Sarinee ChaicharoenVisut BaimaiThatchai UmpraiSuriya Jansaengsri2024-09-032024-09-03199219922024Thesis (M.Sc. (Environmental Biology))--Mahidol University, 1992https://repository.li.mahidol.ac.th/handle/20.500.14594/100735Environmental Biology (Mahidol University 1992)Tissue culture technique applied for mass propagation of Melia spp. is possible. The modified LS basal medium used in this study is composed of macronutrients, micronutrients from LS medium, vitamins of B5 proposed by Gamborg, 6 g/l agar and 10% coconut water. The explants used in this experiment were young leaf, petiole, internode, terminal bud and axillary bud from young plant. The optimun concentration of BA for multiple shoot induction from axillary bud and terminal bud was 1 mg/l. Callus cultures can be readily initiated and proliferated from petiole and internode in the basal medium supplemented with 1 mg/l NAA plus 1 mg/l BA but no callus mass was observed from young leaf explant. The derived callus cultured on basal medium supplemented with 1 mg/l BA regenerated shoots which had a vigorous growth in basal medium with 0.25 regale BA. The individual shootlets regenerated vigorous roots within 7 - 10 days after immersion of the basal cut end into the solution of 1 mg/l IAA and 1 mg/l IBA for 1 day, then transferral to basal medium 85% of the treated shoots rooted. One month old plantlets were then transplanted into pots filled with sterilized vermiculite under high humidity conditions. The survival percentage was about 21%, most of the mortality being due to fungus infection.vi, 46 leaves : ill. (some col.)application/pdfengผลงานนี้เป็นลิขสิทธิ์ของมหาวิทยาลัยมหิดล ขอสงวนไว้สำหรับเพื่อการศึกษาเท่านั้น ต้องอ้างอิงแหล่งที่มา ห้ามดัดแปลงเนื้อหา และห้ามนำไปใช้เพื่อการค้าTissue cultureMaster ThesisMahidol University