AI Article Synopsis

  • * Researchers focused on concanamycin as a target to develop a heterologous expression system for these large BGCs.
  • * By using a bacterial artificial chromosome (BAC) clone containing the entire BGC for concanamycin, they successfully produced concanamycin and two additional compounds in Streptomyces avermitilis, identifying one as JBIR-157.

Article Abstract

The biosynthetic gene clusters (BGCs) for the macrocyclic lactone-based polyketide compounds are extremely large-sized because the polyketide synthases that generate the polyketide chains of the basic backbone are of very high molecular weight. In developing a heterologous expression system for the large BGCs amenable to the production of such natural products, we selected concanamycin as an appropriate target. We obtained a bacterial artificial chromosome (BAC) clone with a 211-kb insert harboring the entire BGC responsible for the biosynthesis of concanamycin. Heterologous expression of this clone in a host strain, Streptomyces avermitilis SUKA32, permitted the production of concanamycin, as well as that of two additional aromatic polyketides. Structural elucidation identified these additional products as ent-gephyromycin and a novel compound that was designated JBIR-157. We describe herein sequencing and expression studies performed on these BGCs, demonstrating the utility of large BAC clones for the heterologous expression of cryptic or near-silent loci.

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Source
http://dx.doi.org/10.1038/s41429-024-00711-9DOI Listing

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