Structural studies of Baeyer-Villiger monooxygenases

Baeyer-Villiger 单加氧酶的结构研究

• 批准号: RGPIN-2019-05067
• 负责人: Berghuis, Albert
• 金额: $ 3.06万
• 依托单位: McGill University
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2019
• 资助国家: 加拿大
• 起止时间: 2019-01-01 至 2020-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=688547
• 关键词: Structural; studies; Baeyer; Villiger; monooxygenases

The Baeyer-Villiger monooxygenases (BMVOs) are flavin enzymes that catalyze the conversion of cyclic ketones into lactones. These enzymes offer exquisite regio- and enantio-specificity, while acting on a wide range of substrates. Furthermore, they only use NADPH and oxygen as co-substrates, and produce NADP+ and water as by products. These properties make BVMOs ideal for use as industrial biocatalysts.*******For the past 10 years, we have pursued structure-function studies of BVMOs. Thus far, we determined the three-dimensional structure for the archetypal BVMO: cyclohexanone mooxygenase (CHMO). We revealed the structural details of substrate/product binding, and modeled the Criegee transition state. These studies allowed for a detailed mechanism of catalysis to be postulated, and rationalize the structural basis for regio- and enantio-specificity for a subset of substrates.*******While our research has revealed much about the structural basis for BVMO catalysis, many details are still unknown. In the coming five years, we plan to examine the following three aspects:*******Substrate binding****We have thus far only examined 6-membered cyclic rings as substrates, and it is unclear how larger substrates are bound. For these substrates, the structural basis for regio- and enantio-specificity also remains to be resolved. We will therefore pursue studies of polycyclic substrates/products in complex with CHMO. Also, the location of the oxygen binding site is not known. Furthermore, the route by which oxygen reaches this site is a matter of speculation. We will address these questions using computational approaches together with structure-function studies.*******Conformational flexibility****BVMOs adopt different conformations during the catalytic cycle. We have begun to probe the relevance of conformational flexibility for catalysis, and note that flexibility has a profound impact on substrate binding and catalytic efficiency. However, the structural basis for this impact is unknown. We will use site-directed mutagenesis, kinetic studies and biophysical approaches to explore this.*******Catalytic activity****In addition to converting cyclic ketones into lactones, BVMOs are able to oxygenate heteroatoms, such as the enantio-selective conversion of sulfides to their corresponding sulfoxides. However, the structural basis for this catalytic activity has not been examined. Thus, we plan to perform structural studies of CHMO in complex with various heteroatom containing substrates/products.******

Baeyer-Villiger 单加氧酶 (BMVO) 是催化环酮转化为内酯的黄素酶。这些酶具有精致的区域特异性和对映体特异性，同时作用于多种底物。此外，它们仅使用 NADPH 和氧气作为共底物，并产生 NADP+ 和水作为副产品。这些特性使 BVMO 非常适合用作工业生物催化剂。********在过去 10 年中，我们一直致力于 BVMO 的结构功能研究。到目前为止，我们确定了原型 BVMO 的三维结构：环己酮单加氧酶 (CHMO)。我们揭示了底物/产物结合的结构细节，并模拟了 Criegee 过渡态。这些研究允许假设详细的催化机制，并合理化底物子集的区域特异性和对映体特异性的结构基础。 ******虽然我们的研究已经揭示了许多关于 BVMO 催化的结构基础，但许多细节仍然未知。未来五年，我们计划研究以下三个方面：********底物结合****迄今为止，我们仅研究了六元环作为底物，尚不清楚更大的底物如何结合。对于这些底物，区域特异性和对映体特异性的结构基础也有待解决。因此，我们将继续研究与 CHMO 复合的多环底物/产物。此外，氧结合位点的位置也是未知的。此外，氧气到达该地点的路线仍是一个推测问题。我们将使用计算方法和结构功能研究来解决这些问题。********构象灵活性****BVMO 在催化循环过程中采用不同的构象。我们已经开始探讨构象灵活性与催化的相关性，并注意到灵活性对底物结合和催化效率具有深远的影响。然而，这种影响的结构基础尚不清楚。我们将使用定点诱变、动力学研究和生物物理方法来探索这一点。********催化活性****除了将环酮转化为内酯外，BVMO 还能够氧化杂原子，例如硫化物对映选择性转化为其相应的亚砜。然而，这种催化活性的结构基础尚未得到研究。因此，我们计划对 CHMO 与各种含杂原子的底物/产物的复合物进行结构研究。******