| Literature DB >> 35147743 |
Sofia Melnyk1, Anastasia Stepanyshyn1, Oleksandr Yushchuk1, Michael Mandler2, Iryna Ostash1, Oksana Koshla1, Victor Fedorenko1, Daniel Kahne2, Bohdan Ostash3.
Abstract
Streptomyces roseochromogenes NRRL 3504 is best known as a producer of clorobiocin, a DNA replication inhibitor from the aminocoumarin family of antibiotics. This natural product currently draws attention as a promising adjuvant for co-application with other antibiotics against Gram-negative multidrug-resistant pathogens. Herein, we expand the genetic toolkit for NRRL 3504 by showing that a set of integrative and replicative vectors, not tested previously for this strain, could be conjugally transferred at high frequency from Escherichia coli to NRRL 3504. Using this approach, we leverage a cumate-inducible expression of cluster-situated regulatory gene novG to increase clorobiocin titers by 30-fold (up to approximately 200 mg/L). To our best knowledge, this is the highest level of clorobiocin production reported so far. Our findings set a working ground for further improvement of clorobiocin production as well as for the application of genetic methods to illuminate the cryptic secondary metabolome of NRRL 3504. Key Points • Efficient system for conjugative transfer of plasmids into NRRL 3504 was developed. • Expression of regulatory genes in NRRL 3504 led to increase in clorobiocin titer. • Secondary metabolome of NRRL 3504 becomes an accessible target for genetic manipulations using the expanded vector set and improved intergeneric conjugation protocol.Entities:
Keywords: Antibiotics; Clorobiocin; Cluster-situated regulatory genes; Conjugative transfer; Integrative plasmids; Streptomyces roseochromogenes NRRL 3504
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Year: 2022 PMID: 35147743 PMCID: PMC9528727 DOI: 10.1007/s00253-022-11814-4
Source DB: PubMed Journal: Appl Microbiol Biotechnol ISSN: 0175-7598 Impact factor: 5.560