Department of Biological and Agricultural Engineering, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA.
Enzyme Microb Technol. 2013 Mar 5;52(3):184-9. doi: 10.1016/j.enzmictec.2012.12.010. Epub 2013 Jan 7.
Direct cellobiose production from cellulose by a genetically modified fungus-Neurospora crassa, was explored in this study. A library of N. crassa sextuple beta-glucosidase (bgl) gene deletion strains was constructed. Various concentrations of cellobiose were detected in the culture broth of the N. crassa sextuple beta-glucosidase (bgl) gene deletion strains when grown on Avicel without exogenous cellulase addition. The sextuple bgl deletion strains expressing one of the three basally transcribed bgl genes are the best cellobiose producers. For most sextuple strains, the multiple bgl gene deletion has no negative effect on the production of other cellulases. The induction of major endoglucanases and exoglucanases on Avicel in most of the sextuple bgl deletions strains was as fast as or faster than that of the wild type, except for strain F4. The best cellobiose producing strain, F5, produced 7.7 g/L of cellobiose from 20 g/L of Avicel in four days and utilized the Avicel as fast as did the wild type (even in the presence of high cellobiose concentration). The cellobiose yield from cellulose was about 48.3%.
本研究探索了通过遗传修饰真菌——粗糙脉孢菌(Neurospora crassa)将纤维素直接转化为纤维二糖。构建了粗糙脉孢菌六倍体β-葡萄糖苷酶(bgl)基因缺失文库。当在不含外源性纤维素酶的微晶纤维素上生长时,在 N. crassa 六倍体β-葡萄糖苷酶(bgl)基因缺失菌株的培养液中检测到各种浓度的纤维二糖。表达三种基础转录的 bgl 基因之一的六倍体 bgl 缺失菌株是最佳的纤维二糖生产菌。对于大多数六倍体菌株,多个 bgl 基因缺失对其他纤维素酶的产生没有负面影响。除了菌株 F4 外,大多数六倍体 bgl 缺失菌株在微晶纤维素上诱导内切葡聚糖酶和外切葡聚糖酶的速度与野生型一样快或更快。最佳的纤维二糖生产菌株 F5 在四天内从 20 g/L 的微晶纤维素中生产了 7.7 g/L 的纤维二糖,并且与野生型一样快速利用微晶纤维素(即使在存在高浓度纤维二糖的情况下)。纤维素的纤维二糖得率约为 48.3%。