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Comamonas

Neopterin cyclic phosphate (92) has been isolated as an intermediate in the biosynthesis of pteridines from GTP in Comamonas Tracer studies show that the phosphoryl group in (92) originates from the... [Pg.148]

A taxonomic note there have been substantial developments in the taxonomy of pseudomonads, and many new genera have been proposed including, for example, Sphingomonas, Comamonas, and Variovorax, while denitrifying organisms described as pseudomonads have been referred to the general Thauera and Azoarcus (Anders et al. 1995). [Pg.66]

Iwaki H, Y Hosegawa, S Wang, MM Kayser, PCK Lau (2002) Cloning and characterization of a gene cluster involved in cyclopentanol metabolism in Comamonas sp. strain NCIMB 9872 and biotransformations effected by Escherichia co/f-expressed cyclopentanone 1,2-monooxygenase. Appl Environ Microbiol 68 5671-5684. [Pg.140]

Locher HH, T Leisinger, AM Cook (1991a) 4-Sulfobenzoate 3,4-dioxygenase. Purification and properties of a desulfonative two-component system from Comamonas testosteroni T-2. Biochem J 274 833-842. [Pg.141]

Schach S, B Tshisuaka, S Fetzner, F Lingens F (1995) Quinoline 2-oxidoreductase and 2-oxo-l,2-dihydro-quinoline 5,6-dioxygenase from Comamonas testosteroni 63. The first two enzymes in quinoline and 3-methylquinoline degradation. EurJ Biochem 232 536-544. [Pg.144]

Wu J-F, C-W Sun, C-Y Jiang, Z-P Liu, S-J Liu (2005) A novel 2-aminophenol 1,6-dioxygenase involved in the degradation of p-chloronitrobenzene by Comamonas strain CNB-1 purification, properties, genetic cloning and expression in Escherichia coli. Arch Microbiol 183 1-8. [Pg.147]

The enzymes from Comamonas testosteroni for hydroxylation of quinoline to quinol-2-one (quinoline 2-oxidoreductase) and the dioxygenase responsible for the introduction of oxygen into the benzenoid ring (2-oxo-l,2-dihydroquinoline 5,6-dioxygenase) have been described (Schach et al. 1995). [Pg.186]

The transport of toluene-4-sulfonate into Comamonas testosteroni has been examined (Locher et al. 1993), and rapid uptake required growth of the cells with toluene-4-sulfonate or 4-methylbenzoate. From the results of experiments with various inhibitors, it was concluded that a toluenesulfonate anion/proton symport system operates rather than transport driven by a difference in electrical potential (A (/), and uptake could not take place under anaerobic conditions unless an electron acceptor such as nitrate was present. [Pg.214]

Hollender J, W Dott, J Hopp (1994) Regulation of chloro- and methylphenol degradation in Comamonas tes-tosteroni JH5. Appl Environ Microbiol 60 2330-2338. [Pg.232]

Junker F, AM Cook (1997) Conjugative plasmids and the degradation of arylsulfonates in Comamonas testos-teroni. Appl Environ Microbiol 63 2403-2410. [Pg.233]

Locher HH, B Poohnan, AM Cook, WN Konings (1993) Uptake of 4-toluene sulfonate by Comamonas tes-tosteroniT-2. J Bacterial 175 1075-1080. [Pg.234]

Mobus E, M Jahn, R Schmid, D Jahn, E Maser (1997) Testosterone-regulated expression of enzymes involved in steroid and aromatic hydrocarbon catabolism in Comamonas testosteroni. J Bacteriol 179 5951-5955. [Pg.235]

Horinouchi M, T Hayashi, H Koshino, T Kurita, T Kudo (2005) Identification of 9,17-dioxo-l,2,3,4,10,11, 19-hexanorandrostan-5-oic acid, 4-hydroxy-2-oxohexanoic acid, and 2-hydroxyhexa-2,4-dienoic acid and related enzymes involved in testosterone degradation in Comamonas testosteroni TA441. Appl Environ Microbiol 71 5275-5281. [Pg.347]

Goyal AK, GJ Zylstra (1996) Molecular cloning of novel genes for polycyclic aromatic hydrocarbon degradation from Comamonas testosteroni. Appl Environ Microbiol 62 230-236. [Pg.419]

Hurtubise Y, D Barriault, J Powlowski, M Sylvestre (1995) Purification and characterization of the Comamonas testosteroni B-356 biphenyl dioxygenase components. J Bacteriol 111 6610-6618. [Pg.420]

Provident MA, JM O Brien, J Ruff, AM Cook, IB Lambert (2006) Metabolism of isovanillate, vanillate, and veratrate by Comamonas testosteroni strain BR6020. J Bacteriol 188 3862-3869. [Pg.444]

Sasoh M, E Masai, S Ishibashi, H Kara, N Kamimura, K Miyauchi, M Fukuda (2006) Characterization of the terephthalate degradation genes of Comamonas sp. strain E6. Appl Environ Microbiol 72 1825-1832. [Pg.445]

Schlafli HR, MA Weiss, T Leisinger, AM Cook (1994) Terephthalate 1,2-dioxygenase system from Comamonas testosteroni T-2 purification and some properties of the oxygenase component. J Bacteriol 176 6644-6652. [Pg.445]

Junker F, R Kiewitz, AM Cook (1997) Characterization of the / -toluenesulfonate operon tsaMBCD and tsaR in Comamonas testosteroni T-2. J Bacteriol 179 919-927. [Pg.508]

The degradation of 3-nitrobenzoate by Pseudomonas sp. strain JS51 and Comamonas sp. strain JS46 is initiated by dioxygenation to 3,4-dihydroxybenzoate with loss of nitrite (Nadeau and Spain 1995) (Figure 9.53b). [Pg.514]

Groenewegen PEG, P Breenwer, JMLM van Helvoort, AAM Langenhoff, EP de Vries, JAM de Bont (1992) Novel degradative pathway of 4-nitrobenzoate in Comamonas acidovorans NBA-10. J Gen Microbiol 138 1599-1605. [Pg.518]

Lessner DJ, GR Johnson, RE Parales, JC Spain, DT Gibson (2002) Molecnlar characterization and snbstrate specificity of nitrobenzene dioxygenase from Comamonas sp. strain JS 765. Appl Environ Microbiol 68 634-541. [Pg.519]

Wu J-f, C-y Jiang, B-j Wang, Y-f Ma, Z-p Liu, S-j Liu (2006) Novel partial reductive pathway for 4-chloro-nitrobenzene and nitrobenzene degradation in Comamonas sp. strain CNB-1. Appl Environ Microbiol 12 1759-1765. [Pg.520]


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