|
|
||||||||
Genetics and Molecular Biology |
Department of Biochemistry and Center for Microbial Pathogenesis, School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14214, USA1
Author for correspondence: Mark R. OBrian. Tel: +1 716 829 3200. Fax: +1 716 829 2725. e-mail: mrobrian{at}buffalo.edu
Bradyrhizobium japonicum expresses both Fur and Irr, proteins that mediate iron-dependent regulation of gene expression. Control of irr mRNA accumulation by iron was aberrant in a fur mutant strain, and Fur repressed an irr::lacZ promoter fusion in the presence of iron. Furthermore, metal-dependent binding of Fur to an irr gene promoter was demonstrated in a region with no significant similarity to the Fur-binding consensus DNA element. These data suggest that the modest control of irr transcription by iron is mediated by Fur. However, Irr protein levels were regulated normally by iron in the fur strain, indicating that Fur is not required for post-transcriptional control of the irr gene. Accordingly, regulation of hemB, a haem biosynthesis gene regulated by Irr, was controlled normally by iron in a fur strain. In addition, the hemA gene was shown to be controlled by Fur, but not by Irr. It was concluded that Fur cannot be the only protein by which B. japonicum cells sense and respond to iron, and that Irr may be involved in Fur-independent signal transduction. Furthermore, iron-dependent regulation of haem biosynthesis involves both Irr and Fur.
Keywords: Bradyrhizobium japonicum, iron metabolism, Fur, Irr, haem metabolism
Abbreviations: ALA,
-aminolevulinic acid
a Present address: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
This article has been cited by other articles:
![]() |
B. M. Carpenter, J. M. Whitmire, and D. S. Merrell This Is Not Your Mother's Repressor: the Complex Role of Fur in Pathogenesis Infect. Immun., July 1, 2009; 77(7): 2590 - 2601. [Full Text] [PDF] |
||||
![]() |
P. A. Zaini, A. C. Fogaca, F. G. N. Lupo, H. I. Nakaya, R. Z. N. Vencio, and A. M. da Silva The Iron Stimulon of Xylella fastidiosa Includes Genes for Type IV Pilus and Colicin V-Like Bacteriocins J. Bacteriol., April 1, 2008; 190(7): 2368 - 2378. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. S. Bender, H.-C. B. Yen, C. L. Hemme, Z. Yang, Z. He, Q. He, J. Zhou, K. H. Huang, E. J. Alm, T. C. Hazen, et al. Analysis of a Ferric Uptake Regulator (Fur) Mutant of Desulfovibrio vulgaris Hildenborough Appl. Envir. Microbiol., September 1, 2007; 73(17): 5389 - 5400. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Kitphati, P. Ngok-ngam, S. Suwanmaneerat, R. Sukchawalit, and S. Mongkolsuk Agrobacterium tumefaciens fur Has Important Physiological Roles in Iron and Manganese Homeostasis, the Oxidative Stress Response, and Full Virulence Appl. Envir. Microbiol., August 1, 2007; 73(15): 4760 - 4768. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Ledala, S. L. Pearson, B. J. Wilkinson, and R. K. Jayaswal Molecular characterization of the Fur protein of Listeria monocytogenes Microbiology, April 1, 2007; 153(4): 1103 - 1111. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Rudolph, G. Semini, F. Hauser, A. Lindemann, M. Friberg, H. Hennecke, and H.-M. Fischer The Iron Control Element, Acting in Positive and Negative Control of Iron-Regulated Bradyrhizobium japonicum Genes, Is a Target for the Irr Protein J. Bacteriol., January 15, 2006; 188(2): 733 - 744. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Diaz-Mireles, M. Wexler, J. D. Todd, D. Bellini, A. W. B. Johnston, and R. G. Sawers The manganese-responsive repressor Mur of Rhizobium leguminosarum is a member of the Fur-superfamily that recognizes an unusual operator sequence Microbiology, December 1, 2005; 151(12): 4071 - 4078. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Martinez, R. A. Ugalde, and M. Almiron Dimeric Brucella abortus Irr protein controls its own expression and binds haem Microbiology, October 1, 2005; 151(10): 3427 - 3433. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Gao and M. R. O'Brian Iron-Dependent Cytochrome c1 Expression Is Mediated by the Status of Heme in Bradyrhizobium japonicum J. Bacteriol., August 1, 2005; 187(15): 5084 - 5089. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. D. King, A. E. Kirby, and T. D. Connell Transcriptional Control of the rhuIR-bhuRSTUV Heme Acquisition Locus in Bordetella avium Infect. Immun., March 1, 2005; 73(3): 1613 - 1624. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. E. Friedman and M. R. O'Brian The Ferric Uptake Regulator (Fur) Protein from Bradyrhizobium japonicum Is an Iron-responsive Transcriptional Repressor in Vitro J. Biol. Chem., July 30, 2004; 279(31): 32100 - 32105. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Platero, L. Peixoto, M. R. O'Brian, and E. Fabiano Fur Is Involved in Manganese-Dependent Regulation of mntA (sitA) Expression in Sinorhizobium meliloti Appl. Envir. Microbiol., July 1, 2004; 70(7): 4349 - 4355. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Diaz-Mireles, M. Wexler, G. Sawers, D. Bellini, J. D. Todd, and A. W. B. Johnston The Fur-like protein Mur of Rhizobium leguminosarum is a Mn2+-responsive transcriptional regulator Microbiology, May 1, 2004; 150(5): 1447 - 1456. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. P. Benson, K. LeVier, and M. L. Guerinot A Dominant-Negative fur Mutation in Bradyrhizobium japonicum J. Bacteriol., March 1, 2004; 186(5): 1409 - 1414. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E. Garrido, M. Bosch, R. Medina, A. Bigas, M. Llagostera, A. M. Perez de Rozas, I. Badiola, and J. Barbe fur-independent regulation of the Pasteurella multocida hbpA gene encoding a haemin-binding protein Microbiology, August 1, 2003; 149(8): 2273 - 2281. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Wexler, J. D. Todd, O. Kolade, D. Bellini, A. M. Hemmings, G. Sawers, and A. W. B. Johnston Fur is not the global regulator of iron uptake genes in Rhizobium leguminosarum Microbiology, May 1, 2003; 149(5): 1357 - 1365. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Loh, R. W. Carlson, W. S. York, and G. Stacey Bradyoxetin, a unique chemical signal involved in symbiotic gene regulation PNAS, October 29, 2002; 99(22): 14446 - 14451. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Panek and M. R. O'Brian A whole genome view of prokaryotic haem biosynthesis Microbiology, August 1, 2002; 148(8): 2273 - 2282. [Full Text] [PDF] |
||||
![]() |
M. Elgrably-Weiss, S. Park, E. Schlosser-Silverman, I. Rosenshine, J. Imlay, and S. Altuvia A Salmonella enterica Serovar Typhimurium hemA Mutant Is Highly Susceptible to Oxidative DNA Damage J. Bacteriol., July 15, 2002; 184(14): 3774 - 3784. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. E. Kirby, D. J. Metzger, E. R. Murphy, and T. D. Connell Heme Utilization in Bordetella avium Is Regulated by RhuI, a Heme-Responsive Extracytoplasmic Function Sigma Factor Infect. Immun., November 1, 2001; 69(11): 6951 - 6961. [Abstract] [Full Text] [PDF] |
||||
![]() |
H.-M. Fischer, L. Velasco, M. J. Delgado, E. J. Bedmar, S. Schären, D. Zingg, M. Göttfert, and H. Hennecke One of Two hemN Genes in Bradyrhizobium japonicum Is Functional during Anaerobic Growth and in Symbiosis J. Bacteriol., February 15, 2001; 183(4): 1300 - 1311. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |