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A synthetic microbial biosensor for high-throughput screening of lactam biocatalysts

Author

Listed:
  • Soo-Jin Yeom

    (KRIBB)

  • Moonjeong Kim

    (KRIBB
    Chungnam National University)

  • Kil Koang Kwon

    (KRIBB)

  • Yaoyao Fu

    (KRIBB)

  • Eugene Rha

    (KRIBB)

  • Sung-Hyun Park

    (KRIBB
    University of Science and Technology)

  • Hyewon Lee

    (KRIBB)

  • Haseong Kim

    (KRIBB
    University of Science and Technology)

  • Dae-Hee Lee

    (KRIBB
    University of Science and Technology)

  • Dong-Myung Kim

    (Chungnam National University)

  • Seung-Goo Lee

    (KRIBB
    University of Science and Technology)

Abstract

Biocatalytic 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.

Suggested Citation

  • Soo-Jin Yeom & Moonjeong Kim & Kil Koang Kwon & Yaoyao Fu & Eugene Rha & Sung-Hyun Park & Hyewon Lee & Haseong Kim & Dae-Hee Lee & Dong-Myung Kim & Seung-Goo Lee, 2018. "A synthetic microbial biosensor for high-throughput screening of lactam biocatalysts," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-07488-0
    DOI: 10.1038/s41467-018-07488-0
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    Cited by:

    1. Elizabeth L. Bell & Gloria Rosetto & Morgan A. Ingraham & Kelsey J. Ramirez & Clarissa Lincoln & Ryan W. Clarke & Japheth E. Gado & Jacob L. Lilly & Katarzyna H. Kucharzyk & Erika Erickson & Gregg T. , 2024. "Natural diversity screening, assay development, and characterization of nylon-6 enzymatic depolymerization," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    2. Dae-yeol Ye & Myung Hyun Noh & Jo Hyun Moon & Alfonsina Milito & Minsun Kim & Jeong Wook Lee & Jae-Seong Yang & Gyoo Yeol Jung, 2022. "Kinetic compartmentalization by unnatural reaction for itaconate production," Nature Communications, Nature, vol. 13(1), pages 1-10, December.

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