首页> 美国卫生研究院文献>EXCLI Journal >On-site cellulase production by Trichoderma reesei 3EMS35 mutant and same vessel saccharification and fermentation of acid treated wheat straw for ethanol production
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On-site cellulase production by Trichoderma reesei 3EMS35 mutant and same vessel saccharification and fermentation of acid treated wheat straw for ethanol production

机译:里氏木霉3EMS35突变体的现场纤维素酶生产以及酸处理的小麦秸秆的相同容器糖化和发酵以生产乙醇

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摘要

Bioethanol production from lignocellulosic raw materials involves process steps like pre-treatment, enzymatic hydrolysis, fermentation and distillation. In this study, wheat straw was explored as feedstock for on-site cellulase production by T. reesei 3EMS35 mutant, and as a substrate for second generation bioethanol production from baker yeast. Scanning electron microscopy (SEM) and X-ray diffractography (XRD) of untreated wheat straw (UWS) and acid treated wheat straw (TWS) were done to understand the structural organization and changes in the cellulase accessibility and reactivity. The effect of delignification and structural modification for on-site cellulase enzyme production was comparably studied. The efficiency of crude cellulase enzyme for digestion of UWS and TWS and then production of ethanol from TWS was studied using same-vessel saccharification and fermentation (SVSF) technique, both in shaking flasks as well as in fermenters. Two different methods of operation were tested, i.e. the UWSEnz method, where UWS was used for on-site enzyme production, and TWSEnz method where TWS was applied as substrate for cellullase production. Results obtained showed structural modifications in cellulose of TWS due to delignification, removal of wax and change of crystallinity. UWS was better substrate than TWS for cellulase production due to the fact that lignin did not hinder the enzyme production by fungus but acted as a booster. On-site cellulase enzyme produced by T. reesei 3EMS35 mutant hydrolyzed most of cellulose (91 %) in TWS within first 24 hrs. Shake flasks experiments showed that ethanol titers and yields with UWSEnz were 2.9 times higher compared to those obtained with TWSEnz method respectively. Comparatively, titer of ethanol in shake flask experiments was 10 % higher than this obtained in 3 L fermenter with UWSEnz. Outcomes from this investigation clearly demonstrated the potential of on-site cellulase enzyme production and SVSF for ethanol production from wheat straw.
机译:从木质纤维素原料生产生物乙醇涉及诸如预处理,酶促水解,发酵和蒸馏之类的工艺步骤。在这项研究中,麦草被用作里氏木霉3EMS35突变体现场纤维素酶生产的原料,并被用作面包酵母第二代生物乙醇生产的底物。对未处理的小麦秸秆(UWS)和酸处理的小麦秸秆(TWS)进行扫描电子显微镜(SEM)和X射线衍射(XRD),以了解纤维素酶的结构组织以及可及性和反应性的变化。比较了去木质素和结构修饰对现场纤维素酶生产的影响。在摇瓶和发酵罐中,使用相同容器的糖化和发酵(SVSF)技术研究了粗纤维素酶消化UWS和TWS,然后从TWS生产乙醇的效率。测试了两种不同的操作方法,即使用UWS进行现场酶生产的UWSEnz方法和使用TWS进行纤维素酶生产的底物的TWSEnz方法。获得的结果显示由于脱木质素,蜡的去除和结晶度的改变,TWS的纤维素中的结构改变。对于纤维素酶生产,UWS比TWS更好的底物,这是因为木质素不会阻碍真菌产生酶,而是起到促进作用。里氏木霉3EMS35突变体产生的现场纤维素酶在最初的24小时内水解了TWS中的大部分纤维素(91%)。摇瓶实验表明,使用UWSEnz的乙醇滴度和收率分别是使用TWSEnz方法获得的乙醇滴度和收率的2.9倍。相比之下,摇瓶实验中的乙醇滴度比用UWSEnz在3 L发酵罐中获得的乙醇滴度高10%。这项调查的结果清楚地证明了现场纤维素酶生产和SVSF在小麦秸秆中生产乙醇的潜力。

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