Two component systems, comprised typically of Histidine Kinase and Response regulator proteins, represent the primary and ubiquitous mechanism in bacteria for initiating cellular response towards a wide variety of environmental conditions. In D. vulgaris Hildenborough, more than 70 such systems have been predicted, but remain mostly uncharacterized. The ability of D. vulgaris to survive in its environment is no doubt linked with the activity of genes modulated by these two component signal transduction systems. These genes in D. vulgaris also present a fascinating set for detailed study. The large number of Histidine kinases are predicted to have arisen from extensive gene duplication (Alm et al 2006), rather than HGT as is predicted to be the case with other microbes such as E. coli and B. subtilis. As a result the Histidine Kinases in D. vulgaris often contain multiple similar domains in a variety of configurations. Further, the majority of both Histidine Kinases and Response regulators in D. vulgaris are mostly encoded in monocistronic operons providing little clue as to the signal they respond to. In order to map Histidine Kinases to their cognate Response regulators and the Response regulators to the genes they may regulate, our project uses a library of purified Histidine Kinase and Response regulator proteins. We use biochemical and array based methods to map histidine kinases to their cognate response regulators and down stream functions.
Engineering solvent tolerant microbes
For microbial fuel production, the efficiency with which fuel can be exported from the cell is likely to have significant influence on production titer. Build-up of fuel molecules may directly reduce titer, and when toxic, also cause significant intracellular stress, leading to feedback inhibition of fuel production. Transport systems, such as efflux pumps and ABC-transport systems in bacteria and yeast, are documented to export a broad range of substrates including solvents and provide a direct engineering route to relieve fuel accumulation-related stress and improve production titer. To address our goal of improving solvent resistance using efflux pumps, we have used a high-throughput approach to create a library efflux pumps in E. coli that can confer tolerance to many candidate fuels. We have also begun exploring export systems in gram positive bacterial hosts for the production of chemicals.
Cellular Engineering in S. cerevisiae
We are interested in understanding the impact of the fuels and biomass inhibitors in S. cereviciae. We hope to develop improved an yeast host that has versatile carbon utilization profiles, ability to produce advanced biofuels and are tolerant to production stresses. We are also developing tools to increase the ease of cellular engineering in yeast.
Signaling and gene regulation in dominant cyanobacteria in Desert soil crusts