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利用基因工程改造菌株大肠杆菌KO11强化啤酒厂废水的乙醇发酵

Enhanced ethanol fermentation of brewery wastewater using the genetically modified strain E. coli KO11.

作者信息

Rao Kripa, Chaudhari Vaibhav, Varanasi Sasidhar, Kim Dong-Shik

机构信息

Department of Chemical and Environmental Engineering, University of Toledo, Toledo, OH 43606, USA.

出版信息

Appl Microbiol Biotechnol. 2007 Feb;74(1):50-60. doi: 10.1007/s00253-006-0643-8. Epub 2006 Oct 17.

Abstract

We have used liquid waste obtained from a beer brewery process to produce ethanol. To increase the productivity, genetically modified organism, Escherichia coli KO11, was used for ethanol fermentation. Yeast was also used to produce ethanol from the same feed stock, and the ethanol production rates and resulting concentrations of sugars and ethanol were compared with those of KO11. In the experiments, first the raw wastewater was directly fermented using two strains with no saccharification enzymes added. Then, commercial enzymes, alpha-amylase, pectinase, or a combination of both, were used for simultaneous saccharification and fermentation, and the results were compared with those of the no-enzyme experiments for KO11 and yeast. Under the given conditions with or without the enzymes, yeast produced ethanol more rapidly than E. coli KO11, but the final ethanol concentrations were almost the same. For both yeast and KO11, the enzymes were observed to enhance the ethanol yields by 61-84% as compared to the fermentation without enzymes. The combination of the two enzymes increased ethanol production the most for the both strains. The advantages of using KO11 were not demonstrated clearly as compared to the yeast fermentation results.

摘要

我们利用啤酒酿造过程产生的废液来生产乙醇。为提高生产率,使用了转基因生物大肠杆菌KO11进行乙醇发酵。还使用酵母从相同原料生产乙醇,并将乙醇生产率以及糖和乙醇的最终浓度与大肠杆菌KO11的进行比较。在实验中,首先在不添加糖化酶的情况下使用两种菌株直接发酵原废水。然后,使用商业酶(α-淀粉酶、果胶酶或两者的组合)进行同步糖化和发酵,并将结果与大肠杆菌KO11和酵母的无酶实验结果进行比较。在有或没有酶的给定条件下,酵母产生乙醇的速度比大肠杆菌KO11快,但最终乙醇浓度几乎相同。对于酵母和大肠杆菌KO11,与无酶发酵相比,观察到酶可使乙醇产量提高61%至84%。两种酶的组合对两种菌株的乙醇产量提高最大。与酵母发酵结果相比,使用大肠杆菌KO11的优势并未得到明显体现。

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