4.3 Article

Towards Area-Based In Vitro Metabolic Engineering: Assembly of Pfs Enzyme onto Patterned Microfabricated Chips

期刊

BIOTECHNOLOGY PROGRESS
卷 24, 期 5, 页码 1042-1051

出版社

WILEY
DOI: 10.1002/btpr.44

关键词

S-adenosylhomocysteine nucleosidase; enzyme assembly; enzyme immobilization; pro-tag; chitosan

资金

  1. Robert W. Deutsch Foundation
  2. Natural Science Foundation [EFRI-735987]
  3. Directorate For Engineering
  4. Emerging Frontiers & Multidisciplinary Activities [1042881] Funding Source: National Science Foundation

向作者/读者索取更多资源

We report an approach for spatially selective assembly of an enzyme onto selected patterns of microfabricated chips. Our approach is based on electrodeposition of the aminopolysaccharide chitosan onto selected electrode patterns and covalent conjugation of a target enzyme to chitosan upon biochemical activation of a genetically fused pro-tag. We report assembly of S-adenosylhomocysteine nucleosidase (Pfs) fused with a C-terminal pentatyrosine pro-tag. Pfs is a member of the bacterial autoinducer-2 biosynthesis pathway, catalyzing the irreversible cleavage of S-adenosylhomocysteine. The assembled Pfs retains its catalytic activity and structure, as demonstrated by retained antibody recognition. Assembly is controlled by the electrode area, resulting in reproducible rates of catalytic conversion for a given area, and thus allowing for area-based manipulation of catalysis and small molecule biosynthesis. Our approach enables optimization of small molecule biosynthesis 1-step as well as multistep enzymatic reactions, including entire metabolic pathways, and we envision a wide variety of potential applications.

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