Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme

Detalhes bibliográficos
Autor(a) principal: Ahmed,S. A.
Data de Publicação: 2013
Outros Autores: Mostafa,F. A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Chemical Engineering
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322013000300003
Resumo: Studies were conducted on the production and extraction of exo-polygalacturonase (PG) in solid-state fermentation (SSF) using orange bagasse (Ob) and molokhia stalks (Ms) as a new solid support by Penicillium pinophlilum Hedg 3503 NRRL. The parameters affecting PG production under SSF were optimized. The maximum PG activity of ~ 3270 U/ g dry solid substrate was obtained from P. pinophlilum Hedg 3503 NRRL grown for 7 days on Ob and Ms in the ratio 1:3 (w/w), moistened with distilled water at 68.2% initial moisture content. Highest enzyme titers occurred in SSF without added nutrients, indicating nutrient sufficiency of the Ob and MS mixture to sustain growth and a high level of pectic substances which induced PG production. The extraction of PG from the fermented biomass was optimized. Among the various solvents tested, the maximum level of enzyme activity was achieved when acetate buffer (0.05 M; pH 5.0) was used. The optimum volume of buffer was 50 mL, an extraction time of 60 min was sufficient to extract most enzyme, which yielded 3269.6 U/ g dry solid substrate of enzyme activity. Repeated washes under the optimum conditions showed that most of the enzyme (about 98%) was recovered in three repeated extractions. Moreover, 68.9% of total activity was achieved in the first wash.
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spelling Utilization of orange bagasse and molokhia stalk for production of pectinase enzymeExo-polygalacturonaseSolid-state fermentationSolid substrateStudies were conducted on the production and extraction of exo-polygalacturonase (PG) in solid-state fermentation (SSF) using orange bagasse (Ob) and molokhia stalks (Ms) as a new solid support by Penicillium pinophlilum Hedg 3503 NRRL. The parameters affecting PG production under SSF were optimized. The maximum PG activity of ~ 3270 U/ g dry solid substrate was obtained from P. pinophlilum Hedg 3503 NRRL grown for 7 days on Ob and Ms in the ratio 1:3 (w/w), moistened with distilled water at 68.2% initial moisture content. Highest enzyme titers occurred in SSF without added nutrients, indicating nutrient sufficiency of the Ob and MS mixture to sustain growth and a high level of pectic substances which induced PG production. The extraction of PG from the fermented biomass was optimized. Among the various solvents tested, the maximum level of enzyme activity was achieved when acetate buffer (0.05 M; pH 5.0) was used. The optimum volume of buffer was 50 mL, an extraction time of 60 min was sufficient to extract most enzyme, which yielded 3269.6 U/ g dry solid substrate of enzyme activity. Repeated washes under the optimum conditions showed that most of the enzyme (about 98%) was recovered in three repeated extractions. Moreover, 68.9% of total activity was achieved in the first wash.Brazilian Society of Chemical Engineering2013-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322013000300003Brazilian Journal of Chemical Engineering v.30 n.3 2013reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/S0104-66322013000300003info:eu-repo/semantics/openAccessAhmed,S. A.Mostafa,F. A.eng2013-09-03T00:00:00Zoai:scielo:S0104-66322013000300003Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2013-09-03T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false
dc.title.none.fl_str_mv Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme
title Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme
spellingShingle Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme
Ahmed,S. A.
Exo-polygalacturonase
Solid-state fermentation
Solid substrate
title_short Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme
title_full Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme
title_fullStr Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme
title_full_unstemmed Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme
title_sort Utilization of orange bagasse and molokhia stalk for production of pectinase enzyme
author Ahmed,S. A.
author_facet Ahmed,S. A.
Mostafa,F. A.
author_role author
author2 Mostafa,F. A.
author2_role author
dc.contributor.author.fl_str_mv Ahmed,S. A.
Mostafa,F. A.
dc.subject.por.fl_str_mv Exo-polygalacturonase
Solid-state fermentation
Solid substrate
topic Exo-polygalacturonase
Solid-state fermentation
Solid substrate
description Studies were conducted on the production and extraction of exo-polygalacturonase (PG) in solid-state fermentation (SSF) using orange bagasse (Ob) and molokhia stalks (Ms) as a new solid support by Penicillium pinophlilum Hedg 3503 NRRL. The parameters affecting PG production under SSF were optimized. The maximum PG activity of ~ 3270 U/ g dry solid substrate was obtained from P. pinophlilum Hedg 3503 NRRL grown for 7 days on Ob and Ms in the ratio 1:3 (w/w), moistened with distilled water at 68.2% initial moisture content. Highest enzyme titers occurred in SSF without added nutrients, indicating nutrient sufficiency of the Ob and MS mixture to sustain growth and a high level of pectic substances which induced PG production. The extraction of PG from the fermented biomass was optimized. Among the various solvents tested, the maximum level of enzyme activity was achieved when acetate buffer (0.05 M; pH 5.0) was used. The optimum volume of buffer was 50 mL, an extraction time of 60 min was sufficient to extract most enzyme, which yielded 3269.6 U/ g dry solid substrate of enzyme activity. Repeated washes under the optimum conditions showed that most of the enzyme (about 98%) was recovered in three repeated extractions. Moreover, 68.9% of total activity was achieved in the first wash.
publishDate 2013
dc.date.none.fl_str_mv 2013-09-01
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=S0104-66322013000300003
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322013000300003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0104-66322013000300003
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 Brazilian Society of Chemical Engineering
publisher.none.fl_str_mv Brazilian Society of Chemical Engineering
dc.source.none.fl_str_mv Brazilian Journal of Chemical Engineering v.30 n.3 2013
reponame:Brazilian Journal of Chemical Engineering
instname:Associação Brasileira de Engenharia Química (ABEQ)
instacron:ABEQ
instname_str Associação Brasileira de Engenharia Química (ABEQ)
instacron_str ABEQ
institution ABEQ
reponame_str Brazilian Journal of Chemical Engineering
collection Brazilian Journal of Chemical Engineering
repository.name.fl_str_mv Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)
repository.mail.fl_str_mv rgiudici@usp.br||rgiudici@usp.br
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