Structural studies of Baeyer-Villiger monooxygenases

Baeyer-Villiger单加氧酶（BMVOs）是黄素酶，催化环酮转化为内酯。这些酶提供精致的区域和对映体特异性，同时作用于广泛的底物。此外，它们只使用NADPH和氧作为共底物，产生NADP+和水作为副产物。这些特性使BVMOs成为工业生物催化剂的理想选择。*******在过去的10年里，我们一直在进行BVMOs的结构和功能研究。至此，我们确定了原型BVMO：环己酮氧合酶（CHMO）的三维结构。我们揭示了底物/产物结合的结构细节，并模拟了Criegee过渡态。这些研究允许对催化的详细机制进行假设，并使底物子集的区域和对映体特异性的结构基础合理化。*******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。在接下来的五年里，我们计划研究以下三个方面：*******底物结合****到目前为止，我们只研究了6元环作为底物，目前还不清楚大底物是如何结合的。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配合的多环底物/产物。此外，氧结合位点的位置尚不清楚。此外，氧气到达这个位置的路线是一个猜测的问题。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在催化循环中采用不同的构象。我们已经开始探索构象柔韧性与催化的相关性，并注意到柔韧性对底物结合和催化效率有深远的影响。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，BVMOs还能够氧化杂原子，例如对映选择性地将硫化物转化为相应的亚砜。然而，这种催化活性的结构基础尚未得到研究。因此，我们计划在各种含杂原子底物/产物的配合物中进行CHMO的结构研究。******

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.******