Microfluidics-driven high-throughput phenotyping and screening in synthetic biology: from single cells to cell-free systems

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dc.contributor.authorTaeok Kim-
dc.contributor.authorMinji Ko-
dc.contributor.authorEugene Rha-
dc.contributor.authorHaseong Kim-
dc.contributor.authorHyewon Lee-
dc.date.accessioned2024-03-11T16:33:09Z-
dc.date.available2024-03-11T16:33:09Z-
dc.date.issued2024-
dc.identifier.issn1226-8372-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/33793-
dc.description.abstractThe interdisciplinary nature of synthetic biology merges engineering principles with biology and provides innovative solutions for issues in the biomanufacturing industry. To develop industrially applicable biocatalysts and/or microbial cell factories, a design-build-test-learn cycle-based iterative process is necessary, which is often time-consuming and labor-intensive. The integration of microfluidic technologies into synthetic biology can accelerate these processes, particularly for achieving high-throughput phenotyping and screening. In this review, we examine the potential of microfluidic technologies to revolutionize synthetic biology. Although commercial microfluidics demonstrate superior throughput for single-cell assays, their application can be limited, for example, in cases where products are retained inside the cells. Droplet microfluidics, on the other hand, is a rather flexible platform and shows high diversity in single-cell, cell-to-cell interaction-based, and cell-free reaction-based analyses. By examining previous studies, we have summarized the potential of microfluidic technologies to foster sustainable biomanufacturing and advanced biological engineering.-
dc.publisherSpringer-
dc.titleMicrofluidics-driven high-throughput phenotyping and screening in synthetic biology: from single cells to cell-free systems-
dc.title.alternativeMicrofluidics-driven high-throughput phenotyping and screening in synthetic biology: from single cells to cell-free systems-
dc.typeArticle-
dc.citation.titleBiotechnology and Bioprocess Engineering-
dc.citation.number0-
dc.citation.endPage33-
dc.citation.startPage25-
dc.citation.volume29-
dc.contributor.affiliatedAuthorTaeok Kim-
dc.contributor.affiliatedAuthorMinji Ko-
dc.contributor.affiliatedAuthorEugene Rha-
dc.contributor.affiliatedAuthorHaseong Kim-
dc.contributor.affiliatedAuthorHyewon Lee-
dc.contributor.alternativeName김태옥-
dc.contributor.alternativeName고민지-
dc.contributor.alternativeName나유진-
dc.contributor.alternativeName김하성-
dc.contributor.alternativeName이혜원-
dc.identifier.bibliographicCitationBiotechnology and Bioprocess Engineering, vol. 29, pp. 25-33-
dc.identifier.doi10.1007/s12257-024-00016-6-
dc.subject.keywordMicrofuidics-
dc.subject.keywordSynthetic biology-
dc.subject.keywordHigh-throughput screening-
dc.subject.keywordBiofoundry-
dc.subject.localSynthetic Biology-
dc.subject.localSynthetic biology-
dc.subject.localsynthetic biology-
dc.subject.localHigh-throughput screening-
dc.subject.localHigh-throughput screening (HTS)-
dc.subject.localhigh-throughput screening-
dc.subject.localhighthroughput screening-
dc.subject.localbiofoundry-
dc.subject.localBiofoundry-
dc.description.journalClassY-
Appears in Collections:
Synthetic Biology and Bioengineering Research Institute > Synthetic Biology Research Center > 1. Journal Articles
Korea Biofoundry > 1. Journal Articles
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