We describe the molecular transformation of Liquidambar styraciflua us
ing Agrobacterium tumefaciens. A binary TI-plasmid vector containing a
chimeric neomycin phosphotransferase gene which confers resistance to
kanamycin and either a chimeric Bacillus thuringiensis toxin gene, a
chimeric E. coli beta-glucuronidase (GUS), or a chimeric tobacco anion
ic peroxidase gene was introduced into sweetgum by co-cultivation with
Agrobacterium tumefaciens. Sweetgum shoots regenerated in the presenc
e of kanamycin were confirmed to be transformed by genomic DNA blots o
r the presence of GUS activity. The optimization of the transformation
protocol and the incorporation of molecular transformation into a rap
id germplasm improvement protocol are discussed.