Beyond vancomycin: recent advances in the modification, reengineering, production, and discovery of improved glycopeptide antibiotics to tackle multi-drug resistant bacteria
Glycopeptide antibiotics (GPA), which include vancomycin and teicoplanin, are important lastresort antibiotics used to treat multidrug-resistant Gram-positive bacterial infections. Whilst second generation GPAs – generated through chemical modification of natural GPAs – have proven successful, the emergence of GPA resistance has underlined the need to develop new members of this compound class. Significant recent advances have been made in GPA research, including gaining an in-depth understanding of their biosynthesis, improving titre in production strains, developing new derivatives via novel chemical modifications, and identifying a new mode of action for structurally diverse Type V GPAs. Taken together, these advances demonstrate significant untapped potential for the further development of GPAs to tackle the growing threat of multidrug resistant bacteria.
Funding
Understanding peptide bond formation in non-ribosomal peptide biosynthesis
Australian Research Council
Find out more...TRR 261: Cellular Mechanisms of Antibiotic Action and Production
Deutsche Forschungsgemeinschaft
Find out more...ARC Centre of Excellence for Innovations in Peptide and Protein Science
Australian Research Council
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