AI Article Synopsis

  • The tropical marine cyanobacterium is found in the Indian and Western Tropical Pacific Oceans, known for producing unique and biologically active natural products.
  • Advanced computational methods, including the ORCA pipeline, were used to analyze samples and identify regional variations in natural product production.
  • The study identified doscadenamide A, a natural product linked to a larger family of compounds, showing potential as an anti-cancer agent when used with lipopolysaccharide (LPS), highlighting the importance of chemogeographic patterns in natural product discovery.

Article Abstract

The tropical marine cyanobacterium occupies a large geographic range across the Indian and Western Tropical Pacific Oceans and is a prolific producer of structurally unique and biologically active natural products. An ensemble of computational approaches, including the creation of the ORCA (Objective Relational Comparative Analysis) pipeline for flexible MS feature detection and multivariate analyses, were used to analyze various samples. The observed chemogeographic patterns suggested the production of regionally specific natural products by . Analyzing the drivers of these chemogeographic patterns allowed for the identification, targeted isolation, and structure elucidation of a regionally specific natural product, doscadenamide A (). Analyses of MS fragmentation patterns further revealed this natural product to be part of an extensive family of herein annotated, proposed natural structural analogs (doscadenamides B-J, 2-10); the ensemble of structures reflect a combinatorial biosynthesis using nonribosomal peptide synthetase (NRPS) and polyketide synthase (PKS) components. Compound displayed synergistic in vitro cancer cell cytotoxicity when administered with lipopolysaccharide (LPS). These discoveries illustrate the utility in leveraging chemogeographic patterns for prioritizing natural product discovery efforts.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7602127PMC
http://dx.doi.org/10.3390/md18100515DOI Listing

Publication Analysis

Top Keywords

natural product
16
chemogeographic patterns
12
product discovery
8
marine cyanobacterium
8
natural products
8
regionally specific
8
specific natural
8
natural
7
applying chemogeographic
4
chemogeographic strategy
4

Similar Publications

Nigrosporinol Sulfoxides A and B, Sulfur-Bridged Heterocyclic Sesquiterpenoids Produced by Cultures of the Fungus .

Org Lett

January 2025

Natural Product Research Unit, Department of Chemistry, and Center of Excellence for Innovation in Chemistry, Faculty of Science Khon Kaen University, Khon Kaen 40002, Thailand.

The sesquiterpenoids nigrosporinol sulfoxides A () and B () have been isolated from cultures of the endophytic fungus harvested from the sunchoke L. collected in Thailand. Nigrosporinol sulfoxides A () and B () have 4/5/5/5/7 heterocyclic skeletons featuring a sulfoxide bridge not previously found in a terpenoid natural product from any living source.

View Article and Find Full Text PDF

We report herein a robust enantioselective ring opening coupling of oxabenzonorbornadienes via Pd(II)-catalyzed domino cyclization of alkynylanilines, which features the formation of three covalent bonds and two contiguous stereocenters with excellent enantio- and diastereoselectivity and a broad substrate scope. The good functional group tolerance of this domino desymmetrization strategy enables efficient late-stage transformation of natural product-derived alkynylanilines. The resulting indolated dihydronaphthols could serve as a valuable platform to streamline the diversity-oriented synthesis of other valuable enantioenriched tetrahydronaphthalene derivatives.

View Article and Find Full Text PDF

In the last few years, many efforts have been devoted to the recovery and valorization of olive oil by-products because of their potentially high biological value. The olive mill wastewater (OMWW), a dark-green brown colored liquid that mainly consists of fruit vegetation water, is particularly exploited in this regard for its great content in phenolic compounds with strong antioxidant properties. In our previous work, we produced different OMWW fractions enriched in hydroxytyrosol- and hydroxytyrosol/oleuropein (i.

View Article and Find Full Text PDF

The proteomic response of to amphotericin B (AmB) reveals the involvement of the RTA-like protein RtaA in AmB resistance.

Microlife

December 2024

Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology, Hans Knöll Institute (HKI), Adolf-Reichwein-Str. 23, 07745 Jena, Germany.

The polyene antimycotic amphotericin B (AmB) and its liposomal formulation AmBisome belong to the treatment options of invasive aspergillosis caused by . Increasing resistance to AmB in clinical isolates of species is a growing concern, but mechanisms of AmB resistance remain unclear. In this study, we conducted a proteomic analysis of exposed to sublethal concentrations of AmB and AmBisome.

View Article and Find Full Text PDF

In October and December 2024, circulating vaccine-derived poliovirus type 2 (cVDPV2) was detected from two wastewater samples in Poland during routine environmental surveillance. The first isolate was characterised and matched previous cVDPV2 isolates detected in Spain in September, as well as in Germany, Finland, and the United Kingdom in November and December 2024. In response to the event, active surveillance for acute flaccid paralysis (AFP) has been strengthened, and the frequency of environmental sample collection has been increased.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!