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菊欧文氏菌3937中dspE和pelD调控的群体行为分析

Population behavior analysis of dspE and pelD regulation in Erwinia chrysanthemi 3937.

作者信息

Peng Quan, Yang Shihui, Charkowski Amy O, Yap Mee-Ngan, Steeber Douglas A, Keen Noel T, Yang Ching-Hong

机构信息

Department of Biological Sciences, University of Wisconsin, Milwaukee 53211, USA.

出版信息

Mol Plant Microbe Interact. 2006 Apr;19(4):451-7. doi: 10.1094/MPMI-19-0451.

Abstract

Erwinia chrysanthemi 3937 (Ech3937) is a phytopathogenic bacterium with a wide host range. The pectinolytic enzymes secreted by the bacterium and the type III secretion system (T3SS) are essential for full virulence. We used the green fluorescent protein gene as a reporter to investigate the expression of dspE (a putative T3SS effector) and pelD (a major pectin-degrading enzyme) in populations of Ech3937 under different conditions. Gene expression was analyzed by measuring the fluorescence intensity of individual cells with a fluorescence-activated cell sorter. Ech3937 dspE was induced in minimal medium (MM) with only a portion of Ech3937 cells (43.03%) expressing dspE after 12 h of culture. The nutrient-rich King's medium B did not fully eliminate the expression of dspE; a small percentage of Ech3937 cells (5.55%) was able to express dspE after 12 h of culture in this medium. In all, 68.95% of Ech3937 cells expressed pelD after 12 h of culture in MM supplemented with polygalacturonic acid (PGA). However, 96.34% of Echl31 cells (an hrpL deletion mutant of Ech3937) expressed pelD after 12 h of culture in MM supplemented with PGA. In potato tubers, 6.32% of the bacterial cells expressed dspE 2 h after inoculation, whereas only 0.25% of the cells expressed pelD. However, after 24 h, the percentage of cells expressing pelD (68.48%) was approximately 3.5 times that of cells expressing dspE (19.39%). In contrast to potato tubers, similar proportion of Ech3937 cells expressing dspE (39.34%) and pelD (40.30%) were observed in Chinese cabbage 24 h after inoculation. From promoter activity and real-time quantitative results, the expression of pelD in Ech3937 was demonstrated to be downregulated by HrpL in MM supplemented with PGA.

摘要

菊欧文氏菌3937(Ech3937)是一种寄主范围广泛的植物病原细菌。该细菌分泌的果胶分解酶和III型分泌系统(T3SS)对其完全致病性至关重要。我们使用绿色荧光蛋白基因作为报告基因,研究了dspE(一种假定的T3SS效应蛋白)和pelD(一种主要的果胶降解酶)在不同条件下Ech3937群体中的表达情况。通过使用荧光激活细胞分选仪测量单个细胞的荧光强度来分析基因表达。Ech3937 dspE在基本培养基(MM)中被诱导,培养12小时后只有一部分Ech3937细胞(43.03%)表达dspE。营养丰富的King's培养基B并未完全消除dspE的表达;在该培养基中培养12小时后,一小部分Ech3937细胞(5.55%)能够表达dspE。总体而言,在补充了聚半乳糖醛酸(PGA)的MM中培养12小时后,68.95%的Ech3937细胞表达了pelD。然而,在补充了PGA的MM中培养12小时后,96.34%的Echl31细胞(Ech3937的hrpL缺失突变体)表达了pelD。在马铃薯块茎中,接种后2小时,6.32%的细菌细胞表达dspE,而只有0.25%的细胞表达pelD。然而,24小时后,表达pelD的细胞百分比(68.48%)约为表达dspE的细胞百分比(19.39%)的3.5倍。与马铃薯块茎不同,接种24小时后,在大白菜中观察到表达dspE(39.34%)和pelD(40.30%)的Ech3937细胞比例相似。从启动子活性和实时定量结果来看,在补充了PGA的MM中,HrpL可下调Ech3937中pelD的表达。

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