Computational Studies on Selected Macrolides Active against Escherichia coli Combined with the NMR Study of Tylosin A in Deuterated Chloroform

Molecules. 2022 Oct 26;27(21):7280. doi: 10.3390/molecules27217280.

Abstract

Although many antibiotics are active against Gram-positive bacteria, fewer also show activity against Gram-negative bacteria. Here, we present a combination of in silico (electron ion-interaction potential, molecular docking, ADMET), NMR, and microbiological investigations of selected macrolides (14-membered, 15-membered, and 16-membered), aiming to discover the pattern of design for macrolides active against Gram-negative bacteria. Although the conformational studies of 14-membered and 15-membered macrolides are abundant in the literature, 16-membered macrolides, and their most prominent representative tylosin A, have received relatively little research attention. We therefore report the complete 1H and 13C NMR assignment of tylosin A in deuterated chloroform, as well as its 3D solution structure determined through molecular modelling (conformational search) and 2D ROESY NMR. Additionally, due to the degradation of tylosin A in deuterated chloroform, other species were also detected in 1D and 2D NMR spectra. We additionally studied the anti-bacterial activity of tylosin A and B against selected Gram-positive and Gram-negative bacteria.

Keywords: 2D ROESY NMR; bacteria; macrolides.

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Chloroform
  • Escherichia coli / metabolism
  • Gram-Negative Bacteria / metabolism
  • Gram-Positive Bacteria / metabolism
  • Macrolides* / chemistry
  • Molecular Docking Simulation
  • Tylosin* / chemistry
  • Tylosin* / pharmacology

Substances

  • Tylosin
  • Macrolides
  • Anti-Bacterial Agents
  • Chloroform