A global approach was used to analyze protein synthesis and stability durin
g the cell cycle of the bacterium Caulobacter crescentus. Approximately one
-fourth (979) of the estimated C. crescentus gene products were detected by
two-dimensional gel electrophoresis, 144 of which showed differential cell
cycle expression patterns. Eighty-one of these proteins were identified by
mass spectrometry and were assigned to a wide variety of functional groups
. Pattern analysis revealed that coexpression groups were functionally clus
tered. A total of 48 proteins were rapidly degraded in the course of one ce
ll cycle. More than half of these unstable proteins were also found to be s
ynthesized in a cell cycle-dependent manner, establishing a strong correlat
ion between rapid protein turnover and the periodicity of the bacterial cel
l cycle. This is, to our knowledge, the first evidence for a global role of
proteolysis in bacterial cell cycle control.