Literature DB >> 25343575

Discovery of catalytic phages by biocatalytic self-assembly.

Yoshiaki Maeda1, Nadeem Javid, Krystyna Duncan, Louise Birchall, Kirsty F Gibson, Daniel Cannon, Yuka Kanetsuki, Charles Knapp, Tell Tuttle, Rein V Ulijn, Hiroshi Matsui.   

Abstract

Discovery of new catalysts for demanding aqueous reactions is challenging. Here, we describe methodology for selection of catalytic phages by taking advantage of localized assembly of the product of the catalytic reaction that is screened for. A phage display library covering 10(9) unique dodecapeptide sequences is incubated with nonassembling precursors. Phages which are able to catalyze formation of the self-assembling reaction product (via amide condensation) acquire an aggregate of reaction product, enabling separation by centrifugation. The thus selected phages can be amplified by infection of Escherichia coli. These phages are shown to catalyze amide condensation and hydrolysis. Kinetic analysis shows a minor role for substrate binding. The approach enables discovery and mass-production of biocatalytic phages.

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Year:  2014        PMID: 25343575      PMCID: PMC6390487          DOI: 10.1021/ja509393p

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  30 in total

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9.  Enzymatic modification of self-assembled peptide structures with tissue transglutaminase.

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  15 in total

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9.  Biocatalysts Based on Peptide and Peptide Conjugate Nanostructures.

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10.  Molecular Self-Assembly Strategy for Generating Catalytic Hybrid Polypeptides.

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