Kung L, Hession A O
Department of Animal Science & Agricultural Biochemistry, University of Delaware, Newark 19717-1303.
J Anim Sci. 1995 Jan;73(1):250-6. doi: 10.2527/1995.731250x.
In vitro fermentations containing a mixed culture of ruminal bacteria (ruminal fluid from a hay-fed steer), buffer, and primarily rapidly degradable substrates (starch, glucose, cellulose, cellobiose, and trypticase) were inoculated with an overnight culture of Megasphaera elsdenii B159. Triplicate flasks were either uninoculated or inoculated to obtain a final concentration of 8.7 x 10(5) and 8.7 x 10(6) colony forming units of M. elsdenii per milliliter of culture fluid. Inoculation with M. elsdenii prevented an accumulation of lactic acid and excessive drop in pH. Lactate peaked at more than 40 mM in untreated cultures. In cultures inoculated with a low dose of M. elsdenii, lactate concentration peaked at approximately 25 mM at 5 h of fermentation but decreased rapidly to less than 5 mM by 7 h of fermentation. With the addition of the high dose of M. elsdenii, lactate was never greater than 2 mM (P < .05) throughout fermentation. Cultures treated with M. elsdenii had greater amounts (P < .05) of isobutyrate, butyrate, isovalerate, and valerate than untreated cultures. After 24 h of fermentation, one-half of the culture fluid was transferred to an equal volume of fresh buffer with substrate but was not inoculated with further quantities of M. elsdenii. Six hours after transfer, cultures that had been originally treated with M. elsdenii had lower (P < .05) amounts of lactate than untreated cultures. Inoculation with M. elsdenii has potential to prevent lactate accumulation in diets containing readily fermentable carbohydrates.
含有瘤胃细菌混合培养物(来自以干草为食的阉牛的瘤胃液)、缓冲液以及主要是快速降解底物(淀粉、葡萄糖、纤维素、纤维二糖和胰蛋白酶)的体外发酵物,用埃氏巨球型菌B159的过夜培养物进行接种。一式三份的烧瓶要么不接种,要么接种以获得每毫升培养液中埃氏巨球型菌的最终浓度为8.7×10⁵和8.7×10⁶菌落形成单位。接种埃氏巨球型菌可防止乳酸积累和pH过度下降。在未处理的培养物中,乳酸峰值超过40 mM。在接种低剂量埃氏巨球型菌的培养物中,乳酸浓度在发酵5小时时达到约25 mM的峰值,但在发酵7小时时迅速降至5 mM以下。添加高剂量的埃氏巨球型菌后,整个发酵过程中乳酸含量从未超过2 mM(P<0.05)。用埃氏巨球型菌处理的培养物中异丁酸、丁酸、异戊酸和戊酸的含量比未处理的培养物更多(P<0.05)。发酵24小时后,将一半的培养液转移到等体积含底物的新鲜缓冲液中,但不接种更多的埃氏巨球型菌。转移6小时后,最初用埃氏巨球型菌处理的培养物中乳酸含量比未处理的培养物更低(P<0.05)。接种埃氏巨球型菌有潜力防止含有易发酵碳水化合物的日粮中乳酸积累。