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

机译:补充酿酒酵母和瘤胃微生物益生菌的日粮的体外发酵特性和瘤胃微生物数量

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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 (P0.05) and bacterial population (P0.05). As compared with control, all treatments reduced protozoa population (P0.05). Combination of S. cerevisiae and MR4 probiotics produced the highest total volatile fatty acids (VFA) and isovalerate (P0.05). 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.
机译:这项研究的目的是选择三种益生酿酒酵母菌株,并评估酿酒酵母和瘤胃细菌分离物(MR4)的添加及其组合对瘤胃发酵能力和瘤胃微生物种群的影响。实验1以4 x 5阶乘随机区组设计进行设计,重复3次。第一个因素是酿酒酵母菌株,包括对照处理(不添加啤酒酵母),NBRC 10217,NRRL Y 567和NRRL 12618,第二个因素是孵育时间为0、1、2、3和4 h 。饲喂量是饲草的基础日粮,饲草与精料之比(F:C)= 60:40。酿酒酵母每次处理的剂量为5 x 1010 cfu / kg定量。实验2设计成随机区组设计,共有4种处理方式:P0 =饲养场的基础日粮; P1 = P0 +酿酒酵母; P2 = P0 + MR4分离株(5 x 107 cfu / kg配比); P3 = P0 +酿酒酵母和MR4分离株。实验1的结果表明,酿酒酵母NRRL 12618的补充具有最高的酿酒酵母种群和增加的瘤胃细菌种群。该菌株在实验2中被选为益生菌。实验2的结果表明,补充益生菌可稳定瘤胃pH值,并产生最高的NH3浓度(P <0.05)和细菌种群(P <0.05)。与对照组相比,所有处理均减少了原生动物种群(P <0.05)。酿酒酵母和MR4益生菌的组合产生最高的总挥发性脂肪酸(VFA)和异戊酸(P <0.05)。结论是,酿酒酵母NRRL 12618具有作为益生菌酵母的潜力。补充该菌株可提高发酵能力,瘤胃异酸并降低A:P比。 MR4瘤胃分离益生菌可以改善这些能力。

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