scholarly journals Alteration of Flower Color in Viola cornuta cv. “Lutea Splendens” through Metabolic Engineering of Capsanthin/Capsorubin Synthesis

Horticulturae ◽  
2021 ◽  
Vol 7 (9) ◽  
pp. 324
Author(s):  
Milena Trajković ◽  
Slađana Jevremović ◽  
Milan Dragićević ◽  
Ana D. Simonović ◽  
Angelina R. Subotić ◽  
...  
Keyword(s):  
Ornamental Plants ◽  
Ectopic Expression ◽  
Shoot Multiplication ◽  
Flower Color ◽  
Phenotypic Characteristics ◽  
Hypocotyl Explants ◽  
Ex Vitro Growth ◽  
Modern Biotechnology ◽  
Lilium Lancifolium

Flower color is an important characteristic that determines the commercial value of ornamental plants. The development of modern biotechnology methods such as genetic engineering enables the creation of new flower colors that cannot be achieved with classical methods of hybridization or mutational breeding. This is the first report on the successful Agrobacterium-mediated genetic transformation of Viola cornuta L. The hypocotyl explants of cv. “Lutea Splendens” variety with yellow flowers were transformed with A. tumefaciens carrying empty pWBVec10a vector (Llccs−) or pWBVec10a/CaMV 35S::Llccs::TNos vector (Llccs+) for capsanthin/capsorubin synthase gene (Llccs) from tiger lily (Lilium lancifolium). A comparative study of shoot multiplication, rooting ability during culture in vitro, as well as phenotypic characteristics of untransformed (control) and transgenic Llccs− and Llccs+ plants during ex vitro growth and flowering is presented. Successful integration of Llccs transgene allows the synthesis of red pigment capsanthin in petal cells that gives flowers different shades of an orange/reddish color. We demonstrate that the ectopic expression of Llccs gene in ornamental plants, such as V. cornuta “Lutea Splendens” could successfully be used to change flower color from yellow to different shades of orange.

scholarly journals The effect of BA and GA3 on the shoot multiplication of in vitro cultures of Polish wild roses

2011 ◽  
Vol 23 (2) ◽  
pp. 145-149 ◽  
Author(s):  
Bożena Pawłowska
Keyword(s):  
Relative Humidity ◽  
Ornamental Plants ◽  
Shoot Multiplication ◽  
In Vitro Cultures ◽  
Multiplication Rate ◽  
Ms Medium ◽  
Naturally Occurring ◽  
Dog Rose ◽  
The University

The effect of BA and GA3on the shoot multiplication ofin vitrocultures of Polish wild rosesThe experiment was conducted using five species of roses naturally occurring in Poland:Rosa agrestis(fieldbriar rose),R. canina(dog rose),R. dumalis(glaucous dog rose),R. rubiginosa(sweetbriar rose), andR. tomentosa(whitewooly rose), from thein vitrocollection of the Department of Ornamental Plants of the University of Agriculture in Kraków. We examined the effect of cytokinin BA (1-10 μM) added to an MS medium (Murashige and Skoog 1962) on auxiliary shoot multiplication. The second group of test media contained BA (1-5 μM) and gibberellin GA3(0.3-1.5 μM). The cultures were maintained at a phytotron temperature of 23/25°C (night/day), 80% relative humidity, with a 16-hour photoperiod and PPFD of 30 μmol m-2s-1, and cultured in five-week cycles. The highest multiplication rate was obtained forR. caninaandR. rubiginosa(4.1 shoots per one explant) andR. dumalis(2.9 shoots per one explant), when shoots were multiplied on an MS medium supplemented with 1 μM BA and 1.5 μM GA3. Multiplication was the weakest inRosa tomentosaindependent of the medium used.

scholarly journals Abnormal symptoms in micropropagation and strategies to overcome

2020 ◽  
Vol 18 (1) ◽  
pp. 23-39
Author(s):  
Ha Thi My Ngan ◽  
Hoang Thanh Tung ◽  
Bui Van Le ◽  
Duong Tan Nhut
Keyword(s):  
Culture System ◽  
Ornamental Plants ◽  
Shoot Multiplication ◽  
Fruit Trees ◽  
Culture Conditions ◽  
Loss Of Function ◽  
Cell Tissue ◽  
Tissue And Organ Culture ◽  
Micro Propagation

Nowaday, plant cell, tissue and organ culture has become a standard and popular propagation method for many crops including ornamental plants, medicinal plants, fruit trees and green vegetables. The advantage of this method is that it can generate a huge number of genetically identical seedlings, effectively control the pathogenicity in order to produce disease-free plants, become a tool for conservation and development of genetic sources and support study of physiological characteristics of plants. However, this method still has some limitations such as abnormal physiological morphology and anatomical structure; necrosis and deformities plants; stomata loss of function, etc. These abnormalities have great impacts on shoot multiplication as well as the growth and development of the plants after transplanted from the culture vessels to the nursery stage. The components of in vitro culture conditions such as culture system, composition and content of nutrients, plant growth regulators used in the culture medium, light, temperature and humidity, age and origin of explants, etc., are the main causes of the abnormalities. Therefore, optimization of culture system to improve the quality of seedlings has always been one of the main targets of commercial micropropagation. In this review, we focused on some frequently abnormal symptoms in micro - propagation such as vitrification, yellowing and abscission of leaves; microbial contamination; necrosis of shoot-tip, roots and tissues culture; browning of explants and medium culture and other restrictions. More over, this report showed some the effective solutions to overcome these abnormal phenomena.

scholarly journals The impact of three bacteria isolated from contaminated plant cultures on in vitro multiplication and rooting of microshoots of four ornamental plants

2013 ◽  
Vol 21 (2) ◽  
pp. 41-51 ◽  
Author(s):  
Marta Zawadzka ◽  
Paweł Trzciński ◽  
Katarzyna Nowak ◽  
Teresa Orlikowska
Keyword(s):  
Root Length ◽  
Ornamental Plants ◽  
Shoot Multiplication ◽  
Shoot Formation ◽  
Axillary Shoot ◽  
Atmospheric Nitrogen ◽  
Tissue Cultures ◽  
Methylobacterium Extorquens ◽  
The Impact

ABSTRACT The strains of bacteria Paenibacillus glucanolyticus, Curtobacterium pusillum and Methylobacterium extorquens were isolated as non-deleterious contaminations from hosta or raspberry tissue cultures. Microshoots of chrysanthemum, gerbera, hosta and rose were inoculated with these bacteria and their influence on shoot multiplication and rooting was evaluated. None of the investigated bacteria caused symptoms of hypersensitivity or vitropathy on the shoot explants at rooting and shoots multiplication. C. pusillum stimulated axillary shoot formation in all studied plant genotypes. Length and number of rose roots and their length were higher but number of roots and their length in chrysanthemum were lower in inoculated than in controls. The number and the length of shoots and roots in gerbera and hosta and the number of shoots in chrysanthemum inoculated with M. extorquens were higher but shoot length of chrysanthemum and rose, and root length of rose were lower as compared with controls. P. glucanolyticus influenced higher number and length of chrysanthemum shoots and root length of chrysanthemum and gerbera than noninoculated control but the number of gerbera and hosta roots was lower and root length of rose was as low as 0.2 cm. All assessed bacteria were able to assimilate atmospheric nitrogen and M. extorquens and P. glucanolyticus were able to produce IAA.

FUTURE PERSPECTIVE OF PLANT BIOTECHNOLOGY: A REVIEW

2020 ◽  
Vol 1 (1) ◽  
pp. 36-41
Author(s):  
Gaurav Ranabhat ◽  
Ashmita Dhakal ◽  
Saurav Ranabhat ◽  
Ananta Dhakal ◽  
Rakshya Aryal
Keyword(s):  
Insect Pest ◽  
Ornamental Plants ◽  
Herbicide Tolerance ◽  
Plant Biotechnology ◽  
Future Perspective ◽  
New Development ◽  
Recent Developments ◽  
Modern Biotechnology ◽  
Stable Yield ◽  
As Stress

Modern biotechnology enables an organism to produce a totally new product which the organism does not or cannot produce normally through the incorporation of the technology of ‘Genetic engineering’. Biotechnology shows its technical merits and new development prospects in breeding of new plants varieties with high and stable yield, good quality, as well as stress tolerance and resistance. Some of the most prevailing problems faced in agricultural ecosystems could be solved with the introduction of transgenic crops incorporated with traits for insect pest resistance, herbicide tolerance and resistance to viral diseases. Plant biotechnology has gained importance in the recent past for increasing the quality and quantity of agricultural, horticultural, ornamental plants, and in manipulating the plants for improved agronomic performance. Recent developments in the genome sequencing will have far reaching implications for future agriculture. From this study, we can know that the developing world adopts these fast-changing technologies soon and harness their unprecedented potential for the future benefit of human being.

Methods of experimental polyploidization and their use in apple breeding

2020 ◽  
Vol 62 ◽  
pp. 85-90
Author(s):  
L. V. Tashmatova ◽  
O. V. Matsneva ◽  
T. M. Khromova ◽  
V. V. Shakhov
Keyword(s):  
Exposure Time ◽  
Cell Walls ◽  
Prolonged Exposure ◽  
Ornamental Plants ◽  
Colchicine Treatment ◽  
Apple Trees ◽  
Open Ground ◽  
High Concentrations ◽  
Diploid Gametes

The article presents methods of experimental polyploidy of fruit, berry and ornamental plants. The purpose of this review is to highlight the problems and prospects of polyploidization of plants in the open ground and in vitro culture and the possibility of their application for apple trees. For the purpose of obtaining apple tetraploids as donors of diploid gametes, seed seedlings were treated with a solution of colchicine in concentrations of 0.1-0.4 % for 24 and 48 hours. Colchicine concentrations of 0.3 % and 0.4 % at 48 hours of treatment had a detrimental eff ect on their development. As a result, tetraploids and chimeras were obtained from seeds from free pollination of the varieties Orlik, Svezhest, Kandil Orlovsky, as well as from seeds obtained from crossing the varieties Svezhest×Bolotovskoe, Moskovskoe Оzherel’e×Imrus, Girlyanda×Venyaminovskoe. The optimal concentration of colchicine was 0.1 %. Methods of colchicine treatment have been studied: 1) adding to the nutrient medium, colchicine concentration: 0.01%, 0.02%, exposure time 24h-19 days; 2) applying amitotic solution to the growth point, colchicine concentration: 0.1 %, 0.2 %, exposure time 24h-7 days. To increase the penetration of colchicine through the cell walls, a 0.1 % dimexide solution was used. Studies have shown that high concentrations and prolonged exposure to colchicine reduce the viability of explants.

Utilization of Different Seedling Explants for in Vitro Propagation of Hibiscus syriacus

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 478e-479
Author(s):  
M.M. Jenderek ◽  
A.J. Olney
Keyword(s):  
Callus Formation ◽  
Adventitious Bud ◽  
Root Explants ◽  
Petiole Explants ◽  
Bud Formation ◽  
Hypocotyl Explants ◽  
Leaf Petiole ◽  
Adventitious Bud Formation ◽  
Hibiscus Syriacus

Hibiscus syriacus is a difficult species in micropropagation due to its endogenous contamination and recalcitrant shoot formation; therefore, studies on using explants other than shoot tip or axillary buds of growing shrubs were initiated. Three different seedling fragments (root, hypocotyl, and leaf petiole) from aseptically germinated seedlings of hibiscus (var. Aphrodite) were evaluated for adventitious bud formation, shoot and leaf development. The explants were cultured on McCown's woody plant basal salt medium supplemented with KNO3 (800 mg/L), adenine sulfate (80 mg/L) and MS vitamins containing BA or 2iP or TDZ at 0.5, 1.0, 2.2, 4.4 and 10 mM. Adventitious buds were present on all of the three different explants grown on medium containing TDZ; however, the most abundant bud formation, with many small leaves originating from callus was observed on hypocotyl explants cultured on medium with 1 mM of TDZ. Petiole explants were the most frequent to develop short shoots (≈15 mm) and one to nine leaves without callus formation, where 70% of hypocotyl and the root explants formed leaves originating from callus. Callus was induced on all explant types regardless of the level or type of cytokinin used. However, the number of shoots produced by any explant type was low, petioles cultured on 0.5 and 1mM of TDZ were the most suitable material for non-callus shoot development in H. syriacus. Hypocotyl explants proved to be an excellent source for adventitious bud formation but their ability to develop shoots needs to be investigated.

scholarly journals Shoot Multiplication and Callus Induction of Labisia pumila var. alata as Influenced by Different Plant Growth Regulators Treatments and Its Polyphenolic Activities Compared with the Wild Plant

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3229
Author(s):  
Mat Yunus Najhah ◽  
Hawa Z. E. Jaafar ◽  
Jaafar Juju Nakasha ◽  
Mansor Hakiman
Keyword(s):  
Callus Induction ◽  
Antioxidant Activities ◽  
Shoot Multiplication ◽  
Wild Plants ◽  
Wild Plant ◽  
Total Phenolic ◽  
Nodal Segment ◽  
Ms Medium ◽  
In Vitro Plantlets

This study aims to investigate whether the in vitro-cultured L. pumila var. alata has higher antioxidant activity than its wild plant. An 8-week-old L. pumila var. alata nodal segment and leaf explants were cultured onto Murashige and Skoog (MS) medium supplemented with various cytokinins (zeatin, kinetin, and 6-benzylaminopurine (BAP)) for shoot multiplication and auxins (2,4-dichlorophenoxyacetic acid (2,4-D) and picloram) for callus induction, respectively. The results showed that 2 mg/L zeatin produced the optimal results for shoot and leaf development, and 0.5 mg/L 2,4-D produced the highest callus induction results (60%). After this, 0.5 mg/L 2,4-D was combined with 0.25 mg/L cytokinins and supplemented to the MS medium. The optimal results for callus induction (100%) with yellowish to greenish and compact texture were obtained using 0.5 mg/L 2,4-D combined with 0.25 mg/L zeatin. Leaves obtained from in vitro plantlets and wild plants as well as callus were extracted and analyzed for their antioxidant activities (DPPH and FRAP methods) and polyphenolic properties (total flavonoid and total phenolic content). When compared with leaf extracts of in vitro plantlets and wild plants of L. pumila var. alata, the callus extract displayed significantly higher antioxidant activities and total phenolic and flavonoid content. Hence, callus culture potentially can be adapted for antioxidant and polyphenolic production to satisfy pharmaceutical and nutraceutical needs while conserving wild L. pumila var. alata.

scholarly journals Human Keratinocytes Adopt Neuronal Fates After In Utero Transplantation in the Developing Rat Brain

2021 ◽  
Vol 30 ◽  
pp. 096368972097821
Author(s):  
Andrea Tenorio-Mina ◽  
Daniel Cortés ◽  
Joel Esquivel-Estudillo ◽  
Adolfo López-Ornelas ◽  
Alejandro Cabrera-Wrooman ◽  
...  
Keyword(s):  
Green Fluorescent Protein ◽  
Fluorescent Protein ◽  
Ectopic Expression ◽  
Neural Induction ◽  
Human Keratinocytes ◽  
Differentiation Potential ◽  
Neuronal Proteins ◽  
Green Fluorescent

Human skin contains keratinocytes in the epidermis. Such cells share their ectodermal origin with the central nervous system (CNS). Recent studies have demonstrated that terminally differentiated somatic cells can adopt a pluripotent state, or can directly convert its phenotype to neurons, after ectopic expression of transcription factors. In this article we tested the hypothesis that human keratinocytes can adopt neural fates after culturing them in suspension with a neural medium. Initially, keratinocytes expressed Keratins and Vimentin. After neural induction, transcriptional upregulation of NESTIN, SOX2, VIMENTIN, SOX1, and MUSASHI1 was observed, concomitant with significant increases in NESTIN detected by immunostaining. However, in vitro differentiation did not yield the expression of neuronal or astrocytic markers. We tested the differentiation potential of control and neural-induced keratinocytes by grafting them in the developing CNS of rats, through ultrasound-guided injection. For this purpose, keratinocytes were transduced with lentivirus that contained the coding sequence of green fluorescent protein. Cell sorting was employed to select cells with high fluorescence. Unexpectedly, 4 days after grafting these cells in the ventricles, both control and neural-induced cells expressed green fluorescent protein together with the neuronal proteins βIII-Tubulin and Microtubule-Associated Protein 2. These results support the notion that in vivo environment provides appropriate signals to evaluate the neuronal differentiation potential of keratinocytes or other non-neural cell populations.

scholarly journals Seed Germination and in vitro Plant Regeneration through Callus Culture of Two Lychnis Species

2015 ◽  
Vol 25 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Kee Hwa Bae ◽  
Eui Soo Yoon
Keyword(s):  
Plant Regeneration ◽  
Seed Germination ◽  
Callus Induction ◽  
In Vitro Propagation ◽  
Ornamental Plants ◽  
Leaf Explants ◽  
Adventitious Shoot ◽  
Temperature Treatment ◽  
In Vitro Plant Regeneration

Lychnis cognate Maxim and Lychnis fulgens Fish. Ex Spreng are two valued ornamental plants in Korea. Soaking of seeds in GA3 solution remarkably promoted germination up to 60%, but the control (0 mg/l) was not effective (> 5%). To select an adequate temperature for seed germination, seeds, previously soaked in a 1000 mg/l GA3 for 24 hrs, were incubated at 15, 20, 25, and 30°C. Seed germination of over 20% was obtained at 15, 20, and 25°C, but only 10% at 30°C. These results indicate that the seeds of L. cognate and L. fulgens are in a such dormant state that they hardly germinate even by dormancy breaker (GA3) and low (15 ? 25°C) temperature treatment. The highest callus induction was observed in the leaf explants of the seedlings on MS containing specific concentrations of 3.0 mg/l BA and 1.0 mg/l NAA. The adventitious shoot was formed < 90% of calli on 1/2 WPM medium. The height of in vitro propagated plantlet was no different media used for regeneration. This in vitro propagation protocol should be useful for conservation of endangered and ornamental plant.Plant Tissue Cult. & Biotech. 25(1): 1-12, 2015 (June)

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