Abstract
Ribosomally synthesized lanthionine-containing peptides (lanthipeptides) have emerged as a promising source of antimicrobials against multidrug resistance pathogens. An effective way to discover and engineer lanthipeptides is through heterologous expression of their biosynthetic gene clusters (BGCs) in a host of choice. Here we report a plug-and-play pathway refactoring strategy for rapid evaluation of lanthipeptide BGCs in Bacillus subtilis based on the T7 expression system. As a proof of concept, we used this strategy to not only observe the successful production of a known lanthipeptide haloduracin β but also discover two new human-microbiota-derived lanthipeptides that previously failed to be produced in Escherichia coli. The resulting B. subtilis plug-and-play T7 expression system should enable the genome mining of new lanthipeptides in a high-throughput manner.
Original language | English (US) |
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Pages (from-to) | 3746-3753 |
Number of pages | 8 |
Journal | ACS synthetic biology |
Volume | 13 |
Issue number | 11 |
Early online date | Oct 31 2024 |
DOIs | |
State | Published - Nov 15 2024 |
Keywords
- Bacillus subtilis
- heterologous expression
- lanthipeptide
- pathway refactoring
- T7 RNA polymerase
ASJC Scopus subject areas
- Biomedical Engineering
- Biochemistry, Genetics and Molecular Biology (miscellaneous)