ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

S-adenosyl-L-methionine is required for DNA cleavage by type III restriction enzymes

Bist, Pradeep and Sistla, Srivani and Krishnamurthy, Vinita and Acharya, Asha and Chandrakala, Basavannachar and Rao, Desirazu N (2001) S-adenosyl-L-methionine is required for DNA cleavage by type III restriction enzymes. In: Journal of Molecular Biology, 310 (1). pp. 93-109.

[img] PDF
S-adenosyl--methionine.pdf - Published Version
Restricted to Registered users only

Download (362kB) | Request a copy
Official URL: http://dx.doi.org/10.1006/jmbi.2001.4744


The requirement of S-adenosyl- -methionine (AdoMet) in the cleavage reaction carried out by type III restriction-modification enzymes has been investigated. We show that DNA restriction by EcoPI restriction enzyme does not take place in the absence of exogenously added AdoMet. Interestingly, the closely related EcoP15I enzyme has endogenously bound AdoMet and therefore does not require the addition of the cofactor for DNA cleavage. By employing a variety of AdoMet analogs, which differ structurally from AdoMet, this study demonstrates that the carboxyl group and any substitution at the epsilon carbon of methionine is absolutely essential for DNA cleavage. Such analogs could bring about the necessary conformational change(s) in the enzyme, which make the enzyme proficient in DNA cleavage. Our studies, which include native polyacrylamide gel electrophoresis, molecular size exclusion chromatography, UV, fluorescence and circular dichroism spectroscopy, clearly demonstrate that the holoenzyme and apoenzyme forms of EcoP15I restriction enzyme have different conformations. Furthermore, the Res and Mod subunits of the EcoP15I restriction enzyme can be separated by gel filtration chromatography in the presence of 2 M NaCl. Reconstitution experiments, which involve mixing of the isolated subunits, result in an apoenzyme form, which is restriction proficient in the presence of AdoMet. However, mixing the Res subunit with Mod subunit deficient in AdoMet binding does not result in a functional restriction enzyme. These observations are consistent with the fact that AdoMet is required for DNA cleavage. In vivo complementation of the defective mod allele with a wild-type mod allele showed that an active restriction enzyme could be formed. Furthermore, we show that while the purified c2-134 mutant restriction enzyme is unable to cleave DNA, the c2-440 mutant enzyme is able to cleave DNA albeit poorly. Taken together, these results suggest that AdoMet binding causes conformational changes in the restriction enzyme and is necessary to bring about DNA cleavage.

Item Type: Journal Article
Publication: Journal of Molecular Biology
Publisher: Elsevier Science
Additional Information: Copyright of this article belongs to Elsevier Science.
Keywords: type III restriction;modification enzymes;AdoMet;apoenzyme; clear plaque mutants;DNA cleavage
Department/Centre: Division of Biological Sciences > Biochemistry
Date Deposited: 03 Oct 2007
Last Modified: 23 Feb 2012 07:09
URI: http://eprints.iisc.ac.in/id/eprint/12034

Actions (login required)

View Item View Item