Abstract
The complete genome sequence of 6.45 Mb is reported here for Pseudomonas trivialis strain IHBB745 (MTCC 5336), which is an efficient, stress-tolerant, and broad-spectrum plant growth-promoting rhizobacterium. The gene-coding clusters predicted the genes for phosphate solubilization, siderophore production, 1-aminocyclopropane-1-carboxylate (ACC) deaminase activity, indole-3-acetic acid (IAA) production, and stress response.
GENOME ANNOUNCEMENT
The genus Pseudomonas belongs to the Gamma subclass of Proteobacteria (1) with 218 species (http://www.bacterio.net/pseudomonas.html). The fluorescent Pseudomonas have received attention due to their widespread distribution and predominance among the rhizobacteria, and versatility for improving plant growth and productivity (2, 3). Pseudomonas trivialis IHBB745, isolated from the rhizosphere of Hippophae rhamnoides growing in the Lahaul-Spiti district, India (31°45′ 33°15″ N 76°21′ 78°40″ E), has been reported as a phosphate solubilizer with high abiotic stress tolerance (4–6). The strain also possesses the attributes of indole-3-acetic acid (IAA) production, 1-aminocyclopropane-1-carboxylate (ACC) deaminase activity, and siderophore production. The complete genome sequence is reported to provide genomic information on the multifunctional plant growth-promoting activities of the strain.
The genomic DNA was isolated using a phenol-chloroform-isoamyl alcohol extraction procedure (7) from 24-h-old cultures. The genomic DNA was quantified by a NanoDrop 2000 UV-Vis spectrophotometer (Thermo Scientific, USA) and Qubit version 2.0 fluorometer (Invitrogen, USA). The genomic DNA was sheared using Covaris g-TUBEs, and quality was checked with a Bioanalyzer DNA 12000 chip (Agilent Technologies, USA). A PacBio SMRTbell library preparation kit version 1.0 was used per the manufacturer’s instructions to prepare the genomic DNA library with a DNA insert size of around 10 kb. The SMRTbell library quantified using a Qubit version 2.0 fluorometer was sequenced on the PacBio RS II system on three SMRT cells, employing a P5 polymerase and C3 chemistry combination (P5-C3) with 180-min movie. The SMRT cells produced 1,259,528,544 bases generated through 295,525 reads (N50 size 5,735 and mean subread length 4,262) (8). The subreads were assembled de novo using the RS Hierarchical Genome Assembly Process (HGAP) protocol version 2.0 in SMRT Analysis version 2.2.0 (Pacific Biosciences, USA). The functional annotations were performed on the Rapid Annotations using Subsystems Technology (RAST) server (9).
The complete circular genome of strain 745 was 6,452,803 bp in size with an estimated GC content of 59.91%. A total of 6,032 protein-coding genes and 84 RNA genes (9) were predicted in the genome. Based on the 16S rRNA gene sequences, the strain IHBB745 is closely related to Pseudomonas trivialis DSM 14937T and P. poae DSM 14936T. The pairwise calculation of the average nucleotide identity using EzBiocloud (http://www.ezbiocloud.net) indicated 86.2% similarity between the genome sequences of strain IHBB745 and Pseudomonas poae RE1-1-14, confirming that the strains belonged to the different species. The annotation predicted gene-coding clusters for phosphate solubilization (6 genes), auxin biosynthesis (4 genes), siderophore production (31 genes), ACC deaminase activity (1 gene), HCN production (7 genes), and ammonia production (2 genes), attesting its multiple plant growth-promoting attribute. The stress tolerance trait of the strain also predicted 205 stress response genes related to osmotic stress (37 genes), oxidative stress (96 genes), cold shock (7 genes), heat shock (16 genes), peripalsmic stress (6 genes), and other stress responses.
Nucleotide sequence accession number.
The genome sequence of Pseudomonas trivialis strain IHBB745 has been deposited in GenBank under the accession number CP011507.
ACKNOWLEDGMENTS
We acknowledge the director of the CSIR-IHBT for the use of laboratory facilities.
This work was financed by the CSIR Network Project “Plant-Microbe-Soil Interactions” (BSC0117, Work Package 06).
Footnotes
Citation Gulati A, Swarnkar MK, Vyas P, Rahi P, Thakur R, Thakur N, Singh AK. 2015. Complete genome sequence of the rhizobacterium Pseudomonas trivialis strain IHBB745 with multiple plant growth-promoting activities and tolerance to desiccation and alkalinity. Genome Announc 3(5):e00943-15. doi:10.1128/genomeA.00943-15.
REFERENCES
- 1.Peix A, Ramirez-Bahena HM, Velázquez E. 2009. Historical evolution and current status of the taxonomy of genus Pseudomonas. Infect Genet Evol 9:1132–1147. doi: 10.1016/j.meegid.2009.08.001. [DOI] [PubMed] [Google Scholar]
- 2.Beneduzi A, Ambrosini A, Passaglia LM. 2012. Plant growth-promoting rhizobacteria (PGPR): their potential as antagonists and biocontrol agents. Genet Mol Biol 35:1044–1051. doi: 10.1590/S1415-47572012000600020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Saleem M, Arshad M, Hussain S, Bhatti AS. 2007. Perspective of plant growth promoting rhizobacteria (PGPR) containing ACC deaminase in stress agriculture. J Ind Microbiol Biotechnol 34:635–648. doi: 10.1007/s10295-007-0240-6. [DOI] [PubMed] [Google Scholar]
- 4.Gulati A, Rahi P, Vyas P. 2008. Characterization of phosphate-solubilizing fluorescent pseudomonads from the rhizosphere of Seabuckthorn growing in the cold deserts of Himalayas. Curr Microbiol 56:73–79. doi: 10.1007/s00284-007-9042-3. [DOI] [PubMed] [Google Scholar]
- 5.Vyas P, Rahi P, Gulati A. 2009. Stress tolerance and genetic variability of phosphate-solubilizing fluorescent Pseudomonas from the cold deserts of the trans-Himalayas. Microb Ecol 58:425–434. doi: 10.1007/s00248-009-9511-2. [DOI] [PubMed] [Google Scholar]
- 6.Vyas P, Gulati A. 2009. Organic acid production in vitro and plant growth promotion in maize under controlled environment by phosphate-solubilizing fluorescent Pseudomonas. BMC Microbiol 9:174. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Marmur J. 1961. A procedure for the isolation of deoxyribonucleic acid from micro-organisms. J Mol Biol 3:208–218. doi: 10.1016/S0022-2836(61)80047-8. [DOI] [Google Scholar]
- 8.Chin CS, Alexander DH, Marks P, Klammer AA, Drake J, Heiner C, Clum A, Copeland A, Huddleston J, Eichler EE, Turner SW, Korlach J. 2013. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data. Nat Methods 10:563–569. doi: 10.1038/nmeth.2474. [DOI] [PubMed] [Google Scholar]
- 9.Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: Rapid Annotations using Subsystems Technology. BMC Genomics 9:75. doi: 10.1186/1471-2164-9-75. [DOI] [PMC free article] [PubMed] [Google Scholar]