Conditions d'apparition d'une embryogénèse somatique sur des cals issus de la culture de tissus foliaires du chêne vert (Quercus ilex)

1989 ◽  
Vol 67 (4) ◽  
pp. 1066-1070 ◽  
Author(s):  
C. Féraud-Keller ◽  
H. Espagnac
Keyword(s):  
Acetic Acid ◽  
Somatic Embryos ◽  
Quercus Ilex ◽  
Foliar Tissue ◽  
Murashige And Skoog's Medium ◽  
Old Trees ◽  
Murashige And Skoog’S Medium

The proliferation of parenchymatous foliar tissue of Quercus ilex was obtained from current year leaves taken from old trees and cultivated in vitro on modified Murashige and Skoog's medium supplemented with benzylaminopurine (4 mg ∙ L−1) and naphthyl acetic acid (0.5 mg ∙ L−1). Only the fragments cultured in October reacted. The neoformations only appeared on calluses that had not been subcultured for 7 months. Primary nodules arising on these calluses were removed and subcultured on the same medium either in the dark or in the light. In the dark only, they produced secondary nodules, which were the source of somatic embryos both in light and dark. Presently, they seem to regulate their structure in the dark but they do not develop in a way that leads to germination.

Plantlet formation from Lycopersicon esculentum leaf callus

1974 ◽  
Vol 52 (6) ◽  
pp. 1429-1432 ◽  
Author(s):  
Vasantha Padmanabhan ◽  
E. F. Paddock ◽  
W. R. Sharp
Keyword(s):  
Acetic Acid ◽  
Lycopersicon Esculentum ◽  
Shoot Formation ◽  
Growth Hormones ◽  
Root Initiation ◽  
Plantlet Formation ◽  
Callus Proliferation ◽  
Murashige And Skoog's Medium ◽  
Murashige And Skoog’S Medium ◽  
Indole 3 Acetic Acid

Explants were obtained from leaves of three strains of tomato and grown on a modified Murashige and Skoog's medium with various combinations of indole-3-acetic acid (IAA) and kinetin. Callus proliferation began by 8–10 days. Root initiation was very common, particularly at 2 mg/liter IAA and 2 mg/liter kinetin. Shoot formation occurred within 30 days but only at a specific combination of concentrations of the two growth hormones (4 mg/liter IAA + 4 mg/liter kinetin). Most shoots became plantlets by 10 days after transfer to basal Murashige and Skoog's medium. Shoot-forming potential was neither correlated with callus-forming potential nor with vigor of strain.

scholarly journals Micropropagation, genetic fidelity assessment and phytochemical studies of Clerodendrum thomsoniae Balf. f. with special reference to its anti-stress properties

2019 ◽  
pp. 09-15 ◽  
Author(s):  
Pallab Kar ◽  
Arnab Kumar Chakraborty ◽  
Malay Bhattacharya ◽  
Tanmayee Mishra ◽  
Arnab Sen
Keyword(s):  
Special Reference ◽  
Genetic Fidelity ◽  
Fidelity Assessment ◽  
Callus Regeneration ◽  
Murashige And Skoog's Medium ◽  
Murashige And Skoog’S Medium ◽  
Phytochemical Studies ◽  
New Crop ◽  
Nodal Culture

Clerodendrum thomsoniae commonly known as bleeding heart vine or bag flower which is a good candidate for a new crop for the floriculture industry. In this study, in-vitro callus regeneration of C. thomsoniae through nodal culture has been attempted. Murashige and Skoog’s medium supplemented with 2 mg/l BAP and 0.5 mg/l

scholarly journals SOMATIC EMBRYOGENESIS OF MUSSAENDA `QUEEN SIRIKIT'

HortScience ◽  
1994 ◽  
Vol 29 (4) ◽  
pp. 251f-251 ◽  
Author(s):  
Christopher S. Cramer ◽  
Mark P. Bridgen
Keyword(s):  
Acetic Acid ◽  
Somatic Embryogenesis ◽  
Somatic Embryo ◽  
Somatic Embryos ◽  
Basal Medium ◽  
Leaf Number ◽  
Callus Production ◽  
Indole 3 Acetic Acid

Disinfected midrib sections of Mussaenda `Queen Sirikit' ≈3 to 4 mm in size were cultured on a basal medium of Murashige and Skoog salts and vitamins, 87.7 mm sucrose, and 5 g Sigma agar/liter supplemented with several concentrations of indole-3-acetic acid (IAA) (0, 5.0, 10.0, 20.0 μm) and 6-benzylaminopurine (BAP) (0, 0.5, 1.0, 2.5, 5.0, 10.0, 25.0, 50.0 μm). Cultures were subculture onto the same treatment after 5 weeks and observed weekly for 15 weeks for the presence of somatic embryos. As somatic embryos were produced, they were subculture onto basal medium supplemented with 0.5, 1.0, 2.5, or 25.0 μm BAP. Callus was first observed at 2 weeks in cultures grown on basal medium supplemented with 5.0–20.0 μm IAA and 0–50.0 μm BAP. Somatic embryos were observed at 8 weeks on basal medium supplemented with 5.0–10.0 μm IAA and 2.5–5.0 μm BAP. Callus cultured on 0–10 μm IAA and 5.0–10.0 μm BAP produced the greatest number of somatic embryos by 15 weeks. Somatic embryos subculture to basal medium supplemented with 25.0 μm BAP proliferated shoots, while eliminating BAP from the medium resulted in root and callus production. Shoots and entire plants were removed from in vitro conditions and successful] y acclimated to greenhouse conditions. Somatic embryo-derived plants flowered sporadically 25 to 35 weeks after removal from in vitro conditions. Variations in sepal number and leaf number per node were observed at 1% to 5%.

Comportement in vitro de bourgeons axillaires de type indéterminé du palmier dattier (Phoenix dactylifera)

1990 ◽  
Vol 68 (9) ◽  
pp. 2004-2009 ◽  
Author(s):  
Nadia Bouguedoura ◽  
Nicole Michaux-Ferrière ◽  
Jean-Louis Bompar
Keyword(s):  
Floral Induction ◽  
Vegetative State ◽  
Phoenix Dactylifera ◽  
Axillary Buds ◽  
Indolebutyric Acid ◽  
Vegetative Buds ◽  
Murashige And Skoog's Medium ◽  
Murashige And Skoog’S Medium

Indeterminate axillary buds excised from young offshoots of date palm (Phoenix dactylifera L.) developed into flowering or vegetative buds when cultured under different in vitro conditions. Floral induction was observed in explants cultured in the dark on Murashige and Skoog's medium supplemented with 50 g∙L−1 of sucrose and several auxins and cytokinins in a ratio favouring the auxins. In contrast, vegetative buds were obtained from explants cultured under a 16-h photoperiod on Murashige and Skoog's medium supplemented with 30 g∙L−1 of sucrose and 1 mg∙L−1 of indolebutyric acid. The results showed that numerous vegetative meristems can be produced from indeterminate buds cultured in vitro. The results also confirmed the observations made during an in vivo study of flowering and vegetative bud development. The importance of the nutritional contribution of the leaves surrounding the flowering buds was pointed out. Key words: Phoenix dactylifera, axillary buds, indeterminate buds, in vitro culture, floral state, vegetative state, morphogenesis.

scholarly journals Somatic Embryogenesis from Roots of Camellia japonica Plantlets Cultured in Vitro

1991 ◽  
Vol 116 (4) ◽  
pp. 753-757 ◽  
Author(s):  
Ana M. Vieitez ◽  
Carmen San-José ◽  
F. Javier Vieitez ◽  
Antonio Ballester
Keyword(s):  
Acetic Acid ◽  
Somatic Embryogenesis ◽  
Dicarboxylic Acid ◽  
Butyric Acid ◽  
Somatic Embryos ◽  
Basal Medium ◽  
Camellia Japonica ◽  
Secondary Embryos ◽  
Indole 3 Acetic Acid

Somatic embryos were induced on the roots of Camellia japonica L. plantlets regenerated from an in vitro clone of juvenile origin. The embryos appeared to differentiate from epidermic cells and to be connected with the root via a few parenchymatous cells. Somatic embryogenesis occurred on basal medium and with or without various combinations of zeatin, BA, and IBA. Secondary embryos were induced on cotyledons and/or hypocotyl regions of somatic embryos. Two morphological types of somatic embryos were developed, seed-like and bud-like types, and their formation was influenced by the presence of BA in the medium. Embryogenic capacity has been maintained for more than 24 months by subculturing secondary embryos at 7- to 8-week intervals. The best gibberellin/auxin combination for inducing the germination of isolated somatic embryos was GA at 5 mg·liter-1 G A3 and IAA at 1 mg·liter-1. P1antlets were successfully established in planting medium and have continued to grow in a greenhouse. Chemical names used: N-(phenylmethyl)-1H-purine-6-amine (BA); (1α, 2β, 4aα, 4bβ, 10β)-2,4a,7-trihydroxy-l-methyl-8-methylenegibb-3-ene-1,10-dicarboxylic acid l,4a-lactone (GA); 1 H -indole-3-acetic acid (IAA); 1 H- indole-3-butyric acid (IBA); 2-methyl-4-(1 H- purine-6-ylamino)-2-buten-l-ol (zeatin).

scholarly journals Rapid In vitro Multiplication of Chirita longgangensis W.T. Wang: An Endemic and Endangered Gesneriaceae Species in China

HortScience ◽  
2007 ◽  
Vol 42 (3) ◽  
pp. 638-641 ◽  
Author(s):  
Zhenghui Tang ◽  
Honghui Lin ◽  
Lei Shi ◽  
Weilun Chen
Keyword(s):  
Acetic Acid ◽  
Somatic Embryos ◽  
Leaf Explants ◽  
Naphthalene Acetic Acid ◽  
Root Induction ◽  
Ms Medium ◽  
Basal Leaf ◽  
Second Stage ◽  
Regenerated Plantlets

Experiments were conducted to establish an efficient protocol for micropropagation of Chirita longgangensis W.T. Wang. Somatic embryos formed directly at the cut edges of C. longgangensis leaf explants on Murashige and Skoog (MS) medium supplemented with benzylaminopurine (BA) and α-naphthalene acetic acid (NAA). During the somatic embryo induction stage, leaf explants and basal leaf explants were used. Leaves were more appropriate explants than the basal leaf explants. The best medium was modified MS macronutrients and micronutrients supplemented with 0.5 mg·L−1 BA and 0.1 mg·L−1 NAA (the best mean number of somatic embryos per explants was 24.10 ± 1.63). The second stage was root induction and elongation. In vitro regenerated plantlets rooted best on MS medium containing 0.1 mg·L−1 indole-3-acetic acid (IAA) and 30 g·L−1 sucrose. Rooted plantlets, following acclimatization in a greenhouse, were successfully transferred to field conditions, and 95% of the plants survived. Application of this protocol has the ability for mass multiplication, in a limited time, of the endangered species C. longgangensis.

In vitro initiation of adventitious buds and its modification by high concentration of benzyladenine in leaf tissues of mulberry (Morus alba)

1981 ◽  
Vol 59 (1) ◽  
pp. 68-74 ◽  
Author(s):  
S. Oka ◽  
K. Ohyama
Keyword(s):  
Leaf Explants ◽  
Morus Alba ◽  
Adventitious Buds ◽  
High Concentration ◽  
Leaf Tissues ◽  
Murashige And Skoog's Medium ◽  
Murashige And Skoog’S Medium ◽  
Bud Initiation ◽  
The Way

Leaf explants of mulberry (Mortis alba L.) derived from aseptically grown shoots and seedlings were cultured on Murashige and Skoog's medium. Normal and abnormal leaves were grown by varying the concentration of benzyladenine. They differed in the way of forming adventitious buds. In normal leaves bud initiation occurred exclusively at the cut ends of midribs after removing petioles, while in abnormal ones buds formed at any region on midribs and petioles. Histological observations were made to study different patterns of bud initiation.

Induction of somatic embryogenesis in carrot by heavy metal ions

1990 ◽  
Vol 68 (10) ◽  
pp. 2301-2303 ◽  
Author(s):  
Tomohiro Kiyosue ◽  
Koujiro Takano ◽  
Hiroshi Kamada ◽  
Hiroshi Harada
Keyword(s):  
Heavy Metal ◽  
Tissue Culture ◽  
Somatic Embryogenesis ◽  
Growth Regulators ◽  
Daucus Carota ◽  
Somatic Embryos ◽  
Heavy Metal Ions ◽  
Metal Chlorides ◽  
Murashige And Skoog's Medium ◽  
Murashige And Skoog’S Medium

A new method for the induction of somatic embryos has been demonstrated. Somatic embryos were formed without a visible interventing callus stage when apical tips from 1-week-old seedlings of carrot (Daucus carota cv. US-Harumakigosun) were cultured for 1–3 weeks on Murashige and Skoog's medium without growth regulators but containing heavy metal chlorides, such as CoCl2, NiCl2, ZnCl2, and CdCl2, and then transferred to Murashige and Skoog's medium. These results suggest that the stresses caused by these chemicals trigger the induction of somatic embryogenesis in carrot. Key words: Daucus carota, somatic embryo, stress, tissue culture.

scholarly journals Freesia plantlets from flower-buds cultivated in vitro.

1975 ◽  
Vol 23 (4) ◽  
pp. 334-337
Author(s):  
R.L.M. Pierik ◽  
H.H.M. Steegmans
Keyword(s):  
Adventitious Buds ◽  
Flower Buds ◽  
Murashige And Skoog's Medium ◽  
Murashige And Skoog’S Medium

Flower-buds of 10 freesia cvs were grown in vitro and were induced to regenerate adventitious buds on a modified Murashige and Skoog's medium containing PBA and IAA. The formation of adventitious buds was strongly enhanced by growing the explants first in darkness and subsequently in light. Subcultured shoots, grown on a medium with IAA, could be rooted easily and viable plants were obtained. (Abstract retrieved from CAB Abstracts by CABI’s permission)

Somatic Embryogenesis and In vitro Plant Regeneration in Vigna trilobata (L.) Verd. - A Potential Pasture Legume

1970 ◽  
Vol 19 (1) ◽  
pp. 89-99
Author(s):  
K. Choudhary ◽  
M. Singh ◽  
M. S. Rathore ◽  
N. S. Shekhawat
Keyword(s):  
Somatic Embryogenesis ◽  
Growth Regulators ◽  
Somatic Embryos ◽  
Basal Medium ◽  
Long Term Study ◽  
Continuous Application ◽  
First Time ◽  
Pasture Legume

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)

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