Issue 26, 2016

Chemoenzymatic synthesis and utilization of a SAM analog with an isomorphic nucleobase

Abstract

SalL, an enzyme that catalyzes the synthesis of SAM from L-methionine and 5′-chloro-5′-deoxyoadenosine, is shown to accept 5′-chloro-5′-deoxythienoadenosine as a substrate and facilitate the synthesis of a synthetic SAM analog with an unnatural nucleobase. This synthetic cofactor is demonstrated to replace SAM in the DNA methylation reaction with M.TaqI.

Graphical abstract: Chemoenzymatic synthesis and utilization of a SAM analog with an isomorphic nucleobase

Supplementary files

Article information

Article type
Communication
Submitted
19 Apr 2016
Accepted
24 May 2016
First published
24 May 2016
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2016,14, 6189-6192

Chemoenzymatic synthesis and utilization of a SAM analog with an isomorphic nucleobase

C. Vranken, A. Fin, P. Tufar, J. Hofkens, M. D. Burkart and Y. Tor, Org. Biomol. Chem., 2016, 14, 6189 DOI: 10.1039/C6OB00844E

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