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Design of Fungal Co-Cultivation Based on Comparative Metabolomics and Bioactivity for Discovery of Marine Fungal Agrochemicals
Microbial co-cultivation is employed for awakening silent biosynthetic gene clusters (BGCs) to enhance chemical diversity. However, the selection of appropriate partners for co-cultivation remains a challenge. Furthermore, competitive interactions involving the suppression of BGCs or upregulation of...
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Published in: | Marine drugs 2020-01, Vol.18 (2), p.73 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Microbial co-cultivation is employed for awakening silent biosynthetic gene clusters (BGCs) to enhance chemical diversity. However, the selection of appropriate partners for co-cultivation remains a challenge. Furthermore, competitive interactions involving the suppression of BGCs or upregulation of known, functional metabolite(s) during co-cultivation efforts is also common. Herein, we performed an alternative approach for targeted selection of the best co-cultivation pair. Eight marine sediment-derived fungi were classified as strong or weak, based on their anti-phytopathogenic potency. The fungi were co-cultured systematically and analyzed for their chemical profiles and anti-phytopathogenic activity. Based on enhanced bioactivity and a significantly different metabolite profile including the appearance of a co-culture specific cluster, the co-culture of
(strong) and
(weak) was prioritized for chemical investigation. Large-scale co-cultivation resulted in isolation of five polyketide type compounds: two 12-membered macrolides, dendrodolide E (
) and its new analog dendrodolide N (
), as well as two rare azaphilones spiciferinone (
) and its new analog 8a-hydroxy-spiciferinone (
). A well-known
-naphtho-γ-pyrone type mycotoxin, cephalochromin (
), whose production was specifically enhanced in the co-culture, was also isolated. Chemical structures of compounds
-
were elucidated by NMR, HRMS and [] analyses. Compound
showed the strongest anti-phytopathogenic activity against
and
with IC
values of 0.9 and 1.7 µg/mL, respectively. |
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ISSN: | 1660-3397 1660-3397 |
DOI: | 10.3390/md18020073 |