“…A CFTR defect leads to, among other problems, the accumulation of abnormal viscous fluids in the lungs of CF patients, which renders the patients susceptible to various bacterial infections. Pseudomonas aeruginosa in its mucoid form is a major source of infection in the CF lung (7,22,24). The mucoid morphology of the bacteria is due to the overproduction of a viscous exopolysaccharide, alginate, which is a high-molecular-weight, linear copolymer of two uronic acids, D-mannuronate and its C-5 epimer, L-guluronate (10).…”