RESUMEN
Aromatic and medicinal plants (AMPs) have great potential for the synthesis of secondary metabolites, which are used by the pharmaceutical and food industry. In addition, they are part of ancestral medicine and the livelihood of many families in regional economies. Argentina has a high number of AMPs. However, the intensive extraction system (overexploitation), together with other anthropic actions, puts them at risk. The "peperina de las lomas" (Hedeoma multiflora Benth. (Lamiaceae)) is within this problem. This native species, xerophyte, is distributed in central Argentina, in stony mountain areas, forming small bushes. In this work, the existing information of the species was collected, covering from its environmental problems to the most recent investigations, oriented towards its conservation and the development of its germplasm. These data will serve to promote activities aimed at preventing the degradation of this resource and promoting its sustainable use.
Las plantas aromáticas y medicinales (PAMs) tienen un gran potencial para la síntesis de metabolitos secundarios, los cuales son utilizados por la industria farmacéutica y alimentaria. Además, son parte de la medicina ancestral y el sustento de muchas familias de las economías regionales. Argentina posee un alto número de PAMs. Sin embargo, el sistema de extracción intensivo (sobreexplotación), junto a otras acciones antrópicas, las coloca en riesgo. La "peperina de las lomas" (Hedeoma multiflora Benth. (Lamiaceae)) se encuentra dentro de esta problemática. Esta especie nativa, xerófita, se distribuye en el centro de Argentina, en zonas pedregosas serranas, formando pequeñas matas. En este trabajo se recopiló la información existente de la especie abarcando, desde su problemática ambiental hasta las investigaciones más recientes, orientadas a su conservación y al desarrollo de su germoplasma. Estos datos servirán para promover actividades destinadas a evitar la degradación de este recurso y propiciar su aprovechamiento sustentable.
Asunto(s)
Plantas Medicinales , Aceites Volátiles , Argentina , Especies en Peligro de Extinción , Desarrollo SostenibleRESUMEN
Sunflower (Helianthus annuus L.) is still considered as a recalcitrant species to in vitro culture and transformation in spite of the publication of different protocols. Here we describe a routine transformation system of this crop which requires mature HA89 genotype seeds and Agrobacterium tumefaciens EHA105 strain for gene delivery, being both easily available. Selection of transformed shoots depends on root development in kanamycin-selective media, instead of shoot color, avoiding selection of escapes. The establishment of this protocol proved successful for the incorporation of both reporter and agronomic important genes and also for the evaluation of the specific expression patterns of different promoters in transgenic sunflower plants. Stable expression of the incorporated transgenes was confirmed by RT-PCR and GUS reporter gene visualization. Stable inheritance of transgenes was successfully followed until T2 generation in several independent lines.
Asunto(s)
Ingeniería Genética/métodos , Helianthus/crecimiento & desarrollo , Helianthus/genética , Agrobacterium tumefaciens/genética , Agrobacterium tumefaciens/crecimiento & desarrollo , Técnicas de Cocultivo , Desinfección , Flores/crecimiento & desarrollo , Técnicas de Transferencia de Gen , Helianthus/fisiología , Plantas Modificadas Genéticamente , Regeneración , Semillas/crecimiento & desarrollo , Suelo , Transformación GenéticaRESUMEN
Six Nierembergia linariaefolia clones were selected for ornamental traits during a native germplasm development program. For fingerprinting diagnosis, 13 anchored inter-simple sequence repeat (ISSR) primers and 6 amplified fragment length polymorphism (AFLP) primer-enzyme combinations were used. Both markers revealed high levels of polymorphism, enabling genetic discrimination of the accessions analyzed by using 443 informative ISSRs and 541 AFLP markers. Both molecular techniques are suitable for monitoring genetic diversity in Nierembergia linariaefolia and, under our experimental conditions, they showed correlation coefficients of 0.629 for similarity matrices and of 0.649 in the cophenetic matrices. These results suggest that ISSRs are a good choice for DNA analysis in N. linariaefolia when simple manipulation and a low budget are required.
Asunto(s)
Solanaceae/genética , Argentina , Secuencia de Bases , Dermatoglifia del ADN , Cartilla de ADN/genética , ADN de Plantas/genética , ADN de Plantas/aislamiento & purificación , Marcadores Genéticos , Repeticiones de Minisatélite , Polimorfismo Genético , Solanaceae/clasificaciónRESUMEN
Sunflower (Helianthus annuus L.) is considered one of the recalcitrant species in terms of transformation and regeneration. A routine transformation system of this crop requires competent cell cultures for efficient plant regeneration as well as an effective method for gene delivery. A transformation system was developed by an Agrobacterium tumefaciens-mediated method using split mature embryonic axis explants from the Ha89 genotype. Mean transformation efficiency obtained (measured as PCR+ plants/treated explants) varied from 1 to 5.2% depending on the use of the EHA105 or the C58 strain containing a plasmid with a gene of agronomic interest. The system developed has applicability to several Agrobacterium strains and plasmids with both reporter genes or genes of agronomic interest. Plants obtained with this protocol were confirmed by PCR and Southern blot. Stable inheritance of transgenes was successfully followed until generation T4 in several independent lines.
Asunto(s)
Agrobacterium tumefaciens/genética , Técnicas de Transferencia de Gen , Helianthus/genética , Plantas Modificadas Genéticamente/genética , Semillas/genética , Transformación Genética , Agrobacterium tumefaciens/crecimiento & desarrollo , Southern Blotting/métodos , Helianthus/embriología , Helianthus/microbiología , Plantas Modificadas Genéticamente/embriología , Plantas Modificadas Genéticamente/microbiología , Reacción en Cadena de la Polimerasa/métodos , Regeneración/genética , Semillas/embriología , Semillas/microbiología , Análisis de Secuencia de ADN/métodosRESUMEN
The objective of the present work was to establish the molecular identification profile for six new varieties of Nierembergia linariaefolia to incorporate the fingerprint, as complementary information to the standard registration data. Total DNA was extracted from young leaves following the protocol of the cetyltrimethylammonium bromide. Anchored microsatellites were used as molecular markers. The amplification reactions were carried out with seven primers. A total of 251 loci were detected, 98 percent of them were polymorphic. The average of polymorphic loci was 35 loci per primer and, 41 loci per genotype. Six out of the seven primers used discriminated all the individuals involved in the present study; consequently, it was possible to generate the molecular identification profile for the six new varieties. This result, supported together with our previous reports, indicates that the anchored microsatellites are a very useful technique for the fingerprints generation in N. linariaefolia.
RESUMEN
The genus Scoparia is native from Argentina. The diversity of colours and shape of their flowers bestows this genus a very interesting ornamental potential. The purpose of the present study is to explore the Scoparia species germplasm by means of in vitro polyploidization in order to improve their ornamental qualities. Accessions of S. montevidiensis var. montevidiensis, S. montevidiensis var. glandulifera, S. nudicaulis, S. hasleriana and S. dulcis were collected and maintained under greenhouse conditions. The Murashige-Skoog medium, supplemented with 0.25 mg/L BAP was used for the nodal segments multiplication of the five Scoparia species. Except for S. hasleriana, the multiplication rate of the other species ranged between 10 and 12 shoots per explant. The colchicine doses tested with S. montevidiensis were: 0.0; 0.1; 0.05; 0.01 and 0.001% (24 and 48 hrs). From a total of 364 recovered plants, 4 solid tetraploid and 16 chimeras were detected. Significant differences were observed for the size of flower, leaves, and the stem diameter among the tetraploid plants and between them and the control. The tissue culture proved to be a powerful tool both to multiply the Scoparia material incorporated to our germplasm collection and to obtain new improved varieties of this beautiful genus.