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Design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast
Saccharomyces cerevisiae plays an important role in the heterologous expression of an array of proteins due to its easy manipulation, low requirements and ability for protein post-translational modifications. The implementation of the preproleader secretion signal of the α-factor mating pheromone fr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038962/ https://www.ncbi.nlm.nih.gov/pubmed/33687500 http://dx.doi.org/10.1007/s00018-021-03793-y |
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author | Aza, Pablo Molpeceres, Gonzalo de Salas, Felipe Camarero, Susana |
author_facet | Aza, Pablo Molpeceres, Gonzalo de Salas, Felipe Camarero, Susana |
author_sort | Aza, Pablo |
collection | PubMed |
description | Saccharomyces cerevisiae plays an important role in the heterologous expression of an array of proteins due to its easy manipulation, low requirements and ability for protein post-translational modifications. The implementation of the preproleader secretion signal of the α-factor mating pheromone from this yeast contributes to increase the production yields by targeting the foreign protein to the extracellular environment. The use of this signal peptide combined with enzyme-directed evolution allowed us to achieve the otherwise difficult functional expression of fungal laccases in S. cerevisiae, obtaining different evolved α-factor preproleader sequences that enhance laccase secretion. However, the design of a universal signal peptide to enhance the production of heterologous proteins in S. cerevisiae is a pending challenge. We describe here the optimisation of the α-factor preproleader to improve recombinant enzyme production in S. cerevisiae through two parallel engineering strategies: a bottom-up design over the native α-factor preproleader (α(nat)) and a top-down design over the fittest evolved signal peptide obtained in our lab (α(9H2) leader). The goal was to analyse the effect of mutations accumulated in the signal sequence throughout iterations of directed evolution, or of other reported mutations, and their possible epistatic interactions. Both approaches agreed in the positive synergism of four mutations (Aα9D, Aα20T, Lα42S, Dα83E) contained in the final optimised leader (α(OPT)), which notably enhanced the secretion of several fungal oxidoreductases and hydrolases. Additionally, we suggest a guideline to further drive the heterologous production of a particular enzyme based on combinatorial saturation mutagenesis of positions 86th and 87th of the α(OPT) leader fused to the target protein. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-021-03793-y. |
format | Online Article Text |
id | pubmed-8038962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-80389622021-04-27 Design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast Aza, Pablo Molpeceres, Gonzalo de Salas, Felipe Camarero, Susana Cell Mol Life Sci Original Article Saccharomyces cerevisiae plays an important role in the heterologous expression of an array of proteins due to its easy manipulation, low requirements and ability for protein post-translational modifications. The implementation of the preproleader secretion signal of the α-factor mating pheromone from this yeast contributes to increase the production yields by targeting the foreign protein to the extracellular environment. The use of this signal peptide combined with enzyme-directed evolution allowed us to achieve the otherwise difficult functional expression of fungal laccases in S. cerevisiae, obtaining different evolved α-factor preproleader sequences that enhance laccase secretion. However, the design of a universal signal peptide to enhance the production of heterologous proteins in S. cerevisiae is a pending challenge. We describe here the optimisation of the α-factor preproleader to improve recombinant enzyme production in S. cerevisiae through two parallel engineering strategies: a bottom-up design over the native α-factor preproleader (α(nat)) and a top-down design over the fittest evolved signal peptide obtained in our lab (α(9H2) leader). The goal was to analyse the effect of mutations accumulated in the signal sequence throughout iterations of directed evolution, or of other reported mutations, and their possible epistatic interactions. Both approaches agreed in the positive synergism of four mutations (Aα9D, Aα20T, Lα42S, Dα83E) contained in the final optimised leader (α(OPT)), which notably enhanced the secretion of several fungal oxidoreductases and hydrolases. Additionally, we suggest a guideline to further drive the heterologous production of a particular enzyme based on combinatorial saturation mutagenesis of positions 86th and 87th of the α(OPT) leader fused to the target protein. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-021-03793-y. Springer International Publishing 2021-03-09 2021 /pmc/articles/PMC8038962/ /pubmed/33687500 http://dx.doi.org/10.1007/s00018-021-03793-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Aza, Pablo Molpeceres, Gonzalo de Salas, Felipe Camarero, Susana Design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast |
title | Design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast |
title_full | Design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast |
title_fullStr | Design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast |
title_full_unstemmed | Design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast |
title_short | Design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast |
title_sort | design of an improved universal signal peptide based on the α-factor mating secretion signal for enzyme production in yeast |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038962/ https://www.ncbi.nlm.nih.gov/pubmed/33687500 http://dx.doi.org/10.1007/s00018-021-03793-y |
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