Green starch nanoparticles production in situ using α-amylase from a newly isolated Bacillus subtilis strain-MA6: statistical designs and characterizations.

IF 4.9 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Mohamed S Hasanin, Mohamed A A Abdella
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引用次数: 0

Abstract

Background: Starch is a carbohydrate polymer, made up of multiple glucose units, connected through glycosidic bonds. Starch nanoparticles (StNPs) are characterized as particles that possess at least one dimension measuring less than 1000 nm, while still being larger than a single molecule, and they have several uses in diverse technological fields. Various studies indicate that synthesizing StNPs through physical and chemical techniques is expensive, requires a lot of energy, and may harm human health and the environment. In contrast, the enzymatic synthesis of StNPs exerts milder impacts on the final products, rendering them more eco-friendly, safe, and healthier. So, amylases can produce StNPs with enhanced solubility, gelation, and viscosity characteristics by hydrolyzing soluble starches.

Results: This study explores the production of starch nanoparticles (StNPs) by α-amylase enzyme in situ from a newly isolated bacterial strain, which was biochemically described, genetically identified, and deposited into the database of GenBank under the designation Bacillus subtilis strain-MA6 (accession number: ON840082). The production medium was adjusted by employing statistical optimization of several parameters using the Plackett-Burman design (P-BD) and Box-Behnken design (B-BD) of the response surface methodology (RSM). Optimization of medium parameters using P-BD and B-BD models caused a 14.5-fold increase in α-amylase production. The StNPs were synthesized from bulk starch using three different α-amylase activities. Based on the B-BD results, trial 5 (B-BD/T5), trial 7 (B-BD/T7), and trial 13 (B-BD/T13) were selected for the StNPs characterization using Fourier-transform infrared spectroscopy (FTIR), Dynamic light scattering (DLS), and high-resolution transmission electron microscopy (HR-TEM) analysis. Trial 13 represented the highest α-amylase activity and observed high stability with an average zeta potential of about - 15.1 ± 3.2 mV. Moreover, HR-TEM showed the StNPs as spheres with an average size of about 43 nm.

Conclusion: StNPs were synthesized from bulk starch using the B. subtilis strain-MA6 α-amylase enzyme. The concentration of α-amylase plays a role in converting bulk starch to nanosized particles, which affects the stability of the produced nanoparticles and their size. This observation offered an optimistic technique to produce StNPs via a green and eco-friendly process.

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利用新分离的枯草芽孢杆菌菌株ma6 α-淀粉酶原位生产绿色淀粉纳米颗粒:统计设计和表征。
背景:淀粉是一种碳水化合物聚合物,由多个葡萄糖单位组成,通过糖苷键连接。淀粉纳米颗粒(StNPs)的特征是具有至少一个尺寸小于1000nm的颗粒,同时仍然大于单个分子,并且它们在不同的技术领域具有多种用途。各种研究表明,通过物理和化学技术合成StNPs价格昂贵,需要大量能源,并且可能危害人类健康和环境。相比之下,酶法合成StNPs对最终产物的影响较小,使其更环保、安全、健康。因此,淀粉酶可以通过水解可溶性淀粉产生具有增强溶解度、凝胶性和粘度特性的StNPs。结果:本研究利用α-淀粉酶原位制备淀粉纳米颗粒(StNPs),对新分离的菌株进行了生化描述和基因鉴定,并将其命名为Bacillus subtilis strain- ma6(登录号:ON840082),存入GenBank数据库。采用响应面法(RSM)的Plackett-Burman设计(P-BD)和Box-Behnken设计(B-BD)对几个参数进行统计优化,调整生产介质。采用P-BD和B-BD模型优化培养基参数,α-淀粉酶产量提高14.5倍。以三种不同α-淀粉酶活性的散装淀粉为原料合成StNPs。基于B-BD结果,选择试验5 (B-BD/T5)、试验7 (B-BD/T7)和试验13 (B-BD/T13)采用傅里叶变换红外光谱(FTIR)、动态光散射(DLS)和高分辨率透射电子显微镜(HR-TEM)分析对StNPs进行表征。试验13 α-淀粉酶活性最高,稳定性较高,平均zeta电位约为- 15.1±3.2 mV。此外,hrtem显示StNPs为平均尺寸约为43 nm的球体。结论:利用枯草芽孢杆菌ma6 α-淀粉酶可从散装淀粉中合成StNPs。α-淀粉酶的浓度在淀粉转化成纳米颗粒过程中起着重要作用,影响了纳米颗粒的稳定性和粒径大小。这一观察结果为通过绿色和生态友好的过程生产StNPs提供了一种乐观的技术。
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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
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