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Bacterial redox homeostasis: Roles of the ABC-type substrate exporter CydDC
Reference
BB/C514174/1
Principal Investigator / Supervisor
Professor Robert K Poole
Co-Investigators /
Co-Supervisors
Professor Cameron McLeod
Institution
University of Sheffield
Department
Molecular Biology and Biotechnology
Funding type
Research
Value (£)
225,781
Status
Completed
Type
Research Grant
Start date
01/09/2005
End date
28/02/2009
Duration
42 months
Abstract
Escherichia coli possesses a well-characterised terminal oxidase of the cytochrome bd class. This oxidase is critical for growth and energy conservation at low oxygen tensions and under diverse conditions of stress (eg. stationary phase, high pH, oxidative stress). In several bacteria, cytochrome bd function is required for pathogenicity. We have discovered a heterodimeric ABC-type transporter. CydDC, that is essential for assembly of functional cytochrome bd. CydDC has intriguing similarities to important eukaryotic transporters like CFTR and xenobiotic-exporting systems. We have recently shown that in E. coli this transporter exports cysteine and glutathione from the cytoplasm to the periplasm, suggesting that the role of CydDC is the establishment and or maintenance of an appropriate redox environment in the periplasm. The aims of the project are (a) to establish the range of metabolites that can be exported by CydDC, (b) to test the hypothesis that cysteine and or GSH export maintains both cytoplasm and periplasm in critical redox states, and investigate the consequences of external redox conditions, (c) to learn more of the mechanism by which transport is achieved by CydDC explored by available site-directed mutants in which cytochrome bd formation in impaired and (d) to study the link between GSH and NO cytotoxicity. This project has considerable potential for commercial exploitation, since CydDC-catalysed export can in principle be utilised in commercial cysteine and glutathione production.
Summary
unavailable
Committee
Closed Committee - Plant & Microbial Sciences (PMS)
Research Topics
Microbiology
Research Priority
X – Research Priority information not available
Research Initiative
X - not in an Initiative
Funding Scheme
X – not Funded via a specific Funding Scheme
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