Pregled bibliografske jedinice broj: 927263
Stereoselective diol production by multi-enzyme system
Stereoselective diol production by multi-enzyme system // Abstract of European Biotechnology Congress 2017 held in Dubrovnik, Croatia during 25 - 27 May 2017 / Dundar, Munis (ur.).
Amsterdam: Elsevier, 2017. str. S10-S10 doi:10.1016/j.jbiotec.2017.06.034 (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 927263 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Stereoselective diol production by multi-enzyme system
Autori
Vrsalović Presečki, Ana ; Pintarić, Lela ; Švarc, Anera ; Vasić-Rački, Đurđa
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Abstract of European Biotechnology Congress 2017 held in Dubrovnik, Croatia during 25 - 27 May 2017
/ Dundar, Munis - Amsterdam : Elsevier, 2017, S10-S10
Skup
European Biotechnology Congress 2017
Mjesto i datum
Dubrovnik, Hrvatska, 25.05.2017. - 27.05.2017
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
multi-enzyme cascade reaction, asymmetric reduction, stereoselectivity, alcohol dehydrogenase, benzoylformate decarboxylase
Sažetak
Within the field of biocatalysis, multi-enzyme cascade reactions are an important strategy for the production of optically active chemicals. This approach is very promising from an environmental and as well the economical point of view since in this manner higher yields and productivities is accomplished, fewer chemicals are spent, isolation of intermediates is avoided and on industrial scale, waste and production costs are reduced. The synthesis of chiral building blocks is always challenging in the field of organic chemistry, especially the production of molecules with two chiral centers, as the chiral 1, 2-diols. These have wide application as synthons for chemical catalysts, agrochemicals and pharmaceuticals and can be produced by chemical and enzymatic methods. The production of specific form of the stereoisomer of 1, 2-diols by enzymatic approach seems to be more attractive since the synthesis takes place under mild conditions and result with high stereoselectivity. An example of multienzyme catalysis for the production of chiral 1, 2 diol will be presented. By coupling stereoselective carboligation reaction catalyzed by benzoylformate decarboxylase, L- selective reduction of carbonyl group with alcohol dehydrogenase and the coenzyme regeneration by formate dehydrogenase, enantiometrically pure diastereoselective diol was successfully produced from inexpensive substrates.
Izvorni jezik
Engleski
Znanstvena područja
Kemijsko inženjerstvo, Biotehnologija
POVEZANOST RADA
Ustanove:
Tekstilno-tehnološki fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Anera Švarc
(autor)
Lela Pintarić
(autor)
Ana Vrsalović Presečki
(autor)
Đurđa Vasić-Rački
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE