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1.
Plantlets produced from meristem culture of six advanced cultivars (Agria, Advanced clone 397007-9, Marfona, Sante, Satina and Ceaser) propagated by single node cuttings arranged in a RCBD base factorial design with ten replications. Factor A was plantlets produced from meristem culture of advanced cultivars and factor B was seven treatments (four concentrations of potassium humate as 0.5, 1, 1.5 and 2 mL, one concentrations of kadostim as 1 mL, compound concentration of potassium humate and kadostim as 1 ml L(-1) MS media culture and without them as control). Produced plantlets transplanted into the planting beds of Pitmass (Biolan) with punce (1:1 v/v) in the greenhouse. Some of traits measured such as average weight and number of mini-tuber per plant after harvesting. Results of analysis of variances showed the significant differences between effects of kadostim and potassium humate on advanced cultivars, for transplantation into the greenhouse, stem solidity and rhizo-genesis characters. So transplantation days decreased from 30 to 13 days in MS media culture with compound of potassium humate + kadostim by concentration of 1 ml L(-1) MS media culture, also decreased to 15 days in MS media culture with kadostim by concentration of 1 ml L(-1) MS media culture and also decreased to 22 days in MS culture with potassium humate by concentration of 1 and 1.5 ml L(-1) MS media culture and plantlets had the highest stem solidity and better rhizo-genesis in all of treatments. Agria, Sante and Marfona transplanted earlier and Ceaser transplanted later than others to the greenhouse. Compound concentration of potassium humate and kadostim 1 ml L(-1) MS media culture had the highest number of mini-tubers per plant and potassium humate 0.5 ml L(-1) MS and Kadostim 1 ml L(-1) MS had the highest mini-tuber weight per plant and average of mini-tuber weight per plant. Agria had the highest number and average of weight of mini-tubers per plant. Potassium humate 0.5 ml L(-1) MS in satina, kadostim 1 ml L(-1) MS in marfona and potassium humate + kadostim 1 ml L(-1) MS in Agria had the highest number of mini-tubers per plant. Increasing rate of weight and number of mini-tubers per plant with potassium humate and kadostim in all of advanced cultivars were more than control.  相似文献   

2.
Summary Potato shoot tips excised from 2-week-old in vitro nodal cuttings were cryopreserved after encapsulation in alginate beads. Encapsulated shoot tips were first precultured in sucroseenriched media, dried over silica gel, and rapidly cooled in liquid nitrogen. After slow rewarming in air at room temperature, alginate beads were transferred to solid culture medium for shoot tip recovery. After cooling in liquid nitrogen, shoot yield depended on preculture duration, sucrose concentration and water content of beads. Survival rates above 60% were obtained for each cultivar tested.  相似文献   

3.
Microtuber size, media growth regulators, incubation period, as well as bud maturity and endogenous abscisic acid content of microtubers were evaluated for their effects on length of dormant period of Kennebec, Russet Burbank and Superior microtubers. The dormant period of microtubers was found to be cultivar-specific and a significant correlation was observed betweenin vitro andin vivo dormant periods. Smaller microtubers (≤250 mg) had longer dormant periods than did those greater than 250 mg. Dormant periods were unaffected by addition of coumarin or 2-(chloroethyl)-trimethylammoniumchloride and 6-benzylaminopurine to the culture media or incubation period (28 and 56 days). Developmental age had no effect on individual buds ability to break dormancy and elongate. A positive correlation was observed between tissue levels of abscisic acid and microtuber dormant periods.  相似文献   

4.
The effect of 2,4-D on tuberization, yield and the starch content of potato tubers produced on stem segments was examined. Potato stem segments were cultured in nutrient agar containing 2,4-D concentrations ranging from 10?7 M to 2 × 10?3 M. The stem segments were incubated in the dark at 25° C and examined after 15 days. The degree of tuberization on stem segments cultured in media containing 10?7 M and 10?6 M 2,4-D was higher than on the control stem segments. Mainly long stolons were observed on stem segments cultured in media containing 10?4 M and 2 × 10?3 M 2,4-D. The percent starch (dry wt. basis) in stolons was higher than that in tubers. However, the total starch content of tubers per stem segment cultured in media containing 10?7 M and 10?6 M 2,4-D was significantly higher than that of stolons obtained from stem segments cultured in media containing higher concentrations of 2,4-D. The total starch content of tubers, except those produced on stem segments cultured in media containing 10?7 M 2,4-D, decreased steadily with increasing concentration of 2,4-D in the culture media.  相似文献   

5.
Summary Tests were made of the influence of selective and nonselective culture media on the rate of production of aluminium tolerant regenerant clones. Regenerants died when selective medium containg Al was continuously applied in tolerance tests. The production of aluminium tolerant clones was dependent on alternating selective and nonselective media. Tests using a medium containing 6 mmol al resulted in 50% growth as compared to control plants. Regenerants showed no growth when a medium with 10 mmol Al was applied. No constant tolerance was obtained when only a nonselective medium was used for regneration.  相似文献   

6.
Plants from 6 potato cultivars uniformly infected with potato virus X (PVX) were exposed to darkness and gradual temperature increases from 37 to 40 C, during a two-week period. This was followed by shoot tip culture to obtain virus free individuals. The procedure was effective in obtaining PVX-free propagation material from 4 of the 6 varieties. Differences were observed in the response of the cultivars to the heat and to thein vitro culture. At least one plant from every cultivar showed repeated negative serological reaction against PVX after the tissue culture regeneration, except Atzimba and Montsama. Tollocan and Murca were the most resistant to heat, developed better duringin vitro culture and resulted in the largest number of PVX-negative plants. Rosita was intermediate, and Juanita did not adapt to heat stress.  相似文献   

7.
PVX infected plantlets from two potato cultivars grownin vitro with 0.3, 3, 30 or 300 ppm kinetin were exposed to temperatures of 28 or 35 C. After 3 wk, axillary buds were isolated and grown aseptically in organogenic media, followed by PVX testing by ELISA. The serological test was also run on whole plantlets at the end of the kinetin-temperature exposure. No donor plants exposed to 28 C nor the plantlets derived from their buds gave an ELISA (-) reaction, regardless of the kinetin content of the media or that of the cultivar. At 35 C the virus was suppressed to undetectable levels in several whole plantlets. In the cultivar Alpha, 2 out of 6 resulting plantlets after isolation of buds were virus-free in the presence of 3.0 mg/1 kinetin during the treatments. From Atzimba, about 15–40% of the regenerated plants were ELISA (-), without any relationship to the cytokinin content in the media. Heat had a stronger influence on virus elimination than kinetin and the results varied with the cultivar.  相似文献   

8.
Summary Mass tuberisation was obtained on plantlets growing from nodal potato cuttings cultured in vitro on Murashige-Skoog (MS) medium under continuous light of 5000 lux at 24–25°C. Tuber formation was stimulated by transferring the plantlets to MS or White-Nitsch-Morel (WhNM) liquid or solid media supplemented with 8% sucrose, 2 mg 1−1 benzyladenine (BAP), 2 mg 1−1 naphthalenacetic acid (NAA) and/or 100 mg 1−1 (2-chloroethyl) trimethylammonium chloride (CCC). Liquid media invariably induced heavier minitubers (390–790 mg each). The process to tuberisation took only two months. Minitubers always produced normal growing plants after dormancy break.  相似文献   

9.
Growth, morphogenesis, and tuberization of potato tissuesin vitro are affected by light. Measurements of the various aspects of light that control development and growth of potato are outlined. Physical parameters like light sources, delivery of the light source, and the degradation of culture media by light are discussed. Irradiance, photoautotrophic growthin vitro, spectral wavelength, and photoperiod modify the responses of potato tissues in culture. Acclimatization of tissue culture plantlets, vegetative growth, and the production, quality, and dormancy of microtubers are modified by light. New light sources such as light-emitting diode (LED) lamps are becoming available forin vitro research and for micropropagation of potato. Pulsed or chopper light has the potential to save energy costs. Light effects on potato protoplasts, anther culture, virus eradication, andin vitro conservation are discussed. Potential new research areas are the effect of the spectral quality of light on regeneration of shoots and somatic embryosin vitro, end-of-day red and far-red light treatments, axillary shoot formation in cultured plantlets, and the use of LEDs. The influence of monochromatic spectral filters on growth and development of potatoes in tissue culture could potentially lead to improvements in productivity. The relationship between daily quantum light integral and photoperiod and their effects on growth and morphogenesis of the potato will provide some useful areas of research.  相似文献   

10.
Growth of 6 potato virus S (PVS)-infected potato clones in tissue culture in temperature regimes alternating between supraoptimal (40°C–45°C) and optimal (25°C) temperatures was compared to incubation of etiolated shoots at constant moderate temperatures (37°C) to obtain virus-free plants by shoot tip culture. Both procedures were effective in obtaining PVS-free propagative material. Virus-free plants were obtained in 5 of 6 clones by the alternating temperatures procedure and in 4 of the 6 clones by the constant 37°C incubation prior to shoot tip isolation. Heat tolerance, virus inactivation, and development of pathogen-free buds from the heat-treated plants depended upon the potato cultivar and the type of culture media in which the tips grew, but these characteristics did not coincide in any clone. The variety Chieftain was the least tolerant to the high temperatures and no virus-free individuals were recovered. White Rose was the most heat resistant, but Russet Burbank resulted with the highest percentage of PVS-free plants. The virus was eliminated from the variety Kennebec only by the alternating temperature treatments. Exposing potato plantlets in the alternating temperature regimes prior to isolation and regeneration of shoot tips was slightly better than the traditional method of incubation of plants at constant moderate temperatures that the plant will withstand and offers a new option in freeing plants of more tenacious viruses.  相似文献   

11.
Microtubers were produced from single nodein vitro cuttings on 43 clonal potato cultivars and selections and two wild species. The microtuberforming cultures were exposed to three temperature regimes over a period of 21 months. At 10 C, cultures continued to produce microtubers after 21 months without subculture or supplementation of the media. Cultures of these single node axillary buds produced an average of 3.3 microtubers each after 21 months. This technique should be very useful in long-term storage of potato germplasm.  相似文献   

12.
Successful isolation of haploids (2n=2x=24) from 4x(2EBN) Mexican species was achieved by using Modified Wenzel (MW) and Nitsch and Nitsch (NN) media for anther culture. Both media, MW and NN, gave consistent regeneration of plantlets from 4x(2EBN) Mexican species, and responses to the media were both species and accession (PI) specific. Plantlets regenerated directly from microspores, by-passing the callus cycle, were mostly haploid (2n=2x=24). Haploid plants appeared smaller and weaker than their parents with a drastic reduction in both male and female fertility. Abnormalities observed during meiosis and the lack of success in crossing confirmed the effect of the meiotic irregularities observed in the haploids. A total of 290 seeds was obtained from the 4x × 2x crosses of 4x Mexican species with irradiated pollen of 2xS. cardiophyllum and 2xS. chancayense; however, no haploid (2n=2x=24) plants resulted. Extraction of haploids from colchicinedoubled 4x (2EBN) or natural 6x(4EBN) Mexican species using a Phureja pollinator was examined to provide clues to the potential of using 2x (1EBN) pollinators for haploid induction in 4x(2EBN) × 2x(1EBN) crosses.  相似文献   

13.
Li J  Bardy J  Yap LY  Chen A  Nurcombe V  Cool SM  Oh SK  Birch WR 《Biointerphases》2010,5(3):FA132-FA142
The standard method for culturing human embryonic stem cells (hESC) uses supporting feeder layers of cells or an undefined substrate, Matrigel(?), which is a basement membrane extracted from murine sarcoma. For stem cell therapeutic applications, a superior alternative would be a defined, artificial surface that is based on immobilized human plasma vitronectin (VN), which is an adhesion-mediating protein. Therefore, VN adsorbed to diverse polymer surfaces was explored for the continuous propagation of hESC. Cells propagated on VN-coated tissue culture polystyrene (TCPS) are karyotypically normal after >10 passages of continuous culture, and are able to differentiate into embryoid bodies containing all three germ layers. Expansion rates and pluripotent marker expression verified that a minimal VN surface density threshold is required on TCPS. Further exploration of adsorbed VN was conducted on polymer substrates with different properties, ranging from hydrophilic to hydrophobic and including cationic and anionic polyelectrolyte coatings. Despite differing surface properties, these substrates adsorbed VN above the required surface density threshold and were capable of supporting hESC expansion for >10 passages. Correlating wettability of the VN-coated surfaces with the response of cultured hESC, higher cell expansion rates and OCT-4 expression levels were found for VN-coated TCPS, which exhibits a water contact angle close to 65°. Importantly, this simple, defined surface matches the performance of the benchmark Matrigel, which is a hydrogel with highly complex composition.  相似文献   

14.
Summary Incorporation of Virazole into potato explant and meristem culture media results in a higher percentage of virus-free progeny plants from virus-infected explant and meristem donor plants than are produced in tissue cultures in the absence of Virazole. Viruses eliminated, singly and as complexes, include potato viruses X, Y, S and M. The need for sensitive virus tests to distinguish between virus suppression and elimination is discussed and protein-A-linked immunoelectron microscopy is described and quantified for potato virus X.
Zusammenfassung In der vorliegenden und einer früheren Arbeit (Cassells & Long, 1980) zeigte Kultivierung von Explantaten auf einem Medium für Gewebekultur mit Virazole (Ribavirin) einen signifikanten Anstieg virusfreier Adventivschosse gegenüber der Kontrolle. Diese Adventivschosse wie auch Kartoffelpflanzen zweiter Generation verhielten sich auch gegenüber den empfindlichsten immunoelektronen-mikroskopischen Tests virusfrei. In Gegenwart von Virazol ergab auch Meristemkultur einen h?heren Anteil virusfreier Pflanzen als bei Fehlen dieser Verbindung. Die Kartoffelviren X, Y, M und S sowie Viruskomplexe konnten aus den Sorten May Queen, King Edward, Kerr's Pink und Golden Wonder eliminiert werden (Tabellen 2 und 3). Die Ergebnisse der Anwendung und der Quantifizierung der Protein A-gebundenen Immuno-Elektronenmikroskopie (PALIEM) werden ebenfalls dargestellt (Abb. 1).
Résumé Cette étude a montré, comme d'autres travaux préliminaires (Cassels & Long, 1980), que le fait de cultiver des boutures sur un milieu de culture de tissus contenant du virazole (ribavirine) permettait d'augmenter de fa?on significative le nombre de tiges aventices indemmes de virus par rapport au témoin. Ces tiges adventices, dans le cas de plants de deuxième génération, sont apparues indemmes de virus par l'analyse des tests les plus sensibles de microscopie immuno-électronique. En présence du virazole, la culture de méristèmes montre également un taux plus élevé de plants indemmes de virus que sans l'application de virazole. Les virus concernés sont les virus X, Y, M, S ainsi, que les complexes viraux, provenant des variétés May Queen, King Edward, Kerr's Pink et Golden Wonder (tableau 2 et 3). Sont également indiqués les résultats qualificatifs et quantitatifs de la microcopie immunoélectronique avec utilisation de la protéine A (PALIEM) (figure 1).
  相似文献   

15.
A two-year study was conducted to determine the effects of (1) jasmonic acid (JA) pre-treatment, (2) JA supplement in culture media, (3) cultivar (Amisk, Atlantic, Russet Burbank, Shepody, and Umatilla Russet), (4) light (0 h, 8 h), and (5) dormancy breaking treatment (Rindite, gibberellic acid) on greenhouse production of minitubers from microtubers andin vitro plantlets. The microtubers were produced under short day (8 h) light conditions and in darkness, from stock plantlets pre-treated with JA and untreated, and on tuberization media with or without JA.In vitro plantlets (the industry choice in nuclear seed potato production) of all five cultivars performed well, meeting the standard criteria for greenhouse production of minitubers. Production of minitubers from microtuber-derived plants of cvs Amisk, Russet Burbank, and Umatilla Russet was similar to that of plantlet-derived plants with regard to number of minitubers. Yields (weight), however, were lower than those from plantlets. Microtuber responses to JA varied with cultivar. Amisk produced the highest number of minitubers per plot from microtubers derived from JA pre-treated plantlets. Jasmonic acid-pretreated microtubers also gave significantly more minitubers in Russet Burbank and Umatilla Russet than the microtubers from other treatments. Shepody did not benefit from JA treatments and JA pre-treated Atlantic microtubers performed poorly, producing significantly lower yields of minitubers than other cultivars. Independently of cultivar, microtubers produced under 8-h photoperiod gave significantly higher yields of minitubers than microtubers produced in the dark. Dormancy release was the key factor influencing microtuber performance. Rindite proved to be a much more effective dormancy breaking treatment than gibberellin. JA conditioning of stock plants prior to tuberization is being proposed as a treatment in production of microtubers for greenhouse production of minitubers.  相似文献   

16.
Summary A bioassay technique is described for assessing growth-regulatory activities of volatile compounds in the potato. Excised potato shoot-tips (3 mm) were cultured aseptically in an aqueous medium in the dark at 25°C. After 7–12 days in culture, growth rates were measured by the increase in length of the treated shoot-tips. The addition of low concentrations (1 μmol/l) of gibberellic acid (GA3) and kinetin to the culture medium enhanced shoot growth. Known sprout suppressants inhibited growth of shoots in the bioassay. Of those tested 1,4-dimethylnaphthalene was found to be the most potent. The effectiveness of these known suppressants of sprout growth of whole potato tubers in inhibiting growth in the bioassay is presented as evidence of the validity of using this bioassay to detect unknown growth inhibitory volatile compounds evolved by stored potatoes.  相似文献   

17.
Ten isolates ofP. infestans collected from blighted potato fields in the U.S. and Canada during the years 1983–1989 were examined for mating type on lima bean, oatmeal, and rye grain media. Two of the ten isolates produced oospores in less than 15 days when cultured in the presence of known A1 mating types from the USA, Mexico, and Europe, indicating they are A2 mating types. When the two A2 isolates (one from Pennsylvania and one from Vancouver, B.C.) were cultured singly or with known A2 isolates, no oospores formed after 6 weeks of culture. Pathogenicity tests showed that both isolates produced typical late blight symptoms on potato foliage and stems, and there appeared to be no difference in virulence between these two A2 and the eight A1 isolates. Inoculations with a mixture of A1 + A2 sporangia also produced oospores in host tissues. This is the first report of the presence of the A2 mating type ofP. infestans in the U.S. and Canada.  相似文献   

18.
利用组织培养法保存野生苎麻资源的研究   总被引：3，自引：0，他引：3  
刘瑛 《中国麻业》2002,24(6):1-3
本试验研究了不同培养基、激素配比、外植体等主要因素对野生苎麻组织培养的影响,野生苎麻茎尖经过诱导不定芽、长苗分化培养和生根培养三个步骤,在相应的培养基上获得完整的试管植株,对野生苎麻资源利用组培法保存效果进行了探讨。  相似文献   

19.
Summary The seaweed concentrate ‘Kelpak’ is used commercially in the greenhouse and field to improve plant quality. ‘Kelpak’ was added to the in vitro culture medium of potato cv. ‘BP1’ and also applied as a leaf/soil drench immediately after transplanting. The addition of 0.25% seaweed concentrate to the medium improved plantlet quality and led to better establishment in the greenhouse. No beneficial effect of seaweed concentrate in the tissue culture medium was observed if a second cutting was part of the micropropagation process. Additional application of 0.5% seaweed concentrate in the greenhouse to plantlet cuttings derived from tissue culture was not beneficial.  相似文献   

20.
影响柑桔球形合子胚离体培养的若干因素   总被引：2，自引：0，他引：2  
通过对柑桔球形合子胚不同发育期的分离培养、不同基本培养基及附加物、蔗糖浓度等因素对柑桔合子胚离体培养影响的研,结果表明:授粉后50d是柑桔合子胚离体培养的最适时期;Whiet基本培养基比MS基本培养基更适于柑桔球形合子胚离体培养。适当增加培养基的渗透压和添加水解乳蛋白,特别是袖子胚乳 ,可提高幼胚的诱导率,有利于柑桔球形胚的发育。比较适宜的蔗糖浓度为10%一 15%,水解乳蛋白浓度为400mg/L  相似文献   

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