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Enhancement of ß-Mannanase Production by Bacillus subtilis ATCC11774 through Optimization of Medium Composition.
Norizan, Nor Amalina Binti Mahamad; Halim, Murni; Tan, Joo Shun; Abbasiliasi, Sahar; Mat Sahri, Miskandar; Othman, Firdaus; Ariff, Arbakariya Bin.
Affiliation
  • Norizan NABM; Bioprocessing and Biomanufacturing Research Centre, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia UPM, Serdang 43400, Selangor, Malaysia.
  • Halim M; Bioprocessing and Biomanufacturing Research Centre, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia UPM, Serdang 43400, Selangor, Malaysia.
  • Tan JS; Department of Bioprocess Technology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia UPM, Serdang 43400, Selangor, Malaysia.
  • Abbasiliasi S; Bioprocess Technology, School of Industrial Technology, Universiti Sains Malaysia, Gelugor 11800, Pulau Pinang, Malaysia.
  • Mat Sahri M; Halal Products Research Institute, Universiti Putra Malaysia UPM, Serdang 43400, Selangor, Malaysia.
  • Othman F; Protein and Food Technology Unit, Product Development and Advisory Services Department, Malaysia Palm Oil Board, Bangi 43600, Selangor, Malaysia.
  • Ariff AB; Milling and Processing Unit, Engineering and Processing Division, Malaysia Palm Oil Board, Bangi 43600, Selangor, Malaysia.
Molecules ; 25(15)2020 Jul 31.
Article in En | MEDLINE | ID: mdl-32752106
ABSTRACT
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 ß-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 ß-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 ß-mannanase activity was 805.12 U/mL, which was close to the predicted ß-mannanas activity. As a comparison, commercial media such as nutrient broth, M9 and Luria bertani were used for the production of ß-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 ß-mannanase activity by Bacillus subtilis ATCC11774.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacillus subtilis / Culture Media / Beta-Mannosidase Type of study: Prognostic_studies Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2020 Type: Article Affiliation country: Malaysia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacillus subtilis / Culture Media / Beta-Mannosidase Type of study: Prognostic_studies Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2020 Type: Article Affiliation country: Malaysia