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Arthrobacter strain

Hormann K, JR Andreesen (1991) A flavin-dependent oxygenase reaction initiates the degradation of pyrrole-2-carboxylate in Arthrobacter strain Pyl (DSM 6386). Arch Microbiol 157 43-48. [Pg.190]

Tam AC, RM Behki, SU Khan (1987) Isolation and characterization of an S-ethyl-V,V-dipropylthiocarbamate-degrading Arthrobacter strain and evidence for plasmid-associated S-ethyl-V,V-dipropylthiocarbamate degradation. Appl Environ Microbiol 53 1088-1093. [Pg.239]

Fig. 8. — Degradation Limit162 of Substrates Having Different Degrees of Esterification, with Pectate Lyase of Arthrobacter, strain 547. Fig. 8. — Degradation Limit162 of Substrates Having Different Degrees of Esterification, with Pectate Lyase of Arthrobacter, strain 547.
Henrick, K., Collyer, C. A., and Blow, D. M. (1989). Structures of o-xylose isomerase from Arthrobacter strain B3728 containing the inhibitors xylitol and n-sorbitol at 2.5 A and 2.3 A resolution, respectively.y. Mol. Biol. 208, 129-157. [Pg.70]

Edgehill, R. U. (1994). Pentachlorophenol removal from slightly acidic mineral salts, commercial sand, and clay soil by recovered Arthrobacter strain ATCC 33790. Applied Microbiology and Biotechnology, 41, 142-8. [Pg.288]

In the amine oxidase from Escherichia coli, the topa quinone was confirmed by a detailed analysis of the cofactor dipeptide X-Asp [67] and the resonance Raman spectrometry of the enzyme and its derivatives[68,69]. The primary structure of the enzyme also contains the cofactor consensus sequence [70]. More bacterial genes were shown to encode proteins containing the topa quinone consensus sequence, such as amine oxidase from Klebsiella aerogenes [71], phenethylamine oxidase and histamine oxidase from Arthrobacter globiformis [72,73], and methylamine oxidase from Arthrobacter strain PI [74]. Amino acid sequences around the position of the cofactor for selected amine oxidases from various sources are given in Table 1. [Pg.1269]

For example, n-p-hydroxyphenylglydne, a key intermediate in the synthesis of semisynthetic cephalosporins and penicillins, is currently manufactured on a multi-thousand ton scale. The hydantoinase-catalysed reaction is also suitable for the production of unnatural D-amino acids, although the in situ racemization of the remaining substrate via keto-enol tautomerization is generally slow. To facilitate the stereoinversion, base or hydantoin racemase of Pseudomonas and Arthrobacter strains is often used. [Pg.165]

Stephen, K.E., Homrighausen, D., DePalma, G., Nakatsu, C.H., and Irudayaraj, J. (2012) Surface enhanced Raman spectroscopy (SERS) for the discrimination of Arthrobacter strains based on variations in cell surface composition. Analyst, 137, 4280-4286. doi 10.1039/C2AN35578G... [Pg.511]

Cabirol, F.L, Gohel, A., CoBier, S.J., liang, J., Mock, M., Mimdorff, E., Novick, S., limanto, J., Smith, D., and Beutner, G. (2012) Biosynthesis of (lR,2R)-2-(3,4-dimethoxyphenethoxy)cyclohexanamine using genetically modified to-aminotransferases for Arthrobacter strain KNK168. PCTInt. Appl, WO 2012024104 A2 20120223. [Pg.205]

Streptomyces sp. AK409 Pyrocoll Arthrobacter strains. Filamentous fungi, pathogenic protozoa, human tumor cell lines Dieter et al. (2003)... [Pg.43]


See other pages where Arthrobacter strain is mentioned: [Pg.523]    [Pg.209]    [Pg.369]    [Pg.216]    [Pg.265]    [Pg.305]    [Pg.200]    [Pg.268]    [Pg.127]    [Pg.1248]    [Pg.1263]    [Pg.1270]    [Pg.117]    [Pg.44]   
See also in sourсe #XX -- [ Pg.1263 , Pg.1267 , Pg.1270 ]

See also in sourсe #XX -- [ Pg.117 , Pg.139 ]




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Arthrobacter

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