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Co-culture fermentation of peanut-soy milk for the development of a novel functional beverage

机译:花生豆浆共培养发酵以开发新型功能性饮料

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Most of the commercial probiotic products are dairy-based, and the development of non-dairy probiotic products could be an alternative for new functional products. The peanut-soy milk (PSM1) was inoculated with six different lactic acid bacteria (LAB), including probiotic strains and yeasts and fermentation was accomplished for 24 h at 37 degrees C and afterwards, another 24 h at +/- 4 degrees C. The Pediococcus acidilactici (UFLA BFFCX 27.1), Lactococcus locus (CCT 0360), Lactobacillus L. rhamnosus (LR 32) probiotic LAB, and the Lactobacillus delbrueckii subsp. bulgaricus (LB 340) yogurt starter culture reached cell concentrations of about 83 log CFU/mL during fermentation. However, these strains were not able to acidify the substrate when inoculated as pure culture. The lactobacillus acidophilus (LACA 4) probiotic produced significant amounts of lactic acid (3.35 g/L) and rapidly lowered the pH (4.6). Saccharomyces cerevisiae (UFLA YFFBM 18.03) did not completely consume the available sugars in PSM and consequently produced low amounts of ethanol (0.24 g/L). In pure culture, S. cerevisiae (UFLA YFFBM 18.03), L rhamnosus (LR 32), L acidophilus (LACA 4), and P. acidilactici (UFLA BFFCX 27.1) promoted the increase of total amino acids (48.02%, 4732%, 46.21% and, 44.07%, respectively). However, when in co-cultured, the strains consumed the free amino acids favoring their growth, and reaching the population of 8 log CFU/mL in PSM. Lactic acid production increased, and 12 h was required to reach a pH value of 4.3. In general, the strains were more efficient in the use of available carbohydrates and release of metabolites in co-cultured than in single culture fermentations. An average of 58% and 78% of available carbohydrates was consumed when single and co-cultures were evaluated, respectively. Higher lactic acid contents were found in a binary culture of P. acidilactici (UFLA BFFCX 27.1) and L acidophilus (LACA 4), and by co-culture of P. acidilactici (UFLA BFFCX 27.1), L. acidophilus (LACA 4) and S. cerevisiae (UFLA YFFBM 18.03) (9.03 and 8.51 g/L, respectively). The final content of ethanol was 0.03% (v/v) or less, which classified the final beverage as non-alcoholic
机译:大多数商业益生菌产品都以乳制品为基础,非乳制品益生菌产品的开发可以替代新功能产品。在花生豆浆(PSM1)中接种六种不同的乳酸菌(LAB),包括益生菌菌株和酵母菌,并在37摄氏度下发酵24小时,然后在+/- 4摄氏度下再发酵24小时。乳酸杆菌(UFLA BFFCX 27.1),乳球菌(CCT 0360),鼠李糖乳杆菌(LR 32)益生菌LAB和德氏乳杆菌亚种。在发酵过程中,保加利亚(LB 340)酸奶发酵剂培养的细胞浓度达到约83 log CFU / mL。然而,当作为纯培养物接种时,这些菌株不能酸化底物。嗜酸乳杆菌(LACA 4)益生菌产生大量乳酸(3.35 g / L),并迅速降低pH(4.6)。酿酒酵母(UFLA YFFBM 18.03)没有完全消耗PSM中的可用糖,因此产生的乙醇量很少(0.24 g / L)。在纯培养物中,酿酒酵母(UFLA YFFBM 18.03),鼠李糖(LR 32),嗜酸乳杆菌(LACA 4)和乳酸乳酸杆菌(UFLA BFFCX 27.1)促进了总氨基酸(48.02%,4732%,分别为46.21%和44.07%)。但是,在共培养时,菌株消耗了有助于其生长的游离氨基酸,并在PSM中达到8 log CFU / mL的种群。乳酸产量增加,需要12小时才能达到4.3的pH值。通常,与单培养发酵相比,在共培养中,菌株在利用可利用的碳水化合物和释放代谢物方面更有效。评估单次培养和共培养时,平均消耗了58%和78%的可用碳水化合物。在乳酸乳酸杆菌(UFLA BFFCX 27.1)和嗜酸乳杆菌(LACA 4)的二元培养中,以及乳酸乳酸杆菌(UFLA BFFCX 27.1),嗜酸乳杆菌(LACA 4)和酿酒酵母(UFLA YFFBM 18.03)(分别为9.03和8.51 g / L)。乙醇的最终含量为0.03%(v / v)或更低,这将最终饮料归类为无酒精

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