Cui Jinyu, Sun Tao, Chen Lei, Zhang Weiwen
Laboratory of Synthetic Microbiology, School of Chemical Engineering & Technology, Tianjin University, Tianjin, China.
Frontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering, Tianjin University, Tianjin, China.
Front Microbiol. 2021 May 18;12:650217. doi: 10.3389/fmicb.2021.650217. eCollection 2021.
The recently isolated cyanobacterium UTEX 2973 (Syn2973) is characterized by a faster growth rate and greater tolerance to high temperature and high light, making it a good candidate chassis for autotrophic photosynthetic microbial cell factories. However, Syn2973 is sensitive to salt stress, making it urgently important to improve the salt tolerance of Syn2973 for future biotechnological applications. Glucosylglycerol, a compatible solute, plays an important role in resisting salt stress in moderate and marine halotolerant cyanobacteria. In this study, the salt tolerance of Syn2973 was successfully improved by introducing the glucosylglycerol (GG) biosynthetic pathway (OD improved by 24% at 60 h). In addition, the salt tolerance of Syn2973 was further enhanced by overexpressing the rate-limiting step of glycerol-3-phosphate dehydrogenase and downregulating the gene , which encodes UDP glucose pyrophosphorylase. Taken together, these results indicate that the growth of the end-point strain M-2522-GgpPS-drfbA was improved by 62% compared with the control strain M-pSI-pSII at 60 h under treatment with 0.5 M NaCl. Finally, a comparative metabolomic analysis between strains M-pSI-pSII and M-2522-GgpPS-drfbA was performed to characterize the carbon flux in the engineered M-2522-GgpPS-drfbA strain, and the results showed that more carbon flux was redirected from ADP-GLC to GG synthesis. This study provides important engineering strategies to improve salt tolerance and GG production in Syn2973 in the future.
最近分离出的蓝藻UTEX 2973(Syn2973)具有生长速度更快、对高温和高光耐受性更强的特点,使其成为自养光合微生物细胞工厂的良好候选底盘。然而,Syn2973对盐胁迫敏感,因此提高其耐盐性对于未来的生物技术应用至关重要。葡糖甘油作为一种相容性溶质,在中度和海洋耐盐蓝藻抵抗盐胁迫中发挥着重要作用。在本研究中,通过引入葡糖甘油(GG)生物合成途径成功提高了Syn2973的耐盐性(60小时时OD提高了24%)。此外,通过过表达3-磷酸甘油脱氢酶的限速步骤并下调编码UDP葡萄糖焦磷酸化酶的基因,进一步增强了Syn2973的耐盐性。综上所述,这些结果表明,在0.5 M NaCl处理下,60小时时终点菌株M-2522-GgpPS-drfbA的生长比对照菌株M-pSI-pSII提高了62%。最后,对菌株M-pSI-pSII和M-2522-GgpPS-drfbA进行了比较代谢组学分析,以表征工程菌株M-2522-GgpPS-drfbA中的碳通量,结果表明更多的碳通量从ADP-GLC重新导向GG合成。本研究为未来提高Syn2973的耐盐性和GG产量提供了重要的工程策略。