Search results for "Murashige and Skoog medium"

showing 10 items of 29 documents

Isolation, culture and plant regeneration from protoplasts of Sideritis angustifolia

1998

Summary Factors promoting high yields of viable protoplasts from leaves of Sideritis angustifolia are reported. Isolated protoplasts divided and gave rise to callus when plated in modified liquid MS medium with growth regulators. Best plating efficiency was obtained when protoplast were cultured in the presence of 6 μM BA and 2 μM NAA. Calli were then transferred onto solidified regeneration media. Adventitious bud differentiation was only observed in calli grown on medium containing 8 μM BA and 2 μM NAA. These buds proliferated quickly when placed on hormone-free medium and subsequendy regenerated new buds and shoots. Once developed shoots were excised, the remaining tissues maintained thi…

Plating efficiencyPhysiologyRegeneration (biology)fungifood and beveragesPlant ScienceProtoplastBiologybiology.organism_classificationMurashige and Skoog mediumCell cultureCallusBotanyShootSideritisAgronomy and Crop Science
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Cryopreservation of Digitalis obscura selected genotypes by encapsulation-dehydration

2001

Shoot-tips from several genotypes of the cardenolide-producing perennial shrub Digitalis obscura L. were successfully cryopreserved using the encapsulation-dehydration technique. Precultivation on MS medium containing 0.5 M sucrose, followed by 2.5 h dehydration (final weight 30 %) induced shoot regrowth in 42 % of cryopreserved shoot-tips. Cold-hardening of the in vitro cultures before sucrose treatment dramatically increased shoot recovery up to 86 %. The optimized cryopreservation protocol was then employed using different shoot cultures from five D. obscura genotypes. Responses to cryopreservation depended mainly on the genotype, best results being obtained when shoot tips from HU3 and …

SucroseDNA PlantGenotypeScrophulariaceaeAcclimatizationDigitalis obscuraPharmaceutical ScienceCapsulesCryopreservationAnalytical ChemistrySomaclonal variationchemistry.chemical_compoundMurashige and Skoog mediumDrug DiscoveryBotanyDesiccationCryopreservationPharmacologyDigitalisbiologyOrganic Chemistryfungifood and beveragesbiology.organism_classificationRandom Amplified Polymorphic DNA TechniqueRAPDCold TemperatureHorticultureComplementary and alternative medicinechemistryShootMolecular MedicinePlant Shoots
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In vitro shoot organogenesis from excised immature cotyledons and microcuttings production in Stone Pine

1994

Adventitious buds were induced on isolated immature cotyledons of Pinus pinea L. in the presence of benzyladenine (BA). The response to different BA concentrations also depended upon the culture medium used (modified MS, SH and GD). A wide range of BA concentrations (5, 25 or 50 μM) can be applied to the GD and SH media, which are the media with the lower nitrogen content, without damaging effects. In the MS medium, which has the highest nitrogen concentration, the range of BA that can be applied was narrower and the highest BA concentration was lethal. The addition of indolebutyric acid (0.05, 0.25 or 0.5 μM) to the induction medium, decreased the response of cotyledons. The increase in th…

Sucrosefood.ingredientfood and beveragesHorticultureBiologychemistry.chemical_compoundTissue cultureMurashige and Skoog mediumfoodchemistryMicropropagationCytokininShootBotanyCotyledonExplant culturePlant Cell, Tissue and Organ Culture
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Regeneration of Sideritis angustifolia (Labiatae) Plants from Single Cell Cultures

1988

Summary Mechanically isolated cells from hypocotyl-derived calli of Sideritis angustifolia Lag. were inoculated on agar-solidified Murashige and Skoog (MS) nutrient medium containing CH and different concentrations and combinations of NAA and BA. Isolated cells underwent continued divisions giving rise to calli after 30 days of culture. Best results were obtained when medium was supplemented with 0.5 μM NAA and 4.4 or 8.8 μM BA or with 5 μM NAA and 4.4μM BA. Calli obtained in the presence of 0.5 μM NAA and 8.8 μM BA regenerated shoot-buds when transferred to MS medium without CH and supplemented or not with these growth regulators. Once shoots were excised, the calli maintained their morpho…

Tissue cultureMurashige and Skoog mediumbiologyPhysiologyInoculationCell culturefungiBotanyShootSideritisPlant Sciencebiology.organism_classificationAgronomy and Crop ScienceJournal of Plant Physiology
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In vitro rescue of zygotic embryos of sour orange, Citrus aurantium L., and their detection based on RFLP analysis

1998

Embryo development in vivo has been studied in four Citrus aurantium L. polyembryonic genotypes. Seeds were collected 65, 85, 105, 125 and 220 days after pollination (DAP). None of the immature seeds harvested 65 and 85 DAP contained visible embryos. A single embryo at a more advanced developmental stage was observed in the central position at the micropylar apex of the embryo sac in about 74% of seeds harvested at 105 DAP, while at 125 and 220 DAP the majority of seeds had two or more embryos at the same developmental stage crowded together. Restriction fragment length polymorphism (RFLP) analysis of low- and high-copy-number nuclear DNA was used to distinguish zygotic from nucellar seedli…

animal structuresPolyembryonyPlant ScienceRepetitive DNANucellar embryonyBiologychemistry.chemical_compoundMurashige and Skoog mediumBotanyGeneticsEmbryo cultureGibberellic acidCitrus aurantiumNucellar embryonyMolecular markersEmbryo cultureEmbryoEmbryo rescueHorticulturechemistryGerminationDNA polymorphismembryonic structuresGrowth regulatorsAgronomy and Crop ScienceApomixis
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Micropropagation of Genista aetnensis [(Raf. ex Biv.)DC]

2015

Genista aetnensis [(Raf. ex Biv.)DC] is a large deciduous shrub or small tree native to the Italian islands of Sardinia and Sicily. Being winter hardy and characterized by high plasticity in altitude and ecology, the species is grown in gardens and landscaping, both for flower and for its attractive shape. Genista species are generally propagate by seed or semi hardwood cuttings. In this report an efficient in vitro technique for propagation of G. aetnensis was investigated. Multiple shoots were induced on nodal segments of a mature plant of Genista aetnensis . The Murashige and Skoog medium, augmented with different concentrations of benzyladenine either singly or in combination with indol…

biologyGenista aetnensisAgriculture (General)food and beveragesForestryPlant ScienceGenistaSettore AGR/04 - Orticoltura E FloricolturaHorticultureSD1-669.5biology.organism_classificationS1-972In vitro rooting growth regulators Mount Etna broom node culture shoot multiplicationchemistry.chemical_compoundMurashige and Skoog mediumMicropropagationchemistryBotanyShootKinetinZeatinAgronomy and Crop ScienceExplant cultureNotulae Botanicae Horti Agrobotanici Cluj-Napoca
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Micropropagation of juvenile and adultDigitalis obscura and cardenolide content of clonally propagated plants

1991

Cultures ofDigitalis obscura L. were established from axillary buds of mature plants or leaves of seedlings obtained under aseptic conditions. Explants were cultured on Murashige and Skoog medium containing benzyladenine and/or naphthaleneacetic acid. Shoot proliferation from axillary buds was not affected by seasonal fluctuations in the stock plants and increased relative to the cytokinin concentration, but auxin reduced the multiplication rate. Differentiation of somatic embryos and adventitious buds from cultured leaves required naphthaleneacetic acid alone or combined with benzyladenine, respectively. Cardenolide pattern and content of the regenerated plants were determined by high perf…

biologySomatic embryogenesisfungiDigitalis obscurafood and beveragesPlant Sciencebiology.organism_classificationchemistry.chemical_compoundMurashige and Skoog mediumMicropropagationchemistryAxillary budBotanyShootCytokininCardenolideBiotechnologyIn Vitro Cellular & Developmental Biology - Plant
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Micropropagation of Lavandula latifolia through nodal bud culture of mature plants

1996

Cultures of Lavandula latifolia Medicus were established from axillary buds of mature field-grown plants. Explants were initially cultured on media with two different macronutrient combinations and benzyladenine or kinetin added either individually or with naphthaleneacetic acid. Subsequently, explants were subcultured in Murashige and Skoog medium supplemented with 20% coconut milk, 0.57 μM indoleacetic acid and 8.88 μM benzyladenine. Shoot proliferation from axillary buds was not affected by seasonal fluctuations in the stock plants but depended on the macronutrient composition and on the type and concentration of cytokinin tested. Best results were obtained in explants initially cultured…

biologyfungiLavandula latifoliafood and beveragesHorticulturebiology.organism_classificationchemistry.chemical_compoundMurashige and Skoog mediumMicropropagationchemistryAxillary budBotanyCytokininShootKinetinExplant culturePlant Cell, Tissue and Organ Culture
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Micropropagation of adultLavandula dentataplants

1998

SummaryA protocol for in vitro propagation of adult Lavandula dentata plants has been achieved. Cultures were established by placing nodal segments on Murashige and Skoog medium containing BA, KIN, and NAA. Highest shoot multiplication rates were obtained when explants grown in the presence of 5.0 μM BA or 20 (JLM KIN were transferred to medium with 8.8 μM BA and 15% coconut milk. Multiplication efficiency through subcultures was significantly affected by the cytokinin concentration in the initial culture medium. Subculture reduced drastically the final number of shoots produced on nodal segments isolated from shoots grown in the presence of 2.0 μM BA or 40.0 μM KIN. Shoots were easily root…

biologyfungifood and beveragesHorticulturebiology.organism_classificationLavandula dentatachemistry.chemical_compoundMurashige and Skoog mediumMicropropagationchemistryShootBotanyCytokininGeneticsKinetinSubculture (biology)Explant cultureThe Journal of Horticultural Science and Biotechnology
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Effect of growth regulators onin vitro propagation ofFicus benjamina cv. Exotica

1994

Stem internodes with axillary buds were excised from 5-year old trees ofFicus benjamina cv. Exotica. The effect of 6-benzylaminopurine (BAP), gibberellic acid (GA3), indole-3-acetic acid (IAA), naphthaleneacetic acid (NAA), and 2,4-dichlorophenoxyacetic acid (2,4-D) on shoot growth and proliferationin vitro was investigated. Multiple shoots were developed after 3–4 weeks from stem internodes with axillary buds incubated in Murashige and Skoog (MS) medium supplemented with phloroglucinol (PG) and BAP. Optimum shoot proliferation took place in the presence of 1.0 mg l−1 BAP. Shoots obtained could be elongated in a medium with 0.5 mg l−1 GA3 prior to their rooting. The root initiation was succ…

chemistry.chemical_classification1-Naphthaleneacetic acidfood and beveragesPlant ScienceHorticultureBiologychemistry.chemical_compoundMurashige and Skoog mediumMicropropagationchemistryAuxinAxillary budShootCytokininBotanyGibberellic acidBiologia plantarum
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