Abstract

Callus was induced from leaves and petioles of in vitro cultred Fragaria moschata shoots. The highest callus formation rate was obtained on MS supplemented with NAA 1.0 mg·1-1 and BA 0.025 mg·1-1. These calli were transferred to eight MS media supplemented with different combinations of NAA and BA. After 18 months with periodic subcultures, callus growth was estimated by their area during a 8-week culture period. The highest growth rate was observed on medium supplemented with NAA 0.1 mg·1-1 and BA 0.25 1 mg·1-1 and the lowest on the one supplemented with NAA 0.5 mg·1-1 and BA 0.025 mg·1-1. Callus weight was measured to determine the fidelity of the callus area calculation method as a non-destructive way of estimation the grwoth rate. High correlation was observed between callus area and callus weight (r2=0.974 to 0.996). Afler 18 months in culture, calli were transferred to different regeneration-inducing media enriched with TDZ, BA, ZEA, IBA and NAA. After nearby four months on these media, the calli regenerated shoots which when transferred to a root-inducing medium, they formed normal roots.

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