Li Fang-Ru, Yang Qian, He Jingyi, Sun Xinru, Pan Xingming, Xu Hui-Min, Rudolf Jeffrey D, Dong Liao-Bin
State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
The Public Laboratory Platform, China Pharmaceutical University, Nanjing, 211198, China.
Chemistry. 2025 Jun 3;31(31):e202500012. doi: 10.1002/chem.202500012. Epub 2025 May 10.
Eunicellane diterpenoids, with over 360 known examples characterized by a cis- or trans-6/10-bicyclic carbon skeleton, exhibit diverse biological activities. To date, five eunicellane cyclases (ECs) have been reported: cis-ECs (Bnd4, CpDTS2 and EcTPS1) and trans-ECs (AlbS and MicA), yet the structural basis and molecular mechanisms governing their distinct cis- or trans-cyclization modes remain unsolved. Here, we present the crystal structure of a cis-EC AriE from Amycolatopsis arida, which catalyzes geranylgeranyl diphosphate to form cis-6/10-fused bicyclic benditerpe-2,6,15-triene (1) in aridacin biosynthesis. Through surface entropy reduction, we obtained the 1.87 Å resolution structure of AriE. Structure-guided mutagenesis identified W73 as a key regulatory hotspot controlling product diversity, with its variants generating diverse diterpene products. Y203A converted AriE into a highly specific (-)-(R)-cembrene A synthase. Our findings provide the first structural insights into this type of terpene synthase and demonstrate the feasibility of engineering EC variants for selective product formation.
链状二萜类化合物有超过360个已知实例,其特征为具有顺式或反式6/10双环碳骨架,展现出多样的生物活性。迄今为止,已报道了五种链状二萜环化酶(ECs):顺式ECs(Bnd4、CpDTS2和EcTPS1)和反式ECs(AlbS和MicA),然而,控制其不同顺式或反式环化模式的结构基础和分子机制仍未解决。在此,我们展示了来自干旱拟无枝酸菌的顺式EC AriE的晶体结构,其在干旱菌素生物合成中催化香叶基香叶基二磷酸形成顺式6/10稠合双环弯曲二萜-2,6,15-三烯(1)。通过表面熵降低,我们获得了分辨率为1.87 Å的AriE结构。基于结构的诱变确定W73是控制产物多样性的关键调控热点,其变体产生多样的二萜产物。Y203A将AriE转化为一种高度特异性的(-)-(R)-西松烯A合酶。我们的研究结果为这类萜类合酶提供了首个结构见解,并证明了改造EC变体以实现选择性产物形成的可行性。