Chang Ai-Ping, Qian Jin, Li Hui, Wang Ying-Lu, Lin Jie-Ying, He Qiao-Mei, Shen Ya-Ling, Zhu Hu
Engineering Research Center of Industrial Biocatalysis, Fujian Provincial Key Laboratory of Advanced Materials Oriented Chemical Engineering, Fujian Provincial Key Laboratory of Polymer Materials, Key Laboratory of OptoElectronic Science and Technology for Medicine of Ministry of Education, College of Chemistry and Materials Science, Fujian Normal University, Fuzhou, China.
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
Front Microbiol. 2021 Feb 9;12:638355. doi: 10.3389/fmicb.2021.638355. eCollection 2021.
Welan gum, a kind of microbial exopolysaccharides, produced by the genus , have great potential for application in many fields, such as the food industry, cement production, and enhanced oil recovery. But there are still challenges to reduce the cost, enhance the production and the quality. Herein, the bioinformatics analysis of gene was preformed, and the characterization and function of WelR, welan gum lyase, from sp. WG were investigated for the first time. The results indicated that 382nd (Asn), 383rd (Met), 494th (Asn), and 568th (Glu) were the key amino acid residues, and C-terminal amino acids were essential to keeping the stability of WelR. The optimal temperature and pH of the enzymatic activity were found to be 25°C and 7.4, respectively. And WelR was good low temperature resistance and alkali resistant. K, Mg, Ca, Mn, and EDTA increased WelR activities, in contrast to Zn. Coupled with the change in glucose concentration and growth profile, the qRT-PCR results indicated that WelR may degrade welan gum existing in the culture to maintain bacterial metabolism when glucose was depleted. This work will lay a theoretical foundation to establish new strategies for the regulation of welan gum biosynthesis.
韦兰胶是一种由[具体菌属]产生的微生物胞外多糖,在食品工业、水泥生产和提高石油采收率等许多领域具有巨大的应用潜力。但在降低成本、提高产量和质量方面仍存在挑战。在此,对[基因名称]进行了生物信息学分析,并首次研究了来自[菌株名称]WG的韦兰胶裂解酶WelR的特性和功能。结果表明,第382位(Asn)、第383位(Met)、第494位(Asn)和第568位(Glu)是关键氨基酸残基,C末端氨基酸对于维持WelR的稳定性至关重要。发现酶活性的最佳温度和pH分别为25°C和7.4。并且WelR具有良好的耐低温和耐碱性。K、Mg、Ca、Mn和EDTA提高了WelR的活性,而Zn则相反。结合葡萄糖浓度的变化和生长曲线,qRT-PCR结果表明,当葡萄糖耗尽时,WelR可能会降解培养物中存在的韦兰胶以维持细菌代谢。这项工作将为建立韦兰胶生物合成调控新策略奠定理论基础。