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大豆幼荚子叶原生质体培养及植株再生 总被引:9,自引:0,他引:9
本文研究了13个栽培大豆(Glycine max L.)品种原生质体培养的再生能力。从大豆幼荚子叶酶解游离原生质体,用Gellan Gum进行株状包埋,悬浮在含2,4-D 0.1-0.2mg/L,BA0.5-1.0mg/L的改良MS液体培养基中,原生质体培养3天后开始第一次分裂,以后持续分裂。供试基因型间的10天植板率差异显著,变幅为33-67%。30天内形成大量的 相似文献
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波缘烟草和枸杞属间原生质体融合再生杂种小植株 总被引:8,自引:0,他引:8
分别利用碘乙酰胺(IOA)和60Co-y射线失活波缘烟草和枸杞的原生质体,然后用改良PEG方法诱导融合。结果表明,异种融合频率为3%左右。利用超氧歧化酶对50个随机选取的细胞系进行同工酶分析发现,9个细胞系为可能的杂种细胞系。对其中4个分化出小植株的可能杂种细胞系进行叶片酯酶同工酶分析,证实它们均为体细胞杂种,杂种小植株在形态上兼有以亲特点且难以生根。细胞学观察指出,这4个杂种细胞系中的3个为可能 相似文献
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苎麻悬浮细胞原生质体培养再生植株 总被引:5,自引:0,他引:5
苎麻品种浏阳大叶绿的子叶在含有2,4-D0.5mg/L、KT0.5mg/L的MSB固体培养基上,形成愈伤组织。愈伤组织经3 ̄4次继代培养后作液体振荡培养,产生悬浮细胞系。从悬浮系分离的原生质体,只有以海藻酸钠包埋方式培养在KM8P培养基中,50天左右才能形成肉眼可见的小愈伤组织。该愈伤组织在附加2,4-D0.2mg/L、6-BA0.1mg/L的MSB生长培养基上增殖,然后转入附加6-BA2.0mg 相似文献
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不同激素条件下大豆原生质体培养和植株再生 总被引:2,自引:0,他引:2
以栽培大豆(Glycine max(L.) Merr.)南农86-21、南农86-4、南农73-935为材料,用K8/K8p基本培养基比较了不同原生质体密度和不同激素种类、水平对未成熟子叶原生质体培养的影响,发现它们的差异表现在植板率、产生愈伤组织的速度和频率、愈伤组织的颜色和结构等几方面。对低激素来源南农73-935的愈伤组织的速度和频率、愈伤组 相似文献
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Influence of genotype and culture medium on callus formation and plant regeneration from immature embryos of Triticum turgidum Desf. cultivars 总被引:2,自引:0,他引:2
Twelve durum wheat cultivars were evaluated for their response to in vitro tissue culture. Zygotic immature embryos were used to induce callus formation using four different Murashige and Skoog‐based media. Each contained 9.05 μM 2,4‐dichlorophenoxy acetic acid but differed in their carbon source (sucrose or maltose) and the presence of NaCl (0 mM or 40 mM). The influence of both genotype and medium on the type and percentage of callus produced was observed. Calli were either compact and frequently embryogenic, or soft and watery. Percentages ranged from 54 to 100%, depending upon genotype and induction medium. All calli were then plated on a regeneration medium containing 20 g/l sucrose, 2.68 μM 1‐naphthaleneacetic acid and 2.22 μ 6‐benzylaminopurine. The regeneration of plantlets was higher from compact than from soft calli, with a strong dependence on genotype and type of induction medium used. MSm induction medium (30 g/l maltose) and MS40s (30 g/l sucrose plus 40 mM NaCl) were best for inducing compact calli, and gave the highest proportion of regenerated plants. The in vitro response (number of total shoots from a compact callus/number of embryos plated) was higher for immature embryos of ‘Baztan’, ‘Bradano’ and ‘Don Pedro’. These cultivars are a good starting material for experiments involving transformation of calli from zygotic immature embryos. 相似文献
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重瓣长寿花叶片组织培养及植株再生的研究 总被引:1,自引:0,他引:1
摘要:以重瓣长寿花幼嫩叶片为试材,筛选各个培养阶段的培养基配方,研究重瓣长寿花的快速繁殖技术。结果表明: 0.1%升汞灭菌4min,外植体污染率为12.5%,死亡率2.5%,效果最佳;愈伤组织诱导培养基以MS+6-BA1.0 mg/L+NAA0.1~0.3 mg/L最佳,不定芽分化和增殖的最适培养基为MS+6-BA0.5 mg/L+NAA0.1 mg/L,生根培养基用1/2MS+NAA0.5mg/L最好,试管苗移栽成活率达99%。 相似文献
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Summary Experiments upon in vitro culture of immature durum wheat embryos, harvested at different growth stages, were made in two consecutive years. Callus formation and plantlet regeneration were obtained. The ability to form callus and the degree of morphogenetic processes varied with the different hormonal treatments used and with the age of the embryos. In the first year the best response for callus growth was observed with 2,4-D 2 mg l-1 plus adenine 50 mg l-1 or 2,4-D 5 mg l-1 alone in the more mature embryos (15 and 20 days after anthesis). On the contrary, NAA 5 mg l-1 had a greater shoot regeneration effect. In the next year, at all 2,4-D concentrations and for the two different ages of the embryos tested, all embryos formed callus. Regeneration of plantlets was obtained in higher percentage in calli originated from the more developed embryos. The effect of changed media upon plantlet regeneration was studied after callus transplant.Investigation by cytophotometry and chromosome counts on different calli showed, practically in all cells, a diploid condition. A histological analysis demonstrated embryogenic somatic characteristics in many samples of callus. The pattern of organogenesis seemed to be via adventitious bud formation but structures resembling embryoids were also observed in the callus. 相似文献
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玫瑰黄链霉菌Men-myco-93-63原生质体形成
和再生条件的初探 总被引:2,自引:0,他引:2
玫瑰黄链霉菌Men-myco-93-63在温室及大田试验中都对棉花黄萎病菌表现出很强的拮抗作用,是一株很有应用潜力的生防菌株。不论是菌丝体本身还是其代谢产物都对多种植物病原菌有很强的抑制作用。对该生防菌株进行深入研究,尤其是分子水平的研究尤为重要。笔者通过研究影响链霉菌原生质体形成的多种条件和因素,包括培养基的选择、培养时间、甘氨酸浓度、溶菌酶浓度、酶解时间等,最终成功的制备出了生防菌Men-myco-93-63的原生质体,初步确定了其形成条件:TSB培养基一级培养24h,用SGGP作为二级培养基培养菌丝体40h(补加甘氨酸2%),将菌丝体加入2mg/ml溶菌酶37℃水浴60min后即可得到原生质体,涂在再生培养基R5上再生培养,再生数可达4.8×106个/ml。为该生防菌原生质体的转化、基因表达等研究奠定了重要的基础。 相似文献
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Incorporation of monoploids in practical breeding requires an efficient method of producing homozygous diploids. This study investigated factors for efficient regeneration of doubled monoploid (DM) potato, crossability of DMs and their field performance. Incorporation of silver thiosulphate (STS) in propagation medium for in vitro monoploid plantlets of Solanum phureja did not affect the frequency of cells with diploid(2x) nuclei but increased those with monoploid (1x) and decreased those with 4x nuclei. Higher shoot regeneration was obtained from leaf explants compared with stem explants. Induction of shoots from calluswas affected neither by light during incubation nor by overnight treatment with a benzyl adenine pulse. Female fertility based on seed set after pollination of DMs with heterozygous diploid clones varied among DMs but encouraged their utilization in practical breeding. 相似文献
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Traditional breeding methods require more than 6 years to obtain homozygous inbred lines, while isolated microspore culture (IMC) is an effective way to cultivate double haploid homozygous lines in only 2 years. However, low embryogenesis induction frequency in Chinese flowering cabbage remains a key obstacle to the practical application of this technique. Thidiazuron was added at different concentrations to NLN‐13 medium to estimate its effects on microspore embryogenesis and plantlet regeneration. Results showed that three genotypes responded positively. Optimum thidiazuron concentrations produced embryo yields of up to 14.67 embryos per bud and increased microspore embryogenesis frequency with up to 100% survival. Plantlet regeneration rates were up to 81.67%, and the treatment groups showed lower callus formation. We obtained up to 552 diploid plants from the tested genotypes, and the percentage of doubled haploid at different TDZ concentrations showed slight differences, and doubled haploid rates in the three genotypes were above 70%. They showed a high uniformity and can be directly used for hybrid breeding. This method accelerates microspore application in Chinese flowering cabbage hybrid breeding. 相似文献
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以番木瓜成年植株茎尖、侧芽为试材,探讨番木瓜种质超低温保存的最适条件。结果表明:用添加3%DMSO的培养基培养3d后,保留2个叶芽长2mm左右的茎尖,在38℃下以60%PVS2溶液处理50min,再用纯PVS2于-4~0℃处理30min,迅速投入液氮中保存24h后,在40℃水浴中解冻后洗涤数次,接种到再生培养基上,存活率51.5%,植株再生率50.1%。 相似文献
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Summary Glume cultures of monogenic recessive mutants PGTSLS1 (Plant Genetics triticale selection large spike 1) and PGTSLG2 (Plant Genetics triticale selection long grain 2) were employed along with their parent PGTS control (Plant Genetics triticale selection control) and their F1 and F2 progenies, to determine the genetic basis of plant regeneration in hexaploid triticale. The mutant PGTSLS1 exhibited greater efficiency of plant regeneration (22.4%) followed by PGTS control (7.6%) and PGTSLG2 did not exhibit any regeneration. All the three F1's exhibited plant regeneration frequency on par with that of control (6.9–7.3%), suggesting dominant nature of control genotype over the isogenic mutants. The F2 results suggested that genetic control over the high frequency regeneration of PGTSLS1 was monogenic recessive in nature, and genetic control over the recalcitrant nature of PGTSLG2 also was monogenic recessive. The F2 of the cross PGTSLS1 × PGTSLG2 segregated into four classes. Of the 114 F2 plants, 19 showed no regeneration, 70 of them exhibited 6–8% regeneration, 20 of them 19–24% regeneration, and 5 of them exhibited highest frequency regeneration (57–60%). These observations suggest dihybrid segregation for regeneration. The highest frequency of plant regeneration (57–60%) exhibited by 5 F2 plants may be due to the interaction of non-allelic genes in recessive condition. These results clearly demonstrate the association of at least two genes with plant regeneration in hexaploid triticale. 相似文献