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Structural investigation of heteroyohimbine alkaloid synthesis reveals active site elements that control stereoselectivity
by
Stavrinides, Anna
, Tatsis, Evangelos C.
, Foureau, Emilien
, Courdavault, Vincent
, Caputi, Lorenzo
, Stevenson, Clare E. M.
, Lawson, David M.
, O'Connor, Sarah E.
in
14/63
/ 631/449/1659
/ 631/449/2667
/ 82
/ 82/80
/ Biosynthesis
/ Catalytic Domain
/ Catharanthus - genetics
/ Catharanthus - metabolism
/ Cell Nucleus - metabolism
/ Cloning, Molecular
/ Dehydrogenases
/ Enzymes
/ Gene Expression Regulation, Plant
/ Humanities and Social Sciences
/ Life Sciences
/ Localization
/ Metabolism
/ Metabolites
/ Models, Molecular
/ Molecular Docking Simulation
/ multidisciplinary
/ Mutagenesis, Site-Directed
/ Plant metabolism
/ Plant Proteins - chemistry
/ Plant Proteins - genetics
/ Plant Proteins - metabolism
/ Protein Conformation
/ Science
/ Science (multidisciplinary)
/ Secologanin Tryptamine Alkaloids - chemistry
/ Secologanin Tryptamine Alkaloids - metabolism
/ Stereoisomerism
/ Vinca Alkaloids - chemistry
/ Vinca Alkaloids - metabolism
2016
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Structural investigation of heteroyohimbine alkaloid synthesis reveals active site elements that control stereoselectivity
by
Stavrinides, Anna
, Tatsis, Evangelos C.
, Foureau, Emilien
, Courdavault, Vincent
, Caputi, Lorenzo
, Stevenson, Clare E. M.
, Lawson, David M.
, O'Connor, Sarah E.
in
14/63
/ 631/449/1659
/ 631/449/2667
/ 82
/ 82/80
/ Biosynthesis
/ Catalytic Domain
/ Catharanthus - genetics
/ Catharanthus - metabolism
/ Cell Nucleus - metabolism
/ Cloning, Molecular
/ Dehydrogenases
/ Enzymes
/ Gene Expression Regulation, Plant
/ Humanities and Social Sciences
/ Life Sciences
/ Localization
/ Metabolism
/ Metabolites
/ Models, Molecular
/ Molecular Docking Simulation
/ multidisciplinary
/ Mutagenesis, Site-Directed
/ Plant metabolism
/ Plant Proteins - chemistry
/ Plant Proteins - genetics
/ Plant Proteins - metabolism
/ Protein Conformation
/ Science
/ Science (multidisciplinary)
/ Secologanin Tryptamine Alkaloids - chemistry
/ Secologanin Tryptamine Alkaloids - metabolism
/ Stereoisomerism
/ Vinca Alkaloids - chemistry
/ Vinca Alkaloids - metabolism
2016
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Structural investigation of heteroyohimbine alkaloid synthesis reveals active site elements that control stereoselectivity
by
Stavrinides, Anna
, Tatsis, Evangelos C.
, Foureau, Emilien
, Courdavault, Vincent
, Caputi, Lorenzo
, Stevenson, Clare E. M.
, Lawson, David M.
, O'Connor, Sarah E.
in
14/63
/ 631/449/1659
/ 631/449/2667
/ 82
/ 82/80
/ Biosynthesis
/ Catalytic Domain
/ Catharanthus - genetics
/ Catharanthus - metabolism
/ Cell Nucleus - metabolism
/ Cloning, Molecular
/ Dehydrogenases
/ Enzymes
/ Gene Expression Regulation, Plant
/ Humanities and Social Sciences
/ Life Sciences
/ Localization
/ Metabolism
/ Metabolites
/ Models, Molecular
/ Molecular Docking Simulation
/ multidisciplinary
/ Mutagenesis, Site-Directed
/ Plant metabolism
/ Plant Proteins - chemistry
/ Plant Proteins - genetics
/ Plant Proteins - metabolism
/ Protein Conformation
/ Science
/ Science (multidisciplinary)
/ Secologanin Tryptamine Alkaloids - chemistry
/ Secologanin Tryptamine Alkaloids - metabolism
/ Stereoisomerism
/ Vinca Alkaloids - chemistry
/ Vinca Alkaloids - metabolism
2016
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Structural investigation of heteroyohimbine alkaloid synthesis reveals active site elements that control stereoselectivity
Journal Article
Structural investigation of heteroyohimbine alkaloid synthesis reveals active site elements that control stereoselectivity
2016
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Overview
Plants produce an enormous array of biologically active metabolites, often with stereochemical variations on the same molecular scaffold. These changes in stereochemistry dramatically impact biological activity. Notably, the stereoisomers of the heteroyohimbine alkaloids show diverse pharmacological activities. We reported a medium chain dehydrogenase/reductase (MDR) from
Catharanthus roseus
that catalyses formation of a heteroyohimbine isomer. Here we report the discovery of additional heteroyohimbine synthases (HYSs), one of which produces a mixture of diastereomers. The crystal structures for three HYSs have been solved, providing insight into the mechanism of reactivity and stereoselectivity, with mutation of one loop transforming product specificity. Localization and gene silencing experiments provide a basis for understanding the function of these enzymes
in vivo
. This work sets the stage to explore how MDRs evolved to generate structural and biological diversity in specialized plant metabolism and opens the possibility for metabolic engineering of new compounds based on this scaffold.
The stereochemistry of the plant heteroyohimbine alkaloids is a key factor determining their diverse biological activities. Here, the authors carry out structural, localization and genetic experiments to understand the mechanism of stereoselectivity for three heteroyohimbine synthases and to identify their function
in vivo
.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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