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Antifungal activity improved by coproduction of cyclodextrins and anabaenolysins in Cyanobacteria

Articolo
Data di Pubblicazione:
2015
Abstract:
Department of Chemistry, Nanoscience Center, University of Jyväskylä, FI-40014, Jyväskylä, Finland Cyclodextrins are cyclic oligosaccharides widely used in the pharmaceutical industry to improve drug delivery and to increase the solubility of hydrophobic compounds. Anabaenolysins are lipopeptides produced by cyanobacteria with potent lytic activity in cholesterolcontaining membranes. Here, we identified the 23- To 24-kb gene clusters responsible for the production of the lipopeptide anabaenolysin. The hybrid nonribosomal peptide synthetase and polyketide synthase biosynthetic gene cluster is encoded in the genomes of three anabaenolysin-producing strains of Anabaena.We detected previously unidentified strains producing known anabaenolysins A and B and discovered the production of new variants of anabaenolysins C and D. Bioassays demonstrated that anabaenolysins have weak antifungal activity against Candida albicans. Surprisingly, addition of the hydrophilic fraction of the whole-cell extracts increased the antifungal activity of the hydrophobic anabaenolysins. The fraction contained compounds identified by NMR as ?-, ?-, and ?-cyclodextrins, which undergo acetylation. Cyclodextrins have been used for decades to improve the solubility and bioavailability of many drugs including antifungal compounds. This study shows a natural example of cyclodextrins improving the solubility and efficacy of an antifungal compound in an ancient lineage of photosynthetic bacteria.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Bioactive compounds; Hydroxyamino fatty acid; Natural products; NRPS; PKS
Elenco autori:
DE BELLIS, Gianluca
Autori di Ateneo:
DE BELLIS GIANLUCA
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/301841
Pubblicato in:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-84946593619&origin=inward
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