Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2013 Apr 25;1(2):e00092-13. doi: 10.1128/genomeA.00092-13

Complete Genome Sequence of Geobacillus sp. Strain GHH01, a Thermophilic Lipase-Secreting Bacterium

Sandra Wiegand a, Ulrich Rabausch b, Jennifer Chow b, Rolf Daniel a, Wolfgang R Streit b, Heiko Liesegang a,
PMCID: PMC3636540  PMID: 23618712

Abstract

Geobacillus sp. strain GHH01 was isolated during a screening for producers of extracellular thermostable lipases. The completely sequenced and annotated 3.6-Mb genome encodes 3,478 proteins. The strain is genetically equipped to utilize a broad range of different substrates and might develop natural competence.

GENOME ANNOUNCEMENT

The genus Geobacillus contains thermophilic strains, which produce a variety of thermostable hydrolytic extracellular enzymes, such as proteases, amylases, and lipases. These features are interesting for future production platforms used in industrial applications (1).

Here, we present the complete genome sequence of Geobacillus sp. strain GHH01, a thermophilic lipase producer. The strain was isolated from an enrichment culture originally sampled at Botanischer Garten, University of Hamburg, Germany, and was cultivated at 60°C with 1.5% native olive oil as the sole carbon source. Recombinant expression in Escherichia coli revealed that the Geobacillus sp. GHH01 lipase (locus tag GHH_c20570) is highly active but only moderately thermostable.

The genome sequence of Geobacillus sp. GHH01 was determined by a combined approach of 454 GS-FLX Titanium XL paired-end sequencing (454 Life Sciences, Branford, CT) and Genome Analyzer II single-read sequencing (TruSeq Chemistry, Illumina, San Diego, CA), resulting in average coverages of 10.91-fold and 33.03-fold, respectively. The assembly employing the MIRA v3.4.1.1 software (2) yielded 84 contigs >3 kbp. Gap closure and quality improvement were performed by PCR-based techniques and subsequent Sanger sequencing (ABI 3730xl, Life Technologies, Carlsbad, CA). Initial gene prediction was performed with IMG/ER (3), followed by manual curation based on comparisons to the Swiss-Prot, TrEMBL (4), and InterPro (5) databases. For the identification of rRNA and tRNA genes, RNAmmer v1.2 and tRNAscan-SE v1.4 (6, 7) were used, respectively.

The complete genome consists of a 3,582,992-bp chromosome with a G+C content of 52.3%. In total, 3,597 genes were identified, including 10 rRNA gene clusters and 88 tRNA genes. The annotation resulted in 2,724 protein-encoding genes with assigned functions.

16S rRNA gene phylogenetic analysis confirmed the affiliation of Geobacillus sp. GHH01 to the genus Geobacillus, whereas an assignment to a described species was not possible. We determined average nucleotide identities (8) of approximately 96% between the Geobacillus sp. GHH01 genome and the genomes of Geobacillus kaustophilus HTA426 (9) and Geobacillus thermoleovorans CCB_US3_UF5 (10). The recently mentioned (10) high synteny between G. thermoleovorans CCB_US3_UF5 and G. kaustophilus HTA426 (97.94%) calls into question their assignment to distinct species. Hence, a sequence similarity-based assignment of Geobacillus sp. GHH01 to a distinct species could not be employed.

Geobacillus sp. GHH01 is predicted to secrete 139 enzymes by the Sec-dependent pathway (11, 12), including the identified lipase, diverse peptidases, proteinases, an amylopullanase (GHH_c32620), an alpha-amylase (GHH_c32630), and an alkaline phosphatase (GHH_c27900). Several substrate-binding proteins of ABC transporters indicate the potential for utilization of a broad range of substrates. The ability to take up extracellular DNA is a crucial mechanism for strain development. Eighteen out of 25 main competence-related structural genes identified for Bacillus subtilis (13) were detected, featuring a possible mechanism of DNA uptake.

Genome comparisons revealed seven distinct GHH01-specific genomic islands (14). Furthermore, 123 putative transposases, five clustered regularly interspaced short palindromic repeat (CRISPR) regions, and nine CRISPR-associated genes of subtype III-B (15) could be detected.

Nucleotide sequence accession number.

The genome sequence of Geobacillus sp. GHH01 has been deposited in GenBank under accession no. CP004008. The strain is available upon request at the Bacillus Genetic Stock Center (BGSC).

ACKNOWLEDGMENTS

This work was supported by the German Federal Ministry of Education and Research (Bundesministerium für Bildung und Forschung) within the network grants GenoMik-Plus and GenoMik-Transfer.

We thank Anja Poehlein for support during sequencing, annotation, and submission and Stefanie Offschanka for technical assistance.

Footnotes

Citation Wiegand S, Rabausch U, Chow J, Daniel R, Streit WR, Liesegang H. 2013. Complete genome sequence of Geobacillus sp. strain GHH01, a thermophilic lipase-secreting bacterium. Genome Announc. 1(2):e00092-13. doi:10.1128/genomeA.00092-13.

REFERENCES

  • 1. McMullan G, Christie JM, Rahman TJ, Banat IM, Ternan NG, Marchant R. 2004. Habitat, applications and genomics of the aerobic, thermophilic genus Geobacillus. Biochem. Soc. Trans. 32:214–217 [DOI] [PubMed] [Google Scholar]
  • 2. 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. CiteSeer, Pennsylvania State University, University Park, PA [Google Scholar]
  • 3. Markowitz VM, Mavromatis K, Ivanova NN, Chen IM, Chu K, Kyrpides NC. 2009. IMG ER: a system for microbial genome annotation expert review and curation. Bioinformatics 25:2271–2278 [DOI] [PubMed] [Google Scholar]
  • 4. UniProt Consortium 2010. The Universal Protein Resource (UniProt) in 2010. Nucleic Acids Res. 37:D169–D174 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Zdobnov EM, Apweiler R. 2001. InterProScan—an integration platform for the signature-recognition methods in InterPro. Bioinformatics 17:847–848 [DOI] [PubMed] [Google Scholar]
  • 6. Lowe TM, Eddy SR. 1997. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 25:955–964 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Lagesen K, Hallin P, Rødland EA, Staerfeldt HH, Rognes T, Ussery DW. 2007. RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res. 35:3100–3108 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Richter M, Rosselló-Móra R. 2009. Shifting the genomic gold standard for the prokaryotic species definition. Proc. Natl. Acad. Sci. U. S. A. 106:19126–19131 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Takami H, Horikoshi K. 2000. Analysis of the genome of an alkaliphilic Bacillus strain from an industrial point of view. Extremophiles 4:99–108 [DOI] [PubMed] [Google Scholar]
  • 10. Muhd Sakaff MKL, Abdul Rahman AY, Saito JA, Hou S, Alam M. 2012. Complete genome sequence of the thermophilic bacterium Geobacillus thermoleovorans CCB_US3_UF5. J. Bacteriol. 194:1239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Petersen TN, Brunak S, Von Heijne G, Nielsen H. 2011. SignalP 4.0: discriminating signal peptides from transmembrane regions. Nat. Methods 8:785–786 [DOI] [PubMed] [Google Scholar]
  • 12. Sonnhammer EL, Von Heijne G, Krogh A. 1998. A hidden Markov model for predicting transmembrane helices in protein sequences. Proc. Int. Conf. Intell. Syst. Mol. Biol. 6:175–182 [PubMed] [Google Scholar]
  • 13. Kovács AT, Smits WK, Mirończuk AM, Kuipers OP. 2009. Ubiquitous late competence genes in Bacillus species indicate the presence of functional DNA uptake machineries. Environ. Microbiol. 11:1911–1922 [DOI] [PubMed] [Google Scholar]
  • 14. Langille MG, Brinkman FS. 2009. IslandViewer: an integrated interface for computational identification and visualization of genomic islands. Bioinformatics 25:664–665 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Makarova KS, Haft DH, Barrangou R, Brouns SJ, Charpentier E, Horvath P, Moineau S, Mojica FJ, Wolf YI, Yakunin AF, Van der Oost J, Koonin EV. 2011. Evolution and classification of the CRISPR-Cas systems. Nat. Rev. Microbiol. 9:467–477 [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES