The formation of multicellular communities requires extensive intracellular communication and although much has been learned about the intricate regulatory network involved in differentiation and biofilm formation, relatively little is known about the signals responsible for initiating bacterial multicellularity. Recently, a novel mechanism for triggering multicellularity in Bacillus subtilis was described and surprisingly, the signaling mechanism involves a histidine kinase activated by potassium leakage. In response to potassium leakage caused by natural products, such as nystatin and surfactin, the histidine kinase KinC initiates a signal transduction cascade that culminates in biofilm formation. Discovery of the novel signaling mechanism provides an opportunity to perform a rigorous functional analysis of the potassium sensing histidine kinase and to determine whether and how other genes are involved in sensing potassium leakage. I propose to address three specific aims: I) evaluate the role of polycyclic terpenoids in signal sensing, II) assess the role of potassium uptake in this signal transduction mechanism, and III) identify key KinC residues involved in signal sensing and determine if there is a cofactor involved. The proposed research is designed to both lay the foundation for future studies of protein kinases capable of sensing changes in intracellular ion concentration and allow me to become proficient using advanced genetic and molecular techniques in a variety of bacterial backgrounds. Studies of this new signaling mechanism will help advance our understanding of large sensory systems and will also have important implications in other research fields, including cancer research and infectious disease research.

Public Health Relevance

Many bacterial and mammalian histidine kinases are homologous and due to structural and functional similarities, it is possible to study model bacterial systems and gain important insight into mammalian systems. By increasing our understanding of the molecular basis for histidine kinase activity in bacteria, it may be possible to design more effective strategies to control or modulate defective mammalian protein kinases that cause cells to become cancerous and/or develop more effective ways to fight infections caused by bacterial biofilms.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32GM087941-01
Application #
7678663
Study Section
Special Emphasis Panel (ZRG1-F13-C (20))
Program Officer
Bender, Michael T
Project Start
2009-09-01
Project End
2012-08-31
Budget Start
2009-09-01
Budget End
2010-08-31
Support Year
1
Fiscal Year
2009
Total Cost
$45,218
Indirect Cost
Name
Harvard University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Gontang, Erin A; Aylward, Frank O; Carlos, Camila et al. (2017) Major changes in microbial diversity and community composition across gut sections of a juvenile Panchlora cockroach. PLoS One 12:e0177189
Neumann, Christopher S; Jiang, Wei; Heemstra Jr, John R et al. (2012) Biosynthesis of piperazic acid via N5-hydroxy-ornithine in Kutzneria spp. 744. Chembiochem 13:972-6
López, Daniel; Gontang, Erin A; Kolter, Roberto (2010) Potassium sensing histidine kinase in Bacillus subtilis. Methods Enzymol 471:229-51