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S-adenosyl-L-methionine is required for DNA cleavage by type III restriction enzymes
P Bist1, S Sistla, V Krishnamurthy
1Department of Biochemistry, Indian Institute of Science, Bangalore, 560 012, India.
Abstract:
The requirement of S-adenosyl-L-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.
Insights
S-adenosyl-L-methionine (AdoMet) is crucial for DNA cleavage by type III restriction enzymes like EcoPI. AdoMet binding induces conformational changes, making the enzyme proficient in DNA restriction.
Area of Science:
- Molecular Biology
- Enzymology
- Biochemistry
Background:
- Type III restriction-modification enzymes utilize S-adenosyl-L-methionine (AdoMet) for DNA cleavage.
- The specific role and necessity of AdoMet in this process vary between related enzymes, such as EcoPI and EcoP15I.
Purpose of the Study:
- To investigate the essential role of AdoMet in the DNA cleavage activity of type III restriction enzymes.
- To elucidate the structural and functional requirements of AdoMet for enzyme activity.
- To understand the conformational changes induced by AdoMet binding in restriction enzymes.
Main Methods:
- Enzyme assays with wild-type and mutant enzymes, and AdoMet analogs.
- Biophysical techniques including native polyacrylamide gel electrophoresis, size exclusion chromatography, UV-Vis, fluorescence, and circular dichroism spectroscopy.
- Subunit separation and reconstitution experiments, and in vivo complementation assays.
Main Results:
- EcoPI requires exogenous AdoMet for DNA restriction, while EcoP15I has bound AdoMet.
- Specific structural features of AdoMet, including the carboxyl group and methionine substitution, are essential for DNA cleavage.
- AdoMet binding induces distinct conformational changes in the EcoP15I holoenzyme and apoenzyme forms.
- Reconstitution of separated subunits demonstrates AdoMet's necessity for forming a restriction-proficient enzyme.
Conclusions:
- AdoMet is indispensable for DNA cleavage by type III restriction enzymes.
- AdoMet binding triggers critical conformational alterations required for enzymatic activity.
- The interaction between AdoMet and the enzyme's subunits is vital for generating a functional restriction system.