State Key Laboratory of Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, PR China.
Biotechnology Research Department, Department of Research and Innovation, Ministry of Education, Kyaukse, The Republic of the Union of Myanmar.
J Appl Microbiol. 2020 Sep;129(3):565-574. doi: 10.1111/jam.14629. Epub 2020 Apr 6.
The aim of the present work was to investigate the overexpression of the wysR gene in Streptomyces albulus var. wuyiensis strain CK-15 based on the ΔwysR3 mutant strain including the effect on morphological development, wuyiencin production and antibacterial activity. At the same time, we report a new rapid method for producing genetically engineered strains for industrial production of wuyiencin.
We developed a method to create a wysR overexpression strain based on the ΔwysR3 mutant strain by direct transformation. In this method, the desired gene fragment to be overexpressed was amplified by polymerase chain reaction (PCR) using Phusion High Fidelity DNA polymerase and fused with the linearized pSETC integrative plasmid by Gibson assembly. The resulting recombinant plasmid was transformed into ΔwysR3 mutant strain by the intergeneric conjugation method. The plasmid was then integrated into the chromosome and the resulting apramycin-resistant overexpression strain was confirmed by PCR using the Apra-F and Apra-R primers. Finally, we successfully screened the genetically engineered strain with overexpression of wysR gene in ΔwysR3 mutant.
We can conclude that overexpression of wysR gene in ΔwysR3 mutant strain proved to be an effective strategy for significantly increasing wuyiencin production together with faster morphological development. Quantitative real-time RT-PCR analysis showed that wysR regulated wuyiencin biosynthesis by modulating other putative regulatory genes and bld, whi, chp, rdl and ram family genes are crucial for the morphological development.
Overexpression of wysR gene in the ΔwysR3 mutant strain named OoWysR strain may increase the efficiency in the industrial fermentation processes for wuyiencin production. The mechanism by which wysR overexpression promotes rapid sporulation and a high yield of wuyiencin production is likely related to modulation of other putative regulatory genes.
本研究旨在基于 ΔwysR3 突变株,通过调查白色链霉菌变种武夷变种 CK-15 中 wysR 基因的过表达对形态发育、武夷菌素产生和抗菌活性的影响,研究 wysR 基因的过表达。同时,我们报告了一种用于产生武夷菌素工业生产的基因工程菌株的新快速方法。
我们开发了一种基于 ΔwysR3 突变株的 wysR 过表达菌株的创建方法,该方法通过聚合酶链反应(PCR)使用 Phusion High Fidelity DNA 聚合酶扩增所需的过表达基因片段,并通过 Gibson 组装将其与线性化的 pSETC 整合质粒融合。通过种间共轭法将所得重组质粒转化入 ΔwysR3 突变株中。然后,质粒整合到染色体中,并用 Apra-F 和 Apra-R 引物进行 PCR 验证得到阿普拉霉素抗性过表达菌株。最后,我们成功筛选出 ΔwysR3 突变株中 wysR 基因过表达的基因工程菌株。
我们可以得出结论,在 ΔwysR3 突变株中过表达 wysR 基因被证明是一种有效策略,可以显著提高武夷菌素的产量,并加速形态发育。定量实时 RT-PCR 分析表明,wysR 通过调节其他假定的调节基因来调节武夷菌素生物合成,而 whi、chp、rdl 和 ram 家族基因对形态发育至关重要。
在 ΔwysR3 突变株中过表达 wysR 基因,命名为 OoWysR 菌株,可能会提高武夷菌素生产的工业发酵过程的效率。wysR 过表达促进快速产孢和高产武夷菌素的机制可能与调节其他假定的调节基因有关。