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Regulation of the p-hydroxybenzoic acid hydroxylase gene (pobA) in plant-growth-promoting Pseudomonas putida WCS358
(Soc General Microbiology, Reading, 2001)
The regulation of the p-hydroxybenzoate hydroxylase gene (pobA) of Pseudomonas putida WC5358 involved in the catabolism of p-hydroxybenzoic acid (PHB) to the central intermediate protocatechuate was studied. Protocatechuic ...
The LysR-type transcriptional regulator CysB controls the repression of hslJ transcription in Escherichia coli
(Microbiology Soc, London, 2003)
The LysR-type transcriptional regulator (LTTR) CysB is a transcription factor in Escherichia coli cells, where as a homotetramer it binds the target promoter regions and activates the genes involved in sulphur utilization ...
Changes of the phagosomal elemental concentrations by Mycobacterium tuberculosis Mramp
(Microbiology-Sgm, 2005)
Pathogenic mycobacteria survive within phagosomes which are thought to represent a nutrient-restricted environment. Divalent cation transporters of the Nramp family in phagosomes and mycobacteria (Mramp) may compete for ...
Molecular characterization of the CmbR activator-binding site in the metC-cysK promoter region in Lactococcus lactis
(Microbiology Soc, London, 2005)
The metC-cysK operon involved in sulphur metabolism in Lactococcus lactis is positively regulated by the LysR-type protein CmbR. Transcription from the metC promoter is activated when concentrations of methionine and ...
Analysis of the Pseudomonas putida CA-3 proteome during growth on styrene under nitrogen-limiting and non-limiting conditions
(Microbiology Soc, London, 2009)
Pseudomonas putida CA-3 is a styrene-degrading bacterium capable of accumulating medium-chain-length polyhydroxyalkanoate (mcIPHA) when exposed to limiting concentrations of a nitrogen source in the growth medium. Using ...
The acetyl xylan esterase of Bacillus pumilus belongs to a family of esterases with broad substrate specificity
(Microbiology Soc, London, 2000)
The Bacillus pumilus gene encoding acetyl xylan esterase tare) was identified and characterized. The axe gene was expressed and the recombinant enzyme produced in Escherichia coli was purified and characterized. The ...