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嗜热葡糖苷芽孢杆菌通过原位微泡气提在连续高产能乙醇发酵中降低毒性

Toxicity reduction in continuous, high productivity ethanol fermentation by Parageobacillus thermoglucosidasius using in situ microbubble gas stripping.

作者信息

Ibenegbu Christopher, Zimmerman William B, Hines Michael, Desai Pratik D, Bandulasena H C Hemaka, Leak David J

机构信息

Department of Life Sciences, University of Bath, Bath, BA2 7AY, UK.

Department of Chemical and Biological Engineering, University of Sheffield, Sheffield, S1 3AD, UK.

出版信息

Microb Cell Fact. 2025 Jun 18;24(1):137. doi: 10.1186/s12934-025-02754-5.

Abstract

Ethanol concentrations above 4% (v/v) are required for economic bioethanol production due to the cost of recovery from dilute solutions. Although thermophilic bacteria have many potential advantages over Saccharomyces cerevisiae as process organisms for second generation bioethanol production, they are known to be less tolerant to ethanol, typically to concentrations less than 4% (v/v). To address this issue we have investigated the application of in situ gas-stripping of ethanol using microbubbles to increase the surface area per unit volume of gas, using fed-batch and continuous cultures of the engineered ethanologenic thermophile Parageobacillus thermoglucosidasius TM242. By using microbubbles generated at room temperature using a Desai-Zimmerman Fluid Oscillator, we initially operated a mixed batch and fed-batch fermentation, followed by a continuous fermentation and finally a chemostat fermentation, under conditions which would have generated in excess of 4% (v/v) ethanol. In all cases, gas stripping maintained the actual dissolved ethanol concentration below, or close to toxic levels. As the focus of this study was on demonstrating the efficiency of in situ microbubble gas stripping, to simplify the operation the latter two processes involved a combination of produced and supplemented ethanol, with the chemostat culture producing a nominal maximum 7.1% v/v based on glucose used (5.1-5.3% (v/v) based on ethanol recovered). This offers a practical way to produce second generation bio-ethanol from thermophiles.

摘要

由于从稀溶液中回收的成本,经济地生产生物乙醇需要乙醇浓度高于4%(v/v)。尽管嗜热细菌作为第二代生物乙醇生产的工艺微生物比酿酒酵母具有许多潜在优势,但已知它们对乙醇的耐受性较低,通常低于4%(v/v)。为了解决这个问题,我们使用工程化的产乙醇嗜热菌嗜热葡萄糖苷芽孢杆菌TM242的分批补料培养和连续培养,研究了利用微泡原位气提乙醇以增加单位体积气体的表面积的应用。通过使用Desai-Zimmerman流体振荡器在室温下产生的微泡,我们首先进行了混合分批和分批补料发酵,然后是连续发酵,最后是恒化器发酵,在会产生超过4%(v/v)乙醇的条件下进行。在所有情况下,气提都将实际溶解的乙醇浓度维持在毒性水平以下或接近毒性水平。由于本研究的重点是证明原位微泡气提的效率,为了简化操作,后两个过程涉及产生的乙醇和补充的乙醇的组合,恒化器培养基于使用的葡萄糖产生名义上最大7.1% v/v(基于回收的乙醇为5.1-5.3%(v/v))。这提供了一种从嗜热菌生产第二代生物乙醇的实用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f03/12177972/786909915c17/12934_2025_2754_Fig3_HTML.jpg

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