scholarly journals Factors Influencing in vitro Germination and Seed Storage Behavior of Couroupita guianensis Aubl. – A Useful Tropical Tree Species

2018 ◽  
Vol 15 (4) ◽  
pp. 957-968
Author(s):  
P. Shiny Arokiamary ◽  
A. Vinoth Alphonse ◽  
R. Ravindhran
Keyword(s):  
Root Length ◽  
Basal Medium ◽  
Seed Storage ◽  
Ms Medium ◽  
Embryo Germination ◽  
Natural Habitats ◽  
Couroupita Guianensis ◽  
Basal Salts ◽  
Mature Seeds

Couroupita guianensis Aubl. popularly known as cannonball tree is widely distributed in the tropical regions. The tree parts are commonly used to treat wounds and tumors. Leaves, flowers, and fruits contain active phytochemicals with significant biological activity. In the recent years, destruction of natural habitats by mankind has reduced its distribution. Natural propagation of C. guianensis by seeds is greatly hindered by poor seed germination and viability. Therefore, the present study was undertaken to optimize the conditions for in vitro embryo germination and to investigate the seed storage behaviour. Mature seeds inoculated on MS basal medium germinated within 10 d with a frequency of 61.6%. Supplementation of plant growth regulators (PGRs) to MS medium improved the embryo germination frequency (100%). Seedlings with highest shoot length (8.10±0.11 cm) and root length (6.27±0.14 cm) were produced in MS medium supplemented with 1.0 mg/l kinetin and 0.1 mg/l indole-3-butyric acid. Among different strength liquid MS basal salts, quarter-strength produced a greater number of secondary roots (8.00±0.28) with average root length of 17.83±0.58 cm. Seed storage behaviour studies clearly proved the recalcitrant nature as only freshly harvested mature seeds retained the germination potential upon storage at 15 ºC for up to 45 d. Desiccation of seeds on exposure to air-dry storage resulted in rapid deterioration of germination. Pre-conditioning of germinated seedlings in liquid MS basal salts was required for their survival under field conditions. Plantlets with well-developed roots were successfully acclimatized to the field with 100% survivability. This protocol facilitates conservation, sustainable utilization and re-introduction of C. guianensis into its natural habitats.

scholarly journals IN VITRO PROPAGATION OF ALGERIAN IVY (HEDERA CANARIENSIS L.)

HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1123g-1124
Author(s):  
Karim H. Al-Juboory ◽  
David J. Williams
Keyword(s):  
Root Length ◽  
In Vitro Propagation ◽  
Inverse Relationship ◽  
Basal Medium ◽  
Shoot Tip ◽  
Ms Medium ◽  
Shoot Tip Explants ◽  
Strength Medium

Shoot tip explants of Algerian Ivy Heder a canariensis were cultured on MS basal medium supplemented with a combination of salt strength and NAA and IBA. More roots per explant developed on full salt strength medium combined with NAA. The most roots per explant were obtained with a combination of IBA and 1/4 MS salt. There was an inverse relationship between an increase in IBA or NAA concentration and root length and number. Shoots proliferated better on full MS salt combined with NAA and IBA. The highest level of NAA (40 uM) and 0.1 uM TDZ produced the most shoots and roots, the longest roots, the highest rooting percentage, the largest plants with the most leaves and the best callus quality per explant. The leaves from in vitro were cultured on MS medium with varying levels of Thidiazuron (TDZ) and NAA in the presence of light produced the highest number of roots.

scholarly journals In Vitro Propagation of Eriostemon myoporoides and Eriostemon `Stardust'

HortScience ◽  
1994 ◽  
Vol 29 (6) ◽  
pp. 686-688 ◽  
Author(s):  
James R. Ault
Keyword(s):  
Root Length ◽  
Basal Medium ◽  
Shoot Proliferation ◽  
Shoot Length ◽  
Axillary Shoot ◽  
Naphthaleneacetic Acid ◽  
Stem Explants ◽  
Ms Medium ◽  
Axillary Shoot Proliferation

Optimal axillary shoot proliferation was obtained from stem explants of a clone of Eriostemon myoporoides DC. on Murashige and Skoog (MS) basal medium containing 0.1 mg BA/liter, and of Eriostemon `Stardust' on MS medium containing 0.5 mg BA/liter. Overall average number of shoots and shoot lengths for all treatments was greater for E. `Stardust' (22.4 shoots and 12.1-mm shoot length) than for E. myoporoides (4.5 shoots and 8.3-mm shoot length). Maximum percent rooting of E. myoporoides (42%) and E. `Stardust' (95%) was obtained on MS medium supplemented with 1.0 mg K-IBA/liter for E. myoporoides and 0.1 mg NAA/liter for E. `Stardust'. Overall average percent rooting and root lengths were greater for E. `Stardust' (42% rooting and 11.0-mm root length) than for E. myoporoides (27% rooting and 2.3-mm root length). For E. `Stardust', reducing sucrose in the rooting medium from 50 to 25 g·liter-1 significantly decreased overall average percent rooting to 1670 and root length to 6.8 mm. Plantlets of both clones were acclimatized in the greenhouse and transferred successfully to soil, although survival was <7070. Chemical names used: N -(phenylmethyl) -l H -purine-6-amine (BA); potassium-l H -indole-3-butyric acid (K-IBA); l-naphthaleneacetic acid (NAA).

scholarly journals IN VITRO PROPAGATION OF ALGERIAN IVY (HEDERA CANARIENSIS L.)

HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1123G-1124 ◽  
Author(s):  
Karim H. Al-Juboory ◽  
David J. Williams
Keyword(s):  
Root Length ◽  
In Vitro Propagation ◽  
Inverse Relationship ◽  
Basal Medium ◽  
Shoot Tip ◽  
Ms Medium ◽  
Shoot Tip Explants ◽  
Strength Medium

Shoot tip explants of Algerian Ivy Heder a canariensis were cultured on MS basal medium supplemented with a combination of salt strength and NAA and IBA. More roots per explant developed on full salt strength medium combined with NAA. The most roots per explant were obtained with a combination of IBA and 1/4 MS salt. There was an inverse relationship between an increase in IBA or NAA concentration and root length and number. Shoots proliferated better on full MS salt combined with NAA and IBA. The highest level of NAA (40 uM) and 0.1 uM TDZ produced the most shoots and roots, the longest roots, the highest rooting percentage, the largest plants with the most leaves and the best callus quality per explant. The leaves from in vitro were cultured on MS medium with varying levels of Thidiazuron (TDZ) and NAA in the presence of light produced the highest number of roots.

scholarly journals Micropropagation of Acacia chundra (Roxb.) DC.

2008 ◽  
Vol 35 (No. 1) ◽  
pp. 22-26 ◽  
Author(s):  
R. Rout G ◽  
K. Senapati S ◽  
S. Aparajeta
Keyword(s):  
Acetic Acid ◽  
Growth Regulators ◽  
Basal Medium ◽  
Multiplication Rate ◽  
Ms Medium ◽  
Leguminous Tree ◽  
Half Strength ◽  
Basal Salts ◽  
Indole 3 Acetic Acid

An <I>in vitro</I> propagation of an economic leguminous tree, <I>Acacia chundra</I>, has been standardized. Induction of bud sprout was obtained from shoot tip and nodal explants derived from <I>in vitro</I> grown plants of <I>A. chundra</I> on the Murashige and Skoog (MS) basal medium supplemented with 6-benzylaminopurine (BA) (1.0 mg/l) and 20 mg/l adenine sulfate (Ads). The rate of multiplication was obtained on MS medium supplemented with 1.5 mg/l BA, 0.01 to 0.05 mg/l (indole-3-acetic acid) IAA and 50 mg/l Ads. The multiplication rate varied from 3 to 6 shoots depending on the growth regulators used. Excised shoots were rooted on half-strength MS basal salts supplemented with 0.25 mg/l indole-3-butyric acid (IBA) or IAA and 20 g/l (w/v) sucrose after 10 to 12 days of culture. The micropropagated plantlets have been acclimatized and successfully transferred to soil.

Genetic transformation of Stella De Oro daylily by particle bombardment

2003 ◽  
Vol 83 (4) ◽  
pp. 873-876 ◽  
Author(s):  
A. N. Aziz ◽  
R. J. Sauvé ◽  
S. Zhou
Keyword(s):  
Southern Blotting ◽  
Basal Medium ◽  
Callus Cultures ◽  
Naphthaleneacetic Acid ◽  
Ms Medium ◽  
Chain Reaction ◽  
Polymerase Chain ◽  
Semi Solid ◽  
Independent Transformation

Daylily (Hemerocallis sp. ‘Stella de Oro’) callus cultures initiated from ovules were bombarded with gold particles coated with plasmid harboring Basta® resistance gene. Resulting putative transgenic calli were selected after 3 wk on semi-solid Murashige and Skoog’s (MS) basal medium supplemented with 10 mg L-1 1-naphthaleneacetic acid, 2 mg L-1 6-benzylaminopurine and 3 mg L-1 phosphinothricin (PPT). Surviving calli regenerated shoots after 2 mo on semi-solid MS medium supplemented with 2 mg L-1 thiadiazuron and 1 mg L-1 PPT. Polymerase chain reaction and Southern blotting were used to confirm independent transformation events. Key words: Basta® resistance, in vitro, Hemerocallis

scholarly journals Micropropagation and in vitro conservation of Alcantarea nahoumii (Bromeliaceae), an endemic and endangered species of the Brazilian Atlantic Forest

2020 ◽  
Vol 42 ◽  
pp. e52940
Author(s):  
Simone Sacramento dos Santos Silva ◽  
Everton Hilo de Souza ◽  
Fernanda Vidigal Duarte Souza ◽  
Cristina Ferreira Nepomuceno ◽  
Maria Angélica Pereira de Carvalho Costa
Keyword(s):  
Atlantic Forest ◽  
Culture Media ◽  
In Vitro Conservation ◽  
Naphthaleneacetic Acid ◽  
High Survival ◽  
Multiplication Rate ◽  
Ms Medium ◽  
Mature Seeds ◽  
Stem Segments

Alcantarea nahoumii (Leme) J. R. Grant is a species native to the Atlantic Forest that stands out for ornamental purposes. The objective of this work was to evaluate the in vitro germination of A. nahoumii seeds and establish a micropropagation protocol for production of seedlings so as to minimize the effects of predatory extractivism and develop an in vitro conservation system. Mature seeds were disinfested, established in three culture media (MS, MS½ and MS⅓) and incubated at four temperatures (20, 25, 30 and 35ºC) in a germination chamber. In the micropropagation experiment, stem segments were introduced in MS medium supplemented with 0.5 μM of 1-naphthaleneacetic acid (NAA) and 0.0, 2.2, 4.4 and 6.6 μM of 6-benzylaminopurine (BAP). For the in vitro conservation, plantlets were established in MS or MS½ medium supplemented with 15 g L-1 or 30 g L-1 of sucrose. The plants were acclimated with commercial substrate. The highest seed germination percentages were promoted by temperature conditions of 20 and 25ºC, with MS culture medium. The highest multiplication rate of shoots was obtained from the treatment without addition of the growth regulator or when combined with 2.2 μM of BAP + 0.5 μM of NAA. The acclimation of the plants occurred with high survival rate. The species can be conserved in vitro under slow growth condition for 24 months when incubated in MS medium supplemented with 30 g L-1 of sucrose.

scholarly journals In vitro regeneration protocol for artificial seed production in an important medicinal plant Mentha arvensis L

2014 ◽  
Vol 20 ◽  
pp. 99-108 ◽  
Author(s):  
MS Islam ◽  
MA Bari
Keyword(s):  
Medicinal Plants ◽  
Seed Production ◽  
In Vitro Regeneration ◽  
Basal Medium ◽  
Nodal Segments ◽  
Ms Medium ◽  
Mentha Arvensis ◽  
Artificial Seed ◽  
Artificial Seed Production

Context: The application of encapsulated shoot tips and nodal segments may contribute to the protection of rare and threatened medicinal plants. Although the artificial seed technique has been reported for more than two decades, for medicinal plants this method has not been developed sufficiently. The main limitations in conventional propagation of some species with medicinal value are: reduced endosperm, low germination rate and seedless varieties. The above mentioned reasons indicate the need for the production of artificial seeds as a technique which combines the advantages of clonal multiplication with those of seed propagation and storage. Objectives: The objective of the present investigation was to standardize artificial seed production technology taking shoot tip and nodal explants in Mentha arvensis and its in vitro regeneration Materials and Methods: Sodium alginate beads were produced by encapsulation of shoot tip and nodal segments of the plant M. arvensis. MS medium was used as basal medium with agar and sodium alginate was used as gelling agent accompanied by CaCl2 solution. Results: Different concentrations and combinations of BAP, Kin and NAA were used in alginate bead in MS basal medium. Among the different concentrations of phytohormone, highest 80% of shoot formation was observed in MS medium containing 2.0 mg/l BAP + 0.2 mg/l NAA from nodal segments of M. arvensis. Highest average number of shoot 9.87 ± 0.58 formation was obtained in the same medium but highest length of shoot 6.27 ± 0.29 cm was found in the medium having 1.0 mg/l BAP + 0.5 mg/l NAA. Conclusion: The present investigation clearly established and demonstrated the method of obtaining the artificial seed production in M. arvensis supported by different hormone concentrations DOI: http://dx.doi.org/10.3329/jbs.v20i0.17722 J. bio-sci.  20:  99-108, 2012

scholarly journals Micropropagation of Cymbidium aloifolium (L.) SW., A Medicinal Orchid by Artificial Seeds Technology

2015 ◽  
Vol 28 ◽  
pp. 42-48 ◽  
Author(s):  
Shreeti Pradhan ◽  
Babu Lal Tiruwa ◽  
Bijay R Subedee ◽  
Bijaya Pant
Keyword(s):  
Basal Medium ◽  
Mass Scale ◽  
Scale Production ◽  
Ms Medium ◽  
Artificial Seeds ◽  
Seed Technology ◽  
Artificial Seed ◽  
Cymbidium Aloifolium ◽  
Medicinal Orchid

Artificial seed technology is a rapidly growing area of research in plant cell and tissue culture. Application of this technology opens an alternative route for mass scale production, efficient delivery of cloned plantlets and fulfils the increasing demand of local growers. An attempt was made to produce artificial seeds and their subsequent regeneration of a highly valuable medicinal orchid of Nepal i.e. Cymbidium aloifolium. Artificial seeds were obtained through encapsulation of protocorms in calcium alginate beads. Protocorms were encapsulated by using 3% sodium alginate and 0.2 M calcium chloride solution. Murashige and Skoog (MS) medium (1962) was used as the basal medium for in vitro germination and seedling development of artificial seed. In Cymbidium aloifolium, 20-25 days old in vitro grown protocorms were used for production of artificial seeds. Artificial seeds were inoculated on two different culture conditions of MS medium i.e. MS solid & MS liquid with four different treatments i.e. strength of 1.0, ½, ¼ and MS media supplemented with plant growth regulators viz. BAP (0.5 mg/l) and NAA (0.5 mg/l). Highest percentage of germination (100%) and plantlet conversion was found on hormone free full strength (1.0 MS) of MS liquid medium after 13-14 weeks of culture. Plantlets regenerated from artificial seeds with well developed shoot and root systems were successfully acclimatized in potting mixture of cocopeat, litter and sphagnum moss in a ratio 2:1:1.J. Nat. Hist. Mus. Vol. 28, 2014: 42-48

scholarly journals In-vitro Regeneration from Direct and Indirect Organogenesis of Crescentia alata Kunth an Important Multipurpose Medicinal Tree

2021 ◽  
pp. 48-58
Author(s):  
R. Abinaya
Keyword(s):  
Shoot Organogenesis ◽  
In Vitro Regeneration ◽  
Basal Medium ◽  
Direct Organogenesis ◽  
Ms Medium ◽  
Indirect Organogenesis ◽  
Medicinal Tree ◽  
Short Period ◽  
In Vitro Clonal Propagation

In this present work, an in-vitro regeneration protocol for Crescentia alata (C. alata) was developed using various explants on Murashige and Skoog (MS) medium augmented with different concentrations and combinations of plant growth regulators (PGRs) for direct and indirect regeneration. The direct organogenesis was established from nodes and internodes on MS medium supplemented with cytokinins and auxins. The indirect organogenesis via callus phase was obtained from leaf, nodes and internodes on MS medium supplemented with different concentrations of PGRs. The high frequency shoot organogenesis were achieved directly from nodal explants were cultured on MS medium supplemented with 3.0 mg/L BAP+0.5 mg/L KIN +1.0 mg/L NAA. Indirect organogenesis callogenic frequency was optimized at the concentration of MS medium containing 1.0 mg/L BAP + 5.0 mg/L IAA. The callus was obtained from all the explants were used, among these explants internodal explants gave best result on MS medium supplemented with different concentrations of cytokinins and auxins for indirect organogenesis experiment. Indirect organogenesis the highest number of shoot regeneration was obtained in MS Basal Medium with 4.0 mg/L BAP + 0.5 mg/L KIN + 2.0 mg/L NAA from internodal explants. For root formation the regenerative shoots which were sub cultured on MS medium containing different ratios of auxins. The rooted plantlets were transferred successfully to the pots containing sterilized soil and were successfully hardened at greenhouse condition for 20 days then exposed to the natural environment. This is the first successful micropropagation report of an efficient and rapid in-vitro clonal propagation protocol for C. alata by direct and indirect shoot organogenesis through various explants, which can be employed for conservation of this important medicinal tree species as well as the utilization of an biologically important active biomolecules. This protocol can be very useful to obtain plants from various explants, without the requirement of meristematic regions, enabling the obtainment of a higher number of plants in short period.

scholarly journals IN VITRO CULTURE OF IMMATURE TAXUS EMBRYOS

HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 698d-698 ◽  
Author(s):  
Ching-yeh Hu ◽  
Lee Wang ◽  
Bernard Wu
Keyword(s):  
Embryo Culture ◽  
Large Population ◽  
Dry Weight ◽  
Ms Medium ◽  
Embryonic Growth ◽  
Embryo Dormancy ◽  
Taxol Production ◽  
Initial Medium ◽  
Mature Seeds

Embryo culture can by-pass yew (Taxus) seed dormancy and produce large population of seedlings to be screened for the anticancer drug, taxol, production. Immature linear embryos from seeds of T. baccata, T. brevifolia. T. cuspidata, and T. media were dissected and cultured. B5 medium supported the best embryonic growth during the initial two week's culture for T. cuspidata and T. baccata. T. brevifolia grew faster on MS medium. Weak embryo dormancy was encountered in T. brevifolia and T. cuspidata from the mature seeds but not from the immature ones. No embryonic growth had been observed in T. media dissected from mature seeds due to strong dormancy. Developing embryos were subsequently transferred to 1/2X B5 medium for germination. Rooting percentage in the mature seed derived T. brevifolia embryos increased from 12.5 to 63.6 when 30 μM GA3 was added to the initial medium. Several hundreds of seedlings of T. baccata. T. brevifolia and T. cuspidata had been acclimatized to the greenhouse conditions. The taxol content of resultant T. cuspidata seedlings was 0.027% (dry weight), while that of T. brevifolia obtained from the wild twig was 0.030%.

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