Search results for "Vomilenine"

showing 6 items of 6 documents

In vivo monitoring of alkaloid metabolism in hybrid plant cell cultures by 2D cryo-NMR without labelling

2003

Non-invasive measurements of alkaloid metabolism in plant cell suspension cultures of a somatic hybrid from Rauvolfia serpentina Benth. ex Kurz and Rhazya stricta Decaisne were carried out. When cell samples were taken sequentially from a stock feeding experiment, measuring times for in vivo NMR of 40 min were sufficient for following conversions of alkaloids at the natural abundance of 13C. Degradation of ajmaline added to the cells at 1.6 mM concentration to raumacline could be monitored after 96 h on a standard 800 MHz NMR instrument (Avance 800). Feeding vinorine an intermediate of ajmaline biosynthesis at 1.8 mM showed with a 500 MHz CryoProbe that the alkaloid enters two metabolic rou…

Magnetic Resonance SpectroscopyTime FactorsClinical BiochemistryCell Culture TechniquesPharmaceutical ScienceHybrid CellsRhazya strictaBiochemistryRauwolfiaIndole AlkaloidsHydroxylationchemistry.chemical_compoundGlucosidesGlucosideRauvolfia serpentinaFreezingDrug Discoverymedicineheterocyclic compoundsMolecular BiologyAjmalineCarbon IsotopesMolecular StructurebiologyApocynaceaeAlkaloidOrganic Chemistrybiology.organism_classificationSecologanin Tryptamine AlkaloidsAjmalinechemistryBiochemistryVomilenineMolecular Medicinemedicine.drugBioorganic & Medicinal Chemistry
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Molecular cloning and functional bacterial expression of a plant glucosidase specifically involved in alkaloid biosynthesis.

2000

Monoterpenoid indole alkaloids are a vast and structurally complex group of plant secondary compounds. In contrast to other groups of plant products which produce many glycosides, indole alkaloids rarely occur as glucosides. Plants of Rauvolfia serpentina accumulate ajmaline as a major alkaloid, whereas cell suspension cultures of Rauvolfia mainly accumulate the glucoalkaloid raucaffricine at levels of 1.6 g/l. Cell cultures do contain a specific glucosidase. known as raucaffricine-O-beta-D-glucosidase (RG), which catalyzes the in vitro formation of vomilenine, a direct intermediate in ajmaline biosynthesis. Here, we describe the molecular cloning and functional expression of this enzyme in…

RauvolfiaDNA ComplementaryStereochemistryMolecular Sequence DataPlant ScienceHorticultureMolecular cloningBiochemistryIndole AlkaloidsSubstrate SpecificityMagnoliopsidaAlkaloidsRauvolfia serpentinamedicineAmino Acid SequenceCloning MolecularMolecular BiologybiologyBase SequenceGeneral Medicinebiology.organism_classificationSecologanin Tryptamine AlkaloidsAjmalineBlotting SouthernBiochemistryVomilenineStrictosidinebiology.proteinHeterologous expressionGlucosidasesGlucosidasesmedicine.drugPhytochemistry
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Vomilenine Reductase — a novel Enzyme catalyzing a crucial Step in the Biosynthesis of the Therapeutically applied Antiarrhythmic Alkaloid Ajmaline

2002

Delineation of the biochemical pathway leading to the antiarrhythmic Rauvolfia alkaloid ajmaline has been an important target in biosynthetic research for many years. The biosynthetic sequence starting with tryptamine and the monoterpene secologanin consists of about 10 different steps. Most of the participating enzymes have been detected and characterized previously, except those catalyzing the reduction of the intermediate vomilenine. A novel NADPH-dependent enzyme that reduces the intermediate has been isolated from Rauvolfia serpentina cell suspension cultures. Vomilenine reductase (M(r )43 kDa, temp opt 30 degrees C, pH opt 5.7-6.2), saturates the indolenine double bond of vomilenine w…

TryptamineRauvolfiaStereochemistryClinical BiochemistryPharmaceutical ScienceReductaseBiochemistryCatalysisRauwolfiaIndole Alkaloidschemistry.chemical_compoundRauvolfia serpentinaDrug DiscoverymedicineSecologanin Tryptamine AlkaloidsMolecular BiologyCells CulturedAjmalineChromatographyMolecular StructurebiologyOrganic ChemistryTemperatureHydrogen-Ion Concentrationbiology.organism_classificationSecologanin Tryptamine AlkaloidsAjmalinechemistryBiochemistryVomilenineMolecular MedicineSecologaninOxidoreductasesAnti-Arrhythmia AgentsNADPmedicine.drugBioorganic & Medicinal Chemistry
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Alkaloids Isolated from Somatic Hybrid Cell Cultures of the Species CombinationRauwolfia serpentinaxrhazya stricta

1995

Abstract The phytochemical analyses of a somatic hybrid cell suspension culture of the genus and species combination Rauwolfia serpentina x Rhazya stricta revealed a number of monoterpenoid indole alkaloids. The alkaloids were identified as tubotaiwine, an isomeric mixture of vallesiachotamine, stemmadenine and vomilenine and were all produced in small amounts < 2mg/litre cell suspension. The hybrid cells showed a greater diversity of alkaloid biosynthesis when compared with the parental cultures.

TubotaiwinebiologyStemmadenineRhazya strictabiology.organism_classificationcomplex mixturesSomatic fusionPhytochemicalCell cultureVomilenineBotanyMolecular MedicineVallesiachotamineheterocyclic compoundsNatural Product Letters
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Enzymatic Formation of Raucaffricine, the Major Indole Alkaloid ofRauwolfia serpentinaCell-Suspension Cultures

1991

The major alkaloid from Rauwolfia serpentina cell-suspension cultures, the glucoalkaloid raucaffricine (2), was enzymatically formed from vomilenine (1) and UDPG in presence of microsomal-bound enzyme. This glucosyltransferase exhibits a relatively high substrate specificity with strong preference for 1 and UDPG. The apparent Km values for 1 and UDPG were 40 μM and 0.8 mM, respectively, for raucaffricine formation. Optimum transferase activity was observed at 50° and pH 6.3. The taxonomic distribution of this enzyme seems to be very limited because transferase can he exclusively detected in raucaffricine-producing plant cells.

chemistry.chemical_classificationIndole alkaloidbiologyAlkaloidOrganic ChemistryPlant cellBiochemistrySuspension cultureCatalysisInorganic ChemistryEnzymeBiochemistrychemistryVomilenineDrug Discoverybiology.proteinTransferaseGlucosyltransferasePhysical and Theoretical ChemistryHelvetica Chimica Acta
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Enzymatic Biosynthesis of Vomilenine, a Key Intermediate of the Ajmaline Pathway, Catalyzed by a Novel Cytochrome P 450-Dependent Enzyme from Plant C…

1995

Abstract Microsomal preparations from Rauwolfia serpentina Benth. cell suspension cultures cata­lyze a key step in the biosynthesis of ajmaline -the enzymatic hydroxylation of the indole alkaloid vinorine at the allylic C-21 resulting in vomilenine. Vomilenine is an important branch-point intermediate, leading not only to ajmaline but also to several side reactions of the biosynthetic pathway to ajmaline. The investigation of the taxonomical distribution of the enzyme indicated that vinorine hydroxylase is exclusively present in ajmaline-producing plant cells. The novel enzyme is strictly dependent on NADPH2 and O2 and can be inhibited by typical cytochrome P450 inhibitors such as cytochrom…

chemistry.chemical_classificationbiologyCytochromeCytochrome P450Plant cellGeneral Biochemistry Genetics and Molecular BiologyCatalysischemistry.chemical_compoundAjmalineEnzymeBiosynthesischemistryBiochemistryVomileninebiology.proteinmedicinemedicine.drugZeitschrift für Naturforschung C
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