Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
J Antibiot (Tokyo). 2018 Aug;71(8):749-752. doi: 10.1038/s41429-018-0057-8. Epub 2018 Apr 20.
Actinoallolides are anti-trypanosomal macrolides isolated from the secondary metabolites of two endophytic actinomycete strains, Actinoallomurus fulvus MK10-036 and K09-0307. A putative actinoallolide biosynthetic gene cluster was predicted from the genome sequence of the strain K09-0307. The gene cluster spans a contiguous 53 kb DNA region that comprises seven genes encoding three PKSs (aalA1, aalA2, and aalA3), cytochrome P450 (aalB), acyl-CoA dehydrogenase (aalC), crotonyl-CoA reductase (aalD), and TetR family regulator (aalR). The entire gene cluster was cloned into a plasmid pYIK1 by assembling DNA fragments, which were obtained from two cosmids containing left and right parts of the gene cluster. Following the introduction of an ermE* promoter at 100bp upstream from the start codon of aalA1, the gene cluster was introduced into Streptomyces coelicolor M1152. Subsequent LC-MS analysis revealed production of actinoallolide A in the culture broth. Thus, the actinoallolide biosynthetic gene cluster was identified by heterologous expression in Streptomyces.
放线紫红素是从两种内生放线菌菌株(Actinoallomurus fulvus MK10-036 和 K09-0307)的次级代谢产物中分离得到的抗锥虫大环内酯类化合物。从菌株 K09-0307 的基因组序列中预测到了一个放线紫红素生物合成基因簇。该基因簇跨越了一个连续的 53kb DNA 区域,包含编码三个聚酮合酶(aalA1、aalA2 和 aalA3)、细胞色素 P450(aalB)、酰基辅酶 A 脱氢酶(aalC)、巴豆酰辅酶 A 还原酶(aalD)和 TetR 家族调节剂(aalR)的七个基因。通过组装来自含有基因簇左右部分的两个 cosmid 的 DNA 片段,将整个基因簇克隆到质粒 pYIK1 中。在 aalA1 起始密码子上游 100bp 处引入 ermE*启动子后,将基因簇引入到 Streptomyces coelicolor M1152 中。随后的 LC-MS 分析显示在发酵液中产生了放线紫红素 A。因此,通过在链霉菌中异源表达鉴定了放线紫红素生物合成基因簇。