Coupling and rearrangement reactions in the biosynthesis of bis-heterocyclic natural products

双杂环天然产物生物合成中的偶联和重排反应

• 批准号: 402631-2011
• 负责人: Ryan, Katherine
• 金额: $ 2.04万
• 依托单位: University of British Columbia
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2015
• 资助国家: 加拿大
• 起止时间: 2015-01-01 至 2016-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=573343
• 关键词: Coupling; rearrangement; reactions; biosynthesis; bis

There is an urgent need for new antibiotic and anticancer agents. One important route to generate new drug molecules is to engineer biosynthetic pathways to existing molecules to create derivatives with improved pharmacological properties. Bacteria are a rich source for such drug molecules and biosynthetic pathways. The clustering of biosynthetic genes in their genomes enables a variety of studies: facile identification of new gene clusters, heterologous expression of entire pathways, and rapid engineering to generate new biosynthetic derivatives. This grant is focused on the biosynthetic pathways to bis-heterocyclic molecules, a group of compounds containing two dimerized, heterocyclic monomers in their structures. Little is known about the mechanisms that lead to the production of such molecules. The objective of this program is to characterize the biosynthetic pathways and key biosynthetic enzymes to two important bis-heterocyclic molecules. My hypothesis is that these two molecules are derived from enzymatic coupling and rearrangement reactions that fuse and contort well-studied heterocyclic monomers into unusual, dimerized molecular skeletons. This hypothesis will be tested by identifying the gene cluster responsible for the production of each molecule and carrying out genetic experiments to test the roles of individual biosynthetic genes. Further, we will biochemically and structurally characterize key enzymes in each pathway. Our proposed biosynthetic studies are significant because they will provide the necessary data and materials to enable studies to generate libraries of structurally related derivatives of these drug molecules. The proposed research is innovative because it focuses on the enzymatic basis for the dimerization and rearrangement of heterocyclic monomers to give bis-heterocyclic natural products and will provide new knowledge about how nature constructs this class of molecules.

迫切需要新的抗生素和抗癌剂。产生新药物分子的一个重要途径是将生物合成途径设计成现有分子，以产生具有改进的药理学性质的衍生物。细菌是这种药物分子和生物合成途径的丰富来源。生物合成基因在其基因组中的聚类使得各种研究成为可能：新基因簇的简易鉴定、整个途径的异源表达以及快速工程化以产生新的生物合成衍生物。该基金主要用于双杂环分子的生物合成途径，双杂环分子是一组在其结构中含有两个二聚杂环单体的化合物。人们对导致这种分子产生的机制知之甚少。该项目的目的是表征两种重要的双杂环分子的生物合成途径和关键生物合成酶。我的假设是，这两个分子是来自酶偶联和重排反应，融合和扭曲充分研究杂环单体到不寻常的，二聚分子骨架。这一假设将通过确定负责生产每个分子的基因簇和进行遗传实验来测试单个生物合成基因的作用来进行测试。此外，我们将生化和结构特征的关键酶在每个途径。我们提出的生物合成研究是重要的，因为它们将提供必要的数据和材料，使研究能够产生这些药物分子的结构相关衍生物的库。拟议的研究是创新的，因为它侧重于杂环单体的二聚化和重排的酶基础，以得到双杂环天然产物，并将提供有关自然界如何构建这类分子的新知识。