文献类型：期刊文献

中文题名：构建伴有β-葡萄糖苷酶表达的乙醇发酵大肠杆菌

英文题名：Construction of an ethanologenic Escherichia coli strain expressing β-glucosidase

作者：张瑶[1];罗紫臣[1];高秋强[1];鲍杰[1]

机构：[1]华东理工大学生物工程学院生物反应器工程国家重点实验室,上海200237

年份：2013

卷号：29

期号：9

起止页码：1254

中文期刊名：生物工程学报

外文期刊名：Chinese Journal of Biotechnology

收录：CSTPCD;;Scopus;北大核心:【北大核心2011】；CSCD:【CSCD2013_2014】；PubMed;

基金：国家重点基础研究发展计划(973计划)(No.2011CB707406);国家高技术研究发展计划(863计划)(No.2012AA022301);中国博士后基金(No.2012M520850);中央高校基本科研业务费专项资金(Nos.WF0913005;WF1314036)资助~~

语种：中文

中文关键词：大肠杆菌;乙醇发酵;β-葡萄糖苷酶;分泌表达;整合生物加工

外文关键词：Escherichia coli, ethanol fermentation, β-glucosidase, secretive expression, consolidated bioprocessing

摘要：研究构建能够分泌表达纤维素酶的产乙醇菌株,实现降解木质纤维素生产乙醇的整合生物加工过程。文中通过克隆来自运动发酵单胞菌Zymomonas mobilis ZM4的丙酮酸脱羧酶基因pdc和乙醇脱氢酶基因adhB,并通过Red重组将二者整合到大肠杆菌Escherichia coli JM109基因组中,首先构建了一株可以利用葡萄糖进行乙醇发酵的重组菌E.coli P81。随后将来源于多粘芽胞杆菌Bacillus polymyxa1.794的β-葡萄糖苷酶基因bglB在E.coli P81中进行了分泌表达,得到了一株可以进行纤维二糖降解和乙醇发酵双重功能的重组菌E.coli P81(pUC19-bglB)。该菌胞外分泌β-糖苷酶活达到84.78 mU/mL菌液,纤维二糖酶活达到了32.32 mU/mL菌液。该重组菌E.coli P81(pUC19-bglB)以纤维二糖为碳源进行乙醇发酵,乙醇得率达到了理论产率55.8%,而在葡萄糖和纤维二糖的共发酵中,其乙醇产量达到了理论产率46.5%。构建得到的此株整合生物加工大肠杆菌能够利用β-葡萄糖苷酶生产乙醇,为构建能利用木质纤维素分解产物生产燃料乙醇的高效、稳定生产用工程菌奠定了良好的基础。
Constructing ethanologenic strains with cellulose activity is important to achieve consolidated bioprocessing of lignocellulose for ethanol production. In this study, we integrated the pyruvate decarboxylase gene pdc and alcohol dehydrogenase gene adhB from Zymomonas mobilis ZM4 into Escherichia coli JM109 by Red recombination method to generatea recombinant strain E. coli P8 lthat could produce ethanol from glucose. Aβ-glucosidase gene bglB from Bacillus polymyxa 1.794 was cloned into the recombinant E. coli P81 and β-glucosidase was expressed to give a new recombinant strain E. coli P81 （pUC19-bglB） with dual functions of cellobiose degradation and ethanol production. The extracellularβ-glucosidaseactivity was 84.78 mU/mL broth and the extracellular cellobiase activity of E. coli P81 （pUC19-bglB） was 32.32 mU/mL broth. E. coli P81 （pUC19-bglB） fermented cellobiose to ethanol with a yield of 55.8% of the theoretical value, and when glucose and cellobiose were co-fermented, the ethanol yield reached 46.5% of thetheoretical value. The construction of consolidated bioprocessing strain opens the possibility to convert cellobiose to ethanol in a single bioprocess.