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Aspergillus hancockii sp. nov., a biosynthetically talented fungus endemic to southeastern Australian soils.
Pitt, John I; Lange, Lene; Lacey, Alastair E; Vuong, Daniel; Midgley, David J; Greenfield, Paul; Bradbury, Mark I; Lacey, Ernest; Busk, Peter K; Pilgaard, Bo; Chooi, Yit-Heng; Piggott, Andrew M.
Affiliation
  • Pitt JI; Commonwealth Scientific and Industrial Research Organisation, North Ryde, Australia.
  • Lange L; Department of Chemical and Biochemical Engineering, Technical University of Denmark, Lyngby, Denmark.
  • Lacey AE; Microbial Screening Technologies, Smithfield, Australia.
  • Vuong D; Microbial Screening Technologies, Smithfield, Australia.
  • Midgley DJ; Commonwealth Scientific and Industrial Research Organisation, North Ryde, Australia.
  • Greenfield P; Commonwealth Scientific and Industrial Research Organisation, North Ryde, Australia.
  • Bradbury MI; Commonwealth Scientific and Industrial Research Organisation, North Ryde, Australia.
  • Lacey E; Microbial Screening Technologies, Smithfield, Australia.
  • Busk PK; Department of Chemical and Biochemical Engineering, Technical University of Denmark, Lyngby, Denmark.
  • Pilgaard B; Department of Chemical and Biochemical Engineering, Technical University of Denmark, Lyngby, Denmark.
  • Chooi YH; School of Chemistry and Biochemistry, University of Western Australia, Crawley, Australia.
  • Piggott AM; Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney NSW, Australia.
PLoS One ; 12(4): e0170254, 2017.
Article in En | MEDLINE | ID: mdl-28379953
ABSTRACT
Aspergillus hancockii sp. nov., classified in Aspergillus subgenus Circumdati section Flavi, was originally isolated from soil in peanut fields near Kumbia, in the South Burnett region of southeast Queensland, Australia, and has since been found occasionally from other substrates and locations in southeast Australia. It is phylogenetically and phenotypically related most closely to A. leporis States and M. Chr., but differs in conidial colour, other minor features and particularly in metabolite profile. When cultivated on rice as an optimal substrate, A. hancockii produced an extensive array of 69 secondary metabolites. Eleven of the 15 most abundant secondary metabolites, constituting 90% of the total area under the curve of the HPLC trace of the crude extract, were novel. The genome of A. hancockii, approximately 40 Mbp, was sequenced and mined for genes encoding carbohydrate degrading enzymes identified the presence of more than 370 genes in 114 gene clusters, demonstrating that A. hancockii has the capacity to degrade cellulose, hemicellulose, lignin, pectin, starch, chitin, cutin and fructan as nutrient sources. Like most Aspergillus species, A. hancockii exhibited a diverse secondary metabolite gene profile, encoding 26 polyketide synthase, 16 nonribosomal peptide synthase and 15 nonribosomal peptide synthase-like enzymes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aspergillus / Fungi Type of study: Prognostic_studies Country/Region as subject: Oceania Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aspergillus / Fungi Type of study: Prognostic_studies Country/Region as subject: Oceania Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Type: Article Affiliation country: Australia