Pregled bibliografske jedinice broj: 331331
Towards understanding enentio-selective enzyme catalysed chemical transformation of pro-drugs
Towards understanding enentio-selective enzyme catalysed chemical transformation of pro-drugs // Abstracts book / Tsantili-Kakoulidou, Anna (ur.).
Atena: University of Athens, 2008. str. 35-35 (predavanje, nije recenziran, sažetak, ostalo)
CROSBI ID: 331331 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Towards understanding enentio-selective enzyme catalysed chemical transformation of pro-drugs
Autori
Tomić, Sanja ; Ceilinger, Igor ; Janežić, Dušanka ; Hodošček, Milan
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Izvornik
Abstracts book
/ Tsantili-Kakoulidou, Anna - Atena : University of Athens, 2008, 35-35
Skup
13th Hellenic Symposium on Medicinal Chemistry
Mjesto i datum
Atena, Grčka, 12.03.2008. - 16.03.2008
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Nije recenziran
Ključne riječi
lipase; reactions; enantioselectivity; QM/MM
Sažetak
Mirror-image versions (enantiomers) of chiral molecules are not structurally identical, and while one enantiomer is acting as a drug, the other may be inactive or even severely harmful. That is why it is important that drugs are enantio-selectively clear. However, production of only one enatiomer in a chemical reaction is often a problem. Bacterial lipases are interesting for biotechnology because of their high enantioselectivity toward chemically and pharmaceutically important compounds. Lipase from bacteria Burkholderia cepacia (BCL) catalyzes esterification of both primary and secondary alcohols with good enantioselectivity producing compounds which are important building blocks for many chiral drugs. Herein we report study of the reaction pathway for BCL using density functional theory based quantum mechanics-molecular mechanics modeling (QM/MM). The reaction was accomplished for two enantiomers of 1-phenoxy-2-hydroxybutane (1), which binding modes were determined previously by molecular dynamics and Monte Carlo conformational search1. The experimentally determined enantiomeric ratio and the calculated one, E=e(-??G/RT) are of the same order of magnitude when the free energy difference, ??G is approximated with the QM/MM energy difference between the modelled hydrated BCL - S-E1 and the BCL - R-E1 tetrahedral complexes. References: 1. Tomič S., Bertoša B., Kojić-Prodić B. and Kolosvary I. Tetrahedron: Asymmetry 15 (2004), 1163-1172.
Izvorni jezik
Engleski
Znanstvena područja
Fizika
POVEZANOST RADA
Projekti:
098-1191344-2860 - Proučavanje biomakromolekula računalnim metodama i razvoj novih algoritama (Tomić, Sanja, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Sanja Tomić
(autor)