Ma Zheng, Rao Zhi-ming, Shen Wei, Fang Hui-ying, Zhuge Jian
Key Laboratory of Industrial Biotechnology, Ministry of Education, China.
Wei Sheng Wu Xue Bao. 2007 Aug;47(4):598-603.
1,3-Propanediol is one of the most important industrial chemicals for its highly desired properties and its wide applications as a key component of an emerging polymer business. Biological production of 1,3-propanediol has been a novel and competitive way. In our previous job, the gene dahB encoding for glycerol dehydratase from Klebsiella and the gene yqhD encoding for 1,3-propanediol oxidoreductase isoenzyme from E. coli were cloned respectively. The two genes were then tandemly ligated and expressed successfully in E. coli. The recombinant E. coli strain could produce 1,3-propanediol from D-glycerol. In the current research, the expression vectors including pGAPZB-yqhD, pGAPZB-dhaB and pYX212-zeocin-pGAP-yqhD-pGAP-dhaB were furtherly constructed on the basis of our previous job. Then the vector pYX212-zeocin-pGAP-yqhD-pGAP-dhaB was introduced into Saccharomyces cerevisiae W303-1A using LiAc transformation method successfully. D-glucose is used as substrate to produce 1,3-propanediol with the recombinant strain after fermentation for 72h. SDS-PAGE analysis showed recombinant products at about 61kD, 43kD, 21kD, 15kD, consistent with the molecular weight from the report. The specific enzymatic activity of the glycerol dehydratase and 1,3-propanediol oxidoreductase isoenzyme of the recombinant yeast strain S. cerevisiae W303-1A/pYX2l2-zeocin-pGAP-yqhD-pGAP-dhaB were 24U/mg protein and 15U/mg protein, respectively, while those of the control were undetectable. In contrast to the wild strain without 1,3-propanediol output, 1,3-propanediol concentration of the recombinant yeast strain S. cerevisiae W303-1A/pYX212-zeocin-pGAP-yqhD-pGAP-dhaB reaches about 1.5g/L. The above results showed that the engineered S. cerevisiae strain which can convert the D-glucose as substrate to produce 1,3-propanediol by one-step fermentation was constructed successfully. This accomplishment bodes well for future construction of recombinant yeast strain which could overproduce 1,3-propanediol with the lower cost feedstock D-glucose by introducing the two genes yqhD and dhaB into the yeast strain overproducing glycerol with D-glucose (e.g. Candida glycerinogenes WL2002-5, which is capable of producing glycerol more than 120g/L with D-glucose as substrate and has been used for the commercial production of glycerol).
1,3 - 丙二醇因其具有高度理想的特性以及作为新兴聚合物业务关键成分的广泛应用,成为最重要的工业化学品之一。1,3 - 丙二醇的生物生产是一种新颖且具有竞争力的方式。在我们之前的工作中,分别克隆了来自克雷伯氏菌的编码甘油脱水酶的基因dahB和来自大肠杆菌的编码1,3 - 丙二醇氧化还原酶同工酶的基因yqhD。然后将这两个基因串联连接并在大肠杆菌中成功表达。重组大肠杆菌菌株能够从D - 甘油生产1,3 - 丙二醇。在当前研究中,基于我们之前的工作进一步构建了表达载体,包括pGAPZB - yqhD、pGAPZB - dhaB和pYX212 - zeocin - pGAP - yqhD - pGAP - dhaB。然后使用醋酸锂转化法将载体pYX212 - zeocin - pGAP - yqhD - pGAP - dhaB成功导入酿酒酵母W303 - 1A。发酵72小时后,用重组菌株以D - 葡萄糖为底物生产1,3 - 丙二醇。SDS - PAGE分析显示重组产物在约61kD、43kD、21kD、15kD处,与报道的分子量一致。重组酿酒酵母菌株S. cerevisiae W303 - 1A/pYX2l2 - zeocin - pGAP - yqhD - pGAP - dhaB的甘油脱水酶和1,3 - 丙二醇氧化还原酶同工酶的比酶活性分别为24U/mg蛋白和15U/mg蛋白,而对照的比酶活性未检测到。与不产生1,3 - 丙二醇的野生菌株相比,重组酿酒酵母菌株S. cerevisiae W303 - 1A/pYX212 - zeocin - pGAP - yqhD - pGAP - dhaB的1,3 - 丙二醇浓度达到约1.5g/L。上述结果表明成功构建了能以D - 葡萄糖为底物通过一步发酵生产1,3 - 丙二醇的工程酿酒酵母菌株。这一成果为未来通过将yqhD和dhaB两个基因导入以D - 葡萄糖过量生产甘油的酵母菌株(例如甘油假丝酵母WL2002 - 5,其能够以D - 葡萄糖为底物生产超过120g/L的甘油且已用于甘油的商业化生产)构建能以低成本原料D - 葡萄糖过量生产1,3 - 丙二醇的重组酵母菌株奠定了良好基础。