Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Scientia Agrícola (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-90162010000200013 |
Resumo: | After harvesting litchi, the red color of the fruit pericarp is rapidly lost resulting in discoloration and browning during storage and marketing. The loss of the red color is caused by the degradation or loss of stability of anthocyanins. The action of peroxidase and polyphenoloxidase is usually related to the browning and discoloration of fruits of various species. This study aimed to evaluate the influence of pH and temperature on peroxidase and polyphenoloxidase activities, in a partially purified preparation of pericarp of the litchi cultivar Bengal. Fruits were harvested at the ripe stage and polyphenoloxidase was partially purified by sequential saturation in 80% ammonium sulfate. At concentrations of 40-50% and 60-70% ammonium sulfate the activities of polyphenoloxidase and peroxidase were, respectively, 124 times and 158 times higher than in the crude extract. The activity of peroxidase and polyphenoloxidase was maximum at pH 6.5 and 7.0, respectively, and no activity was detected at pH 2.5 and 9.5. Pre-incubation of the enzyme extract for 45 min at pH 2.5 or 9.5 completely inactivated the enzymes, with the highest degree of efficiency at pH 2.5. Peroxidase activity was highest at 70ºC and remained active for a period of 120 min at 70 and 80ºC. Peroxidase became completely inactive when maintained at 90ºC for 10 min or 1 min at 100ºC. Polyphenoloxidase activity was highest at 20ºC and remained active for a period of 120 min at 40 and 50ºC and was inactivated after 10 min at 60ºC. Due to the high temperature of inactivation of the peroxidase and polyphenoloxidase activities, the enzymes can be inactivated more easily in fruits using acid or alkaline solutions. |
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Scientia Agrícola (Online) |
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Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarpLitchi Chinensis Sonn.enzyme purificationskin browningAfter harvesting litchi, the red color of the fruit pericarp is rapidly lost resulting in discoloration and browning during storage and marketing. The loss of the red color is caused by the degradation or loss of stability of anthocyanins. The action of peroxidase and polyphenoloxidase is usually related to the browning and discoloration of fruits of various species. This study aimed to evaluate the influence of pH and temperature on peroxidase and polyphenoloxidase activities, in a partially purified preparation of pericarp of the litchi cultivar Bengal. Fruits were harvested at the ripe stage and polyphenoloxidase was partially purified by sequential saturation in 80% ammonium sulfate. At concentrations of 40-50% and 60-70% ammonium sulfate the activities of polyphenoloxidase and peroxidase were, respectively, 124 times and 158 times higher than in the crude extract. The activity of peroxidase and polyphenoloxidase was maximum at pH 6.5 and 7.0, respectively, and no activity was detected at pH 2.5 and 9.5. Pre-incubation of the enzyme extract for 45 min at pH 2.5 or 9.5 completely inactivated the enzymes, with the highest degree of efficiency at pH 2.5. Peroxidase activity was highest at 70ºC and remained active for a period of 120 min at 70 and 80ºC. Peroxidase became completely inactive when maintained at 90ºC for 10 min or 1 min at 100ºC. Polyphenoloxidase activity was highest at 20ºC and remained active for a period of 120 min at 40 and 50ºC and was inactivated after 10 min at 60ºC. Due to the high temperature of inactivation of the peroxidase and polyphenoloxidase activities, the enzymes can be inactivated more easily in fruits using acid or alkaline solutions.Escola Superior de Agricultura "Luiz de Queiroz"2010-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-90162010000200013Scientia Agricola v.67 n.2 2010reponame:Scientia Agrícola (Online)instname:Universidade de São Paulo (USP)instacron:USP10.1590/S0103-90162010000200013info:eu-repo/semantics/openAccessMizobutsi,Gisele PoleteFinger,Fernando LuizRibeiro,Rosilene AntônioPuschmann,RolfNeves,Ludmila Lafetá de MeloMota,Wagner Ferreira daeng2010-04-26T00:00:00Zoai:scielo:S0103-90162010000200013Revistahttp://revistas.usp.br/sa/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpscientia@usp.br||alleoni@usp.br1678-992X0103-9016opendoar:2010-04-26T00:00Scientia Agrícola (Online) - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp |
title |
Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp |
spellingShingle |
Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp Mizobutsi,Gisele Polete Litchi Chinensis Sonn. enzyme purification skin browning |
title_short |
Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp |
title_full |
Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp |
title_fullStr |
Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp |
title_full_unstemmed |
Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp |
title_sort |
Effect of pH and temperature on peroxidase and polyphenoloxidase activities of litchi pericarp |
author |
Mizobutsi,Gisele Polete |
author_facet |
Mizobutsi,Gisele Polete Finger,Fernando Luiz Ribeiro,Rosilene Antônio Puschmann,Rolf Neves,Ludmila Lafetá de Melo Mota,Wagner Ferreira da |
author_role |
author |
author2 |
Finger,Fernando Luiz Ribeiro,Rosilene Antônio Puschmann,Rolf Neves,Ludmila Lafetá de Melo Mota,Wagner Ferreira da |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Mizobutsi,Gisele Polete Finger,Fernando Luiz Ribeiro,Rosilene Antônio Puschmann,Rolf Neves,Ludmila Lafetá de Melo Mota,Wagner Ferreira da |
dc.subject.por.fl_str_mv |
Litchi Chinensis Sonn. enzyme purification skin browning |
topic |
Litchi Chinensis Sonn. enzyme purification skin browning |
description |
After harvesting litchi, the red color of the fruit pericarp is rapidly lost resulting in discoloration and browning during storage and marketing. The loss of the red color is caused by the degradation or loss of stability of anthocyanins. The action of peroxidase and polyphenoloxidase is usually related to the browning and discoloration of fruits of various species. This study aimed to evaluate the influence of pH and temperature on peroxidase and polyphenoloxidase activities, in a partially purified preparation of pericarp of the litchi cultivar Bengal. Fruits were harvested at the ripe stage and polyphenoloxidase was partially purified by sequential saturation in 80% ammonium sulfate. At concentrations of 40-50% and 60-70% ammonium sulfate the activities of polyphenoloxidase and peroxidase were, respectively, 124 times and 158 times higher than in the crude extract. The activity of peroxidase and polyphenoloxidase was maximum at pH 6.5 and 7.0, respectively, and no activity was detected at pH 2.5 and 9.5. Pre-incubation of the enzyme extract for 45 min at pH 2.5 or 9.5 completely inactivated the enzymes, with the highest degree of efficiency at pH 2.5. Peroxidase activity was highest at 70ºC and remained active for a period of 120 min at 70 and 80ºC. Peroxidase became completely inactive when maintained at 90ºC for 10 min or 1 min at 100ºC. Polyphenoloxidase activity was highest at 20ºC and remained active for a period of 120 min at 40 and 50ºC and was inactivated after 10 min at 60ºC. Due to the high temperature of inactivation of the peroxidase and polyphenoloxidase activities, the enzymes can be inactivated more easily in fruits using acid or alkaline solutions. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-04-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-90162010000200013 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-90162010000200013 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-90162010000200013 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Escola Superior de Agricultura "Luiz de Queiroz" |
publisher.none.fl_str_mv |
Escola Superior de Agricultura "Luiz de Queiroz" |
dc.source.none.fl_str_mv |
Scientia Agricola v.67 n.2 2010 reponame:Scientia Agrícola (Online) instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Scientia Agrícola (Online) |
collection |
Scientia Agrícola (Online) |
repository.name.fl_str_mv |
Scientia Agrícola (Online) - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
scientia@usp.br||alleoni@usp.br |
_version_ |
1748936461907918848 |