Cell division properties of temperature-sensitive mutants of Escherichia coli K-12, isolated for ampicillin resistance, altered cell-wall synthesis, and/or cross-linking of peptidoglycan chains were examined. When the incubation temperature of exponentially growing cultures of these mutants was shifted from 32° to 42°, cell division was inhibited and morphological changes were observed. This suggested that inhibition of cell division at 42° was due to a conformational change in temperature-sensitive protein(s). A return to the incubation temperature of 32°, after a short period of growth at 42°, resulted in recovery of cell division. Several of these mutants show recovery in the presence of chloramphenicol indicating that restoration of the normal phenotype occurs by the conformational change of affected protein(s). One mutant which grows into spherical cells at 42° and contains hypercross-linked peptidoglycan chains, will snot regain rod-shaped cell morphology or normal cell division in the presence of nalidixic acid, an inhibitor of DNA synthesis. In this mutant maintenance of cell shape and cell division depends on chromosome replication. These data demonstrate a direct connection between proper biosynthesis and cross-linking of peptidoglycan and cell-shape maintenance and division in E. coll.The peptidoglycan (PG) of Escherichia coli consists of repeating units of N-acetylglucosaminyl-N-acetylmuramyl-tetrapeptide (L-alanyl-D-glutamyl-mesodiaminopimelic acid-D-alanine). This heteropolymer forms a network by forming crosslinks (XL) between the carboxy terminal of the D-alanine and the D-amino terminal of the meso-diaminopimelic acid (1). The extent of this cross-linking in E. coli is 50 % (2). Several functions relating to bacterial cell growth, binding of the chromosomal and plasmid DNA, and decoding of cell surface-related regulatory signals (3) are attributed to this unique heteropolymeric structure.