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Politechniki Gdańskiej

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Enzymes of the L-methionine biosynthesis pathway in Candida albicans as potential novel targets for antifungal chemotherapy

Fungal pathways of essential amino acids biosynthesis provide an abundant source of molecular targets for new antifungal compounds, among which the L-methionine biosynthesis pathway (MBP) may be promising. In this dissertation I characterized three C. albicans enzymes involved in MBP: homoserine O-acetyltransferase (CaMet2p), O-acetyl-L-homoserine sulfhydrylase (CaMet15p), and cystathionine-γ-synthase (CaStr2p). I performed crystallization trials of analyzed proteins, which led to the formation of a CaMet15p crystal of 7 Å resolution. Additionally, I proved that the inhibition of CaMet2p, CaMet15p, and CaStr2p induces fungal growth deficiency dependent on L-methionine (L-Met) presence. Among variety of examined potential inhibitors, I selected L-penicillamine (L-PEN) as the most effective against CaMet2p enzyme, and β-(5-Oxo-3-isoxazolin-2-yl)-L-alanine as an inhibitor of CaMet15p and CaStr2p. Moreover, I have assessed antifungal effect induced by combination of inhibitors, which showed a synergistic effect b

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Informacje dodatkowe

Kategoria
Doktoraty, rozprawy habilitacyjne, nostryfikacje
Typ
praca doktorska pracowników zatrudnionych w PG oraz studentów studium doktoranckiego
Język
angielski
Rok wydania
2024

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