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通过与根癌农杆菌共培养获得的转基因薄荷(Mentha×piperita L.)植株。

Transgenic peppermint (Mentha×piperita L.) plants obtained by cocultivation with Agrobacterium tumefaciens.

作者信息

Niu X, Lin K, Hasegawa P M, Bressan R A, Weller S C

机构信息

Department of Horticulture, Purdue University, 1165 Horticulture Building, West Lafayette, IN 47907-1165, USA Fax no.: +1-765-494-0391 e-mail:

出版信息

Plant Cell Rep. 1998 Jan;17(3):165-171. doi: 10.1007/s002990050372.

Abstract

The first transgenic peppermint (Mentha×piperita L. cultivar Black Mitcham) plants have been obtained by Agrobacterium-mediated transformation by cocultivation with morphogenically responsive leaf explants. Basal leaf explants with petioles, from leaves closest to the apex of in-vitro-culture-maintained shoots (5 cm), exhibited optimal shoot organogenetic responsiveness on medium supplemented with thidiazuron (8.4 µM). Shoot formation occurred at sites of excision on the leaf blade and petiole either directly from cells of the explant or via a primary callus. Analyses of transient GUS activity data indicated that DNA delivery by microprojectile bombardment was more effective than Agrobacterium infection. However, no transgenic plants were obtained from over 22,000 leaf explants after particle bombardment. Cocultivation of leaf explants with Agrobacterium strain EHA 105 and kanamycin selection produced transgenic plants. Greater transient and stable -glucuronidase (GUS) activities were detected in explants or propagules transformed with the construct where gusA was driven by the pBISN1 promoter rather than a CaMV 35S promoter. Eight plants were subsequently regenerated and verified as transgenic based on detection of the nptII transgene by PCR and Southern blot analyses. The Southern analyses indicated that the plants were derived from eight unique transformation events. All transgenic plants appeared morphologically normal. Analyses of GUS activities in leaves sampled from different portions of these transgenic plants, 10 months after transfer to the greenhouse, indicated that six out of the eight original regenerants were uniformly transformed, i.e., did not exhibit chimeric sectors.

摘要

通过与形态发生响应性叶片外植体共培养,利用农杆菌介导的转化方法获得了首批转基因薄荷(Mentha×piperita L. 品种Black Mitcham)植株。带有叶柄的基部叶片外植体取自体外培养的嫩枝(5厘米)最顶端附近的叶片,在添加了噻二唑素(8.4 µM)的培养基上表现出最佳的芽器官发生响应性。芽的形成发生在叶片和叶柄的切割部位,要么直接从外植体细胞产生,要么通过初生愈伤组织产生。对瞬时GUS活性数据的分析表明,通过微粒轰击进行DNA递送比农杆菌感染更有效。然而,在微粒轰击后,超过22000个叶片外植体未获得转基因植株。叶片外植体与农杆菌菌株EHA 105共培养并进行卡那霉素筛选后获得了转基因植株。在用pBISN1启动子而非CaMV 35S启动子驱动gusA的构建体转化的外植体或繁殖体中,检测到更高的瞬时和稳定的葡糖醛酸酶(GUS)活性。随后再生了8株植株,并通过PCR和Southern印迹分析检测nptII转基因,验证为转基因植株。Southern分析表明这些植株来自8个独特的转化事件。所有转基因植株在形态上看起来正常。将这些转基因植株转移到温室10个月后,对从不同部位采集的叶片进行GUS活性分析表明,8株原始再生植株中有6株是均匀转化的,即未表现出嵌合区域。

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