Introduction
Proteobacteria is a major phylum of Gram-negative bacteria, which constitute the largest and most phenotypically diverse division among prokaryotes (Gupta, 2000). They represent nearly a half of the partial and complete prokaryotic genomes hosted at the National Center for Biotechnology Information (NCBI; ftp:// ftp. ncbi.nlm.nih.gov/ genomes/ GENOME_REPORTS/ prokaryotes.txt) (Itävaara et al., 2016). The phylum Proteobacteria comprises 116 validated families according to the List of Prokaryotic Names with Standing in Nomenclature (http://www.bacterio.net/).
The phylum was formally established, using phylogenetic analysis of 16S rRNA gene sequences by Garrity et al. (2005a), with five constituent classes containing all known Gram-negative bacteria: Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, Deltaproteobacteria and Epsilonproteobacteria (William and Kelly, 2013). Further, the molecular analyses using complete multigenome/multiprotein alignments added the sixth (Zetaproteobacteria) and seventh class(Oligoflexis) to the phylum Proteobacteria (Williams et al., 2010; Yutin et al., 2012). The species of Proteobacteria are abundantly present in various ecological niches such as soil (36.5%), plants (62%), the atmosphere (77.9%), seawater (57.9%), and freshwater (61.3%) (Woese et al., 1987; Shin et al., 2015; Kim et al., 2017). Their major functional roles are nitrogen fixation and oxidation of iron, sulfur, and methane (Gupta, 2000).
In Korea, the highest peatland moor is located in the mountainous area of Yongneup (38°12ʹ53ʹN 128°07ʹ30ʹE) in Mt. Daeam, Gangwon Province. Yongneup was designated as a natural reserve in July 1973 owing to its rare and unique plant species (Kim et al., 2015). The peat layers are about 150 cm thick, which have formed over 4,000-5,000 years. This region is characterized by a basic pH, relatively low temperature, and limited environments characterized by the organic matter, released by the plant species in the peatland (Li et al., 2014). The Microorganism Resources Division of the National Institute of Biological Resources(NIBR) collected soil samples from the Yongneup peatland and isolated unrecorded bacterial species. The 16S rRNA sequence similarity provides robust evidence identifying four bacterial strains belonging to the phylum Proteobacteria. In this report, we describe these four bacterial species which are not previously reported in Korea.
Materials and Methods
Soil samples were collected from the Yongneup peatland under aseptic conditions and all the samples were processed separately. Each sample was serially diluted, spread on to R2A agar (Difco, Beckton, Dickinson, and Co., Spake, MD, U.S.A.), and incubated at 30℃ for three days. The isolates colonies were deposited at NIBR, where they were stored at -70℃ until further examinations. Colony morphology and cell size of the strains were observed on R2A agar after cells grown for three days at 30℃ by transmission electron microscopy (LIBRA 120, Carl Zeiss). Transmission electron micrographs of the strains are shown in Fig. 1. Gram staining was performed using a Gram-Staining kit (Sigma-Aldrich). Biochemical characteristics were tested by using API 20NE galleries (bioMerieux) according to manufacturer’s instructions.
Fig. 1. Transmission electron micrographs of the strains isolated in this study. Strains: (A) Curvibacter lanceolatus R-1-5; (B) Massilia brevitalea R-2-13; (C) Pseudomonas lini R-2-1; and (D) Pseudomonas vancouverensis R-1-8.
Genomic DNA was extracted using a DNA extraction kit (AccuPrep Genomic DNA extraction kit, Bioneer, Korea) and 16S rRNA was amplified with PCR (primer sets 27F, 5ʹ-AGAGTTTGATCCTGGCTCAG-3ʹ; 1088R, 5ʹ-GCTCGTTGCGGGACTTAACC-3ʹ, 518F, 5ʹ-CCAGCAGCCGCGGTAATACG-3ʹ; 800R, 5ʹ-TACCAGGGTATCTAATCC-3ʹ) with 30 cycles of denaturation at 95℃ for 30 sec, annealing at 57℃ for 30 sec, and polymerization at 72℃ for 45 sec, and sequenced by Macrogen (Daejeon, Korea). The 16SrRNA gene sequences of the closely related strains were obtained from EzTaxon-e (http://eztaxon-e.ezbiocloud.net). Phylogenetic trees were constructed using the neighbor-joining method (Saitou and Nei, 1987; Thompson et al., 1997) in MEGA5 (Tamura, 2013) with bootstrap values based on 1,000 replications(Felsenstein, 1985).
Results and Discussion
The four bacterial species(R-1-5, R-2-13, R-2-1, R-1- 8) were isolated from peatland soil samples in Korea. The taxonomic composition and identification results are summarized in Table 1. Morphology and physiological characteristics are shown in the species description section. All the four strains belonged to the phylum Proteobacteria, in which R-1-5 and R-2-13 were assigned to the class Betaproteobacteria, and R-2-1 and R-1-8 assigned to the class Gammaproteobacteria. Based on the 16S rRNA phylogenetic analysis(Fig. 2), the strains R-1- 5, R-2-13, R-2-1 and R-1-8 had highest gene sequence similarity with Curvibacter lanceolatus ATCC 14669T (AB021390; 99.93%), Massilia brevitalea byr23-80T (EF546777; 98.7%), Pseudomonas lini CFBP 5737T (AY035996; 99.54%) and Pseudomonas vancouverensis ATCC 700688T (AJ011507; 99.93%), respectively. Here we report on these four unrecorded bacterial species belonging to the phylum Proteobacteria isolated from peatland soil in Korea.
Table 1. Summary of strains isolatèd belonging to the Proteobacteria and their taxonomic affliations.
Fig. 2. Neighbor-joining phylogenetic tree based on 16S rRNA sequences shows the relationship between the strains isolated in this study and their relatives in the genera Curvibacter (A), Massilia (B) and Pseudomonas (C). Bootstrap values (>70%) are shown above nodes for the neighbor-joining. Scale bar: 0.01 changes per nucleotide.
Fig. 2. Continued.
Description of Curvibacter lanceolatus R-1-5
Cells are Gram-negative, non-flagellated, and rodshaped. Colonies are circular, raised, entire, and white colored after 3 days of incubation on R2A agar at 30℃. Oxidase and catalase positive. Using the API 20NE kit, this strain was positive for urease, D-glucose, and gluconate; but negative for nitrate reduction, reduction of nitrates to nitrogen, indole production, glucose acidification, arginine dihydrolase, β-glucosidase, protease, β-galactosidase, L-arabinose, D-mannose, D-mannitol, N-acetyl-glucosamine, D-maltose, caprate, adipate, malate, citrate, and phenyl-acetate. D-Glucose, propionate, valerate, L-histidine, 3-hydroxy-butyrate, 4-hydroxy-benzoate, L-proline, suberate, acetate, DL-lactate, L-alanine, 3-hydroxy-benzoate are utilized. Does not utilize D-mannitol, salicin, D-melibiose, L-fucose, D-sorbitol, L-arabinose, caprate, citrate, 2-ketogluconate, L-rhamnose, N-acetyl-glucosamine, D-ribose, inositol, D-sucrose, D-maltose, itaconate, malonate, 5-ketogluconate, glycogen, and L-serine. DNA G+C mol is 59.1%. Strain R-1-5 (=NIBRBAC000499694) was isolated from peatland soil, Gangwon Province, Korea.
Description of Massilia brevitalea R-2-13
Cells are Gram-negative, motile, and rod-shaped. Colonies are circular, raised, entire, and cream colored after 3 days on R2A agar at 30°C. Oxidase and catalase positive. Using the API 20NE kit, this strain was positive for protease; but negative for nitrate reduction, reduction of nitrates to nitrogen, indole production, glucose acidification, arginine dihydrolase, urease, β-glucosidase, β-galactosidase, D-glucose, L-arabinose, D-mannose, D-mannitol, N-acetyl-glucosamine, D-maltose, gluconate, caprate, adipate, malate, citrate, and phenyl-acetate. In API 32GN, carbon assimilation is positive for salicin, propionate, valerate, L-histidine, 3-hydroxy-butyrate, D-sucrose, itaconate, acetate, DL-lactate, L-alanine, and 5-ketogluconate. Negative for D-mannitol, D-glucose, D-melibiose, L-fucose, D-sorbitol, L-arabinose, caprate, citrate, 2-ketogluconate, 4-hydroxy-benzoate, L-proline, L-rhamnose, N-acetyl-glucosamine, D-ribose, inositol, D-maltose, suberate, malonate, glycogen, 3-hydroxy-benzoate, and L-serine. DNA G+C mol is 64.4%. Strain R-2-13 (=NIBRBAC000500608) was isolated from peatland soil, Gangwon Province, Korea.
Description of Pseudomonas lini R-2-1
Cells are Gram-negative, motile, and rod-shaped. Colonies are circular, raised, entire, and white colored after 3 days on R2A agar at 30°C. Oxidase and catalase positive. Using the API 20NE kit, this strain was positive for nitrate reduction, arginine dihydrolase, urease, D-glucose, D-mannose, D-mannitol, N-acetyl-glucosamine, gluconate, caprate, malate and citrate; but negative for indole production, glucose acidification, β-glucosidase, protease, β-galactosidase, L-arabinose, D-maltose, adipate and phenyl-acetate. In API 32GN, carbon assimilation is positive for D-mannitol, D-glucose, D-sorbitol, propionate, caprate, citrate, L-histidine, 2-ketogluconate, 3-hydroxy-butyrate, L-Proline, L-rhamnose, N-acetyl-glucosamine, acetate, DL-lactate, L-alanine and L-serine. Negative for salicin, D-melibiose, L-fucose, L-arabinose, valerate, 4-hydroxy-benzoate, D-ribose, inositol, D-sucrose, D-maltose, itaconate, suberate, malonate, 5-ketogluconate, glycogen and 3-hydroxy-benzoate. DNA G+C mol is 58.4%. Strain R-2-1 (=NIBRBAC000500607) was isolated from peatland soil, Gangwon Province, Korea.
Description of Pseudomonas vancouverensis R-1-8
Cells are Gram-negative, non-flagellated, and rodshaped. Colonies are circular, raised, entire, and cream colored after 3 days on R2A agar at 30°C. Oxidase and catalase positive. Using the API 20NE kit, this strain was positive for arginine dihydrolase, urease, D-glucose, L-arabinose, gluconate, caprate, malate, citrate and phenyl-acetate; but negative for Nitrate reduction, reduction of nitrates to nitrogen, indole production, glucose acidification, β-glucosidase, protease, β-galactosidase, D-mannose, D-mannitol, N-acetyl-glucosamine, D-maltose and adipate. In API 32GN, carbon assimilation is positive for D-glucose, L-arabinose, propionate, caprate, valerate, citrate, L-histidine, 2-ketogluconate, 3-hydroxy-butyrate, 4-hydroxy-benzoate, L-proline, D-ribose, malonate, acetate, DL-lactate, L-alanine, 3-hydroxy-benzoate and L-serine. Negative for D-mannitol, salicin, D-melibiose, L-fucose, D-sorbitol, L-rhamnose, N-acetyl-glucosamine, inositol, D-sucrose, D-maltose, itaconate, suberate, 5-ketogluconate and glycogen. DNA G+C mol is 60.8%. Strain R-1-8 (=NIBRBAC000500609) was isolated from peatland soil, Gangwon Province, Korea.
AcknowledgeMents
This study was supported by research program from National Institute of Biological Resources funded by the Ministry of Environment (MOE) of the Republic of Korea (NIBR201601113 and NIBR201701107).
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