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介导外生菌根真菌的遗传转化。

-Mediated Genetic Transformation of the Ect-endomycorrhizal Fungus .

机构信息

The Albert Katz International School for Desert Studies, The Jacob Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev, Beer Sheva 84105, Israel.

Avram and Stella Goldstein-Goren Department of Biotechnology Engineering and The Ilse Katz Center for Meso and Nanoscale Science and Technology, Ben-Gurion University of the Negev, Beer Sheva 84105, Israel.

出版信息

Genes (Basel). 2020 Oct 30;11(11):1293. doi: 10.3390/genes11111293.

Abstract

Mycorrhizal desert truffles such as , , and , form mycorrhizal associations with plants of the Cistaceae family. These valued truffles are still collected from the wild and not cultivated under intensive farming due to the lack of basic knowledge about their biology at all levels. Recently, several genomes of desert truffles have been decoded, enabling researchers to attempt genetic manipulations to enable cultivation. To execute such manipulations, the development of molecular tools for genes transformation into truffles is needed. We developed an -mediated genetic transformation system in . This system was optimized for the developmental stage of the mycelia explants, bacterial optical density, infection and co-cultivation durations, and concentrations of the selection antibiotics. The pFPL-Rh plasmid harboring gene conferring hygromycin resistance as a selection marker and the red fluorescent protein gene were used as visual reporters. The optimal conditions were incubation with 200 μM of acetosyringone, attaining a bacterial optical density of 0.3 OD; transfer time of 45 min; and co-cultivation for 3 days. This is the first report on a transformation system for , and the proposed protocol can be adapted for the transformation of other important desert truffles as well as ectomycorrhizal species.

摘要

共生沙漠块菌如 、 、 和 ,与半日花科植物形成共生关系。这些有价值的块菌仍在野外采集,而不是在集约农业下种植,这是因为它们在各级生物学方面的基本知识还很缺乏。最近,一些沙漠块菌的基因组已经被破译,使研究人员能够尝试基因操作以实现种植。为了执行这些操作,需要开发用于将基因转化为块菌的分子工具。我们在 中开发了一种 介导的遗传转化系统。该系统针对菌丝体外植体的发育阶段、细菌光密度、感染和共培养时间以及选择抗生素的浓度进行了优化。携带赋予潮霉素抗性的 基因的 pFPL-Rh 质粒被用作选择标记,而红色荧光蛋白基因被用作可视化报告基因。最佳条件为用 200 μM 的乙酰丁香酮孵育,细菌光密度达到 0.3 OD;转移时间为 45 分钟;共培养 3 天。这是第一个用于 的转化系统报告,所提出的方案也可以适应其他重要的沙漠块菌以及外生菌根物种的转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2be/7693413/716a9f4f0ac5/genes-11-01293-g001.jpg

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