The 30-kDa sporulation-specific peptidoglycan hydrolase CwlC of Bacillus subtilis 168 was purified and characterized. It is an N-acetylmuramoyl-L-alanine amidase (amidase) that is associated with the mother cell wall of sporulating cells, and although it is secreted, it undergoes no N-terminal processing except removal of the initial methionine. It was found that mother cells of a strain insertionally inactivated in cwlC and lytC (the major vegetative amidase gene) did not lyse at the end of sporulation. Mutants with single mutations in cwlC or lytC lysed, and so the two autolysins must have mutually compensatory roles in mother cell lysis. Active CwlC and LytC are present at the time of mother cell lysis; however, reporter gene analysis revealed that lytC transcription ceases early in sporulation, and therefore the function that LytC has in mother cell lysis is performed by material remaining from presporulation expression. Autolytic enzymes similar in molecular mass to CwlC were detected in two other Bacillus species by their cross-reactivity with anti-CwlC antiserum.Autolysins, enzymes that hydrolyze bacterial cell wall peptidoglycan, are ubiquitous among bacteria (11), although their precise roles remain uncertain. In the spore-forming grampositive bacterium Bacillus subtilis, there may be 10 or more peptidoglycan hydrolases (8, 10). Such enzymes have been implicated in several functions during vegetative growth and sporulation (34,41).The differentiation process of sporulation involves a number of events of cell wall rearrangement, in which peptidoglycandegradative enzymes evidently play a fulcral role (10). These include digestion of the asymmetric septum to permit prespore engulfment (5), cortex maturation (1, 42), mother cell lysis, and cortex autolysis during germination (5). Mother cell lysis to release the mature endospore is the final characteristic morphological event that occurs during sporulation. A 30-kDa mother cell-associated autolysin appears during sporulation and has been postulated to be responsible for mother cell lysis (8). A gene, cwlC, which appears to encode this protein has been cloned and sequenced; the deduced gene product is a 255-amino-acid, 27-kDa peptide. Its expression is controlled by K (18), the mother cell-specific, late-sporulation sigma factor (6, 27). However, its role in sporulation was unknown, as the mother cells of a cwlC mutant still lyse (18).LytC is the major vegetative cell amidase of B. subtilis 168 and is also present during sporulation (8). The lytC gene is part of a three-gene operon, lytABC (25). lytR, which is transcribed divergently from lytABC, encodes a putative DNA-binding protein, which represses expression of itself and lytABC (25). lytA encodes an acidic protein that is thought to be membrane associated (20,25). lytB encodes a cell wall-associated modifier protein, which binds to the LytC amidase and enhances its activity (14). A study with a plasmid clone carrying a lytA::lacZ translational fusion suggested that, during vegetative growth, expression ...