Functional Analysis of Plant Monosaccharide Transporters Using a Simple Growth Complementation Assay in Yeast.

Robert Fuhrmeister, Jana Streubel
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Abstract

The study of genes and their products is an essential prerequisite for fundamental research. Characterization can be achieved by analyzing mutants or overexpression lines or by studying the localization and substrate specificities of the resulting proteins. However, functional analysis of specific proteins in complex eukaryotic organisms can be challenging. To overcome this, the use of heterologous systems to express genes and analyze the resulting proteins can save time and effort. Yeast is a preferred heterologous model organism: it is easy to transform, and tools for genomics, engineering, and metabolomics are already available. Here, we describe a well-established and simple method to analyze the activity of plant monosaccharide transporters in the baker's yeast, Saccharomyces cerevisiae, using a simple growth complementation assay. We used the famous hexose-transport-deficient yeast strain EBY.VW4000 to express candidate plant monosaccharide transporters and analyzed their transport activity. This assay does not require any radioactive labeling of substrates and can be easily extended for quantitative analysis using growth curves or by analyzing the transport rates of fluorescent substrates like the glucose analog 2-NBDG. Finally, to further simplify the cloning of potential candidate transporters, we provide level 0 modular cloning (MoClo) modules for efficient and simple Golden Gate cloning. This approach provides a convenient tool for the functional analysis of plant monosaccharide transporters in yeast. Key features Comprehensive, simple protocol for analysis of plant monosaccharide transporters in yeast Includes optional MoClo parts for cloning with Golden Gate method Includes protocol for the production and transformation of competent yeast cells Does not require hazardous solutions, radiolabeled substrates, or specialized equipment.

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植物单糖转运蛋白在酵母中的功能分析。
基因及其产物的研究是基础研究的必要前提。表征可以通过分析突变体或过表达系或通过研究产生的蛋白质的定位和底物特异性来实现。然而,复杂真核生物中特定蛋白质的功能分析可能具有挑战性。为了克服这一点,使用异种系统来表达基因和分析产生的蛋白质可以节省时间和精力。酵母是一种首选的异源模式生物:它很容易转化,基因组学、工程和代谢组学的工具已经可用。在这里,我们描述了一个完善的和简单的方法来分析植物单糖转运蛋白的活性在面包酵母,酿酒酵母,使用简单的生长互补试验。我们使用了著名的己糖转运缺陷酵母菌株EBY。VW4000表达候选植物单糖转运蛋白,并分析其转运活性。该试验不需要对底物进行任何放射性标记,并且可以很容易地扩展到使用生长曲线或通过分析荧光底物(如葡萄糖类似物2-NBDG)的运输速率进行定量分析。最后,为了进一步简化潜在候选转运体的克隆,我们提供了0级模块化克隆(MoClo)模块,用于高效和简单的金门克隆。该方法为酵母中植物单糖转运体的功能分析提供了方便的工具。主要特点:酵母中植物单糖转运体分析的全面,简单的方案包括可选的MoClo部分,用于金门法克隆包括生产和转化合格酵母细胞的方案不需要危险溶液,放射性标记的底物,或专门的设备。
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