Nijland Jeroen G, Driessen Arnold J M
Molecular Microbiology, Groningen Biomolecular Sciences and Biotechnology, University of Groningen, Groningen, Netherlands.
Front Bioeng Biotechnol. 2020 Jan 29;7:464. doi: 10.3389/fbioe.2019.00464. eCollection 2019.
Lignocellulosic biomass yields after hydrolysis, besides the hexose D-glucose, D-xylose, and L-arabinose as main pentose sugars. In second generation bioethanol production utilizing the yeast , it is critical that all three sugars are co-consumed to obtain an economically feasible and robust process. Since is unable to metabolize pentose sugars, metabolic pathway engineering has been employed to introduce the respective pathways for D-xylose and L-arabinose metabolism. However, lacks specific pentose transporters, and these sugars enter the cell with low affinity via glucose transporters of the Hxt family. Therefore, in the presence of D-glucose, utilization of D-xylose and L-arabinose is poor as the Hxt transporters prefer D-glucose. To solve this problem, heterologous expression of pentose transporters has been attempted but often with limited success due to poor expression and stability, and/or low turnover. A more successful approach is the engineering of the endogenous Hxt transporter family and evolutionary selection for D-glucose insensitive growth on pentose sugars. This has led to the identification of a critical and conserved asparagine residue in Hxt transporters that, when mutated, reduces the D-glucose affinity while leaving the D-xylose affinity mostly unaltered. Likewise, mutant Gal2 transporter have been selected supporting specific uptake of L-arabinose. In fermentation experiments, the transporter mutants support efficient uptake and consumption of pentose sugars, and even co-consumption of D-xylose and D-glucose when used at industrial concentrations. Further improvements are obtained by interfering with the post-translational inactivation of Hxt transporters at high or low D-glucose concentrations. Transporter engineering solved major limitations in pentose transport in yeast, now allowing for co-consumption of sugars that is limited only by the rates of primary metabolism. This paves the way for a more economical second-generation biofuels production process.
水解后的木质纤维素生物质除了产生己糖D - 葡萄糖外,还产生D - 木糖和L - 阿拉伯糖作为主要的戊糖。在利用酵母的第二代生物乙醇生产中,至关重要的是所有这三种糖都能被共同消耗,以获得经济上可行且稳定的生产过程。由于酵母无法代谢戊糖,因此已采用代谢途径工程来引入D - 木糖和L - 阿拉伯糖代谢的相应途径。然而,酵母缺乏特定的戊糖转运蛋白,这些糖通过Hxt家族的葡萄糖转运蛋白以低亲和力进入细胞。因此,在存在D - 葡萄糖的情况下,D - 木糖和L - 阿拉伯糖的利用较差,因为Hxt转运蛋白更喜欢D - 葡萄糖。为了解决这个问题,人们尝试了戊糖转运蛋白的异源表达,但由于表达和稳定性差,和/或周转率低,往往成效有限。一种更成功的方法是对内源Hxt转运蛋白家族进行工程改造,并通过进化选择使其在戊糖上对D - 葡萄糖不敏感生长。这导致在Hxt转运蛋白中鉴定出一个关键且保守的天冬酰胺残基,当该残基发生突变时,会降低D - 葡萄糖亲和力,而D - 木糖亲和力大多保持不变。同样,已筛选出支持L - 阿拉伯糖特异性摄取的突变型Gal2转运蛋白。在发酵实验中,转运蛋白突变体支持戊糖的有效摄取和消耗,甚至在工业浓度下使用时也能共同消耗D - 木糖和D - 葡萄糖。通过在高或低D - 葡萄糖浓度下干扰Hxt转运蛋白的翻译后失活可实现进一步改进。转运蛋白工程解决了酵母中戊糖转运的主要限制,现在允许仅受初级代谢速率限制的糖类共同消耗。这为更经济的第二代生物燃料生产过程铺平了道路。