Improving mannanase production in Bacillus subtilis for fibre hydrolysis during solid-state fermentation of palm kernel meal

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biochemical Engineering Journal Pub Date : 2024-09-07 DOI:10.1016/j.bej.2024.109479
Wei Li Ong , Zhi Li , Kian-Hong Ng , Kang Zhou
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Abstract

The primary challenge in utilizing palm kernel meal (PKM, an agricultural by-product) as non-ruminant livestock feed is its high fibre content, predominantly in the form of mannan. Microbial fermentation offers an economically favourable alternative to enzyme supplementation for breaking down fibre in lignocellulosic biomass. In a recent study, our group isolated a B. subtilis strain F6 with a fast response time for mannanase production upon exposure to PKM. This work focuses on improving the mannanase production of the B. subtilis strain to achieve greater fibre hydrolysis of PKM without extending fermentation time. Mannanase GmuG, sourced from B. subtilis F6 and verified for its hydrolytic activity on PKM fibre, was homologously expressed using a replicative plasmid (pBE-S). Enzyme production was systematically improved by optimizing various regulatory elements, including the promoter, ribosome binding site, and signal peptide. Consequently, the neutral detergent fibre content of PKM was substantially reduced by 36.4 % in 22 h of solid-state fermentation using the engineered strain. Lastly, the highest mannanase-producing strain was examined for scaled-up fermentation. The impacts of fermentation on fibre and protein contents, as well as the surface morphology of PKM, were analysed. The outcomes of this study offer an efficient method for robust mannanase expression in B. subtilis and its potential application in the biotransformation of PKM and other mannan-rich bioresources for improved feed utilization.

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提高枯草芽孢杆菌的甘露聚糖酶产量,以便在棕榈仁粕固态发酵过程中水解纤维
利用棕榈仁粕(PKM,一种农副产品)作为非反刍家畜饲料的主要挑战在于其纤维含量高,主要以甘露聚糖的形式存在。微生物发酵为分解木质纤维素生物质中的纤维提供了一种经济上有利的替代酶补充剂。在最近的一项研究中,我们的研究小组分离出了一株枯草芽孢杆菌 F6 菌株,该菌株在接触 PKM 后能快速产生甘露聚糖酶。这项工作的重点是提高枯草芽孢杆菌菌株的甘露聚糖酶产量,以便在不延长发酵时间的情况下,实现更大程度的 PKM 纤维水解。甘露聚糖酶 GmuG 来自枯草芽孢杆菌 F6,其对 PKM 纤维的水解活性已得到验证。通过优化各种调控元件,包括启动子、核糖体结合位点和信号肽,系统地提高了酶的产量。因此,在使用工程菌株进行 22 小时固态发酵后,PKM 的中性洗涤纤维含量大幅降低了 36.4%。最后,对甘露糖产量最高的菌株进行了放大发酵试验。分析了发酵对纤维和蛋白质含量以及 PKM 表面形态的影响。这项研究的成果提供了一种在枯草芽孢杆菌中强力表达甘露聚糖酶的有效方法,并有可能应用于 PKM 和其他富含甘露聚糖的生物资源的生物转化,以提高饲料利用率。
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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