Abstract
Here, we report the draft genome of cyanobacterium Leptolyngbya sp. KIOST-1 isolated from a microalgal culture pond in South Korea. The genome consists of 13 contigs containing 6,320,172 bp, and a total of 5,327 coding sequences were predicted. This genomic information will allow further exploitation of its biotechnological potential for alimentary purposes.
GENOME ANNOUNCEMENT
Cyanobacteria are photosynthetic prokaryotes, and hold promise as producers of sustainable bioresources for foods and other valuable products including bioenergy (1–3). However, selection of candidate strains for biotechnological applications has been a continuing challenge due to potential toxicity and low productivity. The genus Leptolyngbya which classified in the order Pseudanabaenales is filamentous cyanobacteria with a straight trichome, and known to be originated from various environments including extreme conditions (4). Therefore, several Leptolyngbya strains have recently been sequenced to understand its eco-physiological diversity (5–7). Recently, we reported on Leptolyngbya sp. KIOST-1 that possessed a number of advantageous characteristics for alimentary purposes with efficient productivity, high protein content, and lack of potential cytotoxicity (8). Here, we present its genome to exploit its biotechnological potential for industrial biomass production.
Genomic DNA was isolated using the DNeasy mini plant extraction kit (Qiagen) following the manufacturer’s protocols, and directly submitted for sequencing analysis. Genome sequencing was performed at Macrogen, Inc. (South Korea) using the Roche/454 pyrosequencing method on the Genome Sequencer FLX Titanium, and the obtained sequences were assembled using the GS De Novo Assembler software (v2.6). The resultant sequenced data consisted of a total of 366,508,458 bp and 560,014 reads with an average read length of 654.5 bp. Furthermore, the data included 548,755 assembled reads and 4,556 partially assembled reads. The de novo assembly resulted in eight scaffolds, and a total of 13 contigs that were longer than 500 bp were finally recovered after in silico finishing. The assembled draft genome was 6,320,172 bp, and its average G+C content was estimated to be 59.4%.
Genome annotation was acquired from the NCBI Prokaryotic Genome Annotation Pipeline (Bethesda, MD) and revealed 5,542 genes, 5,327 coding sequences, 162 pseudogenes, 7 rRNAs (4 for 5S, 2 for 16S, and 1 for 23S), 45 tRNAs, 1 noncoding RNA, and 26 frameshift genes. Additionally, gene ontology (GO) databases were used to functionally classify the predicted genes, and the results indicated that 23.6%, 25.5%, and 10.8% of the sequences included genes related to biological processes, molecular functions, and cellular components, respectively. However, more than 40% of the predicted genes failed to find a match in the GO database. In the GO category of biological processes, metabolic processes were the predominant subcategory, representing 38.1% of the genes. In the cellular component category, 20.7% of the genes were annotated as unknown, but 40.1% and 16.0% of the genes were associated with cell parts and membrane, respectively. Based on their molecular function, 44.9% of the genes were identified as being associated with catalytic activity.
Although no significant cytotoxicity was detected in our previous study (8), the entire genome of Leptolyngbya sp. KIOST-1 was scanned and no putative cyanotoxin genes were detected in it. This genomic information will contribute to better understanding for the genus Leptolyngbya, and allow further exploitation of its biotechnological potential for alimentary purposes.
Accession number(s).
This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under accession no. JQFA00000000. The version described in this paper is version JQFA01000000.1.
ACKNOWLEDGMENTS
This study was supported by a research grant from the Korea Institute of Ocean Science & Technology (PE99411) and partially supported by a research grant from the Marine Biotechnology Program funded by the Ministry of Oceans and Fisheries (PM59530) and by a research grant from the National Institute of Biological Resources funded by the Ministry of Environment (NIBR201530101) of the South Korean Government.
Footnotes
Citation Kim JH, Kang D-H. 2016. Draft genome sequence of Leptolyngbya sp. KIOST-1, a filamentous cyanobacterium with biotechnological potential for alimentary purposes. Genome Announc 4(5):e00984-16. doi:10.1128/genomeA.00984-16.
REFERENCES
- 1.Gantar M, Svirčev Z. 2008. Microalgae and cyanobacteria: food for thought. J Phycol 44:260–268. doi: 10.1111/j.1529-8817.2008.00469.x. [DOI] [PubMed] [Google Scholar]
- 2.Mata TM, Martins AA, Caetano NS. 2010. Microalgae for biodiesel production and other applications: a review. Renewable Sustain Energy Rev 14:217–232. doi: 10.1016/j.rser.2009.07.020. [DOI] [Google Scholar]
- 3.Prasanna R, Sood A, Jaiswal P, Nayak S, Gupta V, Chaudhary V, Joshi M, Natarajan C. 2010. Rediscovering cyanobacteria as valuable sources of bioactive compounds (Review) Appl Biochem Microbiol 46:119–134. doi: 10.1134/S0003683810020018. [DOI] [PubMed] [Google Scholar]
- 4.Komárek J. 2007. Phenotype diversity of the cyanobacterial genus Leptolyngbya in the maritime Antarctic. Pol Polar Res 28:211–231. [Google Scholar]
- 5.Shih PM, Wu D, Latifi A, Axen SD, Fewer DP, Talla E, Calteau A, Cai F, Tandeau de Marsac N, Rippka R, Herdman M, Sivonen K, Coursin T, Laurent T, Goodwin L, Nolan M, Davenport KW, Han CS, Rubin EM, Eisen JA, Woyke T, Gugger M, Kerfeld CA. 2013. Improving the coverage of the cyanobacterial phylum using diversity-driven genome sequencing. Proc Natl Acad Sci U S A 110:1053–1058. http://dx.doi.org/10.1073/pnas.1217107110. doi: 10.1073/pnas.1217107110. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Paul R, Jinkerson RE, Buss K, Steel J, Mohr R, Hess WR, Chen M, Fromme P. 2014. Draft genome sequence of the filamentous cyanobacterium Leptolyngbya sp. strain Heron Island J, exhibiting chromatic acclimation. Genome Announc 2(1):e01166-13. doi: 10.1128/genomeA.01166-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Shimura Y, Hirose Y, Misawa N, Osana Y, Katoh H, Yamaguchi H, Kawachi M. 2015. Comparison of the terrestrial cyanobacterium Leptolyngbya sp. NIES-2104 and the freshwater Leptolyngbya boryana PCC 6306 genomes. DNA Res 22:403–412 http://dx.doi.org/10.1093/dnares/dsv022. doi: 10.1093/dnares/dsv022. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Kim JH, CHoi W, Jeon SM, Kim T, Park A, Kim J, Heo SJ, Oh C, Shim WB, Kang DH. 2015. Isolation and characterization of Leptolyngbya sp. KIOST-1, a basophilic and euryhaline filamentous cyanobacterium from an open paddle-wheel raceway Arthrospira culture pond in Korea. J Appl Microbiol 119:1597–1612. doi: 10.1111/jam.12961. [DOI] [PubMed] [Google Scholar]
