Anthurium andraeanum Plantlets Produced from Callus Tissues Cultivated in vitro

1976 ◽  
Vol 37 (1) ◽  
pp. 80-82 ◽  
Author(s):  
R. L. M. PIERIK
Keyword(s):  
Anthurium Andraeanum ◽  
Callus Tissues

scholarly journals Isolation of furanocoumarins from Pastinaca sativa L. callus culture

2014 ◽  
Vol 69 (3) ◽  
pp. 193-195 ◽  
Author(s):  
Halina Ekiert ◽  
Wanda Kisiel
Keyword(s):  
Secondary Metabolites ◽  
Callus Culture ◽  
Spectral Methods ◽  
Solid Medium ◽  
Intact Plant ◽  
Pastinaca Sativa ◽  
First Report ◽  
Callus Tissues ◽  
First Time

Four furanocoumarins: bergapten, xanthotoxin, isopimpinellin (linear furanocoumarins) and sphondin (angular furanocoumarin) were isolated for the first time from callus tissues of <em>Pastinaca sativa</em> L.(<em>Apiaceae</em>) cultured in vitro on solid medium. The compounds were identified using spectral methods. They are well-known secondary metabolites of the intact plant. This is the first report on the isolation of sphondin from in vitro plant cultures.

Plantlet formation in callus tissues of Anthurium andraeanum Lind.

1974 ◽  
Vol 2 (2) ◽  
pp. 193-198 ◽  
Author(s):  
R.L.M. Pierik ◽  
H.H.M. Steegmans ◽  
J.A.J. Van Der Meys
Keyword(s):  
Plantlet Formation ◽  
Anthurium Andraeanum ◽  
Callus Tissues

scholarly journals In vitro culture of Anthurium andraeanum

1986 ◽  
Vol 52 (4) ◽  
pp. 343-346 ◽  
Author(s):  
J.F. Finnie ◽  
J. van Staden
Keyword(s):  
In Vitro Culture ◽  
Anthurium Andraeanum

Induction of Anthurium andraeanum “Arizona” tetraploid by colchicine in vitro

Euphytica ◽  
2011 ◽  
Vol 181 (2) ◽  
pp. 137-145 ◽  
Author(s):  
Chao Chen ◽  
Xilin Hou ◽  
Hongxin Zhang ◽  
Guilan Wang ◽  
Limin Tian
Keyword(s):  
Anthurium Andraeanum

scholarly journals Qualitative and Quantitative Evaluation of Active Constituents in Callus of Lavandula angustifolia plant in Vitro

2020 ◽  
Vol 17 (2(SI)) ◽  
pp. 0591
Author(s):  
Zainab Salman et al.
Keyword(s):  
Leaf Explants ◽  
Volatile Oil ◽  
Gas Chromatography Mass Spectrometry ◽  
Naphthalene Acetic Acid ◽  
Fresh Weight ◽  
Lavandula Angustifolia ◽  
Qualitative And Quantitative ◽  
Main Components ◽  
Callus Tissues

This study was conducted to describe a protocol for the callus establishing culture of Lavandula angustifolia plant and estimating their content of volatile oil. The quantity of volatile oil callus tissues was compared with that of leaves production. Callus was induced from leaf explants on Murashige and Skoog medium (MS) supplemented with Naphthalene acetic acid (NAA) and Benzyl adenine (BA) in different concentrations. Maximum callus fresh weight was obtained in the combination of 10 mg/L BA and 3 mg/L NAA which reached 18 g after four weeks. The results of this work showed that the  quantity of volatile oil from the highest fresh weight callus was 6 ml compared with quantity of 18g of leaves which gave 0.5 ml. Volatile oil of leaf and callus extracts were analyzed using gas chromatography mass spectrometry method (GC-MS) which showed linoleic acid (56.61%) and oleic acid (57.93%) as main components.

Analysis of ancient DNA from in vitro grown tissues of 1600-year-old seeds revealed the species as Anagyris foetida

2012 ◽  
Vol 22 (4) ◽  
pp. 279-286 ◽  
Author(s):  
Murat Özgen ◽  
Aslı Özdilek ◽  
Melahat A. Birsin ◽  
Sertaç Önde ◽  
Derya Şahin ◽  
...  
Keyword(s):  
Nuclear Dna ◽  
Adventitious Shoots ◽  
Its Region ◽  
Naphthaleneacetic Acid ◽  
Archaeological Excavation ◽  
Relict Species ◽  
Western Turkey ◽  
Callus Tissues ◽  
Seed Characteristics

AbstractSeven ancient seeds, about 1600 years old, were found during an archaeological excavation in Asar Island which is located in south-western Turkey. These seeds were subjected to germination, in vitro callus induction and molecular characterization experiments to test the viability and plant origin of the seeds. Six of the seven seeds had viable seed components (such as cotyledons) and produced callus tissue in Murashige and Skoog medium supplemented with 2 mg l− 1 6-benzylamino purine (BAP), 0.2 mg l− 1 1-naphthaleneacetic acid (NAA), 20 g l− 1 sucrose, 2 mg l− 1 glycine and 7 g l− 1 agar, but the calli from these seeds failed to yield adventitious shoots. DNA samples from callus tissues produced by ancient seeds in vitro were of good quality. The internal transcribed spacer (ITS) region in nuclear DNA (nDNA) of ancient seeds was amplified successfully. The sequences from amplified ITS DNA products of six ancient seeds indicated that their ITS sequences matched those of Anagyris foetida after subjecting them to BLAST searches in international sequence databases (NCBI). A. foetida is a relict species endemic to the Mediterranean region and used as a herbal medicine. We believe that seed characteristics such as the very hard, extremely smooth and shiny testa, toxic anagyrine alkaloid content and their storage in a pot further improved the longevity of these ancient seeds.

scholarly journals Dr. Ottó Orsós, the forgotten Hungarian pioneer in plant tissue culture

2005 ◽  
Vol 11 (1) ◽  
Author(s):  
M. G. Fári
Keyword(s):  
Tissue Culture ◽  
Plant Tissue Culture ◽  
Plant Tissue ◽  
Cell Biology ◽  
In Vitro Morphogenesis ◽  
Regenerated Plants ◽  
Universal Biology ◽  
History Of ◽  
Callus Tissues

The knowledge of tissue culture deserves attention in respect of understanding the development of universal biology. This study intends to contribute to the past of the plant tissue culture by such data of the history of science which have been unprocessed so far. It seems that the life-work of the Hungarian biologist, Dr. Ottó Orsós is a missing and essential link between those early plant hormone researchers and the representatives of the pioneers of tissue culture schools who have contributed substantially to the development of the modern in vitro plant morphogenesis and plant cell biology. Orsós cultured kohlrabi tuber cubes on White culture medium in a sterile manner. This way, he could efficiently direct the in vitro morphogenesis of the kohlrabi, the regeneration of its shoot and root, and the formation and steps to subculture of pure callus tissues in 1938. He supported the correctness of its statements by means of detailed anatomical examinations. Orsós successfully rooted and aclimatized complete regenerated plants. We may as well call the above system — in remembrance of the creators of the original concept — "Haberlandt-Orsós model". Between the publishing of his main paper in 1938 and 2003, a period of 65 years has lapsed. On the occasion of this anniversary, we bow before this forgotten pioneer.

scholarly journals Regeneration of leaf explants of Anthurium andraeanum Lind. in vitro.

1979 ◽  
Vol 27 (3) ◽  
pp. 221-226 ◽  
Author(s):  
R.L.M. Pierik ◽  
P. van Leeuwen ◽  
G.C.C.M. Rigter
Keyword(s):  
Shoot Regeneration ◽  
Callus Formation ◽  
Leaf Explants ◽  
Growth Substance ◽  
Tween 20 ◽  
Strong Positive Correlation ◽  
Promoting Effect ◽  
Nutrient Agar Medium ◽  
Anthurium Andraeanum

Leaf explants were cultured on a basic nutrient agar medium to which were added growth substances (adenine, benzyladenine, kinetin, 2-iP [isopentenyladenine], zeatin or 2,4-D) and NH4NO3, (NH4)2SO4 or NaNO3 in various concentrations. The effects of using the surfactant Tween 20 during leaf sterilization and of growing explants in light and/or darkness for 20 weeks were also investigated. There was a strong positive correlation between callus formation and shoot regeneration. Regeneration was optimal under the following conditions: addition of 0.25-1.00 ml/litre Tween 20 during leaf sterilization, adding a growth substance (adenine 0.1 mg/litre, zeatin 1 mg/litre, or 2,4-D 0.08 mg/litre), culture during 16 weeks in darkness followed by 4 weeks of light, and including 206 mg/litre NH4NO3 in the medium. The promoting effect of low levels of NH4NO3 on shoot regeneration in callus was caused by the NH4+ ion and not by the NO3- ion. (Abstract retrieved from CAB Abstracts by CABI’s permission)

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