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A. Ahmad, H. Zhong, W. Wang, M. Sticklen (2002)
Shoot apical meristem: In vitro regeneration and morphogenesis in wheat (Triticum aestivum L.)In Vitro Cellular & Developmental Biology - Plant, 38
A. Bennici, P. Cionini, F. D'amato (1976)
Callus formation from the suspensor ofPhaseolus coccineus in hormone-free medium: a cytological and DNA cytophotometric studyProtoplasma, 89
A. Repellin, M. Båga, P. Jauhar, R. Chibbar (2001)
Genetic enrichment of cereal crops via alien gene transfer: New challengesPlant Cell, Tissue and Organ Culture, 64
E. George, M. Hall, G. Klerk (2008)
Micropropagation: Uses and Methods
V. Jiménez, F. Bangerth (2001)
In vitro culture and endogenous hormone levels in immatur zygotic embryos, endosperm and callus cultures of normal and high-lysine Barley genotypes.Journal of applied botany, 75
P. Davies (1995)
The Plant Hormone Concept:Concentration, Sensitivity and Transport
T. Fujimura, A. Komamine (1980)
Mode of action of 2,4-D and zeatin on somatic embryogenesis in a carrot cell suspension cultureZeitschrift für Pflanzenphysiologie, 99
D. Nhựt, B. Lệ, K. Van (2000)
Somatic embryogenesis and direct shoot regeneration of rice (Oryza sativa L.) using thin cell layer culture of apical meristematic tissueJournal of Plant Physiology, 157
F. Eudes, S. Acharya, A. Laroche, L. Selinger, K. Cheng (2003)
A novel method to induce direct somatic embryogenesis, secondary embryogenesis and regeneration of fertile green cereal plantsPlant Cell, Tissue and Organ Culture, 73
A. Trewavas (1981)
How do plant growth substances work? IIPlant Cell and Environment, 14
S. Ganeshan, Sanjay Chodaparambil, M. Båga, D. Fowler, P. Hucl, B. Rossnagel, R. Chibbar (2006)
In vitro regeneration of cereals based on multiple shoot induction from mature embryos in response to thidiazuronPlant Cell, Tissue and Organ Culture, 85
S. Malik, M. Zia, Riaz-ur-Rehman, M. Chaudhary (2007)
In vitro plant regeneration from direct and indirect organogenesis of Memordica charantia.Pakistan journal of biological sciences : PJBS, 10 22
C. Gless, H. Lörz, A. Jähne-Gärtner (1998)
Establishment of a highly efficient regeneration system from leaf base segments of oat (Avena sativa L.)Plant Cell Reports, 17
M. Centeno, A. Rodríguez, I. Feito, B. Fernández (1996)
Relationship between endogenous auxin and cytokinin levels and morphogenic responses inActinidia deliciosa tissue culturesPlant Cell Reports, 16
P. Davies (1995)
Plant hormones : physiology, biochemistry and molecular biology
V. Sharma, R. Hänsch, R. Mendel, J. Schulze (2004)
A highly efficient plant regeneration system through multiple shoot differentiation from commercial cultivars of barley (Hordeum vulgare L.) using meristematic shoot segments excised from germinated mature embryosPlant Cell Reports, 23
Short-term high efficiency protocol for direct shoot regeneration (DSR) and induce of multiple shoot regeneration (MSR) for in vitro plant genetic transformation or propagation was developed for wheat. This tissue culture and regeneration system with no callus formation, takes about 2 months to finish, shorter than any of the available systems requiring 3–4 months. Cutted shoot embryonic meristem (CSEM), shoot embryonic meristem with the scutellum (SEMS), shoot embryonic meristem (SEM) and scutellum (S), were excised from immature embryos and cultured in DSR medium. Rapid inductions of direct shoot buds and multiple shoot regeneration (MSR) in some of explants roots were got. Then, plants were transferred to the soil and showed normal growth and fertility in comparison with the seed-grown plants. The effects of different explants, light conditions and various combinations of plant growth regulators on direct shoot regeneration of wheat were investigated. The best response for multiple shoot regeneration from (SEMS) explants was observed on modified MS medium containing 2 mgl-1 2, 4-D and 10 mgl-1 BAP. Also 4-week period of exposure to darkness followed by light exposure was important for shoot regeneration. The average number of multiplied shoots per explants and explants with multiple shoots per culture dish was 8.38 and 5.46 among the cultivars after 8-9 weeks, respectively.
Journal of Agricultural Engineering and Biotechnology – Bowen Publishing Company Ltd.
Published: Nov 21, 2013
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