scholarly journals Embryological studies of reciprocal crosses between Vicia faba and Vicia narbonensis

2014 ◽  
Vol 67 (1) ◽  
pp. 37-43 ◽  
Author(s):  
Maciej Zenkteler ◽  
Mechtild Tegeder ◽  
Otto Schieder
Keyword(s):  
Vicia Faba ◽  
Pollen Grains ◽  
Pollen Tubes ◽  
Flower Buds ◽  
Reciprocal Crosses ◽  
Globular Embryos ◽  
Vicia Narbonensis ◽  
Whole Number

A study was undertaken to asses the reciprocal crossability between <em>Vicia faba</em> and <em>Vicia narbonensis</em>. Flower buds or only ovaries of several varietes and genotypes were cross-pollinated in vivo (green house and field) and in vitro. Only few pollen tubes passed the style and entered into the ovary. On the whole number of 5320 cross pollinated in vivo and in vitro flowers and ovaries of <em>Vicia narbonensis</em> only 78 globular hybrid embryos were observed. After cross pollination in vivo of 3860 flower buds and ovaries of <em>Vicia faba</em> globular embryos developed in 124 ovules. The highest number of globular embryos were obtained when the <em>Vicia faba</em> line 1/33 was pollinated with <em>Vicia narbonensis</em> lines P3, P5, 150, SE.Embryogenesis proceeded till the 6-10 day after pollination, however, karyological disturbances in the cells of embryos and endosperm were often noticed at earlier stages. In vitro pollen grains of <em>Vicia faba</em> germinated on stigmas and ovaries of <em>Vicia narbonensis</em>, a significant increase in the growth of pollen tubes was noticed after ovary pollination. The technique of in vitro pollination was not suitable for <em>Vicia faba</em> as the inoculated explants died shortly after transferring onto the medium. The results indicate that finding a more suitable genotype for crossing may give a chance to obtain higher number of embryos (example line 1/33) - thus sufficient number for culturing them on media.

scholarly journals Pollen tube growth of Paeonia tenuifolia L. (Paeoniaceae) in vitro and in vivo

1970 ◽  
Vol 40 (1) ◽  
pp. 93-95 ◽  
Author(s):  
Feruzan Dane ◽  
Nuran Ekici
Keyword(s):  
Pollen Tube ◽  
Pollen Germination ◽  
Pollen Viability ◽  
Pollen Grains ◽  
Pollen Tubes ◽  
In Vivo Studies ◽  
In Vivo Growth ◽  
Paeonia Tenuifolia

In vitro and in vivo studies on pollen germination of Paeonia tenuifolia L. (Paeoniaceae) revealed that pollen grains are shed at two-celled stage. Normal and abnormal pollens were observed. Pollen viability was recorded between 55 and 75%. In vitro studies revealed 85% germination and usually the germination was monosphonic. Some pollen tubes with swollen tube tip and undulations were found. Styles and stigma were found to contain many pollen tubes 24 hrs after pollination. Key words: Paeonia tenuifolia; Pollen tube; In vitro growth; In vivo growth  DOI: http://dx.doi.org/10.3329/bjb.v40i1.8003 Bangladesh J. Bot. 40(1): 93-95, 2011 (June)

scholarly journals In vivo and in vitro pollen maturation in Lilium: influence of carbohydrates

2014 ◽  
Vol 65 (1-2) ◽  
pp. 73-82 ◽  
Author(s):  
Christophe Clement ◽  
Daniel Al-Awad ◽  
Jean C. Audran
Keyword(s):  
Germination Rate ◽  
Starch Synthesis ◽  
Pollen Grains ◽  
Second Phase ◽  
Flower Buds ◽  
Flower Bud ◽  
Pollen Maturation ◽  
Microspore Stage

The purpose of this study was to develop a protocol for <em>in vitro</em> conform pollen maturation, as a model to study the involvement of carbohydrates on pollen maturation in <em>Lilium</em>. <em>In vivo</em> and <em>in vitro</em> pollen maturations were followed and compared by transmission electron microscopy, and several <em>in vitro</em> parameters were tested in terms of carbohydrate physiology. <em>In vivo</em>, pollen maturation was initiated at the vacuolated microspore stage, and consisted of two successive phases. The first phase was characterized by reactivation of microspore organelles, followed by microspore mitosis, starch synthesis and vacuole breakdown. During the second phase, starch was progressively degraded whereas lipid and phytine reserves accumulated. <em>In vivo</em>, pollen maturation occured within 14 days and pollen germination rate was 73.6 ± 2.2%. We then attempted to realise <em>in vitro</em> pollen maturation starting from the vacuolated microspore stage. The best results were obtained with flower buds cultivated at 26<sup>o</sup>C, in 100 µmol/m<sup>2</sup>/s light, with a 16h/8h photoperiod on a modified Heller's medium supplemented with NAA (10<sup>-2</sup> mg/l) and sucrose (M/6). In these conditions, pollen maturation occured within 7 days only. <em>In vitro</em> matured pollen is cytologically comparable to <em>in vivo</em> developed pollen grains and the germination rate was 72.4 ± 3.7%. When flower buds were cultivated in the dark, the germination rate decreased, but this could be compensated by providing high sucrose concentrations (1M) in the medium. Further, photosynthesis inhibitors had the same effect on pollen maturation than the darkness, strongly suggesting that photosynthesis occurs in the flower bud and is important for pollen maturation in <em>Lilium</em>.

scholarly journals Bacillus megaterium-Mediated Synthesis of Selenium Nanoparticles and Their Antifungal Activity against Rhizoctonia solani in Faba Bean Plants

2021 ◽  
Vol 7 (3) ◽  
pp. 195
Author(s):  
Amr H. Hashem ◽  
Amer M. Abdelaziz ◽  
Ahmed A. Askar ◽  
Hossam M. Fouda ◽  
Ahmed M. A. Khalil ◽  
...  
Keyword(s):  
Antifungal Activity ◽  
Vicia Faba ◽  
Root Rot ◽  
Antifungal Agents ◽  
Damping Off ◽  
Growth Promoters ◽  
Root Rot Disease ◽  
Rot Disease

Rhizoctonia root-rot disease causes severe economic losses in a wide range of crops, including Vicia faba worldwide. Currently, biosynthesized nanoparticles have become super-growth promoters as well as antifungal agents. In this study, biosynthesized selenium nanoparticles (Se-NPs) have been examined as growth promoters as well as antifungal agents against Rhizoctonia solani RCMB 031001 in vitro and in vivo. Se-NPs were synthesized biologically by Bacillus megaterium ATCC 55000 and characterized by using UV-Vis spectroscopy, XRD, dynamic light scattering (DLS), and transmission electron microscopy (TEM) imaging. TEM and DLS images showed that Se-NPs are mono-dispersed spheres with a mean diameter of 41.2 nm. Se-NPs improved healthy Vicia faba cv. Giza 716 seed germination, morphological, metabolic indicators, and yield. Furthermore, Se-NPs exhibited influential antifungal activity against R. solani in vitro as well as in vivo. Results revealed that minimum inhibition and minimum fungicidal concentrations of Se-NPs were 0.0625 and 1 mM, respectively. Moreover, Se-NPs were able to decrease the pre-and post-emergence of R. solani damping-off and minimize the severity of root rot disease. The most effective treatment method is found when soaking and spraying were used with each other followed by spraying and then soaking individually. Likewise, Se-NPs improve morphological and metabolic indicators and yield significantly compared with infected control. In conclusion, biosynthesized Se-NPs by B. megaterium ATCC 55000 are a promising and effective agent against R. solani damping-off and root rot diseases in Vicia faba as well as plant growth inducer.

scholarly journals Prunus necrotic ringspot virus Early Invasion and Its Effects on Apricot Pollen Grain Performance

2007 ◽  
Vol 97 (8) ◽  
pp. 892-899 ◽  
Author(s):  
Khalid Amari ◽  
Lorenzo Burgos ◽  
Vicente Pallas ◽  
María Amelia Sanchez-Pina
Keyword(s):  
Developmental Stages ◽  
Generative Cell ◽  
Pollen Grains ◽  
Growth Zone ◽  
Pollen Tubes ◽  
Climatic Conditions ◽  
Pollen Grain ◽  
Ringspot Virus ◽  
Prunus Necrotic Ringspot Virus

The route of infection and the pattern of distribution of Prunus necrotic ringspot virus (PNRSV) in apricot pollen were studied. PNRSV was detected both within and on the surface of infected pollen grains. The virus invaded pollen during its early developmental stages, being detected in pollen mother cells. It was distributed uniformly within the cytoplasm of uni- and bicellular pollen grains and infected the generative cell. In mature pollen grains, characterized by their triangular shape, the virus was located mainly at the apertures, suggesting that PNRSV distribution follows the same pattern as the cellular components required for pollen tube germination and cell wall tube synthesis. PNRSV also was localized inside pollen tubes, especially in the growth zone. In vitro experiments demonstrated that infection with PNRSV decreases the germination percentage of pollen grains by more than half and delays the growth of pollen tubes by ≈24 h. However, although PNRSV infection affected apricot pollen grain performance during germination, the presence of the virus did not completely prevent fertilization, because the infected apricot pollen tubes, once germinated, were able to reach the apricot embryo sacs, which, in the climatic conditions of southeastern Spain, mature later than in other climates. Thus, infected pollen still could play an important role in the vertical transmission of PNRSV in apricot.

Broad bean (Vicia faba L.) pods: a rich source of bioactive ingredients with antimicrobial, antioxidant, enzyme inhibitory, anti-diabetic and health-promoting properties

2018 ◽  
Vol 9 (4) ◽  
pp. 2051-2069 ◽  
Author(s):  
Faiza Mejri ◽  
Slimen Selmi ◽  
Alice Martins ◽  
Haifa benkhoud ◽  
Tarek Baati ◽  
...  
Keyword(s):  
Antioxidant Enzyme ◽  
Vicia Faba ◽  
Functional Food ◽  
Broad Bean ◽  
Biological Activities ◽  
Vicia Faba L ◽  
Health Promoting ◽  
Bioactive Ingredients

Broad bean pods have been proven to be a functional food with promising in vitro and in vivo biological activities.

scholarly journals Foliar Application of Boron to Almond Trees Affects Pollen Quality

2000 ◽  
Vol 125 (2) ◽  
pp. 265-270 ◽  
Author(s):  
A.M.S. Nyomora ◽  
P.H. Brown ◽  
K. Pinney ◽  
V.S. Polito
Keyword(s):  
Pollen Germination ◽  
Foliar Application ◽  
Culture Media ◽  
Pollen Viability ◽  
Prunus Dulcis ◽  
Pollen Tubes ◽  
Tube Growth ◽  
Mature Trees

The effect of boron (B) on in vivo and in vitro development of almond [Prunus dulcis (Mill.) D.A. Webb (syn. P. amygdalus Batsch)] pollen and pollen tubes and the resultant effect on fruit set was studied in mature trees. The cultivars Mono (pistil donor) and Butte (pollinizer) in an orchard with low soil B in Fresno, California were sprayed with B at 0, 0.8, 1.7, or 2.5 kg·ha-1 during Fall 1993. Pollen viability as indicated by the fluorescein diacetate method (FDA) was >85% and was not affected by field-applied B, however, in vivo pollen germination and tube growth were enhanced by foliar-applied B. More effect of applied B on in vivo growth appeared as pollen tubes progressed toward the ovary. For in vitro germination, foliar-applied B reduced bursting of tubes, and addition of B to the culture media significantly increased pollen germination and pollen tube growth.

Investigation of the Metabolism of [3H]GA20-13-O-glucoside Vicia faba L. in vivo and in vitro

1987 ◽  
Vol 182 (5) ◽  
pp. 385-391 ◽  
Author(s):  
P. Lattke ◽  
W. Schliemann ◽  
G. Schneider
Keyword(s):  
Vicia Faba ◽  
Vicia Faba L

scholarly journals Comparative analyses of angiosperm secretomes identify apoplastic pollen tube functions and novel secreted peptides

2020 ◽  
Author(s):  
María Flores-Tornero ◽  
Lele Wang ◽  
David Potěšil ◽  
Said Hafidh ◽  
Frank Vogler ◽  
...  
Keyword(s):  
Cell Wall ◽  
Pollen Tube ◽  
Turgor Pressure ◽  
Pollen Grains ◽  
Pollen Tubes ◽  
Secreted Proteins ◽  
Reproductive Tissues ◽  
Small Proteins ◽  
Secreted Peptides

Abstract Key message Analyses of secretomes of in vitro grown pollen tubes from Amborella, maize and tobacco identified many components of processes associated with the cell wall, signaling and metabolism as well as novel small secreted peptides. Abstract Flowering plants (angiosperms) generate pollen grains that germinate on the stigma and produce tubes to transport their sperm cells cargo deep into the maternal reproductive tissues toward the ovules for a double fertilization process. During their journey, pollen tubes secrete many proteins (secreted proteome or secretome) required, for example, for communication with the maternal reproductive tissues, to build a solid own cell wall that withstands their high turgor pressure while softening simultaneously maternal cell wall tissue. The composition and species specificity or family specificity of the pollen tube secretome is poorly understood. Here, we provide a suitable method to obtain the pollen tube secretome from in vitro grown pollen tubes of the basal angiosperm Amborella trichopoda (Amborella) and the Poaceae model maize. The previously published secretome of tobacco pollen tubes was used as an example of eudicotyledonous plants in this comparative study. The secretome of the three species is each strongly different compared to the respective protein composition of pollen grains and tubes. In Amborella and maize, about 40% proteins are secreted by the conventional “classic” pathway and 30% by unconventional pathways. The latter pathway is expanded in tobacco. Proteins enriched in the secretome are especially involved in functions associated with the cell wall, cell surface, energy and lipid metabolism, proteolysis and redox processes. Expansins, pectin methylesterase inhibitors and RALFs are enriched in maize, while tobacco secretes many proteins involved, for example, in proteolysis and signaling. While the majority of proteins detected in the secretome occur also in pollen grains and pollen tubes, and correlate in the number of mapped peptides with relative gene expression levels, some novel secreted small proteins were identified. Moreover, the identification of secreted proteins containing pro-peptides indicates that these are processed in the apoplast. In conclusion, we provide a proteome resource from three distinct angiosperm clades that can be utilized among others to study the localization, abundance and processing of known secreted proteins and help to identify novel pollen tube secreted proteins for functional studies.

scholarly journals Genotoxic effects of the carbamate insecticide Pirimor-50® in Vicia faba root tip meristems and human lymphocyte culture after direct application and treatment with its metabolic extracts

2016 ◽  
Vol 67 (4) ◽  
pp. 266-276 ◽  
Author(s):  
Rafael Valencia-Quintana ◽  
Sandra Gómez-Arroyo ◽  
Juana Sánchez-Alarcón ◽  
Mirta Milić ◽  
José Luis Gómez Olivares ◽  
...  
Keyword(s):  
Vicia Faba ◽  
Human Lymphocyte ◽  
Cell Cycle Progression ◽  
Lymphocyte Culture ◽  
Root Tip ◽  
Genotoxic Effects ◽  
Animal Metabolism ◽  
Index Ratio

Abstract The aim of the study was to evaluate genotoxic effects of Pirimor-50®, a pirimicarb-based formulation (50 % active ingredient), in human lymphocyte cultures and Vicia faba root meristems. Furthermore, the objective was to examine a combined influence of insecticide treatment with mammalian microsomal S9 and vegetal S10 metabolic fractions or S10 mix metabolic transformation extracts (after Vicia faba primary roots treatment with Pirimor-50®). We used sister chromatid exchange assay-SCE and measured cell cycle progression and proliferation (proportion of M1-M3 metaphases and replication index ratio-RI). Two processes were used for plant promutagen activation: in vivo activation-Pirimor-50® was applied for 4 h to the plant and then S10 mix was added to lymphocytes; and, in vitro activation-lymphocytes were treated with Pirimor-50® and S10 or S9 for 2 h. Direct treatment induced significantly higher SCE frequencies in meristems at 0.01 mg mL-1. In lymphocytes, significantly higher SCE was at 1 mg mL-1 with decrease in RI and M1-M3 metaphase proportions at 0.5 mg mL-1 and cell division stop at 2.5 mg mL1. S10 mix lymphocyte treatment showed significantly elevated SCE values at 2-2.5 mg mL-1, with cell death at 3 mg mL-1. Lymphocyte treatment with Pirimor-50® together with S9 or S10 showed slightly elevated SCE frequency but had a significant influence on RI decrease, with lowest values in S9 treatment. Since no data are available on the genotoxicity of Pirimor-50®, this study is one of the first to evaluate and compare its direct effect in two bioassays, animal and vegetal, and also the effect of plant and animal metabolism on its genotoxic potential.

Sign in / Sign up

Export Citation Format

Share Document