首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Separate hydrolysis and fermentation (SHF) of Prosopis juliflora, a woody substrate, for the production of cellulosic ethanol by Saccharomyces cerevisiae and Pichia stipitis-NCIM 3498
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Separate hydrolysis and fermentation (SHF) of Prosopis juliflora, a woody substrate, for the production of cellulosic ethanol by Saccharomyces cerevisiae and Pichia stipitis-NCIM 3498

机译:木本底物Prosopis juliflora的单独水解和发酵(SHF),用于通过酿酒酵母和粘质毕赤酵母生产纤维素乙醇-NCIM 3498

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摘要

Prosopis juliflora (Mesquite) is a raw material for long-term sustainable production of cellulosics ethanol. In this study, we used acid pretreatment, delignification and enzymatic hydrolysis to evaluate the pretreatment to produce more sugar, to be fermented to ethanol. Dilute H_2SO_4 (3.0%, v/v) treatment resulted in hydrolysis of hemicelluloses from lignocellulosic complex to pentose sugars along with other byproducts such as furfural, hydroxymethyl furfural (HMF), phenolics and acetic acid. The acid pretreated substrate was delignified to the extent of 93.2% by the combined action of sodium sulphite (5.0%, w/v) and sodium chlorite (3.0%, w/v). The remaining cellulosic residue was enzymatically hydrolyzed in 0.05 M citrate phosphate buffer (pH 5.0) using 3.0 U of filter paper cellulase (FPase) and 9.0 U of b-glucosidase per mL of citrate phosphate buffer. The maximum enzymatic saccharification of cellulosic material (82.8%) was achieved after 28 h incubation at 50 ℃. The fermentation of both acid and enzymatic hydrolysates, containing 18.24 g/L and 37.47 g/L sugars, with Pichia stipitis and Saccharomyces cerevisiae produced 7.13 g/L and 18.52 g/L of ethanol with corresponding yield of 0.39 g/g and 0.49 g/g, respectively.
机译:胡桃木(Prosopis juliflora)是长期可持续生产纤维素乙醇的原料。在这项研究中,我们使用了酸预处理,去木质素和酶水解作用来评估预处理以生产更多糖并发酵为乙醇。稀H_2SO_4(3.0%,v / v)处理导致半纤维素与其他副产物(例如糠醛,羟甲基糠醛(HMF),酚醛树脂和乙酸)从木质纤维素复合物水解为戊糖。通过亚硫酸钠(5.0%,w / v)和亚氯酸钠(3.0%,w / v)的联合作用,酸预处理的底物被脱木质素至93.2%的程度。使用每毫升柠檬酸磷酸缓冲液3.0 U滤纸纤维素酶(FPase)和9.0 U b-葡萄糖苷酶,在0.05 M柠檬酸磷酸缓冲液(pH 5.0)中酶解剩余的纤维素残留物。在50℃保温28 h后,纤维素物质的最大酶促糖化率为82.8%。酸和酶水解产物(分别含18.24 g / L和37.47 g / L糖)与毕赤酵母和酿酒酵母的发酵产生7.13 g / L和18.52 g / L乙醇,相应产量分别为0.39 g / g和0.49 g / g。

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