Protein synthesis is subject to elaborate transcriptional and post-transcriptional regulation in growing bacterial cells. Such mechanisms ensure that protein synthesis is efficiently coupled to the needs of a rapidly dividing cell when nutrients are not limiting. However, most microbial life exists in a non- proliferating state of quiescence that enables survival during nutrient limitation and in stressful environments. Thus, the needs of quiescent cells are rather different from growing cells as they must minimize energy consumption so as to maximize available resources over a potentially extended period. Protein synthesis is the most energy intensive metabolic process in a cell, accounting for as much as ~70% of total energy consumption in bacteria. Consistently, many bacteria such as Bacillus subtilis are known to substantially reduce protein synthesis when they exit exponential growth. However, quiescent cells need to effectively exploit the emergence of favorable conditions and undergo resuscitation, so this attenuation needs to be rapidly reversible. In addition, as the ribosome is itself the most energetically costly macromolecular machine to synthesize, it must be protected from any degradative processes. And, as with translational attenuation, this protection must be compatible with efficient re-initiation of protein synthesis when conditions improve. Thus, both the inhibitory and protective mechanisms need to be quickly reversible. How the cell balances these two goals is the subject of this research proposal. First, we examine how ribosomes are protected from degradation under metabolic conditions where de novo ribosome biosynthesis is limited. Second, we investigate a reversible mechanism of translation inactivation with particular focus on the role of the nucleotide (p)ppGpp.

Public Health Relevance

Bacteria are often starving and live in stressful environments. To best survive these conditions, most bacteria exist in a state of non-growth. Bacteria must therefore change their metabolism in order to conserve energy and this proposal aims to understand how this occurs.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Unknown (R35)
Project #
1R35GM141953-01
Application #
10206408
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Reddy, Michael K
Project Start
2021-03-17
Project End
2026-01-31
Budget Start
2021-03-17
Budget End
2022-01-31
Support Year
1
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032