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Genes coding for the reversible ADP-ribosylation system of dinitrogenase reductase from Rhodospirillum rubrum
Authors:Wayne P. Fitzmaurice   Leonard L. Saari   Robert G. Lowery   Paul W. Ludden  Gary P. Roberts
Affiliation:(1) Department of Bacteriology, University of Wisconsin, 53706 Madison, WI, USA;(2) Department of Biochemistry, University of Wisconsin, 53706 Madison, WI, USA;(3) Present address: Department of Genetics, North Carolina State University, 27695 Raleigh, NC, USA;(4) Present address: Agricultural Chemicals Department, E.I. Du Pont de Nemous and Co., 19898 Wilmington, DE, USA;(5) Present address: Department of Biology, University of Utah, 84112 Salt Lake City, UT, USA
Abstract:Summary Nitrogen fixation activity in the photosynthetic bacterium Rhodospirillum rubrum is controlled by the reversible ADP-ribosylation of the dinitrogenase reductase component of the nitrogenase enzyme complex. This report describes the cloning and characterization of the genes encoding the ADP-ribosyltransferase (draT) and the ADP-ribosylglycohydrolase (draG) involved in this regulation. These genes are shown to be contiguous on the R. rubrum chromosome and highly linked to the nifHDK genes. Sequence analysis revealed the use of TTG as the initiation codon of the draT gene as well as a potential open reading frame immediately downstream of draG. The mono-ADP-ribosylation system in R. rubrum is the first in which both the target protein and modifying enzymes as well as their structural genes have been isolated, making it the model system of choice for analysis of this post-translational regulatory mechanism.
Keywords:Nitrogen fixation  draT  draG  TTG initiation codon
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