Shuttle vectors with new or improved features were constructed to enable fa
cile genetic manipulations in the plant pathogen Ustilago maydis. Sets of p
lasmids selectable in media containing geneticin, carboxin, nourseothricin,
or hygromycin, able to replicate autonomously, to transform U. maydis by i
ntegration, and to express foreign genes under control of the homologous gl
yceraldehyde-3-phosphate dehydrogenase promoter, were built upon a common p
UC19 vector backbone. This permits a large number of choices for a cloning
site, blue/white screening for recombinant plasmids, rapid transfer of a cl
oned DNA fragment between plasmids, and choice of several dominant drug-res
istance markers for selection in U. maydis.