scholarly journals TISSUE CULTURE MULTIPLICATION OF Paphiopedilum insigne DEPENDING ON THE MEDIUM TYPE, GROWTH REGULATORS AND NATURAL SUPPLEMENTS

2021 ◽  
Vol 20 (4) ◽  
pp. 125-134
Author(s):  
Monika Poniewozik ◽  
Paweł Szot ◽  
Marzena Parzymies
Keyword(s):  
Tissue Culture ◽  
Growth Regulators ◽  
Casein Hydrolysate ◽  
Biologically Active ◽  
Fast Method ◽  
Multiplication Rate ◽  
Ms Medium ◽  
Interior Decoration ◽  
Medium Type

Paphiopedilum is an ornamental orchid used mainly for interior decoration. As the division of plants is uneconomical, a fast method of propagation is needed. The aim of this study was to evaluate the influence of medium type (MS or VW), growth regulators, i.e. BA, KIN, TDZ used separately or in combinations and natural additives, i.e. coconut water, banana pulp, casein hydrolysate, on Paphiopedilum insigne plantlets grown in vitro. It was found out that BA in concentration of 0.5 mg·dm–3 allowed to obtain the highest multiplication rate (2.92), however the use of KIN in concentration of 1 mg·dm–3 resulted in formation of bigger and higher quality plantlets, It is possible to replace cytokinins with other biologically active substance, such as banana pulp. The 1/2 MS medium might be used for Paphiopedilum insigne tissue culture, as there was no difference in terms of multiplication rate and the obtained plantlets were of better quality, especially that it is cheaper and easier to prepare.

scholarly journals IMPACT OF GROWTH REGULATORS ON IN VITRO GROWTH OF BANANA (MUSA SPP) CULTURED: A REVIEW

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Katkam Priyanka
Keyword(s):  
Tissue Culture ◽  
Plant Growth ◽  
Plant Growth Regulators ◽  
Growth Regulators ◽  
Multiplication Rate ◽  
Ms Medium ◽  
In Vitro Growth ◽  
Musa Spp ◽  
Micro Propagation

Banana is important fruit crop in horticulture where it propagates through suckers which takes immense time for production and with low multiplication rate, to overcome these type of situation some protocols have been made such as the micro propagation where the tissue culture of banana is applied with help of plant growth regulators such as auxins and cytokinins are used at different concentration to attain the definite good results till now many studies had been done in the tissue culture of banana. In the present study it was observed that the explants cultured in MS medium containing 4 mg/l BAP + 0.5 mg/l IAA had highest number of shoot buds and number of shoots. Similar result was studied by Muhammad et al. (2007) where the highest multiplication ratio was observed at 4 mg/l BAP along with 1 mg/l IAA. Habiba et al. (2002) and Ahmed et al. (2014) reported that 4 mg/l BAP in combination with 2 mg/l IAA shown remarkable results.

scholarly journals 664 PB 104 AGROBACTERIUM INFECTION OF WHITE ASH (FRAXINUS AMERICANA L.)

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 528a-528
Author(s):  
Sharon A. Bates ◽  
John E. Preece ◽  
John H. Yopp
Keyword(s):  
Tissue Culture ◽  
Plant Growth ◽  
Growth Regulators ◽  
Callus Formation ◽  
High Humidity ◽  
Ms Medium ◽  
Gall Formation ◽  
White Ash ◽  
Seedling Explants

Both greenhouse-grown white ash plants derived from tissue culture and rooted microshoots in high humidity trays were inoculated with 11 tumor-inducing Agrobacterium strains. Eight strains stimulated mutative gall formation. Plants inoculated with strain A281 exhibited a higher frequency of callus formation (greenhouse-22.2%; microshoots-18.8%) than other strains at the site of the wound. Therefore, strain A281 was used to inoculate seed and seedling explants in vitro. Explants were placed on MS medium containiner no plant growth regulators and inoculated at 0, 3, 5, 7, or 10 days after initiation. Plants inoculated at 10 days showed a higher frequency of callus formation (16.4%) than with earlier inoculations. Also, rewounding of the explant at inoculation resulted in a higher frequency of callus formation (11.3%) compared to not rewounding the explant (3.9%).

scholarly journals 901 PB 538 STUDIES ON PROPAGATION OF GLOBE ARTICHOKE THROUGH TISSUE CULTURE TECHNIQUE

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 563b-563 ◽  
Author(s):  
Kh. A. Okasha ◽  
M. E. Ragab
Keyword(s):  
Tissue Culture ◽  
Culture Technique ◽  
Multiplication Rate ◽  
Globe Artichoke ◽  
Ms Medium ◽  
Free Living ◽  
Survival Percentage ◽  
Aseptic Culture ◽  
Low Rate

The aim of this study was to establish an effective method of micropropagation of globe artichoke from shoot-hp. This study involved establishment of an aseptic culture. multiplication of proliferated shook, rooting of these shook in vitro and adaptation of plantlets for free living Highest survival percentage with no contamination was achieved after sterilizing the explants with 70% ethanol (5 Sec.) + 1.5 % sodium hypochlorite for 20 min. The bast results of preventing browning of explants were obtained with 100 mg/1 ascorbic acid. The highest proliferated shook were obtained when shoot tip with 4 mm length (taken in mid March) were cultured on MS medium with 10mg/1 Kin. + 0.5 mg/l IAA. The highest multiplication rate was obtained when recultured on MS medium supplemented with 5 mg/1 Kin. + 0.5 mg/1 IAA. Multiplication rate gradually increased with increasing number of subculturing till Me third subculture but subsequent subculture (4th subculture) had a low rate.

scholarly journals Micropropagation of the Narrow Endemic Hladnikia pastinacifolia (Apiaceae)

2016 ◽  
Vol 75 (2) ◽  
pp. 244-252 ◽  
Author(s):  
Jana Ambrožič-Dolinšek ◽  
Terezija Ciringer ◽  
Mitja Kaligarič
Keyword(s):  
Tissue Culture ◽  
Growth Regulators ◽  
Ex Situ ◽  
Distribution Area ◽  
Ms Medium ◽  
Axillary Shoots ◽  
Culture Techniques ◽  
Narrow Endemic ◽  
Propagation Methods

Abstract The monotypic Hladnikia pastinacifolia Rchb. is a narrow endemic species, with an extremely small distribution area in Slovenia, prone to any kind of threat that could lead to species extinction. Tissue culture techniques are proposed as a conservation measure for rapid propagation and ex-situ conservation. Tissue culture was initiated from seeds and juvenile plants obtained from natural sites on a solid Murashige and Skoog (MS) medium, with and without growth regulators. We tested various combinations and concentrations of growth regulators, and the best proliferation of axillary shoots, on average 14, was obtained on MS medium with 5 μM BAP and 3 μM IBA and 3% sucrose. Rooting was achieved after transferral of the shoots to an MS medium with 2 μM IBA and 3% sucrose. The rooted plants were acclimatized on a mixture of limestone sand, potting soil and vermiculite in a ratio of 10:2:2, with pH in the range of 7.5–8.0. In vitro propagation methods provide an important opportunity for the propagation and preservation of H. pastinacifolia by rapidly increasing the number of plants, without disturbing the wild population.

scholarly journals Plant regeneration from petiole segments of some species in tissue culture

2013 ◽  
Vol 34 (1) ◽  
pp. 5-28 ◽  
Author(s):  
Krystyna Klimaszewska
Keyword(s):  
Tissue Culture ◽  
Plant Regeneration ◽  
Growth Regulators ◽  
Regeneration Ability ◽  
Ms Medium ◽  
Hedera Helix ◽  
Coleus Blumei ◽  
Hibiscus Rosa Sinensis ◽  
Plant Groups

The regeneration ability of 21 plant species belonging to 14 families was tested. The method of tissue culture in vitro was applied, on basic MS medium with an addition of growth regulators from the auxin and cytokinin groups. From among the investigated plant groups <i>Peperomia scandens</i> and <i>Caladium</i> × <i>hortulanum</i> were capable of plant regeneration, <i>Passiilora coerulea</i> regenerated shoots, <i>Hedera helix, Begonia glabra, Coleus blumei, Fuchsia hybrida, Passiflora suberosa </i>and <i>Peperomia eburnea</i> formed callus and roots, <i>Kalanchoe blossfeldiana, Pelargonium grandiflorum, P. peltatum, P. radula, Coleus shirensis</i> and <i>Magnolia soulangeana</i> produced callus, <i>Philodendron scandens, Rhododendron smirnovii, Hibiscus rosa-sinensis, Coprosma baueri, Cestrum purpureum</i> and <i>Solanum rantonnetii</i> did not exhibit any regeneration reactions.

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 Alterations in Microrhizome Induction, Shoot Multiplication and Rooting of Ginger (Zingiber officinale Roscoe) var. Bentong with Regards to Sucrose and Plant Growth Regulators Application

Agronomy ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 320
Author(s):  
Nisar Ahmad Zahid ◽  
Hawa Z.E. Jaafar ◽  
Mansor Hakiman
Keyword(s):  
Plant Growth ◽  
Plant Growth Regulators ◽  
Growth Regulators ◽  
Zingiber Officinale ◽  
Naphthaleneacetic Acid ◽  
Ms Medium ◽  
Zingiber Officinale Roscoe ◽  
Planting Materials ◽  
Disease Free

Ginger (Zingiber officinale Roscoe) var. Bentong is a monocotyledon plant that belongs to the Zingiberaceae family. Bentong ginger is the most popular cultivar of ginger in Malaysia, which is conventionally propagated by its rhizome. As its rhizomes are the economic part of the plant, the allocation of a large amount of rhizomes as planting materials increases agricultural input cost. Simultaneously, the rhizomes’ availability as planting materials is restricted due to the high demand for fresh rhizomes in the market. Moreover, ginger propagation using its rhizome is accompanied by several types of soil-borne diseases. Plant tissue culture techniques have been applied to produce disease-free planting materials of ginger to overcome these problems. Hence, the in vitro-induced microrhizomes are considered as alternative disease-free planting materials for ginger cultivation. On the other hand, Bentong ginger has not been studied for its microrhizome induction. Therefore, this study was conducted to optimize sucrose and plant growth regulators (PGRs) for its microrhizome induction. Microrhizomes were successfully induced in Murashige and Skoog (MS) medium supplemented with a high sucrose concentration (>45 g L−1). In addition, zeatin at 5–10 µM was found more effective for microrhizome induction than 6-benzylaminopurine (BAP) at a similar concentration. The addition of 7.5 µM 1-naphthaleneacetic acid (NAA) further enhanced microrhizome formation and reduced sucrose’s required dose that needs to be supplied for efficient microrhizome formation. MS medium supplemented with 60 g L−1 sucrose, 10 µM zeatin and 7.5 µM NAA was the optimum combination for the microrhizome induction of Bentong ginger. The in vitro-induced microrhizomes sprouted indoors in moist sand and all the sprouted microrhizomes were successfully established in field conditions. In conclusion, in vitro microrhizomes can be used as disease-free planting materials for the commercial cultivation of Bentong ginger.

scholarly journals Influence of growth regulators and explants on shoot regeneration in carnation

2009 ◽  
Vol 36 (No. 4) ◽  
pp. 140-146 ◽  
Author(s):  
J.K. Kanwar ◽  
S. Kumar
Keyword(s):  
Acetic Acid ◽  
Shoot Regeneration ◽  
Growth Regulators ◽  
Dianthus Caryophyllus ◽  
Naphthalene Acetic Acid ◽  
Ms Medium ◽  
Shoot Bud ◽  
Dichlorophenoxy Acetic Acid ◽  
Number Of Shoots

The influence of growth regulators, explants and their interactions on in vitro shoot bud formation from callus was studied in <I>Dianthus caryophyllus</I> L. The leaf and internode explants were cultured on Murashige and Skoog (MS) medium containing different concentrations of growth regulators. The highest callus induction was observed with 2 mg/l 2,4-dichlorophenoxy acetic acid (2,4-D) and 1 mg/l benzyl adenine (BA). Out of twenty seven shoot regeneration media tested, only 2 mg/l thidiazuron (TDZ) and zeatin alone or in combination with naphthalene acetic acid (NAA) and/or indole acetic acid (IAA) could differentiate calli. The highest average number of shoots was observed with 2 mg/l TDZ and 1 mg/l IAA. Significant differences were observed in calli producing shoots and number of shoots per callus in the explants of leaf and internode. The shoots were elongated and multiplied on MS medium supplemented with 1 mg/l BA and solidified with 1% agar. The shoots were rooted and hardened with 76% survival success in pots after six weeks of transfer to the pots.

scholarly journals The Effect of Plant Growth Regulators on Callus Induction and Regeneration of Amygdalus communis

2011 ◽  
Vol 3 (3) ◽  
pp. 97-100
Author(s):  
Naimeh SHARIFMOGHADAM ◽  
Abbas SAFARNEJAD ◽  
Sayed Mohammad TABATABAEI
Keyword(s):  
Tissue Culture ◽  
Plant Growth ◽  
Plant Growth Regulators ◽  
Growth Regulators ◽  
Base Material ◽  
Culture Technique ◽  
Induction Medium ◽  
Root Induction ◽  
Amygdalus Communis

The Almond (Amygdalus communis) is one of the most important and oldest commercial nut crops, belonging to the Rosaceae family. Almond has been used as base material in pharmaceutical, cosmetic, hygienically and food industry. Propagation by tissue culture technique is the most important one in woody plants. In the current research, in vitro optimization of tissue culture and mass production of almond was investigated. In this idea, explants of actively growing shoots were collected and sterilized, then transferred to MS medium with different concentrations and combinations of plant growth regulators. The experiment was done in completely randomized blocks design, with 7 treatment and 30 replications. After 4 weeks, calli induction, proliferation, shoot length and number of shoot per explants were measured. Results showed that the best medium for shoot initiation and proliferation was MS + 0.5 mg/l IAA (Indol-3-Acetic Acid) + 1 mg/l BA (Benzyl Adenine). Autumn was the best season for collecting explants. The shoots were transferred to root induction medium with different concentrations of plant growth regulators. The best root induction medium was MS + 0.5 mg/l IBA (Indol Butyric Acid).

scholarly journals In-Vitro Seed Germination and Effect of Growth Regulators on Subsequent Development of Protocorms of Eulophia Nuda Lindl

2015 ◽  
Vol 3 (2) ◽  
pp. 243-247 ◽  
Author(s):  
Varsha Dawande ◽  
Rajaram Gurav
Keyword(s):  
Seed Germination ◽  
Root Growth ◽  
Growth Regulators ◽  
Subsequent Development ◽  
Ms Medium ◽  
Asymbiotic Seed Germination ◽  
Endangered Orchid ◽  
Maximum Root ◽  
Regenerated Plantlets

Asymbiotic seed germination of Eulophia nuda Lindl. was observed on Knudson C medium. About 90% seeds germinated within 8-10 weeks and formed green protocorms in 11-12 weeks. Effect of BA and IBA was studied on plantlet development from protocorms. BA shows the best results with respect to number and length of shoots. Maximum number (6.45±1.36) and length (3.90±0.99) was observed on MS medium supplemented with 4.44μM.BA. Maximum root growth was also observed on same medium (4.8±0.99 number of roots and 1.43±0.13cm length). The regenerated plantlets were successfully acclimatized and transferred to earthen pots. The results presented here show that in vitro seed germination and plantlet development in Eulophia nuda Lindl., an endangered orchid, can be achieved at a higher rate by this method.Int J Appl Sci Biotechnol, Vol 3(2): 243-247 DOI: http://dx.doi.org/10.3126/ijasbt.v3i2.12476   

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