Cargando…
Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast
BACKGROUND: Identifying the genetic basis of complex microbial phenotypes is currently a major barrier to our understanding of multigenic traits and our ability to rationally design biocatalysts with highly specific attributes for the biotechnology industry. Here, we demonstrate that strain evolutio...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393574/ https://www.ncbi.nlm.nih.gov/pubmed/25866561 http://dx.doi.org/10.1186/s13068-015-0241-z |
_version_ | 1782366180421402624 |
---|---|
author | Pinel, Dominic Colatriano, David Jiang, Heng Lee, Hung Martin, Vincent JJ |
author_facet | Pinel, Dominic Colatriano, David Jiang, Heng Lee, Hung Martin, Vincent JJ |
author_sort | Pinel, Dominic |
collection | PubMed |
description | BACKGROUND: Identifying the genetic basis of complex microbial phenotypes is currently a major barrier to our understanding of multigenic traits and our ability to rationally design biocatalysts with highly specific attributes for the biotechnology industry. Here, we demonstrate that strain evolution by meiotic recombination-based genome shuffling coupled with deep sequencing can be used to deconstruct complex phenotypes and explore the nature of multigenic traits, while providing concrete targets for strain development. RESULTS: We determined genomic variations found within Saccharomyces cerevisiae previously evolved in our laboratory by genome shuffling for tolerance to spent sulphite liquor. The representation of these variations was backtracked through parental mutant pools and cross-referenced with RNA-seq gene expression analysis to elucidate the importance of single mutations and key biological processes that play a role in our trait of interest. Our findings pinpoint novel genes and biological determinants of lignocellulosic hydrolysate inhibitor tolerance in yeast. These include the following: protein homeostasis constituents, including Ubp7p and Art5p, related to ubiquitin-mediated proteolysis; stress response transcriptional repressor, Nrg1p; and NADPH-dependent glutamate dehydrogenase, Gdh1p. Reverse engineering a prominent mutation in ubiquitin-specific protease gene UBP7 in a laboratory S. cerevisiae strain effectively increased spent sulphite liquor tolerance. CONCLUSIONS: This study advances understanding of yeast tolerance mechanisms to inhibitory substrates and biocatalyst design for a biomass-to-biofuel/biochemical industry, while providing insights into the process of mutation accumulation that occurs during genome shuffling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-015-0241-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4393574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43935742015-04-12 Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast Pinel, Dominic Colatriano, David Jiang, Heng Lee, Hung Martin, Vincent JJ Biotechnol Biofuels Research Article BACKGROUND: Identifying the genetic basis of complex microbial phenotypes is currently a major barrier to our understanding of multigenic traits and our ability to rationally design biocatalysts with highly specific attributes for the biotechnology industry. Here, we demonstrate that strain evolution by meiotic recombination-based genome shuffling coupled with deep sequencing can be used to deconstruct complex phenotypes and explore the nature of multigenic traits, while providing concrete targets for strain development. RESULTS: We determined genomic variations found within Saccharomyces cerevisiae previously evolved in our laboratory by genome shuffling for tolerance to spent sulphite liquor. The representation of these variations was backtracked through parental mutant pools and cross-referenced with RNA-seq gene expression analysis to elucidate the importance of single mutations and key biological processes that play a role in our trait of interest. Our findings pinpoint novel genes and biological determinants of lignocellulosic hydrolysate inhibitor tolerance in yeast. These include the following: protein homeostasis constituents, including Ubp7p and Art5p, related to ubiquitin-mediated proteolysis; stress response transcriptional repressor, Nrg1p; and NADPH-dependent glutamate dehydrogenase, Gdh1p. Reverse engineering a prominent mutation in ubiquitin-specific protease gene UBP7 in a laboratory S. cerevisiae strain effectively increased spent sulphite liquor tolerance. CONCLUSIONS: This study advances understanding of yeast tolerance mechanisms to inhibitory substrates and biocatalyst design for a biomass-to-biofuel/biochemical industry, while providing insights into the process of mutation accumulation that occurs during genome shuffling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-015-0241-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-31 /pmc/articles/PMC4393574/ /pubmed/25866561 http://dx.doi.org/10.1186/s13068-015-0241-z Text en © Pinel et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Pinel, Dominic Colatriano, David Jiang, Heng Lee, Hung Martin, Vincent JJ Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast |
title | Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast |
title_full | Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast |
title_fullStr | Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast |
title_full_unstemmed | Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast |
title_short | Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast |
title_sort | deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393574/ https://www.ncbi.nlm.nih.gov/pubmed/25866561 http://dx.doi.org/10.1186/s13068-015-0241-z |
work_keys_str_mv | AT pineldominic deconstructingthegeneticbasisofspentsulphiteliquortoleranceusingdeepsequencingofgenomeshuffledyeast AT colatrianodavid deconstructingthegeneticbasisofspentsulphiteliquortoleranceusingdeepsequencingofgenomeshuffledyeast AT jiangheng deconstructingthegeneticbasisofspentsulphiteliquortoleranceusingdeepsequencingofgenomeshuffledyeast AT leehung deconstructingthegeneticbasisofspentsulphiteliquortoleranceusingdeepsequencingofgenomeshuffledyeast AT martinvincentjj deconstructingthegeneticbasisofspentsulphiteliquortoleranceusingdeepsequencingofgenomeshuffledyeast |