Regeneration of Beauveria bassiana GK2016 protoplasts demonstrated three phases: (1) enlargement, (2) formation of a chain of budding cells, and (3) development of a true germ tube from the original protoplast. Regeneration frequencies of up to 80°7o were obtained when using the stabilizer a m m o n i u m sulphate. Using electroporation, protoplasts were transformed tO methyl 1,2-benzimidazole carbamate (MBC) resistance with the Neurospora crassa MBC-resistant fl-tubulin gene. A transformation efficiency of one to three transformants per 5 ~tg vector D N A was obtained. The MBC phenotype was stable and transformants grew in the presence of 5 Ixg MBC/ml. Southern D N A -D N A by: bridization analysis demonstrated that integration of the vector into the chromosomal D N A had occurred.