Award details

Copper-regulated gene expression in Escherichia coli

ReferenceG14071
Principal Investigator / Supervisor Professor Nigel Brown
Co-Investigators /
Co-Supervisors
Institution University of Birmingham
DepartmentSch of Biosciences
Funding typeResearch
Value (£) 236,104
StatusCompleted
TypeResearch Grant
Start date 01/02/2001
End date 30/08/2004
Duration43 months

Abstract

Copper is an essential metal, but is toxic in excess. The mechanisms whereby E. coli controls intracellular copper concentrations are not understood, although some of the component regulators, copper binding proteins and transport proteins for copper resistance and normal copper management have been identified. This proposal is to use DNA array techniques to identify transcripts and gene products controlled by the chromosomal copper-responsive regulators CutR/CutS and CueR under elevated copper conditions, and to identify copper acquisition genes in order to understand better the global responses to this biologically- important metal. This system provides a model for metal homeostasis in an important model organism and will test the hypothesis that copper-responsive genes form one or more regulons.

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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