Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.2.1.23 (beta-galactosidase)
 14,648 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The virulence regulon of Bordetella pertussis includes a trans-acting regulatory locus, bvg, that is required for expression of several virulence factors. The virulence control system also responds to environmental signals. We have reconstructed a bvg-dependent regulatory system in Escherichia coli by using bacteriophage lambda vectors carrying transcriptional fusions to lacZYA. Single-copy lacZYA fusions to the B. pertussis fhaB locus, which encodes the attachment factor filamentous hemagglutinin, were activated nearly 400-fold by pBR322 replicons carrying sequences that included bvg. In contrast, bvg had no effect on the pertussis toxin operon (ptxA-E) promoter in E. coli as measured by ptxA-lacZ expression. Environmental signals that modulate expression of virulence genes in B. pertussis had a pronounced effect on bvg-mediated activation of fhaB-lacZ. MgSO4, nicotinic acid, and low temperature resulted in decreases in beta-galactosidase activities of 175-, 115-, and 45-fold respectively. Sensory transduction and transcriptional activation were tightly coupled, and both required an intact bvg locus as determined by 5' and 3' deletions that eliminated both activities.
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PMID:Analysis of Bordetella pertussis virulence gene regulation by use of transcriptional fusions in Escherichia coli. 255 78

Streptococcus mitis ATCC 903 aggregated when suspended in salt solutions containing the ions zinc, aluminium, lanthanum and cerium. This aggregation was very rapid as compared to spontaneous aggregation occurring in this strain. It was not inhibited by alkaline pH. Washed bacteria treated previously with zinc sulphate recovered and retained their ability to aggregate spontaneously at a slow rate. No such effect was observed with lanthanum-induced aggregation. The aggregates caused by lanthanum chloride were stable in sodium chloride up to 5 M concentrations. Magnesium sulphate dissociated these aggregates at 250 mM. Aggregation induced by zinc sulphate was less stable in these salts. The spontaneously aggregated cells were dissociated completely at 10 mM magnesium sulphate or 100 mM sodium chloride. Bacteria which had lost their ability to aggregate, owing to trypsin or beta-galactosidase treatment, were re-aggregated after addition of zinc, lanthanum or aluminium ions. Galactosamine inhibited the spontaneous aggregation and aggregation induced by zinc but not the aggregation induced by lanthanum or aluminium ions. In conclusion, the results provide a molecular model of induced and spontaneous aggregations where the two phenomena are qualitatively different.
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PMID:Induction of aggregation in Streptococcus mitis by certain ions. 644 Apr 11

The major targets for improvement of recombinant expression systems in microbial cells are gene dosage, transcriptional control machinery and, to some extent, translation. Here we show that optimization of fermentation conditions by applying statistically designed, multifactorial experiments offers an additional method for potential enhancement of gene expression systems. A chromosomally encoded fusion between the Bacillus subtilis aprE regulatory region and the E. coli lacZ gene carried by the B. subtilis host cells was used. The 2 x SG sporulation medium was used as a basal medium. Among the 11 fermentation factors we examined, the most significant variables influencing beta-galactosidase expression were statistically elucidated for optimization and included peptone, MgSO4.7H2O, and KCl. The optimum concentrations of these variables were predicted by using a second-order polynomial model fitted to the results obtained by applying the Box-Behnken design, a response surface method. Calculated optimum concentrations were predicted to confer a maximum yield of 2,423.5 beta-galactosidase specific activity units. A verification experiment performed under optimal conditions yielded 96% of the predicted specific activity value with an increase by a factor of almost 5 compared with the results obtained under basal conditions.
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PMID:Application of the response surface methodology for optimizing the activity of an aprE-driven gene expression system in Bacillus subtilis. 1109 26

Beta-Galactosidase production by Bifidobacterium longum CCRC 15708, Bifidobacterium longum B6 and Bifidobacterium infantis CCRC 14633 was first examined with B. longum CCRC 15708 showing the highest production of beta-galactosidase and the highest specific activity. Further study with B. longum CCRC 15708 revealed that the highest level of beta-galactosidase was produced with lactose and yeast extract as carbon and nitrogen sources, respectively. Optimal enzyme production occurred at an initial pH of 6.5 and at 37 degrees C. Under these optimum culture conditions, a maximumbeta-galactosidase activity of 18.6 U/ml could be obtained after 16 h of fermentation in a medium contain 4% lactose, 3.5% yeast extract, 0.3% K2HPO4, 0.1% KH2PO4, 0.05% MgSO4.7H2O and 0.03% L-cysteine. The highest transgalactosylation activity was also detected in this culture after 14-16 h of fermentation.
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PMID:Production of beta-galactosidase by Bifidobacteria as influenced by various culture conditions. 1598 5

A locally isolated thermophile, Geobacillus sp. SAB-40, producing thermostable extracellular amylase constitutively and an induced intracellular beta-galactosidase was characterized and identified based on 16S rRNA sequencing. A phylogenetic analysis then revealed its closeness to Geobacillus stearothermophilus. To evaluate the effect of the culture conditions on the coproduction of both enzymes by G. stearothermophilus SAB-40, a Plackett-Burman fractional factorial design was applied to determine the impact of twenty variables. Among the tested variables, CaCl2, the incubation time, MgSO4.7H2O, and tryptone were found to be the most significant for encouraging amylase production. Lactose was found to promote beta-galactosidase production, whereas starch had a significantly negative effect on lactase production. Based on a statistical analysis, a preoptimized medium attained the maximum production of amylase and beta-galactosidase at 23.29 U/ml/min and 12,958 U/mg biomass, respectively, which was 3- and 2-fold higher than the yield of amylase and lactase obtained with the basal medium, respectively.
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PMID:Coproduction of thermostable amylase and beta-galactosidase enzymes by Geobacillus stearothermophilus SAB-40: aplication of Plackett-Burman design to evaluate culture requirements affecting enzyme production. 1846 63