Isolation of MTX-resistant Cell Line NP-19 of Nicotiana plumbaginifolia: Phenotypic, Genetic and Biochemical Study

Several cell lines of Nicotiana plumbaginifolia resistant tomethotrexate (MTX) were isolated upon gradual elevation of theMTX concentration in the growth medium. One of the MTX-resistantcell lines, NP-19, acquired resistance to 10 mmol m^–3MTX, that is, at least 50-fold higher than the lethal dose forthe wild-type cell suspension. Its resistance was stably maintainedupon prolonged withdrawal of the drug. The acquisition of resistancewas accompanied by severe deterioration of regeneration potential.Regenerated shoots still manifested resistance to 50 mmol m^–3.MTX-resistant colonies and tiny shoots were recovered followingasymmetric fusion between -irradiated NP-19 protoplasts andN. plumbaginifolia leaf mesophyll-derived protoplasts on a mediumcontaining 10 mmol m^–3 MTX. The development of the shootsderived both from NP-19 calli and following somatic fusion wasarrested at the stage of 6–8 leaves. No difference wasfound in uptake of ³H-MTX between cell suspension of NP-19 andthe parental cell line. A 30-fold increase in binding of ³H-MTXto protein extract was found in cell line NP-19, suggestingdifferential capacity of MTX binding as a mechanism involvedin the MTX resistance of this cell line. Since differentiatedorgans seem more sensitive to MTX than undifferentiated tissues,this cell line is a promising source for a gene(s) conferringenhanced MTX-tolerance both in non-differentiated and differentiatedtissues. Key words: Methotrexate resistance, MTX-binding capacity, MTX uptake, tobacco cell culture     

Organs and Plantlets Regeneration of Gladiolus through Tissue Culture

Explants from inflorescence stalks of Gladiolus when culturedin vitro regenerated new plantlets within 6–7 weeks. Regenerationwas started by the formation on the basal end of a thin layerof callus and root primordia. This was followed by formationof buds and cormlets, on the distal end. The regeneration ofthe various organs from the explants was found to be polarizedand depended on the levels of growth substances added to thebasal medium, best combination for organ initiation being 10ppm naphthalene-acetic acid and 0.5 ppm of kinetin.     

Geotropic Responses and Pod Development in Gynophore Explants of Peanut (Arachis hypogaea L.) Cultured In Vitro

Peanut gynophore explants cultured in vitro on a defined mediumshow a positive geotropic response in both light and dark whenplanted either horizontally, or vertically with the tip pointingupwards. The growth following the initial curvature dependedon age of the gynophores and on the levels of growth substancesin the medium. In the dark and in presence of 0·01–0·1p.p.m. kinetin, naphthalene acetic acid at concentrations of0·1 p.p.m. and lower promoted gynophore elongation. Athigher concentrations elongation was promoted to a lesser extentin younger explants, caused enlargement of the ovary and formationof pods. Young explants generally elongated more than olderones and pod formation took place inside the medium, while inolder ones it took place above the medium. In the light, theinitial positive geotropic response was followed by elongationbut without any enlargement of the ovary. Decapitation of gynophores1·5–2·0 mm below their tip, removing theovary but leaving most of the intercalary meristem, had no effecton the geotropic response and elongation. The initial geotropicresponse and elongations of explants in vitro was not dependenton the presence of the ovary but on the meristem proximal toit. Changes in growth substances balance during gynophore developmentseem to affect geotropic response, elongation and pod formationin the peanut.     

Pod Formation and Its Geotropic Orientation in the Peanut, Arachis hypogaea L., in Relation to Light and Mechanical Stimulus

Gynophore elongation, pod formation and pod orientation in thepeanut plant (Arachis hypogaea L.) were studied in relationto the effects of light and dark conditions, mechanical stimulus,and growth substances. It was found that the proembryos controlgynophore elongation, probably by secretion of growth regulatorswhich stimulate cell division in the intercalary meristem locatedproximal to the ovules. The stimulus of pod production causesthe development of the proembryo into a mature embryo simultaneouslywith the growth of pod tissues and the cessation of gynophoreelongation. Darkness was found to be an essential factor forthe induction of pod formation. Pod formation did not occurin any of the treatments performed in the light, including theapplication of different growth substances on the ovary. A mechanicalstimulus is needed, in addition to darkness, for the normalthickening and diageotropic orientation of the pod, caused bya higher growth rate of the basal proximal side of the pod.The two ovules are always located on the upper wall of the diageotropicallyoriented pod (ventral suture). A possible mechanism which causessuch an orientation is discussed.     

Photomorphogenesis of the Gynophore, Pod and Embryo in Peanut, Arachis hypogaea L.

Darkened excized gynophores ceased to elongate after 8–10days in vitro and started to form a pod. Gynophore elongationwas inhibited to a greater extent in total darkness than underlow irradiance, while pod and embryo growth was stimulated indarkness only. Intact gynophores, enclosed in transparent vials containingglass beads, continued to elongate in both light and darkness.In light the elongating gynophores thickened as they penetratedbetween the glass beads, forming a seedless pod at the bottomof the vials. In the dark the elongating gynophores producedsmall pods in which the seeds had started to grow. Excized gynophores elongated in vitro under continuous whitelight at a rate similar to that of intact exposed gynophores.The rate of elongation in vitro, was lower under continuousblue or red-enriched light, than under white light, and wasfurther reduced under continuous far-red irradiation. Pods didnot form during any of the continuous irradiation treatmentsbut only after transfer to darkness, the largest pods formingafter continuous far-red irradiation. As little as 10 min daily exposure to red or far-red irradiancehad the same effect on gynophore elongation as continuous irradiation.Pods formed only when the daily periods of far-red irradiationwere 30 min or less. Reducing the daily exposures to 2 min decreasedthe time to onset of pod formation from 30 to 16 days. Far-redfollowing red irradiation was effective in inhibiting gynophoreelongation stimulated by red irradiation. Pod formation in red/far-redirradiation was only 50 per cent of that observed in far-redirradiation. The involvement of light in continual gynophoreelongation and in the concomitant inhibition of proembryo growthis discussed. Arachis hypogaea L., peanut, gynophore, photomorphogenesis, embryo development, pod development, proembryo