Saprolegnia monoica was stably transformed to hygromycin resistance us
ing the plasmids pTH210 and pHAM34H containing a bacterial phosphotran
sferase gene fused to regulatory sequences from genes of another Oomyc
ete. Vectors pBT6, pCM54, used to transform higher fungi, yielded no s
table transformants. DNA hybridizations indicated that transformation
resulted from a single-copy integration of the transforming vector. De
velopment of non-resistant subcultures from transformed colonies revea
led that the transgene could become silent and was not uniformly expre
ssed in the transformants.