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建立一个农杆菌介导的腥黑粉菌转化系统。

Establishment of an Agrobacterium tumefaciens-mediated transformation system for Tilletia foetida.

机构信息

College of Plant Protection, Shenyang Agricultural University, Shenyang 110866, China; State Key Laboratory for Biology of Plant Disease and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China.

State Key Laboratory for Biology of Plant Disease and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China; College of Plant Protection, Gansu Agricultural University, Lanzhou 730070, China.

出版信息

J Microbiol Methods. 2020 Feb;169:105810. doi: 10.1016/j.mimet.2019.105810. Epub 2019 Dec 16.

Abstract

Tilletia foetida causes wheat common smut disease with severe loss of yield production and seed quality. In this study, a low-cost, rapid, and efficient Agrobacterium tumefaciens-mediated transformation (ATMT) system for T. foetida mutagenesis was constructed: Transformants were screened with hygromycin B at 100 μg/ml, cefotaxime sodium concentrations with 200 μg/ml, Acetosyringone (AS) concentration at 200 μmol/l, 1 × 10 T. foetida hypha cells/ml, co-cultivation at 22 °C with 24 h and culture was incubated at 16 °C up to day 7. Fourteen transformants were randomly selected and confirmed using the specific primers to amplify the fragment of hygromycin phosphotransferase gene. At the same time, PCR analysis was performed to detect Agrobacterium tumefaciens Vir gene to eliminate false positives. The transformants were cultivated up to 8 generations on hygromycine B-containing complete medium (CM) and confirmed by PCR. The results indicated that 80% of T. foetida transformants were hygromycine B resistant. In conclusion, our analyses identified an efficient T-DNA insertion system for T. foetida and the results will be useful for further understanding the pathogenic mechanism via generation of the insertional mutants.

摘要

腥黑粉菌引起小麦坚黑穗病,导致严重的产量和种子质量损失。在本研究中,构建了一种用于腥黑粉菌诱变的低成本、快速和高效的根癌农杆菌介导的转化(ATMT)系统:转化体在 100μg/ml 的潮霉素 B、200μg/ml 的头孢噻肟钠、200μmol/l 的乙酰丁香酮(AS)浓度下进行筛选,用 1×10 个腥黑粉菌菌丝/ml 的浓度进行共培养,共培养 22°C 24 小时,培养温度为 16°C,持续 7 天。随机挑选 14 个转化体,并用特异性引物扩增潮霉素磷酸转移酶基因片段进行确认。同时,进行 PCR 分析以检测农杆菌 tumefaciens Vir 基因,以消除假阳性。将转化体在含有潮霉素 B 的完全培养基(CM)中培养至 8 代,并通过 PCR 进行确认。结果表明,80%的腥黑粉菌转化体对潮霉素 B 具有抗性。总之,我们的分析为腥黑粉菌确定了一种有效的 T-DNA 插入系统,该结果将有助于通过产生插入突变体进一步了解致病机制。

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