The secreted, multifunctional enzyme PLB1 (phospholipase B1 protein encoded by the PLB1 gene) is a virulence determinant of the pathogenic fungus Cryptococcus neoformans, but the mechanism of its secretion is unknown. The cryptococcal PLB1 gene encodes putative, N-terminal LP (leader peptide) and C-terminal GPI (glycosylphosphatidylinositol) anchor attachment motifs, suggesting that PLB1 is GPI-anchored before secretion. To investigate the role of these motifs in PLB1 secretion, four cDNA constructs were created encoding the full-length construct (PLB1) and three truncated versions without the LP and/or the GPI anchor attachment motifs [LP−PLB1 (PLB1 expressed without the LP consensus motif), LP−PLB1GPI− (PLB1 expressed without the LP and GPI consensus motifs) and PLB1GPI− (PLB1 expressed without the GPI anchor attachment motif) respectively]. The constructs were ligated into pYES2, and galactose-induced expression was achieved in Saccharomyces cerevisiae. The LP was essential for secretion of the PLB1 protein and its three activities (PLB, lysophospholipase and lysophospholipase transacylase). Deletion of the GPI motif to create PLB1GPI− resulted in a redistribution of activity from the cell wall and membranes to the secreted and cytosolic fractions, with 36–54% of the total activity being secreted as compared with <5% for PLB1. PLB1 produced the maximum cell-associated activity (>2-fold more than that for PLB1GPI−), with 75–86% of this in the cell-wall fraction, 6–19% in the membrane fraction and 3–7% in the cytosolic fraction. Cell-wall localization was confirmed by release of activity with β-glucanase in both S. cerevisiae recombinants and wild-type C. neoformans. The dominant location of PLB1 in the cell wall via GPI anchoring may permit immediate release of the enzyme in response to changing environmental conditions and may represent part of a novel mechanism for regulating the secretion of a fungal virulence determinant.
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Research Article|
July 26 2005
Secretion of cryptococcal phospholipase B1 (PLB1) is regulated by a glycosylphosphatidylinositol (GPI) anchor
Julianne T. Djordjevic;
Julianne T. Djordjevic
1
*Centre for Infectious Diseases and Microbiology, ICPMR and Westmead Millennium Institute, Westmead Hospital, Westmead 2145, NSW, Australia
1To whom correspondence should be addressed (email julianned@icpmr.wsahs.nsw.gov.au).
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Maurizio Del Poeta;
Maurizio Del Poeta
†Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, U.S.A.
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Tania C. Sorrell;
Tania C. Sorrell
*Centre for Infectious Diseases and Microbiology, ICPMR and Westmead Millennium Institute, Westmead Hospital, Westmead 2145, NSW, Australia
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Kylie M. Turner;
Kylie M. Turner
*Centre for Infectious Diseases and Microbiology, ICPMR and Westmead Millennium Institute, Westmead Hospital, Westmead 2145, NSW, Australia
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Lesley C. Wright
Lesley C. Wright
*Centre for Infectious Diseases and Microbiology, ICPMR and Westmead Millennium Institute, Westmead Hospital, Westmead 2145, NSW, Australia
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Publisher: Portland Press Ltd
Received:
January 10 2005
Revision Received:
April 06 2005
Accepted:
April 08 2005
Accepted Manuscript online:
April 08 2005
Online ISSN: 1470-8728
Print ISSN: 0264-6021
The Biochemical Society, London
2005
Biochem J (2005) 389 (3): 803–812.
Article history
Received:
January 10 2005
Revision Received:
April 06 2005
Accepted:
April 08 2005
Accepted Manuscript online:
April 08 2005
Citation
Julianne T. Djordjevic, Maurizio Del Poeta, Tania C. Sorrell, Kylie M. Turner, Lesley C. Wright; Secretion of cryptococcal phospholipase B1 (PLB1) is regulated by a glycosylphosphatidylinositol (GPI) anchor. Biochem J 1 August 2005; 389 (3): 803–812. doi: https://doi.org/10.1042/BJ20050063
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