GROWTH OF ‘PRATA-ANA’ BANANA’S MICROSHOOTS CLONE GORUTUBA FROM SYNTHETIC SEEDS:SUBSTRATES AND BAP CONCENTRATION

ABSTRACT The banana crop stands out as an activity of great social and economic importance in Brazil, which occupies the fifth place in world production. Synthetic seed production is becoming promising for a micropropagation and in vitro conservation. The aim of the study was to analyze the conversion and growth of ‘Prata-anã’ banana’s microshoots clone Gorutuba from synthetic seed in MS medium and vermiculite, different substrates and concentrations of BAP (6-benzylaminopurine) associated with ANA (acetic naphthalene acid) in the constitution of its capsule were tested. The microshoots were immersed in the sodium alginate matrix (3%) and dripped in a solution of CaCl2.2H2O (100 mM) for complexation and then in KNO3 solution (100 mM) to decomplex. The experimental design was completely randomized in a 2 x 5 factorial design (substrate x BAP concentrations), containing different substrates (MS culture medium and vermiculite) and BAP concentrations (2.22, 4.44, 6.66, 8.88 and 13.32 µmol L-1) associated with NAA (naphthalene acetic acid) 0.54 µmol L-1, totaling 10 treatments, with 4 replicates, and that each replicate containing 5 seeds. The evaluations of conversion, number of leaves, leaf length, leaf height, number of roots, root length and oxidation were performed at 30 and 60 days.The use of the MS medium provided better growth results in relation to vermiculite as substrate, in which the different BAP concentrations did not differ from each other. It was found that, in MS culture medium, BAP concentrations above 8.88 µmol L-1 in the capsule composition are not indicated for microshoots growth.

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Callus Induction and Shoot Formation for Mexican Red Bean (Phaseolus vulgaris L.) Pinto Cultivar in Vitro

Iraqi Journal of Science ◽

10.24996/ijs.2020.61.8.5 ◽

2020 ◽

pp. 1887-1893

Author(s):

Rasha K. Mohammed Al-Saedi ◽

Ansam G. Abdulhalem

Keyword(s):

Growth Regulators ◽

Culture Medium ◽

Shoot Formation ◽

Naphthalene Acetic Acid ◽

Ms Medium ◽

Phaseolus Vulgaris L ◽

Different Types ◽

Red Bean ◽

Internode Explants

The current study aimed to adopt a method for inducing callus cells and regenerating the important common red bean using different types of growth regulators such as N6-benzylaminopurine (BAP), Naphthalene acetic acid (NAA), and Thidiazuron (TDZ). Different types of common bean pinto cultivar explants, such as internodes, cotyledons and roots, were inoculated on Murashige and Skoog medium (MS) provided with different combinations of plant growth regulators, including 1- BAP (5 mg/l) 2-BAP (4.5 mg/l) NAA (0.5 mg/l), 3- BAP (4.5 mg/l), and TDZ (0.1mg/l). Callus was initiated on MS culture medium supplied with 5 mg/l BAP for all explants (internodes, cotyledons, and roots) at 50, 20, and 10% respectively, while adding NAA with 0.5mg/l showed a low percentage of callus (30%) only in the internode explants. Optimum results were obtained by growing the internodes on MS medium with 4.5 mg/l BA and either 0.5 mg/l NAA or 0.1 mg/l TDZ, transplanting the derived shoots into internodes and cotyledons with 70 and 10% respectively. This study concludes that the internodes as explants have the best growth results.

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In Vitro Shoot Regeneration and Development of Microcorms of Moroccan Saffron (Crocus sativus L.)

Atlas Journal of Plant Biology ◽

10.5147/ajpb.v0i0.113 ◽

2017 ◽

pp. 50-55

Author(s):

Khalid Lagram ◽

Mohamed Ben El Caid ◽

Souad El Aaouam ◽

Mohamed Lachheb ◽

Abdelhamid El Mousadik ◽

...

Keyword(s):

In Vitro Culture ◽

Culture Medium ◽

Crocus Sativus ◽

Induction Medium ◽

Naphthalene Acetic Acid ◽

Ms Medium ◽

Male Sterile ◽

Indirect Organogenesis ◽

Crocus Sativus L

Crocus sativus L. is a male sterile vegetatively propagated plant. Its flower produces stigmas that when dried, constitute the source of a spice commonly known as Saffron. Slow vegetative propagation and diseases limit the production and the development of saffron. “In vitro” culture could be an effective method to overcome these limitations by improving the quantity and the quality of the planting materials. In this work, Crocus sativus L. segments corms of cultivar from the region of Taliouine (Southeast of Morocco) were used for the propagation through indirect organogenesis. To optimize the in vitro growth conditions, we have used the Murashige and Skoog medium (MS medium), supplemented with 2.4-dichlorophenoxyacetic acid (2.4-D) and with 6-benzylaminopurin (BAP) at combination of various concentrations. Our results showed the formation of callus in 85.42% of explants that grow in a culture medium supplemented with 2,4-D combined with BAP, at a concentration of 1mg/l each. In addition, we observed that increasing the concentration of BAP in the culture medium to 1.5mg/l improved the rate of shoots initiation (0.81). In the meantime, we noted that a combination of BAP (8mg/l) and Naphthalene acetic acid (NAA; 2mg/l) has significantly improved the rate of the formation of advanced shoots (6.65). Finally, the shoots that developed were transferred to an induction medium of roots and corms. As a result, we observed that 50% of shoots tested in ½ MS medium supplemented with 2.4-D and of BAP (1 mg/l each) and 5% sucrose, formed corms. Our study provides a first database for in vitro culture of Moroccan saffron cultivars.

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In vitro morphogenic response from zygotic embryos of Genipa americana

Ciência Rural ◽

10.1590/0103-8478cr20161028 ◽

2017 ◽

Vol 47 (10) ◽

Author(s):

Annie Carolina Araújo de Oliveira ◽

Caroline de Araújo Machado ◽

Leila Albuquerque Resende de Oliveira ◽

Ana Veruska Cruz da Silva ◽

Ana da Silva Lédo

Keyword(s):

Acetic Acid ◽

In Vitro Regeneration ◽

Shoot Length ◽

Naphthalene Acetic Acid ◽

Zygotic Embryos ◽

Ms Medium ◽

Morphogenic Response ◽

Number Of Leaves

ABSTRACT: The aim of this study was to evaluate the in vitro morphogenic potential of genipap (Genipa americana L.) zygotic embryos. Seeds obtained from ripe fruits had their zygotic embryos excised and inoculated in MS medium with 4.44µM of 6-benzylaminopurine (BAP) and supplemented with 0.0; 1.07; 2.14 and 3.21µM of naphthalene acetic acid (NAA). The potential of explants regeneration and the shoot length and number of leaves in plantlets were evaluated. The in vitro regeneration of genipap is possible from the conversion of zygotic embryos in a MS medium with 4.44µM BAP supplemented with 3.21µM NAA.

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Pengaruh Konsentrasi Zat Pengatur Tumbuh Naphthalene Acetic Acid dan Benzil Amino Purin terhadap Pertumbuhan Protokorm Anggrek Dendrobium spectabile pada Kultur In Vitro

Paspalum: Jurnal Ilmiah Pertanian ◽

10.35138/paspalum.v7i1.107 ◽

2019 ◽

Vol 7 (1) ◽

pp. 16

Author(s):

Ujang Siron ◽

Noertjahyani Noertjahyani ◽

Yana Taryana ◽

Romiyadi Romiyadi

Keyword(s):

Research Method ◽

Dry Weight ◽

Naphthalene Acetic Acid ◽

Ms Medium ◽

Randomized Design ◽

Two Factors ◽

Number Of Leaves ◽

Completely Randomized Design ◽

Medium Culture

The aim of the article is to study the interaction effect between NAA and BAP concentration on protocorm growth and to know the proper concentration for growth of Dendrobium spectabile orchid protocorm. This research method using an experimental method which is conducted in the Laboratory of Agriculture Faculty of Winaya Mukti University, Tanjungsari Subdistrict, Sumedang District. The experiment was conducted from June 2017 until September 2017. The experiment used was a Completely Randomized Design (CRD) with the factorial pattern, consisting of two factors and repeated twice. the first factor was the effect of NAA concentration which consisted of five levels, namely without NAA, 0.5 mg kg-1, 1.0 mg kg-1, 1.5 mg kg-1, and 2.0 mg kg-1. The second factor is the BAP concentration which consists of five levels, namel without BAP, 1.0 mg kg-1, 2.0 mg kg-1, 3.0 mg kg-1, and 4.0 mg kg-1. Eksplant is protocorm from orchid D. spectabile which is grown on MS medium (Murashig and Skoog) half recipe as base medium accompanied by each treatment for 12 weeks. The experimental results show that there is an interaction between the effect of NAA and BAP concentration on the number of leaves only. Without NAA or 1.5 mg kg-1 NAA concentration with BAP 2.0 mg kg-1 gives more leaves. Independent of NAA or BAP concentrations did not affect the number of buds, number of roots, root length, fresh and dry weight of plantlets, and also growth ability of plantlets. BAP concentration only affect plant height, and the highest plantlet height is found without add of BAP in medium culture

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An effective protocol for improved regeneration capacity of Kabuli chickpeas

Canadian Journal of Plant Science ◽

10.4141/cjps2011-196 ◽

2012 ◽

Vol 92 (6) ◽

pp. 1057-1064 ◽

Cited By ~ 2

Author(s):

I. S. Yadav ◽

N. P. Singh

Keyword(s):

Shoot Regeneration ◽

Culture Medium ◽

Genetic Manipulation ◽

In Vitro Regeneration ◽

Naphthalene Acetic Acid ◽

Ms Medium ◽

Regeneration Capacity ◽

Regeneration System ◽

Embryonic Axes

Yadav, I. S. and Singh, N. P. 2012. An effective protocol for improved regeneration capacity of Kabuli chickpeas. Can. J. Plant Sci. 92: 1057–1064. An efficient protocol for in vitro regeneration is essential for genetic manipulation and micro-propagation of important plant species. A direct shoot regeneration system has been optimized for Desi chickpeas, but an effective regeneration protocol is still needed for Kabuli chickpeas. An efficient regeneration protocol for Kabuli chickpeas was developed, using whole embryonic axes, an embryonic axes slice and cotyledonary node explants from two genotypes L550 and JGK-1. Depending upon chickpea genotype, type of explant and culture medium, percentage of shoot producing explants (frequency) and the number of shoots per explant (efficiency) varied from 10 to 83% and from 1 to 58, respectively. The shoot regeneration capacity (SRC=frequency×efficiency), which is an indicator of the effectiveness of the protocol, varied from 47 to 2508 shoots per 100 explants cultured. On average, SRC of L550 was 1.8 times higher than JGK-1. Murashige and Skoog's (MS) medium+B5 vitamins supplemented with 8.0 µM benzyl amino purine (BAP)+0.5 µM α- naphthalene acetic acid (NAA) and 0.1 M sucrose plus embryonic axes was found to be the most effective culture medium and type of explants, respectively. Half strength MS medium+2% sucrose supplemented with 4 µM NAA, 3µ M IAA or 4µM IAA produced a high rooting percentage in both chickpea genotypes. The regeneration process starting from explant preparation to establishment of a complete plant in soil took 105–110 d. This optimized regeneration method holds promise for facilitating the insertion of interested genes through genetic transformation for improvement of Kabuli chickpeas.

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RESPONSE OF Cattleya forbesii ORCHID TO INCREASING SILICON CONCENTRATIONS IN VITRO

Revista Caatinga ◽

10.1590/1983-21252016v29n103rc ◽

2016 ◽

Vol 29 (1) ◽

pp. 18-24 ◽

Cited By ~ 4

Author(s):

RONAN CARLOS COLOMBO ◽

VANESSA FAVETTA ◽

RICARDO TADEU DE FARIA ◽

FELIPE ARANHA DE ANDRADE ◽

VANDERLI MARINO MELEM

Keyword(s):

Culture Medium ◽

Culture Media ◽

Average Length ◽

Ms Medium ◽

In Vitro Growth ◽

Shoot Height ◽

Leaf Tissues ◽

Number Of Leaves ◽

Scanning Electron

ABSTRACT: Addition of Silicon (Si) to culture media has been shown to improve the development of seedlings grown in vitro, and to reduce losses during the acclimatization phase. The objective of this study was to evaluate the in vitro growth of Cattleya forbesii (Orchidaceae) in MS medium containing five different concentrations of SiO2 (0.0, 0.5, 1.0, 1.5, and 2.0 g·L−1). At day 200, the following variables were measured: number of roots, average length of the root system, leaf area, number of leaves and shoots, shoot height, fresh and dry masses of roots and shoots, water content of roots and shoots, and pH of the culture medium. Most variables decreased as the concentration of Si increased, reducing the in vitro vegetative growth of C. forbesii. Accumulation of Si in leaf tissues was detected by scanning electron microscopy, confirming uptake by plants. The Si source and concentrations tested showed no beneficial effect on in vitro growth of C. forbesii.

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Multiplicação de anador (Justicia pectoralis) in vitro

Revista Verde de Agroecologia e Desenvolvimento Sustentável ◽

10.18378/rvads.v11i3.3986 ◽

2016 ◽

Vol 11 (3) ◽

pp. 159 ◽

Cited By ~ 1

Author(s):

Rômulo Magno Oliveira Freitas ◽

Narjara Walessa Nogueira ◽

Sidney Carlos Praxedes

Keyword(s):

Plant Material ◽

In Vitro Propagation ◽

Culture Medium ◽

Culture Media ◽

Statistical Design ◽

The Other ◽

Nodal Segments ◽

Ms Medium ◽

Number Of Leaves

O trabalho teve como objetivo desenvolver um protocolo de micropropagação de segmentos nodais de anador (Justicia pectoralis). Para isso foram realizados dois experimentos. O delineamento estatístico utilizado foi o inteiramente casualizado, com 15 repetições. Os segmentos de J. pectoralis, após desinfestados, foram cultivados em meio MS durante 30 dias. No primeiro experimento, esse material foi repicado em três meios de cultura (MS, WPM e B5) e após 77 dias foram avaliados comprimento de plântula, número de raízes, número de folhas e o número de segmentos nodais. Para o segundo experimento foram testadas duas citocininas (BAP e Cinetina) nas seguintes dosagens 0,0; 0,5; 5,0 e 20,0 mM. Aos 60 dias após a repicagem foram avaliadas as seguintes características: números de folhas, número de raízes e número de explantes por planta. O meio MS foi o que apresentou maior comprimento de plântula. As demais variáveis não diferiram entre os meios utilizados. Por isso o meio MS foi utilizado para o segundo experimento onde se verificou que a utilização de BAP proporcionou maior número de folhas e de explantes quando submetido à concentração de 20 mM. Dessa forma, para multiplicação de seg Justicia pectoralis, recomenda-se a utilização de meio MS com adição de 20mM de BAP.In vitro propagation of Justicia pectoralisAbstract: The study aimed to establish a micropropagation protocol for Justicia pectoralis nodal segments. Two experiments were conducted. The statistical design was the completely randomized with 15 repetitions. After disinfestation, the segments of J. pectoralis were inoculated in the MS culture medium for 30 days. In the first experiment, the plant material was transferred to three culture media (MS, WPM and B5). The length of seedlings, number of roots, number of leaves, and number of nodal segments were evaluated at 77 days after transferring. In the second experiment two cytokinins (BAP and Kinetin) were tested in the following concentrations: 0.0; 0.5; 5.0 and 20.0 mM. At 60 days after transplanting the number of leaves, number of roots and number of explants per plant were evaluated. The MS medium induced the highest length of seedlings, but there was no effect for the other variables. Therefore, this medium was used for the second experiment, when it was found that BAP induced a larger number of leaves and explants when applied at 20 mM. Therefore, for multiplying J. pectoralis nodal segments we recommend the use of MS medium with 20 mM BAP.

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Herbicidal potential of Araucaria angustifolia (Bertoloni) Otto Kuntze in lettuce seedlings in vitro

Revista Agrogeoambiental ◽

10.18406/2316-1817v12n220201429 ◽

2020 ◽

Vol 12 (2) ◽

Author(s):

Nayara Clarete da Penha ◽

Priscila Pereira Botrel ◽

Jéssica Azevedo Batista

Keyword(s):

Culture Medium ◽

Herbicidal Activity ◽

Ms Medium ◽

Araucaria Angustifolia ◽

Lettuce Seedling ◽

Extract Concentration ◽

Ethanolic Extracts ◽

Number Of Leaves ◽

Mortality Percentage

Araucaria angustifolia (Bertoloni) Otto Kuntze plants are a viable source of potentially active secondary metabolites; however, deep studies and researches about the activity of these compounds are needed. The objective of this work was to assess the herbicidal activity of ethanolic extracts of plants of the species A. angustifolia in lettuce seedlings in vitro. Ethanolic extracts at different concentrations (0,0%, 12.5%, 25.0%, 50.0%, and 100.0%) were prepared using barks and leaves. A semisolid MS medium with pH adjusted to approximately 5.7 was prepared, solidified with 8g L-1 of agar, and autoclaved at 1.6atm for 20 minutes. The extracts were added to the culture medium during their preparation before the autoclaving, using an automatic pipette containing 0.1mL of A. angustifolia extract per lettuce seedling. The number of leaves per seedling, seedling height, chlorophyll content, root and shoot dry weights, and mortality percentage was determined at 20 days after inoculation. The results showed that the extract from leaves or barks of A. angustifolia plants has herbicidal activity in lettuce seedlings in vitro, and the extract concentration of 100% presented the best inhibitory results for the variables evaluated.

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Influence of growth regulators and explants on shoot regeneration in carnation

Horticultural Science ◽

10.17221/1/2009-hortsci ◽

2009 ◽

Vol 36 (No. 4) ◽

pp. 140-146 ◽

Cited By ~ 4

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 Dianthus caryophyllus 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.

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MODIFICAÇÕES NO MEIO DE CULTURA, FOTOPERÍODO E TEMPO DE CULTIVO AFETAM O ALONGAMENTO E ENRAIZAMENTO IN VITRO DE BANANEIRA CV. PACOVAN

Nativa ◽

10.31413/nativa.v6i1.4731 ◽

2018 ◽

Vol 6 (1) ◽

pp. 27

Author(s):

Marcos Vinícius Marques Pinheiro ◽

Ana Cristina Portugal Pinto De Carvalho ◽

Fabrina Bolzan Martins

Keyword(s):

Plant Height ◽

Culture Medium ◽

Culture Media ◽

Dry Weight ◽

Salt Mixture ◽

Musa Spp ◽

Fresh Biomass ◽

Shoot Dry Weight ◽

Number Of Leaves

No intuito de elevar as taxas de sobrevivência durante a etapa de aclimatização e posterior plantio a campo, avaliou-se o enraizamento in vitro de bananeira cv. Pacovan, em diferentes concentrações de sais MS e de sacarose. Utilizou-se DIC, esquema fatorial (6x2x3), com seis meios de cultura [sendo três concentrações de nutrientes do meio MS (100%; 50% de macronutrientes; e 50% dos sais macro e micronutrientes), e duas concentrações de sacarose (1,5/3,0%)], dois fotoperíodos (12/16 h) e três tempos de cultivo (21, 28 ou 35 dias) e seis repetições/tratamento. Analisaram-se: altura da planta, número de folhas/planta, massas frescas e secas das partes aérea e radicular. Para altura da planta, massa fresca da parte aérea e radicular, o meio MS 50% dos sais + sacarose (1,5%) com fotoperíodo de 16 h e tempo de cultivo de 35 dias foi satisfatório. Para massa seca da parte aérea foi MS 50% de sais + sacarose (3%), e para massa seca da parte radicular, MS 100% + sacarose (3%) (em 12hs/28 dias e 16hs/21 dias). Para o alongamento/enraizamento in vitro da bananeira cv. Pacovan sugere-se MS 50% de sais (macro e micronutrientes), redução ou manutenção de sacarose (1,5 ou 3%) em 16h/35 dias de cultivo.Palavra-chave: Musa spp., propagação in vitro, sistema radicular. CHANGES IN CULTURE MEDIUM, PHOTOPERIOD AND TIME OF CULTIVATION AFFECT THE IN VITRO ELONGATION AND ROOTING OF BANANA CV. PACOVAN ABSTRACT:In order to achieve high rates of survival during the acclimatization and later planting in the field, was evaluated the in vitro of banana cv. Pacovan plants under different concentrations of sucrose and MS basal salt mixture. The experiment was assembled in a DIC, in 6x2x3, six different culture media [three different MS salt mixture concentrations (100%; 50% of macronutrients; and 50% of macro/micronutrients) and two sucrose concentrations (1.5/3%)], two photoperiods (12/16 hours) and three cultivation times (21, 28 or 35 days). Each treatment was composed by 6 replicates. Plant height, number of leaves/plant, fresh and dry weight of roots and shoots, were analyzed. Satisfactory results for plant height and shoot and root fresh biomass were observed in MS with macro/micronutrients (50%) + sucrose (3%), 16 hours/35 days. The highest values of shoot dry weight were observed in MS with macro/micronutrients (50%) + sucrose (3%); the highest root dry weight was achieved with MS 100% + sucrose (3%) (12hs/28 and 16hs/21 days). The suggested medium for the in vitro elongation and rooting stage of banana cv. Pacovan is the MS with 50% of salts (macro and micronutrients), reduction or maintenance of sucrose (1.5 or 3%) in 16h/35 days of cultivation.Keywords: Musa spp., in vitro propagation, root system. DOI:

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