2019
DOI: 10.5713/ajas.18.0282
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Evaluation of in vitro ruminal fermentation of ensiled fruit byproducts and their potential for feed use

Abstract: The results of the in vitro cultivation experiments indicated that not only the composition but also ensiling of FBs affected rumen fermentation patterns and the degree of methane generation. This is primarily because of the compositional changes in the fibrous fraction during ensiling as well as the presence of readily fermented substrates, whereas tannins in these FBs seemed to have little effect on the ruminal fermentation kinetics.

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Cited by 8 publications
(18 citation statements)
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“…We observed in a previous paper [4] that the inclusion of ensiled PS (without absorbent, at that time) decreased in vitro methane generation and that the change was likely dependent on the carbohydrate profile and on the compositional changes in the ensiled byproduct. From this viewpoint, we conceived that compositional changes in absorbents occuring during ensiling may affect in vitro rumen fermentation profile and methane generation.…”
Section: Introductionmentioning
confidence: 57%
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“…We observed in a previous paper [4] that the inclusion of ensiled PS (without absorbent, at that time) decreased in vitro methane generation and that the change was likely dependent on the carbohydrate profile and on the compositional changes in the ensiled byproduct. From this viewpoint, we conceived that compositional changes in absorbents occuring during ensiling may affect in vitro rumen fermentation profile and methane generation.…”
Section: Introductionmentioning
confidence: 57%
“…The procedures for bag silage preparation and fermentation control were described in our previous reports [4,5]. Briefly, we cut PS to a short length (5-10 cm) before combining the inoculum and absorbents and mixed all materials well to ensure even distribution.…”
Section: Silage Preparationmentioning
confidence: 99%
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“…Genomic DNA of the microorganisms was extracted from a precipitant (5,000 × g , 10 min,) of a thawed aliquot using the QIAamp DNA Stool Mini Kit (Qiagen) according to the protocol by the manufacturer, and the nucleic acid material was stored at less than −20°C until analysis. The PCR conditions and primer sequences for total bacteria were as previously reported (Mousa et al, ). Primer sets for real‐time PCR were Eub338F (ACTCCTACGGGAGGCAG) and Eub522R (ACGTCRTCCMCNCCTTCCTC) for total bacteria, qmcrA‐ F (TTCGGTGGATCDCARAGRGC) and qmcrA‐R (GBARGTCGWAWCCGTAGAATCC) for methanogenic Archaea, Fsuc3F (GTTCGGAATTACTGGGCGTAAA) and Fsuc3R (CCCCCGGACACCCAGTAT) for Fibrobacter , and RumFla3F (TGGCGGACGGGTGAGTAA) and RumFla3R (TTACCATCCGTTTCCAGAAGCT) for Ruminococcus flavefaciens .…”
Section: Methodsmentioning
confidence: 99%
“…Genomic DNA of the microorganisms was extracted from a precipitant (5,000 × g, 10 min,) of a thawed aliquot using the QIAamp DNA Stool Mini Kit (Qiagen) according to the protocol by the manufacturer, and the nucleic acid material was stored at less than −20°C until analysis. The PCR conditions and primer sequences for total bacteria were as previously reported (Mousa et al, 2018). Primer sets for real-time (Takara Bio Inc., Otsu, Japan) were applied for real-time PCR.…”
Section: Microbiological and Organic Acid Analysismentioning
confidence: 99%