Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Boris Galunsky"'
Publikováno v:
Journal of the Serbian Chemical Society, Vol 81, Iss 11, Pp 1231-1237 (2016)
An E -chalcone was obtained with very high stereoselectivity for the first time by an enzyme-catalyzed Claisen–Schmidt condensation between benzaldehyde and acetophenone. From a set of lipases, only that from hog pancreas demonstrated promiscuity,
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 59:106-110
The sunflower seed ( Helianthus annuus L.) major aminopeptidase primary specificity has been assessed with a number of specially designed amino acid amides and alkyl esters. Studies with amino acid 4-nitroanilides with straight alkyl side chains sugg
Autor:
Nicolina Stambolieva, Diana Zhiryakova, Ivaylo Ivanov, Sonya Ilieva, Boris Galunsky, Maya Guncheva
Publikováno v:
FEBS Journal. 276:2589-2598
A new set of experimental kinetic data on the hydrolysis of a series of phenylacetyl p-substituted anilides catalyzed by penicillin G acylase from Escherichia coli (PGA) is presented in this article. The Hammett plot of log(k(cat,R)/k(cat,H)) versus
Publikováno v:
Acta Physiologiae Plantarum. 31:199-205
The sunflower seed (Helianthus annuus L.) major peptidase was purified to molecular homogeneity. It is an 80 kDa enzyme with pI of 4.6 and optimal activity at pH 7.5–8.0 and 45–50°C. It is a thiol-dependent aminopeptidase hydrolyzing peptides in
Publikováno v:
Chromatographia. 67:305-308
The present communication describes the novel application of mixed-mode adsorbents for bifunctional chromatography. Oasis MCX mixed-mode adsorbent (Waters GmbH, Eschborn, Germany) shows a high binding capacity for Se-Met. The adsorbed selenoamino aci
Publikováno v:
Analytical and Bioanalytical Chemistry. 384:244-249
In a previous work we described the isolation of selenium organic species from Antarctic krill after enzymatic hydrolysis. In this paper we present the results of the influence of ultrasonication on the enzymatic treatment and the successive isolatio
Publikováno v:
European Journal of Biochemistry. 271:2272-2279
Kinetic experiments with a substrate series of phenylacetyl-arylamides reveal that at least one polar group in the amine moiety is required for the proper orientation of the substrate in the large nucleophile-binding subsite of penicillin acylase of
Publikováno v:
European Journal of Biochemistry. 270:4721-4728
Penicillin amidase from Alcaligenes faecalis is a recently identified N-terminal nucleophile hydrolase, which possesses the highest specificity constant (kcat/Km) for the hydrolysis of benzylpenicillin compared with penicillin amidases from other sou
Autor:
Volker Kasche, Boris Galunsky
Publikováno v:
Advanced Synthesis & Catalysis. 344:1115-1119
Publikováno v:
Monatshefte fuer Chemie/Chemical Monthly. 131:623-632