Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography

In this research, there was purified of β-1,3- endoglucanase from cabbage, having the aim to calculate purification level of enzyme by ion exchange chromatography methods. That process was started by producing enzyme isolated from Gloria osena hybrid of cabbage,then precipitate it using ammonium sul...

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Main Authors: Manuhara, Yosephine Sri Wulan, Puspaningsih, Ni Nyoman Tri, Wahyuningsih, Sri Pudji Astuti
Format: Conference or Workshop Item PeerReviewed
Language:English
English
English
Published: Universitas Teknologi Malasya. 2009
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Online Access:http://repository.unair.ac.id/45612/13/Bukti%20C17%20-%20Purification%20of%20B-1%2C3-Endoglucanase%20from%20Cabbage.pdf
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spelling id-langga.456122017-12-17T16:30:11Z http://repository.unair.ac.id/45612/ Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography Manuhara, Yosephine Sri Wulan Puspaningsih, Ni Nyoman Tri Wahyuningsih, Sri Pudji Astuti QD415-436 Biochemistry QK710-899 Plant physiology S Agriculture In this research, there was purified of β-1,3- endoglucanase from cabbage, having the aim to calculate purification level of enzyme by ion exchange chromatography methods. That process was started by producing enzyme isolated from Gloria osena hybrid of cabbage,then precipitate it using ammonium sulphate with concentration of saturated 40%. The sediment of enzyme was diluted by phosphate citrate then purified by dialysis in order to separate enzyme from other proteins and ammonium sulphate. The next, hydrophobic interaction chromatography eluted by ammonium suphate concentration of saturated 40% in Tris HCl pH 7 (high concentration to low concentration gradient) with Butyl-topearl 650M in ethanol as matrix was done to purify enzyme based on hydrophobic group interaction of protein and absorbent. After that, there was purifying enzyme by ion exchange chromatography in order to separate enzyme based on it’s ion. Enzyme was eluted by NaCl (0- 0.5) M in Tris HCl (low concentration to high concentration gradient) with DEAE-toyopearl 650 M in ethanol as the matrix. The best result of this ion exchange chromatography on first fraction pH 7 had purification level 3.534,1 of initial extract. Universitas Teknologi Malasya. 2009 Conference or Workshop Item PeerReviewed text en http://repository.unair.ac.id/45612/13/Bukti%20C17%20-%20Purification%20of%20B-1%2C3-Endoglucanase%20from%20Cabbage.pdf text en http://repository.unair.ac.id/45612/2/Reviewer%20dan%20Validasi%20Bukti%20C17.pdf text en http://repository.unair.ac.id/45612/19/Bukti%20C17%20-%20Purification%20of%20B-1%2C3-Endoglucanase%20from%20Cabbage.pdf Manuhara, Yosephine Sri Wulan and Puspaningsih, Ni Nyoman Tri and Wahyuningsih, Sri Pudji Astuti (2009) Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography. In: Second International Conference and Workshops on Basic and Applied Sciences and Regional Annual Fundamental Science Seminar 2009 volume iv, 2-4 June 2009, Johor Bahru, Malaysia.
institution Universitas Airlangga
building Universitas Airlangga Library
country Indonesia
collection UNAIR Repository
language English
English
English
topic QD415-436 Biochemistry
QK710-899 Plant physiology
S Agriculture
spellingShingle QD415-436 Biochemistry
QK710-899 Plant physiology
S Agriculture
Manuhara, Yosephine Sri Wulan
Puspaningsih, Ni Nyoman Tri
Wahyuningsih, Sri Pudji Astuti
Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography
description In this research, there was purified of β-1,3- endoglucanase from cabbage, having the aim to calculate purification level of enzyme by ion exchange chromatography methods. That process was started by producing enzyme isolated from Gloria osena hybrid of cabbage,then precipitate it using ammonium sulphate with concentration of saturated 40%. The sediment of enzyme was diluted by phosphate citrate then purified by dialysis in order to separate enzyme from other proteins and ammonium sulphate. The next, hydrophobic interaction chromatography eluted by ammonium suphate concentration of saturated 40% in Tris HCl pH 7 (high concentration to low concentration gradient) with Butyl-topearl 650M in ethanol as matrix was done to purify enzyme based on hydrophobic group interaction of protein and absorbent. After that, there was purifying enzyme by ion exchange chromatography in order to separate enzyme based on it’s ion. Enzyme was eluted by NaCl (0- 0.5) M in Tris HCl (low concentration to high concentration gradient) with DEAE-toyopearl 650 M in ethanol as the matrix. The best result of this ion exchange chromatography on first fraction pH 7 had purification level 3.534,1 of initial extract.
format Conference or Workshop Item
PeerReviewed
author Manuhara, Yosephine Sri Wulan
Puspaningsih, Ni Nyoman Tri
Wahyuningsih, Sri Pudji Astuti
author_facet Manuhara, Yosephine Sri Wulan
Puspaningsih, Ni Nyoman Tri
Wahyuningsih, Sri Pudji Astuti
author_sort Manuhara, Yosephine Sri Wulan
title Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography
title_short Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography
title_full Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography
title_fullStr Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography
title_full_unstemmed Purification of β-1,3-Endoglucanase from Cabbage (Brassicaoleracea cv. capitata L.) by Ion Exchange Chromatography
title_sort purification of β-1,3-endoglucanase from cabbage (brassicaoleracea cv. capitata l.) by ion exchange chromatography
publisher Universitas Teknologi Malasya.
publishDate 2009
url http://repository.unair.ac.id/45612/13/Bukti%20C17%20-%20Purification%20of%20B-1%2C3-Endoglucanase%20from%20Cabbage.pdf
http://repository.unair.ac.id/45612/2/Reviewer%20dan%20Validasi%20Bukti%20C17.pdf
http://repository.unair.ac.id/45612/19/Bukti%20C17%20-%20Purification%20of%20B-1%2C3-Endoglucanase%20from%20Cabbage.pdf
http://repository.unair.ac.id/45612/
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