Isolation and structure elucidation of aromatic polyketides from marine actinomycete with antibiofilm activity against Staphylococcus aureus and Escherichia coli
Paper ID : 1025-ISCHU
Authors
Aya Ramadan Mahmoud *1, Sally Ali2, Hasan Ebrahim3, Ali Hebishy4, Ehab Essawy5, Mohamed Saleh Abdelfattah6
1Science faculty helwan university
2Botany and Microbiology Department, Faculty of Science, Helwan University,
3Faculty of Pharmacy, Helwan University, Ain Helwan
4n University Chemistry Department, Faculty of Science, Helwan University, Ain Helwan, Cairo, Egypt.
5Chemistry Department, Faculty of Science, Helwan University,
6Natural Products Research Unit (NPRU), Chemistry Department, Faculty of Science, Helwan University, Egypt
Abstract
Three pigmented secondary metabolites tetracenomycin D (1), resistomycin (2), and resistoflavin (3) were isolated from Streptomyces sp. EG1 and their antibiofilm activities were evaluated against Staphylococcus aureus and Escherichia coli. The isolated compounds were purified by different chromatographic methods, including Silica gel and Sephadex LH-20, and their chemical structures were elucidated by mass and NMR spectroscopy. Tetracenomycin D (1) inhibited 75% of both pathogens from creating biofilm at 400 µg/ml, whereas resistomycin (2), and resistoflavin (3) inhibited biofilm by more than 80% at the same concentration. The light microscopic investigation revealed that compounds 1-3 inhibit the formation of biofilms and the adhesion of bacterial cells to the surface of glass pieces. As observed by confocal laser scanning microscopy (CLSM), pigmented metabolites 1-3 disrupt the 3D architecture of biofilm-forming bacteria. Molecular docking was used to find out how compounds 1–3 bind to the active sites of the biofilm-forming proteins ClfB and CsgG in S. aureus and E. coli, respectively.
Keywords
Keywords actinomycetes antibiofilm light microscope confocal laser scanning microscope ClfB CsgG molecular docking
Status: Abstract Accepted (Poster Presentation)