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Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast
Metabolites are often unable to permeate cell membranes and are thus accumulated inside cells. We investigate whether engineered microbes can exclusively secrete intracellular metabolites because sustainable metabolite secretion holds a great potential for mass-production of high-value chemicals in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095633/ https://www.ncbi.nlm.nih.gov/pubmed/35546160 http://dx.doi.org/10.1038/s41467-022-30312-9 |
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author | Son, So-Hee Kim, Jae-Eung Park, Gyuri Ko, Young-Joon Sung, Bong Hyun Seo, Jongcheol Oh, Seung Soo Lee, Ju Young |
author_facet | Son, So-Hee Kim, Jae-Eung Park, Gyuri Ko, Young-Joon Sung, Bong Hyun Seo, Jongcheol Oh, Seung Soo Lee, Ju Young |
author_sort | Son, So-Hee |
collection | PubMed |
description | Metabolites are often unable to permeate cell membranes and are thus accumulated inside cells. We investigate whether engineered microbes can exclusively secrete intracellular metabolites because sustainable metabolite secretion holds a great potential for mass-production of high-value chemicals in an efficient and continuous manner. In this study, we demonstrate a synthetic pathway for a metabolite trafficking system that enables lipophilic terpene secretion by yeast cells. When metabolite-binding proteins are tagged with signal peptides, metabolite trafficking is highly achievable; loaded metabolites can be precisely delivered to a desired location within or outside the cell. As a proof of concept, we systematically couple a terpene-binding protein with an export signal peptide and subsequently demonstrate efficient, yet selective terpene secretion by yeast (~225 mg/L for squalene and ~1.6 mg/L for β-carotene). Other carrier proteins can also be readily fused with desired signal peptides, thereby tailoring different metabolite trafficking pathways in different microbes. To the best of our knowledge, this is the most efficient cognate pathway for metabolite secretion by microorganisms. |
format | Online Article Text |
id | pubmed-9095633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90956332022-05-13 Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast Son, So-Hee Kim, Jae-Eung Park, Gyuri Ko, Young-Joon Sung, Bong Hyun Seo, Jongcheol Oh, Seung Soo Lee, Ju Young Nat Commun Article Metabolites are often unable to permeate cell membranes and are thus accumulated inside cells. We investigate whether engineered microbes can exclusively secrete intracellular metabolites because sustainable metabolite secretion holds a great potential for mass-production of high-value chemicals in an efficient and continuous manner. In this study, we demonstrate a synthetic pathway for a metabolite trafficking system that enables lipophilic terpene secretion by yeast cells. When metabolite-binding proteins are tagged with signal peptides, metabolite trafficking is highly achievable; loaded metabolites can be precisely delivered to a desired location within or outside the cell. As a proof of concept, we systematically couple a terpene-binding protein with an export signal peptide and subsequently demonstrate efficient, yet selective terpene secretion by yeast (~225 mg/L for squalene and ~1.6 mg/L for β-carotene). Other carrier proteins can also be readily fused with desired signal peptides, thereby tailoring different metabolite trafficking pathways in different microbes. To the best of our knowledge, this is the most efficient cognate pathway for metabolite secretion by microorganisms. Nature Publishing Group UK 2022-05-11 /pmc/articles/PMC9095633/ /pubmed/35546160 http://dx.doi.org/10.1038/s41467-022-30312-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Son, So-Hee Kim, Jae-Eung Park, Gyuri Ko, Young-Joon Sung, Bong Hyun Seo, Jongcheol Oh, Seung Soo Lee, Ju Young Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast |
title | Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast |
title_full | Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast |
title_fullStr | Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast |
title_full_unstemmed | Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast |
title_short | Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast |
title_sort | metabolite trafficking enables membrane-impermeable-terpene secretion by yeast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095633/ https://www.ncbi.nlm.nih.gov/pubmed/35546160 http://dx.doi.org/10.1038/s41467-022-30312-9 |
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