共查询到18条相似文献,搜索用时 109 毫秒
2.
为获取马尾松(Pinus massoniana)单倍体材料,建立其胚乳组织培养体系,对马尾松胚乳不同的消毒方法进行筛选,并分析不同基本培养基、生长调节剂配比和热激处理对愈伤诱导的影响。结果表明,胚乳的最佳消毒方式为75%酒精处理30 s+2% NaClO消毒15 min,外植体污染率为0,死亡率仅为15.56%;生长素可促进愈伤诱导且是必需的;细胞分裂素浸泡种子可代替培养基中的细胞分裂素,并能取得比较好的胚乳愈伤诱导效果,1.0 mg·mL-1 6-BA浸泡30 min处理的效果最佳,在培养基WPM+NAA 2.0 mg·L-1+2,4-D 1.0 mg·L-1+蔗糖30 g·L-1+琼脂7 g·L-1中,愈伤诱导率高达87.78%;培养基DCR+NAA 2.0 mg·L-1+6-BA 1.0 mg·L-1+蔗糖30 g·L-1+琼脂7 g·L-1的胚乳愈伤诱导率最高(68.75%);热激处理可提高胚乳愈伤的诱导率和质量,以相对湿度85%下45 ℃热激10 min最佳,总愈伤诱导率为66.25%,成团愈伤诱导率达8.75%;增殖培养以培养基WPM+NAA 0.1 mg·L-1+6-BA 2.0 mg·L-1+蔗糖30 g·L-1+琼脂7 g·L-1最佳,增殖率达83.33%。 相似文献
3.
石刁柏已形成细胞的幼嫩胚乳,接种在附加有不同浓度的生长素(NAA)和细胞分裂素(BA)的 MS 培养基上,获得了愈伤组织。愈伤组织的诱导频率随生长素的浓度不同而异,可达65.9—83.1%。将胚乳愈伤组织转移到降低了生长素浓度或只含有低浓度生长素的分化培养基上,可陆续分化芽、根、芽丛和少量胚状体,个别的芽和胚状体能发育成小植株。切取1.5—5cm 长的芽,接种在诱导根的培养基上,或在 IBA50ppm 溶液中浸泡2小时,转移到 MS 基本培养基上,部分芽能生根形成完整植株。 相似文献
5.
首次成功建立阳桃胚乳组织培养并获得胚乳再生植株。胚乳愈伤组织诱导以培养基MS 2,4-D2.0mgL^-1 BA0.2mgL^-1的效果最好,诱导频率可达94.7%,愈伤组织乳白色,结构致密,生长旺盛;将其接种在培养基MS ZT3.0mgL^-1 NAA0.2mgL^-1上,愈伤组织由乳白色致密型转变为淡绿色致密型,进而形成绿色芽点,分化出不定芽,分化频率可达73.3%;胚乳植株在培养基MS ZT2.0-2.5mgL^-1 NAA0.05mgL^-1上进行壮苗和营养繁殖。 相似文献
6.
柑橘愈伤组织是细胞融合、遗传转化等生物技术研究的良好材料。本实验室通过近20年的工作,先后诱导和保存了近80份不同种类和品种的柑橘愈伤组织。这些愈伤组织在MT基本培养基上继代保存。在长期保存过程中,部分材料仍然保持较好的胚胎发生能力。为研究愈伤组织在继代过程中的染色体变异趋势以及这种变异对胚胎发生能力的影响,本文选择有代表性的35份材料作为试材,在4年中连续3次使用流式细胞仪,对细胞DNA含量进行测定。结果发现,待测的35种愈伤组织均存在部分细胞DNA含量加倍的现象,而且,随着时间的推移,除佩奇橘柚、沙漠蒂甜橙、鲁斯脐橙、印度酸橘等4种愈伤组织的DNA含量加倍的细胞有减少的趋势外,其他愈伤组织的DNA含量加倍的细胞均有增加的趋势。数据分析表明,在待测的35种愈伤组织中,有71.4%的基因型的愈伤组织细胞出现了多倍体细胞增加的趋势。对这35种柑橘愈伤组织进行体细胞胚诱导,发现只有9种愈伤组织具有不同程度的胚胎发生能力,其他26种愈伤组织不能再生。相关性分析表明,柑橘愈伤组织细胞DNA含量增加的细胞比例与体细胞胚胎发生能力之间的相关性较小,相关系数为忙-0.10(P〈0.01),未达到显著水平。另外,柑橘胚性愈伤组织继代时间与体细胞胚胎发生能力之间的相关性也不显著。 相似文献
7.
由于胚乳培养在植物遗传研究和育种工作中的潜在价值,多年来不断地有人从事这方面的研究,但仅在少数植物上取得成功。玉米(Zea mays L.)胚乳培养工作虽然开始较早,后来也有一些研究,然而一直未能分化出胚乳植株。1979—1983年我们进行了玉米未成熟胚乳离体培养的工作,诱导出愈伤组织并成功地诱导器官发生,分化出根、苗。现将我们研究的部分结果作一简要报道。 相似文献
9.
植物名称:玉米(Zea mays)品种小金黄。材料类别:幼叶。培养条件:以MS培养基为基本培养基,生长调节物质配比为:(1)2,4-D 4mg╱L(单位下同) NAA2 IAA2;(2)2,4-D8 NAA4 IAA4;(3)2,4—D 8 NAA4 IAA4 ZT0.5 BA0.5 区T 0.5:(4)2,4-DS NAA4 IAA4 ZTl 相似文献
10.
石刁柏(Asparagus officinalis L.)的幼嫩胚乳接种于MS+NAA 5ppm+6-BA 1ppm和MS+NAA 1ppm+6-BA 0.5ppm的培养基上诱导产生愈伤组织。将愈伤组织转移到MS+6-BA 1ppm+NAA 0.5ppm的分化培养基上,培养30天后即可形成胚状体,组织细胞学观察表明:胚状体起源于愈伤组织内或近表层的单个胚性细胞。在胚状体发生的早期阶段,观察到与柳叶菜型和藜型胚胎发育大致相似的细胞分裂方式,从而出现了T型或线型的四个细胞的原胚。在多细胞原胚及球形胚期具有单列或不规则排列的多细胞胚柄。石刁柏胚乳愈伤组织中的胚胎发生是不同步的,在同一块愈伤组织的切片中可以观察到不同发育阶段的胚状体。在外形上还可以观察到一个子叶、两个子叶或四个子叶等多种不同形态的胚状体。一部份胚状体能发育成完整小植株。 相似文献
11.
实验结果表明,孤雌生殖植株根尖体细胞以二倍体细胞最多,占68.9%,其次为非整倍体细胞,占28.7%,其他异倍体和单倍体细胞极少(2.4%)。Pa1植株可分为二倍体和混倍体两类,以二倍体细胞占绝对多数的混倍体植株最多,为83.5%,这些植株生长发育和结实均正常。在花粉母细胞中正常二倍体频率比根尖体细胞明显提高,提高频率为35.3一59.6%,不同材料之间趋势一致。讨论了体细胞染色体变异的来源及其能否延续到生殖细胞。 相似文献
12.
The embryos of maize (Zea mays L.) inbred lines GS02, GS07, GS08, GS11 and GS15 were used as receptor materials to optimize the receptor system from the aspects of genotype, medium components and stress (PEG6000, mannitol, salt and low phosphorus). The results showed that GS07 had the highest induction rate (95.2%). Orthogonal test analysis showed that the best combination of medium components in induction was A2B3C1D3(2), namely, the concentration of 2, 4-dichlorophenoxy acetic acid (2,4-D) was 4 mg·mL-1, the concentration of L-Proline (L-Pro) was 0.8 mg·mL-1, and the concentration of silver nitrate (AgNO3) was 10 mg·mL-1 (or 5 mg·mL). Interestingly, we found that the optimal medium supplemented with 30 g·L-1 PEG6000 or 80 g·L-1 mannitol was suitable for antioxidant enzyme activity and malondialdehyde (MDA) content in GS07 callus. Exogenous 10 mmol·L-1 Ca2+ in the medium components with 100 mmol·L-1 sodium chloride (NaCl) could improve the activity of antioxidant enzymes in GS07 callus. Callus of GS07 could divide normally and grow well in medium components with 27 mg·L-1 KH2PO4. This study enhanced the adaptability of maize callus to stress and optimized the culture conditions. 相似文献
13.
This research uses the immature embryos of inbred maize lines
(GSH9901, Hi01, Hi02, and Chang 7-2) as receptor materials to establish the callus
induction system. These inbred lines provide the receptor materials for the genetic
regeneration of maize and the verification of the genetic functions of maize. The
factor experiment and orthogonal experiments were used to investigate the impacts
of different genotypes, immature embryo size, shield orientation, 2, 4-D
concentration, proline concentration, and folic acid concentration on the induction
rate of embryogenic callus tissue. A sensitivity experiment testing glyphosate (Bar)
and an antibiotic (Cefotaxime sodium) were also conducted. The results indicate
that the immature embryos of inbred maize line GSH9901 were the most effective
for callus tissue induction, and the immature embryos with a length of 1.6-2.0 mm
produce the best result. The upward shield face is more successful for the
formation of induced callus. Using orthogonal analysis, we found that the optimal
combination for the induction system was A 3 (2,4-D concentration 0.25 mg mL -1
),
B 1C 3 (proline concentration 0.8 mg mL -1
), and D 2 (folate Concentration 0.5 mg
mL -1) and the induction rate reached 84%. We found that cold storage at 4 °C for 1
d is more conducive for the formation of embryogenic callus than the other
treatments tested. The sensitivity experiment for callus tissue screening revealed
the critical concentration of glyphosate to be 10 mg ml -1
, and the critical
concentration of antibiotic is 250 mg ml -1
. Using this combination of glyphosate
and antibiotic resulted in regenerated plants. This study established the optimal
conditions for immature embryo callus tissue induction in maize. 相似文献
14.
The endosperm calli were induced on MS basic medium supplemented with lppm 2,4-D, 0.5ppm KT and 5% sucrose. The medium which contained lppm BAP, 0.1ppm NAA and 2% sucrose was used for cell suspension culture. In suspension cell culture, amitosis of cleavage division of nucleus have been observed after 5 days of culture. First the nuclear membrane and nucleolus disappeared. The crevice appeared in the center of the nucleus, and the nucleus divided into two daughter nuclei of similar size and each with a nucleolus. The daughter nucleus resembled an eye in shape. Following the emergence of cell wall, the two new unequal cells were produced. Such amitotic division proceeded repeatedly until the callus developed and eventually plantlet regenerated. 相似文献
16.
以药用寄生植物锁阳的不同部位肉质茎为外植体,研究外植体形态及植物生长调节剂配比对愈伤组织形成、增殖及不定根分化的影响,建立了高效的锁阳肉质茎愈伤组织诱导、增殖和不定根分化体系。结果表明,锁阳茎下部大小为1.5cmx1.5cmxl.5cm的外植体,维管束平行于培养基放置,有利于愈伤组织形成;外植体培养50d,愈伤组织形成。高效的愈伤组织诱导培养基为Ms+6-BA1.0mg.L-1+2,4-D3.0mg·L-1,愈伤组织诱导率可达67%;增殖培养基为Ms+6.BA0.5mg·L-1。+2,4-D1.5mg·L-1,NxsN74%;在Ms+6.BA1.0mg·L-1+NAA2.0mg·L-1。分化培养基中,不定根诱导率达56%。 相似文献
17.
During the early developmental stage of wheat caryopsis the antipodal complex (composed of 20 or more cells) located on the chalazal part of embryo sac gradually turns to degeneration and degradation from its outer part to the innermost, undergoing apparent structural changes of protoplasm. The senescent tissue (antipodals) exports its cell contents continually to support the proliferation and enlargement of the adjacent free-nuclear endosperm and accommodate the dual function of both material transport and nurture supply. The lacking of callose deposition on the boundary wails between antipodals and endosperm is much benefit to the solute transport, but not all cell contents in antipodals undergo thorough degradation until exporting, at least, part of the protoplasm only undergoes limited structural disintegration. The disassembled protoplasmic constituents actively migrate through symplast route in the form of macromolecule. This shows another mode of material transport in feeding endosperm. The occurrence of wide cytoplasmic channel in part of boundary wal ls berween antipodals and endosperm shows a special structural transformation of intercellular connection. Therefore, disassembled nuclear materials, cisternae of endoplasmic reticulum and plastids, mitochondria, etc. could migrate from antipodals into the developing endosperm. It is deduced that this mode of material transport may play an important role in supporting rapid proliferation and enlargement of free-nuclear endosperm in the developing caryopsis. 相似文献
18.
根据已有的猕猴桃自然地理分布资料,通过对中华猕猴桃(Actinidia chinensis)和美味猕猴桃(A.deliciosa)野外分布居群的详细调查,利用流式细胞技术对我国西部高原台地向中东部丘陵平原过渡地带6个纯中华猕猴桃、1个纯美味猕猴桃和5个中华/美味猕猴桃同域分布居群共276个个体的倍性进行了检测。结果表明:(1)中华猕猴桃存在二倍体和四倍体,美味猕猴桃存在四倍体、五倍体和六倍体;(2)中华猕猴桃和美昧猕猴桃在经度和纬度的分布上存在显著差异(P〈0.05),中华猕猴桃在经度上偏东分布而美味猕猴桃偏西,纬度分布上中华猕猴桃偏南而美味猕猴桃偏北;而且不同倍性小种在经、纬度分布上呈现显著差异(P〈0.05),二倍体、四倍体、六倍体的分布在经度上依次从东到西、纬度上从南到北;(3)中华猕猴桃和美味猕猴桃不同倍性小种的海拔分布存在显著性差异(P〈0.05),二倍体小种分布海拔最低,四倍体小种次之,六倍体小种海拔分布最高,但通过LSD分析四倍体个体和六倍体个体在海拔分布上不存在显著差异(P〉0.05)。通过对中华/美味猕猴桃这两种具有重要经济价值的果树的倍性变异及地理分布的探讨,提出了猕猴桃倍性小种分布的上述规律并给猕猴桃种质资源收集、评价、创新和可持续利用方面提供了初步的研究基础,尤其是为我国猕猴桃新品种选育提供了基础数据和科学依据。 相似文献
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