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Infection and Immunity, September 2007, p. 4582-4591, Vol. 75, No. 9
0019-9567/07/$08.00+0     doi:10.1128/IAI.00324-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Expression and Characterization of an Iron-Regulated Hemin-Binding Protein, HbpA, from Leptospira interrogans Serovar Lai{triangledown}

Swapna Asuthkar,1 Sridhar Velineni,1 Johannes Stadlmann,2 Friedrich Altmann,2 and Manjula Sritharan1*

School of Life Sciences, University of Hyderabad, Hyderabad, India,1 Department of Chemistry, Universitaet fuer Bodenkultur, Vienna, Austria2

Received 28 February 2007/ Returned for modification 16 April 2007/ Accepted 4 June 2007

In an earlier study, based on the ferric enterobactin receptor FepA of Escherichia coli, we identified and modeled a TonB-dependent outer membrane receptor protein (LB191) from the genome of Leptospira interrogans serovar Lai. Based on in silico analysis, we hypothesized that this protein was an iron-dependent hemin-binding protein. In this study, we provide experimental evidence to prove that this protein, termed HbpA (hemin-binding protein A), is indeed an iron-regulated hemin-binding protein. We cloned and expressed the full-length 81-kDa recombinant rHbpA protein and a truncated 55-kDa protein from L. interrogans serovar Lai, both of which bind hemin-agarose. Assay of hemin-associated peroxidase activity and spectrofluorimetric analysis provided confirmatory evidence of hemin binding by HbpA. Immunofluorescence studies by confocal microscopy and the microscopic agglutination test demonstrated the surface localization and the iron-regulated expression of HbpA in L. interrogans. Southern blot analysis confirmed our earlier observation that the hbpA gene was present only in some of the pathogenic serovars and was absent in Leptospira biflexa. Hemin-agarose affinity studies showed another hemin-binding protein with a molecular mass of approximately 44 kDa, whose expression was independent of iron levels. This protein was seen in several serovars, including nonpathogenic L. biflexa. Sequence analysis and immunoreactivity with specific antibodies showed this protein to be LipL41.


* Corresponding author. Mailing address: School of Life Sciences, University of Hyderabad, Gachibowli, Hyderabad 500046, India. Phone: 9140-23011763. Fax: 9140-23010120. E-mail: srimanju{at}yahoo.com

{triangledown} Published ahead of print on 18 June 2007.

Editor: F. C. Fang


Infection and Immunity, September 2007, p. 4582-4591, Vol. 75, No. 9
0019-9567/07/$08.00+0     doi:10.1128/IAI.00324-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







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