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Published on: January 13, 2017
Penicillium roqueforti PR toxin gene cluster characterization
Pedro I Hidalgo1, Elisabeth Poirier1, Ricardo V Ullán2
1Université de Brest, EA 3882 Laboratoire Universitaire de Biodiversité et d'Ecologie Microbienne, IBSAM, ESIAB, Technopôle Brest-Iroise, Plouzané, 29280, Brest, France.
Researchers identified the gene cluster responsible for producing PR toxin, a potent mycotoxin from Penicillium roqueforti. Gene silencing confirmed key genes
Area of Science:
- Mycology
- Molecular Biology
- Biochemistry
Background:
- PR toxin is a highly toxic isoprenoid mycotoxin produced by Penicillium roqueforti.
- This mycotoxin poses risks when found in food and animal feed.
- Understanding its biosynthesis is crucial for managing its presence.
Purpose of the Study:
- To identify and characterize the biosynthetic gene cluster for PR toxin in Penicillium roqueforti.
- To elucidate the enzymatic steps involved in PR toxin production.
- To propose a PR toxin biosynthesis pathway.
Main Methods:
- In silico analysis to identify the gene cluster.
- Gene silencing of specific genes (ORF5, ORF6, ORF8).
- Quantification of PR toxin, eremofortin A, and B production in transformants.
Main Results:
- A 22.4-kb gene cluster with 11 open reading frames involved in PR toxin biosynthesis was identified.
- Silencing of three genes (encoding acetyltransferase and P450 monooxygenases) reduced PR toxin production by 20-40%.
- Eremofortin A and B production was affected by gene silencing, suggesting their role as intermediates.
Conclusions:
- The identified gene cluster and its encoded enzymes are essential for PR toxin biosynthesis.
- A novel PR toxin biosynthesis pathway is proposed.
- This research provides a foundation for controlling PR toxin contamination.
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