Pregled bibliografske jedinice broj: 256367
Peptidoglycan monomer and its synthetic derivatives as substrates for N-acetylmuramyl-L-alanine amidase
Peptidoglycan monomer and its synthetic derivatives as substrates for N-acetylmuramyl-L-alanine amidase // Abstracts, 8th European Carbohydrate Symposium, Seville, 02.07.-07.07. 1995.
Sevilla, Španjolska, 1995. (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 256367 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Peptidoglycan monomer and its synthetic derivatives as substrates for N-acetylmuramyl-L-alanine amidase
Autori
Tomašić, Jelka ; Ljevaković, Đurđica ; Vranešić, Branka ; Šporec, Vesna
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Abstracts, 8th European Carbohydrate Symposium, Seville, 02.07.-07.07. 1995.
/ - , 1995
Skup
8th European Carbohydrate Symposium, Seville
Mjesto i datum
Sevilla, Španjolska, 02.07.1995. - 07.07.1995
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
N-acetylmuramyl-L-alanine amidase; peptidoglycan monomer; Boc-Tyr-peptidoglycan monomer; adamantylacetyl-peptidoglycan monomer
Sažetak
N-acetylmuramyl-L-alanine amidase from human serum hydrolyses peptidoglycan monomer (PGM) cleaving the lactylamide bond between lactic acid and L-alanine. The products of hydrolysis are the disaccharide GlcNAc-MurNAc and the pentapeptid, L-Ala-D-isoGln-mesoDAP-D-Ala-D-Ala. Boc-Tyr-PGM and adamantylacetyl-PGM are also good substrates for the amidase yielding the disaccharide and the corresponding hexapeptide and adamantylacetyl-pentapeptide, respectively.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
