Access the full text.
Sign up today, get DeepDyve free for 14 days.
Jen-Tsung Chen, Chung-I Chang, Wei-Chin Chang (1999)
Direct somatic embryogenesis on leaf explants of Oncidium Gower Ramsey and subsequent plant regenerationPlant Cell Reports, 19
J. Dodds, L. Roberts (1982)
Experiments in plant tissue culture
T. Murashige, F. Skoog (1962)
A revised medium for the growth and bioassay with tobacco tissue culture
J. Chen, Wei-Chin Chang (2000)
Efficient plant regeneration through somatic embryogenesis from callus cultures of Oncidium (Orchidaceae).Plant science : an international journal of experimental plant biology, 160 1
T Murashige, F Skoog (1962)
A revised medium for rapid growth and bioassays with tobacco tissue culturesPhysiol. Plant, 15
J. Zimmerman (1993)
Somatic Embryogenesis: A Model for Early Development in Higher Plants.The Plant cell, 5
M. Pedroso, M. Pais (1995)
Factors controlling somatic embryogenesisPlant Cell, Tissue and Organ Culture, 43
C. Chang, Wei-Chin Chang (1998)
Plant regeneration from callus culture of Cymbidium ensifolium var. misericorsPlant Cell Reports, 17
D. Duncan (1955)
MULTIPLE RANGE AND MULTIPLE F TESTSBiometrics, 11
J. Arditti, R. Ernst (1993)
Micropropagation of Orchids
J. Chen, Wei-Chin Chang (2001)
Effects of auxins and cytokinins on direct somatic embryogenesison leaf explants of Oncidium 'Gower Ramsey’Plant Growth Regulation, 34
J. Chen, Wei-Chin Chang (2000)
Plant regeneration via embryo and shoot bud formation from flower-stalk explants of Oncidium Sweet SugarPlant Cell, Tissue and Organ Culture, 62
Y. Ishii, T. Takamura, M. Goi, Michio Tanaka (1998)
Callus induction and somatic embryogenesis of PhalaenopsisPlant Cell Reports, 17
The effects of tissue culture conditions and explant characteristics on direct somatic embryogenesis were studied on Oncidium `Gower Ramsey'. Embryo formation was significantly affected by explant position. Leaf tip segments had a significantly higher embryogenic response than other segments of leaves. Adaxial-side-up orientation significantly promoted embryogenesis in comparison with abaxial-side-up orientation. There was no significant effect of sucrose in a range of concentrations (10–60 g l−1). Modified 1/2-MS medium (containing 85 mg l−1 KH2PO4) supplemented with 170 mg l−1 NaH2PO4 significantly promoted direct somatic embryogenesis. Peptone at 0.5 mg l−1 gave significantly higher emrbyogenic response (80%) on leaf tips than control treatment (50%). The best response on direct embryo formation was obtained on the modified 1/2-MS medium supplemented with 10–20 g l−1 sucrose, 170 mg l−1 NaH2PO4 and 0.5 g l−1 peptone.
Plant Cell, Tissue and Organ Culture – Springer Journals
Published: Oct 13, 2004
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.