Purification and Characterization of protease from Zahdi dates plam seeds (Phoenix dactylifera L.)

Proteinases (E.C.3.4.21) family are widely distributed in the nature; it was present in animals tissues , plants and microbial cell . Protease was purified from Zahdi seed (Phoenix dactylifera L.) by several steps included ammonium sulphite ppt (75%) saturation and dialyzed against the 80mM...

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Main Author: Baghdad Science Journal
Format: Article
Language:Arabic
Published: College of Science for Women, University of Baghdad 2009-12-01
Series:Baghdad Science Journal
Subjects:
Online Access:http://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/1027
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spelling doaj-9bd775822a1b4acb91c775e09aa411dd2020-11-25T02:28:20ZaraCollege of Science for Women, University of BaghdadBaghdad Science Journal2078-86652411-79862009-12-016410.21123/bsj.6.4.633-639Purification and Characterization of protease from Zahdi dates plam seeds (Phoenix dactylifera L.)Baghdad Science Journal Proteinases (E.C.3.4.21) family are widely distributed in the nature; it was present in animals tissues , plants and microbial cell . Protease was purified from Zahdi seed (Phoenix dactylifera L.) by several steps included ammonium sulphite ppt (75%) saturation and dialyzed against the 80mM sodium phosphate buffer at pH 7.5 . The enzyme specific activity was 407.62 unit/mg protein. The obtained extract was purified by DEAE-Cellulose column followed by gel filtration through Sephacyl S-200 column .The enzyme specific activity ,yield and purification fold were 1873.49 unit/mg protein, 22.99 and 58.42% respectively. The results of protease characterization showed that the molecular weight was 25118 daltons as determined by gel filtration. The optimum temperature of the enzyme activity 35 C for 15 minutes and that for stability was 45 C for 15 minutes, using sodium phosphate buffer at pH 7.5, The optimum pH for the enzyme stability and activity were 8.5 for 15 minute and 7.5 respectively. http://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/1027"Protease, Zahdi dates plam seeds, purification and characterization plant proteases"
collection DOAJ
language Arabic
format Article
sources DOAJ
author Baghdad Science Journal
spellingShingle Baghdad Science Journal
Purification and Characterization of protease from Zahdi dates plam seeds (Phoenix dactylifera L.)
Baghdad Science Journal
"Protease, Zahdi dates plam seeds, purification and characterization plant proteases"
author_facet Baghdad Science Journal
author_sort Baghdad Science Journal
title Purification and Characterization of protease from Zahdi dates plam seeds (Phoenix dactylifera L.)
title_short Purification and Characterization of protease from Zahdi dates plam seeds (Phoenix dactylifera L.)
title_full Purification and Characterization of protease from Zahdi dates plam seeds (Phoenix dactylifera L.)
title_fullStr Purification and Characterization of protease from Zahdi dates plam seeds (Phoenix dactylifera L.)
title_full_unstemmed Purification and Characterization of protease from Zahdi dates plam seeds (Phoenix dactylifera L.)
title_sort purification and characterization of protease from zahdi dates plam seeds (phoenix dactylifera l.)
publisher College of Science for Women, University of Baghdad
series Baghdad Science Journal
issn 2078-8665
2411-7986
publishDate 2009-12-01
description Proteinases (E.C.3.4.21) family are widely distributed in the nature; it was present in animals tissues , plants and microbial cell . Protease was purified from Zahdi seed (Phoenix dactylifera L.) by several steps included ammonium sulphite ppt (75%) saturation and dialyzed against the 80mM sodium phosphate buffer at pH 7.5 . The enzyme specific activity was 407.62 unit/mg protein. The obtained extract was purified by DEAE-Cellulose column followed by gel filtration through Sephacyl S-200 column .The enzyme specific activity ,yield and purification fold were 1873.49 unit/mg protein, 22.99 and 58.42% respectively. The results of protease characterization showed that the molecular weight was 25118 daltons as determined by gel filtration. The optimum temperature of the enzyme activity 35 C for 15 minutes and that for stability was 45 C for 15 minutes, using sodium phosphate buffer at pH 7.5, The optimum pH for the enzyme stability and activity were 8.5 for 15 minute and 7.5 respectively.
topic "Protease, Zahdi dates plam seeds, purification and characterization plant proteases"
url http://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/1027
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