Molecular insights into the catalytic promiscuity of a bacterial diterpene synthase

doi:10.1038/s41467-023-39706-9

IOCAS-IR > 实验海洋生物学重点实验室

	Molecular insights into the catalytic promiscuity of a bacterial diterpene synthase
	Li, Zhong 1; Zhang, Lilan 2; Xu, Kangwei 3; Jiang, Yuanyuan 1; Du, Jieke 1; Zhang, Xingwang 1; Meng, Ling-Hong4,5 ; Wu, Qile 1; Du, Lei 1; Li, Xiaoju 1; Hu, Yuechan 2; Xie, Zhenzhen 2; Jiang, Xukai 1; Tang, Ya-Jie 1; Wu, Ruibo 3; Guo, Rey-Ting 2; Li, Shengying 1,5
	2023-07-06
发表期刊	NATURE COMMUNICATIONS
卷号	14 期号:1 页码:15
通讯作者	Wu, Ruibo([email protected]) ; Guo, Rey-Ting([email protected]) ; Li, Shengying([email protected])
摘要	Diterpene synthase VenA catalyses the synthesis of venezuelaene A with a unique 5-5-6-7 tetracyclic skeleton from geranylgeranyl pyrophosphate. Here, the authors report crystal structures of apo- and holo-VenA, provide mechanistic insights into its substrate selectivity and promiscuity, and engineer VenA into a sesterterpene synthase. Diterpene synthase VenA is responsible for assembling venezuelaene A with a unique 5-5-6-7 tetracyclic skeleton from geranylgeranyl pyrophosphate. VenA also demonstrates substrate promiscuity by accepting geranyl pyrophosphate and farnesyl pyrophosphate as alternative substrates. Herein, we report the crystal structures of VenA in both apo form and holo form in complex with a trinuclear magnesium cluster and pyrophosphate group. Functional and structural investigations on the atypical (DSFVSD120)-D-115 motif of VenA, versus the canonical Asp-rich motif of DDXX(X)D/E, reveal that the absent second Asp of canonical motif is functionally replaced by Ser116 and Gln83, together with bioinformatics analysis identifying a hidden subclass of type I microbial terpene synthases. Further structural analysis, multiscale computational simulations, and structure-directed mutagenesis provide significant mechanistic insights into the substrate selectivity and catalytic promiscuity of VenA. Finally, VenA is semi-rationally engineered into a sesterterpene synthase to recognize the larger substrate geranylfarnesyl pyrophosphate.
DOI	10.1038/s41467-023-39706-9
收录类别	SCI
语种	英语
资助项目	National Key Research and Development Program[2021YFA0911500]; National Key Research and Development Program[2019YFA0905100]; National Natural Science Foundation of China[32200017]; National Natural Science Foundation of China[32025001]; National Natural Science Foundation of China[32000039]; National Natural Science Foundation of China[32170088]; China National Postdoctoral Program for Innovative Talents[BX20220191]; China Postdoctoral Science Foundation[2021M701989]; China Postdoctoral Science Foundation[2022M710080]; Shandong Provincial Postdoctoral Innovation Project[SDCX-ZG-202201005]; Shandong Provincial Natural Science Foundation[ZR2019ZD20]; Shandong Provincial Natural Science Foundation[ZR2022QC070]
WOS研究方向	Science & Technology - Other Topics
WOS类目	Multidisciplinary Sciences
WOS记录号	WOS:001026219000027
出版者	NATURE PORTFOLIO
WOS关键词	MAIN-GROUP THERMOCHEMISTRY ; ACTIVE-SITE RESIDUES ; BIOSYNTHETIC MECHANISM ; PENTALENENE SYNTHASE ; TERPENE SYNTHASES ; NATURAL-PRODUCTS ; STRUCTURAL BASIS ; PI INTERACTIONS ; CYCLIZATION ; DYNAMICS
引用统计	被引频次：8[WOS] [WOS记录] [WOS相关记录]
文献类型	期刊论文
条目标识符	http://ir.qdio.ac.cn/handle/337002/182687
专题	实验海洋生物学重点实验室
通讯作者	Wu, Ruibo; Guo, Rey-Ting; Li, Shengying
作者单位	1.Shandong Univ, State Key Lab Microbial Technol, 72 Binhai Rd, Qingdao 266237, Shandong, Peoples R China 2.Hubei Univ, Hubei Collaborat Innovat Ctr Green Transformat Bi, Hubei Key Lab Ind Biotechnol, Hubei Hongshan Lab,Sch Life Sci,State Key Lab Bio, Wuhan, Hubei, Peoples R China 3.Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China 4.Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Nanhai Rd 7, Qingdao, Shandong, Peoples R China 5.Qingdao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Qingdao 266237, Shandong, Peoples R China
推荐引用方式 GB/T 7714	Li, Zhong,Zhang, Lilan,Xu, Kangwei,et al. Molecular insights into the catalytic promiscuity of a bacterial diterpene synthase[J]. NATURE COMMUNICATIONS,2023,14(1):15.
APA	Li, Zhong.,Zhang, Lilan.,Xu, Kangwei.,Jiang, Yuanyuan.,Du, Jieke.,...&Li, Shengying.(2023).Molecular insights into the catalytic promiscuity of a bacterial diterpene synthase.NATURE COMMUNICATIONS,14(1),15.
MLA	Li, Zhong,et al."Molecular insights into the catalytic promiscuity of a bacterial diterpene synthase".NATURE COMMUNICATIONS 14.1(2023):15.