scholarly journals In vitro placental self and cross pollination in some species

2014 ◽  
Vol 60 (1-2) ◽  
pp. 93-97
Author(s):  
Azza Shehata ◽  
Maciej Zenkteler

Excised placentae with ovules of <i>Primula pubescens</i>, <i>P. auricula</i>, <i>Scopolia carniolica</i>, <i>Digitalis purpurea</i>, <i>Torenia fournieri</i> and <i>Chionodoxa luciliae</i> were self pollinated in vitro and the development of seeds was observed. The same method was used for obtaining hybrid globular embryos from crosses between: <i>P. pubescens</i> x <i>P. auricula</i>, <i>Scopolia carniolica</i> x <i>Physochlaina praealta</i>, <i>Melandrium album</i> x <i>Silene saxifraga</i> and <i>M. album</i> x <i>Arenaria pungens</i>.

Zygote ◽  
2008 ◽  
Vol 16 (2) ◽  
pp. 179-186 ◽  
Author(s):  
S.H. Chen ◽  
Y.H. Yang ◽  
J.P. Liao ◽  
A.X. Kuang ◽  
H.Q. Tian

SummaryEgg cells of Torenia fournieri were isolated from embryo sacs 1 day after anthesis using enzymatic digestion or mechanical dissection. About 5% of the egg cells and zygotes (2–3 from 50 ovules) could be mechanically dissected within 2 h. When 0.1% cellulase and 0.1% pectinase were added to the mannitol isolation solution, about 18% of the egg cells (8–10 from 50 ovules) could be isolated within 2 h. The egg cells isolated by mechanical dissection could be used for in vitro fertilization studies without any of the potentially deleterious effects of the enzymes on the plasma membrane of egg cell. The egg cells isolated using enzymatic digestion could be used in the study of the molecular biology of female gamete because more egg cells could be isolated with this technique. Using enzymatic digestion, over 10 zygotes from 50 ovules (over 20%) were isolated from the pollinated ovules. Coupled with our successful isolation of mature sperm cells, the isolation of egg cells of T. fournieri will make in vitro fertilization possible in a dicotyledon plant.


2006 ◽  
Vol 12 (4) ◽  
Author(s):  
P. Vági ◽  
K. Imre ◽  
Z. Kristóf

In contrast to most angiosperms, Torenia contains a naked embryo sac and therefore has been considered since many years as an exciting model plant to study the double fertilization process of flowering seed plants. It is thus not surprising that the isolation of protoplasts from the female gametophyte has been reported already 20 years ago by Mol, the isolation of megaspores and megagametophytes has been published by the authors of this manuscript in 1996 and in 1999. The isolation of the male gametophyte and of sperm cells was published by the authors in 2004. The isolation of viable Torenia sperm cells is a crucial part of the elaboration of an in vitro fertilization system. Torenia sperm cells were isolated from in vivo — in vitro cultured pollen tubes. In this system pollen tubes first grow inside a cut style then follow their elongation in a solid isolation medium. The medium contained agarose in order to detain pollen tube contents. Released sperm cells and enzymatically isolated egg cells were collected and handled using glass micropipettes and transmitted to an electrofusion apparatus or polyethylene glycol containing media for fusion probes.


1993 ◽  
Vol 10 (3) ◽  
pp. 298-300
Author(s):  
Shigeru KOBAYASHI ◽  
Wakanori AMAKI ◽  
Haruzo HIGUCHI

HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1112e-1112
Author(s):  
Masood Hadi ◽  
Mark P. Bridgen

Callus cultures of Torenia fournieri `Compacta Blue' were initiated on a modified Murashige and Skoog salt medium (MS) with 2.26 uM 2,4-dichloro-phenoxy acetic acid. Shoots were regenerated from these cultures using the MS medium amended with 2.46 uM 3-indolebutyric acid and 8.88 uM 6-benzylaminopurine. These shoots were subjected to Tetranychus urticae Koch (twospotted spidermite) and Trialeurodes vaporariorum (Westwood) (greenhouse whitefly) in vitro. Pests were allowed to feed until such time that the pest population started to decrease due to lack of food. Remaining shoot tissue was placed on MS medium amended with 2.28 uM zeatin to -induce shoot formation. Shoots were acclimated to greenhouse conditions and evaluated for resistance to the pest to which they were subjected in vitro. Highly significant differences in pest numbers were found in somaclones when compared to control plants. A wide range of variability was observed within the somaclonal population.


1998 ◽  
Vol 8 (2) ◽  
pp. 179-182
Author(s):  
Masood Z. Hadi ◽  
Mark P. Bridgen ◽  
John P. Sanderson

Procedures were developed to determine if live, adult two-spotted spidermites (Tetranychus urticae Koch) could be surface disinfested before being introduced into in vitro cultures of torenia (Torenia fournieri L.). Three time periods (5, 10, and 15 minutes) and five levels of sodium hypochlorite (0.05% to 0.25%) were evaluated. Surface disinfestation was accomplished by agitating 2 × 3 cm pieces of infested bean leaves in sodium hypochlorite solutions and then drying in a mite drier apparatus. All sodium hypochlorite concentrations disinfested the mites completely, however high concentration levels were lethal to the mites. Exposure periods of 10 and 15 minutes also significantly increased mortality. For optimum disinfestation of two-spotted spidermites with minimum mortality, a concentration of 0.05% sodium hypochlorite and 0.05% Tween-20 for 5 minutes should be used.


2016 ◽  
Vol 8 (2) ◽  
pp. 43 ◽  
Author(s):  
Pauline D. Kasi ◽  
Sumaryono Sumaryono

Development of somatic embryos of sago (Metroxylon sagu Rottb.) on agar-solidified medium are highly varied producing heterogeneous seedlings. Understanding of this phenomenon may help in improving the cultural procedures and conditions of sago<br />somatic embryogenesis to obtain uniform seedlings in a large scale. This experiment was conducted at the laboratory for plant cell culture and micropropagation, Indonesian Biotechnology Research Institute for Estate Crops from January to March 2006 to examine morphological changes i.e. color and development stages of sago during their somatic embryo development on an agar-solidified medium. Twenty single globular somatic embryos of sago with specific color (yellowish, greenish, and reddish) were cultured in a Petri dish supplemented with a solid medium. The medium was a micronutrients-modified MS (MMS) with half strength of macronutrients containing 0.01 mg l-1 ABA, 2 mg l-1 kinetin, 20 g l-1 sucrose, 0.5 g l-1 activated charcoal, and 2 g l-1 gelrite. Parameter observed was the percentage of embryo’s number based on color and developmental stage. The result showed that at the end of 6-week culture passage, most originally greenish (80.8%) and reddish (95.8%) embryos remained unchanged in their colors, whereas almost half of the originally yellowish embryos turned to greenish and only 30%<br />remained yellowish. At the same time, single globular embryos have changed gradually into the next developmental stages, although not all of the embryos were germinated. The initial color of embryo affected the rate of the developmental stage changes. Yellowish and greenish globular embryos developed more rapidly into cotyledon or germinant stages at 58% and 55% respectively, in 6 weeks than the reddish ones (41%). Therefore, the yellowish and greenish embryos are the best sources of material for in vitro mass propagation and synthetic seed production of sago.


2014 ◽  
Vol 16 (1) ◽  
pp. 51 ◽  
Author(s):  
Naivy Lisbet Pérez-Alonso ◽  
Franklyn Arana Labrada ◽  
Alina Capote Pérez ◽  
Anabel Pérez Pérez ◽  
Rafael Sosa ◽  
...  
Keyword(s):  

2007 ◽  
Vol 47 (7) ◽  
pp. 877 ◽  
Author(s):  
S. M. Liu ◽  
S. R. Sykes ◽  
P. R. Clingeleffer

Carina is a significant grape variety grown in Australia to produce dried currants. Its yield and fruit quality are restricted by pollination; however, this can be improved by the judicious use of hormone-based setting sprays. Male fertility and seedless berry set in Carina were investigated by examining pollen viability, the effect of self- and cross-pollination on berry set and in ovulo embryo recovery in comparison with two pollen sterile varieties, Hunisa and Kishmishi. Carina pollen failed to germinate in vitro and gave poor berry set when used to pollinate Hunisa and Kishmishi. Percentage berry set in Carina was unaffected by pollination treatments, but cross-pollination increased berry size. Larger seed traces (>1.2 mm in length) were present in most cross-pollinated Carina berries and their size and number were correlated positively with berry size. In ovulo embryo recovery rates ranged from 19.7 to 49.0% and 6.8 to 13.6% for cross-pollinated combinations of Carina when ovules were cultured at 50 and 75 days after pollination, respectively. In contrast, embryo recovery was zero from self-pollinated ovules. The results indicated that Carina produces sterile or non-functional pollen and is capable of setting seedless fruits through either parthenocarpy and/or stenospermocarpy.


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