Institute of Plasma Physics, Hefei institutes of Physical Science, Chinese Academy of Sciences, Hefei, 230031, China.
University of Science and Technology of China, Hefei, 230026, China.
Bioprocess Biosyst Eng. 2018 May;41(5):729-738. doi: 10.1007/s00449-018-1906-3. Epub 2018 Feb 19.
The production of virginiamycin (VGM) from Streptomyces virginiae was improved by genome shuffling and ribosome engineering companied with a high-throughput screening method integrating deep-well cultivation and the cylinder-plate detecting. First, a novel high-throughput method was developed to rapidly screen large numbers of VGM-producing mutants. Then, the starting population of genome shuffling was obtained through ultraviolet (UV) and microwave mutagenesis, and four mutants with higher productivity of VGM were selected for genome shuffling. Next, the parent protoplasts were inactivated by UV and heat when a fusant probability was about 98%. Streptomycin resistance was used as an evolutionary pressure to extend positive effects on VGM synthesis. Finally, after five rounds of genome shuffling, a genetically stable strain G5-103 was obtained and characterized to be able to yield 251 mg/L VGM, which was 3.1- and 11.6-fold higher than that of the mutant strain UV 1150 and the wild-type strain, respectively.
通过基因组改组和核糖体工程,并结合高通量筛选方法(包括深孔培养和圆柱平板检测),提高了弗氏链霉菌产生维吉尼亚霉素(VGM)的能力。首先,开发了一种新颖的高通量方法,可快速筛选大量产生 VGM 的突变体。然后,通过紫外线(UV)和微波诱变获得基因组改组的起始种群,并选择四个具有更高 VGM 产量的突变体进行基因组改组。接下来,当融合概率约为 98%时,用 UV 和热使亲本体原生质体失活。链霉素抗性被用作进化压力,以延长对 VGM 合成的积极影响。最后,经过五轮基因组改组,获得了遗传稳定的菌株 G5-103,并对其进行了特征分析,结果表明该菌株能够产生 251mg/L 的 VGM,分别比突变株 UV 1150 和野生型菌株提高了 3.1 倍和 11.6 倍。