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1.
Induction of bulbing of tulip shoots in vitro 总被引：2，自引：0，他引：2
Bulbing has been induced in adventitious shoots from floral stem explants of Tulipa ‘Merry Widow’. Incubation of 1-mm thick explants at 20°C on a medium containing 1 mg l−1 NAA and BAP for 14–18 weeks, followed by 4°C for 8 weeks, produced a consistent bulbing response in shoots after transfer back to 20°C. Bulbing was further enhanced by transfer to 25°C and by raising the concentration of sucrose in the medium. Microscopy indicated the presence of developing meristematic centres in shoots 12 weeks of age. Shoots over 16 weeks of age containing meristematic centres gave a variable bulbing response with applied gibberellins and cold incubation, depending on whether gibberellins were supplied continuously in the medium or via a brief soak in sterile gibberellin solutions before sub-culturing. A GA3 “soak” of 1.0 mg l−1 was optimum for bulb production. The possible mechanisms of cold and gibberellin effects are discussed. 相似文献
2.
Shoots have been produced from onion capitulum tissue plated onto agar-solidified media. Up to 98 shoots have been produced per capitulum of cultivar ‘Produre’, the optimal number when explants were cultured upon BDS based medium containing 1.0 mg l−1 BA. The shoots produced in culture were categorised according to their most obvious morphological affinities, and 3 of these categories appeared to be derived by modification of existing floral parts. Shoots could be produced from flower-heads until the meiotic stage in pollen formation of their buds. Over 50% of the shoots produced in each experiment could be regenerated to whole plants, and at maturity they showed no apparent morphological or cytological variation. The value of this method of shoot induction for propagation and breeding purposes, and its usefulness as a site for mutagenic treatments are discussed. 相似文献
3.
A high frequency of sprouting (80.0%) and shoot differentiation was observed in the primary cultures of nodal explants of Morus indica L. cultivar M-5 on MS medium supplemented with 2,4-D (0.3 mg/l). In vitro proliferated shoots were multiplied rapidly by culture of shoot tips on MS medium with BAP (0.5 and 1.0 mg/l) which produced the greatest multiple shoot formation. Multiplication was also achieved by culture of shoot tips on MS medium with BAP (4.0 mg/l) and GA3 (0.05 mg/l) which facilitated the elongation of shoots followed by sprouting of axillary buds of in vitro grown shoots. A high frequency of rooting (86.7%) with development of healthy roots was observed from shoots cultured on medium with 2,4-D (1.0 mg/l). Plants with well developed roots were transferred to soil with a survival frequency of 80%. 相似文献
4.
Explants of Grevillea rosmarinifolia A. Cunn. and Grevillea×semperflorens F.E. Brigs ex Mullig., obtained from vegetative stem segments, were grown on a modified MS medium, which was supplemented with different contents of cytokinins (BA or K) to evaluate optimal conditions for bud proliferation. Auxins (NAA or IBA) were tested to evaluate rooting.
The multiplication rate was often higher in G. rosmarinifolia than in G.×semperflorens. Explant activity varied significantly depending on the cytokinin type and its concentration. The addition of cytokinins to the culture medium often promoted an increase in the number of shoots produced by each propagule, but at the highest BA concentration, shoot differentiation was inhibited in Grevillea×semperflorens. Only the higher concentrations studied (5–10 mg/l) produced better results with K, whereas BA was more effective at 1–2 mg/l. Rooting efficiency of the young shoots was lower in G. rosmarinifolia than in G.×semperflorens. IBA promoted root development in both species and was more effective at the highest concentration (1 mg/l). NAA gave better results at low concentrations (0.2 mg/l) in G. rosmarinifolia, while it had slight or negative effect on rooting of G.×semperflorens. 相似文献
5.
Shoot growth and leaf surface area were recorded during three seasons subsequent to transplanting five deciduous street tree species in Norway: Acer platanoides L., Aesculus hippocastanum L., Prunus avium L., Sorbus aucuparia L. and Tilia x europaea L. ‘Pallida’. Trees were transplanted at four dates, early and late autumn (August 25th and October 23rd), and early and late spring (April 23rd and May 5th–19th, depending on species), with two root ball diameters (3 and 5 times the stem circumference). Control trees were not transplanted. Shoot growth in all species, except S. aucuparia, was reduced by 38 to 86% of control trees and leaf surface area by 13 to 61% in the first season after transplanting. In A. platanoides and A. hippocastanum shoot growth was also reduced in the second season (71 and 81% respectively). All species except A. hippocastanum resumed pre-transplant growth in the third season. Early autumn transplanting was least favourable in all the species, resulting in delayed establishment as well as reduced shoot growth and leaf surface area. Early spring transplanting was found favorable for A. platanoides and P. avium, but unfavorable for S. aucuparia. The experiment confirmed that the larger root balls are preferred over smaller root balls. 相似文献
6.
Anthers of the LiliumבEnchantment’, excised at the uninucleate microspore stage, were cultured on MS media containing 6% sucrose with auxin and cytokinin. When anthers were cultured on the medium with 2 mg l−1 picloram and zeatin, 12–86% of them formed nodular calli. Anthers excised from greenhouse- and field-grown plants showed different responses: anthers of greenhouse-grown plants had a significantly higher capability to form callus and regenerate bulblets than those of field-grown plants. In anthers from greenhouse-grown plants, bulblet formation was dependent on the time at which anthers were excised from donor plants: anthers collected from early forced mother-plants had a higher capability of forming bulblet than others. All regenerated plantlets were diploid, which was substantiated by histological observation showing that the anther-derived calli originated from anther wall tissues. Virus tests by ELISA were made for 49 plantlets selected randomly at transplanting: 20 plantlets (41%) were virus-free, and the rest showed positive reactions for lily symptomless virus, cucumber mosaic virus and/or tulip breaking virus. 相似文献
7.
The aim of the present study was to develop a protocol for in vitro propagation of a grape rootstock, deGrasset, characterized by high tolerance to drought and salinity. Four medium compositions, MS, MS with 1/2 nitrates (MS-1), B5 and WPM, were tested for shoot growth from nodal explants and MS-1 medium produced significantly higher rate of shoot proliferation. MS-1 medium supplemented with 2.0 mg/L BAP was found to be optimum for culture establishment. The first subculturing on the same medium resulted in the production of 4–6, mostly short, hyperhydrated shoots per explant. For subsequent subcultures, a reduced concentration of BAP (1.0 mg/L) was used to prevent hyperhydricity, and that resulted in distinct individual shoot elongation. Three plant growth regulators, BAP, ZEA and TDZ, were tested for further shoot proliferation and BAP at 1.0 mg/L added to MS-1 medium displayed the highest proliferation rate (4.75 new explants per explant inoculated, in 6 weeks). For in vitro rooting of shoots, IAA at 0.2 mg/L was found to be optimum to produce highest response (84%) and an average number of 2.03 roots per shoot whereas use of IBA or NAA resulted in rooting with high frequency of callus formation. The acclimatized plantlets were established in soil under net house conditions with 87% success. 相似文献
8.
Methods to regenerate whole plants from mature leaf explants of Pelargonium rapaceum (L.) L’Hérit were established. To optimize shoot induction, leaf explants were cultured on media containing different types and combinations of plant growth regulators. Growth was initiated within 17–24 days culture, and included callus formation, and root or shoot organogenesis ranging from 20 to 100% regeneration. Shoots were induced only when explants were cultivated on MS medium containing a combination of NAA and kinetin, NAA and BAP, IAA and Kinetin, or IAA and BAP. On media containing NAA and BAP, dark incubation was critical for efficient direct shoot regeneration from explants. Direct shoot formation and the highest number of shoots per explant (17.6) were obtained from leaf explants cultured in the dark for 30 days on MS medium containing 0.1 mg l−1 NAA and 0.1 mg l−1 BAP. Shoots cultured on MS medium containing 0.1 mg l−1 NAA formed tuberous roots with microtubers within 42 days. Healthy regenerated plants were acclimated and transferred to a greenhouse. 相似文献
9.
Hardwood stem cuttings of Damask rose (Rosa damascena Mill.) were dipped in H2SO4 or NaOH prior to application of 0, 1000, 2000 or 3000 mg l−1 indolebutyric acid (IBA) or naphthaleneacetic acid (NAA). Acid pretreatment significantly increased root number, root length and root dry weight per cutting, but did not affect rooting-percentage. Rooting was significantly enhanced by auxin pretreatment, and NAA was superior in increasing root length and root fresh weight; 2000 mg l−1 of auxin was the most suitable concentration for promotion of rooting under the conditions of the study. 相似文献
10.
Diploid callus cells arose from the hypocotyl region of plantlets differentiated by anther culture of Calamondin (Citrus madurensis Lour.). The callus grew vigorously on Murashige and Tucker's medium containing 10 mg l−1 benzyladenine, and differentiated embryoids on a medium with 5% lactose and no plant growth regulators. This embryogenic potential was transferred to protoplasts which regenerated plantlets.
Preculture of callus in liquid medium containing 5% lactose, for 4–7 days prior to protoplast isolation, effected a high yield of protoplasts. Plating efficiency was increased in a medium solidified with agarose and/or layered with liquid medium. 相似文献
11.
The response to IBA treatments in different planting seasons of four plum cultivars, as measured by rooting and field establishment, was investigated during 1986 and 1987. Among the four cultivars, ‘Santa Rosa’ gave the largest rooting percentage, number of primary and secondary roots per cutting, length and diameter of roots and field survival. The European cultivars ‘Greengage’ and ‘Early Transparent Gage’ showed poor rooting and field establishment. The cuttings planted during summer under mist gave better rooting and field establishment than dormant season- or autumn-planted cuttings. Similarly, IBA treatment of cuttings with 2000 mg l−1 during summer and 3000 mg l−1 during dormant and autumn seasons gave the largest rooting and survival percentages, high numbers of primary and secondary roots per cutting, and greater length and diameter of primary roots. 相似文献
12.
Viable shoot cultures and weaned plants were obtained from cultured apical meristems with 10 Buddleia cultivars giving viabilities of 32–72%. The number of shoots produced, the micropropagation rate and the root number produced in vitro was higher in meristem derived shoots compared to those derived from shoot-tips. The subsequent growth rate of meristem derived plants, in the greenhouse, was also greater. The number of roots produced by conventional cuttings collected from meristem derived plants was significantly higher than in cuttings which were collected from plants derived from shoot-tips or from the original stock plants.Endogenous bacteria were not detected in either shoot cultures derived from meristems or in 10-week-old weaned plants derived from meristems whereas those derived from shoot-tips showed the presence of endogenous bacteria when sterilized explants were cultured on nutrient agar or on tryptic soy broth.Factors affecting adventitious bud and shoot production in leaf and internode explants was determined for ‘Lochinch’, ‘Border Beauty’, ‘Ile de France’ and ‘Pink Delight’ using meristem derived shoot cultures. Adventitious shoots appeared after 4 weeks of culture, in both types of explant when cultured on MS supplemented with 0.5–5.0 μM TDZ. The highest percentage regeneration was achieved from bisected internode explants cultured on 0.5 μM TDZ, with 93–100% regeneration among the cultivars whereas BA was less effective. The best response was obtained using 5.0 μM TDZ which gave over 10–11 shoots per explant in all bisected explants for all cultivars. 相似文献
13.
A protocol was developed for organogenesis from immature leaflet explants derived from mature seeds of peanut. Immature leaflets pre-incubated on MS medium supplemented with 13.32 μM BAP + 4.95 μM NAA for 7 days, turned green and enlarged. The enlarged green leaflets produced multiple shoot buds after 1–2 cycles of sub-culture on MS medium supplemented with 13.32 μM BAP. Three cycles of shoot buds on the elongation medium (13.32 μM BAP) produced 6.17 ± 0.47 elongated shoots per explant. The shoot bud formation was genotype independent. All elongated shoots rooted on the medium containing 4.95 μM NAA. The complete protocol gave efficient (>81%) direct organogenesis, leading to the development of plantlets within 4 months. 相似文献
14.
The response of 3-year-old grapevines (Vitis vinifera L. cultivar ‘Thompson Seedless’) to furrow and drip irrigation was quantified in terms of water status, growth, and water use efficiency (WUE). Drip irrigation was applied daily according to best estimates of vineyard evapotranspiration while furrow irrigations were applied when 50% of the plant available soilwater content had been depleted. Drip and furrow irrigated vines showed similar water status (midday leaf water potential, Ψ1) and shoot growth patterns throughout the season. Dry weight partitioning was not significantly different between treatments but root mass was somewhat larger for the furrow than drip irrigated vines. Nitrogen concentrations of the fruit and roots were significantly (P < 0.05) less for the drip irrigated vines when compared with the furrow treatment. Similar WUE (kg water kg−1 fresh fruit wt.) were obtained for both treatments indicating that furrow irrigation was as efficient as drip irrigation under the conditions of this study. The data indicate that drip irrigation may increase the potential for control of vine growth by making vines more dependent on irrigation and N fertilization than furrow irrigation. 相似文献
15.
Multiple shoot formation from the plumular apices excised from mature embryos of cowpea cv. Akkiz was obtained after pulse treatment with 10 mg/l BAP for 5 days followed by culture on MS medium containing 0.25, 0.50, 0.75 and 1.00, 1.25 mg/l BAP – with or without 0.10 mg/l NAA. Callus induction and shoot regeneration was recorded on all cultures containing BAP with or without NAA. However, inclusion of 0.1 mg/l NAA had positive effect on callus diameter and shoot length. Maximum mean number of 7.11 shoots per explant were obtained on MS medium containing 1.00 mg/l BAP. Longer shoots were recorded on MS medium containing various concentration of BAP+ 0.1 mg/l NAA compared to those containing various concentrations of BAP singly. All shoots cultured on MS medium containing 1 mg/l BAP were rooted on MS medium containing 0.50 mg/l IBA. Rooted plants were acclimatized at room temprature in soil contained in pots. All plants flowered and set seeds in the greenhouse after 3 months. 相似文献
16.
BAP、IBA和GA_3对梨砧木BP10030茎尖外殖体的成活率没有明显影响,但0.1mg·1~(-1)GA_3明显促进外殖体的初期生长。外殖体建立阶段以1mg·1~(-1)BAP+0.1mg·1~(-1)IBA+0.1mg·1~(-1)GA_3的处理为宜。BAP与IBA明显影响茎的增殖。茎数量随BAP浓度(1—4mg·1~(-1))的增加而增加,但茎长度明显下降。在BAP存在条件下,增加0.1mg·1~(-1)IBA对茎数量没有明显影响,但显著促进茎增长。高浓度的BAP(4rug·1~(-1))明显导致玻璃苗产生,增施0.1mg·1~(-1)IBA在一定程度上可抑制玻璃苗形成。茎增殖阶段BAP浓度明显影响试管苗生根,其生根率、平均根数与限长度随BAP浓度的增加(1—4rug·1~(-1))而降低。2mg·1~(-1)BAP+0.1mg·1~(-1)IBA为茎增殖阶段的最适浓度。生根阶段2mg·1~(-1)IBA显著提高生根率、根数与根长度,同时也有利于试管苗移栽,促进试管苗初期生长。 相似文献
17.
M. Barghchi P. G. Alderson 《The Journal of Horticultural Science and Biotechnology》2013,88(3):435-445
Proliferating shoot cultures were established from shoot tips and nodal bud segments excised from seedlings germinated aseptically and cultured on Murashige and Skoog medium supplemented with BAP plus NAA. Shoot tip necrosis occurred in some cultures. Cultured shoots were rooted in vitro using MS medium (half strength macronutrients) containing IBA for root initiation, followed by subculture onto hormone-free medium for root development. Rooted shoots were readily established in peat-based compost. 相似文献
18.
A novel micropropagation protocol was established for Capsicum frutescens L. cv. ‘Uchithi’, a pungent chilli cultivar, through induction of axillary shoot proliferation of in vitro raised plantlets by decapitation and using the axillary shoots as explants for multiple shoot bud induction. About 2–6 axillary shoots were induced within 2 weeks when 4-week-old in vitro raised plantlets were decapitated. The axillary shoot-tip explants produced multiple shoot buds when cultured on Murashige and Skoog's (MS) medium containing 8.8–44.4 μM 6-benzylaminopurine (BAP) or 9.3–46.7 μM kinetin alone or 8.8–44.4 μM BAP with 4.6 μM kinetin or 5.7 and 28.5 μM indole-3-acetic acid (IAA). Maximum number of shoots (5.6) were induced on medium containing 22.2 μM BAP in combination with 4.65 μM kinetin. The separated shoots rooted and elongated on medium containing 2.8 μM IAA or 2.4–4.9 μM indole-3-butyric acid (IBA). Rooted plantlets were successfully established in the soil. Efficient mass multiplication of this important food crop was achieved. 相似文献
19.
A protocol was developed for direct shoot and plantlet regeneration from in vitro regenerated leaf explants of male Pistacia vera L. cv. ‘Atl?’. Leaves excised from axenic shoot cultures of pistachio were used to induce organogenesis on a Murashige and Skoog (MS) medium with Gamborg vitamins supplemented with combinations of different concentrations of BAP and IAA. The highest adventitious shoot regeneration in 35% of the explants, with the number of shoots ranging from 2 to 3 per explant, occurred in the explants cultured during the establishment phase in the medium with 1 mg l−1 IAA and 2 mg l−1 BAP. For shoot multiplication, the highest number of new microshoot/explants (5.76) was obtained in a culture medium supplemented with 1 mg l−1 BAP, but it was not significantly different from the number obtained at 2 mg l−1 BAP. A high rooting frequency (84%) for microshoots was recorded on a medium supplemented with 2 mg l−1 IBA. In vitro rooted plantlets were transferred to pots filled with a mixture of soil, sand and peat (1:1:1). They were weaned in a growth room and finally moved to a greenhouse. This protocol could be utilized for in vitro clonal propagation of this economically important plant. 相似文献
20.
提高白菜离体培养植株再生频率的研究 总被引：21，自引：0，他引：21
选用 7个白菜类蔬菜栽培品种和 1个杂交亲本进行离体培养植株再生试验 ,筛选出最佳培养基配方为 1/2倍NH 4 浓度的MS培养基附加BAP 2mg/L、NAA 0 .4 5mg/L和AgNO37.5mg/L ,大幅度提高了植株的再生频率 ,高达 84 .8% ,大大缩短成苗周期 ;子叶—子叶柄接种后 ,最早的仅需 6d即可分化出不定芽 ,从接种到再生苗的移栽最快的仅需 4 0d ,平均一批约需 50d ,达到了高频快速的要求 ;该培养基对白菜类蔬菜的不同品种有着较广的适应性。对不定芽的发生过程进行组织学观察表明 ,在本试验条件下 ,白菜离体培养植株再生方式为外植体直接出芽。再生苗生根后移栽的成活率可达 95%以上。 相似文献