scholarly journals In vitro Micropropagation of Plumbago indica L. Through Induction of Direct and Indirect Organogenesis

1970 ◽  
Vol 19 (2) ◽  
pp. 169-175 ◽  
Author(s):  
S. K. Bhadra ◽  
T. Akhter ◽  
M. M. Hossain
Keyword(s):  
Multiple Shoot ◽  
Nodal Segments ◽  
Old Field ◽  
Indirect Organogenesis ◽  
Shoot Buds ◽  
Wide Range ◽  
Plumbago Indica ◽  
Multiple Shoot Buds ◽  
The Media

Leaf and nodal segments of two months old field grown seedlings of Plumbago indica L. were cultured on agar solidified MS supplemented with different concentrations and combinations of NAA, IAA, 2,4-D and picloram, and BAP and Kn. The nodal segments produced either multiple shoot buds (MSBs) or callus of different nature depending on the combinations of plant growth regulators (PGRs). The callus of light green and nodular shape, on further subculture on wide range of PGRs supplemented media, differentiated into MSBs. These MSBs underwent rapid elongation on different PGRs supplemented media. The elongated shoot buds were rooted on transferring in rooting medium and were acclimated in field with 90% survivability. The leaf segments, however, produced only white and friable calluses failed to undergo any differentiation in some of the media combinations.  Key words: Callus induction, Organogenesis, Plumbago indica D.O.I. 10.3329/ptcb.v19i2.5434 Plant Tissue Cult. & Biotech. 19(2): 169-175, 2009 (December)

scholarly journals In vitro micropropagation of Rauvolfia serpentina (L.) Benth through induction of direct and indirect organogenesis

2013 ◽  
pp. 01-09
Author(s):  
SK Bhadra ◽  
TK Bhowmik ◽  
P Singh
Keyword(s):  
Callus Tissue ◽  
Multiple Shoot ◽  
Nodal Segments ◽  
Nodal Segment ◽  
Ms Medium ◽  
Indirect Organogenesis ◽  
Rauvolfia Serpentina ◽  
Shoot Buds ◽  
Wide Range ◽  
Multiple Shoot Buds

Leaf and nodal segments of two months old field grown seedlings of Rauvolfia serpentina (L.) Benth were aseptically cultured on agar solidified MS medium supplemented with various combinations and concentrations of auxins (NAA, IAA, 2,4-D and picloram) and cytokinins (BAP and Kn). The nodal segments produced highest number of multiple shoot buds (5.85/explant) on MS medium supplemented with 2.0 mgl-1 BAP + 0.2 mgl-1 NAA or 2.0 mgl-1 BAP + 0.1 mgl-1 IAA. Whereas nodal segment produced callus tissue of different nature on MS medium supplemented with 1.5 mgl-1 BAP + 0.5 mgl-1 IAA+ 1.5 mgl-1 2,4-D; 3.0 mgl-1 BAP + 1.0 mgl-1 NAA + 1.5 mgl-1 Kn and 0.1 mgl-1 Pic + 1.0 mgl-1 Kn. The callus tissue of light green and nodular nature on further subculture in a wide range of plant growth regulators (PGRs) supplemented media, differentiated into multiple shoot buds that underwent rapid elongation on 2.0 mg/l BAP and 0.2 mg/l NAA supplemented media. The elongated shoot buds on further subculture in rooting media produced strong and stout roots. Half strength MS with 1.5% (w/v) sucrose was most effective for enhancing rooting. Finally those plantlets were acclimatized in field. Thus a protocol was established for rapid micropropagation of this medicinal plant through induction of direct and indirect organogenesis from nodal explant. DOI: http://dx.doi.org/10.3329/cujbs.v3i1.13401 The Chittagong Univ. J. B. Sci.,Vol. 3(1&2):01-09, 2008

scholarly journals In vitro Regeneration of Aristolochia tagala Champ. A Rare Medicinal Plant of Chittagong Hill Tracts

1970 ◽  
Vol 15 ◽  
pp. 63-67
Author(s):  
Animesh Biswas ◽  
MA Bari ◽  
Mohashweta Roy ◽  
SK Bhadra
Keyword(s):  
Medicinal Plant ◽  
Basal Medium ◽  
Multiple Shoot ◽  
Nodal Segments ◽  
Direct Organogenesis ◽  
Chittagong Hill Tracts ◽  
Efficient Regeneration ◽  
Multiple Shoot Buds ◽  
Half Strength

An efficient regeneration protocol through in vitro direct organogenesis was developed for a valuable medicinal plant Aristolochia tagala Champ. using nodal segments as explants. Multiple shoot buds were induced directly from nodal explants cultured on MS (Murashige and Skoog 1962) basal medium supplemented with 2.0 mg/l BAP (N6- benzylaminopurine) and 0.5 mg/l NAA (a-naphthalenacetic acid). The average number of shoots induced per culture was found to be six. Excised shoot roots were cultured on half-strength MS medium containing 0.5 mg/l IBA. The rooted plantlets were transferred to natural environment after proper acclimatization.  Key words: Aristolochia tagala, rare medicinal plant, direct organogenesis. doi: 10.3329/jbs.v15i0.2204 J. bio-sci. 15: 63-67, 2007      

Plant Regeneration from Excised Cotyledons of Mature Strawberry Achenes

HortScience ◽  
1990 ◽  
Vol 25 (5) ◽  
pp. 569-571 ◽  
Author(s):  
A. Raymond Miller ◽  
Craig K. Chandler
Keyword(s):  
Acetic Acid ◽  
Plant Regeneration ◽  
Multiple Shoot ◽  
Naphthaleneacetic Acid ◽  
Developmental Studies ◽  
Shoot Buds ◽  
Cotyledon Explants ◽  
Multiple Shoot Buds ◽  
Rapid Regeneration ◽  
Dichlorophenoxy Acetic Acid

A protocol was developed for excising and culturing cotyledon explants from mature achenes of strawberry (Fragaria × ananassa Duch.). Cotyledon explants formed callus with multiple shoot buds on agar-solidified Murashige and Skoog media containing several combinations of hormones (1 μm 2,4-D; 10 μm 2,4-D; 1 μm BA + 1 μm 2,4-D; 1 μm BA + 10 μm 2,4-D; 5 μm BA; 5 μm BA + 1 μm 2,4-D; 5 μm BA + 10 μ m 2,4-D; 5 μ m BA + 5 μm NAA; 5 μ m BA + 15 μ m NAA). After three subcultures, only tissues maintained on the medium containing 5 μm BA + 5 μm NAA continued to form shoots. Tissues transferred to other media eventually died (1 μm 2,4-D; 1 μ m BA + 10 μ m 2,4-D; 5 μ m BA; 5 μ m BA + 1 μ m 2,4-D), became unorganized (1 μm BA + 1 μm 2,4-D; 5 μm BA + 10 μm 2,4-D; 5 μm BA + 15 μm NAA), or formed roots (10 μm 2,4-D). Whole plantlets were produced by transferring callus with buds to medium lacking hormones. The rapid regeneration of clonal plantlets from cotyledon explants may be useful for reducing variability in future developmental studies. Chemical names used: N-(phenylmethyl)-1H-purin-6-amine (BA); (2,4-dichlorophenoxy) acetic acid (2,4-D); and 1-naphthaleneacetic acid (NAA).

scholarly journals In vitro Embryo Morphogenesis and Micropropagation of Dendrobium aggregatum Roxb.

2014 ◽  
Vol 23 (2) ◽  
pp. 241-249 ◽  
Author(s):  
Mohammad Musharof Hossain
Keyword(s):  
Seed Germination ◽  
Plant Growth ◽  
Developmental Stages ◽  
Cell Mass ◽  
Multiple Shoot ◽  
Seedling Development ◽  
Ms Medium ◽  
Multiple Shoot Buds ◽  
Half Strength

In vitro embryo morphogenesis and micropropagation of Dendrobium aggregatum Roxb. were described. The gradual developmental stages of embryos to seedlings were traced out. Within two weeks of culture the cells of undifferented embryos underwent repeated aniclinal and periclinal division producing a compact, green parenchymatous cell mass called spherule that emerged out by rupturing the testa. The spherules subsequently differentiated into greenish protocorms were considered as typical seed germination. Germination occurred on both (MS and Phytamax (PM) medium but MS medium proved to be more efficient. The primary protocorms underwent profuse proliferation through production of secondary (2º) protocorms when transferred to different plant growth regulators (PGRs) supplemented MS; the medium fortified with 2.0 mg/l BAP and 1.0 mg/l NAA proved to be most effective for induction of 2º protocorms and seedling development. Multiple shoot buds (MSBs) were induced in pseudobulb segments of the in vitro grown seedlings when cultured on different PGRs supplemented media; and the maximum number of MSBs were obtained MS + 2.0 mg/l BAP + 0.5 mg/l picloram. The MSBs underwent elongation and then they rooted when they were transferred to half strength of MS + 0.5 mg/l IAA. The well rooted plantlets were finally transferred to outside natural environment with 80% survival. D. O. I. http://dx.doi.org/10.3329/ptcb.v23i2.17525 Plant Tissue Cult. & Biotech. 23(2): 241-249, 2013  (December)

scholarly journals In vitro regeneration protocol of Rauvolfia serpentina L.

2018 ◽  
Vol 53 (2) ◽  
pp. 133-138 ◽  
Author(s):  
S Khan ◽  
TA Banu ◽  
S Akter ◽  
B Goswami ◽  
M Islam ◽  
...  
Keyword(s):  
In Vitro Regeneration ◽  
Leaf Explants ◽  
Multiple Shoot ◽  
Nodal Segments ◽  
Root Induction ◽  
Ms Medium ◽  
Regeneration System ◽  
Rauvolfia Serpentina ◽  
Number Of Shoots

An efficient in vitro regeneration system was developed for Rauvolfia serpentina L. through direct and indirect organogenesis from nodal and leaf explants. Among the different growth regulators, MS medium supplemented with 2.0 mg/l BAP, 0.5mg/l IAA and 0.02mg/l NAA found best for the multiple shoot formation from nodal segments. In this combination 98% explants produced multiple shoots and the average number of shoots per explants is 13∙4. The frequency of callus induction and multiple shoot induction from leaves was highest 88% in MS medium supplemented with 2.0 mg/l BAP, where mean number of shoots/explants was 12.5. The highest frequency of root induction (80%) and mean number of roots/plantlets (10) were obtained on half strength of MS medium containing 0.2 mg/l IBA. The rooted plantlets were transferred for hardening following acclimatization and finally were successfully established in the field.Bangladesh J. Sci. Ind. Res.53(2), 133-138, 2018

scholarly journals In vitro propagation of muskmelon (Cucumis melo L.) from nodal segments, shoot tips and cotyledonary nodes

2015 ◽  
Vol 41 ◽  
pp. 71-77
Author(s):  
S. Parvin ◽  
M. Kausar ◽  
M. Enamul Haque ◽  
M. Khalekuzzaman ◽  
B. Sikdar ◽  
...  
Keyword(s):  
Cucumis Melo ◽  
In Vitro Propagation ◽  
Multiple Shoots ◽  
Multiple Shoot ◽  
Shoot Tips ◽  
Nodal Segments ◽  
Ms Medium ◽  
Cotyledonary Nodes ◽  
Cucumis Melo L

A rapid and efficient protocol is outlined for in vitro propagation of muskmelon(Cucumis melo L.) Shoot tips, nodal segments and cotyledonary nodes from invitro grown seedlings were used as explants. The explants were inoculated on MS medium fortified with different combinations and concentrations of growthregulators viz., BAP, NAA, GA3 and IBA for multiple shoot regeneration.Effective result was found on MS medium supplemented with 2.0 mg/l BAP, inwhich 90% and 70% cultures induced multiple shoots from nodal segments andshoot tip explants, respectively. Whereas, 70% cultures of cotyledonary nodeswere found to induced shoots on MS medium with 1.5 mg/l BAP + 0.1 mg/l GA3. In vitro regenerated shoots were subcultured on half strength MS mediumsupplemented with different concentrations of IBA and NAA for successful rootinduction and the effective result (up to 70%) was found in medium with 1 mg/lIBA. Well rooted in vitro grown plantlets were acclimatized in sandy soil, whereas 70% plantlets survived

scholarly journals Effect of Bavistin and Adenine Sulphate on In vitro Shoot Multiplication of Picrorhiza scrophulariiflora

1970 ◽  
Vol 19 (2) ◽  
pp. 237-245 ◽  
Author(s):  
Pranay Bantawa ◽  
Olivia Saha Roy ◽  
Parthadeb Ghosh ◽  
Tapan Kumar Mondal
Keyword(s):  
In Vitro Propagation ◽  
Shoot Multiplication ◽  
Multiple Shoots ◽  
Multiple Shoot ◽  
Virgin Soil ◽  
Adenine Sulphate ◽  
Multiple Shoot Buds ◽  
Picrorhiza Scrophulariiflora ◽  
Regenerated Plantlets

An alternative protocol for in vitro propagation of Picrorhiza scrophulariiflora is described using bavistin and adenine sulphate. The explants differentiated into multiple shoot buds on MS supplemented with various concentrations of bavistin and adenine sulphate ranging from 0 - 400 mg/l either alone or in combination. Maximum number of multiple shoots were obtained on MS containing the combination of bavistin (100 mg/l) and adenine sulphate (100 mg/l). In this combination as high as 28 shoots per explant was achieved and also vetrification of the cultures were not recorded. This study also demonstrates that the bavistin has stronger cytokinin-like activity than adenine sulphate. For instance, it was observed that bavistin alone in the concentration of 300 mg/l produced as high as 24 shoots per explant, however, adenine sulphate (100 mg/l) could produce a maximum of 18 shoots per explant. Moreover, higher or lower concentration did not improve the shoot multiplication. The microshoots were separated from the multiple shoots and transferred to MS containing various concentrations of auxins. Among them, NAA (1 mg/l) produced as high as 6 roots per explant. The regenerated plantlets were hardened in plastic cups (6 x 8 cm) containing 9 : 1 virgin soil and soil at Kyongnosla nursery and acclimated for four weeks. A 90% survival rate of the plants was recorded after 60 days. D.O.I. 10.3329/ptcb.v19i2.5441 Plant Tissue Cult. & Biotech. 19(2): 237-245, 2009 (December)

scholarly journals Influence of the Genotype and TDZ on the in Vitro Regeneration of Hybrid Grapes

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 877B-877
Author(s):  
Maritza I. Tapia ◽  
Paul E Read
Keyword(s):  
In Vitro Regeneration ◽  
Shoot Proliferation ◽  
Multiple Shoot ◽  
Nodal Segments ◽  
Ms Medium ◽  
High Concentrations ◽  
Grape Cultivars

It has been previously demonstrated that thidiazuron (TDZ) enhanced the regeneration and multiple shoot proliferation of vinifera grape cultivars. To determine the effect of TDZ on the multiplication of hybrid grapes, in vitro nodal segments from cultivars Chancellor, Leon Millot, and Valiant were cultured on MS medium supplemented with 0, 0.01, 0.05, 0.1, 0.5, and 1.0 mg TDZ/liter. After 1 month, the higher percentage of rooted shoots was obtained from the explants cultured in medium containing the lowest concentration of TDZ (0.01 mg–liter–1) independent of the genotype. Multiple shoot proliferation was favored by high concentrations of TDZ (0.5 and 1.0 mg–liter–1). An average of 0.39 and 0.39 shoots, respectively, was obtained from `Chancellor' cultures, 0.56 and 0.59 from `Leon Millot', and 1.93 and 2.38 from `Valiant'. Vitrification and teratological structures were observed in all the cultures of the three genotypes, but less vitrification occurred in `Valiant' plantlets.

scholarly journals Plantlets from encapsulated shoot buds of Catalpa ovata G. Don

2014 ◽  
Vol 71 (3) ◽  
pp. 181-186
Author(s):  
Halina Wysokińska ◽  
Katarzyna Lisowska ◽  
Katarzyna Floryanowicz-Czekalska
Keyword(s):  
Woody Plant ◽  
Storage Period ◽  
Shoot Cultures ◽  
Shoot Buds ◽  
Catalpa Ovata ◽  
Alginate Capsules ◽  
Woody Plant Medium ◽  
The Media ◽  
In Vitro Shoot Cultures

Shoot buds isolated from in vitro shoot cultures of <em>Catalpa ovata</em> G. Don were encapsulated using 3% sodium alginate with sucrose (3%) and 50 mM calcium chloride. The morphogenic response of encapsulated buds was affected by such factors, like composition of the media and the presence of growth regulators. The highest frequency of plantlet germination from encapsulated buds (70% within 4 weeks) was obtained on Woody Plant medium (WP) (Lloyd and McCown 1980) containing indole-3-butyric acid (IBA) (1 mg/l). The process was substantially inhibited by cold-storage (4<sup>o</sup>C) of encapsulated buds. In this case, the frequency response ranged from 3% to 22% dependent on storage period (28 or 42 days) and the presence of the paraffin coat covering the alginate capsules. The plantlets developed from both unstored and stored encapsulated buds of <em>C. ovata</em> were transplanted to soil and grew in pots to phenotypically normal plants.

scholarly journals High Frequency In vitro Regeneration of Gynura procumbens (Lour.) Merr.

2017 ◽  
Vol 27 (2) ◽  
pp. 207-216
Author(s):  
Tanjina Akhtar Banu ◽  
Barna Goswami ◽  
Shahina Akter ◽  
Mousona Islam ◽  
Tammana Tanjin ◽  
...  
Keyword(s):  
In Vitro Regeneration ◽  
Leaf Explants ◽  
Multiple Shoots ◽  
Multiple Shoot ◽  
Nodal Segments ◽  
Nodal Segment ◽  
Root Induction ◽  
Petiole Explants ◽  
Number Of Shoots

An efficient rapid in vitro regeneration protocol was described from nodal segment, leaf and petiole explants. MS medium supplemented with 1.0 mg/l BAP and 0.5 mg/l IAA was found best for the multiple shoot formation from nodal segments. In this combination 99% explants produced multiple shoots and the average number of shoots per explants was 20.1 ± 1.96. For petiole and leaf explants best response was observed on MS supplemented with 2.0 mg/l BAP, 1 mg/l IAA and 0.5 mg/l Kn. Petiole explants produced highest mean number of shoots/explant (22.9 ± 1.728) among the three explants when the explants were cultured on MS with 2.0 mg/l BAP, 1 mg/l IAA and 0.5 mg/l Kn. The highest frequency of root induction (100%) and mean number of roots/plantlets (11.75) were obtained on MS. The rooted plantlets were transferred for hardening following acclimatization and finally were successfully established in the field.Plant Tissue Cult. & Biotech. 27(2): 207-216, 2017 (December)

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