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Applied and Environmental Microbiology, December 2004, p. 7311-7320, Vol. 70, No. 12
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.12.7311-7320.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Comparison of Proteolytic Activities Produced by Entomopathogenic Photorhabdus Bacteria: Strain- and Phase-Dependent Heterogeneity in Composition and Activity of Four Enzymes

Judit Marokházi,1 Katalin Lengyel,2 Szilvia Pekár,3 Gabriella Felföldi,1 András Patthy,4 László Gráf,1,4 András Fodor,1 and István Venekei1*

Departments of Biochemistry,1 Genetics,2 Biotechnology Research Group of the Hungarian Academy of Sciences, Eötvös Loránd University, Budapest,4 Department of Agricultural Zoology, Georgikon Faculty of Agriculture, University of Veszprém, Keszthely, Hungary3

Received 12 March 2004/ Accepted 1 August 2004

Twenty strains (including eight phase variant pairs) of nematode-symbiotic and insect-pathogenic Photorhabdus bacteria were examined for the production of proteolytic enzymes by using a combination of several methods, including gelatin liquefaction, zymography coupled to native and sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and activity measurement with two chromogen substrate types. Four protease activities (~74, ~55, ~54, and ~37 kDa) could be separated. The N-terminal sequences of three of the proteases were determined, and a comparison with sequences in databases allowed identification of these proteases as HEXXH metallopeptidases. Thus, the 74-kDa protease (described formerly as Php-B [J. Marokházi, G. Kóczán, F. Hudecz, L. Gráf, A. Fodor, and I. Venekei, Biochem. J. 379:633-640, 2004) is an ortholog of OpdA, a member the thimet oligopeptidase family, and the 55-kDa protease is an ortholog of PrtA, a HEXXH+H peptidase in clan MB (metzincins), while the 37-kDa protease (Php-C) belongs to the HEXXH+E peptidases in clan MA. The 54-kDa protease (Php-D) is a nonmetalloenzyme. PrtA and Php-C were zymographically detected, and they occurred in several smaller forms as well. OpdA could not be detected by zymography. PrtA, Php-C, and Php-D were secreted proteases; OpdA, in contrast, was an intracellular enzyme. OpdA activity was found in every strain tested, while Php-D was detected only in the Brecon/1 strain. There was significant strain variation in the secretion of PrtA and Php-C activities, but reduced activity or a lack of activity was not specific to secondary-phase variants. The presence of PrtA, OpdA, and Php-C activities could be detected in the hemolymph of Galleria melonella larvae 20 to 40 h postinfection. These proteases appear not to be directly involved in the pathogenicity of Photorhabdus, since strains or phase variants lacking any of these proteases do not show reduced virulence when they are injected into G. melonella larvae.

* Corresponding author. Mailing address: Department of Biochemistry, Eötvös Loránd University, Pázmány Péter stny. 1/C, 1117 Budapest, Hungary. Phone: (36)12090555. Fax: (36)13812172. E-mail: venekei{at}cerberus.elte.hu.

Applied and Environmental Microbiology, December 2004, p. 7311-7320, Vol. 70, No. 12
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.12.7311-7320.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Felfoldi, G., Marokhazi, J., Kepiro, M., Venekei, I. (2009). Identification of Natural Target Proteins Indicates Functions of a Serralysin-Type Metalloprotease, PrtA, in Anti-Immune Mechanisms. Appl. Environ. Microbiol. 75: 3120-3126 [Abstract] [Full Text]  
  • Held, K. G., LaRock, C. N., D'Argenio, D. A., Berg, C. A., Collins, C. M. (2007). A Metalloprotease Secreted by the Insect Pathogen Photorhabdus luminescens Induces Melanization. Appl. Environ. Microbiol. 73: 7622-7628 [Abstract] [Full Text]  


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