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Staphylococcus aureus haem biosynthesis: characterisation of the enzymes involved in final steps of the pathway

Lobo, Susana A. L., Scott, Alan, Videira, Marco A. M., Winpenny, David, Gardner, Mark, Palmer, Mike J., Schroeder, Susanne, Lawrence, Andrew D., Parkinson, Tanya, Warren, Martin J., and others. (2015) Staphylococcus aureus haem biosynthesis: characterisation of the enzymes involved in final steps of the pathway. Molecular Microbiology, 97 (3). pp. 472-487. ISSN 0950-382X. (doi:10.1111/mmi.13041) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:50468)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
http://doi.org/10.1111/mmi.13041

Abstract

Haem is a life supporting molecule that is ubiquitous in all major kingdoms. In Staphylococcus aureus, the importance of haem is highlighted by the presence of systems both for the exogenous acquisition and endogenous synthesis of this prosthetic group. In this work, we show that in S.?aureus the formation of haem involves the conversion of coproporphyrinogen III into coproporphyrin III by coproporphyrin synthase HemY, insertion of iron into coproporphyrin III via ferrochelatase HemH, and oxidative decarboxylation of Fe-coproporphyrin III into protohaem IX by Fe-coproporphyrin oxidase/dehydrogenase HemQ. Together, this route represents a transitional pathway between the classic pathway and the more recently acknowledged alternative biosynthesis machinery. The role of the haem biosynthetic pathway in the survival of the bacterium was investigated by testing for inhibitors of HemY. Analogues of acifluorfen are shown to inhibit the flavin-containing HemY, highlighting this protein as a suitable target for the development of drugs against S.?aureus. Moreover, the presence of a transitional pathway for haem biosynthesis within many Gram positive pathogenic bacteria suggests that this route has the potential not only for the design of antimicrobials but also for the selective discrimination between bacteria operating different routes to the biosynthesis of haem.

Item Type: Article
DOI/Identification number: 10.1111/mmi.13041
Subjects: Q Science
Divisions: Divisions > Division of Natural Sciences > Biosciences
Depositing User: Susan Davies
Date Deposited: 11 Sep 2015 09:24 UTC
Last Modified: 05 Nov 2024 10:35 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/50468 (The current URI for this page, for reference purposes)

University of Kent Author Information

Lawrence, Andrew D..

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CReDIT Contributor Roles:

Warren, Martin J..

Creator's ORCID: https://orcid.org/0000-0002-6028-6456
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