Wang Yu, He Huan, Li Siqi, Ren Limei, Li Xiaobing, Wang Xiaoru
College of Chemical Engineering, Shijiazhuang University, Shijiazhuang, Hebei Province, China.
Hebei Provincial University Microbiology Pharmaceutical Application Technology Research and Development Center, Shijiazhuang, China.
Prep Biochem Biotechnol. 2025;55(6):696-706. doi: 10.1080/10826068.2024.2448181. Epub 2025 Jan 2.
Doramectin, a 16-membered macrocyclic lactone that is widely used in the treatment of mammalian parasitic diseases. Doramectin was produced by mutant using cyclohexanecarboxylic acid as a precursor. As a semi-synthetic insecticidal agent produced, the production of doramectin was low, which could not be satisfy the demands of industrial fermentation. In this study, a high-yield mutant strain DA-137 was screened from the starting strain D-11 through a high-throughput screening strategy. D-11 was treated with iterative atmospheric and room temperature plasma mutagenesis to induce mutations. Mutation strains were prescreened by spreading on enhanced doramectin-tolerance plates and were rescreened in 24-deep microtiter plates and via microplate readers to obtain high-producing strains. The resulting mutant strain DA-137 produced 431.5 mg/L doramectin, a 187% increase compared to that of D-11, revealing mutagenesis and doramectin-tolerance screening is an efficient method to enhance doramectin production. Then, fermentation medium was optimized using the response surface method to improve doramectin production. In the optimized fermentation medium, the yield of doramectin was increased to 934.5 mg/L in shake flask. Furthermore, batch culture was carried out in a 50 L fermenter, and the yields of doramectin reached 1217 mg/L at 216 h, which was the highest yield reported to date. This study demonstrates a successful approach for enhancing doramectin production through high-throughput screening strategy and medium optimization, serving as a reference for increasing the yield of other macrocyclic lactone antibiotics.
多拉菌素是一种16元大环内酯类药物,广泛用于治疗哺乳动物的寄生虫病。多拉菌素是由突变体以环己烷羧酸为前体产生的。作为一种半合成杀虫剂,多拉菌素的产量较低,无法满足工业发酵的需求。在本研究中,通过高通量筛选策略从出发菌株D-11中筛选出高产突变菌株DA-137。D-11经迭代常压室温等离子体诱变处理以诱导突变。突变菌株先在增强多拉菌素耐受性平板上进行初筛,然后在24孔深孔板中进行复筛,并通过酶标仪获得高产菌株。所得突变菌株DA-137产生431.5mg/L多拉菌素,比D-11增加了187%,表明诱变和多拉菌素耐受性筛选是提高多拉菌素产量的有效方法。然后,采用响应面法优化发酵培养基以提高多拉菌素产量。在优化的发酵培养基中,摇瓶中多拉菌素的产量提高到934.5mg/L。此外,在50L发酵罐中进行分批培养,216h时多拉菌素产量达到1217mg/L,这是迄今为止报道的最高产量。本研究展示了一种通过高通量筛选策略和培养基优化提高多拉菌素产量的成功方法,为提高其他大环内酯类抗生素的产量提供了参考。