Accumulation of four quinolones by Serratia marcescens was measured fluorom
etrically. The passage of quinolones through the outer membrane was studied
in both lipopolysaccharide-deficient and porin-deficient mutants. The lipo
polysaccharide (LPS) layer formed a partially effective barrier for highly
hydrophobic quinolones such as nalidixic acid. Quinolones with a low relati
ve hydrophobicity coefficient seemed to pass preferentially through the wat
er-filled Omp3 porin channels. Results were confirmed when Omp3 was cloned
in a porin-defective Escherichia coli.