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采用 SO/SnO-kaoline 与 E. coli CCZU-T15 细胞串联催化在甲苯-水介质中由玉米芯衍生木糖转化为糠醛醇。

Chemical-enzymatic conversion of corncob-derived xylose to furfuralcohol by the tandem catalysis with SO/SnO-kaoline and E. coli CCZU-T15 cells in toluene-water media.

机构信息

Platform of Bioethanol, Laboratory of Biochemical Engineering, College of Pharmaceutical Engineering and Life Science, Changzhou University, Changzhou, China; Hubei Collaborative Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial Biotechnology, College of Life Sciences, Hubei University, Wuhan, China; Key Laboratory of Fermentation (Ministry of Education), Hubei University of Technology, Wuhan, China.

Platform of Bioethanol, Laboratory of Biochemical Engineering, College of Pharmaceutical Engineering and Life Science, Changzhou University, Changzhou, China.

出版信息

Bioresour Technol. 2017 Dec;245(Pt A):841-849. doi: 10.1016/j.biortech.2017.08.219. Epub 2017 Sep 4.

Abstract

One-pot synthesis of furfuralcohol from corncob-derived xylose was attempted by the tandem catalysis with solid acid SO/SnO-kaoline and recombination Escherichia coli CCZU-T15 whole-cells in the toluene-water media. Using SO/SnO-kaoline (3.5wt%) as catalyst, the furfural yield of 74.3% was obtained from corncob-derived xylose in the toluene-water (1:2, v:v) containing 10mM OP-10 at 170°C for 30min. After furfural liquor was mixed with corncob-hydrolysate from the enzymatic hydrolysis of oxalic acid-pretreated corncob residue, furfural (50.5mM) could be completely biotransformed to furfuralcohol with Escherichia coli CCZU-T15 whole-cells harboring an NADH-dependent reductase (ClCR) in the toluene-water (1:3, v:v) containing 12.5mM OP-10 and 1.6mM glucose/mM furfural at 30°C and pH 6.5. Furfuralcohol was obtained at 13.0% yield based on starting material corncob (100% furfuralcohol yield for bioreduction of furfural step). Clearly, this one-pot synthesis of furfuralcohol strategy shows high potential application for the effective utilization of corncob.

摘要

尝试采用固体酸 SO/SnO-kaoline 和重组大肠杆菌 CCZU-T15 全细胞串联催化,在甲苯-水(1:2,v/v)介质中从玉米芯来源的木糖一锅合成糠醇。采用 SO/SnO-kaoline(3.5wt%)作为催化剂,在 170°C 下反应 30min,在含有 10mM OP-10 的甲苯-水(1:2,v/v)中,从玉米芯来源的木糖中可获得 74.3%的糠醛收率。糠醛液与草酸预处理玉米芯残渣的酶解玉米芯水解液混合后,在含有 12.5mM OP-10 和 1.6mM 葡萄糖/mmol 糠醛的甲苯-水(1:3,v/v)中,携带有 NADH 依赖型还原酶(ClCR)的大肠杆菌 CCZU-T15 全细胞可将糠醛完全转化为糠醇,反应温度为 30°C,pH 值为 6.5。基于起始原料玉米芯(糠醛还原步骤的 100%糠醇收率),可获得 13.0%的糠醇收率。显然,这种一锅法合成糠醇的策略显示出了有效利用玉米芯的高应用潜力。

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