CYP719B1 is salutaridine synthase, the C-C phenol-coupling enzyme of morphine biosynthesis in opium poppy. - Test2 - elhamkhani - TriplyDB

CYP719B1 is salutaridine synthase, the C-C phenol-coupling enzyme of morphine biosynthesis in opium poppy.

CYP719B1 is salutaridine synthase, the C-C phenol-coupling enzyme of morphine biosynthesis in opium poppy.

http://www.wikidata.org/entity/Q30319073

about

Flavones: From Biosynthesis to Health Benefits Synthesis of Morphinan Alkaloids in Saccharomyces cerevisiae Cytochromes p450 Dirigent Protein Mode of Action Revealed by the Crystal Structure of AtDIR6.Integration of deep transcriptome and proteome analyses reveals the components of alkaloid metabolism in opium poppy cell cultures Characterizing proteins of unknown function: orphan cytochrome p450 enzymes as a paradigm.Integration of deep transcript and targeted metabolite profiles for eight cultivars of opium poppy.A Papaver somniferum 10-gene cluster for synthesis of the anticancer alkaloid noscapine.Towards a molecular understanding of the biosynthesis of amaryllidaceae alkaloids in support of their expanding medical use.De novo sequence assembly and characterization of Lycoris aurea transcriptome using GS FLX titanium platform of 454 pyrosequencing.Comparative transcriptome analysis using high papaverine mutant of Papaver somniferum reveals pathway and uncharacterized steps of papaverine biosynthesis Elucidating steroid alkaloid biosynthesis in Veratrum californicum: production of verazine in Sf9 cells.Rat CYP2D2, not 2D1, is functionally conserved with human CYP2D6 in endogenous morphine formation Identification and differential regulation of microRNAs in response to methyl jasmonate treatment in Lycoris aurea by deep sequencing.Characterization of a flavoprotein oxidase from opium poppy catalyzing the final steps in sanguinarine and papaverine biosynthesis Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs Total biosynthesis of opiates by stepwise fermentation using engineered Escherichia coli.CYP96T1 of Narcissus sp. aff. pseudonarcissus Catalyzes Formation of the Para-Para' C-C Phenol Couple in the Amaryllidaceae Alkaloids.Unusual cytochrome p450 enzymes and reactions.Characterization of plant functions using cultured plant cells, and biotechnological applications.Network analysis for gene discovery in plant-specialized metabolism.Benzylisoquinoline alkaloid metabolism: a century of discovery and a brave new world.Benzylisoquinoline alkaloid biosynthesis in opium poppy.The biocatalytic repertoire of natural biaryl formation.Modern plant metabolomics: advanced natural product gene discoveries, improved technologies, and future prospects.Identification of candidate genes involved in isoquinoline alkaloids biosynthesis in Dactylicapnos scandens by transcriptome analysis.Oxidative Cyclization in Natural Product Biosynthesis Plant science. Morphinan biosynthesis in opium poppy requires a P450-oxidoreductase fusion protein.Mechanism of the P450-Catalyzed Oxidative Cyclization in the Biosynthesis of Griseofulvin.Bifunctional CYP81AA proteins catalyse identical hydroxylations but alternative regioselective phenol couplings in plant xanthone biosynthesis.A Cytochrome P450-Mediated Intramolecular Carbon-Carbon Ring Closure in the Biosynthesis of Multidrug-Resistance-Reversing Lathyrane Diterpenoids.Complexity generation in fungal polyketide biosynthesis: a spirocycle-forming P450 in the concise pathway to the antifungal drug griseofulvin.CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy.(R,S)-tetrahydropapaveroline production by stepwise fermentation using engineered Escherichia coli.Cloning and characterization of canadine synthase involved in noscapine biosynthesis in opium poppy.Flavoenzyme-catalyzed atropo-selective N,C-bipyrrole homocoupling in marinopyrrole biosynthesis.Characterization of the flavoenzyme XiaK as an N-hydroxylase and implications in indolosesquiterpene diversification.Biochemistry and occurrence of o-demethylation in plant metabolism.Metabolic diversification of benzylisoquinoline alkaloid biosynthesis through the introduction of a branch pathway in Eschscholzia californica.Systematic knockdown of morphine pathway enzymes in opium poppy using virus-induced gene silencing.

P2860

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P2860

CYP719B1 is salutaridine synthase, the C-C phenol-coupling enzyme of morphine biosynthesis in opium poppy.

http://www.wikidata.org/entity/Q30319073

description

2009 nî lūn-bûn

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2009 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2009 թվականի հունիսին հրատարակված գիտական հոդված

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2009年の論文

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CYP719B1 is salutaridine synth ...... e biosynthesis in opium poppy.

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CYP719B1 is salutaridine synth ...... e biosynthesis in opium poppy.

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CYP719B1 is salutaridine synth ...... e biosynthesis in opium poppy.

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CYP719B1 is salutaridine synth ...... e biosynthesis in opium poppy.

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CYP719B1 is salutaridine synth ...... e biosynthesis in opium poppy.

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Journal of Biological Chemistry

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CYP719B1 is salutaridine synth ...... e biosynthesis in opium poppy.

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P2093

Andreas Gesell

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Fong-Chin Huang

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Jörg Ziegler

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María Luisa Díaz Chávez

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Megan Rolf

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Toni M Kutchan

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P2860

Production of benzylisoquinoline alkaloids in Saccharomyces cerevisiae

The neighbor-joining method: a new method for reconstructing phylogenetic trees

The purification and characterization of a unique cytochrome P-450 enzyme from Berberis stolonifera plant cell cultures

Molecular cloning and functional heterologous expression of two alleles encoding (S)-N-methylcoclaurine 3'-hydroxylase (CYP80B1), a new methyl jasmonate-inducible cytochrome P-450-dependent mono-oxygenase of benzylisoquinoline alkaloid biosynthesis

Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center

Cloning and expression in Escherichia coli of the obtusifoliol 14 alpha-demethylase of Sorghum bicolor (L.) Moench, a cytochrome P450 orthologous to the sterol 14 alpha-demethylases (CYP51) from fungi and mammals

Canadine synthase from Thalictrum tuberosum cell cultures catalyses the formation of the methylenedioxy bridge in berberine synthesis

THE CARBON MONOXIDE-BINDING PIGMENT OF LIVER MICROSOMES. I. EVIDENCE FOR ITS HEMOPROTEIN NATURE

Comparative macroarray analysis of morphine containing Papaver somniferum and eight morphine free Papaver species identifies an O-methyltransferase involved in benzylisoquinoline biosynthesis.

Molecular characterization of the salutaridinol 7-O-acetyltransferase involved in morphine biosynthesis in opium poppy Papaver somniferum.

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24432-24442

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10.1074/JBC.M109.033373

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36

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284

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2009-06-30T00:00:00Z

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