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利用根癌农杆菌转化玉米幼苗。

The transformation of Zea mays seedlings with Agrobacterium tumefaciens.

机构信息

Department of Biology, University of Toledo, 43606, Toledo, OH, U.S.A..

出版信息

Plant Mol Biol. 1986 Jan;7(1):43-50. doi: 10.1007/BF00020130.

Abstract

Virulent strains of the soil bacterium Agrobacterium tumefaciens infect dicotyledonous plants and elicit a profound neoplastic response which results in crown gall formation (18). The inciting agent has been shown to be a high molecular weight plasmid (Ti) a section of which, the T-DNA, integrates into the host plant's genome (4, 28, 30). Although transformation of this kind was presumed to be limited to dicots, the detection of enzyme activities linked to the expression of T-DNA has been demonstrated in monocots from the families Liliaceae and Amaryllidaceae (10, 11).In this communication, we present evidence that a member of the commercially important Gramineae also is subject to A. tumefaciens directed transformation. This conclusion is based on two observations. First, seedlings of Zea mays that have had the bacteria introduced into wound sites defined by a region which includes the scutellar node and mesocotyl express the activity of enzymes whose synthesis is associated with the translation of T-DNA transcripts. Specifically, strain specific lysopine dehydrogenase activity has been detected in B6 infected material, whereas nopaline dehydrogenase activity is reported only in those plants inoculated with C58N. Second, the detection of either of these activities in extracts made from infected maize plants requires that the assaulting bacterial strain be competent with respect to the transfer of T-DNA. The vir (-) strains, JK195 and 238MX, are not, and transformation does not seem to occur. In this connection, the corresponding opine synthase activities are not observed.

摘要

土壤细菌根癌农杆菌的毒力菌株感染双子叶植物,并引起深刻的肿瘤反应,导致冠瘿形成(18)。已经表明,激发剂是一种高分子质量质粒(Ti),其一部分 T-DNA 整合到宿主植物的基因组中(4、28、30)。虽然这种转化被认为仅限于双子叶植物,但在百合科和石蒜科的单子叶植物中已经检测到与 T-DNA 表达相关的酶活性(10、11)。在本通讯中,我们提供的证据表明,商业上重要的禾本科的一个成员也受到根癌农杆菌的定向转化。这一结论基于两个观察结果。首先,将细菌引入包括盾片节和中胚轴在内的区域定义的玉米幼苗的伤口部位表达与其 T-DNA 转录物翻译相关的酶的活性。具体来说,在 B6 感染的材料中检测到了菌株特异性赖氨酸脱氢酶活性,而只有在接种 C58N 的植物中才报告了胭脂碱脱氢酶活性。其次,从感染的玉米植物提取物中检测到这些活性中的任何一种都需要攻击细菌菌株具有转移 T-DNA 的能力。vir(-)菌株 JK195 和 238MX 不具有这种能力,并且似乎不会发生转化。在这方面,没有观察到相应的同型氨酸合成酶活性。

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