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Biocatalytic cascade to polysaccharide amination

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  • معلومة اضافية
    • Contributors:
      Department of Bioproducts and Biosystems; Protein Technology; University of Toronto; University of Helsinki; Aalto-yliopisto; Aalto University
    • بيانات النشر:
      BioMed Central
    • الموضوع:
      2024
    • Collection:
      Aalto University Publication Archive (Aaltodoc) / Aalto-yliopiston julkaisuarkistoa
    • نبذة مختصرة :
      Publisher Copyright: © The Author(s) 2024. ; Background: Chitin, the main form of aminated polysaccharide in nature, is a biocompatible, polycationic, and antimicrobial biopolymer used extensively in industrial processes. Despite the abundance of chitin, applications thereof are hampered by difficulties in feedstock harvesting and limited structural versatility. To address these problems, we proposed a two-step cascade employing carbohydrate oxidoreductases and amine transaminases for plant polysaccharide aminations via one-pot reactions. Using a galactose oxidase from Fusarium graminearum for oxidation, this study compared the performance of CvATA (from Chromobacterium violaceum) and SpATA (from Silicibacter pomeroyi) on a range of oxidized carbohydrates with various structures and sizes. Using a rational enzyme engineering approach, four point mutations were introduced on the SpATA surface, and their effects on enzyme activity were evaluated. Results: Herein, a quantitative colorimetric assay was developed to enable simple and accurate time-course measurement of the yield of transamination reactions. With higher operational stability, SpATA produced higher product yields in 36 h reactions despite its lower initial activity. Successful amination of oxidized galactomannan by SpATA was confirmed using a deuterium labeling method; higher aminated carbohydrate yields achieved with SpATA compared to CvATA were verified using HPLC and XPS. By balancing the oxidase and transaminase loadings, improved operating conditions were identified where the side product formation was largely suppressed without negatively impacting the product yield. SpATA mutants with multiple alanine substitutions besides E407A showed improved product yield. The E407A mutation reduced SpATA activity substantially, supporting its predicted role in maintaining the dimeric enzyme structure. Conclusions: Using oxidase–amine transaminase cascades, the study demonstrated a fully enzymatic route to polysaccharide amination. Although the activity of ...
    • File Description:
      application/pdf
    • ISSN:
      2731-3654
    • Relation:
      Biotechnology for Biofuels and Bioproducts; Volume 17, issue 1; Feng, X, Hong, S, Zhao, H, Vuong, T V & Master, E R 2024, ' Biocatalytic cascade to polysaccharide amination ', Biotechnology for Biofuels and Bioproducts, vol. 17, no. 1, 34 . https://doi.org/10.1186/s13068-024-02477-6; PURE UUID: 23262504-38a1-482c-8a81-bfc704ab24fe; PURE ITEMURL: https://research.aalto.fi/en/publications/23262504-38a1-482c-8a81-bfc704ab24fe; PURE LINK: http://www.scopus.com/inward/record.url?scp=85185933180&partnerID=8YFLogxK; PURE FILEURL: https://research.aalto.fi/files/141572351/CHEM_Feng_et_al_Biocatalytic_cascade_2024_Biotechnol_Biofuels.pdf; https://aaltodoc.aalto.fi/handle/123456789/127186; URN:NBN:fi:aalto-202403202823
    • الرقم المعرف:
      10.1186/s13068-024-02477-6
    • Rights:
      openAccess
    • الرقم المعرف:
      edsbas.BDC07E5D