Regeneration of Robiniapseudoacacia via somatic embryogenesis

1989 ◽  
Vol 19 (2) ◽  
pp. 285-288 ◽  
Author(s):  
S. A. Merkle ◽  
A. T. Wiecko

Tissue cultures were initiated from developing seeds of black locust (Robiniapseudoacacia L.) collected from three trees at weekly intervals from 1 week following anthesis until early fruit maturity. Explants were cultured on media containing 0, 2, or 4 mg/L 2,4-dichlorophenoxyacetic acid and 0 or 0.25 mg/L 6-benzyladenine. Seeds explanted onto hormone-supplemented media remained on these media for 1 or 3 weeks before being placed on hormone-free media, or were maintained on hormone-supplemented media for the entire study. Direct somatic embryogenesis was observed in a single culture, initiated from a seed collected 4 weeks after anthesis and cultured for 1 week on a medium supplemented with 4 mg/L 2,4-dichlorophenoxyacetic acid and 0.25 mg/L 6-benzyladenine before transfer to basal medium. Although it could not be discerned from which part of the explant somatic embryos were derived, secondary embryogenesis continued from the radicles of cotyledonary-stage somatic embryos. Most somatic embryos were well formed, with two distinct cotyledons. Embryos germinated precociously, producing plantlets that were initially weak but later gained vigor and resembled seedlings.

HortScience ◽  
2006 ◽  
Vol 41 (5) ◽  
pp. 1325-1329 ◽  
Author(s):  
Martín Mata-Rosas ◽  
Ángel Jiménez-Rodríguez ◽  
Victor M. Chávez-Avila

Plants of Magnolia dealbata were regenerated from zygotic embryos through somatic embryogenesis and direct organogenesis. Medium and incubation conditions were determinating factors for the development of morphogenetic responses. Photoperiodic exposure was a limiting factor in the general development of the explants, and incubation in darkness allowed their development. The highest formation of shoots per responding explant were obtained on woody plant (WP) medium supplemented with 13.3 μM or 22.2 μM 6-benzylaminopurine (BA) in combination with 2.26 μM or in absence of 2,4-dichlorophenoxyacetic acid (2,4-D) from which 2.5 shoots per explant were induced. Subcultures on WP medium, supplemented with polyvinylpyrrolidone (PUP) 40,000 1 g·L–1) avoided necrosis of explants. Somatic embryos were formed in 85% of explants cultivated on WP medium with 2,4-D (2.3 μM or 4.5 μM); 20% induced indirect embryogenesis and 65% formed direct somatic embryogenesis. The plants were transferred to soil to acclimatize under greenhouse conditions, achieving 90% survival. Somatic embryo conversion to plantlets was obtained with subculture on WP basal medium without growth regulators. In vitro culture can play a key role in the propagation and conservation of this endangered species.


HortScience ◽  
1992 ◽  
Vol 27 (1) ◽  
pp. 63-65 ◽  
Author(s):  
Les Frey ◽  
Yehoshua Saranga ◽  
Jules Janick

Somatic embryogenesis was induced from internodal callus of `Scania', `Improved White Sim', and `Sandra' carnation (Dianthus caryophyllus L.). The optimum protocol for the induction of somatic embryogenesis included initiation of callus in liquid basal Murashige and Skoog medium supplemented with 3.0 μm 2,4-D followed by transfer to liquid basal medium lacking 2,4-D for embryo development. Somatic embryos originated from single cells and early embryonic development proceeded conventionally (i.e., via globular, heart-shaped, and torpedo stages), but clearly developed apical or root meristems were not always formed. A few embryos developed into seedlings and were acclimatized to ex vitro conditions. Chemical name used: 2,4-dichlorophenoxyacetic acid (2,4-D).


HortScience ◽  
1995 ◽  
Vol 30 (6) ◽  
pp. 1295-1297 ◽  
Author(s):  
Carol Gonsalves ◽  
Baodi Xue ◽  
Dennis Gonsalves

Six summer squash (Cucurbita pepo L.) cultivars were regenerated via somatic embryogenesis using cotyledons excised from germinated or nongerminated seeds. Genotypes included were zucchini, commercial F1 hybrids, `President', `Seneca Zucchini', `Jade'; the noncommercial inbred line `Caserta Inbred 557311'; and two yellow squash hybrids `Dixie' and `Seneca Butterbar'. Somatic embryogenesis was initiated in induction medium containing 22.62 μm 2, 4-D, and embryos were germinated in maturation medium containing 0.27 μm NAA and 0.23 μm kinetin. Plants were elongated and rooted on basal medium without hormones. All media contained carbenicillin at 500 mg·liter–1. Sixty-one percent of the `Seneca Butterbar' cotyledons produced somatic embryos when kept on induction medium for 10 weeks. Overall, 7% of the initial explants produced plantlets, and regeneration efficiency was calculated as 0.3 plantlets per initial explant. The relative production of plants from cotyledons that were kept on induction medium for different time periods were determined for `Caserta Inbred 557311' and `Seneca Zucchini'. All cotyledons produced somatic embryos after 11 to 17 weeks on induction medium. However, plantlet production was optimal with explants kept on induction medium for 13 weeks for `Seneca Zucchini' and for 15 weeks for `Caserta Inbred 557311', producing an average of 4.5 and 9.3 plants per explant, respectively, from 90% to 70% of the explants. We recovered plants from all six cultivars; thus, our regeneration protocol may be applicable to other genotypes. The high percentage of regenerants obtained indicates that the regeneration method is efficient enough to be adapted successfully to squash transformation experiments. Chemical names used: α-carboxybenzylpenicillin (carbenicillin); 2,4-dichlorophenoxyacetic acid (2,4-D); 6-furfurylaminopurine (kinetin); α-napthaleneacetic acid (NAA).


1993 ◽  
Vol 23 (5) ◽  
pp. 835-838 ◽  
Author(s):  
Paula M. Pijut

Immature cotyledonary explants excised from developing fruits of Juglanscinerea L. were cultured in vitro to induce regeneration of somatic embryos. Somatic embryos were initiated directly on cotyledons collected 9 weeks postanthesis and cultured on a Driver and Kuniyuki medium supplemented with 250 mg/L L-glutamine, 0.01 mg/L indole-3-butyric acid, 1 mg/L 6-benzylaminopurine, and 2 mg/L kinetin for 3 weeks, prior to transfer to hormone-free Driverand Kuniyuki medium. Embryogenic callus was initiated on explants collected 8–11 weeks postanthesis and cultured on two different media formulations containing 0.25 mg/L 6-benzylaminopurine and 2 mg/L 2,4-dichlorophenoxyacetic acid for 3 weeks, prior to transfer to hormone-free media. Globular to mature somatic embryos were differentiated, and conversion of somatic embryos into whole plants was incomplete. Competence of embryogenic callus was maintained for 1 year with regular subculturing on hormone-free media.


HortScience ◽  
2009 ◽  
Vol 44 (1) ◽  
pp. 113-118 ◽  
Author(s):  
Nancy Santana-Buzzy ◽  
Guadalupe López-Puc ◽  
Adriana Canto-Flick ◽  
Felipe Barredo-Pool ◽  
Eduardo Balam-Uc ◽  
...  

The ontogenesis of direct high-frequency somatic embryogenesis of C. chinense induced from hypocotyl was characterized through a histological analysis of the different phases in the histodifferentiation process during the development of the somatic embryo. The anatomical analysis was carried out since the hypocotyl segments were placed in the culture medium until 45 days of culture. The somatic embryos were induced and maintained in Murashige and Skoog medium supplemented with 2,4-dichlorophenoxyacetic acid (9.5 μm). Samples of tissues and organs were taken every 24 h, fixed in formalin acetic alcohol, and embedded in plastic resin. They were cut into serial sections (5 μm) and stained with toluidine blue. The analysis revealed that the proembryogenic cells originated just from provascular hypocotyl cells. Provascular cells acquired the embryogenic competence 48 h after induction and an intense mitotic division was observed and embryogenic structures were generated first along the vascular strands, which subsequently evolved into somatic embryos. After 2 weeks, there were observed embryos at different stages of development (preglobular, globular, heart-shaped, torpedo-shaped, and cotyledonary). This is the first report dealing with the ontogenesis of the direct somatic embryogenesis of C. chinense, and it is the most complete histological characterization carried out on somatic embryogenesis in the Capsicum genus to date.


2001 ◽  
Vol 49 (6) ◽  
pp. 753 ◽  
Author(s):  
T. Radhakrishnan ◽  
T. G. K. Murthy ◽  
K. Chandran ◽  
A. Bandyopadhyay

Direct somatic embryogenesis is an efficient method of plant regeneration, allowing rapid multiplication of plants in a short period. Six experiments were conducted to study the influence of auxin level on somatic embryogenesis and to optimise the concentration of auxins. Immature embryo axis was the ideal explant and 20–40 mg L–1 of 2,4-dichlorophenoxyacetic acid was the best concentration range for obtaining the maximum number of free somatic embryos. Significant differences were observed between the genotypes for induction and the number of somatic embryos per explant. The cv. Girnar 1 produced the maximum number of somatic embryos per explant, the number of secondary somatic embryos ranging from 1.5 to 9.4. The overall germination of somatic embryos was 42.8%, and 65% of the plantlets transferred to the field survived. The development of somatic embryos was from the apical region of the embryo axes without undergoing dedifferentiation. The initial cell divided to form a tier of four cells and subsequent anticlinal and periclinal division resulted in the development of globular somatic embryos with small suspensors, followed by heart-shaped, torpedo-shaped and ‘cotyledonary’ stages.


1995 ◽  
Vol 43 (4) ◽  
pp. 385-390 ◽  
Author(s):  
S. Kulothungan ◽  
A. Ganapathi ◽  
A. Shajahan ◽  
K. Kathiravan

Embryogenic callus was induced from seedling leaf explants of cowpea (Vigna unguiculata (L.) Walp. cv. C152 on Murashige and Skoog (MS) medium containing 2.0 mg 1−1 2,4-dichlorophenoxyacetic acid (2,4-D). The maximum frequency of somatic embryogenesis was noticed when this callus was transferred to MS liquid medium supplemented with 2 mg 1−1 2,4-D. Further studies on ontogeny of somatic embryos showed that the cells destined to become somatic embryos divided into spherical or filamentous proembryos. Subsequent divisions in the proembryo led to globular, heart, torpedo-shaped, and cotyledonary-stage somatic embryos. Tiny plantlets were obtained by transferring the cotyledonary-stage somatic embryos to MS liquid medium containing 0.5 mg 1−1 2,4-D.


Author(s):  
T.T.B. Phuong ◽  
V.P. Trung ◽  
N.H. An ◽  
N.D. Tuan ◽  
P.T.T. Nguyen

Background: Dinh Lang [Polyscias fruticosa (L.) Harms] is a medicinal plant widely grown in Vietnam, with proven note-worthy health benefits. However, Dinh Lang’s amounts of triterpenoid saponins could not meet the need of the pharmaceutical industry. Thus, this study’s purpose is to figure out the optimal condition for raising Dinh Lang’s cell biomass, rhizogenesis and somatic embryogenesis to provide materials for bioactive compound productions. Methods: Different 2,4-dichlorophenoxyacetic acid and α-naphthaleneacetic acid concentrations (0.5, 1.0, 1.5 and 2.0 mg/L) were examined to determine the best amount of each plant growth regulator for raising cells’ biomass, rhizogenesis and somatic embryogenesis. In each treatment, two grams of eight-week-old calli were cultured in 50 mL of liquid MS medium. Result: It is demonstrated by the results that liquid MS medium containing 1.5 mg/L α-naphthaleneacetic acid has the capacity of producing the highest numbers of somatic embryos (489 embryos per flask) and rooted cells (259.5 cells per flask), while the fresh weight of cells cultured in the medium given 1.5 mg/L 2,4-dichlorophenoxyacetic acid reached its peak of 5.7 g.


2016 ◽  
Vol 14 (1) ◽  
pp. 63-73
Author(s):  
Vu Thi Hien ◽  
Nguyen Phuc Huy ◽  
Bui Van The Vinh ◽  
Hoang Xuan Chien ◽  
Hoang Thanh Tung ◽  
...  

No report on plant regeneration via somatic embryogenesis of P. vietnamensis has been previously published. In the present study, somatic embryogenesis via callus formation from cultures of leaf transverse thin cell layers (tTCLs) of Vietnamese ginseng (Panax vietnamensis Ha et Grushv.) was investigated. α-naphthaleneacetic acid (NAA), 2,4-dichlorophenoxyacetic acid (2,4-D), 6-benzylaminopurine (BA) and thidiazuron (TDZ) were added separately and in combination into the culture media. Explant necrosis or low callogenesis rates were observed when 1-mm wide leaf tTCLs were cultured on media with TDZ, BA, 2,4-D or NAA. On the other hand, calli were successfully induced from the tTCL explants cultured on medium supplemented with either 2,4-D and BA or 2,4-D and TDZ. Callogenesis was observed under both light and dark conditions. The highest callogenesis rate (100%) was obtained on Murashige and Skoog (MS) basal medium supplemented with 1.0 mg l-1 2,4-D in combination with 0.1 mg l-1 TDZ in darkness after eight weeks of culture. White calli were cut into small pieces (1.0 x 1.0 cm dimension) and placed on MS media containing 1.0 mg l-1 2,4-D, 0.5 mg l-1 NAA and TDZ at various concentrations (0.01; 0.1; 0.2; and 0.5 mg l-1), and the best callus proliferation was recorded on medium containing 1.0 mg l-1 2,4-D and 0.2 mg l-1 TDZ. Somatic embryogenesis, with a success rate of 53.3% and 35 embryos per explant, was achieved when calli were subcultured onto MS medium supplemented with 1.0 mg l-1 2,4-D, 0.5 mg l-1 NAA and 0.2 mg l-1 TDZ.


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