OSMAC method to assess impact of culture parameters on metabolomic diversity and biological activity of marine-derived Actinobacteria
Le Loarer, A.; Dufosse, L.; Bignon, J.; Frédérich, M.; Ledoux, A.; Fouillaud, M.; Gauvin-Bialecki, A. (2024). OSMAC method to assess impact of culture parameters on metabolomic diversity and biological activity of marine-derived Actinobacteria. Mar. Drugs 22(1): 23. https://dx.doi.org/10.3390/md22010023
In: Marine Drugs. Molecular Diversity Preservation International (MDPI): Basel. ISSN 1660-3397; e-ISSN 1660-3397, more
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| Keywords |
Actinobacteria [WoRMS]; Micromonospora Orskov, 1923 [WoRMS]; Salinispora arenicola Maldonado, Fenical, Jensen, Kauffman, Mincer, Ward, Bull & Goodfellow, 2005 [WoRMS]
Marine/Coastal |
| Author keywords |
OSMAC method; Salinispora; Micromonospora; marine-derived actinobacteria; molecular network; specialized metabolites; cytotoxic activity; antiplasmodial activity |
| Authors | | Top |
- Le Loarer, A.
- Dufosse, L.
- Bignon, J.
- Frédérich, M., more
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- Ledoux, A., more
- Fouillaud, M.
- Gauvin-Bialecki, A.
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| Abstract |
Actinobacteria are known for their production of bioactive specialized metabolites, but they are still under-exploited. This study uses the “One Strain Many Compounds” (OSMAC) method to explore the potential of three preselected marine-derived actinobacteria: Salinispora arenicola (SH-78) and two Micromonospora sp. strains (SH-82 and SH-57). Various parameters, including the duration of the culture and the nature of the growth medium, were modified to assess their impact on the production of specialized metabolites. This approach involved a characterization based on chemical analysis completed with the construction of molecular networks and biological testing to evaluate cytotoxic and antiplasmodial activities. The results indicated that the influence of culture parameters depended on the studied species and also varied in relation with the microbial metabolites targeted. However, common favorable parameters could be observed for all strains such as an increase in the duration of the culture or the use of the A1 medium. For Micromonospora sp. SH-82, the solid A1 medium culture over 21 days favored a greater chemical diversity. A rise in the antiplasmodial activity was observed with this culture duration, with a IC50 twice as low as for the 14-day culture. Micromonospora sp. SH-57 produced more diverse natural products in liquid culture, with approximately 54% of nodes from the molecular network specifically linked to the type of culture support. Enhanced biological activities were also observed with specific sets of parameters. Finally, for Salinispora arenicola SH-78, liquid culture allowed a greater diversity of metabolites, but intensity variations were specifically observed for some metabolites under other conditions. Notably, compounds related to staurosporine were more abundant in solid culture. Consequently, in the range of the chosen parameters, optimal conditions to enhance metabolic diversity and biological activities in these three marine-derived actinobacteria were identified, paving the way for future isolation works.
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