Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2017 Apr 13;5(15):e00133-17. doi: 10.1128/genomeA.00133-17

Draft Genome Sequence of Permafrost Bacterium Nesterenkonia sp. Strain PF2B19, Revealing a Cold Adaptation Strategy and Diverse Biotechnological Potential

Purnima Singh a, Neelam Kapse b, Utpal Roy a, Shiv Mohan Singh c,, P K Dhakephalkar b
PMCID: PMC5391407  PMID: 28408669

ABSTRACT

Nesterenkonia sp. strain PF2B19, a psychrophilic bacterium, was isolated from 44,800-year-old permafrost. The draft genome sequence of this strain revealed the presence of genes involved in the production of cold active enzymes, carotenoid biosynthesis, fatty acid biosynthesis, and resistance to heavy metals. These results show the immense potential of the strain.

GENOME ANNOUNCEMENT

Permafrost soils are chronological archives of microorganisms (1). Microbial life has survived in a metabolically active state in the Svalbard permafrost (26). PF2B19, a Gram-positive coccus and aerobic bacterium, was isolated from permafrost (44,800 years old) in Svalbard. In order to unravel the molecular mechanisms underlying the cold adaptation and to identify biotechnologically relevant cold-adapted enzymes, whole-genome sequencing was performed.

The genome of Nesterenkonia sp. strain PF2B19 was sequenced using 316 Chip and 200-bp chemistry on the Ion Torrent PGM platform (Life Technologies, Inc., USA), which generated 2,662,620 bp of reads. The reads were de novo assembled using MIRA assembler version 4.0.5 (7) into 2,924 contigs, yielding a genome of ~2.6 Mb in size, with a G+C content of 67.6%. These results are similar to the sizes (2.59 to 2.81 Mb) and G+C contents (62.2 to 71.5%) detected in the draft genomes of three strains of Nesterenkonia, available in the public databases. The genome was annotated using the Rapid Annotations using Subsystems Technology (RAST) server (8). A total of 3,482 proteins were predicted, including 3,434 coding sequences and 47 total RNAs (nine rRNAs and 38 tRNAs). Digital DNA-DNA hybridization, performed as described by Auch et al. (9), revealed only 30.20%, 26.50%, and 27.40% homology between PF2B19 and Nesterenkonia JCM 19054, Nesterenkonia alba DSM 19423T, and Nesterenkonia sp. strain AN1, respectively, indicating a distinct delineation between the species and also depicting the novelty of strain PF2B19.

Further, the genome of PF2B19 was compared with the available Nesterenkonia genomes, which generated the nucleotide alignments of the genomes by BLASTn using the PF2B19 as the reference and the program BRIG (10). BLASTn results of each genome (Nesterenkonia JCM 19054, Nesterenkonia alba DSM 19423T, and Nesterenkonia sp. AN1) against PF2B19, with results rendered using the BRIG program revealed pronounced gaps in the query genomes highlighting the distinction between PF2B19 and the other Nesterenkonia genomes used.

The Arctic is characterized by harsh cold conditions. A number of genes linked to cold adaptation have been reported in the literature (1114). Analysis of the draft genome of Nesterenkonia sp. PF2B19 revealed multiple genes encoding a repertoire of proteins (a total of 78 genes) associated with cold stress adaptive response. These included cold shock proteins CspA and CspC (nine genes); genes encoding oxidative stress alleviating enzymes namely catalase (24 genes); superoxide dismutases (SodA and SodC- two genes each), a thiol peroxidase (Bcp), thioredoxin and thioredoxin reductase (TrxA and TrxB). Thirty two genes encoding osmotic stress response, transporters for glycine/betaine and other compatible solutes, and choline dehydrogenases were also detected.

Analysis of the annotated genome sequence of PF2B19 revealed the presence of genes involved in the production of α-amylases, including maltase and maltodextrinase, as well as xylanase, highlighting its biotechnological potential.

Thus, by means of genomic analyses, we could elucidate the genetic determinants of the adaptive strategies employed by Nesterenkonia sp. PF2B19 for survival in the cold permafrost soils of the Arctic.

Accession number(s).

The whole-genome shotgun project has been deposited in DDBJ/EMBL/GenBank under accession number MDSS00000000.

ACKNOWLEDGMENTS

We are thankful to Directors of the BITS-Pilani-K.K. Birla Goa campus, NCAOR Goa, and ARI Pune for encouragement and facilities. P.S. thanks DST for financial support (SR/WOS-A/LS-419/2013[G]). We also thank the Department of Science and Technology and Ministry of Earth Sciences for funding support. S.M.S. thanks Simantini Naik for technical help.

Footnotes

Citation Singh P, Kapse N, Roy U, Singh SM, Dhakephalkar PK. 2017. Draft genome sequence of permafrost bacterium Nesterenkonia sp. strain PF2B19, revealing a cold adaptation strategy and diverse biotechnological potential. Genome Announc 5:e00133-17. https://doi.org/10.1128/genomeA.00133-17.

REFERENCES

  • 1.Friedmann EI. 1994. Permafrost as microbial habitat, p 21–26. In Gilichinsky DA (ed). Viable microorganisms in permafrost. Russian Academy of Sciences, Pushchino, Russia. [Google Scholar]
  • 2.Humlum O, Elberling B, Hormes A, Fjordheim K, Hansen OH, Heinemeier J. 2005. Late-Holocene glacier growth in Svalbard, documented by subglacial relict vegetation and living soil microbes. Holocene 15:396–407. doi: 10.1191/0959683605hl817rp. [DOI] [Google Scholar]
  • 3.Singh SM, Sharma J, Gawas-Sakhalkar P, Upadhyay AK, Naik S, Bande D, Ravindra R. 2012. Chemical and bacteriological analysis of soil from the Middle and Late Weichselian from western Spitsbergen, Arctic. Quat Int 271:98–105. doi: 10.1016/j.quaint.2012.03.008. [DOI] [Google Scholar]
  • 4.Hansen AA, Herbert RA, Mikkelsen K, Jensen LL, Kristoffersen T, Tiedje JM, Lomstein BAa, Finster KW. 2007. Viability, diversity and composition of the bacterial community in a high Arctic permafrost soil from Spitsbergen, northern Norway. Environ Microbiol 9:2870–2884. doi: 10.1111/j.1462-2920.2007.01403.x. [DOI] [PubMed] [Google Scholar]
  • 5.Schostag M, Stibal M, Jacobsen CS, Bælum J, Taş N, Elberling B, Jansson JK, Semenchuk P, Priemé A. 2015. Distinct summer and winter bacterial communities in the active layer of Svalbard permafrost revealed by DNA- and RNA-based analyses. Front Microbiol 6:399. doi: 10.3389/fmicb.2015.00399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Singh P, Kapse N, Arora P, Singh SM, Dhakephalkar PK. 2015. Draft genome of Cryobacterium sp. MLB-32, an obligate psychrophile from glacier cryoconite holes of high Arctic. Mar Genomics 21:25–26. doi: 10.1016/j.margen.2015.01.006. [DOI] [PubMed] [Google Scholar]
  • 7.Chevreux B, Wetter T, Suhai S. 1999. Genome sequence assembly using trace signals and additional sequence information, p 45–56. In Computer science and biology. Proceedings of the German Conference on Bioinformatics, GCB ’99. GCB, Hannover, Germany. [Google Scholar]
  • 8.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]
  • 9.Auch AF, von Jan M, Klenk HP, Göker M. 2010. Digital DNA-DNA hybridization for microbial species delineation by means of genome-to-genome sequence comparison. Stand Genomic Sci 2:117–134. doi: 10.4056/sigs.531120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Alikhan NF, Petty NK, Ben Zakour NLB, Beatson SA. 2011. BLAST Ring Image generator (Brig): simple prokaryote genome comparisons. BMC Genomics 12:402. doi: 10.1186/1471-2164-12-402. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Berger F, Morellet N, Menu F, Potier P. 1996. Cold shock and cold acclimation proteins in the psychrotrophic bacterium Arthrobacter globiformis SI55. J Bacteriol 178:2999–3007. doi: 10.1128/jb.178.11.2999-3007.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Médigue C, Krin E, Pascal G, Barbe V, Bernsel A, Bertin PN, Cheung F, Cruveiller S, D’Amico S, Duilio A, Fang G, Feller G, Ho C, Mangenot S, Marino G, Nilsson J, Parrilli E, Rocha EP, Rouy Z, Sekowska A, Tutino ML, Vallenet D, von Heijne G, Danchin A. 2005. Coping with cold: the genome of the versatile marine Antarctica bacterium Pseudoalteromonas haloplanktis TAC125. Genome Res 15:1325–1335. doi: 10.1101/gr.4126905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Methé BA, Nelson KE, Deming JW, Momen B, Melamud E, Zhang X, Moult J, Madupu R, Nelson WC, Dodson RJ, Brinkac LM, Daugherty SC, Durkin AS, DeBoy RT, Kolonay JF, Sullivan SA, Zhou L, Davidsen TM, Wu M, Huston AL, Lewis M, Weaver B, Weidman JF, Khouri H, Utterback TR, Feldblyum TV, Fraser CM. 2005. The psychrophilic lifestyle as revealed by the genome sequence of Colwellia psychrerythraea 34H through genomic and proteomic analyses. Proc Natl Acad Sci U S A 102:10913–10918. doi: 10.1073/pnas.0504766102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Riley M, Staley JT, Danchin A, Wang TZ, Brettin TS, Hauser LJ, Land ML, Thompson LS. 2008. Genomics of an extreme psychrophile, Psychromonas ingrahamii. BMC Genomics 9:210. doi: 10.1186/1471-2164-9-210. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES