State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
Shandong Provincial Key Laboratory of Microbial Engineering, Department of Bioengineering, Qilu University of Technology, Shandong, China.
Biotechnol Bioeng. 2018 Jan;115(1):60-69. doi: 10.1002/bit.26444. Epub 2017 Oct 6.
Despite the well-recognized merits of simultaneous saccharification and co-fermentation (SSCF) on relieving sugar product inhibition on cellulase activity, a practical concomitance difficulty of xylose with inhibitors in the pretreated lignocellulose feedstock prohibits the essential application of SSCF for cellulosic ethanol fermentation. To maximize the SSCF potentials for cellulosic ethanol production, a dry biorefining approach was proposed starting from dry acid pretreatment, disk milling, and biodetoxification of lignocellulose feedstock. The successful SSCF of the inhibitor free and xylose conserved lignocellulose feedstock after dry biorefining reached a record high ethanol titer at moderate cellulase usage and minimum wastewater generation. For wheat straw, 101.4 g/L of ethanol (equivalent to 12.8% in volumetric percentage) was produced with the overall yield of 74.8% from cellulose and xylose, in which the xylose conversion was 73.9%, at the moderate cellulase usage of 15 mg protein per gram cellulose. For corn stover, 85.1 g/L of ethanol (equivalent to 10.8% in volumetric percentage) is produced with the overall conversion of 84.7% from cellulose and xylose, in which the xylose conversion was 87.7%, at the minimum cellulase usage of 10 mg protein per gram cellulose. Most significantly, the SSCF operation achieved the high conversion efficiency by generating the minimum amount of wastewater. Both the fermentation efficiency and the wastewater generation in the current dry biorefining for cellulosic ethanol production are very close to that of corn ethanol production, indicating that the technical gap between cellulosic ethanol and corn ethanol has been gradually filled by the advancing biorefining technology.
尽管同步糖化和共发酵 (SSCF) 在缓解纤维素酶活性的糖产物抑制方面具有公认的优点,但木质纤维素原料预处理中木糖与抑制剂的实际共存困难,限制了 SSCF 在纤维素乙醇发酵中的重要应用。为了最大限度地发挥 SSCF 在纤维素乙醇生产中的潜力,提出了一种从干酸预处理、盘式粉碎和木质纤维素原料的生物解毒开始的干法生物炼制方法。成功地对无抑制剂和保留木糖的木质纤维素原料进行了 SSCF,在使用中等纤维素酶用量和最小废水生成的情况下,达到了创纪录的高乙醇浓度。对于小麦秸秆,在中等纤维素酶用量 15mg 蛋白/g 纤维素的情况下,用 74.8%的纤维素和木糖总收率,其中木糖转化率为 73.9%,生产出 101.4g/L 的乙醇(体积百分比相当于 12.8%)。对于玉米秸秆,用 84.7%的纤维素和木糖总转化率,其中木糖转化率为 87.7%,在最低纤维素酶用量 10mg 蛋白/g 纤维素的情况下,生产出 85.1g/L 的乙醇(体积百分比相当于 10.8%)。最重要的是,SSCF 操作通过生成最少的废水实现了高转化率效率。纤维素乙醇生产中当前的干法生物炼制的发酵效率和废水生成量都非常接近玉米乙醇生产,表明随着生物炼制技术的不断进步,纤维素乙醇和玉米乙醇之间的技术差距正在逐渐缩小。