TY - GEN
T1 - Extracellular metabolite dynamics and temporal organization of metabolic function in E. coli
AU - Robert, Martin
AU - Murray, Douglas
AU - Honma, Masayuki
AU - Nakahigashi, Kenji
AU - Soga, Tomoyoshi
AU - Tomita, Masaru
PY - 2012/10/24
Y1 - 2012/10/24
N2 - Bacteria dynamically exchange with their environment by constantly uptaking nutrients and secreting metabolic products and other biomolecules. While such secreted metabolites may represent a high-level reporter of metabolic activity of the culture, relatively few studies have focused on their characterization. In addition, metabolites may be potential mediators of intercellular interactions. This study aims at identifying candidate mediators of intercellular exchanges and population behavior from temporal patterns of metabolites. To do this, we used capillary electrophoresis mass spectrometry (CE-MS) to monitor secreted metabolites in synchronized continuous culture of E. coli displaying respiratory oscillations. We observed that multiple metabolites are secreted in significant quantities in the extracellular medium, including amino acids and other intermediates of central metabolism. Some of the secreted metabolite dynamics appear linked to the known valine toxicity in E. coli and are also associated with the respiratory oscillations and their dynamics. Moreover, the dynamics in the level of several amino acids appeared well correlated, suggesting organized cycles of secretion/reuptake during respiratory and metabolic shifts linked to valine levels. Overall, the current results suggest that multiple metabolites are produced and likely exchanged by E. coli during continuous growth. These appear to reflect the internal metabolic state of the cell and may form an underappreciated level of information exchange that cell populations use to coordinate activities.
AB - Bacteria dynamically exchange with their environment by constantly uptaking nutrients and secreting metabolic products and other biomolecules. While such secreted metabolites may represent a high-level reporter of metabolic activity of the culture, relatively few studies have focused on their characterization. In addition, metabolites may be potential mediators of intercellular interactions. This study aims at identifying candidate mediators of intercellular exchanges and population behavior from temporal patterns of metabolites. To do this, we used capillary electrophoresis mass spectrometry (CE-MS) to monitor secreted metabolites in synchronized continuous culture of E. coli displaying respiratory oscillations. We observed that multiple metabolites are secreted in significant quantities in the extracellular medium, including amino acids and other intermediates of central metabolism. Some of the secreted metabolite dynamics appear linked to the known valine toxicity in E. coli and are also associated with the respiratory oscillations and their dynamics. Moreover, the dynamics in the level of several amino acids appeared well correlated, suggesting organized cycles of secretion/reuptake during respiratory and metabolic shifts linked to valine levels. Overall, the current results suggest that multiple metabolites are produced and likely exchanged by E. coli during continuous growth. These appear to reflect the internal metabolic state of the cell and may form an underappreciated level of information exchange that cell populations use to coordinate activities.
KW - E. coli
KW - cell-cell communication
KW - dynamics
KW - metabolomics
UR - http://www.scopus.com/inward/record.url?scp=84867635920&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84867635920&partnerID=8YFLogxK
U2 - 10.1109/ICCME.2012.6275650
DO - 10.1109/ICCME.2012.6275650
M3 - Conference contribution
AN - SCOPUS:84867635920
SN - 9781467316163
T3 - 2012 ICME International Conference on Complex Medical Engineering, CME 2012 Proceedings
SP - 197
EP - 202
BT - 2012 ICME International Conference on Complex Medical Engineering, CME 2012 Proceedings
T2 - 6th International Conference on Complex Medical Engineering, CME 2012
Y2 - 1 July 2012 through 4 July 2012
ER -