Electroporation conditions were established for transient expression o
f introduced DNA in banana (Musa spp., cv.'Bluggoe') protoplasts isola
ted from regenerable embryogenic cell suspensions. The following param
eters were found to be highly influential: electroporation buffer, pol
yethylene glycol treatment and its duration before electroporation, us
e of a heat shock, and chimaeric gene constructs. The maximum frequenc
y of DNA introduction as detected by an in situ assay for transient ex
pression of the uidA gene, amounted to 1.8% of total protoplasts. Sinc
e plants have recently been regenerated from banana protoplasts at a h
igh frequency, the present results may contribute to the production of
transgenic banana.