首页> 外文期刊>Asian-Australasian Journal of Animal Sciences >Rumen Microbial Population in the In vitro Fermentation of Different Ratios of Forage and Concentrate in the Presence of Whole Lerak (Sapindus rarak) Fruit Extract
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Rumen Microbial Population in the In vitro Fermentation of Different Ratios of Forage and Concentrate in the Presence of Whole Lerak (Sapindus rarak) Fruit Extract

机译:完整Lerak(Sapindus rarak)果实提取物存在下体外发酵不同发酵液和精料比例的瘤胃微生物种群

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This experiment was designed to investigate the effect of lerak extract on the dynamic of rumen microbes in the in vitro fermentation of diet with different ratios of forage and concentrate. In vitro fermentation was conducted according to the method of Tilley and Terry (1963). The design of experiment was a factorial block design with 2 factors. The first factor was the ratio of forage and concentrate (90:10, 80:20, and 70:30 w/w) and the second factor was the level of lerak extract (0, 0.6, and 0.8 mg/ml). Total volatile fatty acid (VFA) concentration, proportional VFA and NH3 concentration were measured at 4 h incubation. Protozoal numbers in the buffered rumen fluid after 4 and 24 h of incubation were counted under a microscope. Bacterial DNAs of buffered rumen fluid were isolated from incubated samples after 24 h of incubation using a QiaAmp kit. Total bacteria, Fibrobacter succinogenes, Ruminococcus albus, and Prevotella ruminicola were quantified using real time polymerase chain reaction (PCR). Lerak extract markedly reduced protozoal numbers in buffered rumen fluid of all diets after 24 h of incubation. Total bacteria did not change with lerak extract addition. While no difference in F succinogenes was found, there was a slight increase in R. albus number and a significant enhancement in P ruminicola number by increasing the level of lerak extract in all diets. Propionate concentration significantly increased in the presence of lerak extract at level 0.8 mg/ml. It was concluded that the addition of lerak extract could modify rumen fermentation and had positive effects on rumen microbes.
机译:本实验旨在研究在不同饲草和精料比例的日粮体外发酵中,莱拉克提取物对瘤胃微生物动态的影响。根据Tilley和Terry(1963)的方法进行了体外发酵。实验的设计是一个有两个因素的因子分解设计。第一个因素是草料和精料的比例(90:10、80:20和70:30 w / w),第二个因素是青菜提取物的水平(0、0.6和0.8 mg / ml)。在孵育4小时后测量总挥发性脂肪酸(VFA)浓度,比例VFA和NH3浓度。培养4和24小时后,在瘤胃液中的原生动物数在显微镜下计数。孵育24小时后,使用QiaAmp试剂盒从孵育的样品中分离缓冲瘤胃液的细菌DNA。使用实时聚合酶链反应(PCR)定量细菌总数,琥珀酸纤维杆菌,阿鲁米球菌和小球藻。孵育24小时后,所有饮食的缓冲瘤胃液中的Lerak提取物的原生动物数量明显减少。总细菌量没有随添加莱拉克提取物而变化。虽然未发现琥珀酸F的差异,但通过增加所有日粮中的有色提取物水平,白al菌数量略有增加,反刍动物数量显着增加。在有lerak提取物的情况下,浓度为0.8 mg / ml时,丙酸盐浓度显着增加。得出的结论是,添加莱拉克提取物可以改善瘤胃发酵,并对瘤胃微生物产生积极影响。

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