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A streamlined strain engineering workflow with genome-wide screening detects enhanced protein secretion in Komagataella phaffii.
Ito, Yoichiro; Ishigami, Misa; Terai, Goro; Nakamura, Yasuyuki; Hashiba, Noriko; Nishi, Teruyuki; Nakazawa, Hikaru; Hasunuma, Tomohisa; Asai, Kiyoshi; Umetsu, Mitsuo; Ishii, Jun; Kondo, Akihiko.
Afiliación
  • Ito Y; Engineering Biology Research Center, Kobe University, Kobe, Japan.
  • Ishigami M; Graduate School of Science, Technology and Innovation, Kobe University, Kobe, Japan.
  • Terai G; Technology Research Association of Highly Efficient Gene Design (TRAHED), Kobe, Japan.
  • Nakamura Y; Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, University of Tokyo, Chiba, Japan.
  • Hashiba N; Engineering Biology Research Center, Kobe University, Kobe, Japan.
  • Nishi T; Graduate School of Science, Technology and Innovation, Kobe University, Kobe, Japan.
  • Nakazawa H; Technology Research Association of Highly Efficient Gene Design (TRAHED), Kobe, Japan.
  • Hasunuma T; Graduate School of Science, Technology and Innovation, Kobe University, Kobe, Japan.
  • Asai K; Bio-Pharma Research Laboratories, Kaneka Corporation, Takasago, Japan.
  • Umetsu M; Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University, Sendai, Japan.
  • Ishii J; Engineering Biology Research Center, Kobe University, Kobe, Japan.
  • Kondo A; Graduate School of Science, Technology and Innovation, Kobe University, Kobe, Japan.
Commun Biol ; 5(1): 561, 2022 06 08.
Article en En | MEDLINE | ID: mdl-35676418
ABSTRACT
Expression of secreted recombinant proteins burdens the protein secretion machinery, limiting production. Here, we describe an approach to improving protein production by the non-conventional yeast Komagataella phaffii comprised of genome-wide screening for effective gene disruptions, combining them in a single strain, and recovering growth reduction by adaptive evolution. For the screen, we designed a multiwell-formatted, streamlined workflow to high-throughput assay of secretion of a single-chain small antibody, which is cumbersome to detect but serves as a good model of proteins that are difficult to secrete. Using the consolidated screening system, we evaluated >19,000 mutant strains from a mutant library prepared by a modified random gene-disruption method, and identified six factors for which disruption led to increased antibody production. We then combined the disruptions, up to quadruple gene knockouts, which appeared to contribute independently, in a single strain and observed an additive effect. Target protein and promoter were basically interchangeable for the effects of knockout genes screened. We finally used adaptive evolution to recover reduced cell growth by multiple gene knockouts and examine the possibility for further enhancing protein secretion. Our successful, three-part approach holds promise as a method for improving protein production by non-conventional microorganisms.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomycetales Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Idioma: En Revista: Commun Biol Año: 2022 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomycetales Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Idioma: En Revista: Commun Biol Año: 2022 Tipo del documento: Article País de afiliación: Japón