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Biological activities of new secondary metabolite produced by Streptomyces badius

Authors :
Dorota Gudanis
Aleksandra Rajnisz-Mateusiak
Joanna Ziemska
Katarzyna Jakubiec-Krześniak
Robert Kawęcki
Jolanta Solecka
Magdalena Postek
Source :
Proceedings of The 20th International Electronic Conference on Synthetic Organic Chemistry.
Publication Year :
2016
Publisher :
MDPI, 2016.

Abstract

Secondary metabolites obtained from Actinomycetales provide a potential source of many new antibacterial, antitumour, antifungal, antiviral, antiparasitic compounds and others. The majority of discovered substances are widely used as medicines for combating multidrug-resistant Gram-positive and Gram-negative bacterial strains, as well as in veterinary practice, agriculture and industry. Members of the Streptomyces genus are outstanding producers of already known secondary metabolites. In our study we isolated a new metabolite from Streptomyces badius fermentation broth. This compound, 2-acetamido-5-hydroxybenzoic acid (1) was already described in literature, however, not yet discovered as Streptomyces badius product. The compound was firstly isolated from fermentation broth and purified by chromatography methods (ion exchange resin DowexWX40, Solid Phase Extraction C18 Polar Plus; HPLC, dC18). Then, the chemical structure of metabolite was determined by 1H NMR, 13C NMR and 2D homo- and heteronuclear (1H-13C HSQC, 1H-13C HMBC) NMR. The molecular formula of (1), C9H9NO4 was identified by high resolution ESI-MS. The chemical structure was analyzed by the UV and IR methods, as well. Biological activities of 2-acetamido-5-hydroxybenzoic acid were evaluated. The compound shows moderate DD-peptidase 64-575 inhibitory activity as well as antioxidative properties (ABTS radical scavenging). Such chemical moiety may serve as model compound for further modern drug discovery and be a source of active substance in anti-ageing cosmetics.

Details

Database :
OpenAIRE
Journal :
Proceedings of The 20th International Electronic Conference on Synthetic Organic Chemistry
Accession number :
edsair.doi...........6956478ceb20ba4861eb0136a6971383
Full Text :
https://doi.org/10.3390/ecsoc-20-b006