scholarly journals Phloroglucinol Improves Direct Rooting of In Vitro Cultured Apple Rootstocks M9 and M26

Agronomy ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 1079
Author(s):  
Jin-Ho Kim ◽  
Bo-Min Kwon ◽  
Thanh-Tam Ho ◽  
So-Young Park
Keyword(s):  
Adventitious Roots ◽  
Gene Expression Analysis ◽  
Root Formation ◽  
Callus Formation ◽  
The Other ◽  
Endogenous Auxin ◽  
Apple Rootstocks ◽  
Rooting Medium ◽  
Indole 3 Acetic Acid

Advances in micropropagation techniques have helped produce true-to-type clones of many horticulturally important plants. However, several cultivars of apple are difficult to root in vitro. In these cases, adventitious roots are induced together with undesirable formation of callus, which decrease the acclimatization rate of in vitro produced plantlets. In this study, two apple rootstocks, M9 and M26, were subjected to different concentrations of indole-3-butyric acid (IBA) to induce root formation. Although addition of IBA to the medium induced root formation, rhizogenesis was accompanied by the undesirable formation of callus in both cultivars. On the other hand, in gene expression analysis, the indole-3-acetic acid (IAA) synthase genes AAO1 and YUC1 were expressed more highly in M9 than in M26. This suggests that endogenous auxin levels may be higher in M9, which may explain why M9 plantlets are difficult to root and experience high levels of callus formation during propagation. In addition, rooting medium containing 0.1 mg·L−1 IBA was supplemented with different concentrations of phloroglucinol (0, 0.5, 1.0, and 2.0 mM) to examine whether direct rooting efficiency in the M9 could be improved. Addition of 1.0 mM phloroglucinol increased rooting percentage and decreased callus formation in the M9 rootstock. The rootstock M9 is a desirable cultivar but presents a problem with true-to-type direct rooting. Addition of phloroglucinol may improve direct rooting and eliminate callus formation during propagation.

scholarly journals In vitro CULTURE OF BIG-SAGE (Lantana camara L.) PLANT

2020 ◽  
Vol 19 (2) ◽  
pp. 67-73
Author(s):  
Majid Abdulhameed Ibrahim ◽  
Manal Zebari Sabty ◽  
Shaimaa Hussein Mussa
Keyword(s):  
Root Length ◽  
Root Formation ◽  
Callus Formation ◽  
Shoot Multiplication ◽  
Lantana Camara ◽  
The Other ◽  
Ms Medium ◽  
Formation Number ◽  
Number Of Shoots

The study was conducted to mass micropropagation of big sage (Lantana camara L.) plant by shoot multiplication technique. The treatments 2.22 and 2.66 µmol·L–1 BA gave the highest significant increase in the percentage of response to shoot multiplication and number of shoots per explant compared to the other treatments as reached 96.70% and 100.00% and 4.33 and 6.00 shoots, respectively. The results showed that these two treatments did not differ significantly between them. While the 1.33 µmol·L–1 BA gave the lowest values in the percentage of response to shoot multiplication and number of shoots per explant were 80.00% and 2.00 shoots per explant, respectively. The MS medium supplemented with 4.30 or 5.37 µmol·L–1 NAA gave a high response to root formation, number of roots per shoot and root length. While the MS medium supplemented with 6.44 or 7.52 µmol·L–1 NAA gave low values in these characteristics. The MS medium with 2.22 or 2.66 µmol·L–1 concentration of BA or 7.52 µmol·L–1 concentration of NAA recorded the highest significant increase in the percentage of response to callus formation. While the MS medium supplemented with 1.33 µmol·L–1 BA or 4.30 µmol·L–1 NAA gave less response to the callus formation.

scholarly journals In vitro Regeneration, Rooting, and Cloning of Artemisia tridentata

2020 ◽  
Author(s):  
Rachael Barron
Keyword(s):  
Adventitious Roots ◽  
Root Formation ◽  
Callus Formation ◽  
Leaf Explants ◽  
Shoot Formation ◽  
Adventitious Root Formation ◽  
Big Sagebrush ◽  
Nodal Cuttings ◽  
Wyoming Big Sagebrush

Artemisia tridentata (big sagebrush) is an ecologically important shrub found in western North America. In vitro techniques can be applied to big sagebrush for the purpose of studying gene function, genotypic and phenotypic plasticity studies, cloning, genotypic preservation, and restoration. I performed experiments to develop an indirect organogenesis protocol to regenerate whole Wyoming big sagebrush plants from leaf explants. Callus formation frequency was 88% (±4.0%) in leaf explants cultured on medium containing 0.5 mg/l BAP and 1.0 mg/l NAA. Shoot formation frequency was variable between replicates and was the highest when callus tissue was cultured on medium containing 1.5 mg/l BAP and 0.1 mg/l NAA, 37% to 80%. I tested several auxin treatments to induce root formation and concluded the best to be 0.5mg/l IBA, which yielded 42% to 60% rooting. Taking into account all these variables, I estimate the total regeneration efficiency to range between 14% to 43% on this set of treatments. This protocol was also applied to basin big sagebrush. Callus formation was 100% in leaf explants. Shoot formation was 34% (±14.6%), but shoots exhibited a hyperhydric phenotype and were not transferred to root induction medium. The in vitro regeneration protocol developed is a crucial element that would be required to transform big sagebrush using molecular approaches. Experiments were also conducted to determine the feasibility of shoot tip and nodal cuttings to develop adventitious roots in vitro. This method can provide genetically identical material much faster than in vitro regeneration. Adventitious root formation in Wyoming big sagebrush cuttings cultured on two media types was inconsistent, ranging from 10% in some experiments to 80% in others. Limited success was achieved in nodal cuttings cultured on modified MS medium containing auxin and cytokinin 12.5% (±5.6%). No root formation was achieved in mature plant tissue collected in the field. Results indicated that genotypic influences were likely more responsible for variations in rooting than the medium or vessel conditions tested. Cloning experiments in basin big sagebrush further supported this notion. All material for these experiments came from half-sibling individuals that was maintained separately throughout the course of the experiments. Some half-siblings formed no adventitious roots on any treatments tested whereas others had high rates of formation on all treatments. Further studies, utilizing exogenous PGRs, such as auxins, may provide more successful adventitious root formation in shoot tips from both big sagebrush subspecies.

scholarly journals Optimized in vitro plant regeneration of the biodiesel plant Jatropha curcas L.: the effects of using seeds at different stages of maturity as starting materials

2014 ◽  
Vol 5 (1) ◽  
Author(s):  
Sillma Rampadarath ◽  
Daneshwar Puchooa ◽  
Mala Ranghoo-Sanmukhiya
Keyword(s):  
Plant Regeneration ◽  
Jatropha Curcas ◽  
Root Formation ◽  
Callus Formation ◽  
Dichlorophenoxyacetic Acid ◽  
Plantlet Formation ◽  
Seed Maturity ◽  
Rooting Medium ◽  
2,4 Dichlorophenoxyacetic Acid

<em>Jatropha curcas</em> L. is an important biofuel plant that can be regenerated <em>in</em> <em>vitro</em> using seeds. The fruits of <em>J. curcas</em> do not reach maturity at the same time although they are on the same bunch. This study was undertaken to evaluate the effect of seeds, from fruits at different stages of maturity, on <em>in</em> <em>vitro</em> plantlet formation. Callus was induced on Murashige and Skoog medium using different concentrations of 2,4 dichlorophenoxyacetic acid (2,4-D) and 6 benzylaminopurine (BAP). 2,4D at a concentration of 3.0 mg/L and BAP at 1.0 mg/L were found to be optimum for callus formation. <em>In vitro</em> plantlets obtained on BAP were smaller with thicker hypocotyl and thicker roots. On the other hand, seeds from mature fruits gave better results for <em>in</em> <em>vitro</em> plantlet regeneration on 1.0 mg/L BAP without any rooting medium. A combination of sand and soil were used for acclimatization. Best results were obtained when sand and soil were used in equal amounts. Results also showed that seed maturity is an important factor for <em>in vitro</em> plant regeneration of<em> J. curcas</em> and that root formation <em>in vitro</em> does not require additional plant growth regulator substance.

scholarly journals Rhizogenesis in in vitro shoot cultures of passion fruit (Passiflora edulis f. flavicarpa Deg.) is affected by ethylene precursor and by inhibitors

2001 ◽  
Vol 7 (1) ◽  
Author(s):  
W. M. Marota ◽  
W. C. Otoni ◽  
M. Carnelossi ◽  
E. Silva ◽  
A. A. Azevedo ◽  
...  
Keyword(s):  
Ethylene Production ◽  
Time Course ◽  
Root Formation ◽  
Callus Formation ◽  
Passion Fruit ◽  
Shoot Cultures ◽  
Ethylene Inhibitors ◽  
Beneficial Effects ◽  
Ethylene Precursor

The effects of the ethylene precursor ACC and two inhibitors, AgNO3 and AVG, on root formation were tested in in vitro shoots of passion fruit (Passiflora Midis f.flavicalpa Deg.). The organogenic response was assessed on the basis of percentage of shoot-forming. roots, root number and length. The time course of ethylene production was also monitored. ACC inhibited root formation by delaying root emergence and increasine, callus formation at the basis of the shoots. In addition, ACC caused a marked increase in ethylene production, coupled to leaf chlorosis and senescence with lower rooting frequencies, number and length of roots. IAA supplementation increased ethylene production. Both ethylene inhibitors, AgNO3 and AVG, at appropriate concentrations reduced callus formation at the basis of shoots. AVG increased the number of roots per shoot, but drastically reduced length of differentiated roots. Regarding to leaf pigments, ACC promoted a marked reduction on carotenoids and total chlorophyll, whereas AVG and AgNO3 delayed explant senescence and pigments degradation, not differing from IAA supplemented and non-supplemented control treatments. The results confirm previous reports on the beneficial effects of ethylene inhibitors on in vitro rooting and suggest its reliability to be used as an alternative approach to evaluate sensitivity of Passiflora species to ethylene.  

scholarly journals Comparative analyses of stevioside between fresh leaves and in-vitro derived callus tissue from Stevia rebaudiana Bert. using HPLC

2015 ◽  
Vol 49 (4) ◽  
pp. 199-204 ◽  
Author(s):  
S Mahmud ◽  
S Akter ◽  
IA Jahan ◽  
S Khan ◽  
A Khaleque ◽  
...  
Keyword(s):  
Retention Time ◽  
Callus Tissue ◽  
Callus Formation ◽  
Leaf Explants ◽  
Stevia Rebaudiana ◽  
Poor Performance ◽  
The Other ◽  
Ms Medium ◽  
Green Callus

A protocol was developed to produce large amount of callus in short a period of time from leaf explants of Stevia rebaudiana Bert. The highest amount of white callus was obtained on MS medium supplemented with 2.5 mg/l 2, 4-D and 0.5 mg/l BAP after 3 weeks of inoculating leaf segments. On the other hand, 0.5 mg/l BAP and 1.0 mg/l Kn exhibits poor performance towards callus formation while after using 1.0 mg/l Kn alone did not develop any callus. In this experiment, highest amount of green callus was obtained when MS medium supplemented with 2.5 mg/l NAA and 10% coconut water was used. An improved analytical method HPLC was applied to analyze stevioside extracted from the leaf and callus of Stevia rebaudiana. The stevioside in each sample were analyzed by comparing their retention times with those of the standards. The retention time (RT) of stevioside for leaves were found 14.96 and for callus 13.81 mins. The percentage of stevioside content from leaves and callus was 12.19% and 12.62% respectively DOI: http://dx.doi.org/10.3329/bjsir.v49i4.22621 Bangladesh J. Sci. Ind. Res. 49(4), 199-204, 2014

scholarly journals Efficient In Vitro Callus Induction and Plant Regeneration Protocol for Different Polish Tomato Cultivars

2016 ◽  
Vol 44 (2) ◽  
pp. 452-458 ◽  
Author(s):  
Aneta GERSZBERG ◽  
Katarzyna HNATUSZKO-KONKA ◽  
Tomasz KOWALCZYK ◽  
Andrzej K. KONONOWICZ
Keyword(s):  
Regeneration Ability ◽  
Ms Medium ◽  
Regeneration System ◽  
Major Goal ◽  
Rooting Medium ◽  
Ability To Regenerate ◽  
Tomato Cultivars ◽  
Indole 3 Acetic Acid ◽  
Hypocotyl Segments

The major goal of this research was to establish a stable regeneration system for tomato cultivars in order to lay the foundations for the future genetic transformation of the tomato. The regeneration ability of two kinds of explants (cotyledons and hypocotyl segments) was compared for three Polish cultivars of the tomato (Solanum lycopersicum). Explants were cultured on 10 different regeneration media (basal mediums MS or B5, and with a combination of 6-benzylaminopurine (BAP) and indole-3-acetic acid (IAA). It was found that the ability to regenerate was substantially dependent on the cultivars, as well as on the kind of explant. The best explants for inducing shoot regeneration were cotyledons, followed by hypocotyls. It was noticed that the best formulation of the medium for this regeneration from the two types of explants used in this study, is MS with 2 mg/L BA and 0.1 mg/L IAA.  Tomato shoots were transferred to a ½ MS medium and ½ MS complemented with 0.1 mg/L IAA for rooting and all of them responded positively to the rooting medium.

scholarly journals 312 Influence of BAP and CPPU on the in Vitro Shoot and Bud Proliferation of Apple Rootstocks M.111 and M.7

HortScience ◽  
2000 ◽  
Vol 35 (3) ◽  
pp. 445F-446
Author(s):  
Adriano N. Nesi ◽  
Gerson R. de L. Fortes ◽  
Jono B. da Silva ◽  
Adriana C. de M. Dantas
Keyword(s):  
Callus Formation ◽  
Shoot Proliferation ◽  
Shoot Multiplication ◽  
Temperate Climate ◽  
Similar Response ◽  
Multiplication Rate ◽  
Apple Rootstocks ◽  
Shoot Base ◽  
Better Than

This work aims to verify the effect of BAP (6-benzyladenine purine) and CPPU (forchlofenuron) on the in vitro shoot proliferation of apple rootstock cultivars M.111 and M.7 under different concentrations. The experiment was carried out in the tissue culture laboratory at Embrapa Temperate Climate in Pelotas, RS, Brazil. As initial explants, microcuttings were used from in vitro culture. The treatments consisted of the combination of two cultivars with cytokinins and six differents concentrations (0.0, 1.5, 3.0, 4.5, and 6.0 μMol). The explants were inoculated in 250-mL flasks with 40 mL MS medium with agar (7.0 g·L-1), myo-inositol (100.0 g·L-1), NAA (0.005 mg·L-1), and sucrose (40.0 g·L-1). The pH was adjusted to 5.9 before autoclaving. After inoculations the culture was kept for 50 days under 25 ± 2 °C, 16-h photoperiod, and 19 μMol·m-2·s-1 radiation. CPPU performed better than BAP for cultivar M.111 and it had similar response for cultivar M.7 as bud and shoot multiplication and multiplication rate is concerned. The BAP increased the number of shoots with higher length and with no callus formation in the shoot base, contrary to CPPU. The most efficient concentrations were 4.7 and 5.5 μMol for CPPU and BAP, respectively.

scholarly journals Highly Successful Adventitious Root Formation of Zamia L. Stem Cuttings Exhibits Minimal Response to Indole-3-Butyric Acid

HortScience ◽  
2020 ◽  
Vol 55 (9) ◽  
pp. 1463-1467 ◽  
Author(s):  
Benjamin E. Deloso ◽  
Anders J. Lindström ◽  
Frank A. Camacho ◽  
Thomas E. Marler
Keyword(s):  
Butyric Acid ◽  
Root Development ◽  
Adventitious Root ◽  
Adventitious Roots ◽  
Root Formation ◽  
Adventitious Root Formation ◽  
The Other ◽  
Control Group ◽  
Stem Cuttings ◽  
Adventitious Root Development

The influences of indole-3-butyric acid (IBA) concentrations of 0–30 mg·g−1 on the success and speed of adventitious root development of Zamia furfuracea L.f. and Zamia integrifolia L.f. stem cuttings were determined. Root formation success for both species was greater than 95%. The IBA concentrations did not influence the speed of root development for Z. furfuracea, but the Z. integrifolia cuttings that received IBA concentration of 3 mg·g−1 generated adventitious roots more slowly than the cuttings in the control group. The ending dry weights of the stems, leaves, and roots were not influenced by IBA concentration for either species. Our results indicated that adventitious root formation on stem cuttings of these two Zamia species is successful without horticultural application of IBA. Additional IBA studies are needed on the other 300+ cycad species, especially those that are in a threatened category.

scholarly journals Effect of plant growth regulators on the root formation in in vitro culture of Abelmoschus Sagittifolius Kurz

2020 ◽  
Vol 4 (2) ◽  
pp. First
Author(s):  
Trân Huỳnh Ngọc Dương ◽  
Diễm Thị Lê ◽  
Mai Thị Bạch Võ
Keyword(s):  
Plant Growth ◽  
Plant Growth Regulators ◽  
Growth Regulators ◽  
Root Formation ◽  
Callus Formation ◽  
Plant Root ◽  
Germination Rate ◽  
Distribution Area ◽  
Increasing Demand

Abelmoschus sagittifolius Kurz is a medicinal plant with typical pharmacological of ginseng. However, the number of trees in the nature wild is declining rapidly due to the increasing demand for logging along with the narrowing of the distribution area and the low incidence of seed germination, affecting the use for researching and developing gene sources for drug production in many areas. In this plant, root is the most important organ of the plant, so the study of root formation in in vitro has been of great significance in assessing the effect of plant growth regulators on induction roots, as well as creating a source of starting material for studies on the biosynthesis of saponin in in vitro compounds as an alternative to outside planting. The results showed that after 2 weeks of culture, the germination rate was highest (88%) when the seeds were disinfected with HgCl2 0.1%, 3 minutes and then soaked in GA3 20,0 mg/L, 120 minutes, finally seed culture on MS + 20 g/L saccharose + GA3 5.0 mg/L + 7 g/L agar. The callus formation from hypocotyl in the environment on MS medium + 20 g/L sucrose + NAA 0.5 mg/L + BA 1.5 mg/L + 7 g/L agar was appropriate for root reduction and the best root formation was applied in the medium of MS + 20 g/L sucrose + IAA 0.3 mg/L + 7 g/L agar. In conclusion, the method of tissue culture is suitable for the formation of adventitious roots from callus formation from hypocotyl of Abelmoschus sagittifolius Kurz.

scholarly journals Assessment of the Effects of Newly Fabricated CaO, CuO, ZnO Nanoparticles on Callus Formation Maintainance of Alfalfa (Medicago Sativa L.) Under In Vitro Salt Stress

2021 ◽  
Author(s):  
Merve Simsek ◽  
Busra Yazicilar ◽  
Fatma Boke ◽  
Hayrunisa Nadaroglu ◽  
Azize Alayli ◽  
...  
Keyword(s):  
Salt Stress ◽  
Callus Induction ◽  
Callus Formation ◽  
Leaf Explants ◽  
Nacl Stress ◽  
The Other ◽  
Antioxidant Enzyme Activities ◽  
Zno Nps ◽  
Induction Stage

Abstract Nanoparticules plays an important role in plant adaptation to abiotic stress, especially in response to salt stress. In this study, two alfalfa lines (Erzurum, and Muş) were used as the material for the response NaCl to CuO, ZnO and CaO nanoparticules (NPs). CaO is evident to be higher effective than CuO, ZnO in callus induction from leaf explants. The antioxidant enzyme activities were also determined in the callus cultures. The maximum activity in MDA analysis was observed from callus treated of 50 mM NaCl with 0.8 ppm CuO NPs. The callus induction stage without salt treatments indicated a best result in 0.8 ppm CaO NPs for H2O2 value compared to the other NPs. The callus induction stage without salt treatments indicated a best result in 0.8 ppm CaO NPs for POD value compared to the other NPs for POD activity. The best response in protein rate was obtained from callus induction stage and callus formation stage after 50 mM treatment NaCl with 0.8 ppm CuO. LSCM analysis evident that the NPs could migitate the negative effects of NaCl stress by the elimination of stress severity in callus cells. SEM analysis was supported the results obtained by LSCM analysis. Our findings suggest that CuO, CaO and ZnO NPs can offer a simple and effective method to protect alfalfa callus from NaCl stress severity.

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