Production of extracellular tannase enyzme by Aspergillus Niger

Tannase catalyses the hydrolysis reaction of the ester bond present in gallic acid esters and hydrosable tannins.This enzyme is produced by plants and microorganism and used in food industry such as tea industry.In order to produce high yields of tannase enzymes,it needs optimization of parameters w...

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Main Author: Muhamad Syafiq Eidham, Ab Rashid
Format: Undergraduates Project Papers
Language:English
Published: 2012
Subjects:
Online Access:http://umpir.ump.edu.my/id/eprint/5121/
http://umpir.ump.edu.my/id/eprint/5121/
http://umpir.ump.edu.my/id/eprint/5121/1/CD6480.pdf
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recordtype eprints
spelling ump-51212015-03-03T09:23:12Z http://umpir.ump.edu.my/id/eprint/5121/ Production of extracellular tannase enyzme by Aspergillus Niger Muhamad Syafiq Eidham, Ab Rashid TP Chemical technology Tannase catalyses the hydrolysis reaction of the ester bond present in gallic acid esters and hydrosable tannins.This enzyme is produced by plants and microorganism and used in food industry such as tea industry.In order to produce high yields of tannase enzymes,it needs optimization of parameters which normally consuming a lot of time and expensive to be optimized conventionally.In this study, Response Surface Methodology (Central Composite Design) was performed for optimization.Aspergillus niger had been chosen as biomass and glucose as substrate in this study.The fermentation study was take place in the shake flask and was optimized for higher tannase enzyme activity.There are three factors was studied in this study which are the pH of the fermentation medium (pH 3.5-pH 6.0),the substrate concentration (2 w/v%-10 w/v%) and the agitation speed (100 rpm-300 rpm).From one factor at a time (OFAT) analysis, tannase enzyme showed that the optimum tannase activity at pH 5, 6.0 w/v% and 200 rpm with 14.9521 U/ml, 13.1256 U/ml and 12.4301 U/ml.RSM results shows that the optimum values of each parameter were pH 4.75, 6.0 v/w% of substrates concentration and 200 rpm of agitation speed which resulted the optimum tannase activity at 15.3131 U/ml.As a conclusion,RSM is the best tool used to identify the correlation between controlled independent factors and observed dependent responses.For the future research,it is recommended for study the application of genetic engineering in the enzyme production by scale up tannase production using a bioreactor and toxicology studies on tannase enzyme for application in food industry. 2012-01 Undergraduates Project Papers NonPeerReviewed application/pdf en http://umpir.ump.edu.my/id/eprint/5121/1/CD6480.pdf Muhamad Syafiq Eidham, Ab Rashid (2012) Production of extracellular tannase enyzme by Aspergillus Niger. Faculty of Chemical & Natural Resource Engineering, Universiti Malaysia Pahang. http://iportal.ump.edu.my/lib/item?id=chamo:67954&theme=UMP2
repository_type Digital Repository
institution_category Local University
institution Universiti Malaysia Pahang
building UMP Institutional Repository
collection Online Access
language English
topic TP Chemical technology
spellingShingle TP Chemical technology
Muhamad Syafiq Eidham, Ab Rashid
Production of extracellular tannase enyzme by Aspergillus Niger
description Tannase catalyses the hydrolysis reaction of the ester bond present in gallic acid esters and hydrosable tannins.This enzyme is produced by plants and microorganism and used in food industry such as tea industry.In order to produce high yields of tannase enzymes,it needs optimization of parameters which normally consuming a lot of time and expensive to be optimized conventionally.In this study, Response Surface Methodology (Central Composite Design) was performed for optimization.Aspergillus niger had been chosen as biomass and glucose as substrate in this study.The fermentation study was take place in the shake flask and was optimized for higher tannase enzyme activity.There are three factors was studied in this study which are the pH of the fermentation medium (pH 3.5-pH 6.0),the substrate concentration (2 w/v%-10 w/v%) and the agitation speed (100 rpm-300 rpm).From one factor at a time (OFAT) analysis, tannase enzyme showed that the optimum tannase activity at pH 5, 6.0 w/v% and 200 rpm with 14.9521 U/ml, 13.1256 U/ml and 12.4301 U/ml.RSM results shows that the optimum values of each parameter were pH 4.75, 6.0 v/w% of substrates concentration and 200 rpm of agitation speed which resulted the optimum tannase activity at 15.3131 U/ml.As a conclusion,RSM is the best tool used to identify the correlation between controlled independent factors and observed dependent responses.For the future research,it is recommended for study the application of genetic engineering in the enzyme production by scale up tannase production using a bioreactor and toxicology studies on tannase enzyme for application in food industry.
format Undergraduates Project Papers
author Muhamad Syafiq Eidham, Ab Rashid
author_facet Muhamad Syafiq Eidham, Ab Rashid
author_sort Muhamad Syafiq Eidham, Ab Rashid
title Production of extracellular tannase enyzme by Aspergillus Niger
title_short Production of extracellular tannase enyzme by Aspergillus Niger
title_full Production of extracellular tannase enyzme by Aspergillus Niger
title_fullStr Production of extracellular tannase enyzme by Aspergillus Niger
title_full_unstemmed Production of extracellular tannase enyzme by Aspergillus Niger
title_sort production of extracellular tannase enyzme by aspergillus niger
publishDate 2012
url http://umpir.ump.edu.my/id/eprint/5121/
http://umpir.ump.edu.my/id/eprint/5121/
http://umpir.ump.edu.my/id/eprint/5121/1/CD6480.pdf
first_indexed 2023-09-18T22:00:18Z
last_indexed 2023-09-18T22:00:18Z
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