scholarly journals Kultur In Vitro Endosperma, Protokol yang Efisien untuk Mendapatkan Tanaman Triploid secara Langsung

2016 ◽  
Vol 6 (2) ◽  
pp. 107
Author(s):  
Lazarus Agus Sukamto
Keyword(s):  
In Vitro Culture ◽  
Zygotic Embryo ◽  
Direct Organogenesis ◽  
Ploidy Levels ◽  
Endosperm Culture ◽  
Zygotic Embryo Culture ◽  
Seedless Fruits ◽  
Long Time ◽  
Mature Endosperm

<p>In Vitro Culture of Endosperm: An efficient protocol to<br />propagate triploid plants directly. L. Agus Sukamto.<br />Triploid plants are very vigorous and beneficial since they<br />generally produce seedless fruits, bigger flowers, and produce<br />more volume of wood than the diploid counterparts.<br />The triploid plants can be produced by crossing diploid and<br />tetraploid plants, but this method is cumbersome and takes<br />a long time. In vitro culture of endosperm is an alternative<br />method to produce triploid plants directly. The success of<br />endosperm culture is dependent on many factors, such as<br />maturity of endosperm, presence of the zygotic embryo, culture<br />medium, growth regulators, browning, culture period,<br />an plant species. Generally, a mature endosperm needs an<br />initial association with an embryo to induce cell divisions,<br />while proliferation of an immature endosperms is not<br />dependent on the embryo. Endosperm of most parasitic<br />angiosperms shows direct organogenesis without callus<br />formation. Plants produced from endosperm culture are<br />generally triploid, although some plants possess different<br />ploidy levels.</p>

scholarly journals In vitro culture from mature seeds of Passiflora species

2004 ◽  
Vol 61 (1) ◽  
pp. 108-113 ◽  
Author(s):  
Flavia Guzzo ◽  
Stefania Ceoldo ◽  
Filippo Andreetta ◽  
Marisa Levi
Keyword(s):  
In Vitro Culture ◽  
Fruit Juice ◽  
Zygotic Embryo ◽  
South American ◽  
Zygotic Embryo Culture ◽  
In The Wild ◽  
American Tropics ◽  
Mature Seeds ◽  
Continuous Source

The genus Passiflora comprises hundred species, mainly native of the South American tropics and rainforests, which are grouped into 21 subgenera. Some species are widely studied for their economic importance and are chiefly cultivated for production of fruit juice. To obtain a continuous source of material for a screening of secondary metabolites, zygotic embryo culture was attempted for 62 Passiflora species, starting from seeds mainly collected in the wild. Twenty nine of these species produced calli, which had very different growth rates. Plants were successfully regenerated from calli of 13 different species. For 25 of the responsive species this is the first report of in vitro culture.

scholarly journals Coconut Tissue Culture: The Indian Initiatives, Experiences and Achievements

CORD ◽  
2017 ◽  
Vol 33 (2) ◽  
pp. 11
Author(s):  
Anitha Karun
Keyword(s):  
Tissue Culture ◽  
Somatic Embryos ◽  
Culture Media ◽  
Zygotic Embryo ◽  
Shoot Meristem ◽  
Direct Organogenesis ◽  
Zygotic Embryos ◽  
Immature Inflorescence ◽  
High Yielding Varieties

Coconut is one of the principal crops of India cultivated in over 35 districts mainly in the southern states. The productivity of the crop is declining in many of the traditionally cultivated regions owing to ageing plantations as well as biotic and abiotic stresses. These plantations are to be replanted with high yielding varieties/hybrids for which adequate quantity of quality planting material is not available. Even though tissue culture research was initiated in many laboratories in the country, the work was eventually phased out in most of the laboratories for want of a repeatable protocol.  At ICAR-CPCRI, coconut tissue culture programs have been continuing for the past three decades. The attempts made include experimentation with different explants viz., immature inflorescence, plumular tissues, mature palm shoot meristem, ovary and anthers and different culture media supplemented with varying levels and types of hormones. Some of the successful protocols developed at the Institute include coconut zygotic embryo culture for collection and exchange of germplasm, cryopreservation and retrieval of zygotic embryos and pollen and plantlet regeneration from plumular tissues. Even though ICAR-CPCRI has succeeded in obtaining plantlets via direct organogenesis from inflorescence explants, the absence of friable calli formation from explants, the low rate of somatic embryo formation, large number of cultures turning to abnormal shoot development, non conversion of somatic embryos into plantlets, and formation of abnormal somatic embryos remain the major bottlenecks. Gene expression studies are being currently undertaken to decipher the molecular basis of in vitro recalcitrance.

scholarly journals Cultivo in vitro de embrião zigótico de baru influenciado por tipos de vedações e concentrações de sacarose / In vitro culture of zygotic embryo of baru as affected by sealing types and sucrose concentrations

2021 ◽  
Vol 7 (4) ◽  
pp. 42390-42408
Author(s):  
Gabriel Garcia Barbosa ◽  
Victória Maria Ingre Targa ◽  
Wagner Campos Otoni ◽  
Josimara Nolasco Rondon ◽  
Francilina Araújo Costa
Keyword(s):  
In Vitro Culture ◽  
Zygotic Embryo

scholarly journals Standardization of zygotic embryo culture from Nerium oleander L. and comparative analysis of biosynthesized cardiac glycosides within in vitro and acclimatized plants

2021 ◽  
pp. 204-215
Author(s):  
Renu Nimoriya ◽  
Yatendra Singh ◽  
Sumit Kumar Singh ◽  
Pankaj Singh ◽  
Amar Jeet ◽  
...  
Keyword(s):  
Embryo Culture ◽  
Cardiac Glycoside ◽  
Cardiac Glycosides ◽  
Zygotic Embryo ◽  
Germination Percentage ◽  
Zygotic Embryos ◽  
In Vitro Multiplication ◽  
Zygotic Embryo Culture ◽  
In Vitro Plantlets

The primary result of our experiment revealed that the germination percentage of N. oleander mature seeds is only 30%. From this observation, the concept of protocol standardization for zygotic embryo culture of this plant was originated. Zygotic embryo culture was proved an efficient in vitro multiplication system of N. oleander. The maximum germination percentage (96%) of zygotic embryos was observed on ¼ MS medium with 15 gm/L sucrose, whereas the best growth medium was optimized as ½ B5 with same sucrose concentration. The second part of this study was aimed to find out the cardiac glycoside accumulation pattern in both in vitro and acclimatized plants. For this purpose, one-month-old in vitro plantlets and acclimatized plants were subjected to LC-MS analysis and 09 cardiac glycosides were detected and quantified in both the systems. Most of the cardiac glycosides including odoroside A (32.71 mg/gm DW), odoroside H (4.69 mg/gm DW) and oleandrin (0.52 mg/gm DW) were found to be accumulated at maximum level within in vitro plantlets. CG 840b (1.89 mg/gm DW) is the only cardiac glycoside, which was maximally accumulated in acclimatized plants. From this study, it can be concluded that, zygotic embryo culture is a better choice for in vitro multiplication of N. oleander when compared to matured seeds and in vitro grown plantlets of this species favor cardiac glycosides biosynthesis in comparison to acclimatized plants. Therefore, all future research on the enrichment of cardiac glycosides from this plant may be conducted on zygotic embryos derived in vitro grown plantlets or cultures.

scholarly journals In vitro Regeneration and Agrobacterium-mediated Genetic Transformation of Local Varieties of Mungbean (Vigna radiata (L). Wilczek)

2019 ◽  
Vol 29 (1) ◽  
pp. 81-97
Author(s):  
Sujay Kumar Bhajan ◽  
Setara Begum ◽  
Mohammad Nurul Islam ◽  
M Imdadul Hoque ◽  
Rakha Hari Sarker
Keyword(s):  
Genetic Transformation ◽  
Vigna Radiata ◽  
Zygotic Embryo ◽  
In Vitro Regeneration ◽  
Multiple Shoots ◽  
Direct Organogenesis ◽  
Pcr Analysis ◽  
Root Induction ◽  
Half Strength

An efficient Agrobacterium-mediated transformation compatible in vitro regeneration protocol was developed for two important varieties of mungbean (Vigna radiata (L.) Wilczek) cultivated in Bangladesh, namely Binamoog-5 and BARI Mung-6. Two different zygotic embryo derived explants, such as cotyledonary node (CN) and cotyledon attached decapitated embryo (CADE) were used for direct organogenesis of shoot. MS supplemented with 4.0 μM BAP was found to be the best for the development of highest number of multiple shoots from CADE in both the varieties of mungbean. While in case CN the best shoot formation was achieved on MS containing 4.0 μM BAP and 0.5 μM NAA in both varieties. Half strength of MS with 2.0 μM IBA was found to be most effective for producing healthy root from regenerated shoots. Following root induction, the in vitro raised plantlets were successfully transplanted to soil for their establishment. Considering overall responses, genetic transformation efficiency was found to be better with CADE explant using Agrobacterium tumefaciens strain LBA4404 harboring the binary plasmid pBI121 conferring GUS and nptII genes. Different factors influencing transformation was optimized during this study. Selection of transformed shoots was carried out by gradually increasing the concentration of kanamycin and such transformed shoots were eventually selected using 200 mg/l kanamycin. Stable expression of the GUS gene was detected in various parts of regenerated transformed plantlets. Transformed shoots were rooted on half strength MS containing 2.0 μM IBA and 100 mg/l ticarcillin. Rooted transformed plantlets were successfully transferred to soil. Stable integration of GUS and nptII genes in the putative transformed shoots was confirmed through PCR analysis. Plant Tissue Cult. & Biotech. 29(1): 81-97, 2019 (June)

Zygotic embryo culture is an efficient way to optimize in vitro growth in Panax ginseng

2021 ◽  
Vol 167 ◽  
pp. 113497
Author(s):  
Jung-Woo Lee ◽  
Gyung-Ran Do ◽  
Ic-Hyun Jo ◽  
Chi-Eun Hong ◽  
Kyung-Hwan Bang ◽  
...  
Keyword(s):  
Panax Ginseng ◽  
Embryo Culture ◽  
Zygotic Embryo ◽  
In Vitro Growth ◽  
Zygotic Embryo Culture

scholarly journals In Vitro Preservation of Potato Plants

2017 ◽  
Vol 76 (1) ◽  
pp. 69-73
Author(s):  
Danuta Strzelczyk-Żyta
Keyword(s):  
In Vitro Culture ◽  
Good Condition ◽  
Early Developmental Stage ◽  
Potato Plants ◽  
Long Term Storage ◽  
In Vitro Preservation ◽  
Long Time ◽  
Early Developmental

Abstract Potato plants free of viruses, bacteria and viroid could be maintained in vitro for a long time. Proper preparation of potato plants for in vitro culture provide its long-term storage in good condition. First step is to establish in vitro culture from young greenhouse grown plants in early developmental stage. Explants are maintained and propagated by nodal subculture on hormone-free Murashige and Skoog (MS) medium at temperature 20-22°C. After rooting, for longer preservation plants are maintained at temperature 8-10°C.

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