Li Chao, Gai Zhongchao, Wang Kai, Jin Liping
Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, 200092 People's Republic of China.
State Key Laboratory of Microbial Metabolism, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240 People's Republic of China.
Biotechnol Biofuels. 2017 Oct 11;10:235. doi: 10.1186/s13068-017-0920-z. eCollection 2017.
MW3 as a GRAS and thermophilic strain is a promising microorganism for chemical and biofuel production. However, its capacity to co-utilize glucose and xylose, the major sugars found in lignocellulosic biomass, is severely impaired by glucose-mediated carbon catabolite repression (CCR). In this study, a "dual-channel" process was implemented to engineer strain MW3 for simultaneous utilization of glucose and xylose, using l-lactic acid as a target product.
A non-phosphotransferase system (PTS) glucose uptake route was activated via deletion of the glucose transporter gene and introduction of the galactose permease gene . After replacing the promoter of glucokinase gene with the strong promoter , the engineered strain recovered glucose consumption and utilized glucose and xylose simultaneously. Meanwhile, to improve the consumption rate of xylose in this strain, several measures were undertaken, such as relieving the regulation of the xylose repressor XylR, reducing the catabolite-responsive element, and optimizing the rate-limiting step. Knockout of ethanol and acetic acid pathway genes further increased lactic acid yield by 6.2%. The resultant strain, RH15, was capable of producing 121.9 g/L l-lactic acid at high yield (95.3%) after 40 h of fermentation from a mixture of glucose and xylose. When a lignocellulosic hydrolysate was used as the substrate, 99.3 g/L l-lactic acid was produced within 40 h, with a specific productivity of 2.48 g/[L h] and a yield of 94.6%.
Our engineered strain RH15 could thermophilically produced l-lactic acid from lignocellulosic hydrolysate with relatively high concentration and productivity at levels that were competitive with most reported cases of l-lactic acid-producers. Thus, the engineered strain might be used as a platform for the production of other chemicals. In addition to engineering the strain, the "dual-channel" process might serve as an alternative method for engineering a variety of other strains.
MW3作为一种公认安全(GRAS)的嗜热菌株,是用于化学和生物燃料生产的一种很有前景的微生物。然而,其共利用葡萄糖和木糖(木质纤维素生物质中的主要糖类)的能力因葡萄糖介导的碳分解代谢物阻遏(CCR)而严重受损。在本研究中,实施了一种“双通道”方法,以l-乳酸为目标产物对MW3菌株进行工程改造,使其能够同时利用葡萄糖和木糖。
通过缺失葡萄糖转运蛋白基因并引入半乳糖通透酶基因,激活了一种非磷酸转移酶系统(PTS)葡萄糖摄取途径。在用强启动子替换葡萄糖激酶基因的启动子后,工程菌株恢复了葡萄糖消耗并能同时利用葡萄糖和木糖。同时,为提高该菌株中木糖的消耗速率,采取了多项措施,如解除木糖阻遏蛋白XylR的调控、减少分解代谢物反应元件以及优化限速步骤。敲除乙醇和乙酸途径基因进一步使乳酸产量提高了6.2%。所得菌株RH15在以葡萄糖和木糖混合物为底物发酵40小时后,能够高产(95.3%)生产121.9 g/L的l-乳酸。当使用木质纤维素水解产物作为底物时,在40小时内可生产99.3 g/L的l-乳酸,比生产率为2.48 g/[L·h],产率为94.6%。
我们的工程菌株RH15能够在嗜热条件下从木质纤维素水解产物中生产l-乳酸,其浓度和生产率相对较高,与大多数已报道的l-乳酸生产菌株具有竞争力。因此,该工程菌株可作为生产其他化学品的平台。除了对该菌株进行工程改造外,“双通道”方法可能是对多种其他菌株进行工程改造的一种替代方法。