CYP725A4 from yew catalyzes complex structural rearrangement of taxa-4(5),11(12)-diene into the cyclic ether 5(12)-oxa-3(11)-cyclotaxane.
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Isoprenoid pathway optimization for Taxol precursor overproduction in Escherichia coliCytochromes p450Synthesis and In Vitro Evaluation of Taxol oxetane ring D precursors.Advancing secondary metabolite biosynthesis in yeast with synthetic biology tools.Characterization of two genes for the biosynthesis of the labdane diterpene Z-abienol in tobacco (Nicotiana tabacum) glandular trichomes.Plant glandular trichomes as targets for breeding or engineering of resistance to herbivores.A novel pathway for sesquiterpene biosynthesis from Z,Z-farnesyl pyrophosphate in the wild tomato Solanum habrochaites.Distributing a metabolic pathway among a microbial consortium enhances production of natural products.The early stages of taxol biosynthesis: an interim report on the synthesis and identification of early pathway metabolites.Unusual cytochrome p450 enzymes and reactions.Metabolic engineering of plant monoterpenes, sesquiterpenes and diterpenes--current status and future opportunities.Metabolic engineering of plants for artemisinin synthesis.Plant Glandular Trichomes: Natural Cell Factories of High Biotechnological Interest.Synthetic biology for production of natural and new-to-nature terpenoids in photosynthetic organisms.Heterologous expression and characterization of plant Taxadiene-5α-Hydroxylase (CYP725A4) in Escherichia coli.Correlation analysis of the taxane core functional group modification, enzyme expression, and metabolite accumulation profiles under methyl jasmonate treatment.The gymnosperm cytochrome P450 CYP750B1 catalyzes stereospecific monoterpene hydroxylation of (+)-sabinene in thujone biosynthesis in western redcedar.A Cytochrome P450-Mediated Intramolecular Carbon-Carbon Ring Closure in the Biosynthesis of Multidrug-Resistance-Reversing Lathyrane Diterpenoids.Isolation of viable multicellular glands from tissue of the carnivorous plant, Nepenthes.Production of bioactive diterpenoids in the euphorbiaceae depends on evolutionarily conserved gene clusters.Taxadiene-5α-ol is a minor product of CYP725A4 when expressed in Escherichia coli.Expansion of chemical space for natural products by uncommon P450 reactions.P450s controlling metabolic bifurcations in plant terpene specialized metabolism.Accessing low-oxidation state taxanes: is taxadiene-4(5)-epoxide on the taxol biosynthetic pathway?A P450-centric view of plant evolution
P2860
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P2860
CYP725A4 from yew catalyzes complex structural rearrangement of taxa-4(5),11(12)-diene into the cyclic ether 5(12)-oxa-3(11)-cyclotaxane.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
CYP725A4 from yew catalyzes co ...... r 5(12)-oxa-3(11)-cyclotaxane.
@en
CYP725A4 from yew catalyzes co ...... r 5(12)-oxa-3(11)-cyclotaxane.
@nl
type
label
CYP725A4 from yew catalyzes co ...... r 5(12)-oxa-3(11)-cyclotaxane.
@en
CYP725A4 from yew catalyzes co ...... r 5(12)-oxa-3(11)-cyclotaxane.
@nl
prefLabel
CYP725A4 from yew catalyzes co ...... r 5(12)-oxa-3(11)-cyclotaxane.
@en
CYP725A4 from yew catalyzes co ...... r 5(12)-oxa-3(11)-cyclotaxane.
@nl
P2093
P2860
P356
P1476
CYP725A4 from yew catalyzes co ...... er 5(12)-oxa-3(11)-cyclotaxane
@en
P2093
Agnes Lesot
Christophe Sallaud
Danièle Werck-Reichhart
Denis Rontein
Sandrine Onillon
P2860
P304
P356
10.1074/JBC.M708950200
P407
P577
2007-12-31T00:00:00Z