Department of Life Science and Biotechnology, National Institute of Advanced Industrial Science and Technology (AIST), 2-4-7 Aomi, Koto-ku, Tokyo, 135-0064, Japan.
Technology Research Association for Next Generation Natural Products Chemistry, 2-4-7 Aomi, Koto-ku, Tokyo, 135-0064, Japan.
J Antibiot (Tokyo). 2024 May;77(5):288-298. doi: 10.1038/s41429-024-00711-9. Epub 2024 Mar 4.
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.
基于大环内酯的聚酮化合物的生物合成基因簇(BGCs)非常大,因为生成聚酮链的聚酮合酶分子量非常高。为了开发适合生产此类天然产物的大型 BGC 异源表达系统,我们选择康纳霉素作为合适的目标。我们获得了一个带有 211-kb 插入片段的细菌人工染色体 (BAC) 克隆,其中包含负责康纳霉素生物合成的整个 BGC。该克隆在宿主菌株链霉菌属 SUKA32 中的异源表达允许康纳霉素的产生,以及两种额外的芳香聚酮的产生。结构阐明确定这些额外的产物为 ent-gephyromycin 和一种被命名为 JBIR-157 的新型化合物。本文描述了对这些 BGC 进行的测序和表达研究,证明了大型 BAC 克隆在异源表达隐匿或近乎沉默基因座方面的实用性。