Naslov
Pir Proteins of Saccharomyces cerevisiae are Attached to betha-1, 3-Glucan by a New Protein-Carbohydrate Linkage

Autori
Ecker, Margit ; Deutzmann, Rainer ; Lehle, Ludwig ; Mrša, Vladimir ; Tanner, Widmar

Izvornik
Journal of Biological Chemistry (0021-9258) 281 (2006), 17; 11523-11529

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
yeast; cell wall; cell wall proteins; Pir-proteins

Sažetak
A family of covalently linked cell wall proteins of Saccharomyces cerevisiae, called Pir proteins, are characterized by up to 10 conserved repeating units. Ccw5/Pir4p contains only one complete repeating sequence and its deletion caused a release of the protein into the medium. The exchange of each of three glutamines (Gln69, Gln74, Gln76) as well as one aspartic acid (Asp72) within the repeating unit leads to a loss of the protein from the cell wall. Amino acid sequencing revealed that only Gln74 is modified. Release of the protein with mild alkali, changed Gln74 to to glutamic acid, suggesting that Gln74 is involved in the linkage. Analysis by mass spectrometry showed that 5 hexoses are attached to Gln/Glu74. Sugar analysis revealed glucose as the only constituent. It is suggested that Pir proteins form novel, alkali labile ester linkages between the y-carboxyl group of glutamic acids, arising from specific glutamines, with hydroxyl groups of glucoses of betha-1, 3-glucan chains. This transglutaminase-type reaction could take place extracellularly and would energetically proceed on the account of amido group elimination.

Izvorni jezik
Engleski

Znanstvena područja
Biotehnologija

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