State Key Laboratory of Microbial Technology, Shandong University, No. 72, Binhai Road, Qingdao 266237, China.
Int J Mol Sci. 2024 Nov 16;25(22):12306. doi: 10.3390/ijms252212306.
The bioconversion of lignocellulosic biomass, which are abundant and renewable resources, into liquid fuels and bulk chemicals is a promising solution to the current challenges of resource scarcity, energy crisis, and carbon emissions. Considering the separation of some end-products, it is necessary to firstly obtain a high concentration separated fermentable sugar solution, and then conduct fermentation. For this purpose, in this study, using acid catalyzed steam explosion pretreated corn stover (ACSE-CS) and corn cob residues (CCR) as cellulosic substrate, respectively, the batch feeding strategies and enzymatic hydrolysis conditions were investigated to achieve the efficient enzymatic hydrolysis at high solid loading. It was shown that the fermentable sugar solutions of 161.2 g/L and 205 g/L were obtained, respectively, by fed-batch enzymatic hydrolysis of ACSE-CS under 30% of final solid loading with 10 FPU/g DM of crude cellulase, and of CCR at 27% of final solid loading with 8 FPU/g DM of crude cellulase, which have the potential to be directly applied to the large-scale fermentation process without the need for concentration, and the conversion of glucan in ACSE-CS and CCR reached 80.9% and 87.6%, respectively, at 72 h of enzymatic hydrolysis. This study also applied the fed-batch simultaneous saccharification and co-fermentation process to effectively convert the two cellulosic substrates into ethanol, and the ethanol concentrations in fermentation broth reached 46.1 g/L and 72.8 g/L for ACSE-CS and CCR, respectively, at 144 h of fermentation. This study provides a valuable reference for the establishment of "sugar platform" based on lignocellulosic biomass and the production of cellulosic ethanol.
将丰富且可再生的木质纤维素生物质转化为液体燃料和大宗化学品,是解决当前资源短缺、能源危机和碳排放问题的一种有前途的方法。考虑到一些最终产物的分离,首先需要获得高浓度的可发酵糖溶液,然后进行发酵。为此,本研究分别以酸催化蒸汽爆破预处理玉米秸秆(ACSE-CS)和玉米芯残渣(CCR)为纤维素基质,研究了分批进料策略和酶解条件,以在高固体负荷下实现高效酶解。结果表明,在 30%最终固体负荷下,采用分批进料酶解 ACSE-CS,用 10 FPU/g DM 粗纤维素酶进行酶解,可获得 161.2 g/L 的可发酵糖溶液;在 27%最终固体负荷下,用 8 FPU/g DM 粗纤维素酶进行酶解,可获得 205 g/L 的可发酵糖溶液,无需浓缩即可直接应用于大规模发酵过程,且 ACSE-CS 和 CCR 中的葡聚糖转化率分别达到 80.9%和 87.6%,在 72 h 酶解时。本研究还应用分批进料同步糖化共发酵工艺有效地将两种纤维素基质转化为乙醇,在发酵 144 h 时,发酵液中 ACSE-CS 和 CCR 的乙醇浓度分别达到 46.1 g/L 和 72.8 g/L。本研究为建立基于木质纤维素生物质的“糖平台”和生产纤维素乙醇提供了有价值的参考。