Purification, characterisation and inhibition studies of protease from Coriandrum sativum

Protease from coriander leaf (Coriandrum sativum) was evaluated for its ability to detect selected heavy metals using Bradford-protease-casein assay system. Considering the highly polluted environment with heavy metals contributed by industrial wastages and its implications on public health, this pr...

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Main Author:	Gunasekaran, Baskaran
Format:	Thesis
Language:	English
Published:	2011
Subjects:	Proteolytic enzymes Coriander Heavy metals
Online Access:	http://psasir.upm.edu.my/id/eprint/27219/1/FBSB%202011%2030R.pdf
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spelling	my-upm-ir.272192014-01-16T07:42:47Z Purification, characterisation and inhibition studies of protease from Coriandrum sativum 2011-05 Gunasekaran, Baskaran Protease from coriander leaf (Coriandrum sativum) was evaluated for its ability to detect selected heavy metals using Bradford-protease-casein assay system. Considering the highly polluted environment with heavy metals contributed by industrial wastages and its implications on public health, this present study was dedicated to provide a rapid and sensitive assay for the detection of heavy metals in the environmental samples. The basis of the protein assay using casein as a substrate relies upon the inability of the Bradford reagent to stain polypeptide with less than molecular weight of 2 kDa. Casein that has been stained by the Bradford reagent gives a dark blue color. However, the degradation product is not stained by the reagent and the solution remains brown in color. In the presence of heavy metals that inhibit protease activity, casein would remain undigested and the color would remain blue even after incubation. Optimization studies were carried out for this protease prior to heavy metals inhibition studies. The optimization studies include enzyme concentration, substrate concentration, pH, temperature and time of incubation. The optimum concentration of protease, substrate, temperature and incubation time for protease were 0.45 mg/ml protease, 0.43 mg/ml casein, 35oC and 20 min respectively after a period of heavy metals incubation. This enzyme was then purified through anion exchanger using DEAE- Cellulose column and gel filtration using Agilent ZORBAX column. The molecular weight detected was around 55 kDa. Protease activity obtained from coriander was found to be optimum at pH around 8 to 9.5. For this bioassay, two heavy metals showed inhibition towards enzyme activity at a concentration of 1 mg/l. The inhibition shown by the heavy metals on protease activity were around 40% for mercury and 70% for zinc. The IC50 values of mercury and zinc were 3.22 mg/l and 0.73 mg/l respectively. The limits of detection (LOD) for mercury and zinc were 0.24 mg/l and 0.23 mg/l respectively. The limits of quantitation (LOQ) for mercury and zinc were 0.80 mg/l and 0.76 mg/l respectively. This bioassay using coriander protease was found not to be sensitive towards pesticides and xenobiotics. The advantage of the protease bioassay compared to other bioassay relies on its rapidity, simplicity, economical value, stability in severe conditions such as pH and temperature as well as relatively interference free from detergents, solvents and pesticides. Proteolytic enzymes Coriander Heavy metals 2011-05 Thesis http://psasir.upm.edu.my/id/eprint/27219/ http://psasir.upm.edu.my/id/eprint/27219/1/FBSB%202011%2030R.pdf application/pdf en public masters Universiti Putra Malaysia Proteolytic enzymes Coriander Heavy metals Faculty of Biotechnology and Biomolecular Sciences
institution	Universiti Putra Malaysia
collection	PSAS Institutional Repository
language	English
topic	Proteolytic enzymes Coriander Heavy metals
spellingShingle	Proteolytic enzymes Coriander Heavy metals Gunasekaran, Baskaran Purification, characterisation and inhibition studies of protease from Coriandrum sativum
description	Protease from coriander leaf (Coriandrum sativum) was evaluated for its ability to detect selected heavy metals using Bradford-protease-casein assay system. Considering the highly polluted environment with heavy metals contributed by industrial wastages and its implications on public health, this present study was dedicated to provide a rapid and sensitive assay for the detection of heavy metals in the environmental samples. The basis of the protein assay using casein as a substrate relies upon the inability of the Bradford reagent to stain polypeptide with less than molecular weight of 2 kDa. Casein that has been stained by the Bradford reagent gives a dark blue color. However, the degradation product is not stained by the reagent and the solution remains brown in color. In the presence of heavy metals that inhibit protease activity, casein would remain undigested and the color would remain blue even after incubation. Optimization studies were carried out for this protease prior to heavy metals inhibition studies. The optimization studies include enzyme concentration, substrate concentration, pH, temperature and time of incubation. The optimum concentration of protease, substrate, temperature and incubation time for protease were 0.45 mg/ml protease, 0.43 mg/ml casein, 35oC and 20 min respectively after a period of heavy metals incubation. This enzyme was then purified through anion exchanger using DEAE- Cellulose column and gel filtration using Agilent ZORBAX column. The molecular weight detected was around 55 kDa. Protease activity obtained from coriander was found to be optimum at pH around 8 to 9.5. For this bioassay, two heavy metals showed inhibition towards enzyme activity at a concentration of 1 mg/l. The inhibition shown by the heavy metals on protease activity were around 40% for mercury and 70% for zinc. The IC50 values of mercury and zinc were 3.22 mg/l and 0.73 mg/l respectively. The limits of detection (LOD) for mercury and zinc were 0.24 mg/l and 0.23 mg/l respectively. The limits of quantitation (LOQ) for mercury and zinc were 0.80 mg/l and 0.76 mg/l respectively. This bioassay using coriander protease was found not to be sensitive towards pesticides and xenobiotics. The advantage of the protease bioassay compared to other bioassay relies on its rapidity, simplicity, economical value, stability in severe conditions such as pH and temperature as well as relatively interference free from detergents, solvents and pesticides.
format	Thesis
qualification_level	Master's degree
author	Gunasekaran, Baskaran
author_facet	Gunasekaran, Baskaran
author_sort	Gunasekaran, Baskaran
title	Purification, characterisation and inhibition studies of protease from Coriandrum sativum
title_short	Purification, characterisation and inhibition studies of protease from Coriandrum sativum
title_full	Purification, characterisation and inhibition studies of protease from Coriandrum sativum
title_fullStr	Purification, characterisation and inhibition studies of protease from Coriandrum sativum
title_full_unstemmed	Purification, characterisation and inhibition studies of protease from Coriandrum sativum
title_sort	purification, characterisation and inhibition studies of protease from coriandrum sativum
granting_institution	Universiti Putra Malaysia
granting_department	Faculty of Biotechnology and Biomolecular Sciences
publishDate	2011
url	http://psasir.upm.edu.my/id/eprint/27219/1/FBSB%202011%2030R.pdf
_version_	1747811576491016192

Purification, characterisation and inhibition studies of protease from Coriandrum sativum

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