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Microbacterium

Normally amino add synthesis will just satisfy the metabolic demand. In some cases, when the amino add occurs in both biosynthetic and energy production pathways, overproduction of the amino add can take place. This is the case, espedally for L-glutamic add, with Corynebacterium, Brevibacterium, Microbacterium and Arthrobacter. [Pg.241]

Schmidt M, P Roger, F Lingens (1991) Microbial metabolism of quinoline and related compounds XL Degradation of quinoline-4-carboxylic acid by Microbacterium sp. Hj, Agrobacterium sp. IB and Pintelo-bacter simplex 4B anf 5B. Biol Chem Hoppe-Seyler 370 1015-1020. [Pg.551]

Shafiee, A., Motamedi, H. and King, A., Purification, characterization and immobilization of an NADPH-dependent enzyme involved in the chiral specific reduction of the keto ester M, an intermediate in the s3mthesis of an anti-asthma drug, montelukast, from Microbacterium campoquemadoensis (MB5614). App/. Microbiol. Biotechnol., 1998, 49, 709-717. [Pg.78]

Microbacterium sp. (from Halichondria panicea) Glucosylmannosyl glycerolipid 200 [84]... [Pg.225]

Rather than using expensive and possibly toxic chemicals, certain bacteria and other microorganisms have the ability to oxidize As(III) in water, wastes, soils, and sediments (Ehrlich, 2002 Santini, Vanden Hoven and Macy, 2002 Anderson et al., 2002). Microbacterium lacticum (Mokashi and Paknikar, 2002) and Alcaligenes faecalis (Anderson et al., 2002) are examples of bacteria that are known to oxidize As(III). Some bacteria use As(III) as a source of energy, whereas others simply oxidize it as a means of detoxifying their environments (Ehrlich, 2002, 313). [Pg.357]

Further to these results, the microbicidal activities of FIBCIDE-KF and KATHON WT were evaluated. The minimum inhibitory concentrations (MIC) for Pseudomonas aeruginosa, Pseudomonas putida, Bacillus subtilis and Microbacterium sp. are identical for both compounds, so the microbicidal effect has not diminished (Figure 10). It appears that the biocidal effects are similar because the Cl-MIT in the inclusion complex is released into water, as shown in Figure 6. [Pg.215]

Walker, T.E., Han, C.H., Kollman, V.H., London, R.E., Matwiyoff, N.A. (1982). 13C nuclear magnetic resonance studies of the biosynthesis by Microbacterium ammoniaphilum of L-gluta-mate selectively enriched with carbon-13. J. Biol. Chem. 257,1189-1195. [Pg.269]

A main component of the linear ferrioxamine group (63). Reverses inhibition by ferrimycin antibiotics (148) and acts as a growth factor for Microbacterium lacticum (101). From Streptomyces pilosus (8). Also produced by species of Nocardia and Micromonospora, and by a number of species of Streptomyces (148). [Pg.79]

The strains used are either wild types or mutants. Wild types from the genera Arthrobacter, Bacillus, Brevibacterium, Corynebacterium and Microbacterium are mostly employed in glutamic acid and alanine production 48). The yields, depending on the carbon source and bacterial species, are between 10-80%. Other amino acids are also accumulated in wild types however, yields are lower. [Pg.107]

Carbon source11 Corynebacterium glutamicum Nocardia sp. Arthrobacter ilicis Clavibacter rathayi Microbacterium laevaniformans... [Pg.609]

Streptomyces rubiginosus (6) Streptomyces murinus (7) Microbacterium arborescens ... [Pg.897]


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See also in sourсe #XX -- [ Pg.175 ]

See also in sourсe #XX -- [ Pg.241 ]

See also in sourсe #XX -- [ Pg.110 ]




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Microbacterium arborescens

Microbacterium campoquemadoensis

Microbacterium lacticum

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