Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition

Palm kernel cake (PKC) has been largely produced in Malaysia as one of the cheap and abundant agro-waste by-products from the palm oil industry and it contains high fiber (mannan) content. The present study aimed to produce β-mannanase by Bacillus subtilis ATCC11774 via optimization of the medium co...

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Main Authors: Mahamad Norizan, Nor Amalina, Halim, Murni, Tan, Joo Shun, Abbasiliasi, Sahar, Mat Sahri, Miskandar, Othman, Firdaus, Ariff, Arbakariya
Format: Article
Language:English
Published: Multidisciplinary Digital Publishing Institute 2020
Online Access:http://psasir.upm.edu.my/id/eprint/88817/
http://psasir.upm.edu.my/id/eprint/88817/1/Enhancement%20of%20%CE%B2-mannanase%20.pdf
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author Mahamad Norizan, Nor Amalina
Halim, Murni
Tan, Joo Shun
Abbasiliasi, Sahar
Mat Sahri, Miskandar
Othman, Firdaus
Ariff, Arbakariya
author_facet Mahamad Norizan, Nor Amalina
Halim, Murni
Tan, Joo Shun
Abbasiliasi, Sahar
Mat Sahri, Miskandar
Othman, Firdaus
Ariff, Arbakariya
author_sort Mahamad Norizan, Nor Amalina
building UPM Institutional Repository
collection Online Access
description Palm kernel cake (PKC) has been largely produced in Malaysia as one of the cheap and abundant agro-waste by-products from the palm oil industry and it contains high fiber (mannan) content. The present study aimed to produce β-mannanase by Bacillus subtilis ATCC11774 via optimization of the medium composition using palm kernel cake as substrate in semi-solid fermentation. The fermentation nutrients such as PKC, peptone, yeast extract, sodium chloride, magnesium sulphate (MgSO2), initial culture pH and temperature were screened using a Plackett-Burman design. The three most significant factors identified, PKC, peptone and NaCl, were further optimized using central composite design (CCD), a response surface methodology (RSM) approach, where yeast extract and MgSO2 were fixed as a constant factor. The maximum β-mannanase activity predicted by CCD under the optimum medium composition of 16.50 g/L PKC, 19.59 g/L peptone, 3.00 g/L yeast extract, 2.72 g/L NaCl and 0.2 g/L MgSO2 was 799 U/mL. The validated β-mannanase activity was 805.12 U/mL, which was close to the predicted β-mannanas activity. As a comparison, commercial media such as nutrient broth, M9 and Luria bertani were used for the production of β-mannanase with activities achieved at 204.16 ± 9.21 U/mL, 50.32 U/mL and 88.90 U/mL, respectively. The optimized PKC fermentation medium was four times higher than nutrient broth. Hence, it could be a potential fermentation substrate for the production of β-mannanase activity by Bacillus subtilis ATCC11774.
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spelling upm-888172021-10-05T22:41:34Z http://psasir.upm.edu.my/id/eprint/88817/ Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition Mahamad Norizan, Nor Amalina Halim, Murni Tan, Joo Shun Abbasiliasi, Sahar Mat Sahri, Miskandar Othman, Firdaus Ariff, Arbakariya Palm kernel cake (PKC) has been largely produced in Malaysia as one of the cheap and abundant agro-waste by-products from the palm oil industry and it contains high fiber (mannan) content. The present study aimed to produce β-mannanase by Bacillus subtilis ATCC11774 via optimization of the medium composition using palm kernel cake as substrate in semi-solid fermentation. The fermentation nutrients such as PKC, peptone, yeast extract, sodium chloride, magnesium sulphate (MgSO2), initial culture pH and temperature were screened using a Plackett-Burman design. The three most significant factors identified, PKC, peptone and NaCl, were further optimized using central composite design (CCD), a response surface methodology (RSM) approach, where yeast extract and MgSO2 were fixed as a constant factor. The maximum β-mannanase activity predicted by CCD under the optimum medium composition of 16.50 g/L PKC, 19.59 g/L peptone, 3.00 g/L yeast extract, 2.72 g/L NaCl and 0.2 g/L MgSO2 was 799 U/mL. The validated β-mannanase activity was 805.12 U/mL, which was close to the predicted β-mannanas activity. As a comparison, commercial media such as nutrient broth, M9 and Luria bertani were used for the production of β-mannanase with activities achieved at 204.16 ± 9.21 U/mL, 50.32 U/mL and 88.90 U/mL, respectively. The optimized PKC fermentation medium was four times higher than nutrient broth. Hence, it could be a potential fermentation substrate for the production of β-mannanase activity by Bacillus subtilis ATCC11774. Multidisciplinary Digital Publishing Institute 2020 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/88817/1/Enhancement%20of%20%CE%B2-mannanase%20.pdf Mahamad Norizan, Nor Amalina and Halim, Murni and Tan, Joo Shun and Abbasiliasi, Sahar and Mat Sahri, Miskandar and Othman, Firdaus and Ariff, Arbakariya (2020) Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition. Molecules, 25 (15). pp. 1-4. ISSN 1420-3049 https://www.mdpi.com/1420-3049/25/15/3516 10.3390/molecules25153516
spellingShingle Mahamad Norizan, Nor Amalina
Halim, Murni
Tan, Joo Shun
Abbasiliasi, Sahar
Mat Sahri, Miskandar
Othman, Firdaus
Ariff, Arbakariya
Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition
title Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition
title_full Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition
title_fullStr Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition
title_full_unstemmed Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition
title_short Enhancement of β-mannanase production by Bacillus subtilis ATCC11774 through optimization of medium composition
title_sort enhancement of β-mannanase production by bacillus subtilis atcc11774 through optimization of medium composition
url http://psasir.upm.edu.my/id/eprint/88817/
http://psasir.upm.edu.my/id/eprint/88817/
http://psasir.upm.edu.my/id/eprint/88817/
http://psasir.upm.edu.my/id/eprint/88817/1/Enhancement%20of%20%CE%B2-mannanase%20.pdf