~The in uivo functioning of the alanine/D-alanyl-D-alanine pathway of Escherichia cofi was investigated by determining precursor pool levels and specific enzyme activities under various growth conditions. Cells grown on D-or L-alanine showed several remarkable features compared with cells grown on other carbon sources: 10-fold higher values of the D-alanyl-D-alanine and the UDP-MurNAc-pentapeptide pools, a 240-fold increase of the alanine racemase activity, and the absence of bacteriolysis after treatment with D-cycloserine at high concentrations (50 pg m1-l). In cells grown on glucose, D-cycloserine (1 pg ml-l) led to depletion of the D-alanyl-D-alanine pool and to lysis, which was efficiently antagonized by chloramphenicol. A threefold increase of the dipeptide pool was observed when cells were treated with chloramphenicol alone. The alanine racemase activity was lowest in glucose-grown cells and the D-alanine : D-alanine ligase and D-alanyl-D-alanhe-adding activities were the same whatever the carbon source. Molecular masses of 53-56 kDa and 5 6 4 8 kDa were estimated for the partially purified inducible alanine racemase and D-alanine: D-alanine ligase respectively.