scholarly journals In Vitro Long-Term Cultures of Papaya (Carica Papaya L.).

2021 ◽  
Author(s):  
Jose Javier Regalado González ◽  
Manuel López Granero ◽  
Carlos Lopez Encina
Keyword(s):  
Morphological Characteristics ◽  
Basal Medium ◽  
Multiplication Rate ◽  
Ms Medium ◽  
High Quality ◽  
Poor Growth ◽  
Average Multiplication ◽  
Half Strength

Abstract We present the data on proliferation corresponding to 10 years of continuous incubation in vitro of papaya shoots, and propose a reliable method for long-term micropropagation for papaya, using two types of explants: Microshoots from somatic embryos, and from axillary buds of papaya. Three different media were assayed. The proliferation medium (PPRM) allowed to maintain papaya shoots under continuous proliferation during 20 years, maintaining a consistent behaviour. Most of the shoots developed in PPRM rooted during the incubation, and after acclimated easily, maintaining the morphological characteristics of the parental plants, flowering and setting fruits normally. The PPRM medium consist in MS medium supplemented with NAA (0.1 mg l-1), BA (0.5 mg l-1), GA3 (0.5 mg l-1) and Adenine sulphate (40 mg l-1). The average multiplication rate was higher than 20 shoots per explant along the long-term assay. The elongation medium (PELM), was designed to recover shoots with a poor growth, and allowed the development of high quality shoots ready for rooting, and consist in a MS basal medium supplemented with NAA (0.1 mg l-1), Kin (0.5 mg l-1) and GA3 (1 mg l-1). The rooting medium (PROM) was designed to induce high quality roots from non-rooted shoots and consist in a half strength MS medium plus IBA (1mg l-1). On PROM, agar can be exchanged for expanded vermiculite. Acclimation took place inside an acclimatization tunnel under progressive hydric stress. After 4 weeks, the plant recovery rate was 90% for plants maintained under continuous proliferation during ten years.

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.

scholarly journals In Vitro Propagation of Three Moroccan Prickly Pear Cactus Opuntia and Plant Establishment in Soil

2013 ◽  
Vol 5 (1) ◽  
pp. 39-44 ◽  
Author(s):  
Aissam EL FINTI ◽  
Rachida EL BOULLANI ◽  
Naima AIT AABD ◽  
Fouad MSANDA ◽  
Mohammed A. SERGHINI ◽  
...  
Keyword(s):  
Basal Medium ◽  
Prickly Pear ◽  
Multiplication Rate ◽  
In Vitro Micropropagation ◽  
Prickly Pear Cactus ◽  
Half Strength ◽  
Micropropagated Plants ◽  
Large Production ◽  
Pear Cactus

Opuntia is one of the most widespread cacti, primarily due to their edible fruit and vegetable mass used as feed. The high demand for young plants of Opuntia made it necessary to find a rapid method of multiplication of the cactus, the safest method consisting in vitro micropropagation of species belonging to this genus. With aim of large production of plant material, a propagation system of three important prickly pear cactus cultivar (Opuntia ficus-indica) in Morocco was developed. Segments of healthy young cladode (containing one areole) were cultivated in Murashige and Skoog medium (MS) containing adenine sulfate (40 mg/1), monosodium phosphate (50 mg/l), sucrose (50 g/l), phytagel (0.3%) and benzyladenine (BA) at 22.2 μM, to start the process of micropropagation. In vitro-developed shoots from areoles were used as secondary explants to induce shoot development in the MS medium with 5 mg/l of BA. All of the three studied cultivars showed an important multiplication rate in this medium. ‘Sidi Ifni M’ (‘Moussa’) cultivar shows the greatest number of shoots followed by ‘Sidi Ifni A’ (‘Aissa’) and ‘Delahia’ 17.26, 14.12 and 12.13 respectively. Rooting of in vitro-generated shoots was achieved most efficiently on half-strength MS basal medium supplemented with 0.5 mg/l of indole-3-butyric acid (IBA) or IAA. Rooting frequencies were in the range from 95 to 100% and the highest mean number of root (19.1) was obtained with IBA for ‘Delahia’ cultivar. All micropropagated plants were transferred to greenhouse and all of them survived acclimatization process and showed good overall growth.

scholarly journals Clonal fidelity of chrysanthemum regenerated from long term cultures

Genetika ◽  
2006 ◽  
Vol 38 (3) ◽  
pp. 243-249 ◽  
Author(s):  
Sladjana Jevremovic ◽  
Milana Trifunovic ◽  
Marija Nikolic ◽  
Angelina Subotic ◽  
Ljiljana Radojevic
Keyword(s):  
Morphological Characteristics ◽  
Flower Color ◽  
Stem Segment ◽  
Shoot Cultures ◽  
Ms Medium ◽  
Color Changes ◽  
In Vitro Plants ◽  
One Year

Morphological characteristics of flowers of long term regenerated chrysanthemum, cv. "White Spider", after ten years of micropropagation are investigated. Shoot cultures are established and maintained more than ten years by stem segment culture on MS medium supplemented with BAP and NAA (1.0, 0.1 mgL-1, respectively). Rooting of shoots (100 %) has done on MS medium without hormones and it was very successful after ten years, as well as, after two or eight years of micropropagation. Acclimation of rooted chrysanthemum plantlets at greenhouse conditions was excellent and after appropriate photoperiod "in vitro" plants flowered 90.3 % and have the same flower color, shape and size as mother plants. Flower color changes of "in vitro" plants are observed during another flowering cycle one year after acclimatization. Observed variations of chrysanthemum flowers could be attributed to epigenetic factors.

scholarly journals Mass propagation of Bambusa bambos (L.) Voss through in vitro culture

2017 ◽  
Vol 5 (2) ◽  
pp. 15-26 ◽  
Author(s):  
Raihan I Raju ◽  
Shyamal K Roy
Keyword(s):  
In Vitro Culture ◽  
Basal Medium ◽  
Nodal Segments ◽  
Garden Soil ◽  
Root Induction ◽  
Ms Medium ◽  
Mass Propagation ◽  
Surface Sterilization ◽  
Half Strength

Protocol for mass propagation of Bambusa bamboos (L.) Voss was developed through in vitro culture. Nodal segments containing pre-existing axillary bud, after surface sterilization, were inoculated on liquid Murashige and Skoog’s (MS) basal medium containing different concentrations and combinations of cytokinins (BAP, TDZ and Kn). The highest direct shoot induction (90%) was obtained in the MS liquid medium supplemented with 2.0 mg/l BAP and 1.0 mg/l TDZ with maximum average number of shoots (3.14 ± 0.06) per explant. Highest shoot multiplication (16.58 ± 0.24 shoots per culture) with highest average shoot length (9.21 ± 0.13 cm) was obtained when in vitro raised shoots were cultured in gelrite gelled MS medium in conjunction with 2.0 mg/l BAP and 1.0 mg/l TDZ. Incorporation of 10% coconut water with 4% sucrose in the above mentioned medium resulted satisfactory shoot growth and development with an average 26.7 ± 0.60 shoots per culture. For root induction, in vitro raised shoots were divided into clumps of 4-5 shoots in each clump and transferred onto both liquid and gelled half-strength MS medium containing different concentrations and combinations of auxins (IBA and NAA). Maximum rooting (86.67%) was achieved in half-strength of MS medium fortified with 2.5 mg/l IBA and 2.5 mg/l NAA with an average 8.72 ± 0.42 root per shoot. The rooted plantlets were then transferred to polybags containing garden soil, sand and compost mixture with 1:1:1 ratio. After a month the hardened plantlets were then transferred to the larger pots containing garden soil and compost with 1:1 ratio for sufficient growth and finally transplanted to the field. In this process, the highest 100% survivability was recorded from well-established rooted plantlets. The regenerated plants showed well developed root and shoot systems in field condition.Jahangirnagar University J. Biol. Sci. 5(2): 15-26, 2016 (December)

scholarly journals Young capitulum as important explant in in vitro mass propagation of gerbera (Gerbera jamesonii)

2020 ◽  
Vol 12 (2) ◽  
pp. 264-276
Author(s):  
Budi WINARTO ◽  
Kurnia YUNIARTO ◽  
Rudy SOEHENDI
Keyword(s):  
Multiple Shoots ◽  
Shoot Formation ◽  
Leaf Length ◽  
Multiplication Rate ◽  
Ms Medium ◽  
Plantlet Production ◽  
Half Strength ◽  
Flower Stage ◽  
The One

A new route of in vitro propagation of gerbera selected clones was successfully established using young capitula in tight buds and buds that were started to unfold stage as explant source. The one-fourth pieces of young capitula of tight flower stage and half-strength MS medium containing 0.25 mg/l BAP was the suitable for initiation and produced higher number of shoots per explant up to 3.8 shoots. The results were improved by culturing the one-fourth piece of 01.092 capitulums on MS medium fortified by 0.2 mg/l BAP and 0.02 mg/l NAA producing the highest shoot formation up to 8.5 shoots per explant with 28.7 leaves per explant and 2.1 cm leaf length. High multiple shoots were determined in third to fourth subculture periods and reduced thereafter with high multiplication rate noted on 01.092 clone. Shoots were easily rooted on half-strength MS medium supplemented with 2 g/l activated charcoal. Plantlets were transferred to ex vitro condition with 96.4% survivability of 03.045 clone using Cycas rumphii bulk and cocopeat (1:1, v/v) under spraying 1 g/l Growmore (32N:10P:10K) solution once week periodically. The route has high potential applied in qualified plantlet production for other Gerbera’s due to high shoots produced up to 35 shoots per whole young capitulum used. 

scholarly journals IN VITRO PROPAGATION OF PLUM ROOTSTOCK DOCERA 6

2021 ◽  
Vol 37 (37) ◽  
pp. 131-135
Author(s):  
Viktorija Nikolova ◽  
◽  
Vanya Akova ◽  
Marieta Nesheva ◽  
Svetlio Malchev ◽  
...  
Keyword(s):  
In Vitro Propagation ◽  
Basal Medium ◽  
Multiplication Rate ◽  
Culture Techniques ◽  
Rooting Medium ◽  
Different Seasons ◽  
Average Multiplication ◽  
Fruit Growing ◽  
High Concentrations

This paper describes research on the application of tissue culture techniques to the micropropagation of interspecific rootstock ʹDocera 6ʹ. The experimental work was carried out in the period 2017-2018, in the in vitro propagation laboratory of the Fruit Growing Institute Plovdiv. Аxillary buds were employed as initial explantеs in two different seasons (March-May; September-October). The action of the mineral medium was studied in the multiplication stage. The best result was obtained on LS medium included BAP 0.5 mg/l and IAA 0.05 mg/l. Тhe obtained average multiplication rate is 3.08. The concentration of auxin applied to the basal medium influence the quality of the root system Treatment with high concentrations of IBA added to the rooting medium gives the best results (V5). Тhe influence of the season on growth and development of micropropagated ʹDocera 6ʹ rootstock during ex vitro acclimatization is also part of our research. The spring acclimatization gives better results than the autumn.

scholarly journals Effect of activated charcoal and ascorbic acid on in vitro morphogenesis and o-dihydroxyphenols content in Paphiopedilum insigne

2022 ◽  
Author(s):  
Monika Poniewozik ◽  
Marzena Parzymies ◽  
Paweł Szot
Keyword(s):  
Ascorbic Acid ◽  
Phenolic Compounds ◽  
Activated Charcoal ◽  
Root Formation ◽  
Multiplication Rate ◽  
Ms Medium ◽  
In Vitro Morphogenesis ◽  
Half Strength ◽  
Positive Effect

Phenolic compounds limit micropropagation of many orchids in vitro. The aim of the study was to estimate the effect of activated charcoal (AC);1, 2 or 4 g/L) or ascorbic acid (AA; 10, 20 or 30 mg/L) added to the half strength MS medium on the growth and o-dihydroxyphenols content in Paphiopedilum insigne in vitro. A positive effect of AC on the shoot and root formation has been found. The highest multiplication rate (5.6 shoots/explant) and rooting frequency were obtained on medium containing 2 g/L of AC. However, AC reduced the leaf number as compared to the control. The lowest content of o-dihydroxyphenols was marked in Paphiopedilum insigne leaves when the shoots were grown on medium with 10 mg/L AA, followed by AC at 1 or 2 g/L.

scholarly journals Somatic Embryogenesis and Plant Regeneration from in-vitro-grown Leaf Explants of Rose

HortScience ◽  
2004 ◽  
Vol 39 (6) ◽  
pp. 1378-1380 ◽  
Author(s):  
C.K. Kim ◽  
J.Y. Oh ◽  
J.D. Chung ◽  
A.M. Burrell ◽  
D.H. Byrne
Keyword(s):  
Somatic Embryogenesis ◽  
Plant Regeneration ◽  
Somatic Embryos ◽  
Leaf Explants ◽  
Basal Medium ◽  
Shoot Formation ◽  
Ms Medium ◽  
Regeneration Frequency

Somatic embryogenesis was initiated from in vitro-grown leaf explants of rose using an induction period of 4 weeks on MS basal medium supplemented with auxin followed by several subcultures on MS basal medium with cytokinin. `4th of July' showed the highest regeneration frequency (24.4%) on 5.3 μm NAA followed by culture on medium containing 18.2 μm zeatin. `Tournament of Roses' produced somatic embryos when cultured for 4 weeks on medium containing dicamba, 2.3 μm followed by three subcultures on medium containing 18.2 μm zeatin. Embryogenic callus matured on MS media containing 0.5 μm NAA, 6.8 μm zeatin, and 2.9 μm GA3. Long-term cultures were established for both cultivars. Somatic embryos germinated on MS medium containing IBA and BA. Silver nitrate (58.8 μm) enhanced shoot formation and germination of somatic embryos. Plants derived from somatic embryos were acclimatized and successfully established in the greenhouse.

scholarly journals Micropropagation and Polyploid Induction of Acer platanoides ‘Crimson Sentry

2013 ◽  
Vol 31 (4) ◽  
pp. 246-252 ◽  
Author(s):  
Jason D. Lattier ◽  
Darren H. Touchell ◽  
Thomas G. Ranney ◽  
Jeremy C. Smith
Keyword(s):  
In Vitro Rooting ◽  
Naphthaleneacetic Acid ◽  
Multiplication Rate ◽  
Ms Medium ◽  
Norway Maple ◽  
Future Improvement ◽  
Half Strength ◽  
Improvement Programs ◽  
Indole 3 Acetic Acid

Protocols were developed for micropropagation and induction of autopolyploids in a fastigiate cultivar of Norway maple (A. platanoides L. ‘Crimson Sentry’). Murashige and Skoog (MS) medium, woody plant medium (WPM), and Quoirin and Lepoivre medium were supplemented with 2 μM 6-benzylaminopurine (BA), meta-Topolin, 6-(γ,γ-dimethylallylamino) purine, kinetin, or thidiazuron to evaluate microshoot proliferation. Murashige and Skoog medium with 2 μM BA yielded the most microshoots (3.2) and longest microshoots (30.6 mm) per subsample after 5 weeks. The influence of BA concentration on proliferation was evaluated at 0, 2, 4, 8, or 16 μM. Optimal multiplication rate was achieved at 2 or 4 μM BA producing approximately 2.8 microcuttings per subsample after 5 weeks. To induce in vitro rooting, half-strength WPM was supplemented with 0, 5, 10, 20, 40, or 80 μM indole-3-butyric acid (IBA). Optimal in vitro rooting (70%), number of roots (2.5), and root length (15 mm) per subsample were achieved with 10 μM IBA after 8 weeks. To induce polyploidy, microcuttings were pretreated for 7 days on MS medium with 4 μM BA alone or combined with 1 μM IBA, indole-3-acetic acid (IAA), or 1-naphthaleneacetic acid prior to treatment in liquid MS medium containing 15 μM oryzalin for 3 days. Homogenous tetraploids were only obtained from shoots pretreated with IAA. This research provides optimized protocols for micropropagation and autopolyploid induction of A. platanoides ‘Crimson Sentry’ and demonstrates the development of tetraploid lines for use in future improvement programs.

PRELIMINARY STUDY ON IN VITRO PROPAGATION OF Macaranga tanarius (Mahang)

2015 ◽  
Vol 77 (24) ◽  
Author(s):  
Nazirah Abdullah ◽  
Nor Hasnida Hassan ◽  
Muhammad Fuad Yahya ◽  
Rosdi Koter ◽  
Siti Suhaila A. Rahman ◽  
...  
Keyword(s):  
Woody Plant ◽  
Basal Medium ◽  
Medium Size ◽  
Native Plant ◽  
High Quality ◽  
Surface Sterilization ◽  
Half Strength ◽  
Preliminary Study ◽  
Macaranga Tanarius

Macaranga tanarius locally known as Mahang, belongs to Euphorbiaceae family is a native plant in Malaysia. This invasive species is mostly found in disturbed forest. Macaranga genus is a medium size tree and can grow up to 24 m tall. Macaranga genus is a fast growing species, evergreen trees with soft and light wood. M. tanarius wood can be used to produce high quality particle board and pulp besides other usage as good firewood. Phytochemical studies on M. tanarius have discovered the presence of tannin that can be used as toughing agent on fishing net as well as dyeing agent. The leaves extract of this species have shown potential as an antioxidant when tested with 2, 2 – diphenyl-picrylhydrazyl (DPPH) anti-oxidant assay. Due to its benefits in multiple industries, production of sustainable and high quality planting material cannot be avoided. Tissue culture is one of the best approaches to meet this demand. In this preliminary study, surface sterilization protocol for M. tanarius using seed as explants has been developed. 3 different surface sterilization methods have been tested. Based on the percentage of contamination and response, the best method for surface sterilization of M. tanarius  is by using 30% of Chlorox® which produced more than 90% clean culture and the best response among other methods; swelling (38%), formation of roots (8%), shoots (2%) as well as minimum amount of damage tissues. Explants from germinated plantlets in vitro were further tested on four different basal medium to find the most suitable basal medium for M. tanarius growth which were full strength Woody Plant Media (WPM), half strength Woody Plant Media (½ WPM), Murashige and Skoog media (MS) and half strength Murashige and Skoog media (½ MS). Explants cultured on WPM basal medium produced healthy rooted plantlet in terms of size and colour of shoot and leaves. ½ WPM media can also induce rooting in M. tanarius whereas in MS and ½ MS media the explants turn to brown and died. For shoot multiplication experiment, WPM medium supplemented with different types of cytokinin; BAP and TDZ at different concentration have been tested. WPM medium supplemented with 0.1 mg/l TDZ showed the highest percentage of shoot induction with 100% shoot induced and average produces three new shoots per explants.

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