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P. alcaligenes

Pseudomonas stutzeri, P. alcaligenes, and P. putida strains were isolated and proven to remove DBT, benzothiophene, thioxanthene, and thianthrene by decomposition into water-soluble substances [120],... [Pg.84]

Evaluation of P. nitroreducens with quinoline as the sole source of nitrogen showed a reduction of the total nitrogen content by 85%. The partial sequence of the 16S-rRNA gene of this Gram-negative, rod-shaped bacterium was determined and shown to be close to P. alcaligenes and P. stutzeri. [Pg.177]

The characteristics of an extracellular mcl-PHA depolymerase purified from the marine isolate Pseudomonas luteola M13-4 have been reported by Rhee et al. (2006). This enzyme is similar to Pseudomonas alcaligenes LB 19 (Kim et al. 2002) but is different from poly(HB-co-HV) (PHBV) depolymerase of Xanthomonas sp JS02 (Kim et al. 2000a, b, c) the molecular mass is 28 kDa, the isoelectric point is 6.0 with a reactivity optimum at pH 10 and 40°C. Serine residues seem to play an important role in the hydrolysis reaction by analogy with P. alcaligenes LB 19. PHO has been totally degraded polyhydroxyhexanoate (PHH) and a copolymer of (PHB-co-60%HV) have been partially hydrolyzed. [Pg.291]

Rhizobium P. alcaligenes P. cepacia P. diminuta P. fluorescens P. luteola P. maltophilia P. mendocina P. paucimobilis P. pickettii P. pseudoalcaligenes konjaci P. putida P. stutzeri P. testosteroni P. vesicularis R. spp. [Pg.257]

Lipases from C. antarctica and P. cepacia showed higher enantioselectivity in the two ionic liquids l-ethyl-3-methylimidazolium tetrafluoroborate and l-butyl-3-methylimidazolium hexafluoroborate than in THE and toluene, in the kinetic resolution of several secondary alcohols [49]. Similarly, with lipases from Pseudomonas species and Alcaligenes species, increased enantioselectivity was observed in the resolution of 1 -phenylethanol in several ionic liquids as compared to methyl tert-butyl ether [50]. Another study has demonstrated that lipase from Candida rugosa is at least 100% more selective in l-butyl-3-methylimidazolium hexafluoroborate and l-octyl-3-nonylimidazolium hexafluorophosphate than in n-hexane, in the resolution of racemic 2-chloro-propanoic acid [51]. [Pg.15]

Gao X, CL Tan, CC Yeo, CL P (2005) Molecular and biochemical characterization of the x/ D-encoded 3-hydroxybenzoate 6 hydroxylase involved in the degradation of 2,5-xylenol via the gentisate pathway in Pseudomonas alcaligenes NCIMB 9S61. J Bacterial 187 7696-7702. [Pg.138]

Roger P, A Erben, E Lingens (1990) Microbial metabolism of quinoline and related compounds IV. Degradation of isoquinoline by Alcaligenes faecalis Pa and Pseudomonas diminuta 1. Biol Chem Hoppe-Seyler 370 1183-1189. [Pg.191]

Ralstonia eutropha (Alcaligenes eutrophus) strain NH9 is able to degrade 3-chlorobenzene by the modified ortho pathway. The cbnA gene that encodes 3-chlorocatechol-l, 2-dioxygenase was introduced into rice plants (Oryza sativa -p.japonicd) under the control of a virus 35S promoter. 3-Chlorocatechol induced dioxygenase activity in the callus of the plants, and leaf tissues oxidized 3-chlorocatechol with the production of 2-chloromuconate... [Pg.606]

Byrom D (1990) Industrial production of copolymer from Alcaligenes eutrophus. In Dawes EA (ed) Novel biodegradable microbial polymers. Kluwer, Dordrecht, p 113... [Pg.178]

R. eutropha, formerly known as Alcaligenes eutrophus, has been used for the commercial production of P(3HB-co-3HV) [72]. This bacterium grows well in a relatively inexpensive minimal medium and accumulates a large amount of P(3HB) under the unbalanced growth condition. In R. eutropha, acetyl-CoA is converted to P(3HB) by three enzymes (genes) /J-ketothiolase (phaA), aceto-acetyl-CoA reductase (phaB), and PHA synthase (phaC) [6]. [Pg.193]

Lee SY, Choi J, Chang HN (1997) Process development and economic evaluation for the production of polyhydroxyalkanoates by Alcaligenes eutrophus. In Eggink G, Steinbuchel A, Poirier Y, Witholt B (eds) 1996 International Symposium on Bacterial Polyhydroxyalkanoates. NRC Research Press, Ottawa, p 127... [Pg.237]

Roger, P. Erben, A., and Lingens, F., Microbial Metabolism of Quinoline and Related Compounds. IV. degradation of isoquinoline by alcaligenes faecalis pa and pseudomonas diminuta 7. Biol Chem Hoppe Seyler, 1990. 371(6) pp. 511-513. [Pg.221]

Pierik, A. J., Schmelz, M., Ixnz, O., Friedrich, B. and Albracht, S. P. (1998b) Characterization of the active site of a hydrogen sensor from Alcaligenes eutrophus. FEBS Lett., 438, 231-5. [Pg.273]

Hildmann, C., Ninkovic, M., Dietrich, R., Wegener, D., Riester, D., Zimmermann, T, Birch, O.M., Bernegger, C., Loidl, P. and Schwienhorst, A. (2004) A new amidohydrolase from Bordetella or Alcaligenes strain FB188 with similarities to histone deacetylases. Journal of Bacteriology, 186, 2328-2339. [Pg.115]


See other pages where P. alcaligenes is mentioned: [Pg.430]    [Pg.90]    [Pg.292]    [Pg.443]    [Pg.99]    [Pg.217]    [Pg.430]    [Pg.90]    [Pg.292]    [Pg.443]    [Pg.99]    [Pg.217]    [Pg.48]    [Pg.51]    [Pg.59]    [Pg.59]    [Pg.346]    [Pg.264]    [Pg.196]    [Pg.459]    [Pg.580]    [Pg.664]    [Pg.246]    [Pg.28]    [Pg.182]    [Pg.198]    [Pg.311]    [Pg.179]    [Pg.893]    [Pg.196]    [Pg.170]    [Pg.187]    [Pg.188]    [Pg.188]    [Pg.114]    [Pg.60]    [Pg.163]    [Pg.315]    [Pg.101]    [Pg.427]   
See also in sourсe #XX -- [ Pg.112 ]




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