Journal of Industrial Microbiology & Biotechnology

, Volume 36, Issue 9, pp 1199–1213

Chemical induction of silent biosynthetic pathway transcription in Aspergillus niger

  • K. M. Fisch
  • A. F. Gillaspy
  • M. Gipson
  • J. C. Henrikson
  • A. R. Hoover
  • L. Jackson
  • F. Z. Najar
  • H. Wägele
  • R. H. Cichewicz
Original Paper

DOI: 10.1007/s10295-009-0601-4

Cite this article as:
Fisch, K.M., Gillaspy, A.F., Gipson, M. et al. J Ind Microbiol Biotechnol (2009) 36: 1199. doi:10.1007/s10295-009-0601-4

Abstract

Manipulation of the fungal epigenome is hypothesized to be an effective method for accessing natural products from silent biosynthetic pathways. A library of epigenetic modifiers was tested using the fungus Aspergillus niger to determine the impact of small-molecule inhibitors on reversing the transcriptional suppression of biosynthetic genes involved in polyketide (PKS), non-ribosomal peptide (NRPS), and hybrid PKS-NRPS (HPN) production. Examination of expressed sequence tag libraries from A. niger demonstrated that >70% of its PKS-, NRPS-, and HPN-encoding gene clusters were transcriptionally suppressed under standard laboratory culture conditions. Using a chemical epigenetic methodology, we showed that treatment of A. niger with suberoylanilide hydroxamic acid and 5-azacytidine led to the transcriptional upregulation of many secondary-metabolite-encoding biosynthetic gene clusters. Chemical epigenetic modifiers exhibited positional biases for upregulating chromosomally distal gene clusters. In addition, a phylogenetic-based preference was noted in the upregulation of reducing clade I PKS gene clusters, while reducing clade IV PKS gene clusters were largely unaffected. Manipulating epigenetic features in fungi is a powerful method for accessing the products of silent biosynthetic pathways. Moreover, this approach can be readily incorporated into modern microbial screening operations.

Keywords

Aspergillus nigerChemical epigeneticsFungiGene expressionNatural products

Supplementary material

10295_2009_601_MOESM1_ESM.docx (138 kb)
Supplementary material 1 (DOCX 137 kb)

Copyright information

© Society for Industrial Microbiology 2009

Authors and Affiliations

  • K. M. Fisch
    • 1
  • A. F. Gillaspy
    • 2
  • M. Gipson
    • 2
  • J. C. Henrikson
    • 3
  • A. R. Hoover
    • 3
  • L. Jackson
    • 2
  • F. Z. Najar
    • 4
  • H. Wägele
    • 5
  • R. H. Cichewicz
    • 3
    • 6
  1. 1.School of ChemistryUniversity of BristolBristolUK
  2. 2.Laboratory for Genomics and Bioinformatics, Department of Microbiology and ImmunologyUniversity of Oklahoma Health Sciences CenterOklahoma CityUSA
  3. 3.Natural Products Discovery Group, Department of Chemistry and BiochemistryUniversity of OklahomaNormanUSA
  4. 4.Department of Chemistry and BiochemistryUniversity of OklahomaNormanUSA
  5. 5.Zoologisches Forschungsmuseum Alexander KoenigBonnGermany
  6. 6.Graduate Program in Ecology and Evolutionary BiologyUniversity of OklahomaNormanUSA