Issue 21, 2004
From the journal:

Chemical Communications

Photochemical regulation of the activity of an endonuclease BamHI using an azobenzene moiety incorporated site-selectively into the dimer interface

Koji Nakayama,a   Masayuki Endoa  and  Tetsuro Majima*a  

* Corresponding authors

a Institute of Scientific and Industrial Research, Osaka University, 8-1 Mihogaoka, Ibaraki, Osaka, Japan
E-mail: majima@sanken.osaka-u.ac.jp
Fax: +81-6-6879-8499
Tel: +81-6-6879-8495

Abstract

Endonuclease BamHI mutants having an azophenylalanine residue in the dimer interface (azoAla-BamHI) were synthesized; while the activity was almost suppressed using trans-azoAla-BamHI, the cis-isomer generated with photoirradiation recovered its intrinsic activity.

Graphical abstract: Photochemical regulation of the activity of an endonuclease BamHI using an azobenzene moiety incorporated site-selectively into the dimer interface

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Article information

DOI
https://doi.org/10.1039/B409844G
Article type
Communication
Submitted
30 Jun 2004
Accepted
09 Aug 2004
First published
20 Sep 2004

Chem. Commun., 2004, 2386-2387

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Photochemical regulation of the activity of an endonuclease BamHI using an azobenzene moiety incorporated site-selectively into the dimer interface

K. Nakayama, M. Endo and T. Majima, Chem. Commun., 2004, 2386 DOI: 10.1039/B409844G

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