The establishment of high-freguency plant regeneration System of Festuca arundiance
Xuan Huang
Abstract
Xuan Huang
Abstract
Aim To establish a high-freqency regeneration system of tall fescue in order to supply a better receptor system for transformation of relevant genes.Methods Use mature seeds of fescue arundinacea and MS medium were respectively as explants and basical medium to perfume embryonic callus induction,subculture,differentiation and rooting medium.Results After somatic embryos formationon MS medium with 2,4-D 5.0 mg/L,CH 400 mg/L,sucrose 60 g/L and agar 12 g/L,shoots were regenerated on MS medium containing 6-BA 2.0 mg/L+NAA 0.5 mg/L.The ratio of callus differentiation reached higher level of 78.9%.Regenerated shoots were rooted on half strength MS medium supplemented with 0.5 mg/L NAA,rate of rooting reaching 100%.Conclusion MS medium containing 2,4-D 9.0 mg/L was optimal for callus induction;MS medium containing 6-BA 2.0 mg/L+NAA 0.5 mg/L was optimal for differentiateon;Half strength MS medium supplemented with 0.5 mg/L NAA was optmal for rooting.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Aim To establish a high-freqency regeneration system of tall fescue in order to supply a better receptor system for transformation of relevant genes.Methods Use mature seeds of fescue arundinacea and MS medium were respectively as explants and basical medium to perfume embryonic callus induction,subculture,differentiation and rooting medium.Results After somatic embryos formationon MS medium with 2,4-D 5.0 mg/L,CH 400 mg/L,sucrose 60 g/L and agar 12 g/L,shoots were regenerated on MS medium containing 6-BA 2.0 mg/L+NAA 0.5 mg/L.The ratio of callus differentiation reached higher level of 78.9%.Regenerated shoots were rooted on half strength MS medium supplemented with 0.5 mg/L NAA,rate of rooting reaching 100%.Conclusion MS medium containing 2,4-D 9.0 mg/L was optimal for callus induction;MS medium containing 6-BA 2.0 mg/L+NAA 0.5 mg/L was optimal for differentiateon;Half strength MS medium supplemented with 0.5 mg/L NAA was optmal for rooting.
Key concepts: Callus, Subculture (biology), Sucrose, Murashige and Skoog medium, Shoot, Agar, Festuca arundinacea, Botany