Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization.
about
Towards practical biocatalytic Baeyer-Villiger reactions: applying a thermostable enzyme in the gram-scale synthesis of optically-active lactones in a two-liquid-phase system.Engineering non-heme mono- and dioxygenases for biocatalysisMeasurement of oxygen transfer from air into organic solventsRegioselective biooxidation of (+)-valencene by recombinant E. coli expressing CYP109B1 from Bacillus subtilis in a two-liquid-phase system.Role of oxygenases in guiding diverse metabolic pathways in the bacterial degradation of low-molecular-weight polycyclic aromatic hydrocarbons: a review.Engineering of Pseudomonas taiwanensis VLB120 for constitutive solvent tolerance and increased specific styrene epoxidation activity.Synthesis of 1-Naphthol by a Natural Peroxygenase Engineered by Directed Evolution.Enantioselective Benzylic Hydroxylation Catalysed by P450 Monooxygenases: Characterisation of a P450cam Mutant Library and Molecular Modelling.Discovery of a novel styrene monooxygenase originating from the metagenomeSteroid biotransformations in biphasic systems with Yarrowia lipolytica expressing human liver cytochrome P450 genes.The influence of microbial physiology on biocatalyst activity and efficiency in the terminal hydroxylation of n-octane using Escherichia coli expressing the alkane hydroxylase, CYP153A6.Catalytic, mild, and selective oxyfunctionalization of linear alkanes: current challenges.Guidelines for development and implementation of biocatalytic P450 processes.Response of Pseudomonas putida KT2440 to increased NADH and ATP demand.Maximizing the stability of metabolic engineering-derived whole-cell biocatalysts.Proline availability regulates proline-4-hydroxylase synthesis and substrate uptake in proline-hydroxylating recombinant Escherichia coli.Suitability of recombinant Escherichia coli and Pseudomonas putida strains for selective biotransformation of m-nitrotoluene by xylene monooxygenase.Effect of cell permeability and dehydrogenase expression on octane activation by CYP153A6-based whole cell Escherichia coli catalysts.Whole-cell biocatalysis for 1-naphthol production in liquid-liquid biphasic systems.NADH availability limits asymmetric biocatalytic epoxidation in a growing recombinant Escherichia coli strain.Efficient phase separation and product recovery in organic-aqueous bioprocessing using supercritical carbon dioxide.Metabolic response of Pseudomonas putida during redox biocatalysis in the presence of a second octanol phase.High-cell-density cultivation of recombinant Escherichia coli, purification and characterization of a self-sufficient biosynthetic octane ω-hydroxylase.Maximization of cell viability rather than biocatalyst activity improves whole-cell ω-oxyfunctionalization performance.Whole-cell-based CYP153A6-catalyzed (S)-limonene hydroxylation efficiency depends on host background and profits from monoterpene uptake via AlkL.Reaction and catalyst engineering to exploit kinetically controlled whole-cell multistep biocatalysis for terminal FAME oxyfunctionalization.Biocatalytic oxidation reactions - a Chemist's perspective.Production host selection for asymmetric styrene epoxidation: Escherichia coli vs. solvent-tolerant Pseudomonas.
P2860
Q21198740-301BE1DA-3FF6-4CDD-AD1A-FB4B8F006A13Q27022534-827216DA-E6FD-44F3-8674-B8841D337DA1Q28821996-64297F22-40F2-4E9C-8520-02EA1860230CQ33480702-59FFDA9A-2A09-43E5-989D-819360AA3240Q33693798-37412DE7-BBC6-4DA6-B2FA-BF181C3B9B87Q34261206-5106FBBD-D86A-4D9B-8D27-5BBF7D266849Q35871443-CA90DDDE-DE21-4E03-81AE-864ED71406AFQ35876601-7AE4E017-B858-415B-BEEE-56BCC4A5565DQ36136791-16FCAE8B-17BF-489B-99B3-FAFACF0E7AFFQ36531595-C277652B-4126-4485-886D-1E7CA5129C41Q36686957-EFD69C10-F141-4FDB-9810-7DB5B4881E7BQ38045228-3C1F3A5A-DC58-4251-A03C-97968118A4E6Q38344548-DCC24856-71AE-41E0-8B0C-D04CAC5371ABQ38628757-6E698D8E-8B0C-49B2-9D6F-45026A258CD2Q39441761-B53B1E58-9F57-4E6C-A82B-B0EF2613E1F9Q39762292-52305EDC-73E0-4E2C-A83B-11D16FC9DF5BQ39799503-ACA495C1-B8FD-47EF-9EED-F976B2CCD333Q41696380-203325B4-8496-4BEE-9BE6-A8BE7A259D8EQ41831457-C3A34C4A-522F-4694-9E9F-2F2F3E17930AQ42121592-88013B0B-7D29-4ADA-921E-D8946AD82C61Q43000083-CF67D4BF-60C8-48FA-AF67-9D795973216CQ46357643-F42C96E2-53C0-44E5-8F77-CB72B2398C66Q50475286-0FA8B69F-AAE3-48C3-A8F2-A393D395AB1AQ51093711-46F654AF-59F0-47FE-87F6-D05A1AEC12E0Q51843702-307B0A43-DBB7-46F4-B94B-1CE700850414Q53544494-62E77F14-41A1-4450-B085-C1DF3B19A88AQ53835321-4B7DD095-7DBA-4CE3-8191-E4CA96724081Q54338011-0B0F1BFB-8C7D-4C3C-8390-972530EC8BF4
P2860
Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization.
@ast
Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization.
@en
type
label
Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization.
@ast
Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization.
@en
prefLabel
Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization.
@ast
Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization.
@en
P1476
Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization
@en
P2093
Andreas Schmid
P304
P356
10.1016/J.JBIOTEC.2004.03.027
P50
P577
2004-09-01T00:00:00Z