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FEMS Microbiol Lett ; 308(1): 40-7, 2010 Jul 01.
Article in English | MEDLINE | ID: mdl-20487022

ABSTRACT

This study was aimed at describing the spectrum and dynamics of proteins associated with the membrane in the nitrogen-fixing bacterium Herbaspirillum seropedicae according to the availability of fixed nitrogen. Using two-dimensional electrophoresis we identified 79 protein spots representing 45 different proteins in the membrane fraction of H. seropedicae. Quantitative analysis of gel images of membrane extracts indicated two spots with increased levels when cells were grown under nitrogen limitation in comparison with nitrogen sufficiency; these spots were identified as the GlnK protein and as a conserved noncytoplasmic protein of unknown function which was encoded in an operon together with GlnK and AmtB. Comparison of gel images of membrane extracts from cells grown under nitrogen limitation or under the same regime but collected after an ammonium shock revealed two proteins, GlnB and GlnK, with increased levels after the shock. The P(II) proteins were not present in the membrane fraction of an amtB mutant. The results reported here suggest that changes in the cellular localization of P(II) might play a role in the control of nitrogen metabolism in H. seropedicae.


Subject(s)
Cell Membrane/chemistry , Gene Expression Regulation, Bacterial , Gene Expression Regulation, Enzymologic , Herbaspirillum/chemistry , Membrane Transport Proteins/analysis , Proteome/analysis , Quaternary Ammonium Compounds/metabolism , Bacterial Proteins/analysis , Cation Transport Proteins/analysis , Electrophoresis, Gel, Two-Dimensional , Herbaspirillum/physiology , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
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