The ruddy panus, scientifically Panus rudis, is a fungus from the family of stem pore relatives. It is one of the first colonizers of dead deciduous wood, prefers sun-exposed locations and can survive longer dry periods without damage.
However, something else makes it interesting for the pharmaceutical industry. It produces panepoxydone, which belongs to the epoxycyclohexenone (ECH) family of substances. These natural substances are known for their bioactivity.
Panepoxydone is used in biomedical research to interrupt cellular signaling pathways that play a role in inflammation. In addition, studies with panepoxydone have shown an antitumor effect against various breast cancer cells as well as antimicrobial effects.
Decoding fungus
The chemical synthesis of ECHs is difficult, so it is necessary to resort to the biosynthesis of the substances. However, while the enzymes responsible for ECH synthesis in bacteria and tubular fungi (ascomycetes) are already known, this was not previously the case with the class of fungi known as basidiomycetes.
“Even though we know that organisms produce approximately the same active substances, we cannot assume that they do it in the same way,” explains Dirk Hoffmeister, Professor of Pharmaceutical Microbiology at the University of Jena and group leader at the Leibniz-HKI.
Professor Yan-Long Yang, first author of the study, came to the University of Jena from Lanzhou University in China as part of a Humboldt Research Fellowship. Together with Dirk Hoffmeister’s team, he investigated the biosynthesis of panepoxydone in more detail and discovered the enzyme PanH, as revealed in Angewandte Chemie.
Multiple paths
PanH, an enzyme of the cytochrome P450 group, catalyzes the selective epoxidation of cyclohexenones, which is difficult to achieve by chemical synthesis but is essential for the efficacy of the substances.
“The collaboration with Yan-Long Yang was very productive. The exchange of knowledge and methodology worked very well in both directions and both sides made good progress,” Hoffmeister reports.
The result confirms the assumption that not all similar active substances have to be produced by the organisms in the same way. The epoxidation of ECHs in basidiomycetes actually developed in parallel with bacteria and ascomycetes and uses different enzymes.
Multi-talented enzyme
“The next question Yang asked himself was whether the enzyme can also carry out this reaction with other molecules,” reports Hoffmeister.
“And this is the really relevant aspect of the study: if you give the enzyme substrates that do not occur naturally in the cell, epoxidation usually occurs anyway, so the enzyme works quite unspecifically.”
By varying the side chain of the substrates, the team was able to produce a small library of substances. “This enabled us to show that the enzyme is a useful and versatile catalyst with biotechnological significance.” Epoxidation is insertion of an oxygen atom into a molecule, and because single oxygen atoms are quite reactive, this is a huge challenge that needs to be overcome by learning how nature does it. This is peculiar interesting as many pharmaceuticals contain oxygen.
“The long-term goal is to use this enzyme to produce a larger library of substances and test them for improved and more specific activities in the hope of a pharmaceutical application,” concludes Hoffmeister.
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