Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2013 Aug 15;1(4):e00616-13. doi: 10.1128/genomeA.00616-13

Genome Sequence of a Novel Polymer-Grade l-Lactate-Producing Alkaliphile, Exiguobacterium sp. Strain 8-11-1

Xu Jiang a, Yanfen Xue b, Limin Wang a, Bo Yu a,, Yanhe Ma b,c
PMCID: PMC3744680  PMID: 23950124

Abstract

Exiguobacterium sp. strain 8-11-1 is a newly isolated alkaliphile, which was reported to efficiently produce l-lactate using NaOH as the neutralizing agent. Here, we present the first 2.9-Mb assembly of its genome sequence, which may provide useful information related to its efficient lactate production and sodium ion tolerance capacities.

GENOME ANNOUNCEMENT

The genus Exiguobacterium was first described in 1983 by Collins et al. (1), with the characterization of the type species Exiguobacterium aurantiacum. In addition to the type strains, other Exiguobacterium spp. have been isolated from or molecularly detected in a wide range of habitats, including cold and hot environments with temperatures ranging from -12°C to 55°C (2). Many organisms of the genus Exiguobacterium are also haloalkaliphiles (3, 4). Therefore, they have properties of biotechnological interest (5, 6). Exiguobacterium sp. strain 8-11-1, an alkaliphile isolated from soil collected in a salt lake in Inner Mongolia, China, was demonstrated to be a good producer of l-lactic acid from glucose by using NaOH as the neutralizing agent. The high levels of optically pure l-lactic acid produced by Exiguobacterium sp. 8-11-1, combined with the ease of handling and low costs associated with the open fermentation strategy, provide a novel and potentially important approach for future l-lactic acid production (7).

Here, we present the first draft genome sequence of Exiguobacterium sp. 8-11-1, which was obtained by using the Illumina HiSeq 2000 system (300-bp paired-end sequences), which was performed by the Chinese National Human Genome Center at Shanghai, China. A total of 5,212,033 high-quality read pairs were produced for de novo assembly using the Velvet program (8). The reads were assembled into 61 contigs, providing 369-fold coverage. The contig N50 is 127,764 bp and the largest contig assembled was 345,491 bp. The average length of assembled contigs is 47,655 bp, with a total length of 2,906,962 bp.

Gene prediction and genome annotation were performed by the RAST server and the NCBI PAPPC (9, 10). tRNAs were predicted using the tRNAscan software (11). The gene function and classification were performed using the KEGG and Clusters of Orthologous Groups (COG) databases (12). About 2,926 coding sequences (CDSs) (average length, 887 bp), with a G+C content of 54%, were predicted, including 2,165 proteins having identified functions. Fourteen tRNA and 4 rRNA genes were also annotated. The metabolic network of 8-11-1 (determined by RAST) was reconstructed (9). Exiguobacterium sp. 8-11-1 is predicted to possess complete metabolic pathways, including those for glycolysis, the tricarboxylic acid cycle, and the pentose phosphate pathway. In addition, Exiguobacterium sp. 8-11-1 has the genes encoding xylose isomerase, l-lactate dehydrogenase, and permease, which indicates that strain 8-11-1 is a potential producer of l-lactic acid from cellulosic substrate. There are 134 genes for inorganic ion transport and metabolism, including 1 MnhB-type Na+/H+ antiporter and 5 NhaC-type Na+/H+ antiporters, which may contribute to pH homeostasis and the capacity of the cells to lower the cytoplasmic Na+ concentration optimally at the alkaline pH (13). The detailed analysis of the genomic information of strain 8-11-1 will provide further insights into the genetic versatility of Exiguobacterium strains, as well as their extremophilic properties.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession no. ATKK00000000. The version described in this paper is version ATKK01000000.

ACKNOWLEDGMENTS

The work was supported by grants from the Chinese National Programs for High Technology Research and Development (no. 2011AA02A202), the Knowledge Innovation Program of the Chinese Academy of Sciences (no. KSZD-EW-Z-016-3), and the National Natural Science Foundation of China (no. 31270108).

Footnotes

Citation Jiang X, Xue Y, Wang L, Yu B, Ma Y. 2013. Genome sequence of a novel polymer-grade l-lactate-producing alkaliphile, Exiguobacterium sp. strain 8-11-1. Genome Announc. 1(4):e00616-13. doi:10.1128/genomeA.00616-13.

REFERENCES

  • 1. Collins MD, Lund BM, Farrow JAE, Schleifer KH. 1983. Chemotaxonomic study of an alkalophilic bacterium, Exiguobacterium aurantiacum gen. nov., sp. nov. J. Gen. Microbiol. 129:2037–2042 [Google Scholar]
  • 2. Vishnivetskaya TA, Kathariou S, Tiedje JM. 2009. The Exiguobacterium genus: biodiversity and biogeography. Extremophiles 13:541–555 [DOI] [PubMed] [Google Scholar]
  • 3. Tan L, Qu YY, Zhou JT, Li A, Gou M. 2009. Identification and characteristics of a novel salt-tolerant Exiguobacterium sp. for azo dyes decolorization. Appl. Biochem. Biotechnol. 159:728–738 [DOI] [PubMed] [Google Scholar]
  • 4. Lee DH, Oh KH, Kahng HY. 2009. Molecular analysis of antioxidant genes in the extremohalophile marine bacterium Exiguobacterium sp. CNU020. Biotechnol. Lett. 31:1245–1251 [DOI] [PubMed] [Google Scholar]
  • 5. Lee SH, Chung CW, Yu YJ, Rhee YH. 2009. Effect of alkaline protease-producing Exiguobacterium sp. YS1 inoculation on the solubilization and bacterial community of waste activated sludge. Bioresour. Technol. 100:4597–4603 [DOI] [PubMed] [Google Scholar]
  • 6. Carneiro AR, Ramos RT, Dall’Agnol H, Pinto AC, de Castro Soares S, Santos AR, Guimarães LC, Almeida SS, Baraúna RA, das Graças DA, Franco LC, Ali A, Hassan SS, Nunes CI, Barbosa MS, Fiaux KK, Aburjaile FF, Barbosa EG, Bakhtiar SM, Vilela D, Nóbrega F, dos Santos AL, Carepo MS, Azevedo V, Schneider MP, Pellizari VH, Silva A. 2012. Genome sequence of Exiguobacterium antarcticum B7, isolated from a biofilm in Ginger Lake, King George Island, Antarctica. J. Bacteriol. 194:6689–6690 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Jiang X, Xue Y, Wang A, Wang L, Zhang G, Zeng Q, Yu B, Ma Y. 22 June 2013. Efficient production of polymer-grade l-lactate by an alkaliphilic Exiguobacterium sp. strain under nonsterile open fermentation conditions. Bioresour. Technol. [Epub ahead of print.] 10.1016/j.biortech.2013.06.049 [DOI] [PubMed] [Google Scholar]
  • 8. Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 18:821–829 [DOI] [PMC free article] [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. 10.1186/1471-2164-9-75 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Pruitt KD, Tatusova T, Klimke W, Maglott DR. 2009. NCBI reference sequences: current status, policy and new initiatives. Nucleic Acids Res. 37:D32–D36. 10.1093/nar/gkn721 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Schattner P, Brooks AN, Lowe TM. 2005. The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs. Nucleic Acids Res. 33:W686–W689. 10.1093/nar/gki366 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Kanehisa M, Goto S. 2000. KEGG: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 28:27–30 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Ito M, Guffanti AA, Zemsky J, Ivey DM, Krulwich TA. 1997. Role of the nhaC-encoded Na+/H+ antiporter of alkaliphilic bacillus firmus OF4. J. Bacteriol. 179:3851–3857 [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES