Comparative genomics of citric-acid-producing Aspergillus niger ATCC 1015 versus enzyme-producing CBS 513.88

  1. Scott E. Baker4,20
  1. 1Center for Microbial Biotechnology, Department of Systems Biology, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark;
  2. 2Section Fungal Genomics, Laboratory of Microbiology, Wageningen University, Dreijenplein 10, 6703 HB Wageningen, The Netherlands;
  3. 3DSM Biotechnology Center, 2600 MA Delft, The Netherlands;
  4. 4Fungal Biotechnology Team, Pacific Northwest National Laboratory, Richland, Washington 99352, USA;
  5. 5Biomax Informatics AG, D-82152 Martinsried, Germany;
  6. 6Novozymes Inc., Davis, California 95616, USA;
  7. 7Molecular Microbiology and Genetics, Georg-August University, D-37077 Goettingen, Germany;
  8. 8Departamento de Genetica, Universidad de Sevilla, E-41080 Sevilla, Spain;
  9. 9DSM Nutritional Products, 2600 MA Delft, The Netherlands;
  10. 10Novozymes A/S, Hallas Alle 1, BD3.44, DK-4400 Kalundborg, Denmark;
  11. 11CBS Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands;
  12. 12Centre for Structural and Functional Genomics, Concordia University, Montreal, QC, Canada H4B 1R6;
  13. 13Chr. Hansen A/S, Bøge Allé 10-12, DK-2970 Hørsholm, Denmark;
  14. 14U.S. Department of Energy Joint Genome Institute, Walnut Creek, California 94598, USA;
  15. 15Joint Genome Institute, Stanford Human Genome Center, Palo Alto, California 94304, USA;
  16. 16Research Area of Gene Technology and Applied Biochemistry, Institute of Chemical Engineering, Vienna University of Technology, Getreidemarkt 9-1665, A-1060 Vienna, Austria;
  17. 17Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA;
  18. 18Department of Biology, University of New Mexico, Albuquerque, New Mexico 87131, USA
    • 19 Present address: Systems Biology, Department of Chemical and Biological Engineering, Chalmers University of Technology, SE-41296 Göteborg, Sweden.

    Abstract

    The filamentous fungus Aspergillus niger exhibits great diversity in its phenotype. It is found globally, both as marine and terrestrial strains, produces both organic acids and hydrolytic enzymes in high amounts, and some isolates exhibit pathogenicity. Although the genome of an industrial enzyme-producing A. niger strain (CBS 513.88) has already been sequenced, the versatility and diversity of this species compel additional exploration. We therefore undertook whole-genome sequencing of the acidogenic A. niger wild-type strain (ATCC 1015) and produced a genome sequence of very high quality. Only 15 gaps are present in the sequence, and half the telomeric regions have been elucidated. Moreover, sequence information from ATCC 1015 was used to improve the genome sequence of CBS 513.88. Chromosome-level comparisons uncovered several genome rearrangements, deletions, a clear case of strain-specific horizontal gene transfer, and identification of 0.8 Mb of novel sequence. Single nucleotide polymorphisms per kilobase (SNPs/kb) between the two strains were found to be exceptionally high (average: 7.8, maximum: 160 SNPs/kb). High variation within the species was confirmed with exo-metabolite profiling and phylogenetics. Detailed lists of alleles were generated, and genotypic differences were observed to accumulate in metabolic pathways essential to acid production and protein synthesis. A transcriptome analysis supported up-regulation of genes associated with biosynthesis of amino acids that are abundant in glucoamylase A, tRNA-synthases, and protein transporters in the protein producing CBS 513.88 strain. Our results and data sets from this integrative systems biology analysis resulted in a snapshot of fungal evolution and will support further optimization of cell factories based on filamentous fungi.

    Footnotes

    • 20 Corresponding author.

      E-mail scott.baker{at}pnl.gov; fax (509) 372-4732.

    • [Supplemental material is available for this article. The A. niger ATCC 1015 whole genome sequence has been submitted to GenBank (http://www.ncbi.nlm.nih.gov/genbank/) under accession no. ACJE00000000. The sequence data from the phylogeny study have been submitted to GenBank under accession nos. GU296686–GU296739. The microarray data from this study have been submitted to the NCBI Gene Expression Omnibus (GEO) (http://www.ncbi.nlm.nih.gov/geo/) under series accession no. GSE10983. The dsmM_ANIGERa_coll511030F library and platform information have been submitted to GEO under accession no. GPL6758.]

    • Article published online before print. Article, supplemental material, and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.112169.110.

    • Received July 8, 2010.
    • Accepted March 9, 2011.

    Freely available online through the Genome Research Open Access option.

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