Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Life Sciences and Health Engineering, Jiangnan University, Wuxi 214122, PR China; National Engineering Research Center for Cereal Fermentation and Food Biomanufacturing, School of Biotechnology, Jiangnan University, Wuxi 214122, PR China.
Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Life Sciences and Health Engineering, Jiangnan University, Wuxi 214122, PR China; Yixing Institute of Food and Biotechnology Co., Ltd, Yixing 214200, PR China.
Carbohydr Polym. 2023 Jul 15;312:120809. doi: 10.1016/j.carbpol.2023.120809. Epub 2023 Mar 14.
This study reveals the genetic and biochemical changes underlying the enhanced hyaluronan (HA) biosynthesis in Streptococcus zooepidemicus. After multiple rounds of atmospheric and room temperature plasma (ARTP) mutagenesis combined with novel bovine serum albumin/cetyltrimethylammonium bromide coupled high-throughput screening assay, the HA yield of the mutant was increased by 42.9% and reached 0.813 g L with a molecular weight of 0.54 × 10 Da within 18 h by shaking flask culture. HA production was increased to 4.56 g L by batch culture in 5-L fermenter. Transcriptome sequencing exhibits that distinct mutants have similar genetic changes. Regulation in direction of metabolic flow into the HA biosynthesis, by enhancing genes responsible for the biosynthesis of HA including hasB, glmU and glmM, weaking downstream gene (nagA and nagB) of UDP-GlcNAc and significantly down-regulating transcription of wall-synthesizing genes, resulting in the accumulation of precursors (UDP-GlcA and UDP-GlcNAc) increased by 39.74% and 119.22%, respectively. These associated regulatory genes may provide control point for engineering of the efficient HA-producing cell factory.
本研究揭示了马疫链球菌中透明质酸(HA)生物合成增强的遗传和生化变化。经过多轮大气压室温等离子体(ARTP)诱变与新型牛血清白蛋白/十六烷基三甲基溴化铵偶联高通量筛选,突变株摇瓶培养 18 小时后 HA 产量提高了 42.9%,达到 0.813g/L,分子量为 0.54×10 Da。通过 5L 发酵罐分批培养,HA 产量提高到 4.56g/L。转录组测序表明,不同的突变株具有相似的遗传变化。通过增强负责透明质酸生物合成的基因(如 hasB、glmU 和 glmM),使代谢流向透明质酸生物合成方向调控,弱化 UDP-GlcNAc 的下游基因(nagA 和 nagB),并显著下调细胞壁合成基因的转录,导致前体(UDP-GlcA 和 UDP-GlcNAc)分别积累增加 39.74%和 119.22%。这些相关的调控基因可能为高效 HA 生产细胞工厂的工程设计提供了控制点。