Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nijole Dirvianskyte"'
Autor:
Jennifer L. Brennan, Michael Skjøt, Ralf Schweins, Allan Svendsen, Claire Rees, Valdemaras Razumas, Laura Cabo Fernandez, Malin Zackrisson, Paola Nativo, Antonios G. Kanaras, Christian Isak Jørgensen, Nijole Dirvianskyte, T. Robert Tshikhudo, Justas Barauskas, Tommy Nylander, Mathias Brust
Publikováno v:
Langmuir. 26:13590-13599
Variants of lipase were attached to gold nanoparticles (NPs) and their enzymatic activity was studied. The two bioengineered lipase variants have been prepared with biotin groups attached to different residues on the protein outer surface. The biotin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f2a94ac704f3431def3152e009dbc78
https://doi.org/10.1021/la1018604
https://doi.org/10.1021/la1018604
Publikováno v:
Journal für praktische Chemie. 342:715-719
A series of N-formyl-O-acyl-β-phenylserine derivatives 1b-7b were prepared by the interaction of N-acyl-b-phenylserine ethyl esters 1a-7a with formic acid in presence of 1.5% HF. One-pot acyl group N O migration followed N-formylation under elaborat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dd589eb7eb984a19a739b81a3c677c7
https://doi.org/10.1002/1521-3897(200009)342:7<715::aid-prac715>3.0.co
https://doi.org/10.1002/1521-3897(200009)342:7<715::aid-prac715>3.0.co
Autor:
Shamkant Patkar, Jesper Vind, Nijole Dirvianskyte, Allan Svendsen, Nikos S. Hatzakis, Alan E. Rowan, Valdemaras Razumas, Mathias Brust, T. Robert Tshikhudo, Roeland J. M. Nolte, Jennifer L. Brennan
Publikováno v:
Bioconjugate Chemistry, 17, 6, pp. 1373-1375
Bioconjugate Chemistry, 17, 1373-1375
Bioconjugate Chemistry, 17, 1373-1375
A simple and versatile method for the preparation of functional enzyme-gold nanoparticle conjugates using "click" chemistry has been developed. In a copper-catalyzed 1,2,3-triazole cycloaddition, an acetylene-functionalized Thermomyces lanuginosus li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22885b67531b5f74194e130c67e43b67
https://hdl.handle.net/2066/36080
https://hdl.handle.net/2066/36080
Publikováno v:
Zeitschrift fur Naturforschung. C, Journal of biosciences. 58(5-6)
Synthesis of N- and O-acyl derivatives of DL-serine and threo-DL-phenylserine was accomplished by a regioselective acylation of the corresponding amino acid. The residues introduced into amino acid structure contain hydrophobic long chain or aromatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f11ae85b21f1a668569ccba3b60729d
https://pubmed.ncbi.nlm.nih.gov/12872931
https://pubmed.ncbi.nlm.nih.gov/12872931