Simova E D, Beshkova D M, Angelov M P, Dimitrov Zh P
Laboratory of Applied Microbiology, Institute of Microbiology, Bulgarian Academy of Sciences, 26 Maritza Blvd, 4002 Plovdiv, Bulgaria.
J Ind Microbiol Biotechnol. 2008 Jun;35(6):559-67. doi: 10.1007/s10295-008-0317-x. Epub 2008 Feb 14.
By screening for bacteriocin-producing lactic acid bacteria of 1,428 strains isolated from authentic Bulgarian dairy products, Lb. bulgaricus BB18 strain obtained from kefir grain was selected. Out of 11 yogurt starters containing Lb. bulgaricus BB18 and S. thermophilus strains resistant to bacteriocin secreted by Lb. bulgaricus BB18 a yogurt culture (S. thermophilus 11A+Lb. bulgaricus BB18) with high growth and bacteriocinogenic activity in milk was selected. Continuous (pH-stat 5.7) prefermentation processes were carried out in milk at 37 degrees C in a 2l MBR bioreactor (MBR AG, Zurich, Switzerland) with an IMCS controller for agitation speed, temperature, dissolved oxygen, CO2 and pH. Prefermented milk with pH 5.7 coagulated in a thermostat at 37 degrees C until pH 4.8-4.9. S. thermophilus 11A and Lb. bulgaricus BB18 grew independently in a continuous mode at similar and sufficiently high-dilution rates (D=1.83 h(-1)-S. thermophilus 11A; D=1.80 h(-1)-Lb. bulgaricus BB18). The yogurt cultures developed in a stream at a high-dilution rate (D=2.03-2.28 h(-1)). The progress of both processes (growth and bacteriocin production) depended on the initial ratio between the two microorganisms. The continuous prefermentation process promoted conditions for efficient fermentation and bacteriocinogenesis of the starter culture during the batch process: strong reduction of the times for bacteriocin production and coagulation of milk (to 4.5-5.0 h); high cell productivity (lactobacilli-4x10(12) CFU ml(-1), streptococci-6x10(12) CFU ml(-1)); high productivity of bacteriocins (4,500 BU ml(-1))-1.7 times higher than the bacteriocinogenic activity of the batch starter culture.
通过对从正宗保加利亚乳制品中分离出的1428株乳酸菌进行筛选,选择了从开菲尔粒中获得的保加利亚乳杆菌BB18菌株。在11种含有保加利亚乳杆菌BB18和嗜热链球菌菌株的酸奶发酵剂中,这些嗜热链球菌菌株对保加利亚乳杆菌BB18分泌的细菌素具有抗性,从中选择了一种在牛奶中具有高生长和产细菌素活性的酸奶培养物(嗜热链球菌11A + 保加利亚乳杆菌BB18)。在2升的膜生物反应器(MBR AG,瑞士苏黎世)中,于37℃下在牛奶中进行连续(pH值调节为5.7)预发酵过程,该反应器配备有用于搅拌速度、温度、溶解氧、二氧化碳和pH值的IMCS控制器。将pH值为5.7的预发酵牛奶在37℃的恒温器中凝固,直至pH值达到4.8 - 4.9。嗜热链球菌11A和保加利亚乳杆菌BB18以连续模式独立生长,稀释率相似且足够高(D = 1.83 h⁻¹ - 嗜热链球菌11A;D = 1.80 h⁻¹ - 保加利亚乳杆菌BB18)。酸奶培养物以高稀释率(D = 2.03 - 2.28 h⁻¹)在流态中培养。两个过程(生长和细菌素产生)的进展取决于两种微生物之间的初始比例。连续预发酵过程为批式过程中发酵剂培养物的高效发酵和细菌素生成创造了条件:显著缩短了细菌素产生和牛奶凝固的时间(至4.5 - 5.0小时);细胞生产力高(乳酸杆菌 - 4×10¹² CFU/ml,链球菌 - 6×10¹² CFU/ml);细菌素生产力高(4500 BU/ml) - 比批式发酵剂培养物的产细菌素活性高1.7倍。