Biohalogenation: nature's way to synthesize halogenated metabolites.
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The halogenated metabolism of brown algae (Phaeophyta), its biological importance and its environmental significanceInsights into enzymatic halogenation from computational studiesCrystal structure of the novel haloalkane dehalogenase DatA from Agrobacterium tumefaciens C58 reveals a special halide-stabilizing pair and enantioselectivity mechanismCharacterization of a Cyanobacterial Haloperoxidase and Evaluation of its Biocatalytic Halogenation PotentialLaccase catalyzed synthesis of iodinated phenolic compounds with antifungal activityHalogenated indole alkaloids from marine invertebrates.The Vanadium Iodoperoxidase from the marine flavobacteriaceae species Zobellia galactanivorans reveals novel molecular and evolutionary features of halide specificity in the vanadium haloperoxidase enzyme family.Characterization of biosynthetic genes of ascamycin/dealanylascamycin featuring a 5'-O-sulfonamide moiety in Streptomyces sp. JCM9888.Enzymatic functionalization of carbon-hydrogen bonds.Iodide accumulation by aerobic bacteria isolated from subsurface sediments of a 129I-contaminated aquifer at the Savannah River site, South CarolinaChlorinated phenols control the expression of the multidrug resistance efflux pump MexAB-OprM in Pseudomonas aeruginosa by interacting with NalC.Utilizing DART mass spectrometry to pinpoint halogenated metabolites from a marine invertebrate-derived fungus.Effects of Halide Ions on the Carbamidocyclophane Biosynthesis in Nostoc sp. CAVN2.Bioprospecting potential of halogenases from Arctic marine actinomycetes.Specific chlorination of isoquinolines by a fungal flavin-dependent halogenase.Substrate placement influences reactivity in non-heme Fe(II) halogenases and hydroxylases.Natural product research in the Australian marine invertebrate Dicathais orbitaIdentification of a Halogenase Involved in the Biosynthesis of Ochratoxin A in Aspergillus carbonariusActivation of the nuclear factor E2-related factor 2 pathway by novel natural products halomadurones A-D and a synthetic analogueProduction and role of volatile halogenated compounds from marine algae.Functional diversity of organic molecule enzyme cofactors.Genetic and biochemical map for the biosynthesis of occidiofungin, an antifungal produced by Burkholderia contaminans strain MS14.Halogenase Engineering for the Generation of New Natural Product Analogues.Properties and biotechnological applications of natural and engineered haloalkane dehalogenases.Applications of Nonenzymatic Catalysts to the Alteration of Natural Products.Regioselective Dichlorination of a Non-Activated Aliphatic Carbon Atom and Phenolic Bismethylation by a Multifunctional Fungal Flavoenzyme.Bacterial biosynthetic gene clusters encoding the anti-cancer haterumalide class of molecules: biogenesis of the broad spectrum antifungal and anti-oomycete compound, oocydin A.Integrated catalysis opens new arylation pathways via regiodivergent enzymatic C-H activation.Cylindrocyclophanes with proteasome inhibitory activity from the Cyanobacterium Nostoc sp.Merochlorins A-D, cyclic meroterpenoid antibiotics biosynthesized in divergent pathways with vanadium-dependent chloroperoxidasesSuppression of nitric oxide synthase by thienodolin in lipopolysaccharide-stimulated RAW 264.7 murine macrophage cells.Halogenated volatiles from the fungus Geniculosporium and the actinomycete Streptomyces chartreusis.Stereochemistry and biological activity of chlorinated lipids: a study of danicalipin A and selected diastereomers.Efficient total synthesis of dysidenin, dysidin, and barbamide.Formation and structure of the ferryl [Fe[double bond, length as m-dash]O] intermediate in the non-haem iron halogenase SyrB2: classical and QM/MM modelling agree.Evidence That Chlorinated Auxin Is Restricted to the Fabaceae But Not to the Fabeae.Insights into organohalide respiration and the versatile catabolism of Sulfurospirillum multivorans gained from comparative genomics and physiological studies.Organohalide respiration in pristine environments: implications for the natural halogen cycle.A new strategy for aromatic ring alkylation in cylindrocyclophane biosynthesis.Cloning and functional analysis of the naphthomycin biosynthetic gene cluster in Streptomyces sp. CS.
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Biohalogenation: nature's way to synthesize halogenated metabolites.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Biohalogenation: nature's way to synthesize halogenated metabolites.
@en
Biohalogenation: nature's way to synthesize halogenated metabolites.
@nl
type
label
Biohalogenation: nature's way to synthesize halogenated metabolites.
@en
Biohalogenation: nature's way to synthesize halogenated metabolites.
@nl
prefLabel
Biohalogenation: nature's way to synthesize halogenated metabolites.
@en
Biohalogenation: nature's way to synthesize halogenated metabolites.
@nl
P2093
P356
P1476
Biohalogenation: nature's way to synthesize halogenated metabolites.
@en
P2093
Claudia Wagner
Gabriele M König
Mustafa El Omari
P304
P356
10.1021/NP800651M
P577
2009-03-01T00:00:00Z