Applied and Environmental Microbiology, June 2001, p. 2641-2648, Vol. 67, No. 6
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.6.2641-2648.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
MSU-DOE Plant Research Laboratory,1 NSF Center for Microbial Ecology,2 Genetics Program,3 and Department of Microbiology,4 Michigan State University, East Lansing, Michigan 48824
Received 28 November 2000/Accepted 24 March 2001
The regulation of the nutrient-deprivation-induced Sinorhizobium meliloti homogentisate dioxygenase (hmgA) gene, involved in tyrosine degradation, was examined. hmgA expression was found to be independent of the canonical nitrogen regulation (ntr) system. To identify regulators of hmgA, secondary mutagenesis of an S. meliloti strain harboring a hmgA-luxAB reporter gene fusion (N4) was carried out using transposon Tn1721. Two independent Tn1721 insertions were found to be located in a positive regulatory gene (nitR), encoding a protein sharing amino acid sequence similarity with proteins of the ArsR family of regulators. NitR was found to be a regulator of S. meliloti hmgA expression under nitrogen deprivation conditions, suggesting the presence of a ntr-independent nitrogen deprivation regulatory system. nitR insertion mutations were shown not to affect bacterial growth, nodulation of Medicago sativa (alfalfa) plants, or symbiotic nitrogen fixation under the physiological conditions examined. Further analysis of the nitR locus revealed the presence of open reading frames encoding proteins sharing amino acid sequence similarities with an ATP-binding phosphonate transport protein (PhnN), as well as transmembrane efflux proteins.
Present address: INRA/CNRS Laboratoire de Biologie Moleculaire de
Relations Plantes-Microorganismes, 31326 Castanet Tolosan Cedex, France.
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