Determination of assimilator pigment content in cladodes of Opuntia fragilis var. Fragilis …
October 16, 2010
Determination of assimilator pigment content in cladodes of Opuntia fragilis var. Fragilis exposed..
This is an automatically generated default intro template – please do not edit.
General information |
|
Title: | Determination of assimilator pigment content in cladodes of Opuntia fragilis var. Fragilis exposed.. |
Meta keywords: | |
Meta description: | |
Images information |
|
Images path absolute: | |
Images path relative: | |
Thumbs path absolute: | |
Thumbs path relative: | |
Fields information |
|
Article_Title: | Determination of assimilator pigment content in cladodes of Opuntia fragilis var. Fragilis exposed to light of different colors emitted by LEDs |
Authors: | Teodora Iuliana Vidican1, Dorina Cachita-Cosma2 |
Affiliation: | 1 University of Oradea, Romania 2 “Vasile Goldis” Western University of Arad, Romania |
Abstract: | After determining the assimilator pigment content of Opuntia fragilis var. fragilis cladodes, from vitrocultures exposed for 90 days at a light intensity of 1000 lux, different colors (white, blue, yellow, red or green), issued by the LED (Light Emitting Diode), it has been found that in relation to their level, similar vitrocultures illuminated with white fluorescent light (control variant, the reference), only Opuntia vitroplantlets exposed to white light emitted by LEDs held chlorophyll a and carotenoid pigments in quantities close to the value determined from material plant derived from control samples. Instead, those vitroplantlets exposed to emitted red or yellow LEDs light, had a content of more than 50% below the lower chlorophyll a and chlorophyll b, in carotenoid pigments respectively, compared with that recorded in similar vitrocladodes from the culture illuminated with white fluorescent tubes (control variant). The strongest inhibitory effect on the assimilator pigment level gained from Opuntia cladodes mesophyll, regenerated in vitro, it has been challenged by green LED light, the vast majority of the examined pigments, the amount of which were approximately 30% from the parameters that have been registered with prepared extracts from control samples. |
Keywords: | Opuntia, LEDs, light, pigments, vitrocultures |
References: | Behera N., Biswal S., 1990, Effects of pre-storage conditions on storage of in vitro cultures of Nephrolepis exaltata (L.) Schott and Cordyline fruticosa (L.) A. Chev, Plant Cell, Tissue and Organ Culture, vol. 28, no. 2, pp. 167-174. Cachiţă, C.D., Deliu, C., Rakosy-Tican, L., Ardelean, A., 2004, Tratat de biotehnologie vegetală, vol. I, Ed. Dacia, Cluj-Napoca. Folta, K.M., 2004, Green light increases early stem elongation rate, antagonizing light-mediated growth inhibition. Plant Physiol. 135, pp. 1407-1416. Folta, K.M., Spalding E.P., 2001, Opposing roles of phytochrome A and phytochrome B in early cryptochrome-mediated growth inhibition. The Plant Journal. 28, pp. 330 – 340. Heller, R., 1953, Rescherches sur la nutrition minérale des tissus végétaux cultives in vitro, Ann.Sci. Nat. Bot. Veg. Ser.,II, pp. 1-5. Jao, R.C., Fang, W., Chang, S.F., 2005, Effects of red light on the growth of Zantedechia plantlets in vitro tuber formation using Light-emitting diodes, HortScience, vol. 40, no.2, pp. 436-438. Maier J., Schmid R., 1997, Inhibition of pteridine biosynthesis eliminates blue-light dependent stimulation of red-light saturated photosynthesis in Laminaria saccharina (L.)Lamouroux, Journal of Photochemistry Photobiologz B: Biology vol. 38, Issues 2-3, pp. 274-278. Moran, R., Porath, D., 1980, Chlorophyll determination in intact tissues usingN,N-dimethylformamide, Plant Physiol 65, pp. 478-479. Murashige, T.,Skoog, F., 1962, A revised medium for rapid growth and biossays with tabacco tissue cultures, Physiol. Plant., 15; pp. 473 – 497. Pop, L., Cachiţă, C.D., 2007, Preliminary research concerning the reactions of Sequoia sempervirens vitrocultures to „high brightness” LED illumination, Analele Universităţii din Craiova, pp. 215-219. Shemorakov, N., 2001, Plastid mutations, Cultivar, vol. 2, no. 3. Turcuş V.,Cachiţă D, Crăciun C., 2009, Ultrastructural aspects in the rhizome of Drosera rotundifolia L. vitroplantules, Studia Universitatis “Vasile Goldiş”, Seria Ştiințele Vieţii, Arad, vol. 19, nr. 1, pp. 145-150. Vidican I.T., Cachiţă D., Romocea J.E., 2009, The initiation of Echinocactus mihanovichii, Echinopsis chamaecereus f. lutea and Aylostera heliosa vitrocultures, Studia Universitatis “Vasile Goldiş”, Seria Ştiințele Vieţii, Arad, vol. 19, no.2, pp. 351-358. |
Read_full_article: | pdf/20-2010/20-2-2010/SU20-2-10Vidican.pdf |
Correspondence: | Teodora Vidican, University of Oradea, Romania, E-mail: teodora.vidican@gmail.com |
Read full article | |
Article Title: | Determination of assimilator pigment content in cladodes of Opuntia fragilis var. Fragilis exposed to light of different colors emitted by LEDs |
Authors: | Teodora Iuliana Vidican1, Dorina Cachita-Cosma2 |
Affiliation: | 1 University of Oradea, Romania 2 “Vasile Goldis” Western University of Arad, Romania |
Abstract: | After determining the assimilator pigment content of Opuntia fragilis var. fragilis cladodes, from vitrocultures exposed for 90 days at a light intensity of 1000 lux, different colors (white, blue, yellow, red or green), issued by the LED (Light Emitting Diode), it has been found that in relation to their level, similar vitrocultures illuminated with white fluorescent light (control variant, the reference), only Opuntia vitroplantlets exposed to white light emitted by LEDs held chlorophyll a and carotenoid pigments in quantities close to the value determined from material plant derived from control samples. Instead, those vitroplantlets exposed to emitted red or yellow LEDs light, had a content of more than 50% below the lower chlorophyll a and chlorophyll b, in carotenoid pigments respectively, compared with that recorded in similar vitrocladodes from the culture illuminated with white fluorescent tubes (control variant). The strongest inhibitory effect on the assimilator pigment level gained from Opuntia cladodes mesophyll, regenerated in vitro, it has been challenged by green LED light, the vast majority of the examined pigments, the amount of which were approximately 30% from the parameters that have been registered with prepared extracts from control samples. |
Keywords: | Opuntia, LEDs, light, pigments, vitrocultures |
References: | Behera N., Biswal S., 1990, Effects of pre-storage conditions on storage of in vitro cultures of Nephrolepis exaltata (L.) Schott and Cordyline fruticosa (L.) A. Chev, Plant Cell, Tissue and Organ Culture, vol. 28, no. 2, pp. 167-174. Cachiţă, C.D., Deliu, C., Rakosy-Tican, L., Ardelean, A., 2004, Tratat de biotehnologie vegetală, vol. I, Ed. Dacia, Cluj-Napoca. Folta, K.M., 2004, Green light increases early stem elongation rate, antagonizing light-mediated growth inhibition. Plant Physiol. 135, pp. 1407-1416. Folta, K.M., Spalding E.P., 2001, Opposing roles of phytochrome A and phytochrome B in early cryptochrome-mediated growth inhibition. The Plant Journal. 28, pp. 330 – 340. Heller, R., 1953, Rescherches sur la nutrition minérale des tissus végétaux cultives in vitro, Ann.Sci. Nat. Bot. Veg. Ser.,II, pp. 1-5. Jao, R.C., Fang, W., Chang, S.F., 2005, Effects of red light on the growth of Zantedechia plantlets in vitro tuber formation using Light-emitting diodes, HortScience, vol. 40, no.2, pp. 436-438. Maier J., Schmid R., 1997, Inhibition of pteridine biosynthesis eliminates blue-light dependent stimulation of red-light saturated photosynthesis in Laminaria saccharina (L.)Lamouroux, Journal of Photochemistry Photobiologz B: Biology vol. 38, Issues 2-3, pp. 274-278. Moran, R., Porath, D., 1980, Chlorophyll determination in intact tissues usingN,N-dimethylformamide, Plant Physiol 65, pp. 478-479. Murashige, T.,Skoog, F., 1962, A revised medium for rapid growth and biossays with tabacco tissue cultures, Physiol. Plant., 15; pp. 473 – 497. Pop, L., Cachiţă, C.D., 2007, Preliminary research concerning the reactions of Sequoia sempervirens vitrocultures to „high brightness” LED illumination, Analele Universităţii din Craiova, pp. 215-219. Shemorakov, N., 2001, Plastid mutations, Cultivar, vol. 2, no. 3. Turcuş V.,Cachiţă D, Crăciun C., 2009, Ultrastructural aspects in the rhizome of Drosera rotundifolia L. vitroplantules, Studia Universitatis “Vasile Goldiş”, Seria Ştiințele Vieţii, Arad, vol. 19, nr. 1, pp. 145-150. Vidican I.T., Cachiţă D., Romocea J.E., 2009, The initiation of Echinocactus mihanovichii, Echinopsis chamaecereus f. lutea and Aylostera heliosa vitrocultures, Studia Universitatis “Vasile Goldiş”, Seria Ştiințele Vieţii, Arad, vol. 19, no.2, pp. 351-358. |
*Correspondence: | Teodora Vidican, University of Oradea, Romania, E-mail: teodora.vidican@gmail.com |