Robitaille G, Tremblay A, Moineau S, St-Gelais D, Vadeboncoeur C, Britten M
Food Research and Development Centre, Agriculture and Agri-Food Canada, St-Hyacinthe, Quebec, Canada.
J Dairy Sci. 2009 Feb;92(2):477-82. doi: 10.3168/jds.2008-1312.
To prevent textural defects in low-fat and fat-free yogurts, fat substitutes are routinely added to milk. In situ production of exopolysaccharides (EPS) by starter cultures is an acknowledged alternative to the addition of biothickeners. With the aim of increasing in situ EPS production, a recombinant galactose-positive EPS(+) Streptococcus thermophilus strain, RD-534-S1, was generated and compared with the parent galactose-negative EPS(+) strain RD-534. The RD-534-S1 strain produced up to 84 mg/L of EPS during a single-strain milk fermentation process, which represented 1.3 times more than the EPS produced by strain RD-534. Under conditions that mimic industrial yogurt production, the starter culture consisting of RD-534-S1 and (EPS(-)) Lactobacillus bulgaricus L210R strain (RD-534-S1/L210R) led to an EPS production increase of 1.65-fold as compared with RD-534-S1 alone. However, the amount of EPS produced did not differ from that found in yogurts produced using an isogenic starter culture that included the parent S. thermophilus strain RD-534 and Lb. bulgaricus L210R (RD-534/L210R). Moreover, the gel characteristics of set-style yogurt and the rheological properties of stirred-style yogurt produced using RD-534-S1/L210R were similar to the values obtained for yogurts made with RD-534/L210R. In conclusion, it is possible to increase the production of EPS by ropy S. thermophilus strains through genetic engineering of galactose metabolism. However, when used in combination with Lb. bulgaricus for yogurt manufacture, the EPS overproduction of recombinant strain is not significant.
为防止低脂和无脂酸奶出现质地缺陷,通常会向牛奶中添加脂肪替代品。利用发酵剂原位生产胞外多糖(EPS)是一种公认的替代添加生物增稠剂的方法。为了提高EPS的原位产量,构建了一株重组半乳糖阳性EPS(+)嗜热链球菌菌株RD-534-S1,并将其与亲本半乳糖阴性EPS(+)菌株RD-534进行比较。在单菌株牛奶发酵过程中,RD-534-S1菌株产生的EPS高达84 mg/L,比RD-534菌株产生的EPS多1.3倍。在模拟工业酸奶生产的条件下,由RD-534-S1和(EPS(-))保加利亚乳杆菌L210R菌株组成的发酵剂(RD-534-S1/L210R)与单独使用RD-534-S1相比,EPS产量提高了1.65倍。然而,所产生的EPS量与使用包含亲本嗜热链球菌菌株RD-534和保加利亚乳杆菌L210R的同基因发酵剂生产的酸奶中的EPS量没有差异(RD-534/L210R)。此外,使用RD-534-S1/L210R生产的凝固型酸奶的凝胶特性和搅拌型酸奶的流变学特性与使用RD-534/L210R生产的酸奶所获得的值相似。总之,通过半乳糖代谢的基因工程,可以提高粘性嗜热链球菌菌株的EPS产量。然而,当与保加利亚乳杆菌联合用于酸奶生产时,重组菌株的EPS过量生产并不显著。