DC Field | Value | Language |
---|---|---|
dc.contributor.author | S H Son | - |
dc.contributor.author | J E Kim | - |
dc.contributor.author | G Park | - |
dc.contributor.author | Y J Ko | - |
dc.contributor.author | Bong Hyun Sung | - |
dc.contributor.author | J Seo | - |
dc.contributor.author | S S Oh | - |
dc.contributor.author | J Y Lee | - |
dc.date.accessioned | 2022-05-16T15:31:44Z | - |
dc.date.available | 2022-05-16T15:31:44Z | - |
dc.date.issued | 2022 | - |
dc.identifier.issn | 2041-1723 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/26004 | - |
dc.description.abstract | 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. | - |
dc.publisher | Springer-Nature Pub Group | - |
dc.title | Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast | - |
dc.title.alternative | Metabolite trafficking enables membrane-impermeable-terpene secretion by yeast | - |
dc.type | Article | - |
dc.citation.title | Nature Communications | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 2605 | - |
dc.citation.startPage | 2605 | - |
dc.citation.volume | 13 | - |
dc.contributor.affiliatedAuthor | Bong Hyun Sung | - |
dc.contributor.alternativeName | 손소희 | - |
dc.contributor.alternativeName | 김재응 | - |
dc.contributor.alternativeName | 박규리 | - |
dc.contributor.alternativeName | 고영준 | - |
dc.contributor.alternativeName | 성봉현 | - |
dc.contributor.alternativeName | 서종철 | - |
dc.contributor.alternativeName | 오승수 | - |
dc.contributor.alternativeName | 이주영 | - |
dc.identifier.bibliographicCitation | Nature Communications, vol. 13, pp. 2605-2605 | - |
dc.identifier.doi | 10.1038/s41467-022-30312-9 | - |
dc.description.journalClass | Y | - |
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