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水稻悬浮细胞培养的方法. The flasks were set on a gyratory shaker agitated at 120 rpm under fluorescent light of 200-300 lux at 27°C. Cell growth in the R-2 medium was superior to that obtained in B5, Heller, Murashige-Skoog and White media. Plant & CellPhysiol. 14: 1113-1121 (1973).
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The flasks were set on a gyratory shaker agitated at 120 rpm under fluorescent light of 200-300 lux at 27°C. Cell growth in the R-2 medium was superior to that obtained in B5, Heller, Murashige-Skoog and White media. Plant & CellPhysiol. 14: 1113-1121 (1973)
A japonica rice variety, Nackdong, was used for transformation by the Agrobacterium cocultivation method as described previously with the following modifications [14]. Calli were induced from the scutellum of mature seeds on an N6 medium containing 2 mg/l 2,4-D. An A. tumefaciens strain LBA4404 carrying the pGA1647 plasmid was grown for 3 days in an AB liquid medium supplemented with 30 mg/l hygromycin B and 3 mg/l tetracycline. Three-week-old calli were cocultivated with Agrobacterium on a 2N6-As medium supplemented with 1 mM betaine for 2–3 days in darkness at 25 C. The cocultivated calli were washed with sterile water containing 100 mg/l cefotaxime, and incubated on an N6 medium containing 40 mg/l hygromycin B and 250 mg/l cefotaxime for 3 weeks. Actively growing calli were transferred onto a regeneration medium, MS media supplemented with 0.1 mg/l NAA, 2 mg/l kinetin, 2% sorbitol, 1.6% phytagar (Gibco), 50 mg/l hygromycin B, and 250 mg/l cefotaxime. After 2–3 weeks under continuous light (40 mol m2 s1), plantlets were potted and grown in a growth chamber with 10 h light per day. Plant Molecular Biology 39: 35–44, 1999.
NB Basic N6 major salts and iron source (Chu 1975), B5 minor salts and vitamins (Gamborg et al. 1968), 30 g/l sucrose NB NB Basic + 2 mg/l 2,4-dichlorophenoxyacetic acid (2,4-D), 500 mg/l proline, 500 mg/l glutamine, 300 mg/l casein hydrolysate, 2.6 g/l Phytagel, pH 5.8 (Li et al. 1993) R2 Basic R2 major and minor salts, vitamins and iron source (Ohira et al. 1973), 2.5 mg/l 2,4-D CCL R2 Basic + 10 g/l glucose, 100 mM acetosyringone, pH 5.2 liquid co-culture medium CCS CCL + 7 g/l agarose R2S R2 Basic + 30 g/l sucrose, 50 mg/l hygromycin, 400 mg/l cefotaxime, 100 mg/l vancomycine, 7 g/l agarose, pH 6.0 NBS NB Basic + 2.5 mg/l 2,4-D, 500 mg/l proline, 500 mg/l glutamine, 300 mg/l casein hydrolysate, 50 mg/l hygromycin,400 mg/l cefotaxime, 100 mg/l vancomycine,万古霉素 7 g/l agarose, pH 6.0 PRAG NB Basic + 2 mg/l BAP, 1 mg/l NAA, 5 mg/l ABA, 500 mg/l proline, 500 mg/l glutamine, 300 mg/l casein hydrolysate,50 mg/l hygromycin, 100 mg/l cefotaxime, 100 mg/l vancomycine, 7 g/l agarose, pH 5.8预分化 RN NB Basic + 3 mg/l benzylaminopurine, 0.5 mg/l a-naphthaleneacetic acid, 30 g/l sucrose, 50 mg/l hygromycina,4.5 g/l Phytagel, pH 5.8 P MS major and minor salts, vitamins and iron source (Murashige and Skoog 1962), 50 g/l sucrose, 2.6 g/l Phytagel, pH 5.8 Theor Appl Genet (2003) 106:1396–1408
Rice (Oryza sativa L. cv. Nipponbare) was used in this study. Mature rice seeds were husked, sterilized with 70% ethanol for 5 min and 1% NaClO for 30 min. The seeds were washed with sterilized water and allowed to germinate on an agar plate of Murashige and Skoog (MS) medium [17] supplemented with 2 mg·L−1 2,4-dichlorophenoxyacetic acid (2,4-D) and incubated at 25 °C in darkness. Cells were allowed to proliferate for ≈ 1 month and were subcultured in MS medium supplemented with 1 mg·L–1 2,4-D for rice cultured suspension cells. The medium was changed once every 2 weeks during subculturing. To induce regeneration, the rice cultured suspension cells were spread on agar medium containing 0.01 mg·L−1 naphthaleneacetic acid, 0.1 mg·L−1 6-benzyladenine, 4% sucrose, 1% agarose and incubated at 25 °C under continuous light conditions. European Journal of Biochemistry Volume 267 Issue 3 Page 737-745, February 2000
Rice (Oryza sativa L. cv. Nipponbare) was used in this study. To induce regeneration, the rice cultured suspension cells were spread on agar medium containing 0.01 mg/L naphthaleneacetic acid, 0.1 mg/L 6-benzyladenine, 4% sucrose, 1% agarose and incubated at 25 8C under continuous light conditions. Eur. J. Biochem. 267, 737±745 (2000)
In Vitro Binding of Agrobacterium tumefaciens to Plant Cells from Suspension Culture. Plant Physiol. (1979) 63, 382-387 Datura innoxia cells毛曼陀罗 Binding kinetics showed that adherence of bacteria to Datura cells increased gradually during the first 60 minutes and attained a maximum level within 120 minutes of incubation. Maximum binding occurred at pH 6.0. The presence of Ca2+ and Mg2e reduced binding slightly and EDTA had little effect at concentrations of 0.1 to 10 millimolar.
Stable Transformation of Arabidopsis Cell Culture Agrobacteria carrying the pBlN plasmid were grown in YEB medium (0.5% [w/v]) beef extract, 0.5% [w/v] peptone, 0.1 % [w/v] yeast extract, 0.5% [w/v] sucrose, and 10 mM MgSO,, pH 7.2) supplemented with 250 mg/L streptomycin (Duchefa) and 50 mg/L kanamycin (Duchefa) at 28°C to an OD,oo of 1.5. Bacteria were collected by centrifugation (10 min at 4000 rpm) and resuspended in the same amount of cell culture medium. Four days after transfer to fresh medium, Arabidopsis cells (3 g fresh weight per 10 mL of medium) were incubated with 5 mL of an agrobacteria suspension in a Petri dish at 25°C in the dark with gentle agitation (130 rpm). After 48 hr, the cells were loaded onto a nylon net and washed with excess of cell culture medium to remove most of the bacteria. Remaining cells were resuspended in 40 mL of culture media, vortexed vigorously for 20 sec, collected by a short centrifugation (1 min at 600g), and resuspended in fresh cell culture media. This procedure was repeated three times using 250 mg/L timenten (ticarcillin plus clavulanic acid, 151; Smith-Kline Beecham AG, Thorishaus, Switzerland) in the last solution. This antibiotic combination was highly effective in removing the remaining bacteria but had no effect on plant cell growth. Cells were plated on plant cell growth medium with 0.6% Gelrite (Merck), 250 mg/L timenten, and the indicated concentrations of kanamycin (see Results). The dishes were stored at 25°C in the dark until calli formation was observed, usually after 2 or 3 weeks. The Plant Cell, Vol. 9, 2171-2181, December 1997
路铁刚Plant ScienceVolume 167, Issue 2, August 2004, Pages 281-288 T. Murashige and F. Skoog, A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plant15 (1962), pp. 473–479. 21. L. Li, R. Qu, A. de Kochko, C. Fauquet and R.N. Beachy, An improved rice transformation system using the biolistic method. Plant Cell Rep.12 (1993), pp. 250–255. View Record in Scopus | Cited By in Scopus (96) 22. C.C. Chu, C.C. Wang, C.S. Sun, C. Hsu, K.C. Yin, C.Y. Chu and F.Y. Bi, Establishment of an efficient medium for anther culture of rice through comparative experiments on the nitrogen sources. Scientia Sinica5 (1975), pp. 659–668. 23. O.L. Gamborg, R.A. Miller and K. Ojima, Nutrient requirement suspension cultures of soybean root cells. Exp. Cell Res.50 (1968), pp. 151–158. Abstract | Article | PDF (629 K) | View Record in Scopus | Cited By in Scopus (2441)
