condition for callus induction in true leaves was 1. 5 mg/L 2,4-D+0. 1 mg/L KT+MS+0. 8% agar+3% sucrose,with the induction rate of 78% and the browning rate of 8%. The best condition for callus induction in cotyledonspetiole
and stem was 1. 5 mg/L 2,4-D+1. 0 mg/L KT+MS+0. 8% agar+3% sucrose,with the stem showing
the highest callus rate at 96% and no browning, petioles with a callus rate of 92% and a browning rate of 2%,
and cotyledons with a callus rate of 60% and a browning rate of 4%. The condition of 0. 3 mg/LNAA+mg/LKT+
MS+0. 8% agar+3% sucrose was the most suitable for inducing embryogenic callus from cotyledons and petioles.
For true leaves,the best condition was0. 3 mg/L NAA+1. 0 mg/L 6-BA+MS+0. 8% agar+3% sucrose, while
for stem,it was 0. 3 mg/L NAA+0. 5 mg/L KT+MS+0. 8% agar+3% sucrose.【Conclusion】 All four types of
explants were capable of producing callus,which could then be induced todifferentiate into somatic embryos. Among
the four explants,stems had the highest callus induction rate and the lowest Browning rate,making them the most
suitable explants for regeneration.