Naslov
Localization of Scw4p in the Saccharomyces cerevisiae cell wall

Autori
Stuparević, Igor ; Teparić, Renata ; Mrša, Vladimir

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
Abstracts of IV International Conference on Molecular Mechanisms in Fungal Cell Wall Biogenesis / Aebi, Marcus - Varšava : Polish Academy of Sciences, 2009

Skup
IV International Conference on Molecular Mechanisms in Fungal Cell Wall Biogenesis

Mjesto i datum
Varšava, Poljska, 30.08.2009. - 03.09.2009

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
cell wall; Pir proteins; Scw proteins

Sažetak
Yeast cell wall contains proteins that are noncovalently (Scw-proteins) or covalently (Ccw-proteins) bound to β-1, 3-glucan, the latter either through GPI-anchors and β-1, 6-glucan, or by alkali labile ester linkages between γ-carboxyl groups of glutamic acid and hydroxyl groups of glucoses (Pir-proteins, extracted from the cell wall by mild alkali). Disruption of all four genes coding for Pir-proteins revealed that a 67kDa protein still remained in the NaOH extract. Disruption of SCW4, a gene coding for one of the most abundant Scw protein resulted in disappearance of the 67kDa band from the extract, indicating that Scw4p was partly also covalently linked to the cell wall by an apparently new alkali sensitive linkage. Thus Scw4p could be released from cell walls by a treatment with hot SDS, by mild alkali, or by β-1, 3-glucanases. It was shown that noncovalently bound Scw4p (SDS released) undergoes the Kex2p proteolytic maturation. However, when alkali released proteins from wt and kex2 mutant were compared, covalently attached form of Scw4p had the same size indicating that only non-processed form of the protein was attached to β-1, 3-glucan. The SDS-extractable haemagglutinin-tagged Scw4p, from wt strain in which Scw4p was overproduced contained two forms, one processed by Kex2p and the other not. Scw4p protein released from the wall by glucanases or NaOH contained only the non-processed form. As expected, extraction of Scw4p by SDS from kex2 mutant also showed only one form of the protein demonstrating that the other form really was the product of Kex2p processing. To assess the biological role of Scw-proteins, mutants lacking the most prominent of them (scw4, scw10, scw11 and bgl2) and also strains overproducing same proteins were compared with respect of their mortality in the culture and their sensitivity to zymolyase. Generally, it was found that the native concentration of Scw proteins is required for optimal cell wall stability.

Izvorni jezik
Engleski

Znanstvena područja
Biotehnologija

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