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Murashige and Skoog medium

About: Murashige and Skoog medium is a research topic. Over the lifetime, 10125 publications have been published within this topic receiving 148301 citations.


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Journal ArticleDOI
TL;DR: The regeneration of plants from protoplasts of wheat isolated from a regenerable embryogenic suspension culture that was initiated from immature embryo-derived ‘aged’ compact callus produced healthy plants that were successfully transferred to soil and grown in the greenhouse.
Abstract: We describe the regeneration of plants from protoplasts of wheat isolated from a regenerable embryogenic suspension culture that was initiated from immature embryo-derived ‘aged’ compact callus. Proto-colonies were also obtained from a non-regenerable cell line established from friable callus that arose spontaneously on the aged callus, but did not give rise to any plants. Plating efficiencies well in excess of twenty percent were routinely obtained from protoplasts isolated from the regenerable as well as the non-regenerable cell lines in Kao and Michyaluk, as well as Murashige and Skoog based, nutrient media. Four to five week old protocolonies, derived from regenerable suspension culture protoplasts, formed distinct somatic embryos and shoots upon transfer to various regeneration media. Shoots were rooted on transfer to rooting media. Successive transfer of the plantlets to MS or half-strength MS medium, with or without activated charcoal, produced healthy plants that were successfully transferred to soil and grown in the greenhouse.

164 citations

Journal ArticleDOI
TL;DR: Shoot apex, nodal, and leaf explants of Stevia rebaudiana Bertoni can regenerate shoots when cultured on Murashige and Skoog medium supplemented with 6-benzyladenine (BA) and indole-3-acetic acid (5.71 μM).
Abstract: Shoot apex, nodal, and leaf explants of Stevia rebaudiana Bertoni can regenerate shoots when cultured on Murashige and Skoog (MS) medium supplemented with 6-benzyladenine (BA; 8.87 μM) and indole-3-acetic acid (5.71 μM). Rooting of the in vitro-derived shoots could be achieved following subculture onto auxin-containing medium. A survival rate of 70% was recorded at the hardening phase on the substrate cocopeat. The presence of the sweet diterpene glycosides, viz. stevioside and rebaudioside, was confirmed in the in vitro-derived tissues of Stevia using HPTLC techniques. Callus cultured on agar-solidified MS medium supplemented with BA (8.87 μM) and indole-3-butyric acid (9.80 μM) showed the highest sweetener content.

163 citations

Journal ArticleDOI
TL;DR: It is found that melatonin plays an important role in regulating both seminal root length and root growth after germination in monocotyledonous rice plants, and treatment with 0.5 and 1 μm melatonin promoted seminal root growth of the wild type under continuous light.
Abstract: The effect of melatonin on root growth after germination was examined in transgenic rice seedlings expressing sheep serotonin N-acetyltransferase (NAT). Enhanced melatonin levels were found in T(3) homozygous seedlings because of the ectopic overexpression of sheep NAT, which is believed to be the rate-limiting enzyme in melatonin biosynthesis in animals. Compared with wild-type rice seeds, the transgenic rice seeds showed enhanced seminal root growth and an analogous number of adventitious roots 4 and 10 days after seeding on half-strength Murashige and Skoog medium. The enhanced initial seminal root growth in the transgenic seedlings matched their increased root biomass well. We also found that treatment with 0.5 and 1 μM melatonin promoted seminal root growth of the wild type under continuous light. These results indicate that melatonin plays an important role in regulating both seminal root length and root growth after germination in monocotyledonous rice plants. This is the first report on the effects of melatonin on root growth in gain-of-function mutant plants that produce high levels of melatonin.

160 citations

DOI
20 Jan 1973
TL;DR: The results obtained with different materials (different varieties or hybrids of different crosses) varied considerably as discussed by the authors, suggesting that application of the anther culture method to plant breeding is very promising.
Abstract: Anthers of Triticum aestivum L. were cultured in vitro on the MS medium supplemented with auxins, with or without kinetin. Then the pollen grains were successfully, induced to develop into intact plants through a stage of callus formation. Experiments indicated that pollen grains at the mid-uninucleate stage were most favourable for induction to form calli, and that addition of lactalbumin hydrolysate and appropriate increase of the sucrose coneentration had some promoting effects on pollen callus formation. The pollen callus with relatively great differentiating capacity was generally compact in texture and possessed the histological characteristics of the primary meristem. It was noted that the results obtained with different materials (different varieties or hybrids of different crosses) varied considerably. The progeny of the plant induced from F 1, hybrid pollen showed no segregation of characters, suggesting that application of the anther culture method to plant breeding is very promising.

155 citations

Journal ArticleDOI
TL;DR: The effect of thidiazuron (TDZ) was investigated on in vitro shoot proliferation from nodal explants of Rauvolfia tetraphylla and regenerated shoots rooted best on MS medium containing 0.5μM indole-3-butyric acid (IBA).
Abstract: The effect of thidiazuron (TDZ) was investigated on in vitro shoot proliferation from nodal explants of Rauvolfia tetraphylla. Murashige and Skoog (MS) medium containing TDZ (0.5–10μM) was effective in inducing shoot buds and maintaining high rates of shoot multiplication on hormone free medium. The highest shoot regeneration frequency (90%) and mean number (18.50 ± 1.25) of shoots per explant were achieved from nodal segments cultured on MS medium supplemented with 5μM TDZ for 4 weeks prior to transfer to MS medium without TDZ for 8 weeks. The regenerated shoots rooted best on MS medium containing 0.5μM indole-3-butyric acid (IBA). Micropropagated plantlets were hardened to survive ex vitro conditions and were then established into soil.

154 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023160
2022350
2021245
2020268
2019275
2018362