The dogma that ampC genes are located exclusively on the chromosome was dom
inant until about 10 years ago. Since 1989 over 15 different plasmid-encode
d AmpC beta-lactamases have been reported from several countries. Most of t
hese enzymes evolved in two clusters. The major cluster includes several en
zymes with a high similarity to CMY-2 which is the closest related chromoso
mal AmpC enzyme of Citrobacter Freundii: A second cluster centers around CM
Y-1. It is less homogeneous and not closely related chromosomal AmpC enzyme
s. Molecular diversification by amino acid substitutions does not usually t
ranslate into a change in the resistance phenotype. At this time, CMY-2 app
ears to be the most prevalent and widely distributed. Further global increa
se of prevalence and diversity of plasmidic AmpC beta-lactamases have to be
anticipated in the next millenium.