Nichols Nancy N, Quarterman Joshua C, Frazer Sarah E
Bioenergy Research Unit, National Center for Agricultural Utilization Research, Agricultural Research Service, USDA, 1815 N. University Street, Peoria, IL 61604, USA.
Biol Methods Protoc. 2018 Jan 29;3(1):bpx012. doi: 10.1093/biomethods/bpx012. eCollection 2018.
A reporter gene encoding green fluorescent protein (GFP) was introduced into the ascomycete NRRL30616, and fluorescence of cultures was monitored as a measure of cell growth. Fluorescence in the GFP-expressing strain was measured during growth of cells in defined and complex media as well as in the liquor derived from pretreatment of corn stover, an agricultural residue. Fluorescence mirrored growth of cultures, as measured by optical density and counts of colony forming units. Because traditional methods to monitor growth cannot be used in biomass liquors due to its fibrous, dark-colored nature, the speed and convenience of using GFP to monitor growth is advantageous. Fluorescence of cultures in biomass hydrolysate also correlated with the concentration of furfural in hydrolysate. Furfural and other compounds, present in hydrolysate due to physico-chemical pretreatment of biomass, are inhibitory to fermenting microbes. Therefore, measurement of fluorescence in GFP-expressing is a proxy for measures of microbial growth and furfural consumption, and serves as a convenient indicator of metabolism of fermentation inhibitors in biomass hydrolysate.
将编码绿色荧光蛋白(GFP)的报告基因导入子囊菌NRRL30616中,并监测培养物的荧光以衡量细胞生长。在限定培养基、复合培养基以及来源于农业废弃物玉米秸秆预处理液中培养细胞的过程中,对表达GFP的菌株的荧光进行了测量。荧光反映了培养物的生长情况,这通过光密度和菌落形成单位计数来衡量。由于生物质液具有纤维状、深色的特性,传统的生长监测方法无法用于生物质液,因此利用GFP监测生长的速度和便利性具有优势。生物质水解产物中培养物的荧光也与水解产物中糠醛的浓度相关。由于生物质的物理化学预处理,水解产物中存在的糠醛和其他化合物对发酵微生物具有抑制作用。因此,测量表达GFP的微生物中的荧光可替代微生物生长和糠醛消耗的测量,并作为生物质水解产物中发酵抑制剂代谢的便捷指标。