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1.
利用正交实验设计研究了基本培养基、α-吲哚丁酸、α-萘乙酸、蔗糖、暗培养的时间等五个因素对砀山酥、八月红梨的叶片再生苗生根的影响。结果表明,对于砀山酥梨叶片的再生苗生根的适宜培养基为1/4 MS+0.5 mg/l IBA+sucrose 20 g/l,暗培养5 d,生根效果较好。而对于八月红梨叶片的再生苗生根的适宜培养基为1/4 MS+0.3 mg/l IBA+sucrose 30 g/l,暗培养7 d,则生根效果佳。另外,我们还对砀山酥、八月红和红茄梨叶片再生苗进行了二次生根,发现八月红的生根效果最好,生根率达50%,其次是红茄为35%,而砀山酥没有生根。  相似文献   

2.
砀山酥梨叶片培养和植株再生   总被引:8,自引:0,他引:8  
以砀山酥梨叶片为外植体,首次系统地研究了基本培养基、植物生长调节剂、碳源、暗培养时间和琼脂用量等对其再生不定芽的影响。结果表明,砀山酥梨叶片再生不定芽的适宜组合为NN69 6-BA 2.5 mg.L-1 IBA 0.3 mg.L-1 山梨醇20 g.L-1 琼脂8.0 g.L-1,暗培养20 d。叶片再生频率最高为83%,平均再生芽数2.17。叶片再生苗在生根培养基1/4 MS IBA 0.5 mg.L-1 NAA0.3 mg.L-1 蔗糖20 g.L-1 琼脂6.0 g.L-1上已经生根。  相似文献   

3.
越橘组培苗生根培养的正交试验   总被引:2,自引:1,他引:1  
利用正交试验设计研究了不同基本培养基、不同浓度的吲哚丁酸、萘乙酸、蔗糖以及活性炭等因子对越橘组培苗生根的影响。结果表明:5个因子对越橘再生苗生根的影响程度依次为活性炭、吲哚丁酸、基本培养基、萘乙酸和蔗糖。其中,活性炭的添加对越橘的生根有极显著影响,吲哚丁酸的影响较显著,基本培养基有影响但不显著。越橘纽培苗生根的适宜培养基组合为1/2WPMA+IBA2.0mg/L+NA.AO.5mg/L+蔗糖20g/L+活性炭1g/L。  相似文献   

4.
为优化‘砀山酥梨’转基因试管苗的生根条件,解决梨试管苗生根的难题,以‘砀山酥梨’转基因试管苗作为试验材料,研究了基本培养基类型、培养方式、不同的间苯三酚(PG)浓度、不同的IBA浓度和暗培养时间对生根的影响。结果表明:采用两步生根法,试管苗在附加80 mg/L PG和20 mg/L IBA的ASH基本培养基上暗培养7d后转入附加80 mg/L PG的ASH培养基上进行光照培养,生根率达到91.7%。  相似文献   

5.
六月酥梨叶片培养和植株再生   总被引:1,自引:0,他引:1  
以六月酥梨叶片为外植体,研究了基本培养基、不同质量浓度BA和IBA的组合、不同暗培养时间、不同碳源种类和质量浓度、叶片放置方式和乙烯抑制剂AgNO3处理等因素对六月酥梨叶片再生体系的影响。结果表明,六月酥梨叶片再生芽的适宜组合为NN69+BA 5.0 mg/L+IBA 0.3 mg/L+山梨醇40 g/L+琼脂7 g/L,远轴面向下,暗培养30 d。在适宜条件下,六月酥梨叶片再生频率高达83.3%,平均再生芽数为2.84。不同碳源种类和质量浓度对六月酥梨叶片再生有不同的影响,其中40 g/L山梨醇对叶片不定芽诱导效果显著。硝酸银质量浓度为0.1~1.0 mg/L时六月酥梨叶片再生频率高于对照,但无显著差异;当硝酸银质量浓度为2.0 mg/L时,显著降低了叶片再生频率。叶片再生苗在生根培养基1/2MS+IBA 0.5 mg/L+蔗糖20 g/L+琼脂6.5 g/L,暗培养5 d,生根率为50%,平均生根数为3.33。  相似文献   

6.
明水梨叶片不定芽再生体系的建立   总被引:1,自引:0,他引:1  
以‘明水’梨(Akemizu)叶片为外植体,研究了不同基本培养基,不同浓度噻重氮苯基脲(TDZ)和吲哚丁酸(IBA)的组合,不同暗培养时间以及不同浓度的硝酸银(AgNO3)对梨叶片不定芽再生的影响。试验结果表明,在NN69+TDZ 1.5mg/L+IBA0.2 mg/L+AgNO31.0 mg/L中暗培养25 d后,叶片不定芽再生率最高,达到71.8%。  相似文献   

7.
不同处理对丰水梨离体叶片不定芽再生的影响   总被引:3,自引:1,他引:2  
采用多因素组合试验设计,研究了噻重氮苯基腺(TDZ)和吲哚丁酸(IBA)浓度组合、外植体类型、叶片放置方式、暗培养时间以及乙烯抑制剂AgNO3处理等因素对丰水梨离体叶片再生体系建立的影响.结果表明,NN69 TDZ 2.0 mg·L-1 IBA 0.1 mg·L-1处理的叶片再生频率和再生芽数分别达到86.7%和2.92,为丰水梨最佳培养基与植物生长物质组合.同一叶片的基部和中部比顶端更容易产生愈伤并再生形成不定芽.叶片远轴面向下接触培养基比近轴面向下利于叶片不定芽再生.AgNO3质量浓度在0.1~1.5 mg·L-1范围内对离体叶片再生有显著促进作用, NN69 TDZ 2.0 mg·L-1 IBA 0.2 mg·L-1 AgNO3 1.0 mg·L-1以及NN69 TDZ 1.5 mg·L-1 IBA 0.3 mg·L-1 AgNO3 0.1 mg·L-1使丰水梨叶片再生频率均达到100%.  相似文献   

8.
为提高中国龙船花成活率、生根率,缩短生根时间和育苗周期,以中国龙船花为材料,研究不同溶度的吲哚丁酸、萘乙酸、萘乙酸+吲哚丁酸等量混合液对扦插中国龙船花愈伤组织和根发生的影响.结果表明:以浓度为1000 mg/L萘乙酸+吲哚丁酸混合溶液处理的效果最好.  相似文献   

9.
吲哚丁酸和萘乙酸都具有促进葡萄插条生根,提高生根率和成活率,促进根系生长的作用。本试验在统一的管理条件下,使用吲哚丁酸和奈乙酸的不同浓度溶液,不同时间处理葡萄插条,对插条成活率和生根量进行了系统地研究。  相似文献   

10.
长柄扁桃试管苗诱导生根的初步研究   总被引:1,自引:0,他引:1  
应用均匀正交设计UL9(34)方案,对长柄扁桃试管苗诱导生根进行研究。分析了IBA(吲哚丁酸)、AC(活性炭)、蔗糖3种不同浓度及其组合对长柄扁桃试管苗诱导生根培养的影响。结果表明:3种因素的作用大小为AC>IBA>蔗糖,适于诱导长柄扁桃试管苗生根的培养基为1/2MS+IBA 40 mg.L-1+AC0.5 g.L-1+蔗糖40 g.L-1。  相似文献   

11.
以西选二号为试材,运用均匀试验设计方法调整植物生长调节剂的浓度和种类,通过建立回归模型筛选出适宜于西选二号植株愈伤组织形成、不定芽诱导和植株生根的最佳配方.结果表明:以MS+0.5 mg·L-16-BA+0.1 mg·L-1NAA作为愈伤组织的诱导培养基,可以获得92%的愈伤组织诱导率.MS+3.0 mg·L-16-BA +0.1 mg·L-1NAA可作为芽诱导培养基,其芽分化率为90%.使用芽诱导培养基,附加0.6 mg·L-1GA3作为增殖继代培养基为宜.在1/2MS+1.0 mg·L-1 IBA+0.2 mg·L-1NAA培养基中,芽苗诱导生根效果较佳.小植株炼苗移栽成活率达85%.  相似文献   

12.
旨在建立云南榅桲的薄层培养再生体系,并以此为基础进行云南榅桲的多倍体诱导。以云南榅桲茎段薄层为外植体,系统研究各种因素对茎段薄层再生不定芽的影响,以及不同质量浓度秋水仙素对云南榅桲茎段薄层不定芽再生率以及多倍体植株诱导的影响。结果表明,云南榅桲薄层再生不定芽的适宜培养基组合为MS+TDZ 1.5mg·L-1+IBA 0.4mg·L-1+蔗糖30mg·L-1+琼脂7g·L-1,暗培养7d,再生频率最高为35.41%,平均再生芽数2.15。薄层再生苗在生根培养基1/2 MS+NAA 0.3 mg·L-1+蔗糖20g·L-1+琼脂7g·L-1上已经生根。利用薄层再生结合秋水仙素处理诱导出云南榅桲多倍体,经流式细胞仪鉴定,确定获得的多倍体为四倍体植株。  相似文献   

13.
蒙古扁桃单芽茎段培养体系的建立   总被引:1,自引:0,他引:1       下载免费PDF全文
以蒙古扁桃幼龄实生苗单芽茎段为试材,以MS为基本培养基,研究了外植体消毒方法、生长调节剂对初代培养、增殖培养和生根培养效果的影响。结果表明,70%乙醇10s加0.1%HgCl21min消毒效果良好,外植体污染率18.75%,成活率81.25%;MS 6-BA 1.0 mg.L-1 NAA0.2 mg.L-1培养基初代培养,外植体萌芽率为72.2%;MS 6-BA 2.0 mg.L-1 NAA0.2 mg.L-1培养基增殖培养效果最佳,增殖率2.37;1/2MS IBA1.0 mg.L-1培养基上发根最好,14 d时生根率为40%,平均发根量3.5,平均根长2.09 cm。  相似文献   

14.
The pear (Pyrus spp.) is one of the most important temperate fruit crops. The technique of adventitious shoot regeneration from leaves is considered to be one of the shortcuts in the research on pear genetic modification and cellular engineering, which, however, has not been widely used. As the regeneration frequency of pear leaves is usually very low, the research on adventitious shoot regeneration from pear leaves is eagerly needed. In this experiment, the factors affecting shoot and bud regeneration from the leaves of ‘Zhongli 1’ pear were studied, and an efficient protocol for shoot regeneration was established. The results showed that different types of basic media, different combinations of plant growth regulators, leaf placement on medium, periods of dark culture and the use of silver nitrate (AgNO3) on culture media all significantly affected the adventitious shoot regeneration frequency of ‘Zhongli 1’ pear. The details are as follows: (1) Among three kinds of basic media, NN69 was better for ‘Zhongli 1’ shoot regeneration, followed by half (½) MS, while full MS had no effect on shoot regeneration; (2) Thidiazuron (TDZ) was better than 6-benzylaminopurine (6-BA) for ‘Zhongli 1’ regeneration, with an optimal concentration of 1.5 mg · L?1, and the regeneration rate under this concentration could reach 85%, with 2.72 buds per leaf. 0.5 mg · L?1 indole-3-butyric acid (IBA), which induced a higher regeneration frequency, was a better choice for pear regeneration compared with 0.3 mg · L?1 naphthaleneacetic acid (NAA). Among the different combinations of plant growth regulators, TDZ + IBA was better for inducing high regeneration frequency; (3) The abaxial surface of leaves touching the medium was beneficial for leaves to uptake nutrients from the medium, and because of that, the regeneration frequency of leaves was significantly higher than that of leaves touching the medium with their adaxial surfaces (obverse side of leaf); (4) Dark culture was necessary for bud regeneration, and the best duration for dark culture of ‘Zhongli 1’ pear was 21 days; (5) The addition of 1.0 mg · L?1 AgNO3 into the culture medium could promote adventitious shoot regeneration significantly. A high adventitious shoot regeneration frequency was obtained in this research, which will be beneficial for further research on efficient and stable in vitro plant regeneration systems and genetic modification of pear.  相似文献   

15.
以成年态葡萄柚的茎段为材料,研究不同激素组合、基本培养基对丛生芽增殖的影响,以及再生苗生根、炼苗与移栽技术。结果表明:(1)WPM+6-BA 1.0mg·L~(-1)+NAA 0.2mg·L~(-1)+蔗糖40g·L~(-1)为初代培养的最佳培养基,腋芽诱导率达78.33%;(2)继代增殖的最适培养基为WPM+6-BA 0.75mg·L~(-1)+NAA0.2mg·L~(-1)+蔗糖40g·L~(-1),增殖系数达4.93,芽长达2.62cm;(3)培养基1/2WPM+NAA 0.1mg·L~(-1)+IBA 1.0mg·L~(-1)+蔗糖40g·L-1+AC 0.1%的生根效果最好,生根率达63.33%,株高3.03cm,根粗壮;(4)生根苗移栽成活率达78%以上。  相似文献   

16.
以黄山松(Pinus taiwanensis Hayata)成熟胚为试验材料,进行离体培养与植株再生条件的初步研究。结果表明,黄山松成熟胚外植体表面灭菌以75%的乙醇处理1 min,3%的次氯酸钠处理10 min为适宜;愈伤组织诱导培养基以MS + 1.0 mg·L-1 6-BA + 0.2 mg·L-1 NAA为最佳;适宜的不定芽分化培养基为DCR + 1.0 mg·L-1 6-BA + 0.05 mg·L-1 NAA;不定芽伸长以DCR + 0.1 mg·L-1 6-BA + 0.05 mg·L-1 NAA为适宜;生根培养基以1/2 DCR + 2.0 mg·L-1 IBA + 0.05 mg·L-1 NAA为适宜。建立的植株再生体系为黄山松种质资源的保存、遗传改良及优质种苗繁殖等研究提供了参考。  相似文献   

17.
以中国樱桃'泰小红樱'的茎段为外植体,研究WPM和MS不同培养基以及6-BA和NAA不同激素浓度组合对外植体增殖的影响,建立其组织培养的快繁体系。结果表明:(1)泰小红樱茎段最佳的初代培养基为MS+1.0 mg/L6-BA+0.1 mg/L NAA,诱导分化率高,腋芽新梢生长健壮;(2)最佳继代培养基为WPM+1.0 mg/L6-BA+0.1 mg/L NAA,丛芽增殖与腋芽增殖并存,增殖倍数显著提高,高达8.0倍,且芽苗健壮,叶色浓绿;(3)最佳生根培养基为1/2MS+0.5 mg/L IBA+20 g/L蔗糖+5 g/L琼脂,生根率高,根系长且数量多。  相似文献   

18.
This study was undertaken to standardize protocols for in vitro explant establishment, shoot multiplication and in vitro rooting for Pyrus pyrifolia, growing in the Kashmir valley. The explant used was nodal cuttings of 2–3cm size with one or two axillary buds. The highest explant establishment (over 90%) was observed during spring while the lowest (60%) explant establishment frequency was observed during winter season. The shoots sprouted from the axillary buds were excised and subcultured on MS basal medium. The highest shoot multiplication rate (130 shoots from a single nodal cutting) was obtained on MS medium supplemented with BAP 2.2 mg·L?1 and kinetin 1 mg·L?1 after four weeks. The shoots were inoculated for rooting in root induction medium of half strength MS salts supplemented with plant growth regulators like IBA, IAA, NAA, and 2, 4-D. However, the best rooting response (8.50 roots per shoot) was obtained in combination of hormones (IBA + NAA) 0.25 mg·L?1 each. The rooted micro shoots were acclimatized under decreasing humidity regime (95% RH to 75% RH over a period of 5±1 weeks). The highest ex vitro plantlet survival percentage (56.50%) of Pyrus pyrifolia was observed on sand + soil (1:1 v/v).  相似文献   

19.
为建立淡水砂梨离体培养体系,以淡水砂梨品系香水梨为试验材料,以MS为基本培养基,研究生长调节剂不同组合和浓度对腋芽诱导、增殖培养的影响,以及不同生长调节剂的种类和浓度对生根培养的影响。结果表明,香水梨腋芽诱导的最佳培养基配方为MS+6-BA 1.0 mg·L~(-1)+NAA 0.1 mg·L~(-1),诱导率为71.7%;增殖最适宜的培养基配方为MS+6-BA 3.0mg·L~(-1)+NAA 0.20mg·L~(-1),增殖系数为3.2;生根培养基配方为1/2MS+IBA 0.3mg·L~(-1),香水梨生根率为63.3%。研究表明MS为基本培养基添加生长调节剂适于淡水砂梨的离体快繁。  相似文献   

20.
[目的]为野生小花碧冬茄组织快繁技术提供依据,文中研究了组培条件下,不同浓度的6-BA、NAAI、BA处理对野生小花碧冬茄外植体器官分化和植株再生的影响。[方法]以野生小花碧冬茄无菌种子获得的试管苗为材料,筛选其成苗培养和生根培养最适激素组合。[结果]成苗培养中,较高浓度的6-BA配合较低浓度的NAA有利于外植体形成丛生芽,而高水平的NAA会引起愈伤组织的大量产生。对野生小花碧冬茄而言,芽分化最佳培养基组合为MS+蔗糖30 g/L+琼脂粉5 g/L+NAA 0.2 mg/L+6-BA 1.5 mg/L;愈伤组织最佳培养基组合为MS+蔗糖30 g/L+琼脂粉5 g/L+NAA 0.4 mg/L+6-BA 1.0 mg/L;生根最佳培养基组合为1/2MS+蔗糖30 g/L+琼脂粉5 g/L+IBA 1.0 mg/L+NAA 0.4 mg/L。[结论]明确野生小花碧冬茄芽分化、愈伤组织和生根培养的理想激素配比,初步建立了野生小花碧冬茄的高效再生体系。  相似文献   

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