2,4-Dichlorophenoxyacetic acid (2,4-D) utilization by Delftia acidovorans MC1 at alkaline pH and in the presence of dichlorprop is improved by introduction of the tfdK gene
CHEMICAL COMPOUND;
CLONE;
DEGRADATION;
GENE;
HERBICIDE;
PH;
STRAIN;
ARTICLE;
COMPARATIVE STUDY;
DELFTIA ACIDOVORANS;
GENETIC ENGINEERING;
GENETICS;
GROWTH, DEVELOPMENT AND AGING;
KINETICS;
METABOLISM;
PH;
TRANSPORT AT THE CELLULAR LEVEL;
Description of microbial growth behaviour during wash-out phase; Determination of the maximum growth rate
AA Esener JA Roels NWF Kossen JWH Roozenburg 1981 Description of microbial growth behaviour during wash-out phase; determination of the maximum growth rate J. Appl. Microbiol. Biotechnol. 13 141 144
Isolation of phenoxy herbicide-degrading Rhodoferax species from contaminated building material
A Ehrig RH Müller W Babel 1997 Isolation of phenoxy herbicide-degrading Rhodoferax species from contaminated building material Acta Biotechnol. 17 351 356
Alcaligenes eutrophus JMP 134 "2,4-dichlorophenoxyacetate monooxygenase" is an α-ketoglutarate dependent dioxygenase
F Fukumori RP Hausinger 1993a Alcaligenes eutrophus JMP 134 "2,4-dichlorophenoxyacetate monooxygenase" is an α-ketoglutarate dependent dioxygenase J. Bacteriol. 175 2083 2086
Purification and characterization of 2,4-dichlorophenoxyacetate/α- ketoglutarate dioxygenase
F Fukumori RP Hausinger 1993b Purification and characterization of 2,4-dichlorophenoxyacetate/α-ketoglutarate dioxygenase J. Biol. Chem. 268 24311 24317
Structural organization and localization of the chlorocatechol pathway in the 2,4-D degrading alkalitolerant strain Delftia acidovorans P4a
D Hoffmann S Kleinsteuber RH Müller W Babel 2003 Structural organization and localization of the chlorocatechol pathway in the 2,4-D degrading alkalitolerant strain Delftia acidovorans P4a Microbiology 149 2545 2556
The tfdK gene product facilitates uptake of 2,4-dichlorophenoxyacetate by Ralstonia eutropha JMP 134(pJP4)
JHJ Leveau AJB Zehnder JR Van der Meer 1998 The tfdK gene product facilitates uptake of 2,4-dichlorophenoxyacetate by Ralstonia eutropha JMP 134(pJP4) J. Bacteriol. 180 2237 2243
Mineralization and co-metabolic degradation of phenoxyalkanoic acid herbicides by a pure bacterial culture isolated from an aquifer
P Mai SO Jacobsen J Aamand 2001 Mineralization and co-metabolic degradation of phenoxyalkanoic acid herbicides by a pure bacterial culture isolated from an aquifer Appl. Microbiol. Biotechnol. 56 486 490
Formate gradients as a means for detecting the maximum carbon conversion efficiency: Correlation between formate utilization and biomass increase
RH Müller KD Markuske W Babel 1985 Formate gradients as a means for detecting the maximum carbon conversion efficiency: correlation between formate utilization and biomass increase Biotechnol. Bioeng. 17 1599 1602
Phenol and its derivatives as heterotrophic substrates for microbial growth - An energetic comparison
RH Müller W Babel 1994 Phenol and its derivatives as heterotrophic substrates for microbial growth - an energetic comparison Appl. Microbiol. Biotechnol. 42 446 451
Determination of Ks-values during growth of Alcaligenes eutrophus JMP 134 on phenol, 2,4-dichlorophenoxyacetic acid and fructose
RH Müller W Babel 1995a Determination of Ks-values during growth of Alcaligenes eutrophus JMP 134 on phenol, 2,4-dichlorophenoxyacetic acid and fructose Acta Biotechnol. 15 347 353
Transient state cultivation as a means for determining maximum growth rates of microorganisms in inhibition kinetics
RH Müller T Bley W Babel 1995b Transient state cultivation as a means for determining maximum growth rates of microorganisms in inhibition kinetics J. Microbiol. Meth. 22 209 219
Comamonas acidovorans MC1: A new isolate capable of degrading the chiral herbicides dichlorprop and mecoprop and the herbicides 2,4-D and MCPA
RH Müller S Jorks S Kleinsteuber W Babel 1999a Comamonas acidovorans MC1: a new isolate capable of degrading the chiral herbicides dichlorprop and mecoprop and the herbicides 2,4-D and MCPA Microbiol. Res. 154 241 246
A biotechnological approach of detoxifying herbicide-contaminated building rubble
Battelle Press Columbus, Richland
RH Müller RA Müller Y Jahn W Babel 1999b A biotechnological approach of detoxifying herbicide-contaminated building rubble BC Alleman A Leeson Bioremediation of Nitroaromatic and Haloaromatic Compounds Vol 5(7) Battelle Press Columbus, Richland 143 148
Bioremediation of building material contaminated with herbicides
Marcel Dekker New York
RH Müller RA Müller Y Jahn W Babel 2000 Bioremediation of building material contaminated with herbicides DL Wise DJ Trantolt EJ Cichon Remediation of Hazardous Waste Contaminated Soils 2 Marcel Dekker New York 121 131
Physiological and genetic characteristics of two strains utilizing phenoxypropionate and phenoxyacetate herbicides
RH Müller S Kleinsteuber W Babel 2001 Physiological and genetic characteristics of two strains utilizing phenoxypropionate and phenoxyacetate herbicides Microbiol. Res. 156 121 131
Involvement of two α-ketoglutarate-dependent dioxygenases in enantioselective degradation of (R)- and (S)-mecoprop by Sphingomonas herbicidovorans MH
K Nickel MJF Suter HPE Kohler 1997 Involvement of two α-ketoglutarate-dependent dioxygenases in enantioselective degradation of (R)- and (S)-mecoprop by Sphingomonas herbicidovorans MH J. Bacteriol. 179 6674 6679
Stereospecific degradation of the phenoxypropionate herbicide dichlorprop
Saari ER, Hogan DA & Hausinger RP (1999) Stereospecific degradation of the phenoxypropionate herbicide dichlorprop. J. Mol. Catal. B: Enzymatic-6: 421-428
Localization and characterization of two novel genes encoding stereospecific 2(2,4-dichlorophenoxy)propionate cleavage in Delftia acidovorans MC1
KM Schleinitz S Kleinsteuber T Vallaeys W Babel 2004 Localization and characterization of two novel genes encoding stereospecific 2(2,4- dichlorophenoxy)propionate cleavage in Delftia acidovorans MC1 Appl. Environ. Microbiol. 70 5357 5365
Green fluorescent protein-based systems for genetic analysis of bacteria including monocopy application
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Enantioselective degradation of the herbicide mecoprop [2-(2-methyl-4-chlorophenoxy)propionic acid] by mixed and pure bacterial cultures
VA Tett AJ Willetts HM Lappin-Scott 1994 Enantioselective degradation of the herbicide mecoprop [2-(2-methyl-4-chlorophenoxy)propionic acid] by mixed and pure bacterial cultures FEMS Microbiol. Ecol. 14 191 200
Purification and characterization of the enantiospecific dioxygenases from Delftia acidovorans MC1 initiating the degradation of phenoxypropionate and phenoxyacetate herbicides
A Westendorf RH Müller W Babel 2002 Purification and characterization of the enantiospecific dioxygenases from Delftia acidovorans MC1 initiating the degradation of phenoxypropionate and phenoxyacetate herbicides Acta Biotechnol. 23 3 17
The two enantioselective dichlorprop/α-ketoglutarate-dioxygenases from Delftia acidovorans MC1 - Protein data of RdpA and SdpA. Microbiol
A Westendorf RH Müller W Babel 2003 The two enantioselective dichlorprop/α-ketoglutarate-dioxygenases from Delftia acidovorans MC1 - protein data of RdpA and SdpA. Microbiol Res 157 317 322
Westendorf A, (2004) Enantioselektive Verwertung von Phenoxyalkanoat- Herbiziden durch Bakterien - Biochemische Charakterisierung der Dioxygenasen des initialen Abbau-Schrittes. Dissertation, Univ. Leipzig
Complete microbial degradation of both enantiomers of the chiral herbicide Mecoprop [(RS)-2-(4-chloro-2-methylphenoxy)propionic acid] in an enantioselective manner by Sphingomonas herbicidovorans sp. nov
C Zipper K Nickel W Angst HPE Kohler 1996 Complete microbial degradation of both enantiomers of the chiral herbicide Mecoprop [(RS)-2-(4-chloro-2- methylphenoxy)propionic acid] in an enantioselective manner by Sphingomonas herbicidovorans sp. nov Appl. Environ. Microbiol. 62 4318 4322
Enantioselective uptake and degradation of the chiral berbicide dichlorprop [(RS)-2-(2,4-dichlorophenoxy)propionic acid] by Sphingomonas herbicidovorans MH
C Zipper M Bunk AJB Zehnder HEP Kohler 1998 Enantioselective uptake and degradation of the chiral berbicide dichlorprop [(RS)-2-(2,4-dichlorophenoxy) propionic acid] by Sphingomonas herbicidovorans MH J. Bacteriol. 180 3368 3374