Effect of applied and internal hormones on vitrification and apical necrosis of different plants cultured in vitro
β Scribed by Natalia V. Kataeva; Irena G. Alexandrova; Raisa G. Butenko; Elena V. Dragavtceva
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 482 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0167-6857
No coin nor oath required. For personal study only.
β¦ Synopsis
Development of vitrification and apical necrosis was followed in Camellia sinensis, Gerbera jamesonii, Malus domestica and hybrid Populus tremula Γ P. alba shoots cultured in vitro on Murashige & Skoog (MS) medium with different concentrations of growth regulators. High humidity in the culture vessels and excess of BA in the medium were found to be the major factors influencing vitrification. Lack of exogenous cytokinin in the medium during successive subcultures induced apical necrosis in poorrooting species (Malus domestica, Camellia sinensis). The level of internal phytohormones (ABA, IAA, IPA, 2iP, Z, ZR) was determined in the apple shoots by means of ELISA. The content of internal cytokinins in the vitrified apple shoots was several times greater than in normal ones, which supports the hypothesis that excess of cytokinins, inducing rapid divisions of cells in meristems in the atmosphere with high humidity, is responsible for vitrification. Apical necrosis of the plantlets that appeared after cultivation on cytokinin-free medium is the result of deficiency in endogenous hormones in apple shoots and this being confirmed by analysis of endogenous hormones in apple shoots.
π SIMILAR VOLUMES
## Abstract Tumor necrosis factorβΞ± (TNFβΞ±) is known as a pluripotent cell mediator, and it is implicated in the control of uterine cell growth, differentiation and function during estrous cycle and pregnancy. In this study, we investigated the effect of TNFβΞ± on endometrial stromal cells derived f
Storage of in vitro shoot cultures under reduced temperatures was investigated for eight Australian native woody plant species. Survival of multiple-shoot cultures for up to 12 months was best at 10 Β°C in the light. Darkness increased the extent of vitrification and lower temperatures reduced surviv