PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of genannJournal InfoAuthorsPermissionsJournals.ASM.orggenomeA ArticleGenome Announcements
 
Genome Announc. 2017 March; 5(9): e01707-16.
Published online 2017 March 2. doi:  10.1128/genomeA.01707-16
PMCID: PMC5334584

Draft Genome Sequence of Ochrobactrum intermedium Strain SA148, a Plant Growth-Promoting Desert Rhizobacterium

ABSTRACT

Ochrobactrum intermedium strain SA148 is a plant growth-promoting bacterium isolated from sandy soil in the Jizan area of Saudi Arabia. Here, we report the 4.9-Mb draft genome sequence of this strain, highlighting different pathways characteristic of plant growth promotion activity and environmental adaptation of SA148.

GENOME ANNOUNCEMENT

The DARWIN21 project (http://www.darwin21.net/) is an initiative established with the aim of expanding our knowledge on microbial life in deserts. A diverse number of bacterial species were isolated from both soil and plants and were characterized for their potential application in modern agriculture. Within the DARWIN21 collection, diverse bacterial species show enhanced growth of the model plant Arabidopsis thaliana under stress conditions (1, 2). A number of bacterial Ochrobactrum species were isolated on the basis of their plant growth-promoting trait. Ochrobactrum species are widespread in the environment and can colonize a wide variety of habitats, including soil, plants, animals, and humans (3). In an attempt to decipher the genetic basis of the plant growth-promoting activity of a member of the Ochrobactrum species, the genome of strain SA148 was sequenced.

SA148 strain was isolated from the soil samples collected in the Jizan region (16°56.475′N, 42°36.694′E) in the Kingdom of Saudi Arabia. Based on the 16S rRNA gene sequences, the SA148 strain is closely related (99% gene similarity) to Ochrobactrum intermedium strain LMG3301 (accession no. NR_026039.1) (1). The genomic DNA of the SA148 strain was extracted using the Qiagen DNeasy blood and tissue kit, according to the manufacturer’s protocol. The DNA was then sequenced using paired-end Illumina MiSeq, and the library was constructed as described previously (4). Contig assembly was done with SPAdes assembler version 3.6 (5), with a 1-kb contig cutoff size. De novo assembly of MiSeq reads for strain SA148 resulted in 38 contigs with a total length of 4,918,899 bp, a mean contig size of 129,445 bp, an N50 of 419,572 bp, L50 reached with five contigs, and a genome G+C content of 57.5%. MegaBLAST (6) searches of strain SA148 concatenated genomes against the NCBI reference genome database (http://www.ncbi.nlm.nih.gov/genome/) revealed that the closest relative genomes to strain SA148 was O. intermedium strain LMG3301, with sequence coverages of 50% and 35% of chromosomes I and II (accession no. ACQA0100000.1) and similarities of 98% and 99%, respectively. The annotation of strain SA148 was carried out using the default INDIGO pipeline (7), with the exception of open reading frame (ORF) prediction by FragGeneScan (8). SA148 has 3,714 ORFs, three rRNA, 51 tRNA, and 64 noncoding RNA (ncRNA). The annotation predicted a number of enzymes, such as glyphosate resistance enzyme 3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19) first identified in Ochrobactrum anthropi (9), which is targeted by the herbicide glyphosate. We also detected mannitol-1-phosphate 5-dehydrogenase (EC 1.1.1.17) (gene mtlD) as a part of an osmoprotectant synthesis pathway that can be utilized to improve stress tolerance against temperature fluctuation (10). Moreover, a number of genes related to growth-promoting activity, including gene-coding clusters for phosphate solubilization with six genes for pyrroloquinoline quinone synthesis (PQQ) (EC 1.1.5.2) and glucose 1-dehydrogenase (GCD) (EC 1.1.5.2) were found. The genome analysis highlights the presence of 3-phytase (EC 3.1.3.8) (11) and acid phosphatase (EC 3.1.3.2) (12), two enzymes that aid plants during phosphate starvation.

Accession number(s).

The genome of Ochrobactrum intermedium SA148 was deposited at DDBJ/EMBL/GenBank under the accession no. LWEA00000000. The version described in this paper is the first version, LWEA01000000.

ACKNOWLEDGMENTS

Genome sequencing was performed at the Bioscience Core Laboratory of the King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia. We are grateful for the use of Dragon and Snapdragon compute clusters at the Computational Bioscience Research Center (CBRC) of KAUST.

This work was supported by a base fund research grant to H.H. from the King Abdullah University of Science and Technology (KAUST). Computational aspects of this work have been supported by the KAUST Office of Sponsored Research (OSR) under awards URF/1/1976-02 and FCS/1/2448-01 to V.B.B.

Footnotes

Citation Lafi FF, Alam I, Geurts R, Bisseling T, Bajic VB, Hirt H, Saad MM. 2017. Draft genome sequence of Ochrobactrum intermedium strain SA148, a plant growth-promoting desert rhizobacterium. Genome Announc 5:e01707-16. https://doi.org/10.1128/genomeA.01707-16.

REFERENCES

1. Lafi FF, Bokhari A, Alam I, Bajic VB, Hirt H, Saad MM 2016. Draft genome sequence of the plant growth-promoting Cupriavidus gilardii strain JZ4 isolated from the desert plant Tribulus terrestris. Genome Announc 4(4):e00678-16. doi:.10.1128/genomeA.00678-16 [PMC free article] [PubMed] [Cross Ref]
2. Lafi FF, Ramirez-Prado JS, Alam I, Bajic VB, Hirt H, Saad MM 2016. Draft genome sequence of Halomonas elongata strain K4, an endophytic growth-promoting bacterium enhancing salinity tolerance in planta. Genome Announc 4(6):e01214-16. doi:.10.1128/genomeA.01214-16 [PMC free article] [PubMed] [Cross Ref]
3. Bathe S, Achouak W, Hartmann A, Heulin T, Schloter M, Lebuhn M 2006. Genetic and phenotypic microdiversity of Ochrobactrum spp. FEMS Microbiol Ecol 56:272–280. doi:.10.1111/j.1574-6941.2005.00029.x [PubMed] [Cross Ref]
4. Velasco J, Romero C, López-Goñi I, Leiva J, Díaz R, Moriyón I 1998. Evaluation of the relatedness of Brucella spp. and Ochrobactrum anthropi and description of Ochrobactrum intermedium sp. nov., a new species with a closer relationship to Brucella spp. Int J Syst Bacteriol 48:759–768. doi:.10.1099/00207713-48-3-759 [PubMed] [Cross Ref]
5. Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, Pyshkin AV, Sirotkin AV, Vyahhi N, Tesler G, Alekseyev MA, Pevzner PA 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19:455–477. doi:.10.1089/cmb.2012.0021 [PMC free article] [PubMed] [Cross Ref]
6. Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, Madden TL 2009. BLAST plus: architecture and applications. BMC Bioinformatics 10:421. doi:.10.1186/1471-2105-10-421 [PMC free article] [PubMed] [Cross Ref]
7. Alam I, Antunes A, Kamau AA, Ba Alawi WB, Kalkatawi M, Stingl U, Bajic VB 2013. INDIGO—INtegrated data warehouse of MIcrobial GenOmes with examples from the Red Sea extremophiles. PLoS One 8:e82210. doi:.10.1371/journal.pone.0082210 [PMC free article] [PubMed] [Cross Ref]
8. Rho MN, Tang HX, Ye YZ 2010. FragGeneScan: predicting genes in short and error-prone reads. Nucleic Acids Res 38:e191–e191. doi:.10.1093/nar/gkq747 [PMC free article] [PubMed] [Cross Ref]
9. Tian YS, Xu J, Xiong AS, Zhao W, Fu XY, Peng RH, Yao QH 2011. Improvement of glyphosate resistance through concurrent mutations in three amino acids of the Ochrobactrum 5-enopyruvylshikimate-3-phosphate synthase. Appl Environ Microbiol 77:8409–8414. doi:.10.1128/AEM.05271-11 [PMC free article] [PubMed] [Cross Ref]
10. Chiang YJ, Stushnoff C, McSay AE 2005. Overexpression of mannitol-1-phosphate dehydrogenase increases mannitol accumulation and adds protection against chilling injury in petunia. J Am Soc Hort Sci 130:605–610.
11. Vohra A, Satyanarayana T 2003. Phytases: microbial sources, production, purification, and potential biotechnological applications. Crit Rev Biotechnol 23:29–60. doi:.10.1080/713609297 [PubMed] [Cross Ref]
12. Hong YF, Liu CY, Cheng KJ, Hour AL, Chan MT, Tseng TH, Chen KY, Shaw JF, Yu SM 2008. The sweet potato sporamin promoter confers high-level phytase expression and improves organic phosphorus acquisition and tuber yield of transgenic potato. Plant Mol Biol 67:347–361. doi:.10.1007/s11103-008-9324-6 [PubMed] [Cross Ref]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)