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Harnessing Polyketide Natural Product Biosynthesis

Harnessing Polyketide Natural Product Biosynthesis
利用聚酮化合物天然产物生物合成
批准号:
RGPIN-2014-06167
负责人:
Boddy, Christopher
金额:
$7.18万
依托单位:
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2018
资助国家:
加拿大
项目状态:
已结题
起止时间:
2018-01-01 至 2019-12-31

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项目成果

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中文摘要
翻译
酶化学是生产复杂分子的有力工具,但它主要用于产生高纯度的生热中心。酶广泛用于研究和制造的一个主要限制是目前通过酶反应获得的有限的化学多样性。这与合成有机化学形成了鲜明的对比。为了扩大酶在合成中的应用,必须增加可行的酶反应的有限工具箱。**天然产物的结构表明,酶反应可以获得令人难以置信的化学多样性。产生这些天然产物的酶非常适合于满足合成化学家在合成多功能复杂分子时所需的高立体选择性、区域选择性和化学选择性的严格要求。**我的研究计划检查负责聚酮天然产物生产的生物合成途径,以识别和利用能够扩展我们的酶工具箱的酶。虽然我们的长期目标是使用这些酶在体内和体外快速生产不同的分子,但我们的近期目标是开发可用于天然产物的化学酶合成的新催化剂。天然产物全合成是新化学方法学的严格试验场,新酶在这一领域的成功整合将促进它们在研究和制造中的更广泛应用。**为了满足我们扩大现有酶反应工具箱的长期目标,我们提出了三个短期目标:**1)开发硫代酯酶以催化大环化。大环化反应是合成过程中最关键的一步,它可以决定任何合成路线的整体效率。还没有开发出酶法来合成这个关键的官能团。这一目标使我们能够用目前可从聚酮生物合成中获得的酶来快速影响合成社区。**2)化学酶法全合成新贝母内酯。这一目标将成为酶在复杂分子全合成中使用的一个强有力的和第一个此类演示。这项工作有可能改变复杂的聚酮合成,并将证明在全合成的后期阶段使用酶反应的有效性。**3)新的聚酮生物合成途径的发现。这一目标有助于我们对酶的长期发展,以获得新的化学多样性。在新的生物合成途径中,有催化新化学的酶。通过发现这些途径,我们能够开发新的酶。在短期内,这一目标将影响药理学和药物发现,因为聚酮具有强大的生物活性,可以用来改善人类健康。**这些独立但相互关联的方法将扩大通过酶反应获得的化学多样性。最初的两个项目专注于开发基于聚酮生物合成的已知酶来生产复杂分子的新型催化剂。这使得在合成化学家的工具箱中短期引入用于大环化和羟醛反应的酶。最后一个项目描述了我们的长期计划,通过发现新的和独特的聚酮生物合成途径,扩大通过酶化学获得的化学多样性。除了寻找新的酶来利用外,该项目还将对天然产品的发现方法产生重大影响,并影响与天然产品直接相关的所有下游发现,包括识别新的生物活性化合物、其作用机制和目标以及新药的开发。
英文摘要
Enzymatic chemistry is a powerful tool for the production of complex molecules however it has found use mainly in the generation of high purity strereogenic centers. A major limitation to the broad use of enzymes for research and manufacturing is the restricted chemical diversity currently accessible through enzymatic reactions. This is in stark contrast to synthetic organic chemistry. To expand the use of enzymes in synthesis, the limited toolbox of viable enzymatic reactions must be increased.**The structures of natural products show that enzymatic reactions can access incredible chemical diversity. The enzymes that produce these natural products are ideally suited to meet the rigorous demands of high stereo-, regio-, and chemoselectivity that synthetic chemists require for use in the synthesis of polyfunctional complex molecules. **My research program examines the biosynthetic pathways responsible for polyketide natural product production to identify and harness enzymes capable of expanding our enzymatic toolbox. While our long-term goal is to use these enzymes to enable rapid production of diverse molecules in vivo and in vitro, our immediate goals are focused on developing new catalysts that can be used in chemoenzymatic synthesis of natural products. Natural product total synthesis is a rigorous testing ground for new chemical methodology and successful integration of new enzymes in this arena will facilitate their broader application in research and manufacturing. **To meet our long-term goal of expanding the toolbox of available enzymatic reactions, we propose three short-term objectives.**1) The development of thioesterases to catalyze macrocyclization. Macrocyclization is the most decisive step of a synthesis and can define the overall efficiency of any synthetic route. No enzymatic methodology has been developed to synthesize this key functional group. This objective allows us to rapidly impact the synthetic community with currently accessible enzymes from polyketide biosynthesis.**2) The chemoenzymatic total synthesis of neopeltolide. This objective will serve as a powerful and first of its kind demonstration of the use of enzymes in complex molecule total synthesis. This work has the potential to transform complex polyketide synthesis and will demonstrate the effectiveness of using enzymatic reactions in the late stages of a total synthesis.**3) The discovery of new polyketide biosynthetic pathways. This objective contributes to our long-term development of enzymes to access new chemical diversity. Within new biosynthetic pathways are enzymes that catalyze new chemistry. By discovering these pathways, we enable develop the new enzymes. In the short-term this objective will impact the pharmacology and drug discovery as polyketides have potent bioactivity that can be exploited to improve human health.**These separate but interrelated approaches will expand the chemical diversity accessible through enzymatic reactions. The initial two projects focus on developing new catalysts based on known enzymes from polyketide biosynthesis to produce complex molecules. These enable the short-term introduction of enzymes for macrocyclization and aldol reactions into the synthetic chemist's tool box. The last project describes our long-term plans for expanding the chemical diversity accessible through enzymatic chemistry by discovering new and unique polyketide biosynthetic pathways. In addition to finding new enzymes to harness, this project will have a major impact on approaches to natural product discovery and influence all the downstream discoveries directly related to natural products, including identification of new bioactive compounds, their mechanisms of action and targets, and the development of new drugs.
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Harnessing synthesis and biosynthesis to access complex molecules
  • 批准号:
    RGPIN-2019-06859
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $4.66万
  • 财政年份:
    2022
  • 负责人:
    Boddy, Christopher
  • 依托单位:
Harnessing synthesis and biosynthesis to access complex molecules
  • 批准号:
    RGPIN-2019-06859
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $4.66万
  • 财政年份:
    2021
  • 负责人:
    Boddy, Christopher
  • 依托单位:
Harnessing synthesis and biosynthesis to access complex molecules
  • 批准号:
    RGPIN-2019-06859
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $4.66万
  • 财政年份:
    2020
  • 负责人:
    Boddy, Christopher
  • 依托单位:
Peptide synthesizer essential for natural products and chemical biology research
  • 批准号:
    RTI-2021-00791
  • 项目类别:
    Research Tools and Instruments
  • 资助金额:
    $6.32万
  • 财政年份:
    2020
  • 负责人:
    Boddy, Christopher
  • 依托单位:
国内基金
海外基金
裂殖壶菌利用聚酮合成酶(Polyketide synthase, PKS)途径合成二十碳五烯酸代谢机制
  • 批准号:
    31871779
  • 项目类别:
    面上项目
  • 资助金额:
    60.0万元
  • 批准年份:
    2018
  • 负责人:
    何宁
  • 依托单位: