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Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum

β-1,3 glucanase produced from fungi is an important hydrolytic enzymes which can been used as biocontrol agent against plant-pathogenic fungi. The objectives of this study are to determine the best substrates for β-1,3 glucanase production, to evaluate the cultural conditions which stimulate in...

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Main Author: Khairul Ikhsan, Khairul Asma Salsabilla
Format: Thesis
Language:English
Published: 2015
Subjects:
Plant enzymes
Penicillium oxalicum
Online Access:http://psasir.upm.edu.my/id/eprint/84546/1/FBSB%202015%20177%20-%20ir.pdf
http://psasir.upm.edu.my/id/eprint/84546/
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spelling my.upm.eprints.845462021-12-31T08:31:02Z http://psasir.upm.edu.my/id/eprint/84546/ Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum Khairul Ikhsan, Khairul Asma Salsabilla β-1,3 glucanase produced from fungi is an important hydrolytic enzymes which can been used as biocontrol agent against plant-pathogenic fungi. The objectives of this study are to determine the best substrates for β-1,3 glucanase production, to evaluate the cultural conditions which stimulate in vitro production of β-1,3 glucanase and to characterize the β-1,3 glucanase activity and then study the effect of crude β-1,3 glucanase towards fungal hypahe of C. gleosporioides and N. dimidiatum. β-1,3 glucanase production by Penicillium oxalicum T3.3 was investigated using shake flasks under various culture conditions such as different types of carbon and nitrogen sources, initial medium pH, agitation speed and different types of surfactants. The determination of best cultural conditions was carried out by varying and optimizing one variable at a time. The best cultural condition obtained from the shake flask experiment was used for β-1,3 glucanase production in a 2 L stirred tank fermenter where the effect of different impeller speed was investigated. Furthermore, the crude β-1,3 glucanase was characterized to study the enzyme stability. The role of this enzyme in antagonism action against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum, a well-known fungal plant pathogens causing anthracnose disease in dragon fruit also was examined. In this study, seaweed Undaria pinnatifida was chosen as the best substrates for β- 1,3 glucanase production. The highest production of β-1,3 glucanase of 84.73 U/mL was obtained at substrate concentration of 1% (w/v), 0.3% (w/v) peptone and 0.2% (w/v) yeast extract as nitrogen source, initial medium pH 5, temperature at 30ᵒC, agitation speed at 200 rpm and with addition of sodium dodecyl sulfate as surfactant in shake flask condition. The β-1,3 glucanase activity was increased by 38.61% when optimized media and process parameters were used in shake flask culture. The best cultural condition obtained from shake flask was further used for production β- 1,3 glucanase in bioreactor. In bioreactor, the highest production of β-1,3 glucanase was obtained at 250 rpm. However, β-1,3 glucanase production in bioreactor was at par as compared with production in shake flask culture. The crude β-1,3 glucanase obtained was then concentrated by ammonium sulphate precipitation method. Concentrated enzyme was characterized and it was found that the optimum temperature and pH for the enzyme activity were 50ºC and pH 5, respectively. This enzyme can also retain 93.4% and 83.6% of its activity after incubation for 2 h and 4 h, respectively, at 50°C and pH 5. In addition, fungal plant pathogen inhibition assay showed that the crude β-1,3 glucanase produced by P. oxalicum T3.3 was able to hydrolyze the fungal hyphae of C. gloeosporioides and N. dimidiatum. 2015-03 Thesis NonPeerReviewed text en http://psasir.upm.edu.my/id/eprint/84546/1/FBSB%202015%20177%20-%20ir.pdf Khairul Ikhsan, Khairul Asma Salsabilla (2015) Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum. Masters thesis, Universiti Putra Malaysia. Plant enzymes Penicillium oxalicum
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
topic Plant enzymes
Penicillium oxalicum
spellingShingle Plant enzymes
Penicillium oxalicum
Khairul Ikhsan, Khairul Asma Salsabilla
Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum
description β-1,3 glucanase produced from fungi is an important hydrolytic enzymes which can been used as biocontrol agent against plant-pathogenic fungi. The objectives of this study are to determine the best substrates for β-1,3 glucanase production, to evaluate the cultural conditions which stimulate in vitro production of β-1,3 glucanase and to characterize the β-1,3 glucanase activity and then study the effect of crude β-1,3 glucanase towards fungal hypahe of C. gleosporioides and N. dimidiatum. β-1,3 glucanase production by Penicillium oxalicum T3.3 was investigated using shake flasks under various culture conditions such as different types of carbon and nitrogen sources, initial medium pH, agitation speed and different types of surfactants. The determination of best cultural conditions was carried out by varying and optimizing one variable at a time. The best cultural condition obtained from the shake flask experiment was used for β-1,3 glucanase production in a 2 L stirred tank fermenter where the effect of different impeller speed was investigated. Furthermore, the crude β-1,3 glucanase was characterized to study the enzyme stability. The role of this enzyme in antagonism action against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum, a well-known fungal plant pathogens causing anthracnose disease in dragon fruit also was examined. In this study, seaweed Undaria pinnatifida was chosen as the best substrates for β- 1,3 glucanase production. The highest production of β-1,3 glucanase of 84.73 U/mL was obtained at substrate concentration of 1% (w/v), 0.3% (w/v) peptone and 0.2% (w/v) yeast extract as nitrogen source, initial medium pH 5, temperature at 30ᵒC, agitation speed at 200 rpm and with addition of sodium dodecyl sulfate as surfactant in shake flask condition. The β-1,3 glucanase activity was increased by 38.61% when optimized media and process parameters were used in shake flask culture. The best cultural condition obtained from shake flask was further used for production β- 1,3 glucanase in bioreactor. In bioreactor, the highest production of β-1,3 glucanase was obtained at 250 rpm. However, β-1,3 glucanase production in bioreactor was at par as compared with production in shake flask culture. The crude β-1,3 glucanase obtained was then concentrated by ammonium sulphate precipitation method. Concentrated enzyme was characterized and it was found that the optimum temperature and pH for the enzyme activity were 50ºC and pH 5, respectively. This enzyme can also retain 93.4% and 83.6% of its activity after incubation for 2 h and 4 h, respectively, at 50°C and pH 5. In addition, fungal plant pathogen inhibition assay showed that the crude β-1,3 glucanase produced by P. oxalicum T3.3 was able to hydrolyze the fungal hyphae of C. gloeosporioides and N. dimidiatum.
format Thesis
author Khairul Ikhsan, Khairul Asma Salsabilla
author_facet Khairul Ikhsan, Khairul Asma Salsabilla
author_sort Khairul Ikhsan, Khairul Asma Salsabilla
title Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum
title_short Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum
title_full Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum
title_fullStr Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum
title_full_unstemmed Production of β -1,3 glucanase from Penicillium oxalicum T3.3 for biocontrol against Colletotrichum gloeosporioides and Neoscytalidium dimidiatum
title_sort production of β -1,3 glucanase from penicillium oxalicum t3.3 for biocontrol against colletotrichum gloeosporioides and neoscytalidium dimidiatum
publishDate 2015
url http://psasir.upm.edu.my/id/eprint/84546/1/FBSB%202015%20177%20-%20ir.pdf
http://psasir.upm.edu.my/id/eprint/84546/
_version_ 1724075441353916416
score 13.211869

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