1. Hemoglobinase activity of a cysteine protease from the ixodid tick Haemaphysalis longicornis
- Author
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Yamaji, Kayoko, Tsuji, Naotoshi, Miyoshi, Takeharu, Islam, M. Khyrul, Hatta, Takeshi, Alim, M. Abdul, Anisuzzaman, Takenaka, Akio, and Fujisaki, Kozo
- Subjects
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HEMOGLOBINS , *CYSTEINE proteinases , *TICKS , *HAEMAPHYSALIS longicornis , *AMINO acids , *PROTEINS , *GENE expression , *MICROBIAL genetics - Abstract
Abstract: We report here the molecular characterization and possible function of a cysteine protease (termed HlCPL-A) identified in the midgut of the hard tick Haemaphysalis longicornis. HlCPL-A is a 333 amino acid protein belonging to the papain family of the cysteine protease. A construct encoding proHlCPL-A was expressed in Escherichia coli and purified as both procathepsin L and active processed cathepsin L forms. The HlCPL-A gene expression was up-regulated by blood-feeding process. HlCPL-A exhibited substrate specificity against synthetic peptidyl substrates (Z-Phe-Arg-MCA and Z-Arg-Arg-MCA; k cat / K m =0.19 and 0.0023 M−1 S−1, respectively). The proteolytic activity of HlCPL-A was inhibited by leupeptin, antipain and E-64 but was unaffected by pepstatin. HlCPL-A was capable of degrading bovine hemoglobin at pH 3.2 to 5.6. These results suggest that HlCPL-A may play important roles in the digestion of host hemoglobin in ticks. [Copyright &y& Elsevier]
- Published
- 2009
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