Center for Complex Fluids Processing, Multidisciplinary Nanotechnology Center, School of Engineering, Swansea University, Talbort Building, Singleton Park, Wales SA2 8PP, UK.
J Ind Microbiol Biotechnol. 2010 Jul;37(7):727-40. doi: 10.1007/s10295-010-0716-7. Epub 2010 Apr 13.
The aim of this study was to investigate the secondary fermentation of alcoholic green cider by Lactobacillus brevis and Oenococcus oeni in a membrane bioreactor so as to compare the performance of the two organisms to rapidly carry out the malolactic fermentation (MLF), an important step in reducing acidity and enhancing the flavor characteristics of the beverages. First, the growth of both organisms was intensified by using perfusion culture in a membrane bioreactor (MBR). O. oeni and L. brevis were grown up to 12.8 g dry cell weight (DCW) l(-1) and 15.5 g DCW l(-1) in the MBR. Secondly, the resultant cells were then used for the malolactic transformation of green cider in the MBR. The influences of the residence time in the MBR and the ethanol concentration of the green cider on the organic acid transformation were investigated. Both organisms showed a good tolerance against the acidic conditions (pH 3.0-4.0) and ethanol (90 g l(-1)). Good levels of malate removal in the MBR were achieved by both organisms but O. oeni was more tolerant to high ethanol concentrations and was capable of growth and malate removal in 130 g ethanol l(-1) green cider. L. brevis malate removal was significantly inhibited above 110 g ethanol l(-1). The MBR allowed the development of high concentrations of active cells capable of rapid MLF and could be achieved over a prolonged period and over a wide range of conditions thus allowing the control of malate transformation rate. Organism selection for the transformation will be governed by the desired beverage characteristics. There is considerable scope to optimize the process further both with the choice of organisms and the design and operation of the reactor. Rapid beverage maturation on a commercial scale may be possible using MBR and pure cultures of MLF lactic acid bacteria.
本研究旨在通过短乳杆菌和酒香酵母在膜生物反应器中对酒精性青苹果酒进行二次发酵,比较两种微生物快速进行苹果酸-乳酸发酵(MLF)的性能,这是降低酸度和增强饮料风味特征的重要步骤。首先,通过在膜生物反应器(MBR)中进行灌注培养来强化两种微生物的生长。O. oeni 和 L. brevis 在 MBR 中分别达到 12.8 g 干细胞重量(DCW)l(-1)和 15.5 g DCW l(-1)。其次,将得到的细胞用于 MBR 中青苹果酒的苹果酸转化。考察了 MBR 中的停留时间和青苹果酒的乙醇浓度对有机酸转化的影响。两种微生物都对酸性条件(pH 3.0-4.0)和乙醇(90 g l(-1))有很好的耐受性。两种微生物在 MBR 中都能很好地去除苹果酸,但 O. oeni 对高乙醇浓度更耐受,能够在 130 g 乙醇 l(-1)的青苹果酒中生长和去除苹果酸。L. brevis 在乙醇浓度高于 110 g l(-1)时,苹果酸去除明显受到抑制。MBR 允许高浓度的活性细胞生长,从而能够快速进行 MLF,并能在较长时间内和较宽的条件范围内实现,从而可以控制苹果酸转化速率。转化中微生物的选择将取决于所需饮料的特性。通过选择合适的微生物和优化反应器的设计和操作,可以进一步优化该过程。使用 MBR 和 MLF 乳酸菌的纯培养物,可能实现商业规模的快速饮料成熟。