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Published on: December 2, 2022
Alkaloids from Marine Fungi: Promising Antimicrobials
Thomas Willems1, Maarten L De Mol1, Aleksandar De Bruycker1
1Centre for Industrial Biotechnology and Biocatalysis (InBio.be), Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000 Ghent, Belgium.
Abstract:
Resistance of pathogenic microorganisms against antimicrobials is a major threat to contemporary human society. It necessitates a perpetual influx of novel antimicrobial compounds. More specifically, Gram- pathogens emerged as the most exigent danger. In our continuing quest to search for novel antimicrobial molecules, alkaloids from marine fungi show great promise. However, current reports of such newly discovered alkaloids are often limited to cytotoxicity studies and, moreover, neglect to discuss the enigma of their biosynthesis. Yet, the latter is often a prerequisite to make them available through sufficiently efficient processes. This review aims to summarize novel alkaloids with promising antimicrobial properties discovered in the past five years and produced by marine fungi. Several discovery strategies are summarized, and knowledge gaps in biochemical production routes are identified. Finally, links between the structure of the newly discovered molecules and their activity are proposed. Since 2015, a total of 35 new antimicrobial alkaloids from marine fungi were identified, of which 22 showed an antibacterial activity against Gram- microorganisms. Eight of them can be classified as narrow-spectrum Gram- antibiotics. Despite this promising ratio of novel alkaloids active against Gram- microorganisms, the number of newly discovered antimicrobial alkaloids is low, due to the narrow spectrum of discovery protocols that are used and the fact that antimicrobial properties of newly discovered alkaloids are barely characterized. Alternatives are proposed in this review. In conclusion, this review summarizes novel findings on antimicrobial alkaloids from marine fungi, shows their potential as promising therapeutic candidates, and hints on how to further improve this potential.
Insights
Marine fungi yield novel alkaloids with potent antimicrobial activity, particularly against challenging Gram-negative pathogens. Further research into biosynthesis is crucial for developing new antibiotics to combat antimicrobial resistance.
Area of Science:
- Marine natural products chemistry
- Microbiology
- Drug discovery
Background:
- Antimicrobial resistance (AMR) is a critical global health threat, demanding new therapeutic agents.
- Gram-negative pathogens present a significant challenge due to their intrinsic resistance mechanisms.
- Marine-derived alkaloids are a promising source for novel antimicrobial compounds.
Purpose of the Study:
- To review novel antimicrobial alkaloids from marine fungi discovered in the last five years.
- To summarize discovery strategies and identify gaps in understanding their biosynthesis.
- To explore structure-activity relationships of these compounds.
Main Methods:
- Literature review of studies published since 2015 focusing on marine fungal alkaloids with antimicrobial properties.
- Analysis of reported discovery methods and characterization of antimicrobial activity, especially against Gram-negative bacteria.
- Identification of knowledge gaps concerning biosynthetic pathways.
Main Results:
- 35 new antimicrobial alkaloids from marine fungi were identified since 2015.
- 22 of these alkaloids exhibited antibacterial activity against Gram-negative microorganisms.
- Eight alkaloids demonstrated narrow-spectrum activity against Gram-negative bacteria, highlighting their potential as targeted antibiotics.
Conclusions:
- Marine fungi are a valuable source of novel antimicrobial alkaloids with significant potential against Gram-negative pathogens.
- Current discovery and characterization methods are limited, hindering the identification and development of new drug candidates.
- Further investigation into biosynthesis and broader screening protocols are essential to unlock the full therapeutic potential of these compounds.
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