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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College of Science for Women, University of Baghdad
2009-12-01
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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.
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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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