Genetic control of somatic embryogenesis in alfalfa

Genome ◽  
1992 ◽  
Vol 35 (3) ◽  
pp. 474-477 ◽  
Author(s):  
G. A. Kielly ◽  
S. R. Bowley
Keyword(s):  
Tissue Culture ◽  
Somatic Embryogenesis ◽  
Medicago Sativa ◽  
Genetic Control ◽  
In Vitro Regeneration ◽  
Breeding Population ◽  
Medicago Sativa L

The genetic control of somatic embryogenesis in alfalfa (Medicago sativa L.) was studied using one nonembryogenic and three embryogenic genotypes: A70-34, a selection from 'Rangelander'; RA3, a selection from 'Regen-S'; and C2-4, a selection from a breeding population that had A70-34 in its pedigree. Crosses of embryogenic × embryogenic and embryogenic × nonembryogenic and S1 and BC1 testcrosses were evaluated for in vitro regeneration. Selfing reduced the expression of the trait. Somatic embryogenesis was dominant and explained by two loci. All three regenerating genotypes shared a common genetic system.Key words: alfalfa, Medicago sativa, somatic embryogenesis, tissue culture.

A transplant plug technique for production of alfalfa (Medicago sativa L.) plants from somatic embryos

1992 ◽  
Vol 72 (2) ◽  
pp. 483-485 ◽  
Author(s):  
A. R. McElroy ◽  
D. C. W. Brown
Keyword(s):  
Tissue Culture ◽  
Somatic Embryogenesis ◽  
Medicago Sativa ◽  
Somatic Embryos ◽  
Potting Media ◽  
Medicago Sativa L

A transplant plug technique was developed that uses in vitro somatic embryogenesis techniques to mass-multiply alfalfa plants in a form suitable for direct transplanting. The plug contains potting media covered with an agar nutrient cap. Plants develop from embryos placed on the cap and then establish in the potting media.Key words: Hybrid alfalfa, Medicago sativa L., tissue culture, transplant plug, somatic embryogenesis

Genetic control of in vitro regeneration in alfalfa (Medicago sativa L.)

Euphytica ◽  
1988 ◽  
Vol 39 (1) ◽  
pp. 3-9 ◽  
Author(s):  
Y. Wan ◽  
E. L. Sorensen ◽  
G. H. Liang
Keyword(s):  
Medicago Sativa ◽  
Genetic Control ◽  
In Vitro Regeneration ◽  
Medicago Sativa L

Field evaluation following two cycles of backcross transfer of somatic embryogenesis to commercial alfalfa germplasm

1993 ◽  
Vol 73 (1) ◽  
pp. 131-137 ◽  
Author(s):  
S. R. Bowley ◽  
G. A. Kielly ◽  
K. Anandarajah ◽  
B. D. McKersie ◽  
T. Senaratna
Keyword(s):  
Somatic Embryogenesis ◽  
Medicago Sativa ◽  
Seed Yield ◽  
Field Experiments ◽  
Field Evaluation ◽  
Growth Characteristics ◽  
Seed Technology ◽  
Artificial Seed ◽  
Medicago Sativa L

For successful application of artificial seed technology to alfalfa (Medicago sativa L.), parental plants must possess the necessary genes for somatic embryogenesis and produce progeny having high commercial value. A backcross procedure was initiated to transfer the ability to form somatic embryos from genotype A70-34, a selection from the cultivar Rangelander, to multiple-pest-resistant alfalfa germplasm. The objectives of this study were to evaluate the growth characteristics and seed yield of the F1; BC1 and BC2 generations to determine if introgression with commercial germplasm had improved the agronomic features of the embryogenic germplasm. This study consisted of two field experiments, each conducted at two locations. One experiment evaluated herbage growth characteristics and herbage production at Elora and Woodstock, Ontario, and the other evaluated seed yield at Elora and Delhi, Ontario. Significant increases in fall regrowth height, leaflet length:width ratio, and seed yield were detected over the cycles of crossing. By the BC2, fall dormancy and leaflet length:width ratio were similar to those in commercial populations. Although improvements in seed yield were detected, the BC2 was inferior in seed yield compared with commercial germplasm, and further introgression and (or) conscious selection for improved seed yield will be required. Through a population backcross procedure, it appears possible to develop commercial alfalfa germplasm capable of in vitro manipulation. Key words: Alfalfa, Medicago sativa L., somatic embryogenesis, artificial seed, backcross

scholarly journals Improvement of the in vitro regeneration and Agrobacterium-mediated genetic transformation of Medicago sativa L.

2019 ◽  
Vol 43 (1) ◽  
pp. 96-104
Author(s):  
Farzad NOFOUZI ◽  
Muhammet Çağrı OĞUZ ◽  
Saber Delpasand KHABBAZI ◽  
Ali ERGÜL
Keyword(s):  
Genetic Transformation ◽  
Medicago Sativa ◽  
In Vitro Regeneration ◽  
Medicago Sativa L

GENETIC VARIANCE OF PROTEOLYTIC ACTIVITY IN ALFALFA HERBAGE

1987 ◽  
Vol 67 (1) ◽  
pp. 159-165
Author(s):  
S. R. BOWLEY ◽  
B. D. McKERSIE
Keyword(s):  
Medicago Sativa ◽  
Proteolytic Activity ◽  
Genetic Variance ◽  
Effective Means ◽  
Breeding Population ◽  
Narrow Sense ◽  
Nonprotein Nitrogen ◽  
Narrow Sense Heritability ◽  
Medicago Sativa L

Protein hydrolysis can be extensive during ensiling of alfalfa (Medicago sativa L.) herbage. Such hydrolysis lengthens the ensiling phase and reduces the quality of the resultant feed. The objectives of this study were: (1) to estimate the genetic variance and narrow-sense heritability (via a half-sib analysis) of proteolytic activity in an alfalfa breeding population (OAC-A83); and (2) to estimate the genetic diversity among related Medicago subspecies (M. falcata, M. varia, M. praefalcata and M. glomerata), M. sativa introductions, and two cultivars, Iroquois and OAC Minto. An in vitro procedure was used to quantify proteolytic activity, which was expressed as milligrams of trichloroacetic acid (TCA)-soluble leucine equivalents per gram fresh leaf weight, released during a 7-d incubation. Significant (P < 0.05) differences were found among the half-sib families of OAC-A83. The narrow-sense heritability of proteolytic activity was low (13.9%). The expected response to selection for low proteolytic activity, if the top 10% of the plants were recombined, was 5% of the OAC-A83 population mean. Although significant (P < 0.05) differences were obtained among the Medicago introductions, none of the introductions or subspecies tested had lower proteolytic activity than that found in the two cultivars tested (Iroquois and OAC Minto). It was concluded that, although possible, genetic improvement of proteolytic potential in alfalfa may not be easily obtained. In the short term, rapid lowering of silage pH (e.g., bacterial inoculants or acid additives) will likely remain the most effective means of controlling protein degradation in alfalfa silage.Key words: Medicago sativa L., silage, ensiling, soluble nonprotein nitrogen, heritability, alfalfa

Genetic control of somatic embryogenesis in alfalfa (Medicago sativa L. cv. Adriana)

Euphytica ◽  
1995 ◽  
Vol 81 (2) ◽  
pp. 151-155 ◽  
Author(s):  
F. Crea ◽  
M. Bellucci ◽  
F. Damiani ◽  
S. Arcioni
Keyword(s):  
Somatic Embryogenesis ◽  
Medicago Sativa ◽  
Genetic Control ◽  
Medicago Sativa L

scholarly journals EMBRIOGENESIS SOMATIK IN VITRO DAN REGENERASI PLANLET DARI TIGA VARIETAS ALFALFA (Medicago sativa L.)

2019 ◽  
Vol 6 (1) ◽  
pp. 83
Author(s):  
Sulastri Sulastri ◽  
Winda Nawfetrias ◽  
Djatmiko Pinardi ◽  
Henti Rosdayanti
Keyword(s):  
Somatic Embryogenesis ◽  
Medicago Sativa ◽  
Callus Induction ◽  
Plantlet Regeneration ◽  
Dichlorophenoxyacetic Acid ◽  
Naphthaleneacetic Acid ◽  
Medicago Sativa L ◽  
Embryogenic Callus Induction ◽  
2,4 Dichlorophenoxyacetic Acid

In Vitro Somatic Embryogenesis and Plantlet Regeneration of Three Varieties of Alfalfa (Medicago sativa L.)ABSTRACTAlfalfa (Medicago sativa L.) is a valuable plant as a source of food for animal, forage, pharmaceutical, medicine, food supplement, and human consumption.  In vitro selection technology combined with induction or spontaneous mutagenesis has been effective in altering or isolating genetic variability for desirable characters.  Consequently, a reproducible in vitro propagation technique of that plant is mandatory. The aim of the research was to obtain information on the embryogenic callus induction, somatic embryogenesis, and plantlet regeneration of three varieties of alfalfa. The results showed that an optimum embryogenic callus induction (82%) was obtained on Murashige & Skoog (MS) basal medium containing 2 ppm 2,4-dichlorophenoxyacetic acid (2,4-D), 2 ppm kinetin and 2 ppm a-naphthaleneacetic acid (NAA). Those embryogenic calli could subsequently develop into somatic embryos, which germinated and regenerated into normal plantlets on R1 medium consisting of MS nutrients without the addition of plant growth regulator.Keywords: alfalfa, callus, embryogenic, plantlets, regeneration ABSTRAKAlfalfa (Medicago sativa) adalah tanaman berharga sebagai sumber makanan untuk hewan, yaitu hijauan pakan ternak, farmasi, obat-obatan, suplemen makanan dan konsumsi manusia. Teknologi seleksi in vitro yang dikombinasikan dengan induksi atau mutagenesis spontan telah terbukti efektif dalam mengubah atau mengisolasi variabilitas genetik untuk karakter yang diinginkan. Oleh sebab itu, keberhasilan teknik perbanyakan in vitro yang telah terbukti dapat direproduksi dari tanaman tersebut menjadi syarat yang harus terpenuhi. Tujuan dari penelitian ini adalah untuk mendapatkan informasi mengenai induksi kalus embriogenik, embriogenesis somatik dan regenerasi planlet dari tiga varietas alfalfa. Hasil penelitian menunjukkan bahwa induksi kalus embriogenik optimal (82%) didapat pada media Murashige & Skoog (MS) dengan  2 ppm 2,4-dichlorophenoxyacetic acid (2,4-D), 2 ppm kinetin dan 2 ppm a-naphthaleneacetic acid (NAA). Kalus embriogenik tersebut dapat membentuk embrio somatik, embrionya berkecambah dan beregenerasi membentuk planlet normal pada perlakuan media R1 yaitu nutrisi MS tanpa penambahan zat pengatur tumbuh.Kata Kunci: alfalfa, embriogenik, kalus, planlet, regenerasi

Inheritance of somatic embryogenesis in alfalfa (Medicago sativa L.)

Genome ◽  
1989 ◽  
Vol 32 (2) ◽  
pp. 318-321 ◽  
Author(s):  
M. M. Hernández-Fernández ◽  
B. R. Christie
Keyword(s):  
Tissue Culture ◽  
Somatic Embryogenesis ◽  
Medicago Sativa ◽  
Key Words ◽  
Complete Dominance ◽  
Callus Production ◽  
Medicago Sativa L

To study the inheritance of somatic embryogenesis in alfalfa (Medicago sativa L.), three alfalfa genotypes were self-pollinated and intercrossed. A70-34 is a highly embryogenic genotype; R3 produced callus but not embryos; and MK does not produce callus. Callus production was controlled by one locus with complete dominance. In a survey of 107 alfalfa genotypes, the dominant and recessive alleles were present in equal frequencies. Embryogenesis among those plants producing callus was controlled by two complementary loci with additivity within each locus. The suggested designations for the two genes are Rna and Rnb.Key words: alfalfa, Medicago sativa L., tissue culture, somatic embryogenesis, inheritance.

Insecticidal Active Rotenoids from Plant Parts and Callus Culture of Medicago sativa L. from a Semiarid Region of India (Rajasthan)

2020 ◽  
Vol 16 (6) ◽  
pp. 937-941
Author(s):  
Sharad Vats ◽  
Preeti Mehra
Keyword(s):  
Medicago Sativa ◽  
Callus Culture ◽  
Point Of View ◽  
Semiarid Region ◽  
Disease Vectors ◽  
Vector Borne Diseases ◽  
Plant Parts ◽  
Resistant Varieties ◽  
Medicago Sativa L

Background: Vector-borne diseases are quite prevalent globally and are one of the major causes of deaths due to infectious diseases. There is an availability of synthetic insecticides, however, their excessive and indiscriminate use have resulted in the emergence of resistant varieties of insects. Thus, a search for novel biopesticide has become inevitable. Methods: Rotenoids were isolated and identified from different parts of Medicago sativa L. This group of metabolites was also identified in the callus culture, and the rotenoid content was monitored during subculturing for a period of 10 months. Enhancement of the rotenoid content was evaluated by feeding precursors in a tissue culture medium. Results: Four rotenoids (elliptone, deguelin, rotenone and Dehydrorotenone) were identified, which were confirmed using spectral and chromatographic techniques. The maximum rotenoid content was found in the seeds (0.33±0.01%), followed by roots (0.31±0.01%) and minimum in the aerial parts (0.20±0.05%). A gradual decrease in the rotenoid content was observed with the ageing of subcultured tissue maintained for 10 months. The production of rotenoids was enhanced up to 2 folds in the callus culture using amino acids, Phenylalanine and Methionine as precursors as compared to the control. The LC50 value of the rotenoids was found to be 91 ppm and 162 ppm against disease vectors of malaria and Dracunculiasis, respectively. Conclusion: The study projects M. sativa as a novel source of biopesticide against the disease vectors of malaria and Dracunculiasis. The use of precursors to enhance the rotenoid content in vitro can be an effective venture from a commercial point of view.

Sign in / Sign up

Export Citation Format

Share Document