Abstract
The transport of organophosphates across the cytoplasma membrane is mediated by organophosphate:phosphate antiporter proteins. In this work, we present the application of a recombinant phosphoenolpyruvate:phosphate antiporter for isotopic labeling experiments in E. coli strains. The antiporters UhpT, UhpT-D388C, and PgtP were investigated regarding transport activity and growth on phosphoenolpyruvate as sole carbon source. The expression of the protein variant UhpT-D388C in a shikimic acid producing E. coli strain was used to show the successful isotopic labeling of shikimic acid from extracellular phosphoenolpyruvate. The results demonstrate the possibility of a direct incorporation of exogenously applicated glycolysis intermediates into E. coli cells for 13C-labeling experiments. The described work demonstrates the possibility of a direct incorporation of exogenously applicated glycolysis intermediates into E. coli cells for labeling or perturbation experiments.
Original language | English |
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Pages (from-to) | 52-61 |
Number of pages | 10 |
Journal | FEMS Microbiology Letters |
Volume | 361 |
Issue number | 1 |
DOIs | |
State | Published - 1 Dec 2014 |
Keywords
- Isotopic labeling
- Organophosphate:phosphate antiporter
- Phosphoenolpyruvate
- Shikimic acid