A simple method for large-scale isolation and regeneration of Arabidop
sis thaliana green protoplasts utilizing a novel starting material is
presented. This technique takes advantage of shooty/embryogenic masses
regenerating from fresh or cultured roots. There is no time-consuming
mechanical isolation of starting material. Economical Bacto agar is u
sed as an embedding agent. Plating efficiencies are between 5% and 10%
. Seventy-six percent of protoplast-derived colonies produce shoots.