Thioesterase-mediated side chain transesterification generates potent Gq signaling inhibitor FR900359.
Thioesterase-mediated side chain transesterification generates potent Gq signaling inhibitor FR900359.
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DOI:
10.1038/s41467-020-20418-3
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发表时间:
2021-01-08
影响因子:
16.6
通讯作者:
Crüsemann M
中科院分区:
文献类型:
--
作者:
Hermes C;Richarz R;Wirtz DA;Patt J;Hanke W;Kehraus S;Voß JH;Küppers J;Ohbayashi T;Namasivayam V;Alenfelder J;Inoue A;Mergaert P;Gütschow M;Müller CE;Kostenis E;König GM;Crüsemann M
The potent and selective Gq protein inhibitor depsipeptide FR900359 (FR), originally discovered as the product of an uncultivable plant endosymbiont, is synthesized by a complex biosynthetic system comprising two nonribosomal peptide synthetase (NRPS) assembly lines. Here we characterize a cultivable bacterial FR producer, enabling detailed investigations into biosynthesis and attachment of the functionally important FR side chain. We reconstitute side chain assembly by the monomodular NRPS FrsA and the non-heme monooxygenase FrsH, and characterize intermolecular side chain transesterification to the final macrocyclic intermediate FR-Core, mediated by the FrsA thioesterase domain. We harness FrsA substrate promiscuity to generate FR analogs with altered side chains and demonstrate indispensability of the FR side chain for efficient Gq inhibition by comparative bioactivity, toxicity and docking studies. Finally, evolution of FR and side chain biosynthesis is discussed based on bioinformatics analyses. Side chain transesterification boosts potency and target affinity of selective Gq inhibitor natural products. FR900359 (FR) is a Gq protein inhibitor depsipeptide isolated from an uncultivable plant endosymbiont and synthesized by non-ribosomal peptide synthetases. Here, the authors discover a cultivable bacterial FR producer and show that FrsA thioesterase domain catalyses intermolecular transesterification of the FR side chain to the depsipeptide core during biosynthesis, improving Gq inhibition properties.
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影响因子:
9.2
作者:
Kautsar SA;van der Hooft JJJ;de Ridder D;Medema MH
通讯作者:
Medema MH
影响因子:
8.6
作者:
Klapper, Martin;Braga, Daniel;Stallforth, Pierre
通讯作者:
Stallforth, Pierre
影响因子:
7.3
作者:
Kuschak, Markus;Namasivayam, Vigneshwaran;Mueller, Christa E.
通讯作者:
Mueller, Christa E.
影响因子:
15
作者:
He, Hai-Yan;Tang, Man-Cheng;Tang, Gong-Li
通讯作者:
Tang, Gong-Li
DOI:
10.1073/pnas.1511688112
发表时间:
2015-11-10
影响因子:
11.1
作者:
Hillenmeyer, Maureen E.;Vandova, Gergana A.;Charkoudian, Louise K.
通讯作者:
Charkoudian, Louise K.