2020
DOI: 10.5713/ajas.19.0308
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Effects of wild or mutated inoculants on rye silage and its rumen fermentation indices

Abstract: Objective: This study was conducted to confirm the effects of new inoculants producing-antifungal or esterase substances on rye silage and its rumen fermentation indices by comparing wild with mutated types.Methods: Rye harvested at dough stage was ensiled into 3 L mini bucket silo (1 kg) for 90 d in triplicate following: distilled water at 20 μL/g (CON); <i>Lactobacillus brevis</i> 100D8 (AT) and its inactivation of antifungal genes (AT-m) at 1.2×10<sup>5</sup> cfu/g, respectively; and… Show more

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Cited by 17 publications
(34 citation statements)
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“…Application of IN and SA had no effects on rumen fermentation and nutrient digestibility of SBM substrate but increased IVDMD of BGH substrate. Ruminal pH and total SCFA concentration in the present study were similar to the previous studies [ 13 , 23 , 24 ]. The GA decreased total SCFA concentration resulting from the fermentation of both substrates and decreased also IVDNDF of the BGH substrate.…”
Section: Discussionsupporting
confidence: 92%
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“…Application of IN and SA had no effects on rumen fermentation and nutrient digestibility of SBM substrate but increased IVDMD of BGH substrate. Ruminal pH and total SCFA concentration in the present study were similar to the previous studies [ 13 , 23 , 24 ]. The GA decreased total SCFA concentration resulting from the fermentation of both substrates and decreased also IVDNDF of the BGH substrate.…”
Section: Discussionsupporting
confidence: 92%
“…Carbon dioxide gas was flushed into each incubation bottle continuously to maintain anaerobic conditions. Each treatment was prepared in triplicate along with three blanks and incubated at 39 °C for 72 h [ 13 ].…”
Section: Methodsmentioning
confidence: 99%
“…The WCR before and after ensiling were sub-sampled at 500 g, respectively, to analyses chemical composition and in vitro digestibility. Also, 20 g of ensiled WCR was sub-sampled and blended with 200 mL of sterile ultrapure water for 30 sec, and then filtered through two layers of cheesecloth to make silage extraction [3][4][5]. The fresh silage extraction was used to analyze pH and microbial counts.…”
Section: Inoculant Preparationmentioning
confidence: 99%
“…Silage extract (first dilution) was continued in several dilutions (10 -3 [3][4][5]. Visible colonies were counted from the plates and the number of cfu was expressed per gram of silage.…”
Section: Microbial Countsmentioning
confidence: 99%
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