Enhanced Production of Phytase, A Feed Enzyme, from Pichia kudriavzevii using Mutagenesis and Improved Culture Conditions

Pichia kudriavzevii WB17-1, a phytase-producing yeast isolated from duck excrement, was found to produce both cell-bound and extracellular phytases. To enhance extracellular phytase, P. kudriavzevii WB17-1 was subjected to induced mutation. Ethylmethane sulfonate (EMS)-induced mutation resulted in 2...

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Main Authors: Wanatchaporn Boontham, Natsuda Srivanichpoom, Pumin Nutaratat, Savitree Limtong, Nantana Srisuk
Language:English
Published: Science Faculty of Chiang Mai University 2019
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Online Access:http://it.science.cmu.ac.th/ejournal/dl.php?journal_id=10134
http://cmuir.cmu.ac.th/jspui/handle/6653943832/66022
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-660222019-08-21T09:18:19Z Enhanced Production of Phytase, A Feed Enzyme, from Pichia kudriavzevii using Mutagenesis and Improved Culture Conditions Wanatchaporn Boontham Natsuda Srivanichpoom Pumin Nutaratat Savitree Limtong Nantana Srisuk phytase optimisation mutagenesis Pichia kudriavzevii yeast Pichia kudriavzevii WB17-1, a phytase-producing yeast isolated from duck excrement, was found to produce both cell-bound and extracellular phytases. To enhance extracellular phytase, P. kudriavzevii WB17-1 was subjected to induced mutation. Ethylmethane sulfonate (EMS)-induced mutation resulted in 2,400 mutants. The mutant P. kudriavzevii WB17-1 EMS3 showed the highest extracellular phytase activity. This mutant possessed a 6.2-fold increase in enzyme activity compared to the wild type level. The wild type and mutant were subjected to characterization of PHYPk, a gene encoding P. kudriavzevii phytase. An open reading frame of 1,071 bp encoding 357 amino acids with a predicted protein molecular mass of 40.056 kDa was identified. To optimize the extracellular phytase activity of P. kudriavzevii WB17-1 EMS3, a response surface methodology (RSM) was employed. The highest extracellular phytase activity was obtained in the medium containing 2.95% dextrose and 0.58% peptone with an initial pH of 5.8. The optimized phytase activity was 2.3 times the level obtained under un-optimized conditions and was 14.4 times the wild type level. The results obtained here show successful yeast strain improvement and optimization of extracellular phytase by yeast using RSM. 2019-08-21T09:18:19Z 2019-08-21T09:18:19Z 2019 Chiang Mai Journal of Science 46, 3 (May 2019), 431 - 443 0125-2526 http://it.science.cmu.ac.th/ejournal/dl.php?journal_id=10134 http://cmuir.cmu.ac.th/jspui/handle/6653943832/66022 Eng Science Faculty of Chiang Mai University
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
topic phytase
optimisation
mutagenesis
Pichia kudriavzevii
yeast
spellingShingle phytase
optimisation
mutagenesis
Pichia kudriavzevii
yeast
Wanatchaporn Boontham
Natsuda Srivanichpoom
Pumin Nutaratat
Savitree Limtong
Nantana Srisuk
Enhanced Production of Phytase, A Feed Enzyme, from Pichia kudriavzevii using Mutagenesis and Improved Culture Conditions
description Pichia kudriavzevii WB17-1, a phytase-producing yeast isolated from duck excrement, was found to produce both cell-bound and extracellular phytases. To enhance extracellular phytase, P. kudriavzevii WB17-1 was subjected to induced mutation. Ethylmethane sulfonate (EMS)-induced mutation resulted in 2,400 mutants. The mutant P. kudriavzevii WB17-1 EMS3 showed the highest extracellular phytase activity. This mutant possessed a 6.2-fold increase in enzyme activity compared to the wild type level. The wild type and mutant were subjected to characterization of PHYPk, a gene encoding P. kudriavzevii phytase. An open reading frame of 1,071 bp encoding 357 amino acids with a predicted protein molecular mass of 40.056 kDa was identified. To optimize the extracellular phytase activity of P. kudriavzevii WB17-1 EMS3, a response surface methodology (RSM) was employed. The highest extracellular phytase activity was obtained in the medium containing 2.95% dextrose and 0.58% peptone with an initial pH of 5.8. The optimized phytase activity was 2.3 times the level obtained under un-optimized conditions and was 14.4 times the wild type level. The results obtained here show successful yeast strain improvement and optimization of extracellular phytase by yeast using RSM.
author Wanatchaporn Boontham
Natsuda Srivanichpoom
Pumin Nutaratat
Savitree Limtong
Nantana Srisuk
author_facet Wanatchaporn Boontham
Natsuda Srivanichpoom
Pumin Nutaratat
Savitree Limtong
Nantana Srisuk
author_sort Wanatchaporn Boontham
title Enhanced Production of Phytase, A Feed Enzyme, from Pichia kudriavzevii using Mutagenesis and Improved Culture Conditions
title_short Enhanced Production of Phytase, A Feed Enzyme, from Pichia kudriavzevii using Mutagenesis and Improved Culture Conditions
title_full Enhanced Production of Phytase, A Feed Enzyme, from Pichia kudriavzevii using Mutagenesis and Improved Culture Conditions
title_fullStr Enhanced Production of Phytase, A Feed Enzyme, from Pichia kudriavzevii using Mutagenesis and Improved Culture Conditions
title_full_unstemmed Enhanced Production of Phytase, A Feed Enzyme, from Pichia kudriavzevii using Mutagenesis and Improved Culture Conditions
title_sort enhanced production of phytase, a feed enzyme, from pichia kudriavzevii using mutagenesis and improved culture conditions
publisher Science Faculty of Chiang Mai University
publishDate 2019
url http://it.science.cmu.ac.th/ejournal/dl.php?journal_id=10134
http://cmuir.cmu.ac.th/jspui/handle/6653943832/66022
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