The applicability of beta-glucuronidase and chloramphenicol acetyltran
sferase reporter genes to a carnation (Dianthus caryophyllus L.) trans
formation procedure was analyzed. Transgenic tobacco (Nicotiana tabacu
m L.) plants expressing the respective reporter genes were prepared an
d used as the enzyme source. Carnation leaf extract strongly inhibited
enzymatic activity of beta-glucuronidase, but not that of chloramphen
icol acetyltransferase. One or more carnation phenolic compounds, acti
ng in a noncompetitive manner, is suggested as the cause of the observ
ed inhibition of fluorometrically assayed beta-glucuronidase activity.
This inhibition was eliminated by treating the carnation leaf extract
with polyvinylpolypyrrolidone.