Li Yun-Cheng, Gou Zi-Xi, Liu Ze-Shen, Tang Yue-Qin, Akamatsu Takashi, Kida Kenji
College of Light Industry Textile and Food Engineering, Sichuan University, Chengdu, 610064, Sichuan, China.
Biotechnol Lett. 2014 Oct;36(10):2011-21. doi: 10.1007/s10529-014-1581-7. Epub 2014 Jun 26.
In the industrial production of bioethanol from lignocellulosic biomass, a strain of Saccharomyces cerevisiae that can ferment xylose in the presence of inhibitors is of utmost importance. The recombinant, industrial-flocculating S. cerevisiae strain NAPX37, which can ferment xylose, was used as the parent to delete the gene encoding p-nitrophenylphosphatase (PHO13) and overexpress the gene encoding transaldolase (TAL1) to evaluate the synergistic effects of these two genes on xylose fermentation in the presence of weak acid inhibitors, including formic, acetic, or levulinic acids. TAL1 over-expression or PHO13 deletion improved xylose fermentation as well as the tolerance of NAPX37 to all three weak acids. The simultaneous deletion of PHO13 and the over-expression of TAL1 had synergistic effects and improved ethanol production and reduction of xylitol accumulation in the absence and presence of weak acid inhibitors.
在从木质纤维素生物质工业生产生物乙醇的过程中,一株能够在抑制剂存在的情况下发酵木糖的酿酒酵母菌株至关重要。重组的工业絮凝酿酒酵母菌株NAPX37能够发酵木糖,以此为亲本删除编码对硝基苯磷酸酶(PHO13)的基因,并过表达编码转醛醇酶(TAL1)的基因,以评估这两个基因在甲酸、乙酸或乙酰丙酸等弱酸抑制剂存在的情况下对木糖发酵的协同作用。TAL1的过表达或PHO13的缺失改善了木糖发酵以及NAPX37对所有三种弱酸的耐受性。在不存在和存在弱酸抑制剂的情况下,同时删除PHO13和过表达TAL1具有协同作用,提高了乙醇产量并减少了木糖醇积累。