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

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 p...

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Autores principales: Fuhrmeister, Robert, Streubel, Jana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bio-Protocol 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415198/
https://www.ncbi.nlm.nih.gov/pubmed/37575400
http://dx.doi.org/10.21769/BioProtoc.4733
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author Fuhrmeister, Robert
Streubel, Jana
author_facet Fuhrmeister, Robert
Streubel, Jana
author_sort Fuhrmeister, Robert
collection PubMed
description 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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spelling pubmed-104151982023-08-12 Functional Analysis of Plant Monosaccharide Transporters Using a Simple Growth Complementation Assay in Yeast Fuhrmeister, Robert Streubel, Jana Bio Protoc Methods Article 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 Bio-Protocol 2023-08-05 /pmc/articles/PMC10415198/ /pubmed/37575400 http://dx.doi.org/10.21769/BioProtoc.4733 Text en ©Copyright : © 2023 The Authors; This is an open access article under the CC BY-NC license https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/).
spellingShingle Methods Article
Fuhrmeister, Robert
Streubel, Jana
Functional Analysis of Plant Monosaccharide Transporters Using a Simple Growth Complementation Assay in Yeast
title Functional Analysis of Plant Monosaccharide Transporters Using a Simple Growth Complementation Assay in Yeast
title_full Functional Analysis of Plant Monosaccharide Transporters Using a Simple Growth Complementation Assay in Yeast
title_fullStr Functional Analysis of Plant Monosaccharide Transporters Using a Simple Growth Complementation Assay in Yeast
title_full_unstemmed Functional Analysis of Plant Monosaccharide Transporters Using a Simple Growth Complementation Assay in Yeast
title_short Functional Analysis of Plant Monosaccharide Transporters Using a Simple Growth Complementation Assay in Yeast
title_sort functional analysis of plant monosaccharide transporters using a simple growth complementation assay in yeast
topic Methods Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415198/
https://www.ncbi.nlm.nih.gov/pubmed/37575400
http://dx.doi.org/10.21769/BioProtoc.4733
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