Callus protoplasts of sour cherry clone CAB4D entered sustained division in Murashige and Skoog's (1962) medium with 1-naphthaleneacetic acid, 6-beneylaminopurine and zeatin. Further to callusing, organogenesis was induced from the protoplastderived callus, in a basal regeneration medium with these
Micropropagation of sour cherry (Prunus cerasusL.) cv.
✍ Scribed by Radosav Cerović; Djurdina Ružić
- Book ID
- 104620950
- Publisher
- Springer
- Year
- 1987
- Tongue
- English
- Weight
- 302 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0167-6857
No coin nor oath required. For personal study only.
✦ Synopsis
Sour cherry cv. ~umadinka (Prunus cerasus L.) is the leading Yugoslav cultivar for production orchards. A method of micropropagation has been developed for the purpose of growing '~umadinka' on its own roots and for rapid multiplication.
Aseptic cultures were initiated from shoot explants 1-2 mm long on Murashige & Skoog medium with (in mg 1 -~) 6-benzylaminopurine (BAP): 1, indole -3-yl butyric acid (IBA): 1 and gibberellic acid (GA3): 0-1.
The best medium for proliferation was MS with (in mg 1-~ ): BAP 0.5, IBA 0.1, GA 3 0.1, but media with (in mgl-1): BAP 0.5, NAA 0.1, GA3 0.1 and BAP 1, NAA 0.1 and GA3 0.1 were also shown to be good. A higher degree of proliferation obtained with some media did not necessarily result in a better quality of plantlets produced.
For rooting the best combination of culture medium was achieved with pretreatment 10 days in MS I/2 with 1 mgl -t IBA, followed by transfer to a hormone-free medium after 5-10 days, resulting in 88% success.
The rooted plants were planted in containers and acclimatized under mist, with over 90% of plants surviving transplantation.
📜 SIMILAR VOLUMES
Diurnal and seasonal net photosynthetic rates (Pn) of sour cherry were determined. Leaf Pn was not significantly affected by shoot excision. Under constant environmental conditions (PFD, 1200/zmol m-2 s-~ ; temp. 25; relative humidity, 80-90%) there was no significant diurnal fluctuation in Pn for i