通过嗜盐古菌 Y2 进行启动子工程以在低盐环境中生产高浓度海藻糖。
Promoter engineering for high ectoine production in a lower saline medium by Halomonas hydrothermalis Y2.
机构信息
State Key Laboratory of Microbial Technology, Institute of Microbial Technology, Shandong University, Qingdao, 266237, People's Republic of China.
出版信息
Biotechnol Lett. 2021 Apr;43(4):825-834. doi: 10.1007/s10529-021-03084-3. Epub 2021 Jan 27.
OBJECTIVES
For the stress from fermenters, downstream processing equipment, and wastewater treatment to be alleviated, lowering salt-dependence in the ectoine synthesis process is of great significance in the moderately halotolerant Halomonas hydrothermalis Y2.
RESULTS
In H. hydrothermalis Y2, the σ- and σ-controlled promoters of ectA are predicted to be involved in the osmotic regulation of ectoine synthesis. By substituting the ectA promoter with a promoter P that identified in the outer membrane pore protein E of H. hydrothermalis Y2, the salt dependence of ectoine synthesis was significantly decreased. In the 500-ml flask containing various NaCl contents, the engineered strain (p/Y2/△ectD/△doeA) showed a remarkably enhanced ability in ectoine synthesis, especially under lower saline stress. After a 36-h fed-batch fermentation in the 1-l fermenter, p/Y2/△ectD/△doeA synthesized 11.5 g ectoine l in the presence of 60 g NaCll, with a high 0.32 g ectoine l h productivity, a specific productivity of 512.2 mg ectoine per g cell dry weight (CDW), and an excretion ratio of 67 % ectoine.
CONCLUSIONS
As no impaired growth was observed in strain p/Y2/△ectD/△doeA while ectoine synthesis was increased, this promoter engineering strategy provides a practical protocol for lowering the salt-dependence of ectoine synthesis in this moderately halotolerant strain.
目的
为了减轻发酵罐、下游处理设备和废水处理的压力,降低嗜盐古菌盐依赖型生产章鱼胺的工艺过程具有重要意义。
结果
在中度嗜盐古菌盐氢单胞菌 Y2 中,预测 σ-和 σ 控制的 ectA 启动子参与章鱼胺合成的渗透调节。通过用 H. hydrothermalis Y2 的外膜孔蛋白 E 鉴定的启动子 P 取代 ectA 启动子,显著降低了章鱼胺合成的盐依赖性。在含有不同 NaCl 含量的 500-ml 摇瓶中,工程菌株(p/Y2/△ectD/△doeA)在合成章鱼胺方面表现出显著增强的能力,特别是在低盐胁迫下。在 1-l 发酵罐中进行 36 小时补料分批发酵后,p/Y2/△ectD/△doeA 在 60g NaCl 存在下合成了 11.5g 章鱼胺 l,具有 0.32g ectoine l h 的高生产力、512.2mg ectoine 每克细胞干重的比生产力(CDW)和 67%的章鱼胺排泄比。
结论
在没有观察到菌株 p/Y2/△ectD/△doeA 生长受损的情况下,同时增加了章鱼胺的合成,这种启动子工程策略为降低该中度嗜盐菌株中章鱼胺合成的盐依赖性提供了一种实用方案。