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. 2015 May 21;3(3):e00398-15. doi: 10.1128/genomeA.00398-15

Genome Sequence of Leucobacter sp. 4J7B1, a Plant-Osmoprotectant Soil Microorganism

M Manzanera 1,, J I Vílchez 1, C García-Fontana 1, C Calvo 1, J González-López 1
PMCID: PMC4440946  PMID: 25999566

Abstract

We report the first genome sequence for Leucobacter sp. 4J7B1, a newly described desiccation-tolerant strain. The complete genome sequence of Leucobacter sp. 4J7B1 has been sequenced and is estimated to be around 3.5 Mb in size, with an average GC content of 62.18%. We predict 2,953 protein-coding sequences.

GENOME ANNOUNCEMENT

The genus Leucobacter belongs to the class of high-GC-content, Gram-positive, nonsporulating Actinobacteria. Species of Leucobacter have been recovered from diverse ecological niches, including plants’ phyllosphere (1). Leucobacter sp. 4J7B1 is a desiccation-tolerant bacterium isolated from a Nerium oleander rhizosphere subjected to severe drought (2). Isolation of other desiccation-tolerant microorganisms from this environment, including the new species Arthrobacter siccitolerans 4J27, has been reported recently (3, 4). The production of xeroprotectants, such as glycerol, by many desiccation-tolerant microorganisms protects themselves against damage caused by drought and salts (511) and other stressors (12). Thus, the combination of soy plants and Leucobacter sp. 4J7B1 in the presence of 200-mM NaCl results in significant protection of the plant by the microorganism. This protection effect might be the result of glycerol production, a well-known osmoprotectant. To our knowledge, the complete genome sequence of the genus Leucobacter sp. 4J7B1 has not been deposited in the DDBJ/EMBL/GenBank databases. In this research, we determine the whole-genome sequence of Leucobacter sp. 4J7B1 with pyrosequencing technology as implemented at the 454 Life Science-Roche platform with a combined approach of shotgun and 8-Kb mate-pair sequencing (12).

A total of 150,575 reads were produced, with an average read length of 603 bases for the shotgun and 123,838 sequences with an average read length of 389,53 bases for the mate-pair sequencing strategy. The total number of sequenced bases is 129,339,181, representing a sequencing depth of around 38×. De novo assembly was performed with default parameters by using the Newbler version 2.6 assembler. The assembly resulted in 432 contigs, 149 of which were larger than 500 bp. The N50 of the contig assembly was 871,355 bp, and the largest contig was 1,030,920 bp. Most of these contigs were ordered in two scaffolds (based on mate-pair information), where the largest scaffold was 3,069,722 bp. This combination of scaffolds and contigs resulted in an estimated genome size of 3.5 Mb. Gap closure was attempted using gap-spanning clones and PCR products. Putative coding sequences were predicted and genes were annotated with a pipeline implemented at Lifesequencing S.L. (Valencia, Spain). Briefly, protein-coding sequences were predicted by the combined use of Glimmer (1315), RNAmmer (16), tRNAScan (17, 18), and BLAST (19, 20). The complete genomic information for Leucobacter sp. 4J7B1 was found to contain 2,953 protein-coding genes, 5 rRNA operons, and 49 tRNA genes, with an average GC content for that chromosome of 62.18%.

Analysis of this genome sequence data led to propose the presence of several genes involved in glycerol metabolism in bacteria, such as tagD, glpF, or glpQ1, among others. This knowledge can lead to advance biotechnological applications in osmoprotection engineering (6, 8, 21).

In summary, the complete genome sequence of Leucobacter sp. 4J7B1 will contribute to improving the knowledge of plants’ osmoprotection by microorganisms.

Nucleotide sequence accession numbers.

The complete genome sequence of Leucobacter sp. 4J7B1 has been deposited in the TBL/EMBL/GenBank databases under accession numbers CDWJ01000001 to CDWJ01000432.

ACKNOWLEDGMENTS

This research was funded by the Ministry of Science and Innovation in Spain, the Andalusian regional government (Spain), within the context of research projects P11-RNM-7844 and CTM2009-09270. M. Manzanera received a Ramón y Cajal research grant from the Ministry of Science and Innovation, as well as support from European Regional Development Funds (EU).

Footnotes

Citation Manzanera M, Vílchez JI, García-Fontana C, Calvo C, González-López J. 2015. Genome sequence of Leucobacter sp. 4J7B1, a plant-osmoprotectant soil microorganism. Genome Announc 3(3):e00398-15. doi:10.1128/genomeA.00398-15.

REFERENCES

  • 1.Behrendt U, Ulrich A, Schumann P. 2008. Leucobacter tardus sp. nov., isolated from the phyllosphere of Solanun tuberosum L. 2008. Int J Syst Envol Micrbiol 58:2574–2578. doi: 10.1099/ijs.0.2008/001065-0. [DOI] [PubMed] [Google Scholar]
  • 2.Narváez-Reinaldo JJ, Barba I, González-López J, Tunnacliffe A, Manzanera M. 2010. Rapid method for isolation of desiccation-tolerant strains and xeroprotectants. Appl Environ Microbiol 76:5254–5262. doi: 10.1128/AEM.00855-10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Manzanera M, Santa-Cruz-Calvo L, Vílchez JI, García-Fontana C, Silva-Castro GA, Calvo C, González-López J. 2014. Genome sequence of Arthrobacter siccitolerans 4J27, a xeroprotectant-producing desiccation-tolerant microorganism. Genome Announc 2(3): e00526-14. doi: 10.1128/genomeA.00526-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.SantaCruz-Calvo L, González-López J, Manzanera M. 2013. Arthrobacter siccitolerans sp. nov., a highly desiccation-tolerant, xeroprotectant-producing strain isolated from dry soil. Int J Syst Envol Micrbiol 63:4174–4180. doi: 10.1099/ijs.0.052902-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Vilchez S, Manzanera M. 2011. Biotechnological uses of desiccation-tolerant microorganisms for the rhizoremediation of soils subjected to seasonal drought. Appl Microbiol Biotechnol 91:1297–1304. doi: 10.1007/s00253-011-3461-6. [DOI] [PubMed] [Google Scholar]
  • 6.Manzanera M, García de Castro A, Tøndervik A, Rayner-Brandes M, Strøm AR, Tunnacliffe A. 2002. Hydroxyectoine is superior to trehalose for anhydrobiotic engineering of Pseudomonas putida KT2440. Appl Environ Microbiol 68:4328–4333. doi: 10.1128/AEM.68.9.4328-4333.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Manzanera M, Vilchez S, Tunnacliffe A. 2004. High survival and stability rates of Escherichia coli dried in hydroxyectoine. FEMS Microbiol Lett 233:347–352. doi: 10.1016/j.femsle.2004.03.005. [DOI] [PubMed] [Google Scholar]
  • 8.Julca I, Alaminos M, González-López J, Manzanera M. 2012. Xeroprotectants for the stabilization of biomaterials. Biotechnol Adv 30:1641–1654. doi: 10.1016/j.biotechadv.2012.07.002. [DOI] [PubMed] [Google Scholar]
  • 9.Manzanera M, Vilchez S, Tunnacliffe A. 2004. Plastic encapsulation of stabilized Escherichia coli and Pseudomonas putida. Appl Environ Microbiol 70:3143–3145. doi: 10.1128/AEM.70.5.3143-3145.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Billi D, Wright DJ, Helm RF, Prickett T, Potts M, Crowe JH. 2000. Engineering desiccation tolerance in Escherichia coli. Appl Environ Microbiol 66:1680–1684. doi: 10.1128/AEM.66.4.1680-1684.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Crowe JH, Crowe L, Carpenter JF, Wistrom A 1987. Stabilization of dry phospholipid-bilayers and proteins by sugars. Biochem J 242:1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Margulies M, Egholm M, Altman WE, Attiya S, Bader JS, Bemben LA, Berka J, Braverman MS, Chen YJ, Chen Z, Dewell SB, Du L, Fierro JM, Gomes XV, Godwin BC, He W, Helgesen S, Ho CH, Ho CH, Irzyk GP. 2005. Genome sequencing in microfabricated high-density picolitre reactors. Nature 437:376–380. doi: 10.1038/nature03959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Delcher AL, Harmon D, Kasif S, White O, Salzberg SL. 1999. Improved microbial gene identification with GLIMMER. Nucleic Acids Res 27:4636–4641. doi: 10.1093/nar/27.23.4636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Salzberg SL, Delcher AL, Kasif S, White O. 1998. Microbial gene identification using interpolated Markov models. Nucleic Acids Res 26:544–548. doi: 10.1093/nar/26.2.544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Delcher AL, Bratke KA, Powers EC, Salzberg SL. 2007. Identifying bacterial genes and endosymbiont DNA with glimmer. Bioinformatics 23:673–679. doi: 10.1093/bioinformatics/btm009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Lagesen K, Hallin P, Rødland EA, Staerfeldt HH, Rognes T, Ussery DW. 2007. RNammer: consistent and rapid annotation of rRNA genes. Nucleic Acids Res 35:3100–3108. doi: 10.1093/nar/gkm160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Schattner P, Brooks AN, Lowe TM. 2005. The tRNA scan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs. Nucleic Acids Res 33:W686–W689. doi: 10.1093/nar/gki366. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Lowe TM, Eddy SR. 1997. Program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res 25:955–964. doi: 10.1093/nar/25.5.0955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. 1990. Basic local alignment search tool. J Mol Biol 215:403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  • 20.Morgulis A, Coulouris G, Raytselis Y, Madden TL, Agarwala R, Schäffer AA. 2008. Database indexing for production MegaBLAST searches. BioInformatics 24:1757–1764. doi: 10.1093/bioinformatics/btn322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Vílchez S, Tunnacliffe A, Manzanera M. 2008. Tolerance of plastic-encapsulated Pseudomonas putida KT2440 to chemical stress. Extremophiles 12:297–299. doi: 10.1007/s00792-007-0123-9. [DOI] [PubMed] [Google Scholar]

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