Search results for "Micropropagation"

showing 10 items of 71 documents

Use of carbon dioxide enrichment to obtain adult morphology of grapevinein vitro

1993

A procedure has been developed forin vitro propagation ofVitis vinifera ‘Pinot noir’ from lateral-bud cuttings under high CO2 concentration (1200 µmol mol−1). Because of inhibition of rooting by CO2, this procedure requires a rooting pre-culture of explants on medium with sucrose before the CO2-enriched culture on sucrose-free medium. Shoot growth was enhanced by CO2 enrichment as a result of both a higher rate of leaf production and greater internode elongation. Leaf expansion and tendril growth were promoted and better rooting was obtained. The more significant effect of CO2 enrichment was to promote adult morphology with, in particular, the tendril pattern. Thus, for the first time, grap…

Sucrosefood and beveragesPlant physiologyHorticultureBiologychemistry.chemical_compoundCuttingchemistryMicropropagationBotanyShootTendrilPropagation of grapevinesExplant culturePlant Cell, Tissue and Organ Culture
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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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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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Plant hormones and Agrobacterium tumefaciens strain 82.139 induce efficient plant regeneration in the cardenolide-producing plant Digitalis minor

2002

Summary Shoot formation in explants of Digitalis minor was achieved, through axillary bud proliferation and adventitious bud differentiation, by varying the amount and source of plant hormones. Shoot regeneration was also obtained after infection of D. minor with the wild-type Agrobacterium tumefaciens strain 82.139, which induced shooty tumours. These shoots were not transgenic, as revealed by nopaline assays and the use of a C58pMP90/T139GUS-INT strain harbouring the intron inactivated gusA gene. Plants were easily rooted and transplanted into the greenhouse. Shoot cultures of D. minor accumulated up to 226 μg cardenolides per g dry mass when cultured on agar-solidified medium. Cardenolid…

biologyPhysiologyfungiHyperhydricityfood and beveragesPlant ScienceAgrobacterium tumefaciensbiology.organism_classificationchemistry.chemical_compoundchemistryMicropropagationAxillary budShootBotanyCardenolideNopalineAgronomy and Crop ScienceExplant cultureJournal of Plant Physiology
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Plant regeneration from juvenile and adult Anthyllis cytisoides, a multipurpose leguminous shrub

1997

Summary Anthyllis cytisoides , a legume shrub used for afforestation and reclamation of degraded Mediterranean areas, was successfully micropropagated from expiants of juvenile (cotyledonary nodes and apical buds) and adult origin (axillary buds). Multiple shoot formation was dependent on the presence of benzyladenine in the induction medium. Of the salt formulation and expiants examined, the higher proliferation rates were obtained when axillary buds from adult plants were cultured on a modified Schenk and Hildebrandt medium. Following the preferred protocol, shoot yield reached values greater than 100 shoots per expiant. Plants were easily rooted and transplanted into greenhouse.

biologyPhysiologyved/biologyfungived/biology.organism_classification_rank.speciesfood and beveragesAnthyllisPlant ScienceAnthyllis cytisoidesbiology.organism_classificationShrubMicropropagationAxillary budShootBotanyJuvenileMultipurpose treeAgronomy and Crop ScienceJournal of Plant Physiology
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Selection and long-term cultures of high-yielding Digitalis obscura plants: RAPD markers for analysis of genetic stability

1996

Fifteen wild-growing plants of Digitalis obscura collected in three differents regions were characterized according to their capacities to biosynthesize cardenolides and to proliferate in vitro. Great genotype-dependent variabilities were found in both parameters. Selected genotypes were differentiated using randomly amplified polymorphic DNA (RAPD) markers. Once an elite genotype with high-yielding properties was isolated and micropropagated during 2 years, identity of the donor plant and the regenerants was confirmed by RAPD analysis.

biologyScrophulariaceaeDigitalis obscurafood and beveragesPlant ScienceGeneral Medicinebiology.organism_classificationRAPDTissue cultureMicropropagationBotanyGenotypeGeneticsGenetic variabilityAgronomy and Crop ScienceSelection (genetic algorithm)Plant Science
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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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Factors controlling adventitious bud induction and plant regeneration in matureJuniperus oxycedrus leaves cultured in vitro

1994

The morphogenetic capacity of matureJuniperus oxycedrus L. leaves cultured in vitro has been studied, noting nutritive, hormonal, and environmental factors inducing differentiation and development of adventitious shoots. Bud primordia formed directly from the leaves. Highest bud differentiation rates were obtained when the explants were cultured for at least 21 days on a modified Schenk and Hildebrandt solidified medium containing 0.5 μM benzyladenine under a 16-h photoperiod. Maximum bud development and elongation was achieved on cytokinin-free medium containing 4% (wt/vol) sucrose and 0.05% (wt/vol) activated charcoal. Regenerated shoots were excised and induced to root on media with auxi…

chemistry.chemical_classification1-Naphthaleneacetic acidbiologyfood and beveragesPlant Sciencebiology.organism_classificationchemistry.chemical_compoundchemistryMicropropagationAuxinBotanyCytokininShootPrimordiumJuniperus oxycedrusBiotechnologyExplant cultureIn Vitro Cellular & Developmental Biology - Plant
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