Pregled bibliografske jedinice broj: 1154442
Macrodomain hydrolase SCO6735 from Streptomyces coelicolor reverses genotoxic stress induced by T- linked DNA ADP-ribosylation
Macrodomain hydrolase SCO6735 from Streptomyces coelicolor reverses genotoxic stress induced by T- linked DNA ADP-ribosylation // FEBS Advances Lectures Course PARP2021:PARP Research on the family of poly(ADP-ribose) polymerases : Book of abstracts
Barcelona, 2021. str. 60-60 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1154442 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Macrodomain hydrolase SCO6735 from Streptomyces
coelicolor reverses genotoxic stress induced by T-
linked DNA ADP-ribosylation
Autori
Hloušek-Kasun, Andrea ; Mikolčević, Petra ; Tromans-Coia, Callum ; Jankevicius, Gytis ; Matković, Marija ; Bertoša, Branimir ; Ahel, Ivan ; Mikoč, Andreja
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
FEBS Advances Lectures Course PARP2021:PARP Research on the family of poly(ADP-ribose) polymerases : Book of abstracts
/ - Barcelona, 2021, 60-60
Skup
PARP2021: Research on the Family of Poly(ADP-ribose) Polymerases
Mjesto i datum
Barcelona, Španjolska, 07.09.2021. - 10.09.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
ADP-ribosylation ADP-ribosyl transferase ADP-ribosyl hydrolase PARP ; PARG Macrodomain Toxin-antitoxin system
Sažetak
Streptomyces species of bacteria have a very lively ADP-ribosylation metabolism. ADP- ribosylation is involved in the regulation of morphological differentiation and antibiotic production. More than 15 proteins that constitute ADP-ribosylation metabolic cycle have been found in Streptomyces coelicolor. We focused on the member of the macrodomain ADP-ribosylhydrolase SCO6735, whose disruption has been shown to increase the production of antibiotic actinorhodin. We structurally and biochemically characterized SCO6735 protein. SCO6735, shares a 19% similarity with DarG from toxin/antitoxin DarT/DarG bacterial system and 25% with human TARG1. Molecular dynamic simulations of SCO6735 WT and mutants in complex with substrate suggest a novel, substrate-assisted, catalytic mechanism. We showed that SCO6735 can reverse thymidine-linked ADP-ribosylation in vitro and in vivo. Experiments in vitro showed that SCO6735 is active on both protein and DNA modified substrates ; although it reverses DNA ADP-ribosylation on thymidines (modified by toxin DarT) much more efficiently. SCO6735 activity in vivo has been shown in heterologous (E. coli) and homologous (S. coelicolor) system. Both in vivo systems SCO6735 rescued from the toxic effect of DarT suggesting the SCO6735 might be a defence mechanism hydrolase, protecting the cell from genotoxic stress.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Biotehnologija
POVEZANOST RADA
Projekti:
HRZZ-IP-2016-06-4242 - Istraživanje uloge proteinske modifikacije ADP-ribozilacije kod bakterija (ADPRIBAC) (Mikoč, Andreja, HRZZ - 2016-06) ( CroRIS)
EK-H2020-867468 - Unlocking the antibiotic production potential in soil bacteria Streptomyces coelicolor (STREPUNLOCKED) (Mikoč, Andreja; Mikolčević, Petra, EK - H2020-WF-01-2018) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Andrea Hloušek-Kasun
(autor)
Marija Matković
(autor)
Branimir Bertoša
(autor)
Andreja Mikoč
(autor)
Ivan Ahel
(autor)
Petra Mikolčević
(autor)