Sustainable menaquinone-7 production through continuous fermentation in biofilm bioreactors.

IF 3.5 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Bioprocess and Biosystems Engineering Pub Date : 2024-07-01 Epub Date: 2024-06-12 DOI:10.1007/s00449-024-03040-1
Aydin Berenjian, Ehsan Mahdinia, Ali Demirci
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Abstract

Menaquinone-7 (MK-7), a vital vitamin with numerous health benefits, is synthesized and secreted extracellularly by the formation of biofilm, dominantly in Bacillus strains. Our team developed an innovative biofilm reactor utilizing Bacillus subtilis natto cells to foster biofilm growth on plastic composite supports to produce MK-7. Continuous fermentation in biofilm reactors offers a promising strategy for achieving sustainable and efficient production of Menaquinone-7 (MK-7). Unlike conventional batch fermentation, continuous biofilm reactors maintain a steady state of operation, which reduces resource consumption and waste generation, contributing to sustainability. By optimizing fermentation conditions, MK-7 production was significantly enhanced in this study, demonstrating the potential for sustainable industrial-scale production. To determine the optimal operational parameters, various dilution rates were tested. These rates were selected based on their potential to enhance nutrient supply and biofilm stability, thereby improving MK-7 production. By carefully considering the fermentation conditions and systematically varying the dilution rates, MK-7 production was significantly enhanced during continuous fermentation. The MK-7 productivity was found to increase from 0.12 mg/L/h to 0.33 mg/L/h with a dilution rate increment from 0.007 to 0.042 h-1). This range was chosen to explore the impact of various nutrient supply rates on MK-7 production and to identify the optimal conditions for maximizing productivity. However, a further increase in the dilution rate to 0.084 h-1 led to reduced productivity at approximately 0.16 mg/L/h, likely due to insufficient retention time for effective biofilm formation. Consequently, a dilution rate of 0.042 h-1 exhibited the highest productivity of 0.33 mg/L/h, outperforming all investigated dilution rates and demonstrating the critical balance between nutrient supply and retention time in continuous fermentation. These findings validate the feasibility of operating continuous fermentation at a 0.084 h-1 dilution rate, corresponding to a 48 h retention time, to achieve the highest MK-7 productivity compared to conventional batch fermentation. The significant advancements achieved in enhancing Menaquinone-7 (MK-7) productivity through continuous fermentation at optimal dilution rates in the present work indicate promising prospects for even greater efficiency and sustainability in MK-7 production through future developments.

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通过生物膜生物反应器中的连续发酵实现可持续的 Menaquinone-7 生产。
Menaquinone-7 (MK-7)是一种对健康有诸多益处的重要维生素,主要由枯草杆菌菌株通过形成生物膜在细胞外合成和分泌。我们的团队开发了一种创新的生物膜反应器,利用枯草芽孢杆菌纳豆细胞在塑料复合支架上促进生物膜生长,以生产 MK-7。生物膜反应器中的连续发酵为实现可持续高效生产 Menaquinone-7 (MK-7) 提供了一种前景广阔的策略。与传统的间歇发酵不同,连续生物膜反应器能保持稳定的运行状态,从而减少资源消耗和废物产生,有助于实现可持续发展。本研究通过优化发酵条件,显著提高了 MK-7 的产量,证明了可持续工业规模生产的潜力。为确定最佳操作参数,对各种稀释率进行了测试。选择这些稀释率的依据是它们在提高营养供应和生物膜稳定性方面的潜力,从而提高 MK-7 的产量。通过仔细考虑发酵条件并系统地改变稀释率,MK-7 的产量在连续发酵过程中得到了显著提高。稀释率从 0.007 增至 0.042 h-1),MK-7 的产量从 0.12 mg/L/h 增至 0.33 mg/L/h。选择这一范围是为了探索各种营养供应率对 MK-7 产量的影响,并确定使产量最大化的最佳条件。然而,稀释率进一步提高到 0.084 h-1 后,生产率降低到约 0.16 mg/L/h,这可能是由于有效形成生物膜所需的滞留时间不足。因此,稀释率为 0.042 h-1 时的生产率最高,达到 0.33 mg/L/h,超过了所有研究过的稀释率,证明了连续发酵中营养供应和保留时间之间的关键平衡。这些发现验证了以 0.084 h-1 的稀释率(相当于 48 小时的保留时间)进行连续发酵的可行性,与传统的间歇发酵相比,它能获得最高的 MK-7 生产率。本研究以最佳稀释率进行连续发酵,在提高萘醌-7(MK-7)生产率方面取得了重大进展,这预示着未来的发展有望提高 MK-7 生产的效率和可持续性。
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来源期刊
Bioprocess and Biosystems Engineering
Bioprocess and Biosystems Engineering 工程技术-工程:化工
CiteScore
7.90
自引率
2.60%
发文量
147
审稿时长
2.6 months
期刊介绍: Bioprocess and Biosystems Engineering provides an international peer-reviewed forum to facilitate the discussion between engineering and biological science to find efficient solutions in the development and improvement of bioprocesses. The aim of the journal is to focus more attention on the multidisciplinary approaches for integrative bioprocess design. Of special interest are the rational manipulation of biosystems through metabolic engineering techniques to provide new biocatalysts as well as the model based design of bioprocesses (up-stream processing, bioreactor operation and downstream processing) that will lead to new and sustainable production processes. Contributions are targeted at new approaches for rational and evolutive design of cellular systems by taking into account the environment and constraints of technical production processes, integration of recombinant technology and process design, as well as new hybrid intersections such as bioinformatics and process systems engineering. Manuscripts concerning the design, simulation, experimental validation, control, and economic as well as ecological evaluation of novel processes using biosystems or parts thereof (e.g., enzymes, microorganisms, mammalian cells, plant cells, or tissue), their related products, or technical devices are also encouraged. The Editors will consider papers for publication based on novelty, their impact on biotechnological production and their contribution to the advancement of bioprocess and biosystems engineering science. Submission of papers dealing with routine aspects of bioprocess engineering (e.g., routine application of established methodologies, and description of established equipment) are discouraged.
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