TY - JOUR
T1 - Capability of a large bacterial artificial chromosome clone harboring multiple biosynthetic gene clusters for the production of diverse compounds
AU - Kudo, Kei
AU - Nishimura, Takehiro
AU - Izumikawa, Miho
AU - Kozone, Ikuko
AU - Hashimoto, Junko
AU - Fujie, Manabu
AU - Suenaga, Hikaru
AU - Ikeda, Haruo
AU - Satoh, Nori
AU - Shin-ya, Kazuo
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to the Japan Antibiotics Research Association 2024.
PY - 2024/5
Y1 - 2024/5
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85186566429
UR - https://www.scopus.com/pages/publications/85186566429#tab=citedBy
U2 - 10.1038/s41429-024-00711-9
DO - 10.1038/s41429-024-00711-9
M3 - Article
C2 - 38438499
AN - SCOPUS:85186566429
SN - 0021-8820
VL - 77
SP - 288
EP - 298
JO - Journal of Antibiotics
JF - Journal of Antibiotics
IS - 5
ER -