Response Surface Methodology for the production of endopolygalacturonase by a novel Bacillus licheniformis
Background: Polygalacturonase is one of the most important commercial pectinase. The production cost and the mesophilic nature of the present polygalacturonase is a big problem in its application in the juice industry. A lot of work is going on for the isolation of thermophilic bacterial strains whi...
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doaj-bc8946a96bd4406cbe003274309233252020-11-25T00:41:47Zeng University of the PunjabAdvancements in Life Sciences2310-53802310-53802018-09-0154204210Response Surface Methodology for the production of endopolygalacturonase by a novel Bacillus licheniformisSaqib Hussain Hadri0Muhammad Javaid Asad1Muhammad Zeeshan Hyder2Syed Muhammad Saqlan Naqvi3Tariq Mukhtar4Raja Tahir Mehmood5JH David Wu6Department of Biochemistry, Pir Mehr Ali Shah Arid Agriculture University, Rawalpindi, PakistanDepartment of Biochemistry, Pir Mehr Ali Shah Arid Agriculture University, Rawalpindi, PakistanDepartment of Bioscience, COMSATS Institute of Information and Technology, Islamabad, PakistanDepartment of Biochemistry, Pir Mehr Ali Shah Arid Agriculture University, Rawalpindi, PakistanDepartment of Biochemistry, Pir Mehr Ali Shah Arid Agriculture University, Rawalpindi, PakistanDepartment of Biotechnology, Mirpur University of Science and Technology (MUST), Mirpur Azad Jamu and Kashmir, PakistanDepartment of Chemical Engineering, University of Rochester, Rochester, NY, USABackground: Polygalacturonase is one of the most important commercial pectinase. The production cost and the mesophilic nature of the present polygalacturonase is a big problem in its application in the juice industry. A lot of work is going on for the isolation of thermophilic bacterial strains which can utilize pectin as the only carbon source. Methods: Bacterial strains were isolated from rotten fruits and vegetables and cultured at 50 – 70oC. The strains were than screened for endopolygalacturonase activity and identified on the basis of 16S rRNA sequence. Different growth parameters for the production of endopolygalacturonase by Bacillus licheniformis IEB-8 were optimized using Response Surface Methodology under Center Composite Design using JMP-12 software. Endopolygalacturonase was purified in two steps; ammonium sulfate precipitation and then by size exclusion column chromatography. Results: Only four strains, IEB-8, IEB-11, IEB-12 and IEB-13 showed growth above 60oC. Among these four, only IEB-8 was found to be endopolygalacturonase positive, which was identified as Bacillus licheniformis by 16S rRNA gene sequence. Purification fold of 2.57 and 7.48 in the specific activity were achieved using ammonium sulfate precipitation and gel filtration chromatography respectively. Molecular weight of the purified endopolygalacturonase was found to be 42 kDa. The purified endopolygalacturonase showed an optimum pH of 7 and optimum temperature of 55oC. Conclusion: Bacillus licheniformis IEB-8 is a novel bacteria which can efficiently be utilized in the industry for the production of endopolygalacturonase very cheaply. Furthermore, the high optimum working temperature of endopolygalacturonase, increases its significance for its industrial applications. http://www.als-journal.com/549-18/EndopolygalacturonaseBacillus licheniformisThermophilicResponse Surface MethodologyAmmonium sulfate precipitation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Saqib Hussain Hadri Muhammad Javaid Asad Muhammad Zeeshan Hyder Syed Muhammad Saqlan Naqvi Tariq Mukhtar Raja Tahir Mehmood JH David Wu |
spellingShingle |
Saqib Hussain Hadri Muhammad Javaid Asad Muhammad Zeeshan Hyder Syed Muhammad Saqlan Naqvi Tariq Mukhtar Raja Tahir Mehmood JH David Wu Response Surface Methodology for the production of endopolygalacturonase by a novel Bacillus licheniformis Advancements in Life Sciences Endopolygalacturonase Bacillus licheniformis Thermophilic Response Surface Methodology Ammonium sulfate precipitation |
author_facet |
Saqib Hussain Hadri Muhammad Javaid Asad Muhammad Zeeshan Hyder Syed Muhammad Saqlan Naqvi Tariq Mukhtar Raja Tahir Mehmood JH David Wu |
author_sort |
Saqib Hussain Hadri |
title |
Response Surface Methodology for the production of endopolygalacturonase by a novel Bacillus licheniformis |
title_short |
Response Surface Methodology for the production of endopolygalacturonase by a novel Bacillus licheniformis |
title_full |
Response Surface Methodology for the production of endopolygalacturonase by a novel Bacillus licheniformis |
title_fullStr |
Response Surface Methodology for the production of endopolygalacturonase by a novel Bacillus licheniformis |
title_full_unstemmed |
Response Surface Methodology for the production of endopolygalacturonase by a novel Bacillus licheniformis |
title_sort |
response surface methodology for the production of endopolygalacturonase by a novel bacillus licheniformis |
publisher |
University of the Punjab |
series |
Advancements in Life Sciences |
issn |
2310-5380 2310-5380 |
publishDate |
2018-09-01 |
description |
Background: Polygalacturonase is one of the most important commercial pectinase. The production cost and the mesophilic nature of the present polygalacturonase is a big problem in its application in the juice industry. A lot of work is going on for the isolation of thermophilic bacterial strains which can utilize pectin as the only carbon source.
Methods: Bacterial strains were isolated from rotten fruits and vegetables and cultured at 50 – 70oC. The strains were than screened for endopolygalacturonase activity and identified on the basis of 16S rRNA sequence. Different growth parameters for the production of endopolygalacturonase by Bacillus licheniformis IEB-8 were optimized using Response Surface Methodology under Center Composite Design using JMP-12 software. Endopolygalacturonase was purified in two steps; ammonium sulfate precipitation and then by size exclusion column chromatography.
Results: Only four strains, IEB-8, IEB-11, IEB-12 and IEB-13 showed growth above 60oC. Among these four, only IEB-8 was found to be endopolygalacturonase positive, which was identified as Bacillus licheniformis by 16S rRNA gene sequence. Purification fold of 2.57 and 7.48 in the specific activity were achieved using ammonium sulfate precipitation and gel filtration chromatography respectively. Molecular weight of the purified endopolygalacturonase was found to be 42 kDa. The purified endopolygalacturonase showed an optimum pH of 7 and optimum temperature of 55oC.
Conclusion: Bacillus licheniformis IEB-8 is a novel bacteria which can efficiently be utilized in the industry for the production of endopolygalacturonase very cheaply. Furthermore, the high optimum working temperature of endopolygalacturonase, increases its significance for its industrial applications. |
topic |
Endopolygalacturonase Bacillus licheniformis Thermophilic Response Surface Methodology Ammonium sulfate precipitation |
url |
http://www.als-journal.com/549-18/ |
work_keys_str_mv |
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