3,4-Dihydroxyphenylalanine (DOPA)-containing peptides and proteins provide attractive design paradigms for pharmaceutical applications and engineering of synthetic polymers. An efficient and selective route to DOPA peptides by oxidation of L-tyrosine derivatives with tyrosinase is reported. The efficiency of the procedure was tested by using successively recycled tyrosinase immobilized on Eupergit®C250L and coated with polyelectrolytes by the layer-by-layer method.

Selective Synthesis of DOPA and DOPA Peptides by Native and Immobilized Tyrosinase in Organic Solvent / Botta, G., Delfino, M., Guazzaroni, M., Crestini, C., Onofri, S., Saladino, R.. - In: CHEMPLUSCHEM. - ISSN 2192-6506. - 78:4(2013), pp. 325-330. [10.1002/cplu.201200300]

Selective Synthesis of DOPA and DOPA Peptides by Native and Immobilized Tyrosinase in Organic Solvent

Saladino R
2013

Abstract

3,4-Dihydroxyphenylalanine (DOPA)-containing peptides and proteins provide attractive design paradigms for pharmaceutical applications and engineering of synthetic polymers. An efficient and selective route to DOPA peptides by oxidation of L-tyrosine derivatives with tyrosinase is reported. The efficiency of the procedure was tested by using successively recycled tyrosinase immobilized on Eupergit®C250L and coated with polyelectrolytes by the layer-by-layer method.
2013
biocatalysis; DOPA peptides; synthetic methods
01 Pubblicazione su rivista::01a Articolo in rivista
Selective Synthesis of DOPA and DOPA Peptides by Native and Immobilized Tyrosinase in Organic Solvent / Botta, G., Delfino, M., Guazzaroni, M., Crestini, C., Onofri, S., Saladino, R.. - In: CHEMPLUSCHEM. - ISSN 2192-6506. - 78:4(2013), pp. 325-330. [10.1002/cplu.201200300]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1766436
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