共查询到19条相似文献,搜索用时 98 毫秒
1.
麻栎成熟合子胚外植体体胚发生和植株再生 总被引:1,自引:0,他引:1
为探索麻栎快速繁殖技术新途径,以成熟合子胚为外植体诱导体胚发生,进一步培养形成幼苗。结果表明:体胚诱导以MS+1.0mg.L-1 6-BA+1.0mg.L-1 IBA+1.0g.L-1谷氨酰胺+0.5g.L-1脯氨酸为最优,培养30d诱导率达70.0%;体胚成熟以1/2MS+2.0mg.L-1 6-BA+0.5mg.L-1 IBA+2.0mg.L-1 ABA+4.0g.L-1谷氨酰胺+2.0g.L-1脯氨酸为佳,培养60d,体胚完全成熟;体胚萌发最适培养基为1/2MS+0.2mg.L-1 6-BA+10g.L-1山梨醇,且冷处理有利于体胚的萌发,萌发率高达100%,萌发培养80d,形成再生植株。 相似文献
2.
以苦荞子叶和下胚轴为外植体,进行了不同浓度激素组合的MS和SH固体培养基对胚性愈伤组织诱导及植株再生的研究。结果发现,MS培养基比SH培养基更有利于胚性愈伤组织诱导;2,4-D是诱导愈伤组织的有效激素,KT能有效促进胚状体的形成;下胚轴和子叶都能有效诱导出胚性愈伤组织和再生植株。下胚轴在MS 1.5mg·L-12,4-D 1.5mg·L-1BA培养基,子叶在MS 2mg·L-12,4-D 0.5~1.5mg·L-1BA上能高效诱导出愈伤组织;愈伤组织在MS 2mg·L-12,4-D 0.1mg·L-1KT培养基中继代,能有效诱导胚性愈伤组织;来自下胚轴的胚性愈伤组织在1/2MS 2.0mg·L-1BA 0.5mg·L-1KT 0.1mg·L-1NAA培养基上能够高频再生出芽,来自子叶的胚性愈伤组织在1/2MS 1.0mg·L-1BA 0.1mg·L-1KT 0.1mg·L-1NAA培养基上芽诱导率较高;MS 1mg·L-1NAA是适宜的再生苗生根培养基。 相似文献
3.
非洲紫罗兰叶片体细胞胚培养及快繁技术研究 总被引:4,自引:0,他引:4
以非洲紫罗兰叶片为材料进行胚状体诱导及快繁技术研究.结果表明:.在MS NAA0.1mg/L BA0.1 mg/L 2,4-D1.0 mg/L的培养基上培养15d利于诱导胚性细胞分化,起始黑暗培养5~10d可提高胚性细胞分化率;在MS BA0.05~1mg/L的培养基上可诱导胚状体大量发生;在MS NAA0.1mg/L十BA0.1 mg/L的培养基上能够获得茎芽快速增殖;在1/2MS NAA0.01mg/L的培养基上可以生根. 相似文献
4.
5.
油茶优良无性系子叶体细胞胚植株再生 总被引:15,自引:0,他引:15
以油茶优良无性系‘湘林4号’子叶为外植体,采用附加不同种类激素的MS培养基对其进行组织培养实验。研究结果表明:子叶形成胚性愈伤组织的最适合培养基为MS+2.0mg.L-12,4-D+1.0mg.L-1KT;经胚状体诱导产生不定芽分化的最适合培养基为MS+2.5mg.L-16-BA+1.5mg.L-1IAA;油茶优良无性系的生根培养基以MS+7.0mg.L-1NAA最适;通过对植株再生过程中各阶段的组培材料进行RAPD鉴定分析表明,DNA水平上未发现变异,说明通过组织培养建立的油茶优良无性系再生植株同原无性系无明显差别,最终获得的组培苗木能够保持原无性系的优良特性,其遗传是稳定的。 相似文献
6.
亚麻品种'双亚5号'的胚性愈伤组织诱导和体细胞胚胎发生 总被引:2,自引:0,他引:2
亚麻品种'双亚5号'的种子在MS 1.0 mg·L-1 2,4-D 30 g·L-1蔗糖培养基上可诱导出愈伤组织,将其转入MS 0.5mg·L-1KT 0.5mg·L-1NAA培养基上培养10周后诱导出大量胚性愈伤组织,结构较致密,浅黄色,表面有成团的紧密粘附在一起的小颗粒形态.但其继代周期不宜太长,继代次数不宜多,否则易回到非胚性化状态.胚性愈伤组织转A.MS 1.5 mg·L-1(T 1.0 mg·L-1 2,4-D分化培养基上培养40 d后可获得大量的球形胚状体.少量球形体胚可萌发形成正常的子叶胚初期形态,较多的球形体胚形成次生体胚或仅有单极性的畸形胚状体.组织解剖学观察表明,诱导出的是亚麻胚性愈伤组织和胚状体. 相似文献
7.
2,4-D、BA对人参体细胞胚胎发生过程的影响研究 总被引:1,自引:0,他引:1
以人参芽胞、二年生人参根、实生苗(茎、叶)为外植体研究了体细胞胚的发生条件,并对其发生过程中可溶性蛋白、相关酶活性及内源激素的变化等进行了研究。结果表明,诱导愈伤组织的培养基为MS+2,4-D4.0mg/L+BA0.2mg/L;在MS+2,4-D1.0mg/L+KT0.2mg/L培养基上继代培养,可获得胚性愈伤组织;在无2,4-D的培养基上可诱导出胚状体。将胚状体转入无任何激素的MS培养基上继续培养,之后转入1/2MS培养基上获得再生植株。在体细胞胚胎发生过程中,可溶性多糖和可溶性淀粉含量在早期胚时较低,可溶性蛋白含量、POD及PPO活性在早期胚时最高;IAA在早期胚时期含量最高,在成熟胚时期ABA含量最高,而ABA/IAA比值在成熟胚时较高,利于体细胞胚的发育成熟。 相似文献
8.
9.
紫斑牡丹胚培养与植株再生(简报) 总被引:20,自引:0,他引:20
紫斑牡丹专性种子繁殖,效率极低。通过胚培养,种胚在1/2MS+BA1.0mg/L(单位下同)+IAA1.0培养基上可以较快生长并分化出不定芽,不定芽在1/2MS+BA1.0 IAA0.2培养基上可实现快速增殖,40d平均增殖倍数为6.5,增殖芽在1/2MS+IAA0.2培养基上可快速高效生根。 相似文献
10.
11.
激素对百合植株再生的影响 总被引:11,自引:0,他引:11
本研究设计了 1 5种不同配比的激素组合研究 2 ,4 -D和 6 -BA对百合鳞片叶器官发生和体细胞胚胎发生的影响。结果表明 :在 MS培养基上 ,BA可诱导外植体直接分化不定芽 ,其中 1 .0~ 2 .0 mg/L BA诱导不定芽的分化频率最高 ,6 .0 mg/L BA抑制不定芽分化 ;2 ,4 -D可诱导直接体细胞胚胎发生 ,其中 4 .0 mg/L2 ,4 -D诱导体细胞胚胎发生的频率最高 ,而 6 .0 mg/L 2 ,4 -D诱导体细胞胚胎发生的频率降低 ;当培养基中同时含有 BA和 2 ,4 -D时 ,既出现不定芽 ,又出现体细胞胚。当再生苗移入无激素的 MS培养基和含有 1 .0mg/L和 2 .0 mg/L IAA的 MS培养基上时 ,只有无激素的 MS培养基有利于根的形成。此外 ,鳞片叶的大小和外植体的接种方向也影响外植体分化 相似文献
12.
本文报告了黑穗醋栗(Ribes nigrum L.)三个栽培品种中的薄皮黑豆未受精胚珠(花粉发育到单核晚期)在MS基本培养基附加植物激素BA,2.4-D和GA_3中形成了体细胞胚状体。长度约为0.5—1.0cm大小的胚状体在生根培养基中可以形成完整的再生植株。经过筛选得到了体细胞胚性愈伤组织无性系,继代培养二年多仍能保持胚状体形成能力。试验结果表明:诱导体细胞胚胎发生受品种和接种时期的影响,适宜的接种时期为花粉发育到单核晚期。培养基中的BA为诱导胚胎发生和保持胚性愈伤组织无性系所必需。 相似文献
13.
2.4-D、6-BA对人参体细胞胚胎发生过程的影响研究 总被引:1,自引:0,他引:1
本实验以人参芽胞、二年生人参根、实生苗的茎、叶为外植体研究了体细胞胚的发生条件,并对其发生过程中可溶性蛋白、相关酶活性及内源激素的变化等进行了研究。结果表明,诱导愈伤组织的培养基为MS+2,4-D 4.0mg/L + BA 0.2mg/L;在MS+2,4-D 1.0mg/L + KT 0.2 mg/L培养基上继代培养,可获得胚性愈伤组织;在无2,4-D的培养基上可诱导出胚状体。将胚状体转入无任何激素的MS培养基上继续培养,之后转入1/2MS培养基上获得再生植株。组织细胞学观察表明人参胚状体的起源方式为单细胞起源。在体细胞胚胎发生过程中,多糖和淀粉含量在早期胚时较低,可溶性蛋白含量、POD及PPO活性在早期胚时最高;IAA在早期胚时期含量最高,在成熟胚时期ABA含量最高,而ABA/IAA比值在成熟胚时较高,利于体细胞胚的发育成熟。cDNA-AFLP 分析表明胚状体发育不同时期的人参培养物基因表达不同,从而导致了分化和发育。培养物HPLC分析表明胚胎发生试管苗总皂苷含量比子叶胚时期高4倍多。单体皂苷差异较大。 相似文献
14.
This paper deals with the study on the condition of callus formation, embryogenesis, organogenesis, plant regeneration and protoplast culture of wild cotton (G. davidsonii) Callus cultures derived from several organs such as root, stem, leaf, cotyledon and hypocotyl. The results obtained in these cultures showed that the modified MS medium containing 2,4-D 1.0+KT 0.1; 2,4-D 0.1+KT 0.01; NAA (IAA) 2.0+KT 0.1 and NAA (IAA) 1.0+KT 0.1 mg/L were favorable to callus formation. Modified MS medium containing 2,4-D was suitable for initiated callus of G. davidsonii Besides, suspension cultures from callus of G. davidsonii were saccessfully initiated. Optimum concentration of 6BA (or ZT, or 2ip) and NAA (IAA) was for shooting, somatic embryo or leaf formation. Plantlets regenerated from somatic embryo at lower concentration of 6BA, or ZT, or 2ip. As to protoplast culture of this species, the age and physiological condition of callus or suspension cells and concentration of enzymes used for protoplast isolation affected the yield and survival of protoplasts. Protoplast of this species cultured in modified MS medium containing 2,4-D 0.5+NAA 0.5+ZT 0.1–0.2 mg/L. and divied after 3–4 days. The rate of division was 3--4% and cell cluster formed after 14 days, then these cells died. 相似文献
15.
Excised seedling leaf segments of winged bean [Psophocarpus tetragonolobus (L.) DC.] underwent direct somatic embryogenesis under appropriate incubation conditions. Initiation and development of the somatic embryos occurred using a two-step culture method. The culture procedure involved incubation for 28 days on MS basal medium supplemented with 0.1–0.5 mg/l NAA and 1.0–2.0 mg/l BA (induction medium) before transfer to MS medium supplemented with 0.1 mg/l IAA and 2.0 mg/l BA (embryo development medium). The initial exposure to low levels of NAA coincident with high levels of BA in the induction medium was essential for embryogenic induction. Maximum embryogenesis (43.3%) was obtained with 0.2 mg/l NAA and 2.0 mg/l BA, and at least 14 days on induction medium were required prior to transfer to the embryo development medium. The conversion frequency of cotyledonary embryos was 53.3% upon culture on MS medium containing 0.1 mg/l ABA for 7 days followed by transfer to MS medium supplemented with 0.1 mg/l IBA and 0.2 mg/l BA. Following conversion, the regenerated plantlets were transferred to soil and showed normal morphological characteristics.Abbreviations
MS
Murashige and Skoog (1962) medium
-
2,4-D
2,4-dichlorophenoxyacetic acid
-
NAA
1-naphthaleneacetic acid
-
IAA
indole-3-acetic acid
-
IBA
indole-3-butyric acid
-
BA
6-benzylaminopurine
-
ABA
abscisic acid 相似文献
16.
A rapid protocol for somatic embryogenesis from immature leaflets of groundnut (Arachis hypogaea L.)
P. Venkatachalam P. B. Kavi Kishor N. Geetha M. Thangavelu N. Jayabalan 《In vitro cellular & developmental biology. Plant》1999,35(5):409-412
Summary Plant regeneration via somatic embryogenesis was developed in two groundnut varieties. Somatic embryogenesis was induced from
immature leaflets on MS medium with different concentrations of the auxins 2,4-dichlorophenoxyacetic acid (2,4-D) or naphthaleneacetic
acid (NAA) in combination with 0.5 mg/l of the cytokinin BA. The highest frequency of somatic embryo formation occurred on
MS medium fortified with 20 mg 2,4-D per l. Of the two auxins tested individually 2,4-D was more effective for induction of
embryogenesis as well as production of embryos. Embryo development and maturation was achieved on MS medium supplemented with
N6-benzyladenine (BA) (0.5–2.0 mg/l) and 2,4-D (0.5 mg/l). Plant conversion frequency from somatic embryos was highest in presence
of 2.0 mg BA per l and 0.5 mg NAA per l. The frequency of embryogenesis and plant regeneration was higher in the VRI-2 cultivar
than in the other cultivar tested. Regenerated plants were transferred to soil, grown to maturity, and produced viable seeds. 相似文献
17.
Pradeep C. Deo Mary Taylor Robert M. Harding Anand P. Tyagi Douglas K. Becker 《Plant Cell, Tissue and Organ Culture》2010,100(3):283-291
Embryogenic callus was initiated by culturing in vitro taro corm slices on agar-solidified half-strength MS medium containing
2.0 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D) for 20 days followed by transfer to 1.0 mg/L thidiazuron (TDZ). Callus was
subsequently proliferated on solid medium containing 1.0 mg/L TDZ, 0.5 mg/L 2,4-D and 800 mg/L glutamine before transfer to
liquid medium containing the same components but with reduced glutamine (100 mg/L). After 3 months in liquid culture on an
orbital shaker, cytoplasmically dense cell aggregates began to form. Somatic embryogenesis was induced by plating suspension
cells onto solid media containing reduced levels of hormones (0.1 mg/L TDZ, 0.05 mg/L 2,4-D), high concentrations of sucrose
(40–50 g/L) and biotin (1.0 mg/L). Embryo maturation and germination was then induced on media containing 0.05 mg/L benzyladenine
(BA) and 0.1 mg/L indole-3-acetic acid (IAA). Histological studies of the developing embryos revealed the presence of typical
shoot and root poles suggesting that these structures were true somatic embryos. The rate of somatic embryos formation was
500–3,000 per mL settled cell volume while approximately 60% of the embryos regenerated into plants. 相似文献
18.
Somatic embryos were obtained from callus cultures derived from leaf explants of the winged bean, Psophocarpus tetragonolobus (L.) DC. Initiation and development of the somatic embryos occurred with a two-step culture method. Callus cultures initiated on MS medium with NAA and BAP, upon transfer to a new medium with IAA and BAP, produced somatic embryos. Maximum embryogenesis of 60% was obtained on induction medium with 0.5 mg/l NAA plus 1.0 mg/l BAP followed by transfer to a secondary medium with 0.1 mg/l IAA and 2.0 mg/l BAP. Optimal embryo germination and plantlet development was achieved on MS medium with 0.2 mg/l BAP plus 0.1 mg/l IBA. The regenerated plants were successfully transferred to glasshouse conditions.Abbreviations MS
Murashige and Skoog (1962) medium
- 2,4-D
2,4-dichlorophenoxyacetic acid
- NAA
1-naphthaleneacetic acid
- IAA
Indole-3-acetic acid
- IBA
Indole-3-butyric acid
- BAP
6-benzylaminopurine
- KN
Kinetin 相似文献
19.
Pinsan Xu Zhiling Zhang Bo Wang Xiuying Xia Jun Jia 《Plant Cell, Tissue and Organ Culture》2012,111(3):393-397
Somatic embryogenesis was induced from leaf and stem of chrysanthemum (cv. Yuukou) using various combinations of plant growth regulators. About 93 and 63?% of somatic embryogenesis were respectively induced from leaf and stem cultured in Murashige and Skoog (MS) medium supplemented with 6-benzyladenine (BA) and a-naphthalene acetic acid (NAA). Somatic embryogenesis was more readily induced from leaf, yielding 100?% regeneration rate in MS medium supplement with 0.6?mg/L BA and 1.8?mg/L NAA. Plants were efficiently regenerated from leaf in medium lacking growth regulators, yielding a regeneration rate of 98?%. Micro-morphology analysis revealed the presence of individual somatic embryo and there is no vascular bundle connection between the new embryo structure and the parental tissue. In this study, an efficient system for plant regeneration via somatic embryogenesis from leaves and stems of chrysanthemum was achieved. The result may facilitate mass production of high-quality chrysanthemum seedings for the commercial market. 相似文献