Laboratory of Applied Microbiology and Biotechnology, Department of Molecular Biology and Genetics, Democritus University of Thrace, Alexandroupolis, Greece.
Food Biotechnology Group, Section of Analytical Environmental and Applied Chemistry, Department of Chemistry, University of Patras, Patras, Greece.
J Sci Food Agric. 2020 Jun;100(8):3319-3327. doi: 10.1002/jsfa.10363. Epub 2020 Mar 18.
The aim of the present study was to evaluate the fermentation efficiency of freeze-dried immobilized kefir culture on natural supports (apple pieces, delignified cellulosic material) in cider making at various temperatures (5-45 °C) in comparison with freeze-dried free cells. Freeze-dried cells were initially tested in apple juice fermentations at 30 °C, and then the freeze-dried cultures produced with no cryoprotectants were assessed in repeated batch fermentations.
Repeated batch fermentations lasted for longer than 5 months. High malic acid conversion rates (up to 78.5%) and ethanol productivity values (up to 37.9 g L day ) were recorded for freeze-dried immobilized cells. Polymerase chain reaction - denaturing gradient gel electrophoresis (PCR-DGGE) analysis showed that freeze-drying had no effect on the microbial diversity of kefir culture. Higher alcohols were significantly reduced at low fermentation temperatures. Application of principal component analysis (PCA) revealed that both the fermentation temperature and the nature of the freeze-dried kefir culture affected significantly the minor volatiles determined by gas chromatography/mass spectrometry (GC/MS). Notably, all ciders produced were of high quality and were accepted by the tasting panel.
Freeze-dried immobilized kefir culture on natural supports with no cryoprotectants was found to be suitable for simultaneous alcoholic and malolactic cider fermentation at various temperatures (5-45 °C). The high operational stability of the systems was confirmed and the results obtained are of great interest for the industrial sector as they could be exploited for cider, low-alcohol cider, or 'soft' cider production. © 2020 Society of Chemical Industry.
本研究的目的是评估在不同温度(5-45°C)下,与冻干自由细胞相比,在 cider 制作中,将冻干固定化开菲尔培养物在天然载体(苹果片、脱木质素纤维素材料)上的发酵效率。首先在 30°C 的苹果汁发酵中测试了冻干细胞,然后评估了在重复分批发酵中生产的无冷冻保护剂的冻干培养物。
重复分批发酵持续了 5 个多月。对于冻干固定化细胞,记录了高达 78.5%的高苹果酸转化率和高达 37.9 g·L 天 的乙醇生产率值。聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)分析表明,冻干对开菲尔培养物的微生物多样性没有影响。在低温发酵时,高级醇显著降低。主成分分析(PCA)的应用表明,发酵温度和冻干开菲尔培养物的性质都显著影响了气相色谱/质谱(GC/MS)测定的挥发性物质。值得注意的是,生产的所有 cider 都具有高品质,并且被品尝小组所接受。
发现无冷冻保护剂的天然载体上的冻干固定化开菲尔培养物适合在不同温度(5-45°C)下进行同时进行酒精和苹果酸乳酸发酵。系统的高操作稳定性得到了证实,所获得的结果对工业界具有很大的兴趣,因为它们可用于 cider、低酒精 cider 或“软” cider 的生产。© 2020 化学工业协会。