Abstract:Striga and Orobanche seeds germinate in response to a host-derived germination stimulant. Dose-response curves of the synthetic strigolactone analogues GR 24 and Nijmegen 1 were determined, and their activities were compared to that of the naturally occurring stimulant sorgolactone. Typical sigmoidal curves were obtained. ED(50) values for GR 24 were in the order of 10(-)(9)-10(-)(8) mol/L; for Nijmegen 1 these values were 3 orders of magnitude higher. Both synthetic stimulants are appreciably active at low co… Show more
“…Successful surface sterilization and germination of parasite seeds is prerequisite for derivation of in vitro culture. It is well known, that Striga and Orobanche seeds germinate in response to native or synthetic (GR24 and Nijmegen 1) germination stimulants (Wigchert et al 1999). Different combinations of plant growth regulators were studied for establishment of in vitro cultures of Orobanche ramosa, O. minor, O. aegyptica (Zhou et al 2004), C. reflexa (Srivastava & Dwivedi 2001), C. japonica (Furuhashi 1991) and C. trifolli (Bakos et al 1995).…”
Agrobacterium tumefaciens-mediated transformation of callus culture, combined with a visual selection of GFPtagged fimbrin actin binding domain (FABD2) expression is described for parasitic species (Cuscuta europaea). The conditions for callus induction from 1 cm-long explants from the basal part of 7-day-old dodder seedlings were defined. We obtained light-green calli, which were transformed with A. tumefaciens bacterial strain GV3101 carrying plasmid pCB302 (35S::ABD2:gfp) with neomycin phosphotransferase (nptII) gene. The limitations of selection procedures based on antibiotics were avoided using green fluorescent protein (GFP) detection, as a visual selection marker subcellularly targeted to the actin cytoskeleton. Fluorescence microscopy analyses demonstrated a network of nucleus-associated actin arrays and dense cortical actin arrangements in stably transformed Cuscuta callus cells. RT-PCR analyses confirmed gfp expression in transformed calli 7, 14 and 21 days after transformation. Although the GFP fluorescence associated with the actin cytoskeleton has retained for at least six months without silencing, no shoot regeneration was observed. It can be concluded that, C. europaea callus cells are competent for transformation, but under given conditions, these cells failed to realize their morphogenic and regeneration potentials.
“…Successful surface sterilization and germination of parasite seeds is prerequisite for derivation of in vitro culture. It is well known, that Striga and Orobanche seeds germinate in response to native or synthetic (GR24 and Nijmegen 1) germination stimulants (Wigchert et al 1999). Different combinations of plant growth regulators were studied for establishment of in vitro cultures of Orobanche ramosa, O. minor, O. aegyptica (Zhou et al 2004), C. reflexa (Srivastava & Dwivedi 2001), C. japonica (Furuhashi 1991) and C. trifolli (Bakos et al 1995).…”
Agrobacterium tumefaciens-mediated transformation of callus culture, combined with a visual selection of GFPtagged fimbrin actin binding domain (FABD2) expression is described for parasitic species (Cuscuta europaea). The conditions for callus induction from 1 cm-long explants from the basal part of 7-day-old dodder seedlings were defined. We obtained light-green calli, which were transformed with A. tumefaciens bacterial strain GV3101 carrying plasmid pCB302 (35S::ABD2:gfp) with neomycin phosphotransferase (nptII) gene. The limitations of selection procedures based on antibiotics were avoided using green fluorescent protein (GFP) detection, as a visual selection marker subcellularly targeted to the actin cytoskeleton. Fluorescence microscopy analyses demonstrated a network of nucleus-associated actin arrays and dense cortical actin arrangements in stably transformed Cuscuta callus cells. RT-PCR analyses confirmed gfp expression in transformed calli 7, 14 and 21 days after transformation. Although the GFP fluorescence associated with the actin cytoskeleton has retained for at least six months without silencing, no shoot regeneration was observed. It can be concluded that, C. europaea callus cells are competent for transformation, but under given conditions, these cells failed to realize their morphogenic and regeneration potentials.
“…Sigmoidalshaped curves display a suboptimal (linear) zone at low strigolactone concentrations, reaching an optimal (saturation) zone at high concentrations. Bell-shaped curves show also a supraoptimal zone, characterized by a decline of the response at considerably high strigolactone concentrations (Wigchert et al 1999). This pattern could hold true also for GR24 inhibition of axillary buds.…”
The role of strigolactones as plant growth regulators
has been demonstrated through research on biosynthesis
and signaling mutant plants and through the use of
GR24, a synthetic analog of this class of molecules. Strigolactone
mutants show a bushy phenotype and GR24 application
inhibits the growth of axillary buds in these mutants,
thus restoring the phenotype of a wild plant, which is characterized
by a stronger apical dominance. In this work, we
tested the effectiveness of this chemical on pea (Pisum sativum)
plants following apex removal, which disrupts apical
dominance and leads to axillary bud outgrowth. Moreover,
we searched for relationships between the response to the
strigolactone and gibberellin metabolism by applying GR24
to both climbing and dwarf peas, the latters being mutants
for gibberellin biosynthesis. The results suggest that the
endogenous level of the bioactive gibberellin GA1 might
modulate the response of decapitated pea plants to GR24, by
changing bud sensitivity to the applied strigolactone
“…Compounds structurally related to strigolactone are potent synthetic germination stimulants for many Striga and Orobanche/Phelipanche species (Zwanenburg & Wigchert 1998;Wigchert et al 1999) but their usage in the field has not been practical up to now due to the high cost involved in their synthesis and also their instability in soils with high pH (Dhanapal & Struik 1996;Kroschel 2001;Lopez-Raez et al 2008). Therefore, detailed studies are needed to solve the issues about the cost and the formulation of the substances, which are affecting the efficiency and stability of them in the field conditions.…”
Section: Resultsmentioning
confidence: 99%
“…The application of germination stimulants to induce suicidal seed germination of parasitic weeds appears attractive for biosafety reasons, rapid soil decomposition, and high biological activity at very low application rates (Elzein & Kroschel 2004). Compounds structurally related to strigolactone are potent synthetic germination stimulants for many Orobanche species (Zwanenburg & Wigchert 1998;Wigchert et al 1999). Synthetic strigolactone analogues of the strigolactones have been synthesized by several working groups: Johnson, Welzel, Zwanenburg (Wegman 2006).…”
Broomrapes (Orobanche/Phelipanche spp.) are considered as the most important problem of some cultivated plants, especially belonging to Solanaceae and Fabaceae families. Phelipanche ramosa L. and Phelipanche aegyptiaca (L.) Pers. cause serious problems especially in tomato grown areas in Turkey and the other Mediterranean countries. This study was conducted to determine the effect of some synthetic stimulant substances and root exudates on the germination rate of the broomrape species under controlled laboratory conditions. GR24 (0.1-1 ppm), GR7 (0.1-1 ppm) and GA3 (10 ppm) were used as synthetic germination stimulant substances; otherwise flax, cotton, soybean, bean, pea, cowpea, tomato, lentil, cucumber and tobacco seedlings were used for root exudates. According to average results of the trials; synthetic stimulants and root secretions increased the germination rate of P. ramosa at the range of 50-77% and 0-16% respectively, otherwise average data for P. aegyptiaca are 62-95% and 0-63%. As a result of the studies it was determined that synthetic stimulants were significantly increased the germination rate of Phelipanche species.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.