文冠果体细胞胚发生中钙的超微细胞化学定位

用电镜细胞化学定位的方法,对文冠果种胚诱导体细胞胚发生过程中非胚性愈伤组织、胚性愈伤组织及球形胚、鱼雷胚发育期间Ca2 的分布动态进行超微结构水平上的定位比较研究.结果表明:非胚性细胞Ca2 的含量最少,集中分布在细胞壁和细胞间隙中;胚性愈伤组织的细胞Ca2 的含量明显增加,集中分布在液泡膜、质膜和细胞质中;球形胚时,质膜上Ca2 积累的颗粒较大,但量相对较少;鱼雷胚期ca2 的含量明显增多,集中分布在胚芽端和胚根端,胚根最外层细胞的外侧的细胞壁明显增厚,其细胞壁的外侧Ca2 分布多.推测Ca2 与文冠果体细胞胚发生过程中细胞的发育时期密切相关.     

滇楸体胚发生及生理生化特性研究

探讨了滇楸体细胞胚胎发生和发育过程中形态学和解剖学特征及变化,对其发生和发育过程中的一些生理生化特性进行了初步研究.结果表明:(1)滇楸非胚性和胚性愈伤组织在细胞形态和组织结构上差异明显,滇楸体胚起源于单个胚性细胞,经历了单细胞、多细胞、球形胚、心形胚、鱼雷胚和子叶胚各阶段.(2)在胚性愈伤组织和体细胞胚胎诱导形成及发育早期,3种抗氧化酶(SOD、POD和CAT)活性均提高,而在后期体胚成熟和萌发的过程中3种抗氧化酶的活性变化趋势差异明显.(3)碳、氮类营养物质在胚性愈伤组织内大量积累,为体细胞胚胎发生奠定能量和物质基础;在体胚发育的不同阶段,碳、氮代谢呈现明显的差异.     

天山云杉体细胞胚的成熟及萌发条件

【目的】建立天山云杉体细胞胚成熟及萌发阶段的适宜培养条件,为该树种的体细胞胚大规模繁殖和工厂化生产提供基础。【方法】以天山云杉成熟合子胚为外植体所诱导形成的胚性愈伤组织为材料,通过14个株系、4种成熟培养基、接种量(100、150、200mg的新鲜胚性愈伤组织)、ABA浓度(1.9、3.8、7.6、19、38μmol·L^-1)等体细胞胚成熟培养条件,以及对不同起源(体细胞胚、合子胚和种子)的幼苗形态特征的比较,筛选出最优的天山云杉体细胞胚成熟与萌发条件。采用SPSS18.0等统计软件对体细胞胚进行统计分析。【结果】1)天山云杉14个株系诱导体细胞胚的结果表明,不同株系在同一成熟培养基上诱导体细胞胚的数量存在差异;其中4个株系及其接种量对体细胞胚形成数量影响的结果表明,不同株系及其接种量诱导体细胞胚的数量也存在差异,当接种量为100mg时,T36株系的体细胞胚诱导数量最高,为3470±546个,显著高于其他接种量和株系(P<0.05)。2)在4种不同成熟培养基上,均形成了成熟的体细胞胚,在1/2BLG+30g·L^-1麦芽糖培养基上形成的体细胞胚数量高于其他培养基,分别为2044个(T6株系)和2282个(T36株系),且与其他培养基差异显著(P<0.05)。3)不同ABA浓度对天山云杉体细胞胚诱导数量的影响无显著性差异(P>0.05),在ABA浓度为1.9~38μmol·L^-1时,其体细胞胚平均诱导数量为2850~2913个,其中以7.6μmol·L^-1ABA的浓度处理效果较好,平均获得2913个正常体细胞胚,高于其他处理。4)将不同起源(体细胞胚、合子胚和成熟种子)萌发的小植株进行对比,结果表明,体细胞胚和合子胚幼苗发育阶段基本一致,但合子胚的幼苗比体细胞胚的幼苗约大1倍,但二者间差异不显著(P>0.05);体细胞胚与合子胚子叶的平均数量一致,二者无显著差异(P>0.05),多数幼苗子叶数量为7~8个。【结论】天山云杉体细胞胚成熟阶段的适宜培养条件为胚性愈伤组织接种量100mg,1/2BLG培养基添加7.6μmol·L^-1的ABA及75%PEG4000、30g·L^-1麦芽糖,并添加750mg·L^-1的L-谷氨酰胺或50mg·L^-1L-天冬酰胺。不同株系在诱导体细胞胚的数量上存在差异。体细胞胚再生植株与合子胚植株在形态上相似。研究结果可为天山云杉体细胞胚的大规模繁殖和工厂化生产提供基础。     

火炬松体细胞胚胎发生体系的优化

[目的]建立和优化火炬松体胚发生技术体系，为火炬松优良基因型体胚繁育及遗传转化体系建立提供技术支撑。[方法]以火炬松优良基因型的未成熟合子胚为材料，从基因型、球果采集期、基本培养基、植物外源激素组合及浓度等方面对胚性愈伤组织诱导条件进行优化；选取增殖效果好、具有胚性胚柄细胞团（ESM）的胚性愈伤组织开展体胚成熟的正交试验，选择发育正常的子叶胚进行萌发，8周后移栽。[结果]基因型、球果采集期、基本培养基和外源激素（PGR）组合及浓度等因子均对胚性愈伤组织诱导有不同程度的影响。火炬松6种基因型中荣山52胚性愈伤组织诱导率最高，达63.33%；处于裂生多胚期的合子胚为外植体的最佳采样期（7月20日左右）；6种基本培养基中，在DCR基本培养基上胚性愈伤组织诱导率最高，达40.00%；不同PGR组合及浓度中，以0.5 mg·L^-1 6-BA+1.0 mg·L^-1 2,4-D+2.0 mg·L^-1 NAA+5.0 mg·L^-1ABA的胚性愈伤组织诱导率最高，达50.00%。胚性愈伤组织在基本培养基MLP上培养1...     

刺槐未成熟合子胚的体细胞胚胎发生和植株再生

以刺槐不同胚龄的未成熟合子胚为外植体,采用混合正交试验设计,研究幼胚胚龄和不同外源激素种类及质量浓度对刺槐胚性愈伤组织的诱导和体细胞胚分化、萌发的影响.结果表明:开花后8周(55天左右)是胚性愈伤组织和体胚诱导的最佳外植体取材时期;MS+2,4-D 5.0 mg·L-1 +BA0.5 mg·L-1是诱导胚性愈伤组织的最佳培养基,出愈率最高为95.42％±0.02％;MS +NAA0.5 mg·L-1 +BA0.5 mg·L-1+谷氨酰胺250 mg·L-1+水解酪蛋白500 mg·L-1是体细胞胚诱导和分化的最佳培养基,直接体细胞胚发生率最高为92.40％±0.12％,通过愈伤组织诱导体细胞胚发生的频率最高为90.73％ ±0.49％.一旦形成球形胚,将培养物转接到不含任何生长调节剂的MS培养基上,体细胞胚经成熟萌发可进一步形成完整小植株.     

杂交榛子体细胞胚发生研究

不同培养基、激素种类及浓度和外植体对杂交榛子体细胞胚直接和间接诱导的影响的结果表明,MS培养基为杂交榛子体细胞胚发生最佳培养基;激素对杂交榛子体细胞胚直接诱导无显著影响,均可诱导成熟植株;筛选出杂交榛子愈伤组织培养最佳培养为:MS+6-BA2.0 mg/L+NAA1.5 mg/L;再生植株分化最佳培养基为:MS+6-BA2.0mg/L+N AA1.5 mg/L转入MS+6-BA 5.0 mg/L+N AA 0.01+GA3 0.5 mg/L;杂交榛子体细胞胚发生以子叶诱导率最高,以龙榛胚性愈伤组织诱导率最高。     

白刺花胚性愈伤组织诱导及体细胞胚发生

【目的】探讨不同植物生长调节剂对白刺花胚性愈伤组织诱导的作用,以及培养基中氮源和无机盐浓度对白刺花体细胞胚发生和植株再生的影响,以期建立白刺花体细胞胚发生、发育及调控技术体系,为白刺花种苗快速繁殖体系建立及遗传转化研究提供参考。【方法】以白刺花叶片为外植体,研究生长调节剂2,4-D(1.0、2.0、3.0、4.0 mg ·L -1 )、NAA(0、0.5、0.8、1.0 mg ·L -1 )、6-BA(0.2、0.5、1.0、2.0 mg ·L -1 )和TDZ(0、0.2、0.5、1.0 mg ·L -1 )组合对胚性愈伤组织诱导,及NAA(0、0.2、0.5 mg ·L -1 )、6-BA(0、0.5、1.0 mg ·L -1 )和TDZ(0、0.2、0.5 mg ·L -1 )组合对体细胞胚发生的调控作用,筛选最优生长调节剂组合;并研究培养基中KNO 3和NH 4NO 3比例对体细胞胚发生的作用,及MS培养基中无机盐浓度(1/5MS 、1/4MS、1/3MS、1/2MS)对体细胞胚萌发的影响,筛选最佳的体细胞胚发育及成熟萌发条件。【结果】白刺花叶片外植体胚性愈伤组织诱导适宜培养基为MS + 2,4-D 3.0 mg ·L -1 + NAA 0.5 mg ·L -1 + 6-BA 0.2 mg ·L -1 + TDZ 1.0 mg ·L -1 +蔗糖40 g ·L -1 +琼脂7.0 g ·L -1 ,诱导率为42.0%。采用MS基本培养基时,最佳的体细胞胚发生培养基为MS + NAA 0.5 mg ·L -1 + 6-BA 1.0 mg ·L -1 + TDZ 0.5 mg ·L -1 +蔗糖40 g ·L -1 +谷氨酰胺100 mg ·L -1 +琼脂7.0 g ·L -1 ,体细胞胚发生率为78.46%,总胚数为对照的3.6倍;MS培养基中,KNO 3浓度提高1倍、NH 4NO 3降至1/2时,体细胞胚发生率可提高至91.33%,总胚数为采用MS基本培养基时的1.4倍;1/3MS培养基有利于体细胞胚的萌发,萌发率为82.75%,幼苗长势良好,单株平均鲜质量为76 mg,幼苗驯化移栽1个月后成活率达90%以上。【结论】白刺花叶片接种于添加2,4-D、NAA、6-BA和TDZ不同组合的诱导培养基上,可脱分化形成愈伤组织或胚性愈伤组织,2,4-D浓度对愈伤组织形态和质地有较大影响。TDZ有利于体细胞胚的形成,适宜浓度的生长素与细胞分裂素组合及硝态氮和铵态氮的比例对体细胞胚的形成和发育具有调控作用,降低MS无机盐浓度可提高体细胞胚萌发率,本试验体系的再生植株移栽成活率达90%以上。     

火炬松成熟合子胚体胚发生与成熟试验

以火炬松成熟合子胚为外植体,开展成熟合子胚体胚诱导、胚性胚柄细胞团(ESM)维持与增殖培养及体胚成熟试验。结果表明:火炬松成熟合子胚体胚诱导率为3%,远远低于未成熟合子胚;诱导获得的多数ESM在连续的增殖培养中难以生存;不同胚性细胞系体胚发育和成熟能力不同,胚性细胞系AL-225经无植物生长调节剂培养基预培养后转入AL+ABA 50 mg·L-1+15%PEG8000培养基,体胚进一步发育,但未能获得完全成熟体胚。     

黑松合子胚和体细胞胚发育阶段的形态特征比较

为掌握黑松合子胚和体细胞胚发育进程,以未成熟合子胚为外植体,建立了黑松体细胞胚胎发生体系。对合子胚和体细胞胚发育阶段的形态特征进行观察和比较,结果表明,合子胚和体细胞胚的发育进程均可划分为8个阶段,两者同一阶段的形态特征大致相同,只有第2阶段和第4阶段有细微差别。     

核桃体细胞胚诱导的初步研究

将5月中旬至6月上旬的核桃未成熟幼胚在改良DKW培养基+6-BA1.0mg/L中黑暗培养30天左右,从外植体表面直接产生或通过胚性愈伤组织间接形成体细胞胚。在体细胞胚诱导培养基上连续多代培养,培养材料仍可保持胚性分生能力。发育正常的体细胞胚在无激素的发芽培养基中黑暗培养15天左右可发芽成苗。     

花曲柳体胚发生和植株再生

以花曲柳合子胚的单片子叶为外植体成功诱导出体胚并获得再生植株。未成熟合子胚的子叶在添加400mg·L-1水解酪蛋白、0.25mg·L-16-BA、1.5mg·L-1NAA、70g.L-1蔗糖和6g·L-1琼脂的MS1/2培养基上可以成功诱导产生体胚,诱导率达到34.7%,每个外植体上体胚数量为2～9个。成熟合子胚的子叶在添加0.25mg·L-16-BA、2mg·L-1NAA的MS1/2培养基(其他成分同上)上可以成功诱导产生体胚,诱导率为10.0%。体胚在MS1/2培养基上经过成熟培养后可以正常萌发,萌发率87.6%。萌发的体胚植株在MS1/2+0.01mg·L-1NAA培养基上生长较好,具备实生幼苗的外观特征。经炼苗后的体胚苗移植到栽培基质(草炭土:蛭石:珍珠岩体积比为5:4:1)中可以正常生长,成活率为75.0%。     

Somatic embryogenesis and plant regeneration inAcanthopanax sciadophylloides

Somatic embryos ofAcanthopanax sciadophylloides Franch. et Sav. were differentiated from both zygotic and somatic embryos and calli, and plants were regenerated from these somatic embryos. A zygotic embryo, enclosed within a small portion of the endosperm, was incubated on Murashige and Skoog (MS) media supplemented with various combinations (range 0–10.0 mg/l) of 6-benzylaminopurine (BAP) and 2,4-dichlorophenoxyacetic acid (2,4-D). After 4 months, swelling of the zygotic embryos and callus formation was observed. When the swollen embryos were transferred to MS medium supplemented with 0.5 mg/l of 2,4-D, somatic embryos were formed in one to two months. After subculture on the same medium, new embryos were differentiated from various parts of the older somatic embryos. The calli were cultured on medium supplemented with 2.0 mg/l of 2,4-D and BAP for three weeks. Proliferated calli were transferred to medium supplemented with 1.0 mg/l of 2,4-D and BAP. Somatic embryos were differentiated from the calli within one to two months. Somatic embryos were germinated on half-strength MS medium without plant growth regulators and the plantlets were grown in soil. A part of this paper was presented at the 106th Annual Meeting of the Japanese Forestry Society (1995) & First Asia-Pacific Symposium on Forest Tree Genetic Improvement (Beijing).     

水曲柳体细胞胚与合子胚发生的细胞学研究

水曲柳(Fraxinus mandshurica)属木犀科(Oleaceae)白蜡树属,是我国东北重要珍贵硬阔树种之一,主要分布于小兴安岭、长白山、辽宁东部山地等地区, 以材质优良而著称.由于长期不合理的采伐利用,目前可利用的资源急剧减少,已被列为国家三级保护植物(傅立国,1992).进行水曲柳体细胞胚胎发生的研究,在资源保护、树种快繁和基因工程育种上有其重要的现实意义.     

Somatic Embryogenesis and Plantlet Regeneration in Callus Cultures Derived from Mature Zygotic Embryos of Slash Pine

1TheworkwassupportedbyChineseNationalHighTechnologyDevelopmentProgram"863project"IntroductionSomaticembryogenesishasagreatpotentiaIforrapidProPaationofsuPCriorconifcrspccics.ThefirstreportonsomaticembryogenesisandplantlctrcgencrationinconifersPeCieswasach…     

火炬松体细胞胚胎发生和干化体细胞的氧化物酶活性(英文)

培养于附加2,4-D、BA和KT的愈伤组织诱导培养基上的火炬松成熟合子胚在培养3-9周后形成白色、半透明、有光泽的粘性愈伤组织。这类愈伤组织形成于成熟合子胚的子叶,但当用NAA或者IBA代替愈伤组织诱导培养基中的2,4-D时,它的诱导频率明显降低。这种粘性愈伤组织在分化培养基上形成体细胞胚。体细胞胚经过去50μm ABA和8.5%PEG600处理后成为耐干化胚。扫描电镜观察表明,萌发处理36小时后,耐干化胚恢复到干化处理之前的状态且大小和形态正常,而不耐干化胚不能恢复到干化处理之前的状态且表面撕裂。过氧化物酶活性的分析结果表明,耐干化胚有更高的过氧化物酶活性。耐干化胚的高过氧化物酶活性可能与催化H2O2的分解和保护体细胞胚免受氧化的伤害有关。     

Using synergistic exogenous phytohormones to enhance somatic embryogenesis from leaf explants of a Eucalyptus grandis clone

Somatic embryogenesis (SE) in Eucalyptus spp. has been limited to germinated seeds, flowers, lignotubers or zygotic embryos. The low yield of somatic embryos from leaf explants has hampered progress, even though leaves offer a more viable source of clonal explants from superior selected genotypes. It was hypothesised that SE from leaf explants could be enhanced through pairing of synergistic exogenous plant growth regulators, such as natural auxins with natural cytokinins. Callus and embryo induction using 2,4-dichlorophenoxyacetic acid (2,4-D), α-naphthalene acetic acid (NAA), indole acetic acid (IAA), and indole butyric acid (IBA), each at either 1.0 or 3.0?mg L^?1, indicated that IAA and IBA favoured significantly higher numbers of embryos compared with 2,4-D or NAA. Hence, IAA and IBA were used for subsequent experiments, combining them (at 1.0?mg L^?1) with either the synthetic cytokinin, kinetin, or the natural cytokinin, trans-zeatin, both at 0.1?mg L?1. The combination of trans-zeatin and either IAA or IBA resulted in a significant increase in SE (e.g. 86 ± 17.2% and 23 ± 3.2% for IAA with trans-zeatin and kinetin, respectively), compared with kinetin, or with these auxins alone. Embryo maturation and plantlet regeneration was highest in those calli that were induced with IAA and trans-zeatin, indicating that maturation was dependent on auxin depletion, based on the stability of the analogue used for induction. For the E. grandis clone under study, the use of synergistic plant growth regulators significantly enhanced SE from leaf explants, thus presenting the opportunity to benefit from the advantages that SE offers over conventional organogenesis.     

核桃体细胞胚发生与转基因研究进展

总结了核桃体细胞胚发生的研究进展,列表统计已报道的核桃５个种和３个杂种体细胞胚发生的外植体与诱导条件,重点论述了影响核桃体细胞胚发生与次生胚发生的因素,介绍了核桃体细胞胚萌发与转化的方法。还总结核桃转基因研究的进展,提出了用核桃体细胞胚发生系统进行外源基因转移的操作模式。     

Somatic embryo production and plant regeneration of Japanese black pine (Pinus thunbergii)

Somatic embryogenesis in Pinus thunbergii was initiated from megagametophytes containing immature zygotic embryos. Embryogenic cultures were maintained and proliferated in medium supplemented with 2,4-dichlorophenoxyacetic acid and 6-benzylaminopurine. High maturation frequencies of somatic embryos were obtained on maturation media containing maltose, activated charcoal, abscisic acid, and polyethylene glycol as osmotic agent. The best result among the cell lines tested was achieved with the cell line T-205-3. More than 900 somatic embryos per petri dish, on average, were obtained after about 8 weeks of culture on maturation medium. Sixty percent of somatic embryos tested germinated after transfer to plant growth regulator-free medium and then 85% of them converted into plantlets.     

Efficient plant regeneration of Hinoki cypress (Chamaecyparis obtusa) via somatic embryogenesis

This report describes the efficient plant regeneration of Chamaecyparis obtusa Sieb et Zucc. via somatic embryogenesis. Embryogenic cultures were initiated from megagametophytes containing immature zygotic embryos. Embryogenic cultures were maintained and proliferated by 2–3-week interval subcultures in medium supplemented with 2,4-dichlorophenoxyacetic acid and 6-benzylaminopurine. High maturation frequencies of cotyledonary embryos were obtained on maturation medium containing maltose, polyethylene glycol, activated charcoal, and abscisic acid. Somatic embryos germinated readily after transfer to plant growth regulator-free medium. Growth of regenerated emblings has been monitored in a greenhouse.     

Pine somatic embryogenesis: analyses of seed tissue and medium to improve protocol development

The shift from vegetative to embryogenic growth requires tissue to enter a radically different program of development and can be studied in vitro through the development of somatic embryos. From an applied perspective somatic embryogenesis (SE) is expected to play an important role in increasing productivity, sustainability, and uniformity of future forests. For commercial use, SE technology must work with a variety of genetically diverse trees. Since the first reports of SE in Picea abies and Larix decidua in 1985, many different coniferous species have shown the ability to produce embryogenic tissue. However, initiation frequency is often low, many desired seed sources are recalcitrant, and culture survival is often poor, raising costs of somatic seedlings produced from successful genotypes. A number of tools are now available to improve embryogenic tissue initiation and somatic embryo development in vitro that have resulted from analytical studies of seed tissues, the seed environment and gene expression in megagametophyte, zygotic embryos and somatic embryos. Benefits have occurred from medium supplementation with hormones, plant growth regulators, hormone inhibitors and polyamines. Somatic embryo growth has been enhanced with medium supplementation of nutritional components including specific sugar types, vitamins, organic acids, and redox potential modifiers. Control of environmental factors including, water potential, pH, adsorption of medium components by activated carbon and liquid versus gelled medium have also led to SE protocol improvements. The use of analytical studies to duplicate the seed environment in vitro is improving protocol development resulting in increased initiation, improved yields and higher-quality somatic embryos.