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Natural variation among restriction enzymes

ReferenceG10881
Principal Investigator / Supervisor Professor Steve Halford
Co-Investigators /
Co-Supervisors
Institution University of Bristol
DepartmentBiochemistry
Funding typeResearch
Value (£) 213,556
StatusCompleted
TypeResearch Grant
Start date 01/02/1999
End date 01/02/2002
Duration36 months

Abstract

Most type II restriction enzymes are dimers that cut duplex DNA at palindromic sites. Each active site in the protein is placed to cut one strand, so one turnover of the enzyme cuts both strands at a single site. However, some type II enzymes behave differently from this paradigm. For example, SfiI interacts with two copies of its recognition site before DNA cleavage, while FokI seems to need two copies of the protein at one site. The objective of this study is to elucidate the range of different behaviours displayed by type II restriction enzymes; to assess the prevalence of enzymes in this category that act differently from the paradigms such as EcoRV and EcoRI; and to characterise the mode of action of BspMI and some other enzymes that act in non-standard ways, with respect to their protein assemblies and their mechanisms for DNA recognition and cleavage.

Summary

unavailable
Committee Closed Committee - Genes & Developmental Biology (GDB)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
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