نتایج جستجو برای: corynebacterium glutamicum
تعداد نتایج: 5369 فیلتر نتایج به سال:
Regulation of glnA expression and glutamine synthetase I activity was analyzed in Corynebacterium glutamicum. Transcription is regulated by the global repressor protein AmtR, essential for derepression of glnA transcription are GlnK and uridylyltransferase, key proteins of the C. glutamicum nitrogen regulatory system. Glutamine synthetase I activity is controlled by adenylylation/deadenylylatio...
Sucrose uptake by Corynebacterium glutamicum involves a phosphoenolpyruvate-dependent sucrose phosphotransferase (PTS), but in the absence of fructokinase, further metabolism of the liberated fructose requires efflux of the fructose and reassimilation via the fructose PTS. Mutant strains lacking detectable fructose-transporting PTS activity accumulated fructose extracellularly but consumed sucr...
Duncan, D. B. (1955) Biornetrics 11, 1-42 Gomez, E. C. & Frost, P. (1972) Ado. Biol. Skin 12,367-379 Hamilton, J. B. & Montagna, W. (1950) Am. J . Anot. 86, 191-233 Katchen, B. & Buxbaum, S. (1975) J . C/i/i. Etic/oci.i/io/. Metab. 41, 373-379 Liao, S., Howell, D. K. & Chang, T. (1974) Endocrinology 94, 1205-1208 Lutsky, B. N., Casmer, C. & Koziol, P. (1974) Lipid.x 9,43-48 Lutsky, B. N., Budak...
This paper studies microlocal regularity properties of the distributions f on a strongly noncharacteristic submanifold E of a hypoanalytic manifold M that arise as the boundary values of solutions on wedges in M with edge E. The hypo-analytic wave-front set of f in the sense of Baouendi-Chang-Treves is constrained as a consequence of the fact that f extends as a solution to a wedge.
L-Lysine is an essential amino acid with high commercial importance, as it has to be available in sufficient quantities in animal and human feeds to meet their nutritional requirement. As there is constant increase in L-lysine demand every year, to meet the increasing demand it is necessary to produce L-lysine in large scale. Generally, L-lysine is produced by batch fermentation. In the present...
The following several lines of evidence demonstrate that lactose permease (LacY) of Escherichia coli is assembled into the cytoplasmic membrane of gram-positive Corynebacterium glutamicum, expressing the lacY gene, as a functional carrier protein. (i) LacY was detected immunologically in the cytoplasmic membrane fraction of the heterologous host. (ii) Recombinant C. glutamicum cells bearing the...
The complete genome sequence of Corynebacterium glutamicum strain R was determined to allow its comparative analysis with other corynebacteria. The biology of corynebacteria was explored by refining the definition of the subset of genes that constitutes the corynebacterial core as well as those characteristic of saprophytic and pathogenic ecological niches. In addition, the relative scarcity of...
Auxotrophic proA mutants of Escherichia coli were complemented by two different classes of Corynebacterium glutamicum genes. One of these was the asd gene. The E. coli asd gene also complements the same proA alleles. Complementation of proA by the asd+ gene requires a high asd dosage and the proB and the proC gene products. The reciprocal complementation pattern (asd by the proA+ gene) was not ...
Corynebacterium glutamicum is widely used for the biotechnological production of amino acids. Amino acid producing strains have been improved classically by mutagenesis and screening as well as in a rational manner using recombinant DNA technology. Metabolic flux analysis may be viewed as the first systems approach to C. glutamicum physiology since it combines isotope labeling data with metabol...
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