bioRxiv preprint doi: https://doi.org/10.1101/2021.04.14.439929; this version posted April 16, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Phylogeny Reveals Novel HipA-Homologous Kinase Families and Toxin – Antitoxin Gene Organizations Kenn Gerdes1*, Rene Bærentsen2 & Ditlev E. Brodersen2* 1) Centre of Excellence for Bacterial Stress Response and Persistence, Section for Functional Genomics, Department of Biology, University of Copenhagen, DK-2200, Copenhagen N, Denmark. 2) Department of Molecular Biology and Genetics, Aarhus University, DK-8000 Aarhus C, Denmark. * To whom correspondence should be addressed:
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[email protected] Running Head: Phylogeny of High Persister A-Homologous Kinases Keywords: High Persister A, HipB, HipS, HipT, HIRAN, Stl, GltX, TrpS bioRxiv preprint doi: https://doi.org/10.1101/2021.04.14.439929; this version posted April 16, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Abstract Toxin – Antitoxin modules function in the genetic stability of mobile genetic elements, bacteriophage defense, and antibiotic tolerance. A gain-of-function mutation of the Escherichia coli K-12 hipBA module can induce antibiotic tolerance in a subpopulation of bacterial cells, a phenomenon known as persistence. HipA is a Ser/Thr kinase that phosphorylates and inactivates glutamyl tRNA synthetase, inhibiting cellular translation and inducing the stringent response.