Escherichia coli possesses multiple systems for uptake and utilization of the \beta-glucoside sugars salicin, arbutin and cellobiose. However, these genes are not expressed in the wild-type organism. Activating mutations at three different loci, the bgl operon, the cel operon, and the asc system, enable E. coli to utilize these sugars (see Mukerji and Mahadevan 1997 for a review). Of the three, the bgl operon, involved in uptake and degradation of the aromatic \beta-glucosides arbutin and salicin, is best characterized (Prasad and Schaefler 1974; Reynolds et al. 1981; Mahadevan et al. 1987; Schnetz and Rak 1987)
Escherichia coli normally cannot utilize the beta-glucoside sugar cellobiose as a carbon and energy ...
The genomes of bacterial species are very dynamic. For example in Escherichia coli, individual isola...
The phytopathogenic bacterium Erwinia chrysanthemi, unlike other members of the family Enterobac-ter...
Escherichia coli possesses multiple systems for uptake and utilization of the \beta-glucoside sugars...
The ability to metabolize aromatic beta-glucosides such as salicin and arbutin varies among members ...
The bglA gene of Escherichia coli encodes phospho-beta-glucosidase A capable of hydrolyzing the plan...
The bglA gene of Escherichia coli encodes phospho--glucosidase A capable of hydrolyzing the plant-de...
The ability to metabolize aromatic β-glucosides such as salicin and arbutin varies among members of ...
Utilization of β-glucosides is markedly variable in the members of the family Enterobacteriaceae. Th...
The cryptic bgl operon in E. coli can be activated via mutation under starvation conditions to enabl...
The chb operon of Escherichia coli is involved in the utilization of chitooligosaccharides. While ac...
Utilization of the aryl-beta-glucosides salicin or arbutin in most wild-type strains of E. coli is a...
The genes for utilization of cellobiose are normally cryptic in both laboratory strains and natural ...
The aromatic beta-glucosides of plant origin, salicin and arbutin, serve as carbon sources for the s...
Evolution of aromatic beta-glucoside utilization by 1 successive mutational steps in Escherichia col...
Escherichia coli normally cannot utilize the beta-glucoside sugar cellobiose as a carbon and energy ...
The genomes of bacterial species are very dynamic. For example in Escherichia coli, individual isola...
The phytopathogenic bacterium Erwinia chrysanthemi, unlike other members of the family Enterobac-ter...
Escherichia coli possesses multiple systems for uptake and utilization of the \beta-glucoside sugars...
The ability to metabolize aromatic beta-glucosides such as salicin and arbutin varies among members ...
The bglA gene of Escherichia coli encodes phospho-beta-glucosidase A capable of hydrolyzing the plan...
The bglA gene of Escherichia coli encodes phospho--glucosidase A capable of hydrolyzing the plant-de...
The ability to metabolize aromatic β-glucosides such as salicin and arbutin varies among members of ...
Utilization of β-glucosides is markedly variable in the members of the family Enterobacteriaceae. Th...
The cryptic bgl operon in E. coli can be activated via mutation under starvation conditions to enabl...
The chb operon of Escherichia coli is involved in the utilization of chitooligosaccharides. While ac...
Utilization of the aryl-beta-glucosides salicin or arbutin in most wild-type strains of E. coli is a...
The genes for utilization of cellobiose are normally cryptic in both laboratory strains and natural ...
The aromatic beta-glucosides of plant origin, salicin and arbutin, serve as carbon sources for the s...
Evolution of aromatic beta-glucoside utilization by 1 successive mutational steps in Escherichia col...
Escherichia coli normally cannot utilize the beta-glucoside sugar cellobiose as a carbon and energy ...
The genomes of bacterial species are very dynamic. For example in Escherichia coli, individual isola...
The phytopathogenic bacterium Erwinia chrysanthemi, unlike other members of the family Enterobac-ter...