Search results for "Biosynthesis"

showing 10 items of 523 documents

Production of 6-pentyl-?-pyrone byTrichoderma harzianum from 18?n fatty acid methyl esters

1992

Biosynthesis of 6-pentyl-α-pyrone byTrichoderma harzianum in two different media was evaluated. Best yields were found in nitrogen deficient medium (C/N=60). Limited growth seems to favour the production of this lactone. When fungal cells, precultured in low nitrogen medium, were incubated on methyl ricinoleate (10 g/l, C/N=60) an increase in 6-pentyl-α-pyrone production was observed in comparison with the media containing methyl oleate or methyl linoleate.

chemistry.chemical_classificationbiologyStereochemistryTrichoderma harzianumFatty acidchemistry.chemical_elementBioengineeringGeneral MedicineFungi imperfectibiology.organism_classificationApplied Microbiology and BiotechnologyNitrogenPyronechemistry.chemical_compoundBiosynthesischemistryLactoneUnsaturated fatty acidBiotechnologyBiotechnology Letters
researchProduct

The gene encoding polyneuridine aldehyde esterase of monoterpenoid indole alkaloid biosynthesis in plants is an ortholog of theα/β hydrolase super fa…

2000

The biosynthesis of the anti-arrhythmic alkaloid ajmaline is catalysed by more than 10 specific enzymes. In this multistep process polyneuridine aldehyde esterase (PNAE) catalyses a central reaction by transforming polyneuridine aldehyde into epi-vellosimine, which is the immediate precursor for the synthesis of the ajmalane skeleton. PNAE was purified from cell suspension cultures of Rauvolfia serpentina. The N-terminal sequence and endoproteinase LysC fragments of the purified protein were used for primer design and for the amplification of specific PCR products leading to the isolation of PNAE-encoding cDNA from a R. serpentina library. The PNAE cDNA was fused with a C-terminal His-tag, …

chemistry.chemical_classificationbiologyStereochemistrymedicine.disease_causebiology.organism_classificationBiochemistryPolyneuridine-aldehyde esterasechemistry.chemical_compoundEnzymeBiosynthesischemistryBiochemistryRauvolfia serpentinaComplementary DNAHydrolasemedicineHeterologous expressionEscherichia coliEuropean Journal of Biochemistry
researchProduct

Metabolic cross-talk between pathways of terpenoid backbone biosynthesis in spike lavender

2015

Abstract The metabolic cross-talk between the mevalonate (MVA) and the methylerythritol phosphate (MEP) pathways in developing spike lavender ( Lavandula latifolia Med) was analyzed using specific inhibitors and on the basis of 13 C-labeling experiments. The presence of mevinolin (MEV), an inhibitor of the MVA pathway, at concentrations higher than 0.5 μM significantly reduced plant development, but not the synthesis of chlorophylls and carotenoids. On the other hand, fosmidomycin (FSM), an inhibitor of the MEP pathway, at concentrations higher than 20 μM blocked the synthesis of chlorophyll, carotenoids and essential oils, and significantly reduced stem development. Notably, 1.2 mM MVA cou…

chemistry.chemical_classificationbiologyTerpenesPhysiologyLavandula latifoliaPlant ScienceReductasebiology.organism_classificationFosmidomycinchemistry.chemical_compoundCytosolLavandulaEnzymeBiosynthesischemistryBiochemistryHydroxymethylglutaryl-CoA-Reductases NADP-dependentGeneticsmedicineLamiaceaeCarotenoidPlant ShootsPlant Proteinsmedicine.drugPlant Physiology and Biochemistry
researchProduct

An Uncommon Pathway in the Biosynthesis of Acetylenic Fatty Acids in Mosses

1995

Although more than 600 acetylenic compounds of various structures have been found in plants [1], hardly anything is known about the formation of the triple bonds. The acetylenes so far known from Bryophytes, have been identified as long chain fatty acids with a characteristic arrangement of one triple bond and one to three double bonds.

chemistry.chemical_classificationchemistry.chemical_compoundBiosynthesischemistryDouble bondStereochemistryAcetylenic acidAcetylenic CompoundsTriple bondLong chainStearidonic acid
researchProduct

Metabolism of Chemical Carcinogens

1989

Most chemical carcinogens are chemically unreactive per se and need metabolic activation to the ultimate carcinogenic species. The enzyme pattern responsible for the generation and disposition of reactive metabolites constitutes one important early contribution to the control of chemical carcinogenesis. Especially well studied is the group of enzymes responsible for the control of reactive epoxides. Many natural as well as manmade foreign compounds, including pharmaceuticals, possess olefinic or aromatic double bonds. Such compounds can be transformed to epoxides by microsomal monooxygenases present in many mammalian organs. By virtue of their electrophilic reactivity such epoxides may spon…

chemistry.chemical_classificationchemistry.chemical_compoundEnzymeBiosynthesischemistryBiochemistryEpoxide HydrolasesMetabolismMonooxygenaseEpoxide hydrolaseCarcinogenDNA
researchProduct

Measurement of Protein Synthesis: In Vitro Comparison of 68Ga-DOTA-Puromycin, [3H]Tyrosine, and 2-Fluoro-[3H]tyrosine

2012

Aim: Puromycin has played an important role in our understanding of the eukaryotic ribosome and protein synthesis. It has been known for more than 40 years that this antibiotic is a universal protein synthesis inhibitor that acts as a structural analog of an aminoacyl-transfer RNA (aa-tRNA) in eukaryotic ribosomes. Due to the role of enzymes and their synthesis in situations of need (DNA damage, e.g., after chemo- or radiation therapy), determination of protein synthesis is important for control of antitumor therapy, to enhance long-term survival of tumor patients, and to minimize side-effects of therapy. Multiple attempts to reach this goal have been made through the last decades, mostly u…

chemistry.chemical_classificationchemistry.chemical_compoundEnzymeProtein synthesis inhibitorchemistryBiochemistryPuromycinProtein biosynthesisTyrosineCycloheximideRibosomeAmino acid
researchProduct

ChemInform Abstract: Enzymatic Biosynthesis of Raumacline

2010

chemistry.chemical_classificationchemistry.chemical_compoundRaumaclineEnzymeBiosynthesischemistryBiochemistryGeneral MedicineChemInform
researchProduct

Alkaloids from Rauwolfia serpentina cell cultures treated with ajmaline

1993

Abstract A group of new alkaloids, the raumaclines, and some related alkaloids were isolated from Rauwolfia serpentina cell suspensions fed with high levels of ajmaline; their structures were determined and syntheses developed providing an essential prerequisite to the further study of their biosynthesis at the enzymatic level.

chemistry.chemical_classificationendocrine systemorganic chemicalsCellPlant ScienceGeneral MedicineHorticultureBiologycomplex mixturesBiochemistryAjmalinechemistry.chemical_compoundmedicine.anatomical_structureEnzymeBiosynthesischemistryBiochemistryCell culturemedicineheterocyclic compoundsMolecular Biologymedicine.drugPhytochemistry
researchProduct

Carnitine transport in volume-overloaded rat hearts

1995

Carnitine concentration in tissue is generally related to mitochondrial volume-density and ability to oxidize fatty acids. The highest tissue carnitine has been detected in ventricular myocardium which, compared to other tissues, presents elevated rates of oxidative phosphorylation [1]. The ability of cardiac mitochondria to oxidize long chain fatty acids is also much higher when compared to skeletal muscle or liver sarcosomes (Table 1). Paradoxically enough, it has been known for many years [3–5] that the heart is missing γ-butyrobetaine hydroxylase [6, 7], the last enzyme of carnitine synthesizing pathway, and that in the myocardium of different species including man, the carnitine synthe…

chemistry.chemical_classificationmedicine.medical_specialtyKidneySkeletal muscleLipid metabolismOxidative phosphorylationCarnitine transportEnzymeEndocrinologymedicine.anatomical_structurechemistryInternal medicineCarnitine biosynthesismedicineCarnitinemedicine.drug
researchProduct

Biosynthesis of Monoterpenoid Indole Alkaloid Ajmaline Catalyzed by Novel Reductases1

2006

chemistry.chemical_compoundAjmalineBiosynthesischemistryIndole alkaloidStereochemistryAlkaloidmedicineOrganic chemistryGeneral ChemistryReductaseCatalysismedicine.drugChemical Research in Chinese Universities
researchProduct