Enzymatic Release of Antioxidants for Human Low-Density Lipoprotein from Grape Pomace

Enzyme-assisted release of phenolic antioxidants from grape pomace from wine production was examined. The enzymes used were Grindamyl pectinase from Aspergillus niger and Celluclast from Trichoderma reesei. Total phenols released ranged from 820 to 6055 mg/L gallic acid equivalents (GAE) and varied...

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Veröffentlicht in:Journal of agricultural and food chemistry 1998-07, Vol.46 (7), p.2439-2446
Hauptverfasser: Meyer, Anne S, Jepsen, Signe M, Sørensen, Nina S
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container_issue 7
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container_title Journal of agricultural and food chemistry
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creator Meyer, Anne S
Jepsen, Signe M
Sørensen, Nina S
description Enzyme-assisted release of phenolic antioxidants from grape pomace from wine production was examined. The enzymes used were Grindamyl pectinase from Aspergillus niger and Celluclast from Trichoderma reesei. Total phenols released ranged from 820 to 6055 mg/L gallic acid equivalents (GAE) and varied in response to enzyme type, time of enzyme treatment, particle size of the pomace, and type of extraction solvent employed. The yield of total phenols was correlated to the degree of plant cell wall breakdown of grape pomace (r > 0.6, P < 0.01). Grindamyl pectinase catalyzed degradation of grape pomace polysaccharides (P < 0.001), whereas Celluclast did not. Reduction of the particle size of grape pomace to 125−250 μm increased the enzymatic polysaccharide hydrolysis and the recovery of phenols. The grape pomace extracts significantly retarded human low-density lipoprotein oxidation in vitro. When evaluated at 3.0 μM GAE, phenolic extracts of Grindamyl pectinase treated pomace of small particle size (125−250 μm) appeared to release more active antioxidant phenols than the other types of enzyme treatments tested (P < 0.05). Keywords: Pectinase; cellulase; phenols; plant cell wall degradation; LDL oxidation
doi_str_mv 10.1021/jf971012f
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The enzymes used were Grindamyl pectinase from Aspergillus niger and Celluclast from Trichoderma reesei. Total phenols released ranged from 820 to 6055 mg/L gallic acid equivalents (GAE) and varied in response to enzyme type, time of enzyme treatment, particle size of the pomace, and type of extraction solvent employed. The yield of total phenols was correlated to the degree of plant cell wall breakdown of grape pomace (r &gt; 0.6, P &lt; 0.01). Grindamyl pectinase catalyzed degradation of grape pomace polysaccharides (P &lt; 0.001), whereas Celluclast did not. Reduction of the particle size of grape pomace to 125−250 μm increased the enzymatic polysaccharide hydrolysis and the recovery of phenols. The grape pomace extracts significantly retarded human low-density lipoprotein oxidation in vitro. When evaluated at 3.0 μM GAE, phenolic extracts of Grindamyl pectinase treated pomace of small particle size (125−250 μm) appeared to release more active antioxidant phenols than the other types of enzyme treatments tested (P &lt; 0.05). 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Homeopathy. Health food ; Pharmacology. 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Agric. Food Chem</addtitle><description>Enzyme-assisted release of phenolic antioxidants from grape pomace from wine production was examined. The enzymes used were Grindamyl pectinase from Aspergillus niger and Celluclast from Trichoderma reesei. Total phenols released ranged from 820 to 6055 mg/L gallic acid equivalents (GAE) and varied in response to enzyme type, time of enzyme treatment, particle size of the pomace, and type of extraction solvent employed. The yield of total phenols was correlated to the degree of plant cell wall breakdown of grape pomace (r &gt; 0.6, P &lt; 0.01). Grindamyl pectinase catalyzed degradation of grape pomace polysaccharides (P &lt; 0.001), whereas Celluclast did not. Reduction of the particle size of grape pomace to 125−250 μm increased the enzymatic polysaccharide hydrolysis and the recovery of phenols. The grape pomace extracts significantly retarded human low-density lipoprotein oxidation in vitro. When evaluated at 3.0 μM GAE, phenolic extracts of Grindamyl pectinase treated pomace of small particle size (125−250 μm) appeared to release more active antioxidant phenols than the other types of enzyme treatments tested (P &lt; 0.05). 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Drug treatments</subject><subject>PHENOLIC COMPOUNDS</subject><subject>PLANT CELL WALL DEGRADATION</subject><subject>POLIGALACTURONASA</subject><subject>POLISACARIDOS</subject><subject>POLYGALACTURONASE</subject><subject>POLYHOLOSIDE</subject><subject>POLYSACCHARIDES</subject><subject>RENDEMENT</subject><subject>RENDIMIENTO</subject><subject>SOUS PRODUIT</subject><subject>SUBPRODUCTOS</subject><subject>TAMANO DE LA PARTICULA</subject><subject>TRICHODERMA LONGIBRACHIATUM</subject><subject>VID</subject><subject>VIGNE</subject><subject>YIELDS</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNptkMFO4zAQhi20SHQLBx4AyQc4cAjrceI4PlbdbkGqAFF6tqaOjdxt4sgOWsrTb1BWPe1c5vB_82v0EXIJ7A4Yhx87pyQw4O6ETEBwlgmA6huZsCHMKlHCGfme0o4xVgnJJmSzaD8PDfbe0Be7t5gsDY7O2t6HD19j2yfqQqT37w22dBX-ZD9tm3x_oCvfhS6G3vqWuhgauozYWfocGjT2nJw63Cd78W9PyebX4nV-n62elg_z2SrDAnif1TV3VcEBtk4wW4HI61wpsFUtiqJWZitkCcAMwpYrkJAbQMVLYHWJxbaQ-ZTcjr0mhpSidbqLvsF40MD0lw999DGw1yPbYTK4dxFb49PxgOfDsK_KbMR86u3HMcb4W5cyl0K_Pq-1LEUh1o9SPw781cg7DBrf4lC5WYNSalAshpen5GbM0SS9C--xHYT8572_ftCCSA</recordid><startdate>19980701</startdate><enddate>19980701</enddate><creator>Meyer, Anne S</creator><creator>Jepsen, Signe M</creator><creator>Sørensen, Nina S</creator><general>American Chemical Society</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19980701</creationdate><title>Enzymatic Release of Antioxidants for Human Low-Density Lipoprotein from Grape Pomace</title><author>Meyer, Anne S ; Jepsen, Signe M ; Sørensen, Nina S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a412t-dd2f84211bf50e8153d3991e8d544d9cb576110ca1b291713c1a92610d6a4b473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>ANTIOXIDANTES</topic><topic>ANTIOXIDANTS</topic><topic>ANTIOXYDANT</topic><topic>ASPERGILLUS NIGER</topic><topic>Biological and medical sciences</topic><topic>BYPRODUCTS</topic><topic>CELL WALLS</topic><topic>CELLULASE</topic><topic>CELULASA</topic><topic>COMPOSE PHENOLIQUE</topic><topic>COMPUESTOS FENOLICOS</topic><topic>CORRELATION</topic><topic>DOSAGE EFFECTS</topic><topic>EFECTOS DE DOSIFICACION</topic><topic>EFFET DOSE</topic><topic>ENZYME TREATMENT</topic><topic>EXPERIMENTACION IN VITRO</topic><topic>EXPERIMENTATION IN VITRO</topic><topic>General pharmacology</topic><topic>GENERO HUMANO</topic><topic>GENRE HUMAIN</topic><topic>GRAPEVINES</topic><topic>GROSSEUR DES PARTICULES</topic><topic>HIDROLISIS</topic><topic>HYDROLYSE</topic><topic>HYDROLYSIS</topic><topic>IN VITRO EXPERIMENTATION</topic><topic>LIPOPROTEINAS</topic><topic>LIPOPROTEINE</topic><topic>LIPOPROTEINS</topic><topic>MANKIND</topic><topic>Medical sciences</topic><topic>OXIDACION</topic><topic>OXIDATION</topic><topic>OXYDATION</topic><topic>PARED CELULAR</topic><topic>PAROI CELLULAIRE</topic><topic>PARTICLE SIZE</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>PHENOLIC COMPOUNDS</topic><topic>PLANT CELL WALL DEGRADATION</topic><topic>POLIGALACTURONASA</topic><topic>POLISACARIDOS</topic><topic>POLYGALACTURONASE</topic><topic>POLYHOLOSIDE</topic><topic>POLYSACCHARIDES</topic><topic>RENDEMENT</topic><topic>RENDIMIENTO</topic><topic>SOUS PRODUIT</topic><topic>SUBPRODUCTOS</topic><topic>TAMANO DE LA PARTICULA</topic><topic>TRICHODERMA LONGIBRACHIATUM</topic><topic>VID</topic><topic>VIGNE</topic><topic>YIELDS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meyer, Anne S</creatorcontrib><creatorcontrib>Jepsen, Signe M</creatorcontrib><creatorcontrib>Sørensen, Nina S</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meyer, Anne S</au><au>Jepsen, Signe M</au><au>Sørensen, Nina S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzymatic Release of Antioxidants for Human Low-Density Lipoprotein from Grape Pomace</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>1998-07-01</date><risdate>1998</risdate><volume>46</volume><issue>7</issue><spage>2439</spage><epage>2446</epage><pages>2439-2446</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Enzyme-assisted release of phenolic antioxidants from grape pomace from wine production was examined. The enzymes used were Grindamyl pectinase from Aspergillus niger and Celluclast from Trichoderma reesei. Total phenols released ranged from 820 to 6055 mg/L gallic acid equivalents (GAE) and varied in response to enzyme type, time of enzyme treatment, particle size of the pomace, and type of extraction solvent employed. The yield of total phenols was correlated to the degree of plant cell wall breakdown of grape pomace (r &gt; 0.6, P &lt; 0.01). Grindamyl pectinase catalyzed degradation of grape pomace polysaccharides (P &lt; 0.001), whereas Celluclast did not. Reduction of the particle size of grape pomace to 125−250 μm increased the enzymatic polysaccharide hydrolysis and the recovery of phenols. The grape pomace extracts significantly retarded human low-density lipoprotein oxidation in vitro. When evaluated at 3.0 μM GAE, phenolic extracts of Grindamyl pectinase treated pomace of small particle size (125−250 μm) appeared to release more active antioxidant phenols than the other types of enzyme treatments tested (P &lt; 0.05). Keywords: Pectinase; cellulase; phenols; plant cell wall degradation; LDL oxidation</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/jf971012f</doi><tpages>8</tpages></addata></record>
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source American Chemical Society Journals
subjects ANTIOXIDANTES
ANTIOXIDANTS
ANTIOXYDANT
ASPERGILLUS NIGER
Biological and medical sciences
BYPRODUCTS
CELL WALLS
CELLULASE
CELULASA
COMPOSE PHENOLIQUE
COMPUESTOS FENOLICOS
CORRELATION
DOSAGE EFFECTS
EFECTOS DE DOSIFICACION
EFFET DOSE
ENZYME TREATMENT
EXPERIMENTACION IN VITRO
EXPERIMENTATION IN VITRO
General pharmacology
GENERO HUMANO
GENRE HUMAIN
GRAPEVINES
GROSSEUR DES PARTICULES
HIDROLISIS
HYDROLYSE
HYDROLYSIS
IN VITRO EXPERIMENTATION
LIPOPROTEINAS
LIPOPROTEINE
LIPOPROTEINS
MANKIND
Medical sciences
OXIDACION
OXIDATION
OXYDATION
PARED CELULAR
PAROI CELLULAIRE
PARTICLE SIZE
Pharmacognosy. Homeopathy. Health food
Pharmacology. Drug treatments
PHENOLIC COMPOUNDS
PLANT CELL WALL DEGRADATION
POLIGALACTURONASA
POLISACARIDOS
POLYGALACTURONASE
POLYHOLOSIDE
POLYSACCHARIDES
RENDEMENT
RENDIMIENTO
SOUS PRODUIT
SUBPRODUCTOS
TAMANO DE LA PARTICULA
TRICHODERMA LONGIBRACHIATUM
VID
VIGNE
YIELDS
title Enzymatic Release of Antioxidants for Human Low-Density Lipoprotein from Grape Pomace
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