Targeting the alternative oxidase (AOX) for human health and food security, a pharmaceutical and agrochemical target or a rescue mechanism?

Author:

Szibor Marten12ORCID,Schenkl Christina1,Barsottini Mario R. O.34,Young Luke3,Moore Anthony L.3ORCID

Affiliation:

1. 1Department of Cardiothoracic Surgery, and Center for Sepsis Control and Care (CSCC), Jena University Hospital, DE-07747 Jena, Germany

2. 2Faculty of Medicine and Health Technology, Tampere University, FI-33520 Tampere, Finland

3. 3Biochemistry & Biomedicine, School of Life Sciences, University of Sussex, Brighton BN1 9QG, U.K.

4. 4Genomics and BioEnergy Laboratory, Institute of Biology, University of Campinas, Campinas – SP 13083-862, Brazil

Abstract

Some of the most threatening human diseases are due to a blockage of the mitochondrial electron transport chain (ETC). In a variety of plants, fungi, and prokaryotes, there is a naturally evolved mechanism for such threats to viability, namely a bypassing of the blocked portion of the ETC by alternative enzymes of the respiratory chain. One such enzyme is the alternative oxidase (AOX). When AOX is expressed, it enables its host to survive life-threatening conditions or, as in parasites, to evade host defenses. In vertebrates, this mechanism has been lost during evolution. However, we and others have shown that transfer of AOX into the genome of the fruit fly and mouse results in a catalytically engaged AOX. This implies that not only is the AOX a promising target for combating human or agricultural pathogens but also a novel approach to elucidate disease mechanisms or, in several cases, potentially a therapeutic cure for human diseases. In this review, we highlight the varying functions of AOX in their natural hosts and upon xenotopic expression, and discuss the resulting need to develop species-specific AOX inhibitors.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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