scholarly journals (292) In Vitro Rooting of Bigtooth Maple Microshoots

HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1081D-1081
Author(s):  
Clare Bowen-O'Connor ◽  
John Hubstenberger ◽  
Dawn Van Leeuwen ◽  
Rolston St. Hilaire
Keyword(s):  
Culture Media ◽  
Shoot Proliferation ◽  
Leaf Size ◽  
Root Induction ◽  
Auxin Treatment ◽  
Tissue Culture Media ◽  
Acer Grandidentatum ◽  
Number Of Leaves ◽  
Bigtooth Maple

Double-node microshoots of bigtooth maple (Acer grandidentatum Nutt.) were rooted in vitro on Driver-Kuniyuki Walnut (DKW) tissue culture media containing indole acetic acid (IAA). Microshoots represented six sources from three locations within Texas and New Mexico. Microshoots were placed in Phytatrays II™ containing DKW media with no plant growth regulator (DKW0) to reduce the high cytokinin levels used for shoot proliferation. Microshoots were induced to form roots for 15 days by placing them on DKW media containing IAA at 0.01, 1, 2.5, 5, 10, 15 or 20 μmol. Rooting frequency, the number of leaves and callus area were recorded every 30 days for 60 days. Rooting frequency increased up to 29% as IAA concentration increased (P= 0.004). However, as much as 71% of shoots for one of the three Guadalupe Mountain, Texas, sources rooted without auxin treatment after 30 days. The IAA concentration also affected the number of leaves per shoot (P= 0.0228) which averaged seven and callus area (P= <0.0001) which averaged 52 mm2. Average leaf size was 307 mm2. We conclude that IAA induces rooting in microshoots of bigtooth maple after 15 days of root induction. However, one source rooted without auxin treatment. The presence of callus does not interfere with root formation.

scholarly journals PERTUMBUHAN KULTUR TUNAS AKSILAR KENTANG (Solanum tuberosum L.) DENGAN PENAMBAHAN SUPER FOSFAT DAN KNO3 PADA MEDIA AB MIX SECARA IN VITRO

2019 ◽  
Vol 20 (2) ◽  
pp. 71
Author(s):  
Hamami Alfasani Dewanto ◽  
Desi Saraswati ◽  
Oetami Dwi Hadjoeningtijas
Keyword(s):  
Culture Media ◽  
Raw Materials ◽  
Solanum Tuberosum L ◽  
Leaf Color ◽  
Tissue Culture Media ◽  
Randomized Design ◽  
Plantlet Growth ◽  
Number Of Leaves ◽  
Dark Green

Murashige&Skoog-based medium Potatoes are one commodity that has the potential to be developed as a resource in the context of food diversification, farmers' income riser, non fossil export commodities and raw materials for processing industry. The objective of this research was to find out the effect of SP-36 fertilizer, KNO3 fertilizer, as well as the interaction between the two fertilizers on the growth of potato nodal culture on AB Mix media in vitro. The results of this study are expected to provide economical potato tissue culture media development. This research used factorial complete randomized design. The treatment were SP-36 concentration: 0 ppm; 50 ppm; 100 ppm; and 200 ppm, in combination with KNO3 concentration: 0 ppm; 100 ppm; 200 ppm; 400 ppm; and 600 ppm, The variables observed included number of leaves, leaf color, length of plantlets, fresh weight of plantlets and percentage of plantlets growth. Based on the results of the analysis of variance (ANOVA) F. Calculate < F. Table with the average success of plantlet growth between 87.5-100%. In addition, there are four types of leaf color produced, namely the color of yellowish green, pale green leaves, green, and dark green. Research showed that the interaction between SP-36 fertilizer and KNO3 fertilizer on AB Mix media had no significant effect on all observed variables.

scholarly journals Clonal Propagation and Karyomorphological Study of Solanum torvum Swartz: An Ethnobotanical Species of Tripura, India

2018 ◽  
Vol 28 (1) ◽  
pp. 69-76
Author(s):  
H Reshmi Singha ◽  
Sangram Sinha ◽  
Rabindra Kumar Sinha
Keyword(s):  
Clonal Propagation ◽  
Culture Media ◽  
Shoot Proliferation ◽  
Induction Phase ◽  
Root Induction ◽  
Metaphase Chromosomes ◽  
Solanum Torvum ◽  
Regenerated Plants ◽  
Bud Induction

An efficient method of clonal propagation through nodal culture of Solanum torvum Swartz. is described. Different concentrations of BAP/Kn alone or in combination with IAA were tested for direct shoot bud induction and proliferation. Lower concentration of BAP/Kn alone produced better shoot proliferation and elongation. Maximum number of shoot proliferation was achieved from MS supplemented with Kn 0.5 mg/l with an average 4.0 ± 1.41 shoots during 28 days of culture. Addition of IAA to the culture media in combination with BAP/ Kn significantly reduced the number of shoot formation. Regenerated plants also produced roots during subsequent culture in the same media supplemented with BAP/Kn alone or in combination with IAA. The easy nature of in vitro rooting of S. torvum was recorded without any separate root induction phase. Regenerated plants were successfully transferred to the field condition. Clonal feature was cytologically confirmed through the study of mitotic metaphase chromosomes of regenerated plants which reveals 2n = 24 somatic chromosomes. Comparative karyomorphological details between the mother and regenerated plants of S. torvum revealed close similarity in their chromosomal complements and falls under the category of "1B" Stebbin’s symmetric index suggesting true to type nature of the regenerated plant.Plant Tissue Cult. & Biotech. 28(1): 69-76, 2018 (June)

scholarly journals Enhanced Axillary Branching and Pigment Development of Double-Node Explants of Bigtooth Maple

HortScience ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 755D-755
Author(s):  
Clare A. Bowen-O'Connor* ◽  
Rolston St. Hilaire ◽  
John Hubsten-berger ◽  
Dawn VanLeeuwen
Keyword(s):  
Tissue Culture ◽  
Culture Media ◽  
Shoot Proliferation ◽  
Tissue Culture Media ◽  
Royal Horticultural Society ◽  
Significant Difference ◽  
Murashige Skoog ◽  
Bigtooth Maple ◽  
Bigtooth Maples ◽  
Managed Landscapes

Bigtooth maple (Acer grandidentatum Nutt.) is indigenous to the southwestern United States. This species is not widely used in managed landscapes but the plant holds promise as a useful ornamental tree. Micropropagation might provide additional sources of selected genotypes for the nursery industry, but tissue culture has not been used successfully to propagate this species. We cultured double-node explants from greenhouse-grown, 2-year old seedlings of bigtooth maples that originated from Utah, Texas and New Mexico. Seedling height ranged from 15-90 cm. The shoot region was divided into three equal zones designated as terminal, intermediate and basal. Explants were selected from each of those zones. Explants were established on Murashige-Skoog (MS), Linsmaier-Skoog (LS), Woody Plant Medium (WPM) and Driver-Kuniyuki (DKW) tissue culture media. Shoot proliferation, area of the plate covered by callus and foliar pigment development (hue as determined by Royal Horticultural Society Color charts) were monitored for 17 weeks. Media affected shoot proliferation (P = 0.0042) but the zone of origin (P = 0.6664) of the explant did not. Callus area showed no significant difference among the four media and three zones (P = 0.2091) and averaged 3.60 centimeters2. After four subcultures, each lasting 30 days, explants on DKW media produced 10 shoots per explant. This media might hold promise for the micropropagation of bigtooth maple. Twenty-nine percent of all explants expressed foliar pigmentation, which ranged from red-purple to orange-red. Whether foliar pigment development in tissue culture correlates with expressed pigmentation in nature warrants further investigation.

scholarly journals Micropropagation of Vanda tricolor Lindl. var. suavis with various concentrations of organic growth supplements

2021 ◽  
Vol 886 (1) ◽  
pp. 012004
Author(s):  
M Tuwo ◽  
A I Latunra ◽  
E T Ana
Keyword(s):  
Tissue Culture ◽  
Culture Media ◽  
Good Alternative ◽  
Control Treatment ◽  
Tissue Culture Media ◽  
Organic Growth ◽  
Randomized Design ◽  
Significant Difference ◽  
Number Of Leaves

Abstract Plant propagation through in vitro culture is increasingly being used to produce hybrid orchids. Plant tissue culture provides a good alternative to produce plants in large numbers in a short time. The provision of organic growth supplements in tissue culture media plays an important role as a substitute for growth regulators in stimulating the growth of explants. In this study, young coconut water, banana extract (cv. ambon), and tomato extract were used to stimulate the growth of the Vanda tricolor Lindl. Var suavis protocorm. Data were analyzed using a completely randomized design (CRD) with five replications using the Kruskal-Wallis test and continued with the Mann-Whitney test if there was a significant difference between each treatment and its concentration. Parameters observed were the percentage of the number of shoots and the number of leaves. The results showed that there was a significant difference between the treatments given to the number of leaves. Mann-Whitney further test results on the number of leaves showed a significant difference in the banana extract treatment and the control treatment.

scholarly journals In Vitro Propagation of HS314 Rootstock (Prunus amygdalus × P. persica)

HortScience ◽  
2011 ◽  
Vol 46 (6) ◽  
pp. 928-931
Author(s):  
Jalil Dejampour ◽  
Islam Majidi ◽  
Solmaz Khosravi ◽  
Sevil Farhadi ◽  
Atena Shadmehr
Keyword(s):  
Culture Media ◽  
Shoot Proliferation ◽  
Nodal Segments ◽  
Naphthaleneacetic Acid ◽  
Root Induction ◽  
Prunus Amygdalus ◽  
Indole Butyric Acid ◽  
Half Strength

A micropropagation protocol was developed for the HS314 rootstock, a hybrid between almond and peach that could be used as an alternative rootstock instead of GF677. Surface-sterilized nodal segments were cultured in a modified DKW medium containing 3% sucrose, 100 mg·L−1 of Phloroglucinol, 0.7% plant agar, and 0.5 mg·L−1 benzyl amino purine (BAP). Explants were transferred to the same culture media supplemented with 0.5, 1, or 2 mg·L−1 BAP and 0, 0.1, or 0.5 mg·L−1 indole butyric acid (IBA) for further shoot proliferation. The maximum number of shoots produced on a medium containing 2 mg·L−1 BAP. Microshoots were transferred to the DKW medium supplemented with 0.5, 1, 2, or 4 mg·L−1 IBA or naphthaleneacetic acid (NAA) for root induction. The highest root number and the greatest root length were gained on a medium containing 2 mg·L−1 IBA. Rooting percentage was improved from 66% to more than 85% by reducing the concentration of DKW salts to half strength. Finally, rooted plantlets were successfully acclimatized and transferred in vivo conditions.

scholarly journals In Vitro Micropropagation of the Medicinal Plant Physalis angulata L.

2016 ◽  
Vol 8 (2) ◽  
pp. 161-163
Author(s):  
Owk ANIEL KUMAR ◽  
Songa RAMESH ◽  
Sape SUBBA TATA
Keyword(s):  
Large Scale ◽  
Leaf Disc ◽  
Basal Medium ◽  
Shoot Proliferation ◽  
Shoot Multiplication ◽  
Medicinal Herb ◽  
Root Induction ◽  
Survival Percentage ◽  
Physalis Angulata

Physalis angulata L. is an important medicinal herb. An efficient direct adventitious plant regeneration protocol was developed for large scale propagation using leaf disc as explants. The explants were cultured on MS basal medium supplemented with 0.25-3.0 mg/L 6-benzyl amino purine (BAP) for primary shoot proliferation. Inclusion of indole-3-acetic acid (IAA) and gibberellic acid (GA3) in the culture medium along with BAP promoted a higher rate of shoot multiplication. The maximum number of shoots was produced in MS + BAP (1.0 mg/L) + IAA (0.5 mg/L) + GA3 (0.20 mg/L) after the third subculture. An average of 152.8 ± 0.40 shoots were produced from each leaf disc. For root induction the shootlets were transferred to MS medium supplemented with different concentrations of indole-3-butyric acid (IBA). The highest percentage of root induction was observed in 1.0 mg/L (IBA). Rooted plants were successfully established in the soil after hardening. The survival percentage of rooted plants on soil was found to be 85%. This result will facilitate the conservation and propagation of the important medicinal herb Physalis angulata L.

scholarly journals MODIFICAÇÕES NO MEIO DE CULTURA, FOTOPERÍODO E TEMPO DE CULTIVO AFETAM O ALONGAMENTO E ENRAIZAMENTO IN VITRO DE BANANEIRA CV. PACOVAN

Nativa ◽  
2018 ◽  
Vol 6 (1) ◽  
pp. 27
Author(s):  
Marcos Vinícius Marques Pinheiro ◽  
Ana Cristina Portugal Pinto De Carvalho ◽  
Fabrina Bolzan Martins
Keyword(s):  
Plant Height ◽  
Culture Medium ◽  
Culture Media ◽  
Dry Weight ◽  
Salt Mixture ◽  
Musa Spp ◽  
Fresh Biomass ◽  
Shoot Dry Weight ◽  
Number Of Leaves

No intuito de elevar as taxas de sobrevivência durante a etapa de aclimatização e posterior plantio a campo, avaliou-se o enraizamento in vitro de bananeira cv. Pacovan, em diferentes concentrações de sais MS e de sacarose. Utilizou-se DIC, esquema fatorial (6x2x3), com seis meios de cultura [sendo três concentrações de nutrientes do meio MS (100%; 50% de macronutrientes; e 50% dos sais macro e micronutrientes), e duas concentrações de sacarose (1,5/3,0%)], dois fotoperíodos (12/16 h) e três tempos de cultivo (21, 28 ou 35 dias) e seis repetições/tratamento. Analisaram-se: altura da planta, número de folhas/planta, massas frescas e secas das partes aérea e radicular. Para altura da planta, massa fresca da parte aérea e radicular, o meio MS 50% dos sais + sacarose (1,5%) com fotoperíodo de 16 h e tempo de cultivo de 35 dias foi satisfatório. Para massa seca da parte aérea foi MS 50% de sais + sacarose (3%), e para massa seca da parte radicular, MS 100% + sacarose (3%) (em 12hs/28 dias e 16hs/21 dias). Para o alongamento/enraizamento in vitro da bananeira cv. Pacovan sugere-se MS 50% de sais (macro e micronutrientes), redução ou manutenção de sacarose (1,5 ou 3%) em 16h/35 dias de cultivo.Palavra-chave: Musa spp., propagação in vitro, sistema radicular. CHANGES IN CULTURE MEDIUM, PHOTOPERIOD AND TIME OF CULTIVATION AFFECT THE IN VITRO ELONGATION AND ROOTING OF BANANA CV. PACOVAN ABSTRACT:In order to achieve high rates of survival during the acclimatization and later planting in the field, was evaluated the in vitro of banana cv. Pacovan plants under different concentrations of sucrose and MS basal salt mixture. The experiment was assembled in a DIC, in 6x2x3, six different culture media [three different MS salt mixture concentrations (100%; 50% of macronutrients; and 50% of macro/micronutrients) and two sucrose concentrations (1.5/3%)], two photoperiods (12/16 hours) and three cultivation times (21, 28 or 35 days). Each treatment was composed by 6 replicates. Plant height, number of leaves/plant, fresh and dry weight of roots and shoots, were analyzed. Satisfactory results for plant height and shoot and root fresh biomass were observed in MS with macro/micronutrients (50%) + sucrose (3%), 16 hours/35 days. The highest values of shoot dry weight were observed in MS with macro/micronutrients (50%) + sucrose (3%); the highest root dry weight was achieved with MS 100% + sucrose (3%) (12hs/28 and 16hs/21 days). The suggested medium for the in vitro elongation and rooting stage of banana cv. Pacovan is the MS with 50% of salts (macro and micronutrients), reduction or maintenance of sucrose (1.5 or 3%) in 16h/35 days of cultivation.Keywords: Musa spp., in vitro propagation, root system. DOI:

scholarly journals In vitro development of Encyclea cordigera in different concentrations of honey

2015 ◽  
Vol 46 (4) ◽  
pp. 590-592 ◽  
Author(s):  
Cibele Mantovani ◽  
Kathia Fernandes Lopes Pivetta
Keyword(s):  
Culture Media ◽  
Leaf Length ◽  
In Vitro Development ◽  
Randomized Design ◽  
Sucrose Medium ◽  
Number Of Leaves ◽  
Completely Randomized Design ◽  
Set Up ◽  
Vitro Development

ABSTRACT: The objective of this paper was to evaluate the effects of different honey concentrations in culture media, in comparison to sucrose medium, for the in vitro development of the epiphytic Encyclea cordigera orchid, in order to improve the process of propagation of the species. The in vitro germination was prepared on a reduced Murashige & Skoog (MS) medium. After 90 days, the seedlings were divided into different treatments, where they remained for another 90 days. Six treatments were set up (30g L-1 of sucrose; 15, 30, 45, and 60g L-1 of honey; and absence of any carbohydrates) in a completely randomized design. Plants were removed from the vials 270 days after the start of the experiment, and the number of roots, length of the largest leaf, length of the longest root, number of leaves, and fresh and dry masses were evaluated. Data concerning the number of leaves and roots were (x+1)1/2 transformed and subjected to an analysis of variance (ANOVA); the means were compared by a Tukey's test set at 5% probability. Medium containing 60g L-1 of honey proved to be superior to the sucrose medium traditionally used, favoring the in vitro growth and development of Encyclea cordigera. This medium can therefore be recommended for the propagation of this species, which is usually cultivated as an ornamental plant.

AFLP Analysis and Improved Phytoextraction Capacity of Transgenic gshI-Poplar Clones (Populus x canescens L.) for Copper in vitro

2005 ◽  
Vol 60 (3-4) ◽  
pp. 300-306 ◽  
Author(s):  
Gábor Gyulai ◽  
Mervyn Humphreys ◽  
András Bittsánszky ◽  
Kirsten Skøtc ◽  
József Kiss ◽  
...  
Keyword(s):  
Culture Media ◽  
Leaf Disc ◽  
Aflp Analysis ◽  
Polymorphism Analysis ◽  
Tissue Culture Media ◽  
Dna Fragment ◽  
High Concentrations ◽  
Cu Uptake ◽  
Concentration Series

Abstract Clone stability and in vitro phytoextraction capacity of vegetative clones of P. x canescens (2n = 4x = 38) including two transgenic clones (ggs11 and lgl6) were studied as in vitro leaf disc cultures. Presence of the gshI-transgene in the transformed clones was detected in PCR reactions using gshI-specific primers. Clone stability was determined by fAFLP (fluorescent amplified DNA fragment length polymorphism) analysis. In total, 682 AFLP fragments were identified generated by twelve selective primer pairs after EcoRIDMseI digestion. Four fragments generated by EcoAGTDMseCCC were different (99.4% genetic similarity) which proves an unexpectedly low bud mutation frequency in P. \ canescens. For the study of phytoextraction capacity leaf discs (8 mm) were exposed to a concentration series of ZnSO4 (10-1 to 10-5 ᴍ) incubated for 21 days on aseptic tissue culture media WPM containing 1 μᴍ Cu. Zn2+ caused phytotoxicity only at high concentrations (10-1 to 10-2 ᴍ). The transgenic poplar cyt-ECS (ggs11) clone, as stimulated by the presence of Zn, showed elevated heavy metal (Cu) uptake as compared to the non-transformed clone. These results suggest that gshI-transgenic poplars may be suitable for phytoremediation of soils contaminated with zinc and copper.

scholarly journals In vitro propagation of Citrullus lanatus Thumb. from nodal explants culture

1970 ◽  
Vol 8 (2) ◽  
pp. 203-206 ◽  
Author(s):  
MM Khatun ◽  
MS Hossain ◽  
MA Haque ◽  
M Khalekuzzaman
Keyword(s):  
Citrullus Lanatus ◽  
In Vitro Regeneration ◽  
Shoot Proliferation ◽  
Multiple Shoot ◽  
Nodal Explants ◽  
Root Induction ◽  
Ms Medium ◽  
Nodal Explant ◽  
Grown Plant

A standard protocol was established for rapid in vitro propagation of watermelon (Citrullus lanatus Thumb.) from nodal explants of field grown plant. Multiple shoot proliferation was achieved from nodal explants on MS medium supplemented with 1.0 mg/l BAP + 0.2 mg/l NAA within 30 days of inoculation. The elongation of shoots was obtained on the same medium. Highest percentage of root induction was achieved on MS medium supplement with 1.0 mg/l IBA within 25 days of culture. Well rooted plantlets were transferred to small pots and after proper acclimatization the plantlets were transplanted in the field condition, where 80% plantlets were survived and grew successfully. Keywords: In vitro regeneration; Nodal explant; Citrullus lanatus DOI: 10.3329/jbau.v8i2.7926 J. Bangladesh Agril. Univ. 8(2): 203-206, 2010  

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