Transcriptional Profiling of Nitrogen Fixation in Azotobacter vinelandii

Author:

Hamilton Trinity L.1,Ludwig Marcus2,Dixon Ray3,Boyd Eric S.1,Dos Santos Patricia C.4,Setubal João C.56,Bryant Donald A.12,Dean Dennis R.7,Peters John W.18

Affiliation:

1. Department of Chemistry and Biochemistry and Astrobiology Biogeocatalysis Research Center, Montana State University, Bozeman, Montana 59717

2. Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania 16802

3. Department of Molecular Microbiology, John Innes Centre, Norwich NR4 7UH, United Kingdom

4. Department of Chemistry, Wake Forest University, Winston-Salem, North Carolina 27109

5. Virginia Bioinformatics Institute, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061

6. Department of Computer Science, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061

7. Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061

8. Department of Microbiology, Montana State University, Bozeman, Montana 59717

Abstract

ABSTRACT Most biological nitrogen (N 2 ) fixation results from the activity of a molybdenum-dependent nitrogenase, a complex iron-sulfur enzyme found associated with a diversity of bacteria and some methanogenic archaea. Azotobacter vinelandii , an obligate aerobe, fixes nitrogen via the oxygen-sensitive Mo nitrogenase but is also able to fix nitrogen through the activities of genetically distinct alternative forms of nitrogenase designated the Vnf and Anf systems when Mo is limiting. The Vnf system appears to replace Mo with V, and the Anf system is thought to contain Fe as the only transition metal within the respective active site metallocofactors. Prior genetic analyses suggest that a number of nif -encoded components are involved in the Vnf and Anf systems. Genome-wide transcription profiling of A. vinelandii cultured under nitrogen-fixing conditions under various metal amendments (e.g., Mo or V) revealed the discrete complement of genes associated with each nitrogenase system and the extent of cross talk between the systems. In addition, changes in transcript levels of genes not directly involved in N 2 fixation provided insight into the integration of central metabolic processes and the oxygen-sensitive process of N 2 fixation in this obligate aerobe. The results underscored significant differences between Mo-dependent and Mo-independent diazotrophic growth that highlight the significant advantages of diazotrophic growth in the presence of Mo.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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