Collaborative Research: Molecular Design of Thermophilic Alcohol Dehydrogenase for Chiral Synthesis

合作研究：用于手性合成的嗜热醇脱氢酶的分子设计

• 批准号: 0445750
• 负责人: J. Gregory Zeikus
• 金额: $ 33.38万
• 依托单位: Michigan State University
• 依托单位国家: 美国
• 项目类别: Continuing Grant
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-03-15 至 2009-02-28
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=0445750&HistoricalAwards=false
• 关键词: Collaborative; Research; Molecular; Design; Thermophilic

In this collaborative project, the biochemistry and molecular biology of Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase (TeSADH) will be investigated. This enzyme has a novel metabolic biochemistry, since physiologically it synthesizes ethanol in two reductive steps from acetyl-CoA. This, in part, explains its natural broad substrate specificity. In this project, TeSADH will be used as a model system to understand the physicochemical bases for substrate specificity and stereospecificity of enzymes. Genetic engineering studies of TeSADH will include: 1) Rational design of the small substrate-binding pocket to determine its role in (S)- versus (R)-enantiospecificity; 2) Evolving TeSADH by directed evolution from an (S)-specific enzyme into an enzyme with high (R)-enantiospecificity; and 3) Changing TeSADH cofactor specificity from NADP+ towards NAD+. TeSADH is uniquely suited for these investigations because of its high thermostability and its broad substrate specificity. The effects of the mutations will be evaluated in terms of substrate specificity, kinetic parameters, and enantiomeric specificity. Broader Impacts: The modified enzymes resulting from this research could be potentially used in preparation of chiral intermediates in commercial synthesis. The results of the proposed research are likely to make a significant intellectual contribution to a greater understanding or the physical biochemical basis of enzymatic stereospecificity, as well as to provide novel biocatalysts with potential industrial utility. The project's outreach program includes training multidisciplinary graduate and undergraduate students, including minorities; disseminating knowledge in courses at the grantee institutions; and presenting papers at national chemistry, biochemistry, chemical engineering, and microbiology meetings.

本合作项目对嗜热厌氧乙醇菌仲醇脱氢酶（TeSADH）的生物化学和分子生物学进行了研究。这种酶具有新的代谢生物化学，因为它在生理上以两个还原步骤从乙酰辅酶A合成乙醇。这在一定程度上解释了其天然的广泛底物特异性。在这个项目中，TeSADH将被用作模型系统，以了解酶的底物特异性和立体特异性的物理化学基础。TeSADH的基因工程研究将包括：1）合理设计小底物结合口袋，以确定其在（S）-对（R）-对映体特异性中的作用; 2）通过定向进化将TeSADH从（S）-特异性酶进化为具有高（R）-对映体特异性的酶; 3）将TeSADH辅因子特异性从NADP+变为NAD+。TeSADH由于其高热稳定性和广泛的底物特异性而独特地适合于这些研究。将根据底物特异性、动力学参数和对映体特异性评价突变的影响。更广泛的影响：本研究所得到的修饰酶可用于手性中间体的制备。拟议的研究结果可能会作出重大的智力贡献，更好地理解或酶的立体专一性的物理生化基础，以及提供新的生物催化剂与潜在的工业实用性。该项目的外展计划包括培训多学科研究生和本科生，包括少数族裔;在受资助机构的课程中传播知识;以及在国家化学、生物化学、化学工程和微生物学会议上发表论文。