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Investigating genetic markers and mechanisms of CO dehydrogenase regulation in response to atmospheric mercury
Secondary Supervisor(s): Professor Yin Chen
University of Registration: University of Birmingham
BBSRC Research Themes:
Project Outline
Volcanic emissions are a natural source of mercury (Hg) to the atmosphere and geologists have shown that volcanoes, like Mt. Etna (Italy), is a major natural source of Hg to the atmosphere. This has clear environmental impacts as mercury is a toxic heavy metal that bioaccumulates and biomagnificates in the environment. Volcanic emissions also release significant amounts of trace gases, such as carbon monoxide (CO), carbon dioxide, and methane, and we have found genes encoding enzymes responsible for the oxidation of CO in particular.
The enzyme responsible for CO oxidation is the carbon monoxide dehydrogenase (CODH). This enzyme in our model organism (Oligotropha carvoxidovorans) contains a unique active site composed of a molybdenum/copper bimetallic centre. Mercury-resistant bacteria harbour the mer operon that includes merA a mercury ion reductase, which catalyses the conversion of Hg2+ to Hg0. In this PhD proposal, we hypothesise that mercury resistance genes are widespread within bacterial populations and that the mercury reductase, which also contains copper sites, might compete with CODH for available copper and downregulate CODHs, which will decrease CO uptake. This will have negative consequences for atmospheric pollution, as CO concentrations will be higher when mercury concentrations are high.
In this DTP project, the student will determine how mercury exposure affects CO dehydrogenase activity and expression, and whether exposure to Hg alters the regulation of CO oxidation pathways in CO-oxidising bacteria. This will establish how metal stress influences microbial energy metabolism and the regulation of competing metal-dependent processes.
The student will join sampling campaigns in Italy, prepare microcosm incubations and learn interdisciplinary techniques including qPCR, gas-chromatography, enrichment and isolation of bacteria, proteomics and metagenomics.