Sompop PrathanturarugRungthipwan PheakkoetThaya JenjittikulWongsatit ChuakulPromchit SaralampMahidol University2018-06-112018-06-112012-07-01Physiology and Molecular Biology of Plants. Vol.18, No.3 (2012), 281-286097158942-s2.0-84863447330https://repository.li.mahidol.ac.th/handle/20.500.14594/13433In vitro propagation of Stemona hutanguriana W. Chuakul, an endangered species of Stemonaceae, was established. Nodal and internodal explants were cultured on Murashige and Skoog (MS) medium supplemented with thidiazuron (TDZ) alone or in combination with 1-naphthaleneacetic acid (NAA). When cultured on MS medium supplemented with 18. 16 μM TDZ with 0. 54 μM NAA for 8 weeks and then on MS medium without plant growth regulator (PGR) for 8 weeks, nodal explants demonstrated a responding frequency of 91. 67 % and a shoot regeneration rate of 5. 46 shoots/responding explant. Furthermore, internodal explants demonstrated a responding frequency of 17. 17 % with 11. 17 shoots/responding explant. The regenerated shoots were rooted using a two-step protocol by culturing for 4 weeks on MS medium supplemented with various concentrations of NAA and Indole-3-butyric acid (IBA) and 8 weeks on MS medium without PGR. When 5. 40 μM NAA was used as a PGR, the maximum root induction rate was 69. 45 %. Regenerated plantlets were successfully transferred to soil. © 2012 Prof. H.S. Srivastava Foundation for Science and Society.Mahidol UniversityAgricultural and Biological SciencesBiochemistry, Genetics and Molecular BiologyArticleSCOPUS10.1007/s12298-012-0116-8