Yao He, Hongxing Li, Liyuan Chen, Liyuan Zheng, Chunhui Ye, Jin Hou, Xiaoming Bao, Weifeng Liu, Yu Shen
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引用次数: 5
摘要
木糖醇商业规模生产产生的木糖母液废液和玉米芯渣产量过高,造成了环境问题。为了减少浪费,一株耐WXML的酿酒酵母菌株被赋予了表达木糖还原酶基因的能力,木糖还原酶是一种木糖特异性转运蛋白,也是戊糖磷酸途径的酶。该菌株以葡萄糖为共底物,在WXML中以木糖为原料生产木糖醇的能力很高。此外,设计了一种同时糖化和发酵(SSF)工艺,利用玉米芯渣和纤维素酶代替直接添加葡萄糖作为共底物。采用20% WXML、55 g DCW l-1脱木素玉米芯渣和11.8 FPU cellulose-1纤维素酶在35°条件下发酵,木糖醇滴度和产率分别为91.0 g l-1和1.26±0.01 g l-1 h-1。本研究证明了固体燃料利用废弃物进行木糖醇发酵的良好策略。
Production of xylitol by Saccharomyces cerevisiae using waste xylose mother liquor and corncob residues
Exorbitant outputs of waste xylose mother liquor (WXML) and corncob residue from commercial-scale production of xylitol create environmental problems. To reduce the wastes, a Saccharomyces cerevisiae strain tolerant to WXML was conferred with abilities to express the genes of xylose reductase, a xylose-specific transporter and enzymes of the pentose phosphate pathway. This strain showed a high capacity to produce xylitol from xylose in WXML with glucose as a co-substrate. Additionally, a simultaneous saccharification and fermentation (SSF) process was designed to use corncob residues and cellulase instead of directly adding glucose as a co-substrate. Xylitol titer and the productivity were, respectively, 91.0 g l-1 and 1.26 ± 0.01 g l-1 h-1 using 20% WXML, 55 g DCW l-1 delignified corncob residues and 11.8 FPU gcellulose-1 cellulase at 35° during fermentation. This work demonstrates the promising strategy of SSF to exploit waste products to xylitol fermentation process.
期刊介绍:
Microbial Biotechnology publishes papers of original research reporting significant advances in any aspect of microbial applications, including, but not limited to biotechnologies related to: Green chemistry; Primary metabolites; Food, beverages and supplements; Secondary metabolites and natural products; Pharmaceuticals; Diagnostics; Agriculture; Bioenergy; Biomining, including oil recovery and processing; Bioremediation; Biopolymers, biomaterials; Bionanotechnology; Biosurfactants and bioemulsifiers; Compatible solutes and bioprotectants; Biosensors, monitoring systems, quantitative microbial risk assessment; Technology development; Protein engineering; Functional genomics; Metabolic engineering; Metabolic design; Systems analysis, modelling; Process engineering; Biologically-based analytical methods; Microbially-based strategies in public health; Microbially-based strategies to influence global processes