scholarly journals Evidence of somatic embryogenesis from root tip explants of the rattan Calamus manan

1999 ◽  
Vol 35 (5) ◽  
pp. 424-427 ◽  
Author(s):  
D. K. S. Goh ◽  
N. Michaux-Ferrière ◽  
O. Monteuuis ◽  
M. -C. Bon
2006 ◽  
Vol 18 (1) ◽  
pp. 45-54 ◽  
Author(s):  
Hervé Etienne ◽  
E Dechamp ◽  
D Barry-Etienne ◽  
Bernóit Bertrand

In coffee, bioreactors are the most promising way for scaling-up micropropagation processes, particularly somatic embryogenesis. The availability of an efficient somatic embryogenesis process would allow the rapid mass production of heterozygous materials such as selected Coffea canephora clones and F1 Arabica hybrid varieties. For the last fifteen years, bioreactors (mechanically or pneumatically agitated bioreactors, temporary immersion bioreactors) have mostly been used on coffee to optimize the mass regeneration of somatic embryos from embryogenic tissues. This review presents the main results, obtained with several bioreactor models, concerning the different steps of the micropropagation process : i) the multiplication of embryogenic tissues, ii) the somatic embryo mass regeneration and iii) the production of pre-germinated embryos and plantlets in bioreactors. The literature shows that scaling-up can be successful, since very efficient embryo production has been achieved for both C. arabica and C. canephora. Moreover, it was proven that the pre-germinated coffee embryos - i.e. embryonic axis elongation (10-12 mm), root tip formation, cotyledon expansion and greening - obtained in temporary immersion bioreactors were photoautotrophic and able to regenerate vigorous plantlets after sowing under nursery conditions. The feasibility to apply the bioreactor technology in an industrial micropropagation procedure is also discussed in the particular socio-economic context of coffee growing.


1998 ◽  
Vol 1 (3) ◽  
pp. 216-222 ◽  
Author(s):  
Muhammad Shahidul Haque ◽  
Tomikichi Wada ◽  
Kazumi Hattori

2014 ◽  
Vol 12 (1) ◽  
pp. 1-6 ◽  
Author(s):  
MN Hassan ◽  
MS Haque ◽  
MM Hassan ◽  
MS Haque

Genetic improvement of garlic through conventional breeding is very difficult due to sterile nature of its flower. Hence, an alternative system is desirable to induce genetic variation. Tissue culture could be a good opportunities and somatic embryogenesis is one of the potential techniques of tissue culture for in vitro regeneration of garlic plant. The successes and production of somatic embryo depends on several factors such as optimization of media components, genotypes and explant type. Therefore, in the present investigation, garlic root tips were used as explant for callus and somatic embryo induction under different plant growth regulator combination. It was found that MS+1.0 mg l-1 2,4-D was the most favorable (86.10% regeneration with 2.19 cm callus diameter) for callus induction. This concentration also induced and produced good quality somatic embryo. In addition, MS+2.0 mg l-1 Kinetin gave better regeneration of somatic embryo and yielded the highest number (4.670) and longest length (7.0 cm) of shoots per callus. The procedure used a single hormonal signal for callus and somatic embryo induction as well as hormone free medium for further development of plantlet. Besides, maximum duration for callus induction and somatic embryo production was 17 and 10.67 days respectively. Thus, it appears that the protocol is cheap and time bound and particularly useful for conducting experiment for genetic improvement of garlic. Furthermore, as the protocol is cost effective, it can be further tested for commercial feasibility. DOI: http://dx.doi.org/10.3329/jbau.v12i1.20747 J. Bangladesh Agril. Univ. 12(1): 1-6, June 2014


HortScience ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 545F-546 ◽  
Author(s):  
Shailaja Sinha ◽  
Madhuri Sharon

Somatic embryogenesis from apical meristem, cell elongation zone, and cell differentiation zone of roots of Punica granatum L. var. Ganesh was obtained. The basal medium used was Gamborg's B5. 2, 4-D induced white globular callus in root tip explants, which on further subculture to medium containing 0.5 mg/L BAP, produced somatic embryos from the outer surface of the callus. Direct somatic embryogenesis occurred from all the three zones of the root in presence of 2 mg/L kinetin. BAP induced embryogenic callus in elongation and cell differentiation zone segments of the roots, which, on further subculture onto the same medium, produced somatic embryos. NAA caused rhizogenesis in all the three root segments. Differentiation of somatic embryos into plantlets took place on B5 medium supplemented with 0.01 mg/L NAA + 0.5 mg/l BAP + 2 mg/L kinetin.


Author(s):  
James Cronshaw ◽  
Jamison E. Gilder

Adenosine triphosphatase (ATPase) activity has been shown to be associated with numerous physiological processes in both plants and animal cells. Biochemical studies have shown that in higher plants ATPase activity is high in cell wall preparations and is associated with the plasma membrane, nuclei, mitochondria, chloroplasts and lysosomes. However, there have been only a few ATPase localization studies of higher plants at the electron microscope level. Poux (1967) demonstrated ATPase activity associated with most cellular organelles in the protoderm cells of Cucumis roots. Hall (1971) has demonstrated ATPase activity in root tip cells of Zea mays. There was high surface activity largely associated with the plasma membrane and plasmodesmata. ATPase activity was also demonstrated in mitochondria, dictyosomes, endoplasmic reticulum and plastids.


1995 ◽  
Vol 94 (4) ◽  
pp. 605-612 ◽  
Author(s):  
Marc Kreuger ◽  
Erik Postma ◽  
Yvon Brouwer ◽  
Gerrit-Jan van Holst

1970 ◽  
Vol 19 (1) ◽  
pp. 89-99
Author(s):  
K. Choudhary ◽  
M. Singh ◽  
M. S. Rathore ◽  
N. S. Shekhawat

This long term study demonstrates for the first time that it is possible to propagate embryogenic Vigna trilobata and to subsequently initiate the differentiation of embryos into complete plantlets. Initiation of callus was possible on 2,4-D. Somatic embryos differentiated on modified MS basal nutrient medium with 1.0 mg/l  of 2,4-D and 0.5 mg/l  of Kn. Sustained cell division resulted in globular and heart shape stages of somatic embryos. Transfer of embryos on to a fresh modified MS basal medium with 0.5 mg/l of Kn and 0.5 mg/l of GA3 helped them to attain maturation and germination. However, the propagation of cells, as well as the differentiation of embryos, were inhibited by a continuous application of these growth regulators. For this reason, a long period on medium lacking these growth regulators was necessary before the differentiation of embryos occurred again. The consequences for improving the propagation of embryogenic cultures in Vigna species are discussed. Key words: Pasture  legume, Vigna trilobata, Globular, Heart shape, somatic embryogenesis D.O.I. 10.3329/ptcb.v19i1.4990 Plant Tissue Cult. & Biotech. 19(1): 89-99, 2009 (June)


1996 ◽  
Author(s):  
Michael P. Amaranthus ◽  
Debbie Page-Dumroese ◽  
Al Harvey ◽  
Efren Cazares ◽  
Larry F. Bednar

1950 ◽  
Author(s):  
Gabriel Baldovinos de la Pena
Keyword(s):  

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