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1.
INTRODUCTIONCreepingbentgrass (AgrostispalustrisHuds.)isanoutstandingcool seasonspeciesavailableforuseongolfcourseputtinggreens,tees,andcloselymowedfairways.Althoughco lonialbentgrass (AgrostistenuisSibth .Fl.Ox en .)isnotwelladaptedtotheverylowmowingheig…  相似文献   

2.
Embryogenic calli were induced from the seeds of creeping bentgrass (Agrostis palustris Huds.) cv. Regent and colonial bentgrass (Agrostis Tenuis Sibth. Fl. Oxen.) cv. Tiger. The embryogenic calli were precultured on fresh medium for 4–7 days and then co-cultivated withAgrobacterium tumefaciens, LBA4404. which contains plasmid vector-pSBGM harboring bar coding region, synthetic green fluorescent protein (sGFP) coding region and matrix attachment region (MAR). After 3 days of co-cultivation, the calli were washed thoroughly and transferred to MS medium containing 2 mg/L of 2, 4-D, 12–15 mg/L phosphinothricin (PPT) and 250 mg/L of cefotaxime. After 2–3 months of selection, the actively growing calli of ‘Regent’ and ‘Tiger’ were transferred to MS medium with 12–15 mg/L PPT and 250 mg/L cefotazime for regeneration. The putative transformants were maintained on MS medium with 3 mg/L PPT for long period but control died within 1 month. After establishing in greenhouse, the transformants also showed strong resistance to 0.4% of herbicide Basta but control plants died within 2 weeks. Under confocal microscope, both young leaves and roots showed significant GFP expression. PCR analysis revealed the presence of a DNA fragment of GFP gene at the expected size (380 bp) in the transformants and its absence in a randomly selected control plant.  相似文献   

3.
朱缨花愈伤组织的诱导   总被引:1,自引:0,他引:1  
研究了不同外植体和不同生长调节剂对朱缨花愈伤组织诱导的影响.结果表明:不同外植体的愈伤组织诱导能力为茎段〉带节茎段〉叶柄〉叶片,茎段和带节茎段是愈伤组织诱导的最佳外植体;诱导朱缨花茎段愈伤组织的最佳生长调节剂组合为MS+NAA1mg/L和MS+BA0.5mg/L+NAA1mg/L;诱导朱缨花带节茎段愈伤组织的最佳生长调节剂组合为MS+BA2mg/L+NAA1.5mg/L.  相似文献   

4.
番茄ACC合成酶反义基因在转基因猕猴桃中表达的初步研究   总被引:4,自引:0,他引:4  
利用从番茄(Lycopersicum esculentumMill.)果实中分离到的ACC合成酶cDNA基因,反向置于CaMV35S启动子的控制之下(所用根癌杆农菌中合有改建后分别携带嵌合NPT Ⅱ基因和番茄的ACC合成酶反义基因的质粒),并转入美味猕猴桃(Actinidiadeliciosa cv.Hayward)的愈伤组织中。通过分化,2周后获得了能在附加羧苄青霉素(Carbenicillin,500mg/l)和卡那霉素(Kanamycin,50mg/l)的MSA(MS盐类,3.0mg/lBA,0.2mg/l IAA)培养基上生长的抗性愈伤组织。经过半年多的继代培养并筛选,获得了大量的抗卡那霉素(50mg/l)的丛芽以及由抗性芽发育形成的抗性试管苗。探讨了在用卡那霉素进行筛选的条件下影响愈伤组织诱导率的一些因素。  相似文献   

5.
刘恺  贾春凤 《保定师专学报》2007,20(2):51-52,62
较系统地对甜柿(Diospyros kakiThunb.)品种“富有”柿组培苗的继代增殖、叶片不定芽再生和生根的培养条件进行研究.试验结果表明:“富有”柿的最佳长期继代培养基为MS ZT2.0m g/L IAA 0.1m g/L;高效不定芽再生体系在培养基MS(1/2N) TDZ 0.4m g/L ZT1.0m g/L培养30d之后,转入培养基M S(1/2N) IAA 0.1mg/L ZT 2.0mg/L中,其分化率达到90.3%以上,外植体平均芽数为4.6;生根选取在培养基1/2M S IBA 1.0mg/L培养基中暗培养8d,生根率为93.1%.  相似文献   

6.
刘恺  贾春凤 《保定师专学报》2007,20(2):51-52,62
较系统地对甜柿(Diospyros kaki Thunb.)品种"富有"柿组培苗的继代增殖、叶片不定芽再生和生根的培养条件进行研究.试验结果表明:"富有"柿的最佳长期继代培养基为MS+ZT2.0 mg/L+IAA 0.1 mg/L;高效不定芽再生体系在培养基MS(1/2N)+TDZ 0.4 mg/L+ZT1.0 mg/L培养30 d之后,转入培养基MS(1/2 N)+IAA 0.1 mg/L+ZT 2.0 mg/L中,其分化率达到90.3%以上,外植体平均芽数为4.6;生根选取在培养基1/2 MS+IBA 1.0 mg/L培养基中暗培养8 d,生根率为93.1%.  相似文献   

7.
以黄山贡菊的茎尖、叶片及根为外植体,进行了黄山贡菊芽的诱导、继代增殖培养、瓶外生根壮苗试验.结果表明MS+6-BA2mg/L+0.1NAAmg/L是诱导黄山贡菊芽形成的最佳培养基,茎尖诱导率最高达95%;MS+6-BA2mg/L+0.01NAAmg/L是黄山贡菊芽继代增殖的最佳培养基,增殖系数达13.2;在生产上,可采用试管苗瓶外生根方法进行黄山贡菊的快速繁殖.  相似文献   

8.
为降低软籽石榴组培过程中外植体褐化程度,从外植体表面消毒时间、转瓶间隔时间、培养基的硬度、吸附剂的使用方面进行了综合试验。结果表明:表面消毒最适时间为7~9min,10d转瓶1次降低褐化的效果较好;使用硬度为5g/L琼脂的MS培养基,并添加0.1 mg/LNAA+0.1mg/LIBA+1.0mg/L6-BA+30g/L蔗糖+聚乙烯吡咯烷酮(PVP)2g/L可有效控制褐变并获得较高的愈伤诱导率。  相似文献   

9.
以菘蓝离体叶片为外植体,研究了激素种类和浓度、接种方式、光照条件等因素对叶片再生的影响,建立了菘蓝离体叶片高频再生体系.结果表明:以MS+6-BA2.0 mg/L+NAA0.2 mg/L+3%蔗糖为培养基,接种后暗培养5天转到光下培养,叶片远轴面向下接触培养基对不定芽的再生最为有效,不定芽不经过愈伤组织阶段直接从叶片上分化产生,再生率高达93.10%.以1/2MS为培养基附加0.1 mg/LNAA可使不定芽生根率达到100%.  相似文献   

10.
In vitro cultures of loquat cultivar Mardan were established using shoot apices after treating with NaOCl (5%, 7%, 10%, 12%, 14% (v/v)) for 12 min and HgCl2 (0.01%, 0.05%, 0.10%, 0.20%, 0.25% (w/v)) for 2 min. A maximum survival rate of 70% was recorded after surface sterilization with 10% NaOCl. Caulogenic response was assessed on Murashige and Skoog (MS) medium fortified with assorted combinations of the cytokinins, benzylaminopurine (BAP), kinetin, and N6-(2-isopentyl)adenine (2iP). Treatment of BAP 1.5 mg/L combined with 2iP 9.0 mg/L and kinetin 1.5 mg/L was found to be optimum for shoot morphogenesis in terms of the number and subsequent growth of shoots, while the highest shoot length was yielded by the combination of BAP 0.5 mg/L, kinetin 0.5 mg/L, and 2iP 3 mg/L. Higher levels of cytokinins induced callogenesis, vitrification and stunted growth to some extent. For rhizogenesis, uniform sized micro-shoots were excised and transferred to half-strength MS medium containing auxins. The best rooting expression was observed with naphthaleneacetic acid (NAA) 1 mg/L combined with indole-3-butyric acid (IBA) 2 mg/L and paclobutrazol (PBZ) 1 mg/L.  相似文献   

11.
何首乌的快速繁殖技术   总被引:1,自引:0,他引:1  
文章对何首乌的快速繁殖技术进行了研究。结果表明:采用MS+6-BA2.0mg/L+IBA0.1mg/L的培养基对诱导带侧芽茎段芽的分化效果最好,通过继代培养,出现芽增殖现象。诱导生根,以1/2MS+IBA0.25-0.5mg/L和1/2MS+NAA0.25-0.5mg/L效果较好。  相似文献   

12.
用MS+2,4-D1.0 mg/L+6%蔗糖培养基诱导三种柚叶片愈伤组织,悬浮培养法扩大培养.进行有效成分分析.结果表明沙田柚含有较高黄酮物质、柚皮苷和野漆树苷,结溪蜜柚次之,江津柚含量最低,约为沙田柚的50-60%.柚苷元在三个品种愈伤组织中含量相似.该结果为柚类进一步遗传转化和改良提供了基础数据.  相似文献   

13.
以绞股蓝茎尖、茎段、叶片为外植体,研究了不同种类、不同浓度配比的外源激素对绞股蓝愈伤组织诱导的影响。结果表明:茎尖在培养基MS+6- BA 1.0 mg·L-1+NAA 0.02 mg·L-1中的诱导效果最好,其诱导率为75.0%;茎段在培养基MS+6- BA 2.0 mg·L-1+NAA 0.2 mg·L-1中的诱导效果最好,其诱导率为81.8%;叶片在培养基MS+6- BA 1.0 mg·L-1+NAA 0.15 mg·L-1中的诱导效果较好,其诱导率为69.2%。  相似文献   

14.
皱叶忍冬的组织培养与快速繁殖初步研究   总被引:5,自引:0,他引:5  
以宜州当地主要金银花品种皱叶忍冬的茎段为外植体材料,于MSt和1/2MS附加不同激素配比的基本培养基上,探讨丛生芽诱导及生根诱导的条件。试验结果表明:丛生芽诱导和继代培养的培养基为MS 6-BA0.5mg/L IBA0.05mg/L,生根培养基为1/2MS IBA1.0mg/L NAA0.05mg/L.  相似文献   

15.
为了获得高质量的罗汉果组培苗,本文主要探究罗汉果从外植体诱导到幼苗移栽的整个过程。实验结果表明:外植体消毒的最佳方法为10%过氧化氢,消毒3min,污染率最低,而外植体成活率高达80%。MS+IBA0.5mg/L+6-BA1.0mg/L和MS+IBA0.5mg/L+6-BA1.5mg/L有利于罗汉果的增殖,其增殖系数达4.45,1/2MS+6-BA1.0mg/L+IBA0.5mg/L最适合罗汉果根的分化。移栽初期有光照并经过炼苗的移栽方法成活率最高,幼苗移栽成活率在80%以上。  相似文献   

16.
以大花蕙兰的茎尖为外植体,探讨了不同培养基对原球茎增殖、分化和小苗诱导及壮苗生根的影响.结果表明:1)大花蕙兰组织培养的原球茎诱导和增殖都可以用培养基1/2MS BA1.0mg/L NAA0.5mg/L;2)适合大花蕙兰组织培养原球茎芽苗诱导的培养基配方为1/2MS BAl.5mg/L NAA0.5mg/L;3)适合大花蕙兰壮苗生根的培养基配方为1/2MS NAA0,1mg/L GAl.0mg/L的组合.  相似文献   

17.
瀑布兰组织培养快速繁殖技术的研究   总被引:1,自引:0,他引:1  
采用植物组织培养技术,开展瀑布兰的诱导分化、芽苗增殖、壮苗培养、生根和移栽等系列研究.结果表明:瀑布兰适宜的诱导分化培养基为:MS+BA2.0mg/L+NAA0.2mg/L,其分化率可达69.8%;增殖培养基为:MS+BA3.0mg/L+NAA0.2mg/L,培养60d的增殖系数达到4.9;壮苗培养基为:1/2MS+NAA0.2mg/L+BA0.5mg/L+香蕉泥10%;生根培养基为:1/2MS+NAA0.5ms/L;当幼苗长高至3-4cm,生根5-7条,根长至1-2cm时,移栽至水草中,成活率达75%以上.  相似文献   

18.
以散叶生菜大速生为试材,以MS为基本培养基,采用不同激素配比,确定生菜高效诱芽培养基为MS 1.5 mg/L 6-BA 0.2mg/L IAA;抗生素敏感性试验表明,筛选培养基中适宜的潮霉素选择压为20 mg/L,抑菌剂羧苄青霉素的适宜质量浓度为300 mg/L;通过根癌农杆菌介导的叶盘法将携带O型和A型口蹄疫抗原决定簇融合基因O21-O14-A21-HBcAg转入大速生散叶生菜,PCR检测转化率达50%。  相似文献   

19.
以丽格海棠巴科斯品系叶片为材料,进行外植体的诱导培养、不定芽继代增殖培养、无根苗生根培养等组织培养技术研究,探索其适宜的培养基和培养条件.结果表明:在MS+BA1.0mg/L+NAA0.2mg/L培养基上丽格海棠叶片诱导不定芽效果最好;在MS+BA0.1mg/L+NAA0.0lmg/L培养基上继代增殖效果较好;在1/2MS+NAA0.2mg/L培养基生根诱导培养效果较好.苗高6cm可出瓶过渡移栽,并保持90%以上的空气湿度,温度为(25±3)℃,成活率最高.  相似文献   

20.
用百合叶片及其鳞茎叶片离体诱导不定芽   总被引:1,自引:0,他引:1  
以MS为基本培养基,附加不同浓度配比的NAA、6-BA、TDZ、2.4-D等激素,分别对5种百合的鳞片叶和叶片进行培养.结果显示,叶片经MS TDZ0.5mg/L和MS 2.4-D0.2mg/L TDZ2.0mg/L诱导可产生不定芽,诱导率最高为20%.MS NAA0.03mg/L、MS NAA0.05mg/L和MS 6-BA2.0mg/L 2.4-D0.2mg/L的培养基都不同程度诱导鳞片叶产生多个不定芽。以MS NAA0.05mg/L芽诱导率最高,不定芽经过继代培养,可长出新鳞茎.  相似文献   

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