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质粒pPNptGreen在绿针假单胞菌菌株S1Bt23中绿色荧光蛋白的表达消除了对终极腐霉的生防活性。

Plasmid pPNptGreen Expression of Green Fluorescent Protein in Pseudomonas chlororaphis Strain S1Bt23 Abrogates Biocontrol Activity Against Pythium ultimum.

作者信息

Akuma Mercy, Chi Sylvia Ighem, Xu Renlin, Thapa Indira, Blackwell Barbara, Tambong James Tabi

机构信息

Ottawa Research and Development Centre, Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.

University of Ottawa, Ottawa, Ontario, Canada.

出版信息

Environ Microbiol Rep. 2025 Apr;17(2):e70083. doi: 10.1111/1758-2229.70083.

Abstract

Pseudomonas chlororaphis is a highly effective plant root coloniser and biocontrol agent. To monitor the colonisation of tomato and canola roots, P. chlororaphis S1Bt23 was transformed with the pPNptGreen plasmid encoding for green fluorescent protein (S1Bt23-GFP). Seedling roots inoculated with S1Bt23-GFP were examined after 2 and 5 h using confocal laser fluorescence microscopy. Roots exposed to S1Bt23-GFP showed pronounced biofilm formation around the root surface, and fluorescing cells were localised in the epidermis and metaxylem after 2 and 5 h of inoculation, respectively. The canola roots also showed upward active translocation of the S1Bt23-GFP cells in xylem vessels in real time. S1Bt23-GFP was also evaluated for antagonistic activity against Pythium ultimum. While S1Bt23 WT exhibited 65.70%-71.4% inhibition of radial growth of Py. ultimum, the S1Bt23-GFP strain did not demonstrate any antagonistic effects. Thin layer chromatography and liquid chromatography mass spectrometry analyses of culture extracts of S1Bt23-GFP did not detect phenazines or pyrrolnitrin, antifungal metabolites identified in S1Bt23 wild type. Expressions of phenazine and pyrrolnitrin genes showed no differences in S1Bt23-GFP and wild type. This suggests that the abrogation of these metabolites occurred post-transcriptionally, probably due to a high cellular molecular load in GFP production. This could negatively impact the ecological fitness of S1Bt23-GFP.

摘要

绿针假单胞菌是一种高效的植物根系定殖菌和生物防治剂。为了监测番茄和油菜根系的定殖情况,用编码绿色荧光蛋白的pPNptGreen质粒转化绿针假单胞菌S1Bt23(S1Bt23-GFP)。接种S1Bt23-GFP的幼苗根系在2小时和5小时后用共聚焦激光荧光显微镜检查。暴露于S1Bt23-GFP的根系在根表面周围显示出明显的生物膜形成,接种2小时和5小时后,荧光细胞分别位于表皮和后生木质部。油菜根系还实时显示出S1Bt23-GFP细胞在木质部导管中向上的活跃转运。还评估了S1Bt23-GFP对终极腐霉的拮抗活性。虽然S1Bt23野生型对终极腐霉的径向生长表现出65.70%-71.4%的抑制作用,但S1Bt23-GFP菌株未表现出任何拮抗作用。对S1Bt23-GFP培养提取物的薄层色谱和液相色谱质谱分析未检测到吩嗪或吡咯菌素,这两种物质是在S1Bt23野生型中鉴定出的抗真菌代谢产物。吩嗪和吡咯菌素基因的表达在S1Bt23-GFP和野生型中没有差异。这表明这些代谢产物的消除发生在转录后,可能是由于GFP产生过程中细胞分子负荷过高。这可能会对S1Bt23-GFP的生态适应性产生负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8374/12002801/0633c72c56bb/EMI4-17-e70083-g001.jpg

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