TY - JOUR
T1 - High-Yield Lasso Peptide Production in a Burkholderia Bacterial Host by Plasmid Copy Number Engineering
AU - Fernandez, Hannah N.
AU - Kretsch, Ashley M.
AU - Kunakom, Sylvia
AU - Kadjo, Adjo E.
AU - Mitchell, Douglas A.
AU - Eustáquio, Alessandra S.
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/1/19
Y1 - 2024/1/19
N2 - The knotted configuration of lasso peptides confers thermal stability and proteolytic resistance, addressing two shortcomings of peptide-based drugs. However, low isolation yields hinder the discovery and development of lasso peptides. While testing Burkholderia sp. FERM BP-3421 as a bacterial host to produce the lasso peptide capistruin, an overproducer clone was previously identified. In this study, we show that an increase in the plasmid copy number partially contributed to the overproducer phenotype. Further, we modulated the plasmid copy number to recapitulate titers to an average of 160% relative to the overproducer, which is 1000-fold higher than previously reported with E. coli, reaching up to 240 mg/L. To probe the applicability of the developed tools for lasso peptide discovery, we targeted a new lasso peptide biosynthetic gene cluster from endosymbiont Mycetohabitans sp. B13, leading to the isolation of mycetolassin-15 and mycetolassin-18 in combined titers of 11 mg/L. These results validate Burkholderia sp. FERM BP-3421 as a production platform for lasso peptide discovery.
AB - The knotted configuration of lasso peptides confers thermal stability and proteolytic resistance, addressing two shortcomings of peptide-based drugs. However, low isolation yields hinder the discovery and development of lasso peptides. While testing Burkholderia sp. FERM BP-3421 as a bacterial host to produce the lasso peptide capistruin, an overproducer clone was previously identified. In this study, we show that an increase in the plasmid copy number partially contributed to the overproducer phenotype. Further, we modulated the plasmid copy number to recapitulate titers to an average of 160% relative to the overproducer, which is 1000-fold higher than previously reported with E. coli, reaching up to 240 mg/L. To probe the applicability of the developed tools for lasso peptide discovery, we targeted a new lasso peptide biosynthetic gene cluster from endosymbiont Mycetohabitans sp. B13, leading to the isolation of mycetolassin-15 and mycetolassin-18 in combined titers of 11 mg/L. These results validate Burkholderia sp. FERM BP-3421 as a production platform for lasso peptide discovery.
KW - bacteria
KW - Burkholderiaceae
KW - heterologous expression
KW - lasso peptide
KW - natural product
KW - RiPP
KW - secondary metabolite
UR - http://www.scopus.com/inward/record.url?scp=85182560476&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85182560476&partnerID=8YFLogxK
U2 - 10.1021/acssynbio.3c00597
DO - 10.1021/acssynbio.3c00597
M3 - Article
C2 - 38194362
AN - SCOPUS:85182560476
SN - 2161-5063
VL - 13
SP - 337
EP - 350
JO - ACS synthetic biology
JF - ACS synthetic biology
IS - 1
ER -