Cargando…
A common inducer molecule enhances sugar utilization by Shewanella oneidensis MR-1
Shewanella oneidensis MR-1 is an electroactive bacterium that is a promising host for bioelectrochemical technologies, which makes it a common target for genetic engineering, including gene deletions and expression of heterologous pathways. Expression of heterologous genes and gene knockdown via CRI...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10549210/ https://www.ncbi.nlm.nih.gov/pubmed/37537149 http://dx.doi.org/10.1093/jimb/kuad018 |
_version_ | 1785115373431947264 |
---|---|
author | Gruenberg, Megan C TerAvest, Michaela A |
author_facet | Gruenberg, Megan C TerAvest, Michaela A |
author_sort | Gruenberg, Megan C |
collection | PubMed |
description | Shewanella oneidensis MR-1 is an electroactive bacterium that is a promising host for bioelectrochemical technologies, which makes it a common target for genetic engineering, including gene deletions and expression of heterologous pathways. Expression of heterologous genes and gene knockdown via CRISPRi in S. oneidensis are both frequently induced by β-D-1-thiogalactopyranoside (IPTG), a commonly used inducer molecule across many model organisms. Here, we report and characterize an unexpected phenotype; IPTG enhances the growth of wild-type S. oneidensis MR-1 on the sugar substrate N-acetylglucosamine (NAG). IPTG improves the carrying capacity of S. oneidensis growing on NAG while the growth rate remains similar to cultures without the inducer. Extracellular acetate accumulates faster and to a higher concentration in cultures without IPTG than those with it. IPTG appears to improve acetate metabolism, which combats the negative effect that acetate accumulation has on the growth of S. oneidensis with NAG. We recommend using extensive experimental controls and careful data interpretation when using both NAG and IPTG in S. oneidensis cultures. |
format | Online Article Text |
id | pubmed-10549210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105492102023-10-05 A common inducer molecule enhances sugar utilization by Shewanella oneidensis MR-1 Gruenberg, Megan C TerAvest, Michaela A J Ind Microbiol Biotechnol Metabolic Engineering and Synthetic Biology Shewanella oneidensis MR-1 is an electroactive bacterium that is a promising host for bioelectrochemical technologies, which makes it a common target for genetic engineering, including gene deletions and expression of heterologous pathways. Expression of heterologous genes and gene knockdown via CRISPRi in S. oneidensis are both frequently induced by β-D-1-thiogalactopyranoside (IPTG), a commonly used inducer molecule across many model organisms. Here, we report and characterize an unexpected phenotype; IPTG enhances the growth of wild-type S. oneidensis MR-1 on the sugar substrate N-acetylglucosamine (NAG). IPTG improves the carrying capacity of S. oneidensis growing on NAG while the growth rate remains similar to cultures without the inducer. Extracellular acetate accumulates faster and to a higher concentration in cultures without IPTG than those with it. IPTG appears to improve acetate metabolism, which combats the negative effect that acetate accumulation has on the growth of S. oneidensis with NAG. We recommend using extensive experimental controls and careful data interpretation when using both NAG and IPTG in S. oneidensis cultures. Oxford University Press 2023-08-03 /pmc/articles/PMC10549210/ /pubmed/37537149 http://dx.doi.org/10.1093/jimb/kuad018 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society of Industrial Microbiology and Biotechnology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Metabolic Engineering and Synthetic Biology Gruenberg, Megan C TerAvest, Michaela A A common inducer molecule enhances sugar utilization by Shewanella oneidensis MR-1 |
title | A common inducer molecule enhances sugar utilization by Shewanella oneidensis MR-1 |
title_full | A common inducer molecule enhances sugar utilization by Shewanella oneidensis MR-1 |
title_fullStr | A common inducer molecule enhances sugar utilization by Shewanella oneidensis MR-1 |
title_full_unstemmed | A common inducer molecule enhances sugar utilization by Shewanella oneidensis MR-1 |
title_short | A common inducer molecule enhances sugar utilization by Shewanella oneidensis MR-1 |
title_sort | common inducer molecule enhances sugar utilization by shewanella oneidensis mr-1 |
topic | Metabolic Engineering and Synthetic Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10549210/ https://www.ncbi.nlm.nih.gov/pubmed/37537149 http://dx.doi.org/10.1093/jimb/kuad018 |
work_keys_str_mv | AT gruenbergmeganc acommoninducermoleculeenhancessugarutilizationbyshewanellaoneidensismr1 AT teravestmichaelaa acommoninducermoleculeenhancessugarutilizationbyshewanellaoneidensismr1 AT gruenbergmeganc commoninducermoleculeenhancessugarutilizationbyshewanellaoneidensismr1 AT teravestmichaelaa commoninducermoleculeenhancessugarutilizationbyshewanellaoneidensismr1 |