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. 2016 Mar 10;4(2):e00098-16. doi: 10.1128/genomeA.00098-16

Draft Genome Sequences of Rhodosporidium toruloides Strains ATCC 10788 and ATCC 10657 with Compatible Mating Types

Jie Hu 1, Lianghui Ji 1,
PMCID: PMC4786659  PMID: 26966203

Abstract

Rhodosporidium toruloides ATCC 10788 (haploid, A1 mating type) and ATCC 10657 (haploid, A2 mating type) were derived from the same diploid parent strain Rhodotorula glutinis ATCC 90781 and are important strains for metabolic engineering. Draft genome sequences of both strains are reported here. The current assembly of strain ATCC 10788 comprises 61 scaffolds with a total size of 20.75 Mbp and a GC content of 62.01%, while that of strain ATCC 10657 comprises 137 scaffolds with a total size of 21.49 Mbp and a GC content of 61.81%. Genome annotation predicts 7,730 and 7,800 protein encoding genes for strain ATCC 10788 and strain ATCC 10657, respectively.

GENOME ANNOUNCEMENT

Rhodosporidium toruloides has attracted increasing interest since the 1980s because of its capability for high-cell-density fermentation and high-level lipid production (13). It is a promising production host for renewable fuels and chemicals. Four genome sequences of R. toruloides strains have been published since 2012, i.e., MTCC 457 (4), NP 11 (5), CECT 1137 (6), and ATCC 204091 (previously Rhodotorula glutinis) (7). Haploid strains ATCC 10788 and ATCC 10657, obtained from the American Type Culture Collection, were derived from the same parent strain Rhodotorula glutinis ATCC 90781 with A1 and A2 mating types, respectively, and have been targets for metabolic engineering for the production of high-value bioproducts (810).

Whole-genome sequencing was carried out by Macrogen, Inc. (Republic of Korea) with the Illumina HiSeq 2000 platform using paired-end (insert length of 200 bp) and mate-pair (10-kb insert) libraries. Approximately 5 Gb of raw data (101-bp reads with about 100× sequencing depth) were generated from each strain. Several de novo assemblies, like SOAPdenovo (11), ALLPATHS-LG (12), CLC genomics workbench (Qiagen), Velvet (13), ABySS (14), IDBA-UD (15), and MaSuRCA (16), were used to perform the assembly. The best assemblies (by ALLPATHS-LG) were evaluated and chosen by the quality assessment tool for genome assemblies (QUAST) (17). The genes were predicted by GeneMark-ES (18) and MAKER2 (19). Gene functions and evolutionary relationship were identified by BLAST (20) against the NCBI nonredundant databases (nt and nr).

The draft genome sequence of ATCC 10788 comprises 61 scaffolds with a total size of 20.75 Mbp and a GC content of 62.01%, while that of strain ATCC 10657 comprises 137 scaffolds, with a total size of 21.49 Mbp and a GC content of 61.81%. A total of 7,730 genes for strain ATCC 10788 and 7,800 genes for strain ATCC 10657 were predicted by GeneMark-ES without a reference annotated genome, whereas 7,181 and 7,085 for ATCC 10788 and ATCC 10657, respectively, were predicted by MAKER2 based on the Rhodotorula glutinis ATCC 204091 protein database. A comparison of the genome assemblies to published ones by QUAST (genome fraction %) reveals that 98.78 to 99.63% of contig bases of ATCC 10788 could be aligned to the genome of MTCC 457 (4), NP 11 (5), or CECT 1137 (6), while 0.14% could be aligned to the genome of ATCC 204091 (7). On the other hand, 99.51% of the contig bases of ATCC 10657 could be aligned to the genome of ATCC 204091, but 0.11 to 0.16% could be aligned to the genome of MTCC 457 (4), NP 11 (5), or CECT 1137 (6). These data suggest that R. toruloides of different mating types have diversified extensively in nucleotide sequences and gene organizations.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession numbers LNQQ00000000 and LNKU00000000.

ACKNOWLEDGMENTS

This work was supported by the Singapore National Research Foundation under CRP award no. NRF-CRP8-2011-02 and by the Temasek Trust.

Footnotes

Citation Hu J, Ji L. 2016. Draft genome sequences of Rhodosporidium toruloides strains ATCC 10788 and ATCC 10657 with compatible mating types. Genome Announc 4(2):e00098-16. doi:10.1128/genomeA.00098-16.

REFERENCES

  • 1.Zhao X, Hu C, Wu S, Shen H, Zhao ZK. 2011. Lipid production by Rhodosporidium toruloides Y4 using different substrate feeding strategies. J Ind Microbiol Biotechnol 38:627–632. doi: 10.1007/s10295-010-0808-4. [DOI] [PubMed] [Google Scholar]
  • 2.Li Y, Zhao Z, Bai F. 2007. High-density cultivation of oleaginous yeast Rhodosporidium toruloides Y4 in fed-batch culture. Enzyme Microb Technol 41:312–317. doi: 10.1016/j.enzmictec.2007.02.008. [DOI] [Google Scholar]
  • 3.Pan JG, Kwak MY, Rhee JS. 1986. High density cell culture of rhodotorula glutinis using oxygen-enriched air. Biotechnol Lett 8:715–718. doi: 10.1007/BF01032568. [DOI] [Google Scholar]
  • 4.Kumar S, Kushwaha H, Bachhawat AK, Raghava GP, Ganesan K. 2012. Genome sequence of the oleaginous red yeast Rhodosporidium toruloides MTCC 457. Eukaryot Cell 11:1083–1084. doi: 10.1128/EC.00156-12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Zhu Z, Zhang S, Liu H, Shen H, Lin X, Yang F, Zhou YJ, Jin G, Ye M, Zou H, Zhao ZK. 2012. A multi-omic map of the lipid-producing yeast Rhodosporidium toruloides. Nat Commun 3:1112. doi: 10.1038/ncomms2112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Morin N, Calcas X, Devillers H, Durrens P, Sherman DJ, Nicaud JM, Neuvéglise C. 2014. Draft genome sequence of Rhodosporidium toruloides CECT1137, an oleaginous yeast of biotechnological interest. Genome Announc 2(4):e00641-14. doi: 10.1128/genomeA.00641-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Paul D, Magbanua Z, Arick M II, French T, Bridges SM, Burgess SC, Lawrence ML. 2014. Genome sequence of the oleaginous yeast Rhodotorula glutinis ATCC 204091. Genome Announc 2(1):e00046-14. doi: 10.1128/genomeA.00046-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Liu Y, Koh CM, Ngoh ST, Ji L. 2015. Engineering an efficient and tight d-amino acid-inducible gene expression system in Rhodosporidium/Rhodotorula species. Microb Cell Fact 14:170. doi: 10.1186/s12934-015-0357-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Koh CM, Liu Y, Moehninsi, Du M, Ji L. 2014. Molecular characterization of KU70 and KU80 homologues and exploitation of a KU70-deficient mutant for improving gene deletion frequency in Rhodosporidium toruloides. BMC Microbiol 14:50. doi: 10.1186/1471-2180-14-50. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Liu Y, Koh CM, Sun L, Hlaing MM, Du M, Peng N, Ji L. 2013. Characterization of glyceraldehyde-3-phosphate dehydrogenase gene RtGPD1 and development of genetic transformation method by dominant selection in oleaginous yeast Rhodosporidium toruloides. Appl Microbiol Biotechnol 97:719–729. doi: 10.1007/s00253-012-4223-9. [DOI] [PubMed] [Google Scholar]
  • 11.Xie Y, Wu G, Tang J, Luo R, Patterson J, Liu S, Huang W, He G, Gu S, Li S, Zhou X, Lam TW, Li Y, Xu X, Wong GK, Wang J. 2014. SOAPdenovo-Trans: de novo transcriptome assembly with short RNA-Seq reads. BioInformatics 30:1660–1666. doi: 10.1093/bioinformatics/btu077. [DOI] [PubMed] [Google Scholar]
  • 12.Gnerre S, Maccallum I, Przybylski D, Ribeiro FJ, Burton JN, Walker BJ, Sharpe T, Hall G, Shea TP, Sykes S, Berlin AM, Aird D, Costello M, Daza R, Williams L, Nicol R, Gnirke A, Nusbaum C, Lander ES, Jaffe DB. 2011. High-quality draft assemblies of mammalian genomes from massively parallel sequence data. Proc Natl Acad Sci USA 108:1513–1518. doi: 10.1073/pnas.1017351108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18:821–829. doi: 10.1101/gr.074492.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Simpson JT, Wong K, Jackman SD, Schein JE, Jones SJ, Birol I. 2009. ABySS: a parallel assembler for short read sequence data. Genome Res 19:1117–1123. doi: 10.1101/gr.089532.108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Peng Y, Leung HC, Yiu SM, Chin FY. 2012. IDBA-UD: a de novo assembler for single-cell and metagenomic sequencing data with highly uneven depth. BioInformatics 28:1420–1428. doi: 10.1093/bioinformatics/bts174. [DOI] [PubMed] [Google Scholar]
  • 16.Zimin AV, Marçais G, Puiu D, Roberts M, Salzberg SL, Yorke JA. 2013. The MaSuRCA genome assembler. Bioinformatics 29:2669–2677. doi: 10.1093/bioinformatics/btt476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Gurevich A, Saveliev V, Vyahhi N, Tesler G. 2013. QUAST: quality assessment tool for genome assemblies. Bioinformatics 29:1072–1075. doi: 10.1093/bioinformatics/btt086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Borodovsky M, Lomsadze A. 2011. Eukaryotic gene prediction using GeneMark.hmm-E and GeneMark-ES. Curr Protoc Bioinformatics 35:4.6.1–4.6.10. doi: 10.1002/0471250953.bi0406s35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Holt C, Yandell M. 2011. MAKER2: an annotation pipeline and genome-database management tool for second-generation genome projects. BMC Bioinformatics 12:491. doi: 10.1186/1471-2105-12-491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, Madden TL. 2009. BLAST+: architecture and applications. BMC Bioinformatics 10:421. doi: 10.1186/1471-2105-10-421. [DOI] [PMC free article] [PubMed] [Google Scholar]

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