipid are present in small amounts. The main fatty acid is the unsaturated straight-chain fatty acid 18 : 17c. Other significant fatty acids (>3 %) include 16 : 0, 18 : 17c 11Me and 19 : 0 cyclo 8c. Hydroxy fatty acids are present in small amounts. Phylogenetically a member of the family ‘Phyllobacteriaceae’. The DNA G+C content of the type species is 53·1 mol%.
The type species of the genus is Hoeflea marina.
Description of Hoeflea marina sp. nov.
Hoeflea marina (ma.ri'na. L. fem. adj. marina of the sea, marine, referring to the isolation source of this micro-organism, sea water).
In addition to the properties listed in the genus description, the following properties are reported. Colonies on nutrient agar are circular, convex, white–cream, opaque and usually 1–3 mm in diameter, within 7 days at 28 °C. Cells are short rods of 0·7–0·9x1·1–1·4 µm. Optimal growth occurs at 3 % NaCl. Optimal growth temperature and pH are 28 °C and 7, respectively. Does not produce arginine dihydrolase, and hydrolysis of gelatin is weak and slow. Utilizes glucose, L-arabinose, mannose, mannitol, maltose and malate, but not N-acetylglucosamine, gentiobiose, caproate, adipate, citrate or phenylacetate. Fatty acids are listed in Table 1
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The type strain, and so far the only strain, is LMG 128T (=ATCC 25654T), which was isolated from the Baltic Sea, off the coast of Germany. The DNA G+C content is 53·1 mol%.
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ACKNOWLEDGEMENTS |
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REFERENCES |
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TOPABSTRACTMAIN TEXTREFERENCES |
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Ahrens, R. & Rheinheimer, G. (1967). Über einige sternbildende Bakterien aus der Ostsee. Kiel Meeresforsch 23, 127–136 (in German).
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Bambauer, A., Rainey, F. A., Stackebrandt, E. & Winter, J. (1998). Characterization of Aquamicrobium defluvii gen. nov., sp. nov., a thiophene-2-carboxylate-metabolizing bacterium from activated sludge. Arch Microbiol 169, 293–302.[CrossRef][Medline]
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Rivas, R., Willems, A., Subba-Rao, N. S., Mateos, P. F., Dazzo, F. B., Martínez-Molina, E., Gillis, M. & Velázquez, E. (2003). Description of Devosia neptuniae sp. nov. that nodulates and fixes nitrogen in symbiosis with Neptunia natans, an aquatic legume from India. Syst Appl Microbiol 26, 47–53.[CrossRef][Medline]
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1·0 %); ND, not detected.