Li Hui, Zhang Zaimei, Liu Jianlin, Guo Zhongrui, Chen Mengqi, Li Benchao, Xue Han, Ji Sixue, Li Hang, Qin Lijian, Zhu Ling, Wang Jiqian, Zhu Hu
State Key Laboratory of Heavy Oil Processing and Centre for Bioengineering and Biotechnology, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao, China.
Engineering Research Center of Industrial Biocatalysis, Fujian-Taiwan Science and Technology Cooperation Base of Biomedical Materials and Tissue Engineering, College of Chemistry and Materials Science, Fujian Normal University, Fuzhou, China.
Front Bioeng Biotechnol. 2022 May 27;10:918687. doi: 10.3389/fbioe.2022.918687. eCollection 2022.
As an important microbial exopolysaccharide, the sphingan WL gum could be widely used in petroleum, food, and many other fields. However, its lower production is still limiting its wider application. Therefore, to gain insights into the bottlenecks of WL gum production by identifying the key enzymes in the WL gum biosynthesis pathway, more than 20 genes were over-expressed in sp. WG and their effects on WL gum production and structure were investigated. Compared to the control strain, the WL gum production of over-expression strain was increased by 19.0 and 21.0% at 36 and 84 h, respectively. The WL gum production of both and over-expression strains reached 47 g/L, which was approximately 34.5% higher than that of the control strain at 36 h. Therefore, WelB, AtrB, and AtrD may be the key enzymes in WL production. Interestingly, the broth viscosity of most over-expression strains decreased, especially the over-expression strain whose viscosity decreased by 99.3% at 84 h. Polysaccharides' structural features were investigated to find the critical components in viscosity control. The uronic acid content and total sugar content was affected by only a few genes, therefore, uronic acid and total sugar content may be not the key composition. In comparison, the acetyl degrees were enhanced by over-expression of most genes, which meant that acetyl content may be the critical factor and negatively correlated with the apparent viscosity of WL gum. This work provides useful information on the understanding of the bottlenecks of WL gum biosynthesis and will be helpful for the construction of high WL gum-yielding strains and rheological property controlling in different industries.
作为一种重要的微生物胞外多糖,斯氏糖胶WL胶可广泛应用于石油、食品等诸多领域。然而,其产量较低仍限制了其更广泛的应用。因此,为了通过鉴定WL胶生物合成途径中的关键酶来深入了解WL胶生产的瓶颈,在斯氏菌WG中过表达了20多个基因,并研究了它们对WL胶产量和结构的影响。与对照菌株相比,过表达菌株在36小时和84小时时的WL胶产量分别提高了19.0%和21.0%。AtfB和AtrD过表达菌株的WL胶产量均达到47 g/L,在36小时时比对照菌株高出约34.5%。因此,WelB、AtrB和AtrD可能是WL胶生产中的关键酶。有趣的是,大多数过表达菌株的发酵液粘度降低,尤其是AtfB过表达菌株,其在84小时时粘度降低了99.3%。研究了多糖的结构特征以找出粘度控制中的关键成分。糖醛酸含量和总糖含量仅受少数基因影响,因此,糖醛酸和总糖含量可能不是关键组成部分。相比之下,大多数基因的过表达提高了乙酰化程度,这意味着乙酰基含量可能是关键因素,且与WL胶的表观粘度呈负相关。这项工作为理解WL胶生物合成的瓶颈提供了有用信息,将有助于构建高产WL胶的菌株以及控制不同行业中的流变学性质。