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Pseudomonas chlororaphis

Oinuma K-I, Y Hashimoto, K Konishi, M Goda, T Noguchi, H Higashibata, M Kobayashi (2003) Novel aldox-ime dehydratase involved in carbon-nitrogen triple bond synthesis of Pseudomonas chlororaphis B23. J Biol Chem 278 29600-29608. [Pg.143]

Potrawfke T, J Armangaud, R-M Wittich (2001) Chlorocatechols substituted at positions 4 and 5 are substrates of the broad-spectrum chlorocatechol 1,2-dioxygenase of Pseudomonas chlororaphis RW71. J Bacteriol 183 997-1011. [Pg.481]

Potrawfke T, KN Timmis, R-M Wittich (1998) Degradation of 1,2,3,4-tetrachlorobenzene by Pseudomonas chlororaphis. Appl Environ Microbiol 64 3798-3806. [Pg.481]

Inoue H, O Takimura, K Kawaguchi, T Nitoda, H Euse, K Murakami, Y Yamaoka (2003) Tin-carbon cleavage of organotin compounds by pyoverdine from Pseudomonas chlororaphis. Appl Environ Microbiol 69 878-883. [Pg.594]

Chin-A-Woeng TFC, D van den Broek, G de Voer, KMGK van der Drift, S Tuinman, JE Thomas-Oates, BJJ Lugtenberg, GV Bloemberg (2001) Phenazine-l-carboxamide production in the biocontrol strain Pseudomonas chlororaphis PC L 1391 is regulated by multiple factors secreted into the growth medium. Mol Plant-Microbe Interact 14 869-879. [Pg.614]

Chin-A-Woeng TFC, GV Bloemberg, IHM Mulders, LC Dekkers, BJJ Lugtenberg (2000) Root comonization by phenazine-l-carboxamide-producing bacterium Pseudomonas chlororaphis PCL 1391 is essential for biocontrol of tomato foot and root rot. Mol Plant-Microbe Interact 13 1340-1345. [Pg.614]

Tjeerd van Rij E, G Girard, BJJ Lugtenberg, GV Bloemberg (2005) Influence of fusaric acid on phenazine-1-carboxamide synthesis and gene expression of Pseudomonas chlororaphis strain PCL1391. Microbiology (UK) 151 2805-2814. [Pg.618]

Tjeerd van Rij E, M Wesselink, TEC Chin-A-Woeng, GV Bloemberg, BJJ Lugtenberg (2004) Influence of environmental conditions on the production of phenazine-l-carboxamide by Pseudomonas chlororaphis PCL 1391. Mol Plant-Microbe Interact 17 557-566. [Pg.618]

Siunova, T., Anokhina, T., Mashukova, A., Kochetkov, V., and Boronin, A., Rhizosphere strain of Pseudomonas chlororaphis capable of degrading naphthalene in the presence of cobalt/nickel, Microbiology, 76 (2), 182-188, 2007. [Pg.428]

Barelmann I, Uria Fernandez D, Budzikiewicz H, Meyer JM (2003) The Pyoverdine from Pseudomonas chlororaphis D-TR133 Showing Mutual Acceptance with the Pyoverdine from Pseudomonas fluorescens CHAO. BioMetals 16 263... [Pg.54]

Hohlneicher U, Hartmann R, Taraz K, Budzikiewicz H (1995) Pyoverdin, Ferribactin, Azotobactin - a new Triad of Siderophores from Pseudomonas chlororaphis ATTC 9446 and its Relation to Pseudomonas fluorescens ATCC 13525. Z Naturforsch 50c 337... [Pg.61]

Phenazine-l-carboxamide (137) is known as oxychlororaphine and has been isolated from cultures of Pseudomonas chlororaphis it has some limited inhibitory properties, but the inhibitory action of phenazines is generally disappointing. Some phenazine derivatives have insecticidal properties thus, phenazine itself has been found to be toxic to the clothes moth, the Hawaiian beet webworm, the rice weevil and larva of the codling moth, but under trial conditions its toxicity to plant material, as evidenced by severe burning of foliage, was found to be too high to make it of practical value. [Pg.196]

S. M. Cooper, J. E. Gavagan, B. Stieglitz, S. M. Hennessey, and R. DiCosimo, 5-Cyanovaleramide production using immobilized Pseudomonas chlororaphis B23, Bioorgan. Med. Chem. 1999, 7, 2239-2245. [Pg.203]

Pseudomonas chlororaphis B23 with high NHase activity was isolated as an isobutyronitrile-assimilating bacterium [47], The NHase acts well on acrylonitrile to form acrylamide but the amidase hardly acts on acrylamide in this strain. When resting cells of P. chlororaphis B23 were added to the reaction mixture and incubated at 10 °C for 7.5 h, more than 400 g of acrylamide per liter was accumulated. More than 99% of the substrate was converted to acrylamide without the formation of any by-products. [Pg.56]

Candida famata Cryptococcus sp. UFMG-Y28 Cryptococcusflavus UFMG-Y61 Comamonas testosteroni ATCC 55744 Klebsiella oxytoca 38.1.2 Myrothecium verrucaria Pseudomonas chlororaphis B23 (PERM BP-187)... [Pg.371]

Hann, E.C., Eisenberg, A., Eager, S.K., et al. 1999.5-Cyanovaleramide production using immobilized Pseudomonas chlororaphis B23. Bioorganic and Medicinal Chemistry, 7 2239-45. [Pg.407]

Rynno, K., Nagasawa, T., and Yamada, H. 1988. Isolation of advantageons mntants of Pseudomonas chlororaphis B23 for the enzymatic prodnction of acrylamide. A,gric /ZfMraZ and Biological Chemistry, 52 1813-6. [Pg.412]

Howard, G. T., Ruiz, C. Newton, N. P. (1999). Growth of Pseudomonas chlororaphis on a polyester-polyurethane and the purification and characterization of a polyurethanase-esterase enzyme. International Biodeterioration and Biodegradation, 43, 7-12. [Pg.231]

Stern, R. V. Howard, G. T. (2000). The polyester polyurethanase gene (pueA) from Pseudomonas chlororaphis encodes a lipase. FEMS Microbiology Letters,... [Pg.234]

Rhodococcus sp. N-774 and Pseudomonas chlororaphis B23 resting cells have been used at industrial scale (as first- and second-generation biocatalysts) for the biological production of acrylamide from acrylonitrile since the 1980s [21]. Currently Rhodococcus rhodochrous J1 is being adopted as a third-generation biocatalyst (Mitsubishi Rayon Co.). The industrial production of nicotinamide from 3-cyanopyridine is also operated with this strain (Lonza AG). However, despite the enormous potentiality of nitrile-hydrolyzing biocatalysts for industrial applications, only a few commercial processes have been realized [22]. [Pg.273]


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