首页> 外文OA文献 >High frequency plant regeneration from mature seed of elite, recalcitrant Malaysian indica rice (Oryza sativaL.) CV. MR 219
【2h】

High frequency plant regeneration from mature seed of elite, recalcitrant Malaysian indica rice (Oryza sativaL.) CV. MR 219

机译:精子,顽拗马来西亚籼稻成熟种子的高频植株再生( ud Oryza sativa ud L.)CV。 mR 219

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

An efficient in vitro plant regeneration system was established for elite, recalcitrant Malaysian indica rice,udOryza sativa L. CV. MR 219 using mature seeds as explant on Murashige and Skoog and Chu N6 mediaudcontaining 2,4-dichlorophenoxy acetic acid and kinetin either alone or in different combinations.udL-proline, casein hydrolysate and L-glutamine were added to callus induction media for enhancement ofudembryogenic callus induction. The highest frequency of friable callus induction (84%) was observedudin N6 medium containing 2.5 mg lud–1 2,4-dichlorophenoxy acetic acid, 0.2 mg lud–1 kinetin, 2.5 mg lud–1udL-proline, 300 mg l-1 casein hydrolysate, 20 mg lud–1 L-glutamine and 30 g lud–1 sucrose under culture inudcontinuous lighting conditions. The maximum regeneration frequency (71%) was observed, whenud30-day-old N6 friable calli were cultured on MS medium supplemented with 3 mg lud–1 6-benzyl aminopurine,ud1 mg lud–1 naphthalene acetic acid, 2.5 mg lud–1 L-proline, 300 mg lud–1 casein hydrolysate and 3% maltose.udDeveloped shoots were rooted in half strength MS medium supplemented with 2% sucrose and wereudsuccessfully transplanted to soil with 95% survival. This protocol may be used for other recalcitrantudindica rice genotypes and to transfer desirable genes in to Malaysian indica rice cultivar MR219 for cropudimprovement.
机译:建立了高效的体外植物再生系统,为Elite,顽皮的马来西亚籼稻, udoryza sativa L.CV。 219 219先生使用成熟种子作为Murashige and Skoog和Chu N6培养基 Udcontaining 2,4-二氯苯氧基乙酸和运动蛋白,单独或以不同的组合。 Udl-脯氨酸,酪蛋白水解产物和L-谷氨酰胺被加入愈伤组织诱导培养基提高 udembryogencic愈伤组织诱导。观察到易碎愈伤组织诱导的最高频率(84%)含有2.5mg L UD-1 2,4-二氯苯氧基乙酸,0.2mg l ud-1 kinetin,2.5mg l ud-1 UDL-脯氨酸,300mg L-1酪蛋白水解产物,20mg L UD-1 L-谷氨酰胺和30GL UD-1蔗糖在培养下,在培养下 Ud连续照明条件。观察到最大再生频率(71%),当 Ud30日旧的N6易碎的Calli培养在补充有3mg L UD-1 6-苄基氨基嘌呤的MS培养基上时, UD1 Mg L UD-1萘乙酸酸,2.5mg l ud-1 l-脯氨酸,300mg l ud-1酪蛋白水解酸盐和3%麦芽糖。 uddeveloped枝条植根于补充有2%蔗糖的半强度Ms培养基,并呈 udsuccessplectle地移植到土壤中95%生存。该方案可用于其他氯普氏素 udindica水稻基因型,并转移到马来西亚籼稻品种MR219中的期望基因进行作物 UDIMPROVEMENT。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号