The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions

Anabas testudineus (A. testudineus) is a freshwater fish that belongs to the family of Anabantidae and its local name in Malaysia is ‘Ikan Puyu’. It can be used as a bioindicator for heavy metal contamination as it is quite sturdy and ideally suited for experimentation in laboratory for a longer per...

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Main Author: Abdul Wahab Sha'arani, Shakirah
Format: Project Paper Report
Language:English
Published: 2015
Online Access:http://psasir.upm.edu.my/id/eprint/85089/1/FBSB%202015%2077%20-%20IR.pdf
http://psasir.upm.edu.my/id/eprint/85089/
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Institution: Universiti Putra Malaysia
Language: English
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spelling my.upm.eprints.850892021-09-22T12:24:37Z http://psasir.upm.edu.my/id/eprint/85089/ The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions Abdul Wahab Sha'arani, Shakirah Anabas testudineus (A. testudineus) is a freshwater fish that belongs to the family of Anabantidae and its local name in Malaysia is ‘Ikan Puyu’. It can be used as a bioindicator for heavy metal contamination as it is quite sturdy and ideally suited for experimentation in laboratory for a longer period. The present study aimed to partially purify cholinesterase (ChE) from the brain extract of A. testudineus and to study the optimization of assay conditions and inhibition effect towards ChE. The result showed that ChE was successfully partially purified from the brain extract of A. testudineus using DEAE-cellulose through ion exchange chromatography. The serial purification method gave 2.80 fold of purification with a recovery of 17.38%. ChE was successfully purified in protein analysis through non-denaturing polyacrylamide gel electrophoresis (native-PAGE) and it proved that DEAE-cellulose matrix can serve as an effective medium to separate protein molecules. The optimum conditions for ChE assay was found to be at pH 9 in Tris-HCl and temperature of 35°C. Substrate specificity profile showed acetylcholinesterase (AChE) as the predominant enzyme which resides in partially purified samples because it indicated the highest Vmax and lowest Km when using acetylthiocholine iodide (ATC) as substrate. Inhibition study showed mercury as a strong inhibitor because it gave the highest percentage of inhibition effect (68.1%) towards ChE. Secondary screening found that half maximal inhibitory concentration (IC50) value for mercury was 1.8 mg/L. These finding suggested that partially purified ChE from brain extract of A. testudineus is suitable to be applied as biosensor to detect the presence of heavy metal in the environment. 2015-06 Project Paper Report NonPeerReviewed text en http://psasir.upm.edu.my/id/eprint/85089/1/FBSB%202015%2077%20-%20IR.pdf Abdul Wahab Sha'arani, Shakirah (2015) The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions. [Project Paper Report]
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Anabas testudineus (A. testudineus) is a freshwater fish that belongs to the family of Anabantidae and its local name in Malaysia is ‘Ikan Puyu’. It can be used as a bioindicator for heavy metal contamination as it is quite sturdy and ideally suited for experimentation in laboratory for a longer period. The present study aimed to partially purify cholinesterase (ChE) from the brain extract of A. testudineus and to study the optimization of assay conditions and inhibition effect towards ChE. The result showed that ChE was successfully partially purified from the brain extract of A. testudineus using DEAE-cellulose through ion exchange chromatography. The serial purification method gave 2.80 fold of purification with a recovery of 17.38%. ChE was successfully purified in protein analysis through non-denaturing polyacrylamide gel electrophoresis (native-PAGE) and it proved that DEAE-cellulose matrix can serve as an effective medium to separate protein molecules. The optimum conditions for ChE assay was found to be at pH 9 in Tris-HCl and temperature of 35°C. Substrate specificity profile showed acetylcholinesterase (AChE) as the predominant enzyme which resides in partially purified samples because it indicated the highest Vmax and lowest Km when using acetylthiocholine iodide (ATC) as substrate. Inhibition study showed mercury as a strong inhibitor because it gave the highest percentage of inhibition effect (68.1%) towards ChE. Secondary screening found that half maximal inhibitory concentration (IC50) value for mercury was 1.8 mg/L. These finding suggested that partially purified ChE from brain extract of A. testudineus is suitable to be applied as biosensor to detect the presence of heavy metal in the environment.
format Project Paper Report
author Abdul Wahab Sha'arani, Shakirah
spellingShingle Abdul Wahab Sha'arani, Shakirah
The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions
author_facet Abdul Wahab Sha'arani, Shakirah
author_sort Abdul Wahab Sha'arani, Shakirah
title The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions
title_short The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions
title_full The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions
title_fullStr The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions
title_full_unstemmed The assessment of cholinesterase from the brain of Anabas testudineus as detection of metal ions
title_sort assessment of cholinesterase from the brain of anabas testudineus as detection of metal ions
publishDate 2015
url http://psasir.upm.edu.my/id/eprint/85089/1/FBSB%202015%2077%20-%20IR.pdf
http://psasir.upm.edu.my/id/eprint/85089/
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