Media formulation using statistical methodology to enhance α-amylase production for green synthesis of Au-NPs by Bacillus subtilis VSP4 under solid-state fermentation.

IF 4.8 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2025-06-03 eCollection Date: 2025-01-01 DOI:10.3389/fbioe.2025.1569902
Vimalkumar S Prajapati, Vaibhavkumar N Mehta, Swati K Patel
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引用次数: 0

Abstract

In recent years, gold nanoparticles (Au-NPs) have garnered popularity for their remarkable and promising applications in various areas. Here, we report the synthesis of Au-NPs using extracellular amylase produced by Bacillus subtilis VSP4 under solid-state fermentation (SSF) through the reduction of AuCl4 with retention of enzymatic activity in the complex. Accordingly, B. subtilis VSP4 was exploited to enhance α-amylase production under SSF using the Plackett-Burman design, followed by the central composite design (CCD) of response surface methodology (RSM). According to our analysis, the most significant components in the medium are starch, yeast extract, and CaCl2 (significance >95%, ANOVA), which prominently enhance enzyme production. The optimum levels of these three selected variables were evaluated using CCD-RSM (20 runs), and it was confirmed that 0.05 g of starch, 0.1 g of yeast extract, and 5 mM of CaCl2 per 5 g of wheat bran under SSF produced the maximum α-amylase yield (169.72 U/gds). The F-value of the quadratic model (18.36) implies that the model is significant, while the F-value of the lack of fit (3.17) indicates that the lack of fit is not significant, meaning that the model has good fit. The coefficient of variance was found to be 0.369, which denotes that the experiments performed herein are reliable (R2 = 0.94) (multiple correlation coefficient), and the standard deviation for the quadratic model was found to be 4.72. We also performed separate validation experiments to confirm the adequacy of the quadratic model. The present work highlights α-amylase production by B. subtilis VSP4 under SSF, which was prominently enhanced by adopting a statistical experimental design, leading to the formation of Au-NPs of average size 5.17 ± 0.85 nm showing a surface plasmon resonance peak at 528 nm.

采用统计学方法制备培养基,提高枯草芽孢杆菌VSP4固态发酵下绿色合成Au-NPs的α-淀粉酶产量。
近年来,金纳米颗粒(Au-NPs)因其在各个领域的卓越应用而广受欢迎。在这里,我们报道了利用枯草芽孢杆菌VSP4产生的胞外淀粉酶在固态发酵(SSF)下通过还原AuCl4合成Au-NPs的过程,同时保留了复合物中的酶活性。利用Plackett-Burman设计和响应面法的中心复合设计(CCD),利用枯草芽孢杆菌VSP4在SSF条件下提高α-淀粉酶的产量。根据我们的分析,培养基中最显著的成分是淀粉、酵母提取物和CaCl2(显著性为95%,方差分析),它们显著提高了酶的产量。结果表明,在SSF条件下,淀粉用量为0.05 g,酵母浸膏用量为0.1 g, CaCl2用量为5 mM /g /g时,α-淀粉酶产率最高(169.72 U/gds)。二次模型的f值(18.36)表示模型显著,而缺乏拟合的f值(3.17)表示缺乏拟合不显著,表示模型拟合良好。方差系数为0.369,表明本文所做的实验是可靠的(R2 = 0.94)(多重相关系数),二次模型的标准差为4.72。我们还进行了单独的验证实验,以确认二次模型的充分性。采用统计实验设计,研究了枯草芽孢杆菌VSP4在SSF作用下α-淀粉酶的产量显著增加,形成平均尺寸为5.17±0.85 nm的Au-NPs,在528 nm处出现表面等离子体共振峰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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