Several factors influencing reliability of the quantitative fluorimetr
ic beta-glucuronidase (GUS) assay in transgenic plant tissue have been
investigated. We obtained linear dependence of fluorescence on both t
he duration of hydrolysis and the extract concentration. The stability
of the enzyme in the homogenate was fairly high, the same as the stab
ility of the substrate solution and of the final reaction product. The
modification of the extraction/incubation buffer was proposed, result
ing in several times higher activity in comparison with original proce
dure.