Literature DB >> 28922556

Structure and Mechanism of the Monoterpene Cyclolavandulyl Diphosphate Synthase that Catalyzes Consecutive Condensation and Cyclization.

Takeo Tomita1, Masaya Kobayashi1, Yuma Karita2, Yoko Yasuno2, Tetsuro Shinada2, Makoto Nishiyama1, Tomohisa Kuzuyama1.   

Abstract

We report the three-dimensional structure of cyclolavandulyl diphosphate (CLPP) synthase (CLDS), which consecutively catalyzes the condensation of two molecules of dimethylallyl diphosphate (DMAPP) followed by cyclization to form a cyclic monoterpene, CLPP. The structures of apo-CLDS and CLDS in complex with Tris, pyrophosphate, and Mg2+ ion were refined at 2.00 Å resolution and 1.73 Å resolution, respectively. CLDS adopts a typical fold for cis-prenyl synthases and forms a homo-dimeric structure. An in vitro reaction using a regiospecifically 2 H-substituted DMAPP substrate revealed the intramolecular proton transfer mechanism of the CLDS reaction. The CLDS structure and structure-based mutagenesis provide mechanistic insights into this unprecedented terpene synthase. The combination of structural and mechanistic insights advances the knowledge of intricate terpene synthase-catalyzed reactions.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  biosynthesis; crystal structure; cyclization; head-to-middle condensation; terpene synthases

Year:  2017        PMID: 28922556     DOI: 10.1002/anie.201708474

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  5 in total

1.  Structure of undecaprenyl pyrophosphate synthase from Acinetobacter baumannii.

Authors:  Tzu Ping Ko; Chi Hung Huang; Shu Jung Lai; Yeh Chen
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2018-11-16       Impact factor: 1.056

2.  Catalytic Role of Conserved Asparagine, Glutamine, Serine, and Tyrosine Residues in Isoprenoid Biosynthesis Enzymes.

Authors:  Satish R Malwal; Jian Gao; Xiangying Hu; Yunyun Yang; Weidong Liu; Jian-Wen Huang; Tzu-Ping Ko; Liping Li; Chun-Chi Chen; Bing O'Dowd; Rahul L Khade; Yong Zhang; Yonghui Zhang; Eric Oldfield; Rey-Ting Guo
Journal:  ACS Catal       Date:  2018-04-06       Impact factor: 13.084

Review 3.  Terpene synthases in disguise: enzymology, structure, and opportunities of non-canonical terpene synthases.

Authors:  Jeffrey D Rudolf; Chin-Yuan Chang
Journal:  Nat Prod Rep       Date:  2020-03-25       Impact factor: 13.423

4.  Engineering of a Plant Isoprenyl Diphosphate Synthase for Development of Irregular Coupling Activity.

Authors:  Iryna Gerasymenko; Yuriy V Sheludko; Ismael Navarro Fuertes; Volker Schmidts; Lara Steinel; Elisabeth Haumann; Heribert Warzecha
Journal:  Chembiochem       Date:  2021-11-05       Impact factor: 3.461

Review 5.  Structure, catalysis, and inhibition mechanism of prenyltransferase.

Authors:  Hsin-Yang Chang; Tien-Hsing Cheng; Andrew H-J Wang
Journal:  IUBMB Life       Date:  2020-11-27       Impact factor: 4.709

  5 in total

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