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Journal of Bacteriology, January 2008, p. 78-86, Vol. 190, No. 1
0021-9193/08/$08.00+0     doi:10.1128/JB.00792-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Agrobacterium tumefaciens C58 Uses ActR and FnrN To Control nirK and nor Expression{triangledown}

Seung-Hun Baek, Angela Hartsock, and James P. Shapleigh*

Department of Microbiology, Wing Hall, Cornell University, Ithaca, New York 14853-8101

Received 22 May 2007/ Accepted 10 October 2007

Agrobacterium tumefaciens can grow anaerobically via denitrification. To learn more about how cells regulate production of nitrite and nitric oxide, experiments were carried out to identify proteins involved in regulating expression and activity of nitrite and nitric oxide reductase. Transcription of NnrR, required for expression of these two reductases, was found to be under control of FnrN. Insertional inactivation of the response regulator actR significantly reduced nirK expression and Nir activity but not nnrR expression. Purified ActR bound to the nirK promoter but not the nor or nnrR promoter. A putative ActR binding site was identified in the nirK promoter region using mutational analysis and an in vitro binding assay. A nirK promoter containing mutations preventing the binding of ActR showed delayed expression but eventually reached about 65% of the activity of an equivalent wild-type promoter lacZ fusion. Truncation of the nirK promoter revealed that truncation up to and within the ActR binding site reduced expression, but fragments lacking the ActR binding site and retaining the NnrR binding site showed expression as high as or higher than the full-length fragment. Additional experiments revealed that expression of paz, encoding the copper protein pseudoazurin, was highly reduced in the actR or fnrN mutants and that ActR binds to the paz promoter. Inactivation of paz reduced Nir activity by 55%. These results help explain why Nir activity is very low in the actR mutant even though a nirK promoter with mutations in the ActR binding site showed significant expression.

* Corresponding author. Mailing address: Department of Microbiology, Wing Hall, Cornell University, Ithaca, NY 14853-8101. Phone: (607) 255-8535. Fax: (607) 255-3904. E-mail: jps2{at}cornell.edu

{triangledown} Published ahead of print on 2 November 2007.

Journal of Bacteriology, January 2008, p. 78-86, Vol. 190, No. 1
0021-9193/08/$08.00+0     doi:10.1128/JB.00792-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



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