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1.
Appl Biochem Biotechnol ; 185(4): 1029-1043, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29404908

RESUMEN

Carboxypeptidase A (CPA) is a metalloexopeptidase that catalyzes the hydrolysis of the peptide bonds that are adjacent to the C-terminal end of a polypeptide chain. The enzyme preferentially cleaves over C-terminal L-amino acids with aromatic or branched side chains. This is of main importance for food industry because it can be employed for manufacturing functional foods from different protein sources with reduced hydrophobic amino acid content for patients with deficiencies in the absorption or digestion of the corresponding amino acids. In that way, strategies for effective multipoint covalent immobilization of CPA metalloenzyme on chitosan beads have been developed. The study of the ability to produce several chemical modifications on chitosan molecules before, during and after its coagulation to form carrier beads lead in a protective effect of the polymer matrix. The chemical modification of chitosan through the use of an N-alkylation strategy produced the best derivatives. N-alkyl chitosan derivative beads with D-fructose presented values of 0.86 for immobilization yield, 314.6 IU g-1 bead for initial activity of biocatalyst and were 5675.64-fold more stable than the free enzyme at 55 °C. Results have shown that these derivatives would present a potential technological application in hydrolytic processes due to both their physical properties, such as low swelling capacity, reduced metal chelation ability and bulk mesoporosity, and increased operational stability when compared with soluble enzyme.


Asunto(s)
Carboxipeptidasas A/química , Quitosano/química , Enzimas Inmovilizadas/química , Biocatálisis , Estabilidad de Enzimas , Fructosa/química , Calor
2.
PLoS One ; 10(10): e0139550, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26465145

RESUMEN

Milk whey proteins are well known for their high biological value and versatile functional properties, characteristics that allow its wide use in the food and pharmaceutical industries. In this work, a 24 kDa protein from buffalo cheese whey was analyzed by mass spectrometry and presented homology with Bos taurus beta-lactoglobulin. In addition, the proteins present in buffalo cheese whey were hydrolyzed with pepsin and with different combinations of trypsin, chymotrypsin and carboxypeptidase-A. When the TNBS method was used the obtained hydrolysates presented DH of 55 and 62% for H1 and H2, respectively. Otherwise for the OPA method the DH was 27 and 43% for H1 and H2, respectively. The total antioxidant activities of the H1 and H2 samples with and without previous enzymatic hydrolysis, determined by DPPH using diphenyl-p-picrylhydrazyl radical, was 4.9 and 12 mM of Trolox equivalents (TE) for H2 and H2Dint, respectively. The increased concentrations for H1 and H2 samples were approximately 99% and 75%, respectively. The in vitro gastrointestinal digestion efficiency for the samples that were first hydrolyzed was higher compared with samples not submitted to previous hydrolysis. After in vitro gastrointestinal digestion, several amino acids were released in higher concentrations, and most of which were essential amino acids. These results suggest that buffalo cheese whey is a better source of bioavailable amino acids than bovine cheese whey.


Asunto(s)
Queso/análisis , Análisis de los Alimentos/métodos , Hidrolisados de Proteína/química , Proteína de Suero de Leche/química , Suero Lácteo/metabolismo , Aminoácidos/química , Animales , Antioxidantes/química , Compuestos de Bifenilo/química , Búfalos , Carboxipeptidasas A/química , Bovinos , Cromanos/química , Quimotripsina/química , Tracto Gastrointestinal/metabolismo , Hidrólisis , Lactoglobulinas/química , Lactosa/química , Espectrometría de Masas , Péptidos/química , Picratos/química , Tripsina/química
3.
Biotechnol Prog ; 19(2): 565-74, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12675602

RESUMEN

This paper presents stable carboxypeptidase A (CPA)-glyoxyl derivatives, to be used in the controlled hydrolysis of proteins. They were produced after immobilizing-stabilizing CPA on cross-linked 6% agarose beads, activated with low and high concentrations of aldehyde groups, and different immobilization times. The CPA-glyoxyl derivatives were compared to other agarose derivatives, prepared using glutaraldehyde as activation reactant. The most stabilized CPA-glyoxyl derivative was produced using 48 h of immobilization time and high activation grade of the support. This derivative was approximately 260-fold more stable than the soluble enzyme and presented approximately 42% of the activity of the soluble enzyme for the hydrolysis of long-chain peptides (e.g., cheese whey proteins previously hydrolyzed with immobilized trypsin and chymotrypsin) and of the small substrate N-benzoylglycyl-l-phenylalanine (hippuryl-l-Phe). These results were much better than those achieved using the conventional support, glutaraldehyde-agarose. Amino acid analysis of the products of the acid hydrolysis of CPA (both soluble and immobilized) showed that approximately four lysine residues were linked on the glyoxyl agarose beads, suggesting the existence of an intense multipoint covalent attachment between the enzyme and the support. The maximum temperature of hydrolysis was increased from 50 degrees C (soluble enzyme) to 70 degrees C (most stable CPA-glyoxyl derivative). The most stable CPA-glyoxyl derivative could be efficiently used in the hydrolysis of long-chain peptides at high temperature (e.g., 60 degrees C), being able to release 2-fold more aromatic amino acids (Tyr, Phe, and Trp) than the soluble enzyme, under the same operational conditions. This new CPA derivative greatly increased the feasibility of using this protease in the production of protein hydrolysates that must be free of aromatic amino acids.


Asunto(s)
Carboxipeptidasas A/química , Carboxipeptidasas A/síntesis química , Hidrocarburos Aromáticos/química , Proteínas de la Leche/química , Fenilalanina/análogos & derivados , Fenilalanina/química , Ingeniería de Proteínas/métodos , Hidrolisados de Proteína/síntesis química , Aminoácidos/química , Quimotripsina/química , Diseño de Fármacos , Activación Enzimática , Estabilidad de Enzimas , Enzimas Inmovilizadas/síntesis química , Enzimas Inmovilizadas/química , Concentración de Iones de Hidrógeno , Especificidad por Sustrato , Temperatura , Tripsina/química
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