Regulation of gene expression: Cryptic β-glucoside (bgl) operon of Escherichia coli as a paradigm

Bacteria have evolved various mechanisms to extract utilizable substrates from available resources and consequently acquire fitness advantage over competitors. One of the strategies is the exploitation of cryptic cellular functions encoded by genetic systems that are silent under laboratory conditions, such as the bgl (β-glucoside) operon of E. coli. The bgl operon of Escherichia coli, involved in the uptake and utilization of aromatic β-glucosides salicin and arbutin, is maintained in a silent state in the wild type organism by the presence of structural elements in the regulatory region. This operon can be activated by mutations that disrupt these negative elements. The fact that the silent bgl operon is retained without accumulating deleterious mutations seems paradoxical from an evolutionary view point. Although this operon appears to be silent, specific physiological conditions might be able to regulate its expression and/or the operon might be carrying out function(s) apart from the utilization of aromatic β-glucosides. This is consistent with the observations that the activated operon confers a Growth Advantage in Stationary Phase (GASP) phenotype to Bgl+ cells and exerts its regulation on at least twelve downstream target genes.

Degradation of toluene and benzene by Trametes versicolor.

In this study, biological degradation of non-polar monoaromatic compounds, benzene and toluene, by one of the white rot fungi, namely Trametes versicolor was analyzed and the biomass formed was determined. The studies were carried out in mediums which contain basic nutrients in certain amounts, toluene and benzene at concentrations of 50, 100, 200, 250 and 350 mg/l, pH at 5, temperature at 28 degrees C and rpm at 150. Within an incubation period of 48 hours, it was observed that, removal was completed in 4 hours when toluene concentration was 50 mg/l and was completed in 36 hours when concentration was 300 mg/l. Biodegradation was completed at the end of 4th hour at benzene concentration of 50 mg/l while it continued for 42 hours at the concentration of 300 mg/l. With the addition of veratryl alcohol (3,4-Dimethoxybenzyl alcohol) to the basic feed medium, the operation of the enzyme system gained speed and biodegradation completed in a shorter time period.