Enhancement of β-Mannanase Production by Bacillus subtilis ATCC11774 through Optimization of Medium Composition

棕榈仁 枯草芽孢杆菌 食品科学 酵母抽提物 发酵 作文(语言) 响应面法 化学 基质(水族馆) 中心组合设计 酵母 萃取(化学) 生物化学 色谱法 生物 细菌 棕榈油 哲学 遗传学 语言学 生态学
作者
Nor Amalina Binti Mahamad Norizan,Murni Halim,Joo Shun Tan,Sahar Abbasiliasi,Miskandar Mat Sahri,Firdaus Othman,Arbakariya B. Ariff
出处
期刊:Molecules [MDPI AG]
卷期号:25 (15): 3516-3516 被引量:17
标识
DOI:10.3390/molecules25153516
摘要

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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