Cargando…
Laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting S. cerevisiae strain reveals mutations in GAL2 that enable glucose-insensitive l-arabinose uptake
Cas9-assisted genome editing was used to construct an engineered glucose-phosphorylation-negative S. cerevisiae strain, expressing the Lactobacillus plantaruml-arabinose pathway and the Penicillium chrysogenum transporter PcAraT. This strain, which showed a growth rate of 0.26 h(−1) on l-arabinose i...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044391/ https://www.ncbi.nlm.nih.gov/pubmed/29860442 http://dx.doi.org/10.1093/femsyr/foy062 |
_version_ | 1783339475166822400 |
---|---|
author | Verhoeven, Maarten D Bracher, Jasmine M Nijland, Jeroen G Bouwknegt, Jonna Daran, Jean-Marc G Driessen, Arnold J M van Maris, Antonius J A Pronk, Jack T |
author_facet | Verhoeven, Maarten D Bracher, Jasmine M Nijland, Jeroen G Bouwknegt, Jonna Daran, Jean-Marc G Driessen, Arnold J M van Maris, Antonius J A Pronk, Jack T |
author_sort | Verhoeven, Maarten D |
collection | PubMed |
description | Cas9-assisted genome editing was used to construct an engineered glucose-phosphorylation-negative S. cerevisiae strain, expressing the Lactobacillus plantaruml-arabinose pathway and the Penicillium chrysogenum transporter PcAraT. This strain, which showed a growth rate of 0.26 h(−1) on l-arabinose in aerobic batch cultures, was subsequently evolved for anaerobic growth on l-arabinose in the presence of d-glucose and d-xylose. In four strains isolated from two independent evolution experiments the galactose-transporter gene GAL2 had been duplicated, with all alleles encoding Gal2(N376T) or Gal2(N376I) substitutions. In one strain, a single GAL2 allele additionally encoded a Gal2(T89I) substitution, which was subsequently also detected in the independently evolved strain IMS0010. In (14)C-sugar-transport assays, Gal2(N376S), Gal2(N376T) and Gal2(N376I) substitutions showed a much lower glucose sensitivity of l-arabinose transport and a much higher K(m) for d-glucose transport than wild-type Gal2. Introduction of the Gal2(N376I) substitution in a non-evolved strain enabled growth on l-arabinose in the presence of d-glucose. Gal2(N376T, T89I) and Gal2(T89I) variants showed a lower K(m) for l-arabinose and a higher K(m) for d-glucose than wild-type Gal2, while reverting Gal2(N376T, T89I) to Gal2(N376) in an evolved strain negatively affected anaerobic growth on l-arabinose. This study indicates that optimal conversion of mixed-sugar feedstocks may require complex ‘transporter landscapes’, consisting of sugar transporters with complementary kinetic and regulatory properties. |
format | Online Article Text |
id | pubmed-6044391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60443912018-07-19 Laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting S. cerevisiae strain reveals mutations in GAL2 that enable glucose-insensitive l-arabinose uptake Verhoeven, Maarten D Bracher, Jasmine M Nijland, Jeroen G Bouwknegt, Jonna Daran, Jean-Marc G Driessen, Arnold J M van Maris, Antonius J A Pronk, Jack T FEMS Yeast Res Research Article Cas9-assisted genome editing was used to construct an engineered glucose-phosphorylation-negative S. cerevisiae strain, expressing the Lactobacillus plantaruml-arabinose pathway and the Penicillium chrysogenum transporter PcAraT. This strain, which showed a growth rate of 0.26 h(−1) on l-arabinose in aerobic batch cultures, was subsequently evolved for anaerobic growth on l-arabinose in the presence of d-glucose and d-xylose. In four strains isolated from two independent evolution experiments the galactose-transporter gene GAL2 had been duplicated, with all alleles encoding Gal2(N376T) or Gal2(N376I) substitutions. In one strain, a single GAL2 allele additionally encoded a Gal2(T89I) substitution, which was subsequently also detected in the independently evolved strain IMS0010. In (14)C-sugar-transport assays, Gal2(N376S), Gal2(N376T) and Gal2(N376I) substitutions showed a much lower glucose sensitivity of l-arabinose transport and a much higher K(m) for d-glucose transport than wild-type Gal2. Introduction of the Gal2(N376I) substitution in a non-evolved strain enabled growth on l-arabinose in the presence of d-glucose. Gal2(N376T, T89I) and Gal2(T89I) variants showed a lower K(m) for l-arabinose and a higher K(m) for d-glucose than wild-type Gal2, while reverting Gal2(N376T, T89I) to Gal2(N376) in an evolved strain negatively affected anaerobic growth on l-arabinose. This study indicates that optimal conversion of mixed-sugar feedstocks may require complex ‘transporter landscapes’, consisting of sugar transporters with complementary kinetic and regulatory properties. Oxford University Press 2018-05-31 /pmc/articles/PMC6044391/ /pubmed/29860442 http://dx.doi.org/10.1093/femsyr/foy062 Text en © FEMS 2018. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Verhoeven, Maarten D Bracher, Jasmine M Nijland, Jeroen G Bouwknegt, Jonna Daran, Jean-Marc G Driessen, Arnold J M van Maris, Antonius J A Pronk, Jack T Laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting S. cerevisiae strain reveals mutations in GAL2 that enable glucose-insensitive l-arabinose uptake |
title | Laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting S. cerevisiae strain reveals mutations in GAL2 that enable glucose-insensitive l-arabinose uptake |
title_full | Laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting S. cerevisiae strain reveals mutations in GAL2 that enable glucose-insensitive l-arabinose uptake |
title_fullStr | Laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting S. cerevisiae strain reveals mutations in GAL2 that enable glucose-insensitive l-arabinose uptake |
title_full_unstemmed | Laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting S. cerevisiae strain reveals mutations in GAL2 that enable glucose-insensitive l-arabinose uptake |
title_short | Laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting S. cerevisiae strain reveals mutations in GAL2 that enable glucose-insensitive l-arabinose uptake |
title_sort | laboratory evolution of a glucose-phosphorylation-deficient, arabinose-fermenting s. cerevisiae strain reveals mutations in gal2 that enable glucose-insensitive l-arabinose uptake |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044391/ https://www.ncbi.nlm.nih.gov/pubmed/29860442 http://dx.doi.org/10.1093/femsyr/foy062 |
work_keys_str_mv | AT verhoevenmaartend laboratoryevolutionofaglucosephosphorylationdeficientarabinosefermentingscerevisiaestrainrevealsmutationsingal2thatenableglucoseinsensitivelarabinoseuptake AT bracherjasminem laboratoryevolutionofaglucosephosphorylationdeficientarabinosefermentingscerevisiaestrainrevealsmutationsingal2thatenableglucoseinsensitivelarabinoseuptake AT nijlandjeroeng laboratoryevolutionofaglucosephosphorylationdeficientarabinosefermentingscerevisiaestrainrevealsmutationsingal2thatenableglucoseinsensitivelarabinoseuptake AT bouwknegtjonna laboratoryevolutionofaglucosephosphorylationdeficientarabinosefermentingscerevisiaestrainrevealsmutationsingal2thatenableglucoseinsensitivelarabinoseuptake AT daranjeanmarcg laboratoryevolutionofaglucosephosphorylationdeficientarabinosefermentingscerevisiaestrainrevealsmutationsingal2thatenableglucoseinsensitivelarabinoseuptake AT driessenarnoldjm laboratoryevolutionofaglucosephosphorylationdeficientarabinosefermentingscerevisiaestrainrevealsmutationsingal2thatenableglucoseinsensitivelarabinoseuptake AT vanmarisantoniusja laboratoryevolutionofaglucosephosphorylationdeficientarabinosefermentingscerevisiaestrainrevealsmutationsingal2thatenableglucoseinsensitivelarabinoseuptake AT pronkjackt laboratoryevolutionofaglucosephosphorylationdeficientarabinosefermentingscerevisiaestrainrevealsmutationsingal2thatenableglucoseinsensitivelarabinoseuptake |