Christian Bassi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Christian Bassi has a total of 21 co-authors. Here are the top co-authors by number of shared publications:
- Barrie Wilkinson
Department of Molecular Microbiology, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK
2 shared publications - Daniel C. L. Van
Astbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology University of Leeds Leeds UK
2 shared publications - Edward S. Hems
Department of Molecular Microbiology, John Innes Centre Norwich Research Park Norwich UK
2 shared publications - Glyn R. Hemsworth
Astbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology University of Leeds Leeds UK
2 shared publications - Julius S. P. Adamson
Department of Molecular Microbiology, John Innes Centre Norwich Research Park Norwich UK
2 shared publications - Justin E. Clarke
Astbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology University of Leeds Leeds UK
2 shared publications
Latest Publications
- Open Access
- 6 May 2026
- Published by Wiley in Angewandte Chemie
- Vol. 138 (26) , e11349
Discovery and Biosynthesis of the Novel Glycotetrapeptide Antibiotic Biffamycin A
The clinical deployment of antibiotics is undermined by antimicrobial resistance. Without new agents to treat antibiotic‐resistant bacterial infections, mortality rates are predicted to reach 10 million people per year by 2050. Most antibiotics are derived from natural products (NPs) produced by bacteria; however, this resource was abandoned by industry because of high rediscovery rates. We are amid a natural product renaissance fuelled by inexpensive access to genome sequencing and sophisticated bioinformatic tools, which have highlighted that most of the biosynthetic pathways for NPs are not expressed in the laboratory. Here, we engineered the expression of a silent biosynthetic gene cluster harboured by an environmental isolate of Streptomyces albidoflavus . Using a bioinformatics‐guided approach, we isolated and structurally characterised a novel glycopeptide antibiotic (GPA) named biffamycin A, which is the smallest GPA known and harbours unprecedented 5‐chloro‐4‐methoxy tryptophan and 3‐hydroxy(α‐D‐mannoysl)‐D‐lysine moieties. Biffamycin A possesses antimycobacterial and antistaphylococcal bioactivity, including against methicillin‐ and vancomycin‐resistant Staphylococcus aureus .
- 6 May 2026
- Published by Wiley in Angewandte Chemie
- Vol. 138 (26) , e11349
Open AccessDiscovery and Biosynthesis of the Novel Glycotetrapeptide Antibiotic Biffamycin A
The clinical deployment of antibiotics is undermined by antimicrobial resistance. Without new agents to treat antibiotic‐resistant bacterial infections, mortality rates are predicted to reach 10 million people per year by 2050. Most antibiotics are derived from natural products (NPs) produced by bacteria; however, this resource was abandoned by industry because of high rediscovery rates. We are amid a natural product renaissance fuelled by inexpensive access to genome sequencing and sophisticated bioinformatic tools, which have highlighted that most of the biosynthetic pathways for NPs are not expressed in the laboratory. Here, we engineered the expression of a silent biosynthetic gene cluster harboured by an environmental isolate of Streptomyces albidoflavus . Using a bioinformatics‐guided approach, we isolated and structurally characterised a novel glycopeptide antibiotic (GPA) named biffamycin A, which is the smallest GPA known and harbours unprecedented 5‐chloro‐4‐methoxy tryptophan and 3‐hydroxy(α‐D‐mannoysl)‐D‐lysine moieties. Biffamycin A possesses antimycobacterial and antistaphylococcal bioactivity, including against methicillin‐ and vancomycin‐resistant Staphylococcus aureus .
- Open Access
- 6 May 2026
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 65 (26) , e11349
Discovery and Biosynthesis of the Novel Glycotetrapeptide Antibiotic Biffamycin A
The clinical deployment of antibiotics is undermined by antimicrobial resistance. Without new agents to treat antibiotic‐resistant bacterial infections, mortality rates are predicted to reach 10 million people per year by 2050. Most antibiotics are derived from natural products (NPs) produced by bacteria; however, this resource was abandoned by industry because of high rediscovery rates. We are amid a natural product renaissance fuelled by inexpensive access to genome sequencing and sophisticated bioinformatic tools, which have highlighted that most of the biosynthetic pathways for NPs are not expressed in the laboratory. Here, we engineered the expression of a silent biosynthetic gene cluster harboured by an environmental isolate of Streptomyces albidoflavus . Using a bioinformatics‐guided approach, we isolated and structurally characterised a novel glycopeptide antibiotic (GPA) named biffamycin A, which is the smallest GPA known and harbours unprecedented 5‐chloro‐4‐methoxy tryptophan and 3‐hydroxy(α‐D‐mannoysl)‐D‐lysine moieties. Biffamycin A possesses antimycobacterial and antistaphylococcal bioactivity, including against methicillin‐ and vancomycin‐resistant Staphylococcus aureus .
- 6 May 2026
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 65 (26) , e11349
Open AccessDiscovery and Biosynthesis of the Novel Glycotetrapeptide Antibiotic Biffamycin A
The clinical deployment of antibiotics is undermined by antimicrobial resistance. Without new agents to treat antibiotic‐resistant bacterial infections, mortality rates are predicted to reach 10 million people per year by 2050. Most antibiotics are derived from natural products (NPs) produced by bacteria; however, this resource was abandoned by industry because of high rediscovery rates. We are amid a natural product renaissance fuelled by inexpensive access to genome sequencing and sophisticated bioinformatic tools, which have highlighted that most of the biosynthetic pathways for NPs are not expressed in the laboratory. Here, we engineered the expression of a silent biosynthetic gene cluster harboured by an environmental isolate of Streptomyces albidoflavus . Using a bioinformatics‐guided approach, we isolated and structurally characterised a novel glycopeptide antibiotic (GPA) named biffamycin A, which is the smallest GPA known and harbours unprecedented 5‐chloro‐4‐methoxy tryptophan and 3‐hydroxy(α‐D‐mannoysl)‐D‐lysine moieties. Biffamycin A possesses antimycobacterial and antistaphylococcal bioactivity, including against methicillin‐ and vancomycin‐resistant Staphylococcus aureus .
- 1 July 2021
- Published by Elsevier in Pancreatology
- Vol. 21, S52
iCyst: 1 year, 1000 and more simulations through an app
- 1 July 2021
- Published by Elsevier in Pancreatology
- Vol. 21, S52
iCyst: 1 year, 1000 and more simulations through an app