Pregled bibliografske jedinice broj: 802714
Ispitivanje procesiranja Scw4p proteina stanične stijenke u stanicama kex2 i 5ypsΔkex2 mutanata kvasca S. cerevisiae
Ispitivanje procesiranja Scw4p proteina stanične stijenke u stanicama kex2 i 5ypsΔkex2 mutanata kvasca S. cerevisiae, 2015., diplomski rad, preddiplomski, Prehrambeno-biotehnološki fakultet, Zagreb
CROSBI ID: 802714 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Ispitivanje procesiranja Scw4p proteina stanične stijenke u stanicama kex2 i 5ypsΔkex2 mutanata kvasca S. cerevisiae
(Investigation of the processing of yeast cell wall protein Scw4p in the kex2 and 5ypsΔkex2 mutant of S. cerevisiae)
Autori
Glavan, Martina
Vrsta, podvrsta i kategorija rada
Ocjenski radovi, diplomski rad, preddiplomski
Fakultet
Prehrambeno-biotehnološki fakultet
Mjesto
Zagreb
Datum
08.07
Godina
2015
Stranica
34
Mentor
Teparić, Renata
Ključne riječi
Saccharomyces cerevisiae; stanična stijenka kvasca; protein Scw4p; Kex2p; japsinske proteaze
(Saccharomyces cerevisiae; yeast cell wall; Scw4p protein; Kex2p protease; aspartic proteases yapsins)
Sažetak
Protein Scw4p is one of the most abundant non-covalently linked cell wall proteins in yeast and its role in the cell has not yet been discovered. It was previously shown that the protein is linked to the yeast cell wall by two different mechanisms - covalently and non-covalently. It is assumed that proteolytic enzymes which might have a role in processing of Scw4p are Kex2p and a family of aspartic proteases called yapsins and that non-covalently bound forms of Scw4p underwent the proteolytic processing, while the covalently bound Scw4p was not processed. Depending on the processing three forms of Scw4p in the cell wall with different molecular weights could be found. In this work Western blot analysis of Scw4p protein, isolated from 5ypsΔkex2 and kex2 mutant yeast transformed with native and mutated forms of the gene SCW4, was performed in order to get a better insight into the processing of Scw4p protein. Another object of this study was to determinate the impact of protein Scw4p overexpression on the viability of wild-type cells, kex2, 5ypsΔ and 5ypsΔkex2 mutants to gather information about the possible physiological role and possible differences in the activities of the various forms of this protein in the yeast cell wall.
Izvorni jezik
Hrvatski
Znanstvena područja
Biotehnologija
POVEZANOST RADA
Projekti:
058-0580477-2240 - Molekularni mehanizmi ugradnje proteina u staničnu stijenku kvasca (Mrša, Vladimir, MZOS ) ( CroRIS)
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb
Profili:
Renata Teparić
(mentor)