Secondary Metabolites from Marine Endophytic Fungi: Emphasis on Recent Advances in Natural Product Research

Bramhachari, Pallaval Veera; Anju, S; Sheela, G. Mohana; Komaraiah, T. Raja; Peddaboina, Venkataiah; Prathyusha, A. M. V. N.

doi:10.1007/978-3-030-03589-1_15

Cited by 4 publications

(1 citation statement)

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“…Another endophytic fungus from a marine alga, Aspergillus nidulans var. acristatus , was found to be the producer of arugosins G and H, which showed significant antitumor activity [ 65 ]. Marine fungi from Talaromyces genus and Alternaria sp.…”

Section: Resultsmentioning

confidence: 99%

Metabolomic study of marine Streptomyces sp.: Secondary metabolites and the production of potential anticancer compounds

et al. 2020

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Resorting to a One Strain Many Compounds (OSMAC) approach, the marine Streptomyces sp. BRB081 strain was grown in six different media settings over 1, 2, 3 or 7 days. Extractions of mycelium and broth were conducted separately for each media and cultivation period by sonication using methanol/acetone 1:1 and agitation with ethyl acetate, respectively. All methanol/acetone and ethyl acetate crude extracts were analysed by HPLC-MS/MS and data treatment was performed through GNPS platform using MZmine 2 software. In parallel, the genome was sequenced, assembled and mined to search for biosynthetic gene clusters (BGC) of secondary metabolites using the AntiSMASH 5.0 software. Spectral library search tool allowed the annotation of desferrioxamines, fatty acid amides, diketopiperazines, xanthurenic acid and, remarkably, the cyclic octapeptides surugamides. Molecular network analysis allowed the observation of the surugamides cluster, where surugamide A and the protonated molecule corresponding to the B-E isomers, as well as two potentially new analogues, were detected. Data treatment through MZmine 2 software allowed to distinguish that the largest amount of surugamides was obtained by cultivating BRB081 in SCB medium during 7 days and extraction of culture broth. Using the same data treatment, a chemical barcode was created for easy visualization and comparison of the metabolites produced overtime in all media. By genome mining of BRB081 four regions of biosynthetic gene clusters of secondary metabolites were detected supporting the metabolic data. Cytotoxic evaluation of all crude extracts using MTT assay revealed the highest bioactivity was also observed for extracts obtained in the optimal conditions as those for surugamides production, suggesting these to be the main active compounds herein. This method allowed the identification of compounds in the crude extracts and guided the selection of best conditions for production of bioactive compounds.

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Section: Resultsmentioning

confidence: 99%