Li Hui, Chen Mengqi, Zhang Zaimei, Li Benchao, Liu Jianlin, Xue Han, Ji Sixue, Guo Zhongrui, Wang Jiqian, Zhu Hu
State Key Laboratory of Heavy Oil Processing and Centre for Bioengineering and Biotechnology, China University of Petroleum (East China), Qingdao, China.
Engineering Research Center of Industrial Biocatalysis, Fujian Province Universities, College of Chemistry and Materials Science, Fujian Normal University, Fuzhou, China.
Front Microbiol. 2022 Mar 1;13:792315. doi: 10.3389/fmicb.2022.792315. eCollection 2022.
sp. WG produced WL gum with commercial utility potential in many industries. A hybrid sensor histidine kinase/response regulator WelA was identified to regulate the WL gum biosynthesis, and its function was evaluated by gene deletion strategy. The WL gum production and broth viscosity of mutant Δ was only 44% and 0.6% of wild type strain at 72 h. The transcriptomic analysis of differentially expressed genes showed that WelA was mapped to CckA; ChpT, and CtrA in the CckA-ChpT-CtrA pathway was up-regulated. One phosphodiesterase was up-regulated by CtrA, and the intracellular c-di-GMP was decreased. Most genes involved in WL gum biosynthesis pathway was not significantly changed in Δ except the up-regulated and and the down-regulated . Furthermore, the up-regulated regulators , , and may participate in the regulation of flagellar biogenesis and influenced motility. These results suggested that CckA-ChpT-CtrA pathway and c-di-GMP were involved in WL gum biosynthesis regulation. This work provides useful information on the understanding of molecular mechanisms underlying WL gum biosynthesis regulation.
sp. WG产生的WL胶在许多行业具有商业应用潜力。鉴定出一种杂合传感器组氨酸激酶/反应调节因子WelA来调节WL胶的生物合成,并通过基因缺失策略评估其功能。在72小时时,突变体Δ的WL胶产量和发酵液粘度仅为野生型菌株的44%和0.6%。差异表达基因的转录组分析表明,WelA映射到CckA;CckA-ChpT-CtrA途径中的ChpT和CtrA上调。一种磷酸二酯酶被CtrA上调,细胞内c-di-GMP降低。除了上调的 和 以及下调的 外,WL胶生物合成途径中涉及的大多数基因在Δ中没有显著变化。此外,上调的调节因子 、 和 可能参与鞭毛生物合成的调节并影响运动性。这些结果表明,CckA-ChpT-CtrA途径和c-di-GMP参与了WL胶生物合成的调节。这项工作为理解WL胶生物合成调节的分子机制提供了有用信息。