Study on Tissue Culture Techniques for Stem Segment of Millettia speciosa Champ.
Bilan Huang
Abstract
Bilan Huang
Abstract
[Objective] The study was to provide the basis for the scale production of Millettia speciosa Champ.and protect its wild resource.[Method] With tender stem segments of M.speciosa as explants,the techniques of its tissue culture and rapid propagation in vitro were studied.[Result] The explants were treated by 0.1% HgCl2 for 20 min and the asepsis material could be obtained.With MS+6-BA 1.0 mg/L+ IBA 0.1 mg/L as the initial medium,the induction rate could reach 100%.After inoculation for 20 d,the axillary buds begun to germinate and normally grow.With MS+6-BA 2.0 mg/L+ IBA 0.1 mg/L as the multiplication medium,after culture for 30 d,the multiplication coefficient reached 7.0,and there were a few callus emerged,but the growth and development of adventitious buds were normal.When the medium of 1/2 MS+ IBA 0.5 mg/L+ IAA 0.5 mg/L was used for rooting culture,the rooting effect was the best and the rooting rate reached 80%,and the growth of root was good.When the rooted small seeding were transplanted into the matrix of coconut bran and sand(3∶1),and the plastic film was covered on it for keeping moisture for 15 d,the survival rate reached more than 85%.[Conclusion] The optimum rooting medium for stem segments culture of M.speciosa was 1/2 MS+ IBA 0.5 mg/L+ IAA 0.5 mg/L.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
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.
[Objective] The study was to provide the basis for the scale production of Millettia speciosa Champ.and protect its wild resource.[Method] With tender stem segments of M.speciosa as explants,the techniques of its tissue culture and rapid propagation in vitro were studied.[Result] The explants were treated by 0.1% HgCl2 for 20 min and the asepsis material could be obtained.With MS+6-BA 1.0 mg/L+ IBA 0.1 mg/L as the initial medium,the induction rate could reach 100%.After inoculation for 20 d,the axillary buds begun to germinate and normally grow.With MS+6-BA 2.0 mg/L+ IBA 0.1 mg/L as the multiplication medium,after culture for 30 d,the multiplication coefficient reached 7.0,and there were a few callus emerged,but the growth and development of adventitious buds were normal.When the medium of 1/2 MS+ IBA 0.5 mg/L+ IAA 0.5 mg/L was used for rooting culture,the rooting effect was the best and the rooting rate reached 80%,and the growth of root was good.When the rooted small seeding were transplanted into the matrix of coconut bran and sand(3∶1),and the plastic film was covered on it for keeping moisture for 15 d,the survival rate reached more than 85%.[Conclusion] The optimum rooting medium for stem segments culture of M.speciosa was 1/2 MS+ IBA 0.5 mg/L+ IAA 0.5 mg/L.
Key concepts: Explant culture, Tissue culture, Inoculation, Axillary bud, Horticulture, Biology, Botany, Murashige and Skoog medium