In vitro Fermentation Characteristics and Rumen Microbial Population of Diet Supplemented with Saccharomyces cerevisiae and Rumen Microbe Probiotics

Lilis Riyanti, Suryahadi, D. Evvyernie
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引用次数: 3

Abstract

The objective of this study was to select three strains of probiotic Saccharomyces cerevisiae and to evaluate the effect of S. cerevisiae and rumen bacteria isolate (MR4) supplementation and their combination on rumen fermentability and rumen microbial population. Experiment 1 was designed in a 4 x 5 factorial randomized block design with 3 replications. The first factor was S. cerevisiae strain consisted of control treatment (without S. cerevisiae supplementation), NBRC 10217, NRRL Y 567 and NRRL 12618, and the second factor was incubation time consisted of 0, 1, 2, 3, and 4 h. Ration was basal ration for feedlot with forage to concentrate ratio (F:C)= 60:40. Dosage of each treatment with S. cerevisiae was 5 x 1010 cfu/kg ration. Experiment 2 was designed in randomized block design with 4 treatments: P0= basal ration of feedlot; P1= P0 + S. cerevisiae; P2= P0 + MR4 isolate (5 x 107 cfu/kg ration); P3= P0 + S. cerevisiae and MR4 isolate. The result of experiment 1 showed that supplementation of S. cerevisiae NRRL 12618 had the highest S. cerevisiae population and increased rumen bacterial population. This strain was selected as probiotic in experiment 2. The result from experiment 2 showed that probiotic supplementation stabilized rumen pH and produced the highest NH3 concentration (P<0.05) and bacterial population (P<0.05). As compared with control, all treatments reduced protozoa population (P<0.05). Combination of S. cerevisiae and MR4 probiotics produced the highest total volatile fatty acids (VFA) and isovalerate (P<0.05). It was concluded that strain S. cerevisiae NRRL 12618 had potential as probiotic yeast. Supplementation with this strain increased fermentability, rumen isoacid and decreased A:P ratio. Those abilities could be improved with MR4 rumen isolate probiotic.
添加酿酒酵母和瘤胃微生物益生菌的日粮体外发酵特性及瘤胃微生物种群
本试验旨在筛选3株酿酒酵母菌,研究添加酿酒酵母菌和瘤胃分离菌(MR4)及其组合对瘤胃发酵能力和瘤胃微生物种群的影响。试验1采用4 × 5因子随机区组设计,设3个重复。第一个影响因素是由对照处理(不添加酿酒酵母)、NBRC 10217、NRRL Y 567和NRRL 12618组成的酿酒酵母菌株,第二个影响因素是孵育时间为0、1、2、3和4 h。饲粮为基础日粮,料精比(F:C)= 60:40。酿酒酵母每次处理的剂量为5 × 1010 cfu/kg日粮。试验2采用随机区组设计,共设4个处理:P0=饲场基础日粮;P1= P0 +酿酒葡萄球菌;P2= P0 + MR4分离物(5 × 107 cfu/kg);P3= P0 +酿酒葡萄球菌和MR4分离株。试验1结果表明,添加酿酒葡萄球菌NRRL 12618后,酿酒葡萄球菌数量最高,瘤胃细菌数量增加。试验2选用该菌株作为益生菌。试验2结果表明,添加益生菌稳定了瘤胃pH,产生了最高的NH3浓度(P<0.05)和细菌数量(P<0.05)。与对照组相比,各处理均减少了原生动物种群数量(P<0.05)。酿酒葡萄球菌与MR4益生菌组合产生的总挥发性脂肪酸和异戊酸最高(P<0.05)。综上所述,酿酒葡萄球菌NRRL 12618具有作为益生菌酵母的潜力。添加该菌株可提高发酵率、瘤胃异酸,降低A:P比。MR4瘤胃分离菌可以提高这些能力。
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