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Zeatin</title> <meta name="description" content="Search results for: Zeatin"> <meta name="keywords" content="Zeatin"> <meta name="viewport" content="width=device-width, initial-scale=1, minimum-scale=1, maximum-scale=1, user-scalable=no"> <meta charset="utf-8"> <link href="https://cdn.waset.org/favicon.ico" type="image/x-icon" rel="shortcut icon"> <link href="https://cdn.waset.org/static/plugins/bootstrap-4.2.1/css/bootstrap.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/plugins/fontawesome/css/all.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/css/site.css?v=150220211555" rel="stylesheet"> </head> <body> <header> <div class="container"> <nav class="navbar navbar-expand-lg navbar-light"> <a class="navbar-brand" href="https://waset.org"> <img src="https://cdn.waset.org/static/images/wasetc.png" alt="Open Science Research Excellence" title="Open Science Research Excellence" /> </a> <button class="d-block d-lg-none navbar-toggler ml-auto" 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class="input-group"> <i class="fas fa-search"></i> <input type="text" class="search-query" name="q" placeholder="Author, Title, Abstract, Keywords" value="Zeatin"> <input type="submit" class="btn_search" value="Search"> </div> </div> </form> </div> </div> <div class="row mt-3"> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 8</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: Zeatin</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">8</span> Anatomy Study of Seeds of Calligonium comosum in Vitro</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abobkar%20Saad">Abobkar Saad</a>, <a href="https://publications.waset.org/abstracts/search?q=Qasmia%20Abdalla"> Qasmia Abdalla</a>, <a href="https://publications.waset.org/abstracts/search?q=Fatma%20Emhemed"> Fatma Emhemed</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Eighty-four of Calligonum comosum were cultured on Murashige and Skoog medium on every combination supplemented with different concentrations of IAA, BA, Zeatin, and GA3. When 84 seeds were inoculated on MS free hormones, different types of cells contain dense cytoplasm were observed ater 23 days and long thick wall cells arranged in layers. In case of using MS +BA(0.5mg/L), different types and shapes of parenchyma cells contain dense cytoplasm were detected after four weeks. In the case of using MS + BA(1mg/L) + GA3 (3mg/L), thick wall parenchyma cells contain dense cytoplasm after 19 days, but many layers of parenchyma cells contain dense cytoplasm after 28 days. When MS +kin(0.5mg/L) a thick cells wall as Sclereids were observed after 29 days. No any response were observed on Zeatin (0.5, 1 mg/L). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=anatomy" title="anatomy">anatomy</a>, <a href="https://publications.waset.org/abstracts/search?q=Calligonum%20comosum" title=" Calligonum comosum"> Calligonum comosum</a>, <a href="https://publications.waset.org/abstracts/search?q=in%20vitro" title=" in vitro"> in vitro</a>, <a href="https://publications.waset.org/abstracts/search?q=aeeds" title=" aeeds"> aeeds</a> </p> <a href="https://publications.waset.org/abstracts/54176/anatomy-study-of-seeds-of-calligonium-comosum-in-vitro" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/54176.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">418</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">7</span> Artificial Seed Production in Stipagrostis pennata</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Masoumeh%20Asadi%20Aghbolaghi">Masoumeh Asadi Aghbolaghi</a>, <a href="https://publications.waset.org/abstracts/search?q=Beata%20Dedicova"> Beata Dedicova</a>, <a href="https://publications.waset.org/abstracts/search?q=Farzad%20Sharifzadeh"> Farzad Sharifzadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Mansoor%20Omidi"> Mansoor Omidi</a>, <a href="https://publications.waset.org/abstracts/search?q=Ulrika%20Egertsdotter"> Ulrika Egertsdotter</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Stipagrostis pennata is one of the valuable fodder plants and is very resistant to drought, due to the low capacity of seed production, the use of asexual reproduction methods, including somatic embryogenesis and artificial seed, can increase its reproduction on a large scale. This study was conducted in order to obtain optimal treatments for the production of artificial seeds of this plant through the somatic embryo encapsulating. Embryonic calluses were encapsulated using sodium alginate and calcium chloride and then sowed in a germination medium. The experiment was conducted as a factorial based on a completely randomized design with three replications. The treatments include three concentrations of sodium alginate (1.5, 2.5, and 3.5 percent), two ion exchange times (20 and 30 minutes,) and two artificial seed germination media (hormone free MS and MS containing zeatin riboside and L-proline). Germination percentage and number of days until the beginning of germination were investigated. The highest percentage of artificial seed germination was obtained when 2.5% sodium alginate was used for 30 minutes (ion exchange time) and the seeds were placed on the germination medium containing zeatin riboside and L-proline. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=somatic%20embryogenesis" title="somatic embryogenesis">somatic embryogenesis</a>, <a href="https://publications.waset.org/abstracts/search?q=Stipagrostis%20pennata" title=" Stipagrostis pennata"> Stipagrostis pennata</a>, <a href="https://publications.waset.org/abstracts/search?q=synthetic%20seed" title=" synthetic seed"> synthetic seed</a>, <a href="https://publications.waset.org/abstracts/search?q=tissue%20culture" title=" tissue culture"> tissue culture</a> </p> <a href="https://publications.waset.org/abstracts/154985/artificial-seed-production-in-stipagrostis-pennata" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/154985.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">99</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">6</span> Recovering Taraxacum Taraxacum kok-saghyz Rodin via Seed and Callus Culture</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=K.%20Uteulin">K. Uteulin</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Mukhambetzhanov"> S. Mukhambetzhanov</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Rakhimbaiev"> I. Rakhimbaiev</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This experiment was performed to optimize the medium for tissue culture of Taraxacum kok-saghyz Rodin. Different tissue culture approaches such as shoot regeneration from seed, callus formation from leaf explants and plant regeneration from callus were investigated in this study. All the explants were cultured on MS basal medium supplemented with 20 g/l sucrose, 7 g/l agar and different plant growth regulators. Seeds of Taraxacum kok-saghyz were cultured on media containing different levels of BA and 2,4-D (0,5 and 1,0 and 3,0 mg/L) to direct shoot regeneration study. Leaf explants were cultured in different combination of BA (at three levels: 0.5, 1.0 and 3.0 mg/L) and zeatin (at two levels: 0.5 and 1.0 mg/L) to examine callus formation. After the callus formation the formed calli were cultured on different combinations of BA and NAA for shoot regeneration. BA at three levels (0.5 and 1.0 and 3.0 mg/L) and NAA at two levels (0.5 and 1.0 mg/L) in all possible combinations were used for shoot regeneration from callus. The results showed that the treatment containing 1.0 mg/L 2,4-D in combination with 1.0 mg/L BA was found to be the best one for shoot regeneration from seeds. The treatment with 1.0 mg/L BA in combination with 1.0 mg/L zeatin were found to be suitable treatments for callus production from leaf explants, as well. Moreover, 0.5 mg/L BA alone or in combination with 1.0 mg/L NAA were found to be the best treatments for shoot regeneration from callus. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Taraxacum%20kok-saghyz%20Rodin" title="Taraxacum kok-saghyz Rodin">Taraxacum kok-saghyz Rodin</a>, <a href="https://publications.waset.org/abstracts/search?q=shoot%20regeneration" title=" shoot regeneration"> shoot regeneration</a>, <a href="https://publications.waset.org/abstracts/search?q=callus" title=" callus"> callus</a>, <a href="https://publications.waset.org/abstracts/search?q=plant" title=" plant"> plant</a> </p> <a href="https://publications.waset.org/abstracts/7790/recovering-taraxacum-taraxacum-kok-saghyz-rodin-via-seed-and-callus-culture" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/7790.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">241</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">5</span> Single Protoplast of Murraya paniculata L. Jack Regenerated Into Plantlets</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hasan%20Basri%20Jumin">Hasan Basri Jumin</a>, <a href="https://publications.waset.org/abstracts/search?q=Danil%20Endriand%20Basri">Danil Endriand Basri</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Isolated protoplast from embryogenic callus of orange Jessamine (Murraya paniculata L. (Jack) cultured and maintained under growth chamber at the temperature +25oC. The parameter observed are the plating efficiency, the number of spherical embryos, heard-shaped embryos-like structure, shoot formation, and plantlets obtained. Treatment was arranged with 0.0, 0.001, 0.01, 0.1 or 1.0 mg 1-1 Naphthalene acetic acid (NAA), and 0, 300, 500 mg 1/l malt extract (ME) and 0.M sorbitol in the medium with 2.5 % sucrose. Interaction between 0.001 mg/l NAA and 500 mg/l was observed the higher percentage of planting efficiency. For embryo development from callus, the media was added to 0.0 mg/l, 0.001 mg/l, 0.01 ,mg/l, 0.1 mg/l, 1.0 mg/l NAA, and 1.0 %, 2.0 %, 3.0 %, 4.0 % sucrose. Media supplemented with 0.01mg/l NAA, and 1.0% sucrose was found to be a suitable medium for the development of spherical somatic embryos. A combination of 0.1 mg/ indole acetic acid (IAA) and 0.1 mg/l zeatin constituted the spherical somatic embryo became heart-shaped embryos-like structure. A combination between GA3 0.1 mg 1/l GA3 and 0.1 mg 1-1 zeatin is looking high, growing the heart-shaped embryos-like structure to form a shoot. Cells were developed into spherical embryos and grew into heart-shaped embryos, and then spherical somatic embryos developed into shoot formation. Sequence from single protoplast to plantlets was obtained by using a low concentration of plant growth regulator and sucrose; This recovery of single protoplast to be completed plantlets is a new technology in plant cell culture, and this could be used in genetic engineering in citrus. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=heart-shaped-embryos-like-structure" title="heart-shaped-embryos-like-structure">heart-shaped-embryos-like-structure</a>, <a href="https://publications.waset.org/abstracts/search?q=Muraya-paniculata" title=" Muraya-paniculata"> Muraya-paniculata</a>, <a href="https://publications.waset.org/abstracts/search?q=plant-growth-regulator" title=" plant-growth-regulator"> plant-growth-regulator</a>, <a href="https://publications.waset.org/abstracts/search?q=spherical-%20somatic-embryo" title=" spherical- somatic-embryo"> spherical- somatic-embryo</a>, <a href="https://publications.waset.org/abstracts/search?q=single%20protoplast" title=" single protoplast"> single protoplast</a>, <a href="https://publications.waset.org/abstracts/search?q=glucose" title=" glucose"> glucose</a> </p> <a href="https://publications.waset.org/abstracts/153880/single-protoplast-of-murraya-paniculata-l-jack-regenerated-into-plantlets" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/153880.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">110</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4</span> Rapid Proliferation of Tissue Culture Using of Olive (Olea Europea L.) cv.Zard</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Majid%20Gharaipour%20Abbasabad">Majid Gharaipour Abbasabad</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This research is studying the effects that various densities of Zeatin, and BA hormones may have on the scale of transformation of plant nodes to new shoots, among seedlings produced by seed germination, and also surveys the amount of produced shoots and their lengths, inside the specific Olive seed lab medium (OM). It is also concerned with the effects that various densities of IBA hormone, and inoculating the shoots with Agrobacterium Rhizogenez A4 can have on shoots' root production. This is a totally random research, and each attendance group has had three occurrences, and ten samples per a hectare. The average amounts have been compared using Duncan's test method, which was done in 5% level. The results indicated that the highest rate of transformation of micro samples to shoots happened in the seed germination environments, containing Zetain with 5 mg, and also 15 mg per a liter densities. (respectively, 95% and 94%), while the highest rate of plants' stem production ,in micro samples, happened in the lab medium environments with 5mg per a liter Zetain density (4.5). In lab medium environments with 15 mg Zetain per liter, a decrease was observed in the number of produced stems (3.88). According to the produced stems' lenght, the longest stem length was observed in environments with 5 mg and also 15 mg per a liter Zetain, and 25 mg per a liter BA densities (respectively, 8.45 cm, 45.66 cm, 8.53 cm). Meanwhile, the lowest amount of transformation of micro samples to shoots, the lowest number of produced shoots, and the shortest shoots were observed in the environments without any hormones (respectively, 3.32 cm, 1.13, 19.66%). The results of root production in Olive indicated that attendance groups which were exposed to different hormones did not vary, and Agrobacterium Rhizogenez A4 had no effect on them, as well. The lowest root's growth rate (22%) happened in environments without any hormones and also, in environment with Agrobacterium Rhizogenez A4 (19.66%). The largest number of roots was observed in the environments, containing Agrobacterium Rhizogenez A4 plus IBA (10 mg/l) and Agrobacterium Rhizogenez A4 plus IBA (10 mg/l), (respectively, 8.46 and 8.70), which had a significant difference with environments merely containing 10 mg and 20 mg of IBA per a litre (respectively, 3.06 and 3.2). So it can be concluded that even though Agrobacterium Rhizogenez A4 had no impact on root's growth among shoots, it had an impact on the number of produced roots. It should be noted that even when the environment contained merely Agrobacterium Rhizogenez A4 without any hormones, only (1.16) roots were produced, which is significantly different from the attendance group with hormones (1.06). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=olive-effect%20of%20hormones-germination%20of%20seed" title="olive-effect of hormones-germination of seed">olive-effect of hormones-germination of seed</a>, <a href="https://publications.waset.org/abstracts/search?q=densities%20of%20zeatin" title=" densities of zeatin"> densities of zeatin</a>, <a href="https://publications.waset.org/abstracts/search?q=BA%20hormones" title=" BA hormones"> BA hormones</a>, <a href="https://publications.waset.org/abstracts/search?q=agriculture" title=" agriculture"> agriculture</a> </p> <a href="https://publications.waset.org/abstracts/14822/rapid-proliferation-of-tissue-culture-using-of-olive-olea-europea-l-cvzard" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/14822.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">292</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">3</span> In vitro Culture of Stem Node Segments of Maerua crassifolia</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abobaker%20Abrahem%20M.%20Saad">Abobaker Abrahem M. Saad</a>, <a href="https://publications.waset.org/abstracts/search?q=Asma%20Abudasalam"> Asma Abudasalam</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The stem node segments were cultured on Murashige and Skoog (MS) medium. In the case of using MS+ Zeatin (1 mg/l), small shoot buds were formed directly in 70% of explants after 15 days, their length range between 0.1 to 0.3 cm after two weeks and reached 0.3 cm in length and three shoots in numbers after 4 weeks. When those small shoots were sub cultured on the same medium, they increased in length, number and reached 0.4 cm with 4 shoots, 0.4 cm with 5 shoots after six, eight and ten weeks respectively. In the case of using MS free hormones, MS+IAA (0.2mg/l) +BA (0.5mg/l), MS + kin(0.5mg/l), MS + kin (3mg/l) and MS +NAA (3mg/l) +BA (1mg/l), no sign of responses were noticed and only change in color in some cases. Different types of parenchyma cells and many layers of thick wall sclerenchyma cells were observed on MS+BA (1mg/l). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Maerua" title="Maerua">Maerua</a>, <a href="https://publications.waset.org/abstracts/search?q=stem%20node" title=" stem node"> stem node</a>, <a href="https://publications.waset.org/abstracts/search?q=shoots" title=" shoots"> shoots</a>, <a href="https://publications.waset.org/abstracts/search?q=buds" title=" buds"> buds</a>, <a href="https://publications.waset.org/abstracts/search?q=In%20vitro" title=" In vitro"> In vitro</a> </p> <a href="https://publications.waset.org/abstracts/59982/in-vitro-culture-of-stem-node-segments-of-maerua-crassifolia" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/59982.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">312</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2</span> Bioproduction of Phytohormones by Liquid Fermentation Using a Mexican Strain of Botryodiplodia theobromae</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Laredo%20Alcal%C3%A1%20Elan%20I%C3%B1aky">Laredo Alcal谩 Elan I帽aky</a>, <a href="https://publications.waset.org/abstracts/search?q=Hernandez%20Castillo%20Daniel"> Hernandez Castillo Daniel</a>, <a href="https://publications.waset.org/abstracts/search?q=Martinez%20Hernandez%20Jos%C3%A9%20Luis"> Martinez Hernandez Jos茅 Luis</a>, <a href="https://publications.waset.org/abstracts/search?q=Arredondo%20Valdes%20Roberto"> Arredondo Valdes Roberto</a>, <a href="https://publications.waset.org/abstracts/search?q=Gonzalez%20Gallegos%20Esmeralda"> Gonzalez Gallegos Esmeralda</a>, <a href="https://publications.waset.org/abstracts/search?q=Anguiano%20Cabello%20Julia%20Cecilia"> Anguiano Cabello Julia Cecilia</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Plant hormones are a group of molecules that control different processes ranging from the growth and development of the plant until their response to biotic and abiotic stresses. In this study, the capacity of production of various phytohormones was evaluated from a strain of Botryodiplodia theobromae by liquid fermentation system using the modified Mierch medium added with a hydrolyzate compound of mead all in a reactor without agitation at 28 掳C for 15 days. Quantification of the metabolites was performed using high performance liquid chromatography techniques. The results showed that a microbial broth with at least five different types of plant hormones was obtained: gibberellic acid, zeatin, kinetin, indoleacetic acid and jasmonic acid, the last one was higher than the others metabolites produced. The production of such hormones using a single type of microorganism could be in the future a great alternative to reduce production costs and similarly reduce the use of synthetic chemicals. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biosystem" title="biosystem">biosystem</a>, <a href="https://publications.waset.org/abstracts/search?q=plant%20hormones" title=" plant hormones"> plant hormones</a>, <a href="https://publications.waset.org/abstracts/search?q=Botryodiplodia%20theobromae" title=" Botryodiplodia theobromae"> Botryodiplodia theobromae</a>, <a href="https://publications.waset.org/abstracts/search?q=fermentation" title=" fermentation"> fermentation</a> </p> <a href="https://publications.waset.org/abstracts/43134/bioproduction-of-phytohormones-by-liquid-fermentation-using-a-mexican-strain-of-botryodiplodia-theobromae" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/43134.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">403</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1</span> Somatic Embryogenesis Derived from Protoplast of Murraya Paniculata L. Jack and Their Regeneration into Plant Flowering in vitro</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hasan%20Basri%20Jumin">Hasan Basri Jumin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The in vitro flowering of orange jessamine plantlets derived from protoplast was affected by the manipulation of plant growth regulators, sugar and light conditions. MT basal medium containing 5% sucrose and supplemented with 0.001 mg 1-1 indole-acetic-acid was found to be a suitable medium for development of globular somatic embryos derived from protoplasts to form heart-shaped somatic embryos with cotyledon-like structures. The highest percentage (85 %) of flowering was achieved with plantlet on half-strength MT basal medium containing 5% sucrose and 0.001 mg1-1 indole-acetic-acid in light. Exposure to darkness for more than 3 weeks followed by re-exposure to light reduced flowering. Flowering required a 10-day exposure to indole-acetic-acid. Photoperiod with 18 h and 79.4 碌mol m-2 s-1 light intensity promoted in vitro flowering in high frequencies. The sucrose treatment affected the flower bud size distribution. Flower buds originating from plantlet derived from protoplasts developed into normal flowers. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=indole-acetc-acid" title="indole-acetc-acid">indole-acetc-acid</a>, <a href="https://publications.waset.org/abstracts/search?q=light-intensity" title=" light-intensity"> light-intensity</a>, <a href="https://publications.waset.org/abstracts/search?q=Murraya-paniculata" title=" Murraya-paniculata"> Murraya-paniculata</a>, <a href="https://publications.waset.org/abstracts/search?q=photoperiod" title=" photoperiod"> photoperiod</a>, <a href="https://publications.waset.org/abstracts/search?q=plantlet" title=" plantlet"> plantlet</a>, <a href="https://publications.waset.org/abstracts/search?q=Zeatin" title=" Zeatin"> Zeatin</a> </p> <a href="https://publications.waset.org/abstracts/28393/somatic-embryogenesis-derived-from-protoplast-of-murraya-paniculata-l-jack-and-their-regeneration-into-plant-flowering-in-vitro" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/28393.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">418</span> </span> </div> </div> </div> </main> <footer> <div id="infolinks" class="pt-3 pb-2"> <div class="container"> <div style="background-color:#f5f5f5;" class="p-3"> <div class="row"> <div class="col-md-2"> <ul class="list-unstyled"> About <li><a href="https://waset.org/page/support">About Us</a></li> <li><a href="https://waset.org/page/support#legal-information">Legal</a></li> <li><a target="_blank" rel="nofollow" href="https://publications.waset.org/static/files/WASET-16th-foundational-anniversary.pdf">WASET celebrates its 16th 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