scholarly journals In Vitro Callus Culture and Plant Regeneration from Different Explants of Groundnut(Arachis hypogaea L.).

1996 ◽  
Vol 46 (4) ◽  
pp. 315-320
Author(s):  
Perumal Venkatachalam ◽  
Adaikalam Subramaniampillai ◽  
Narayanasamylpillai Jayabalan
1992 ◽  
Vol 70 (6) ◽  
pp. 1186-1192 ◽  
Author(s):  
R. Gill ◽  
Praveen K. Saxena

An efficient procedure has been developed for inducing direct somatic embryogenesis, organogenesis, and regeneration of plants from tissue cultures of peanut (Arachis hypogaea L.). Thin transverse sections of the cotyledons and juvenile leaves were cultured on Murashige and Skoog medium supplemented with N6-benzylaminopurine (BAP) or a substituted phenylurea, thidiazuron (TDZ). Somatic embryos or shoot buds differentiated from cut surfaces of the cotyledons and midrib region of the leaves. The application of BAP induced differentiation of shoot buds whereas the treatment with TDZ resulted in the production of somatic embryos. Somatic embryos developed into plants after subculturing on a basal meduim. Agar-solidified medium was found to be superior to the liquid medium for the development of embryos and shoot buds. The procedure of TDZ-induced somatic embryogenesis and plant regeneration was successfully applied to three genotypes of peanut. A distinct feature of this study is the induction of the morphogenic competence in cultures of seedling expiants of peanut that so far have remained recalcitrant to somatic embryogenesis in vitro. Key words: peanut, Arachis hypogaea, shoot regeneration, somatic embryogenesis, thidiazuron, plant regeneration.


1981 ◽  
Vol 59 (5) ◽  
pp. 826-830 ◽  
Author(s):  
L. A. Mroginski ◽  
K. K. Kartha ◽  
J. P. Shyluk

The in vitro regeneration of buds, shoots, and roots from immature leaves of 3- to 5-day-old peanut (Arachis hypogaea L. cv. Colorado Manfredi) seedlings was studied under defined nutritional, hormonal, and environmental conditions. The first two leaves (2–5 mm in length) removed from aseptically germinated seeds were cultured on Murashige and Skoog medium containing vitamins as in B5 medium and 0.8% agar, supplemented with 12 combinations of naphthaleneacetic acid (NAA) (0.01 to 4 mg/L) and benzyladenine (BA) (1 and 3 mg/L). Bud regeneration occurred in all hormone combinations, but the maximum number of buds was regenerated at a concentration of 1 mg/L each of NAA and BA. Although bud regeneration was maximum with 2- to 5-mm-long leaflets, some success was also obtained with leaflets 8–13 mm long. However, no buds were regenerated when fully expanded leaflets were cultured.Development of buds into shoots was readily achieved by transferring regenerated buds into fresh medium containing 0.01 mg/L NAA and 1 mg/L BA. A few roots were induced to grow when callus with buds was also transferred to medium devoid of hormones. So far, bud regeneration from immature leaves has been induced in vitro in 5 of the 10 cultivars tested.


1992 ◽  
Vol 19 (2) ◽  
pp. 78-82 ◽  
Author(s):  
Tallury P. S. Rau ◽  
H. T. Stalker ◽  
H. E. Pattee ◽  
P. Reece

Abstract Arachis hypogaea L. cv. NC 4 was used as a model plant system in an effort to develop an in vitro embryo rescue protocol which could have application to interspecific hybrid embryos, which often abort at very early growth stages. Embryo growth and development was studied in 1- to 4-day-old peg tips containing proembryos equivalent to a stage where many interspecific hybrid embryos abort. Three independent experiments were conducted to 1) determine the most favorable basal media, 2) evaluate the effects of auxins and cytokinins on growth, and 3) determine a favorable combination of auxins and cytokinins for in vitro peanut embryo growth. The results indicated that MS (Murashige and Skoog) medium with 3% sucrose was the most favorable basal medium among seven media and two sucrose concentrations analyzed. IAA (indole-3-acetic acid) at 1.5 mg L-1 in combination with a range of KN (kinetin) levels from 0.5 to 1.25 mg L-1 were the growth regulator combinations of choice. Proembryo growth reached the multicellular globular stage, but differentiation into heart-shaped embryos did not occur.


1994 ◽  
Vol 21 (2) ◽  
pp. 112-115 ◽  
Author(s):  
D. W. Gorbet ◽  
R. L. Stanley ◽  
D. A. Knauft

Abstract Livestock production enterprises in the southern USA depend primarily on forage for feed. With the development of peanut (Arachis hypogaea L.) lines with good late leaf spot (Cercosporidium personatum (Berk. & Curt.) Deighton) resistance in the Florida breeding program, studies were initiated in 1983 at Marianna to evaluate their forage potential. Peanut breeding lines were grown without fungicide applications for leaf spot control and cuttings were made to evaluate forage production. Two forage cuttings were compared to a single cutting or harvest for each genotype. Pod yields were taken at the end of each season. Some lines produced dry matter forage yields exceeding 9000 kg ha-1 with two cuttings, with some single harvest yields exceeding 7000 kg ha-1. Significant differences were observed among genotypes, years, and forage harvest treatments. Two cuttings always produced the greatest forage yield but reduced pod yields as much as 50% for some entries. Some genotypes produced pod yields of 4000 kg ha-1 with the single forage harvest. Crude protein values for the forage were generally higher for two cuttings (14.0 − 19.6%), as compared to the single cutting or harvest (12.5 − 15.1%). In vitro organic matter digestibility (IVOMD) ranged from 59.6 − 72% for forage samples. These protein and digestibility values compare favorably to alfalfa (Medicago sativa L.) and perennial rhizoma peanut cultivars of A. glabrata Benth.


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