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通过化学酶级联催化将玉米芯转化为糠醇和糠酸。

Valorisation of corncob into furfuryl alcohol and furoic acid via chemoenzymatic cascade catalysis.

作者信息

Ni Jiacheng, Di Junhua, Ma Cuiluan, He Yu-Cai

机构信息

National-Local Joint Engineering Research Center of Biomass Refining and High-Quality Utilization, School of Pharmacy, Changzhou University, Changzhou, China.

State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, China.

出版信息

Bioresour Bioprocess. 2021 Nov 16;8(1):113. doi: 10.1186/s40643-021-00466-3.

Abstract

Heterogeneous tin-based sulfonated graphite (Sn-GP) catalyst was prepared with graphite as carrier. The physicochemical properties of Sn-GP were captured by FT-IR, XRD, SEM and BET. Organic acids with different pKa values were used to assist Sn-GP for transforming corncob (CC), and a linear equation (Furfural yield  = - 7.563 ×  pKa  + 64.383) (R  =  0.9348) was fitted in acidic condition. Using sugarcane bagasse, reed leaf, chestnut shell, sunflower stalk and CC as feedstocks, co-catalysis of CC (75.0 g/L) with maleic acid (pKa  =  1.92) (0.5 wt%) and Sn-GP (3.6 wt%) yielded the highest furfural yield (47.3%) for 0.5 h at 170 °C. An effective furfural synthesis was conducted via co-catalysis with Sn-GP and maleic acid. Subsequently, E. coli CG-19 and TS completely catalyzed the conversion of corncob-derived FAL to furfurylalcohol and furoic acid, respectively. Valorisation of available renewable biomass to furans was successfully developed in tandem chemoenzymatic reaction.

摘要

以石墨为载体制备了非均相锡基磺化石墨(Sn-GP)催化剂。通过傅里叶变换红外光谱(FT-IR)、X射线衍射(XRD)、扫描电子显微镜(SEM)和比表面积分析仪(BET)对Sn-GP的物理化学性质进行了表征。使用具有不同pKa值的有机酸辅助Sn-GP转化玉米芯(CC),并在酸性条件下拟合得到线性方程(糠醛产率=-7.563×pKa+64.383)(R=0.9348)。以甘蔗渣、芦苇叶、板栗壳、向日葵秸秆和玉米芯为原料,将CC(75.0 g/L)与马来酸(pKa=1.92)(0.5 wt%)和Sn-GP(3.6 wt%)共同催化,在170℃下反应0.5 h,糠醛产率最高(47.3%)。通过Sn-GP和马来酸的共同催化实现了有效的糠醛合成。随后,大肠杆菌CG-19和TS分别完全催化了玉米芯衍生的FAL转化为糠醇和糠酸。通过串联化学酶促反应成功地将可用的可再生生物质转化为呋喃。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dd0/10991097/10ddf88d94f4/40643_2021_466_Fig1_HTML.jpg

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