Statistical versus neural network-embedded swarm intelligence optimization of a metallo-neutral-protease production: activity kinetics and food industry applications.

IF 2 4区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS Preparative Biochemistry & Biotechnology Pub Date : 2024-10-01 Epub Date: 2024-03-16 DOI:10.1080/10826068.2024.2328681
Maurice George Ekpenyong, Sylvester Peter Antai
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Abstract

An integrated approach involving response surface methodology (RSM) and artificial neural network-ant-colony hybrid optimization (ANN-ACO) was adopted to develop a bioprocess medium to increase the yield of Bacillus cereus neutral protease under submerged fermentation conditions. The ANN-ACO model was comparatively superior (predicted r2 = 98.5%, mean squared error [MSE] = 0.0353) to RSM model (predicted r2 = 86.4%, MSE = 23.85) in predictive capability arising from its low performance error. The hybrid model recommended a medium containing (gL-1) molasses 45.00, urea 9.81, casein 25.45, Ca2+ 1.23, Zn2+ 0.021, Mn2+ 0.020, and 4.45% (vv-1) inoculum, for a 6.75-fold increase in protease activity from a baseline of 76.63 UmL-1. Yield was further increased in a 5-L bioreactor to a final volumetric productivity of 3.472 mg(Lh)-1. The 10.0-fold purified 46.6-kDa-enzyme had maximum activity at pH 6.5, 45-55 °C, with Km of 6.92 mM, Vmax of 769.23 µmolmL-1 min-1, kcat of 28.49 s-1, and kcat/Km of 4.117 × 103 M-1 s-1, at 45 °C, pH 6.5. The enzyme was stabilized by Ca2+, activated by Zn2+ but inhibited by EDTA suggesting that it was a metallo-protease. The biomolecule significantly clarified orange and pineapple juices indicating its food industry application.

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金属中性蛋白酶生产的统计与神经网络嵌入式群集智能优化:活性动力学与食品工业应用。
采用响应面方法(RSM)和人工神经网络-蚁群混合优化(ANN-ACO)的综合方法开发了一种生物工艺培养基,以提高浸没发酵条件下蜡样芽孢杆菌中性蛋白酶的产量。ANN-ACO 模型的预测能力(预测 r2 = 98.5%,均方误差 [MSE] = 0.0353)相对优于 RSM 模型(预测 r2 = 86.4%,MSE = 23.85),因为其性能误差小。混合模型推荐的培养基含(gL-1)糖蜜 45.00、尿素 9.81、酪蛋白 25.45、Ca2+ 1.23、Zn2+ 0.021、Mn2+ 0.020 和 4.45%(vv-1)接种物,使蛋白酶活性从 76.63 UmL-1 的基线提高了 6.75 倍。在 5 升生物反应器中,产量进一步提高,最终体积生产率为 3.472 mg(Lh)-1。10.0 倍纯化的 46.6-kDa 酶在 pH 6.5、45-55 °C 条件下具有最大活性,Km 为 6.92 mM,Vmax 为 769.23 µmolmL-1 min-1,kcat 为 28.49 s-1,kcat/Km 为 4.117 × 103 M-1 s-1。该酶受 Ca2+ 稳定,受 Zn2+ 激活,但受 EDTA 抑制,表明它是一种金属蛋白酶。该生物大分子能明显澄清橙汁和菠萝汁,表明其在食品工业中的应用。
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来源期刊
Preparative Biochemistry & Biotechnology
Preparative Biochemistry & Biotechnology 工程技术-生化研究方法
CiteScore
4.90
自引率
3.40%
发文量
98
审稿时长
2 months
期刊介绍: Preparative Biochemistry & Biotechnology is an international forum for rapid dissemination of high quality research results dealing with all aspects of preparative techniques in biochemistry, biotechnology and other life science disciplines.
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