Establishment of a Tissue Culture and Rapid Propagation System for Erythropalum scandens Based on Orthogonal Test
To solve the problem of breeding excellent seedlings of Erythropalum scandens,research has been con-ducted on the establishment and optimization of tissue culture and rapid propagation systems of E.scandens by taking apical bud-induced aseptic seedlings as the material.Explant sterilization,callus induction,callus differentiation,test-tube rooting and transplanting and domestication were studied.The results are as follows:the best ratio of sterilization was 60 seconds of 75%alcohol+10 minutes of 0.1%HgCl2,and the success rate was 48.89%.The best formula for callus induc-tion by aseptic seedling leaf was MS+0.5 mg·L-1 6-BA+1.0 mg·L-1 2,4-D+1.0 mg·L-1 IBA,for 30 days,and the induction rate was 71.11%,with compact green and strong differentiation potential.The best formula for callus induction by aseptic seedling shoot was MS+1.0 mg·L-1 6-BA+0.5 mg·L-1 2,4-D+1.0 mg·L-1 IBA,for 30 days,and the induction rate was 70.00%;The most suitable medium for induction of callus propagation and differentiation was MS+2.0 mg·L-16-BA+0.5 mg·L-1 TDZ+1.0 mg·L-1 IBA,bud differentiation rate was 98.89%,and coefficient of propagation was 3.33.The most suitable medium for rootage was MS+1.5 mg·L-1 6-BA+0.5 mg·L-1 IBA,achieving a 100%rootage rate with 2.2 of the average number.Plantlets were transplanted to small particle peat soil,and 88.89%of rooted plants survived.The re-search has established the tissue culture and rapid propagation system of E.scandens,which can be applied in produc-tion and serve as a foundation for providing seedlings and factory production.
Erythropalum scandenstissue culture and rapid propagationaseptic seedlingcallusinduction and proli-feration