GcsR, a TyrR-Like Enhancer-Binding Protein, Regulates Expression of the Glycine Cleavage System in Pseudomonas aeruginosa PAO1

Author:

Sarwar Zaara1,Lundgren Benjamin R.1,Grassa Michael T.1,Wang Michael X.1,Gribble Megan2,Moffat Jennifer F.2,Nomura Christopher T.134ORCID

Affiliation:

1. Department of Chemistry, State University of New York—College of Environmental Science and Forestry, Syracuse, New York, USA

2. Department of Microbiology and Immunology, State University of New York Upstate Medical University, Syracuse, New York, USA

3. Center for Applied Microbiology, State University of New York—College of Environmental Science and Forestry, Syracuse, New York, USA

4. Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, College of Life Sciences, Hubei University, Wuhan, People’s Republic of China

Abstract

Glycine is required for various cellular functions, including cell wall synthesis, protein synthesis, and the biosynthesis of several important metabolites. Regulating levels of glycine metabolism allows P. aeruginosa to maintain the metabolic flux of glycine through several pathways, including the metabolism of glycine to produce other amino acids, entry into the trichloroacetic acid cycle, and the production of virulence factors such as hydrogen cyanide. In this study, we characterized GcsR, a transcriptional regulator that activates the expression of genes involved in P. aeruginosa PAO1 glycine metabolism. Our work reveals that GcsR is the founding member of a novel class of TyrR-like EBPs that likely regulate glycine metabolism in Pseudomonadales .

Funder

HHS | National Institutes of Health

National Science Foundation

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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