AI-Accelerated Structure Elucidation of Boavistamides A <b>–</b> C, Cyclic Depsipeptides from a Marine Filamentous Cyanobacterium Collected in Cabo Verde

Boavistamide A ( 1 ), a new alkyne-containing cyclic depsipeptide featuring the rare 3-amino-2-methyl-7-octynoic acid (AMOYA) moiety, was discovered along with two structurally related analogs, boavistamides B and C ( 2 and 3 ), from a filamentous marine cyanobacterium collected on Boa Vista Island, Cabo Verde. Their isolation was guided by antiplasmodial activity, GNPS MS/MS molecular networking, LC-MS profiling, and dereplication using the MarinLit database. The planar structures of boavistamides A–C ( 1 – 3 ) were elucidated through comprehensive HRMS and 1D/2D NMR analyses, with annotation support from AI-based tools SMART-NMR 2.1 and DeepSAT. The absolute configurations were established using Marfey’s analysis and l -Phe-OMe coupling, complemented by NMR-based conformational studies. Boavistamides A and B exhibited moderate antiplasmodial activity with no mammalian cell cytotoxicity. Microscopic observations and metagenomic binning identified the producer strain as belonging to the genus Okeania (Microcoleaceae). These results expand the chemical diversity of AMOYA-containing cyanobacterial metabolites and highlight the utility of integrated metabolomics and AI-assisted workflows for natural product discovery from environmental samples.

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Publication Details

Journal
Journal of Natural Products
Published
2026-06-24
DOI
https://doi.org/10.1021/acs.jnatprod.6c00391
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

AI-Accelerated Structure Elucidation of Boavistamides A – C, Cyclic Depsipeptides from a Marine Filamentous Cyanobacterium Collected in Cabo Verde

Byeol Ryu, Krittikorn Kümpornsin, Thaiz R. Teixeira, Case W. McNamara et al.
Journal of Natural Products
Microbial Natural Products and Biosynthesis
article

AI-Accelerated Structure Elucidation of Boavistamides A – C, Cyclic Depsipeptides from a Marine Filamentous Cyanobacterium Collected in Cabo Verde

Byeol Ryu, Krittikorn Kümpornsin, Thaiz R. Teixeira, Case W. McNamara, Evgenia Glukhov, Marine Cuau, Pedro N. Leão, Mariana Laureano de Souza, Nicole E. Avalon, Jehad Almaliti, William H. Gerwick, Elizabeth A. Winzeler, Adriana Rego, Joseph Chen, Conor R. Caffrey, Vitor Vasconcelos, Alma Trinidad-Javier, Mai Shingyoji
article en

Abstract

Boavistamide A ( 1 ), a new alkyne-containing cyclic depsipeptide featuring the rare 3-amino-2-methyl-7-octynoic acid (AMOYA) moiety, was discovered along with two structurally related analogs, boavistamides B and C ( 2 and 3 ), from a filamentous marine cyanobacterium collected on Boa Vista Island, Cabo Verde. Their isolation was guided by antiplasmodial activity, GNPS MS/MS molecular networking, LC-MS profiling, and dereplication using the MarinLit database. The planar structures of boavistamides A–C ( 1 – 3 ) were elucidated through comprehensive HRMS and 1D/2D NMR analyses, with annotation support from AI-based tools SMART-NMR 2.1 and DeepSAT. The absolute configurations were established using Marfey’s analysis and l -Phe-OMe coupling, complemented by NMR-based conformational studies. Boavistamides A and B exhibited moderate antiplasmodial activity with no mammalian cell cytotoxicity. Microscopic observations and metagenomic binning identified the producer strain as belonging to the genus Okeania (Microcoleaceae). These results expand the chemical diversity of AMOYA-containing cyanobacterial metabolites and highlight the utility of integrated metabolomics and AI-assisted workflows for natural product discovery from environmental samples.

Journal of Natural Products
Scripps Institution of Oceanography (US), Universidade do Porto (PT), University of California, Irvine (US), Mahidol University (TH), University of California San Diego (US), Scripps (United States) (US), California Institute for Biomedical Research (US), Center for Discovery (US), University of Montana (US)
Life below water
Openalex Percentile: Top 8%
Microbial Natural Products and Biosynthesis
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