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根瘤菌感染大豆根瘤中基因表达的生物发光可视化标记。

Visualization of bioluminescence as a marker of gene expression in rhizobium-infected soybean root nodules.

机构信息

Bioluminescence Laboratory, Department of Biochemistry, University of Georgia, 30602, Athens, GA, USA.

出版信息

Plant Mol Biol. 1988 Sep;10(5):387-99. doi: 10.1007/BF00014945.

Abstract

The linked structural genes lux A and lux B, encoding bacterial luciferase of a marine bacterium Vibrio harveyi, were fused with the nitrogenase nifD promoter from Bradyrhizobium japonicum and with the P1 promoter of pBR322. Both fusions were integrated into the B. japonicum chromosome by site-specific recombination. Soybean roots infected with the two types of rhizobium transconjugants formed nitrogen-fixing nodules that produced bright blue-green light. Cells containing the P1 promoter/lux AB fusion resulted in continuously expressed bioluminescence in both free-living rhizobium and in nodule bacteriods. However, when under control of the nifD promoter, luciferase activity was found only in introgen-fixing nodules. Light emission from bacteroids allowed us to visualize and to photograph nodules expressing this marker gene fusion in vivo at various levels of resolution, including within single, living plant cells. Localization of host cells containing nitrogen-fixing bacteroids within nodule tissue was accomplished using low-light video microscopy aided by realtime image processing techniques developed specifically to enhance extreme low-level luminescent images.

摘要

海洋细菌哈维氏弧菌的细菌荧光素的连接结构基因 luxA 和 luxB 与根瘤菌属的固氮酶 nifD 启动子和 pBR322 的 P1 启动子融合。这两个融合物通过位点特异性重组整合到根瘤菌属的染色体中。感染了这两种类型的根瘤菌转导子的大豆根形成了固氮的根瘤,产生了亮蓝色的绿光。含有 P1 启动子/luxAB 融合物的细胞导致游离根瘤菌和根瘤细菌中持续表达生物发光。然而,当受 nifD 启动子控制时,只有在固氮的根瘤中才发现荧光酶活性。从细菌体中发出的光使我们能够在不同的分辨率水平下对活体植物细胞中的表达这种标记基因融合的根瘤进行可视化和拍照。利用专门开发的实时图像处理技术,借助低光视频显微镜,对根瘤组织中的含固氮细菌体的宿主细胞进行定位,该技术专门用于增强极端低水平的发光图像。

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