A synthetic microbial biosensor for highthroughput screening of lactam biocatalysts

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dc.contributor.authorSoo Jin Yeom-
dc.contributor.authorMoonjeong Kim-
dc.contributor.authorKil Koang Kwon-
dc.contributor.authorY Fu-
dc.contributor.authorEugene Rha-
dc.contributor.authorSung-Hyun Park-
dc.contributor.authorHyewon Lee-
dc.contributor.authorHaseong Kim-
dc.contributor.authorDae-Hee Lee-
dc.contributor.authorD M Kim-
dc.contributor.authorSeung Goo Lee-
dc.date.accessioned2019-01-23T16:30:54Z-
dc.date.available2019-01-23T16:30:54Z-
dc.date.issued2018-
dc.identifier.issn2041-1723-
dc.identifier.uri10.1038/s41467-018-07488-0ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18235-
dc.description.abstractBiocatalytic cyclization is highly desirable for efficient synthesis of biologically derived chemical substances, such as the commodity chemicals ε-caprolactam and δ-valerolactam. To identify biocatalysts in lactam biosynthesis, we develop a caprolactam-detecting genetic enzyme screening system (CL-GESS). The Alcaligenes faecalis regulatory protein NitR is adopted for the highly specific detection of lactam compounds against lactam biosynthetic intermediates. We further systematically optimize the genetic components of the CL-GESS to enhance sensitivity, achieving 10-fold improvement. Using this highly sensitive GESS, we screen marine metagenomes and find an enzyme that cyclizes ω-amino fatty acids to lactam. Moreover, we determine the X-ray crystal structure and catalytic residues based on mutational analysis of the cyclase. The cyclase is also used as a helper enzyme to sense intracellular ω-amino fatty acids. We expect this simple and accurate biosensor to have wide-ranging applications in rapid screening of new lactam-synthesizing enzymes and metabolic engineering for lactam bio-production.-
dc.publisherSpringer-Nature Pub Group-
dc.titleA synthetic microbial biosensor for highthroughput screening of lactam biocatalysts-
dc.title.alternativeA synthetic microbial biosensor for highthroughput screening of lactam biocatalysts-
dc.typeArticle-
dc.citation.titleNature Communications-
dc.citation.number0-
dc.citation.endPage5053-
dc.citation.startPage5053-
dc.citation.volume9-
dc.contributor.affiliatedAuthorSoo Jin Yeom-
dc.contributor.affiliatedAuthorMoonjeong Kim-
dc.contributor.affiliatedAuthorKil Koang Kwon-
dc.contributor.affiliatedAuthorEugene Rha-
dc.contributor.affiliatedAuthorSung-Hyun Park-
dc.contributor.affiliatedAuthorHyewon Lee-
dc.contributor.affiliatedAuthorHaseong Kim-
dc.contributor.affiliatedAuthorDae-Hee Lee-
dc.contributor.affiliatedAuthorSeung Goo Lee-
dc.contributor.alternativeName염수진-
dc.contributor.alternativeName김문정-
dc.contributor.alternativeName권길광-
dc.contributor.alternativeNameFu-
dc.contributor.alternativeName나유진-
dc.contributor.alternativeName박성현-
dc.contributor.alternativeName이혜원-
dc.contributor.alternativeName김하성-
dc.contributor.alternativeName이대희-
dc.contributor.alternativeName김동명-
dc.contributor.alternativeName이승구-
dc.identifier.bibliographicCitationNature Communications, vol. 9, pp. 5053-5053-
dc.identifier.doi10.1038/s41467-018-07488-0-
dc.description.journalClassY-
Appears in Collections:
Korea Biofoundry > 1. Journal Articles
Synthetic Biology and Bioengineering Research Institute > Synthetic Biology Research Center > 1. Journal Articles
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