Biotransformation of natural and synthetic isoflavonoids by two recombinant microbial enzymes.
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Structural Insight into the Expanded PCB-Degrading Abilities of a Biphenyl Dioxygenase Obtained by Directed EvolutionRetuning Rieske-type Oxygenases to Expand Substrate RangeEpoxide formation on the aromatic B ring of flavanone by biphenyl dioxygenase of Pseudomonas pseudoalcaligenes KF707Burkholderia xenovorans LB400 harbors a multi-replicon, 9.73-Mbp genome shaped for versatility.Optimizing Polychlorinated Biphenyl Degradation by Flavonoid-Induced Cells of the Rhizobacterium Rhodococcus erythropolis U23A.Remarkable ability of Pandoraea pnomenusa B356 biphenyl dioxygenase to metabolize simple flavonoidsMetabolism of Doubly para-Substituted Hydroxychlorobiphenyls by Bacterial Biphenyl Dioxygenases.Drug activity screening based on microsomes-hydrogel system in predicting metabolism induced antitumor effect of oroxylin AHas the bacterial biphenyl catabolic pathway evolved primarily to degrade biphenyl? The diphenylmethane case.Flavonoids biotransformation by bacterial non-heme dioxygenases, biphenyl and naphthalene dioxygenase.Common features of environmental and potentially beneficial plant-associated Burkholderia.Prospects for using combined engineered bacterial enzymes and plant systems to rhizoremediate polychlorinated biphenyls.Bioremediation of petroleum hydrocarbons: catabolic genes, microbial communities, and applications.Biotransformation of chloro-substituted indoles to indigoids by phenol hydroxylase from Arthrobacter sp. W1.Flavone Biotransformation by Aspergillus niger and the Characterization of Two Newly Formed Metabolites.Commonalities and differences in regulation of N-acyl homoserine lactone quorum sensing in the beneficial plant-associated burkholderia species cluster.Second acyl homoserine lactone production system in the extreme acidophile Acidithiobacillus ferrooxidans.From PCBs to highly toxic metabolites by the biphenyl pathway.Plant exudates promote PCB degradation by a rhodococcal rhizobacteria.Identifying 6,7,4'-trihydroxyisoflavone as a potent tyrosinase inhibitor.Using tyrosinase as a monophenol monooxygenase: A combined strategy for effective inhibition of melanin formation.Microbial transformations of 7-hydroxyflavanone
P2860
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P2860
Biotransformation of natural and synthetic isoflavonoids by two recombinant microbial enzymes.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh
2003年學術文章
@zh-hant
name
Biotransformation of natural a ...... recombinant microbial enzymes.
@en
Biotransformation of natural a ...... recombinant microbial enzymes.
@nl
type
label
Biotransformation of natural a ...... recombinant microbial enzymes.
@en
Biotransformation of natural a ...... recombinant microbial enzymes.
@nl
prefLabel
Biotransformation of natural a ...... recombinant microbial enzymes.
@en
Biotransformation of natural a ...... recombinant microbial enzymes.
@nl
P2093
P2860
P1476
Biotransformation of natural a ...... recombinant microbial enzymes.
@en
P2093
Beatriz Cámara
Carolina Mascayano
Emilio Ponce
Liliana Muñoz
Lorenzo Mejías
Michael Seeger
Myriam González
Silvia Sepúlveda-Boza
Yesseny Vásquez
P2860
P304
P356
10.1128/AEM.69.9.5045-5050.2003
P407
P577
2003-09-01T00:00:00Z