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Journal of Bacteriology, March 2007, p. 1698-1710, Vol. 189, No. 5
0021-9193/07/$08.00+0     doi:10.1128/JB.01526-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Biosynthetic Analysis of the Petrobactin Siderophore Pathway from Bacillus anthracis{triangledown}

Jung Yeop Lee,1 Brian K. Janes,2 Karla D. Passalacqua,2 Brian F. Pfleger,1 Nicholas H. Bergman,2,3 Haichuan Liu,4 Kristina Håkansson,4 Ravindranadh V. Somu,5 Courtney C. Aldrich,5 Stephen Cendrowski,6 Philip C. Hanna,2 and David H. Sherman1*

Life Sciences Institute and Department of Medicinal Chemistry, University of Michigan, Ann Arbor, Michigan 48109,1 Department of Microbiology and Immunology,2 Bioinformatics Program, University of Michigan Medical School, Ann Arbor, Michigan 48109,3 Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109,4 Center for Drug Design, Academic Health Center, University of Minnesota, Minneapolis, Minnesota 55455,5 Medical Technology Program and Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan 488246

Received 29 September 2006/ Accepted 14 December 2006

The asbABCDEF gene cluster from Bacillus anthracis is responsible for biosynthesis of petrobactin, a catecholate siderophore that functions in both iron acquisition and virulence in a murine model of anthrax. We initiated studies to determine the biosynthetic details of petrobactin assembly based on mutational analysis of the asb operon, identification of accumulated intermediates, and addition of exogenous siderophores to asb mutant strains. As a starting point, in-frame deletions of each of the genes in the asb locus (asbABCDEF) were constructed. The individual mutations resulted in complete abrogation of petrobactin biosynthesis when strains were grown on iron-depleted medium. However, in vitro analysis showed that each asb mutant grew to a very limited extent as vegetative cells in iron-depleted medium. In contrast, none of the B. anthracis asb mutant strains were able to outgrow from spores under the same culture conditions. Provision of exogenous petrobactin was able to rescue the growth defect in each asb mutant strain. Taken together, these data provide compelling evidence that AsbA performs the penultimate step in the biosynthesis of petrobactin, involving condensation of 3,4-dihydroxybenzoyl spermidine with citrate to form 3,4-dihydroxybenzoyl spermidinyl citrate. As a final step, the data reveal that AsbB catalyzes condensation of a second molecule of 3,4-dihydroxybenzoyl spermidine with 3,4-dihydroxybenzoyl spermidinyl citrate to form the mature siderophore. This work sets the stage for detailed biochemical studies with this unique acyl carrier protein-dependent, nonribosomal peptide synthetase-independent biosynthetic system.


* Corresponding author. Mailing address: Life Sciences Institute, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI 48109-2216. Phone: (734) 615-9907. Fax: (734) 615-3641. E-mail: davidhs{at}umich.edu.

{triangledown} Published ahead of print on 22 December 2006.


Journal of Bacteriology, March 2007, p. 1698-1710, Vol. 189, No. 5
0021-9193/07/$08.00+0     doi:10.1128/JB.01526-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




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