Maeda Yoshiaki, Javid Nadeem, Duncan Krystyna, Birchall Louise, Gibson Kirsty F, Cannon Daniel, Kanetsuki Yuka, Knapp Charles, Tuttle Tell, Ulijn Rein V, Matsui Hiroshi
Department of Chemistry and Biochemistry, Hunter College, City University of New York , 695 Park Avenue, New York, New York 10065, United States.
J Am Chem Soc. 2014 Nov 12;136(45):15893-6. doi: 10.1021/ja509393p. Epub 2014 Oct 29.
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.
发现适用于苛刻水相反应的新型催化剂具有挑战性。在此,我们描述了一种通过利用所筛选催化反应产物的局部组装来选择催化噬菌体的方法。将一个覆盖10⁹个独特十二肽序列的噬菌体展示文库与非组装前体一起孵育。能够催化自组装反应产物形成(通过酰胺缩合)的噬菌体获得反应产物聚集体,从而能够通过离心分离。如此筛选出的噬菌体可通过感染大肠杆菌进行扩增。这些噬菌体被证明能催化酰胺缩合和水解反应。动力学分析表明底物结合作用较小。该方法能够实现生物催化噬菌体的发现和大规模生产。