کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5371425 | 1388819 | 2010 | 7 صفحه PDF | دانلود رایگان |

The immobilization of cells or enzymes is a promising tool for the development of biosensors, yet the interactions between the fixative materials and the cells are not fully understood, especially with respect to their impact on both cell metabolism and cell-to-cell signaling. We show that the spatiotemporal dynamics of waves of metabolic synchronization of yeast cells provides a new criterion to distinguish the effect of different gels on the cellular metabolism, which otherwise could not be detected. Cells from the yeast Saccharomyces carlsbergensis were immobilized into agarose gel, silica gel (TMOS), or a mixture of TMOS and alginate. We compared these immobilized cells with respect to their ability to generate temporal, intracellular oscillations in glycolysis as well as propagating, extracellular synchronization waves. While the temporal dynamics, as measured by the period and the number of oscillatory cycles, was similar for all three immobilized cell populations, significant differences have been observed with respect to the shape of the waves, wave propagation direction and velocity in the three gel matrices used.
Graphical AbstractResearch Highlights⺠Yeast cells immobilized in gels are still active and perform oscillatory glycolysis. ⺠Gel-immobilized yeast cells induce traveling waves of metabolites. ⺠Traveling waves provide for spatial self-organization and synchronization of gel-immobilized yeast cells. ⺠Immobilization prolongs the periods of glycolytic oscillations.
Journal: Biophysical Chemistry - Volume 153, Issue 1, December 2010, Pages 54-60