首页> 美国卫生研究院文献>Asian-Australasian Journal of Animal Sciences >The Effect of Forage Level and Oil Supplement on Butyrivibrio fibrisolvens and Anaerovibrio lipolytica in Continuous Culture Fermenters
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The Effect of Forage Level and Oil Supplement on Butyrivibrio fibrisolvens and Anaerovibrio lipolytica in Continuous Culture Fermenters

机译:饲料水平和补油对连续培养发酵罐中纤维溶酪伯和解脂拟革细菌的影响。

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摘要

The objective of this study was to evaluate the effects of forage level and oil supplement on selected strains of rumen bacteria believed to be involved in biohydrogenation (BH). A continuous culture system consisting of four fermenters was used in a 4×4 Latin square design with a factorial arrangement of treatments, with four 10 d consecutive periods. Treatment diets were: i) high forage diet (70:30 forage to concentrate (dry matter basis); HFC), ii) high forage plus oil supplement (HFO), iii) low forage diet (30:70 forage to concentrate; LFC), and iv) low forage plus oil supplement (LFO). The oil supplement was a blend of fish oil and soybean oil added at 1 and 2 g/100 g dry matter, respectively. Treatment diets were fed for 10 days and samples were collected from each fermenter on the last day of each period 3 h post morning feeding. The concentrations of vaccenic acid (t11C18:1; VA) and c9t11 conjugated linoleic acid (CLA) were greater with the high forage diet while the concentrations of t10 C18:1 and t10c12 CLA were greater with the low forage diet and addition of oil supplement increased their concentrations at both forage levels. The DNA abundance of Anaerovibrio lipolytica, and Butyrivibrio fibrisolvens vaccenic acid subgroup (Butyrivibrio VA) were lower with the low forage diets but not affected by oil supplement. The DNA abundance of Butyrivibrio fibrisolvens stearic acid producer subgroup (Butyrivibrio SA) was not affected by forage level or oil supplement. In conclusion, oil supplement had no effects on the tested rumen bacteria and forage level affected Anaerovibrio lipolytica and Butyrivibrio VA.
机译:这项研究的目的是评估饲草水平和油脂补充对选定的瘤胃细菌菌株的影响,这些菌株被认为与生物氢化(BH)有关。由4个发酵罐组成的连续培养系统采用4×4拉丁方形设计,采用因子分解处理,连续四个10 d。治疗饮食为:i)高饲草饮食(以浓缩饲料为70:30(以干物质为基础); HFC),ii)高饲草加油补充剂(HFO),iii)低饲草饮食(以30:70为浓缩的草料; LFC )和iv)低草料加油脂补充剂(LFO)。油补充剂是分别以1和2 g / 100 g干物质添加的鱼油和大豆油的混合物。治疗饮食喂养10天,并在早晨喂养后3小时的每个时期的最后一天从每个发酵罐收集样品。高饲草饲料中的痘苗酸(t11C18:1; VA)和c9t11共轭亚油酸(CLA)的浓度较高,而低饲草饲料和添加油补充剂中的t10 C18:1和t10c12 CLA的浓度较高在两个饲草水平上均增加了其浓度。饲喂低饲草饲料的人,脂解阿纳罗氏弧菌和纤维状解百维酸亚群(Butyrivibrio VA)的DNA丰度较低,但不受油脂补充的影响。饲草水平或补充油脂不会影响纤维状丁酸弧菌硬脂酸生产者组(Butyrivibrio SA)的DNA丰度。总之,补充油对测试的瘤胃细菌没有影响,并且饲草水平影响解脂阿那罗布韦和VA。

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