Abstract
Transport of vinylglycolate (2-hydroxy-3-butenoic acid) via the lactate transport system is the limiting step for covalent labeling of membrane vesicles prepared from E. coli ML 308-225. Thus, the rate and extent of vinylglycolate labeling is stimulated about 10-fold by ascorbate-phenazine methosulfate, and stimulation is abolished by 2,4-dinitrophenol and by phospholipase treatment, neither of which affect the rate of vinylglycolate oxidation. [(3)H]Vinylglycolate of high specific activity has been prepared, and vesicles have been labeled with this compound in the presence of ascorbate-phenazine methosulfate. Examination of these preparations by high resolution radioautography in the electron microscope demonstrates that virtually all of the vesicles are labeled. The experiments provide a strong indication that most, if not all, of the membrane vesicles in these preparations catalyze active transport.
MeSH Terms
Ascorbic Acid/pharmacology
Autoradiography
Biological Transport, Active/drug effects
Catalysis
Cell Membrane/metabolism,ultrastructure
Dinitrophenols/pharmacology
Escherichia coli/metabolism,ultrastructure
Glucose/metabolism
Hydroxy Acids/metabolism
Microscopy, Electron
Phenazines/pharmacology
Phosphoenolpyruvate
Phosphotransferases/metabolism
Tritium
Vinyl Compounds/metabolism
Chemicals
Dinitrophenols
Hydroxy Acids
Phenazines
Vinyl Compounds
Tritium
Phosphoenolpyruvate
Phosphotransferases
Glucose
Ascorbic Acid
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Short S A
Kaback H R
Kaczorowski G
Fisher J
Walsh C T
Silverstein S C
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17 references, click to expand
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