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Journal of Bacteriology, May 2007, p. 3414-3424, Vol. 189, No. 9
0021-9193/07/$08.00+0     doi:10.1128/JB.01835-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Mycoplasma hyopneumoniae mhp379 Is a Ca2+-Dependent, Sugar-Nonspecific Exonuclease Exposed on the Cell Surface{triangledown}

Jonathan A. Schmidt, Glenn F. Browning,* and Philip F. Markham

Veterinary Preclinical Centre, Department of Veterinary Science, The University of Melbourne, Parkville, Victoria 3010, Australia

Received 7 December 2006/ Accepted 9 February 2007

Mycoplasma hyopneumoniae mhp379 is a putative lipoprotein that shares significant amino acid sequence similarity with a family of bacterial thermostable nucleases. To examine the nuclease activity of mhp379, the gene was cloned and expressed in Escherichia coli following the deletion of the amino-terminal signal sequence and prokaryotic lipoprotein cleavage site and mutagenesis of the mycoplasma TGA tryptophan codons to TGG. The recombinant fusion protein yielded a 33-kDa thrombin cleavage product, corresponding in size to the mature mhp379 protein. Exonuclease activity was indicated by agarose gel electrophoresis analysis of the reaction products that were released when different nucleic acid substrates were used. Endonuclease activity was also indicated by the digestion of closed circular plasmid DNA. The recombinant mhp379 fusion protein completely digested single-stranded DNA, double-stranded DNA (dsDNA), and RNA. The optimal reaction conditions were determined with a novel nuclease assay based on the enhancement of fluorescence of SYBR green I bound to dsDNA. Optimal activity was observed in the presence of calcium ions at a concentration of 15 mM and a pH of 9.5. No nuclease activity was observed in the absence of calcium ions. Mycoplasmas do not have the ability to synthesize nucleic acid precursors, and thus, nucleases are likely to be important in the acquisition of precursors for the synthesis of nucleic acids. Homologs of an ATP-binding cassette (ABC) transport system were identified immediately downstream of the gene encoding mhp379, and two homologs of M. pneumoniae lipoprotein multigene family 2 were also identified immediately upstream. Homologs of mhp379 were identified in the sequenced genomes of a number of mycoplasma species, and in most cases the homologous ABC transport system was identified immediately downstream of the homologous gene; in several cases a homolog of M. pneumoniae lipoprotein multigene family 2 was also identified immediately upstream. These observations suggest that mhp379 comprises part of a conserved ABC transport operon in mycoplasmas and that the exonuclease activity of mhp379 may be associated with the conserved function of the ABC transport system in the import of nucleic acid precursors. This is the first study to identify the gene and characterize the activity of a mycoplasma exonuclease.

* Corresponding author. Mailing address: Veterinary Preclinical Centre, Department of Veterinary Science, The University of Melbourne, Parkville, Victoria 3010, Australia. Phone: 61 3 8344 7342. Fax: 61 3 8344 7374. E-mail: glenfb{at}unimelb.edu.au

{triangledown} Published ahead of print on 16 February 2007.

Journal of Bacteriology, May 2007, p. 3414-3424, Vol. 189, No. 9
0021-9193/07/$08.00+0     doi:10.1128/JB.01835-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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