Characterization of PIR 32, a candida albicans cell wall protein. (c2009)

2009 ◽  
Author(s):  
Wael G. Bahnan
2010 ◽  
Vol 165 (3) ◽  
pp. 250-258 ◽  
Author(s):  
Peter Hayek ◽  
Leila Dib ◽  
Pascal Yazbeck ◽  
Berna Beyrouthy ◽  
Roy A. Khalaf

Yeast ◽  
2003 ◽  
Vol 20 (5) ◽  
pp. 417-426 ◽  
Author(s):  
Lahcen Jaafar ◽  
Isma�l Moukadiri ◽  
Jes�s Zueco
Keyword(s):  

1990 ◽  
Vol 94 (4) ◽  
pp. 1897-1902 ◽  
Author(s):  
Susan M. Kleis-San Francisco ◽  
Mary L. Tierney

1994 ◽  
Vol 162 (1-2) ◽  
pp. 33-40
Author(s):  
W. Jenq ◽  
Chi Lan Chen ◽  
Chun Chang ◽  
Richard F. E. Crang
Keyword(s):  

2015 ◽  
Vol 62 (4) ◽  
pp. 825-835 ◽  
Author(s):  
Karolina Seweryn ◽  
Justyna Karkowska-Kuleta ◽  
Natalia Wolak ◽  
Oliwia Bochenska ◽  
Sylwia Kedracka-Krok ◽  
...  

2013 ◽  
Vol 457 (2) ◽  
pp. 347-360 ◽  
Author(s):  
Emeline Fabre ◽  
Ghenima Sfihi-Loualia ◽  
Marilyne Pourcelot ◽  
Bernadette Coddeville ◽  
Frédéric Krzewinski ◽  
...  

Candida albicans is a yeast responsible for serious infections in immunocompromised patients. In the present paper, we report the identification of an enzyme that initiates the synthesis of a bioactive cell wall carbohydrate antigenic factor, the β-mannans.


1994 ◽  
Vol 40 (1) ◽  
pp. 35-44 ◽  
Author(s):  
Srabani Banerjee ◽  
Judy Little ◽  
Maria Chan ◽  
Brian T. Luck ◽  
Colette Breuil ◽  
...  

A sensitive immunological tool has been developed to detect the sapstaining fungus Ophiostoma piceae 3871, which plagues the wood industry. Monoclonal antibodies (1F3(1), 4G3(14), 4G2(4), and 2B6(24)) produced against cell wall protein extracts of this fungus were specific. Specificity was estimated by enzyme linked immunosorbent assay, western blotting, and light and electron microscopy using the immunogold technique. Electron microscopy revealed gold particles localized on the outer surface of the cell wall. When screened against 24 biological control fungi the antibodies showed pratically no cross-reactivity (< 4%). When tested against 19 other staining fungi, the antibodies recognized three strains of Ophiostoma piceae, 1F3(1) recognized Phialophora botulispora, and the antibodies showed less than 5% reactivity with the other fungi. Chemical and enzymatic modification of the antigen revealed that the epitopes recognized by the monoclonal antibodies were glycospecific. Although the antibodies were produced against the cell wall protein extracts of the fungus grown in liquid culture, they also recognized the fungus growing in wood and therefore can be employed to investigate wood colonization by this fungus.Key words: Ophiostoma piceae, monoclonal antibodies, glycoprotein.


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