Biochemical characterization of StyAB from Pseudomonas sp. strain VLB120 as a two-component flavin-diffusible monooxygenase
about
Robust in vitro activity of RebF and RebH, a two-component reductase/halogenase, generating 7-chlorotryptophan during rebeccamycin biosynthesisEngineering non-heme mono- and dioxygenases for biocatalysisStructure and Ligand Binding Properties of the Epoxidase Component of Styrene Monooxygenase,Crystal Structures of NADH:FMN Oxidoreductase (EmoB) at Different Stages of CatalysisCharacterization of Chlorophenol 4-Monooxygenase (TftD) and NADH:FAD Oxidoreductase (TftC) of Burkholderia cepacia AC1100Structural and Catalytic Differences between Two FADH2-Dependent Monooxygenases: 2,4,5-TCP 4-Monooxygenase (TftD) from Burkholderia cepacia AC1100 and 2,4,6-TCP 4-Monooxygenase (TcpA) from Cupriavidus necator JMP134Structure and Mechanism of Styrene Monooxygenase Reductase: New Insight into the FAD-Transfer ReactionThe Oxygen Dilemma: A Severe Challenge for the Application of Monooxygenases?Highly regio- and enantioselective multiple oxy- and amino-functionalizations of alkenes by modular cascade biocatalysisEnantioselective substrate binding in a monooxygenase protein model by molecular dynamics and docking.The interplay of StyR and IHF regulates substrate-dependent induction and carbon catabolite repression of styrene catabolism genes in Pseudomonas fluorescens ST.Engineering of Pseudomonas taiwanensis VLB120 for constitutive solvent tolerance and increased specific styrene epoxidation activity.Isolation of a gene responsible for the oxidation of trans-anethole to para-anisaldehyde by Pseudomonas putida JYR-1 and its expression in Escherichia coli.Characterization of a self-sufficient trans-anethole oxygenase from Pseudomonas putida JYR-1Enzymatic chemistry of cyclopropane, epoxide, and aziridine biosynthesis.Discovery of a novel styrene monooxygenase originating from the metagenomeResponse of Pseudomonas putida KT2440 to increased NADH and ATP demand.Variability in subpopulation formation propagates into biocatalytic variability of engineered Pseudomonas putida strains.pH-dependent studies reveal an efficient hydroxylation mechanism of the oxygenase component of p-hydroxyphenylacetate 3-hydroxylase.Identification and characterization of the flavin:NADH reductase (PrnF) involved in a novel two-component arylamine oxygenase.Styrene oxide isomerase of Rhodococcus opacus 1CP, a highly stable and considerably active enzyme.FAD C(4a)-hydroxide stabilized in a naturally fused styrene monooxygenase.Nature of the reaction intermediates in the flavin adenine dinucleotide-dependent epoxidation mechanism of styrene monooxygenase.NADH availability limits asymmetric biocatalytic epoxidation in a growing recombinant Escherichia coli strain.Biochemical and genetic analysis of the gamma-resorcylate (2,6-dihydroxybenzoate) catabolic pathway in Rhizobium sp. strain MTP-10005: identification and functional analysis of its gene clusterIdentification of a novel self-sufficient styrene monooxygenase from Rhodococcus opacus 1CP.StyA1 and StyA2B from Rhodococcus opacus 1CP: a multifunctional styrene monooxygenase systemCatalytic and hydrodynamic properties of styrene monooxygenases from Rhodococcus opacus 1CP are modulated by cofactor binding.One-component styrene monooxygenases: an evolutionary view on a rare class of flavoproteins.Stabilization of C4a-hydroperoxyflavin in a two-component flavin-dependent monooxygenase is achieved through interactions at flavin N5 and C4a atoms.Expression and characterization of styrene monooxygenases of Rhodococcus sp. ST-5 and ST-10 for synthesizing enantiopure (S)-epoxides.The oxidation of alkylaryl sulfides and benzo[b]thiophenes by Escherichia coli cells expressing wild-type and engineered styrene monooxygenase from Pseudomonas putida CA-3.Metabolic response of Pseudomonas putida during redox biocatalysis in the presence of a second octanol phase.Enzymatic cascades for the stereo-complementary epimerisation of in situ generated epoxy alcohols.Engineering Styrene Monooxygenase for Biocatalysis: Reductase-Epoxidase Fusion Proteins.Chimeric Styrene Monooxygenase with Increased Efficiency in Asymmetric Biocatalytic Epoxidation.Enhancing Indigo Production by Over-Expression of the Styrene Monooxygenase in Pseudomonas putida.Purification and characterization of salicylate 5-hydroxylase, a three-component monooxygenase from Ralstonia sp. strain U2.A mechanistic study on SMOB-ADP1: an NADH:flavin oxidoreductase of the two-component styrene monooxygenase of Acinetobacter baylyi ADP1.Microbial production of the aromatic building-blocks (S)-styrene oxide and (R)-1,2-phenylethanediol from renewable resources.
P2860
Q24555783-AC21C8CC-96F1-4B6D-9FE1-4B762E71BD6CQ27022534-389C155C-44B4-418E-AD8A-BCA81AC238C7Q27646752-B5D01F7F-4164-4178-B338-2CF482F2C7B9Q27651551-D2FE1F84-16E2-42B7-B621-CD761E50709CQ27658188-A5CD154A-3FD7-4E15-810B-AED62894D623Q27672273-23E1B711-3EFC-4B1C-BDC1-D5FDC096E4E3Q27679342-33EAA6A9-C861-4367-930A-F9BB32855312Q28070112-7197CE23-9552-4BDB-A966-B79A0567DB32Q28829942-843177F7-A711-43F7-91DC-9561380FFFCBQ30356250-57E07C1E-91BB-4CD4-A1C9-886B065DF4EBQ33343109-EAEB2CD3-A049-4E93-9B74-A19D5DE0C2CFQ34261206-54B0288E-99B7-42F2-A56E-4A3FD1B41419Q34275468-FC8AA2FC-2B49-4406-993E-23A9F55954C1Q34996998-50AA43A5-EB52-4010-9C13-5AD66B9DEFE3Q35785144-80C24305-7B38-4DF5-AB37-BC708369C726Q36136791-AEB4E4AE-9271-4427-A7C1-ACF1F5D83D44Q38628757-A5C3A209-DC3A-4A6D-ADCD-445DA43827EFQ41548175-D6CCA04A-93A6-4704-8924-8FAEBBAAED2DQ41556740-6E802AB1-833A-48CF-A509-EA56C5003E64Q41983662-5DB8EADF-241F-438B-99BE-B176EB5DD791Q42064807-A92D9608-5A3B-4966-A59F-FB6900FF6BFEQ42082251-9717692B-CC92-41E7-B73D-C3D7F11CE086Q42120766-EBB1974A-C993-4DE4-B5D5-70BE1B60B243Q42121592-115D5644-B347-473F-AEA7-3C6354719105Q42144483-F46823E5-C0BA-42FD-B9AB-9831ACB7A638Q42232506-881FCEA7-1F9C-4576-9A48-01DDAA6C85B4Q42421275-6AD36395-32BB-4338-9424-9AD74C8F9FE9Q42573539-2BE94419-209F-4627-8B4B-3D658BD71DADQ42645359-1E1E2BF3-0917-4724-A9AE-03F0330990B0Q42856849-E5E73A42-CE55-4257-B1CF-D9853D40C75DQ44376315-B25D41FE-9C13-4074-A4B4-8D818B97B8A2Q45716641-09D4902A-A4AC-4C97-A79C-8E08D468CAB6Q46357643-59E7B35A-7399-4959-99D6-0C2D80CE630EQ48156261-23DE5053-5370-4C49-AF7B-7C94B0CE03E1Q48235032-5489A800-39E9-4A54-B2FF-AB4462E0AF54Q49603770-6FD463F8-1881-4E2B-BE9C-261FDFD35E11Q50202190-A282993C-F42A-4BD2-A124-59820F677616Q51035175-B516EF99-4C62-44A7-AEFD-224AB8E38586Q51419610-ECA3009C-1B52-410C-836B-7302EE506E5BQ52641752-99DB77DB-80D1-4DA2-B540-D489A2FCE840
P2860
Biochemical characterization of StyAB from Pseudomonas sp. strain VLB120 as a two-component flavin-diffusible monooxygenase
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on August 2004
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Biochemical characterization o ...... lavin-diffusible monooxygenase
@en
Biochemical characterization o ...... avin-diffusible monooxygenase.
@nl
type
label
Biochemical characterization o ...... lavin-diffusible monooxygenase
@en
Biochemical characterization o ...... avin-diffusible monooxygenase.
@nl
prefLabel
Biochemical characterization o ...... lavin-diffusible monooxygenase
@en
Biochemical characterization o ...... avin-diffusible monooxygenase.
@nl
P2093
P2860
P1476
Biochemical characterization o ...... lavin-diffusible monooxygenase
@en
P2093
Andreas Schmid
Bernard Witholt
Karin Hofstetter
Katja Otto
Martina Röthlisberger
P2860
P304
P356
10.1128/JB.186.16.5292-5302.2004
P407
P577
2004-08-01T00:00:00Z