26 research outputs found

    Effects of pH and Concentrations of Linoleic and Linolenic Acids on Extent and Intermediates of Ruminal Biohydrogenation in Vitro

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    Three experiments were conducted by in vitro incubations in ruminal fluid to investigate the effects of pH and amounts of linoleic and linolenic acids on the extent of their biohydrogenation, the proportions of conjugated linoleic acid (CLA) and trans-C18:1 as intermediates, and the ratio trans-10:trans-11 intermediates. The effects of pH and amount of linoleic acid were investigated in kinetic studies, and effects of the amount of linolenic acid were studied with 6-h incubations. With identical initial amounts of linoleic acid, its disappearance declined when the mean pH during incubation was under 6.0 compared with a mean pH over 6.5, and when the amount of linolenic acid increased from 10 to 180 mg/160-ml flask, suggesting an inhibition of the isomerization step of the biohydrogenation. Low pH decreased the ratio of trans-10:trans-11 intermediates. With initial amounts of linoleic acid increasing from 100 to 300 mg, the percentage of linoleic acid disappearance declined, but the amount that disappeared increased, without modification of the trans-10:trans-11 ratio, suggesting a maximal capacity of isomerization rather than an inhibition. Moreover, increasing initial linoleic acid resulted in high amounts of trans-C18:1 and an increase of C18:0 that was a linear function of time, suggesting a maximal capacity for the second reduction step of biohydrogenation. High amounts of initial linolenic acid did not affect the amounts of CLA, trans-C18:1, or the ratio trans-10:trans-11. Based on these experiments, a ruminal pH near neutrality with high amount of dietary linoleic acid should modulate the reactions of biohydrogenation in a way that supports CLA and trans-11C18:1 in the rumen

    Effects of live yeast on the fatty acid biohydrogenation by ruminal bacteria

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    Addition of live yeasts in high concentrate diets for ruminants has been shown to help maintaining the ruminal pH above 6, which could enhance the microbial biohydrogenation of unsaturated dietary fatty acids. Moreover, yeasts improve the growth of Megasphera elsdenii, a bacteria which favors the trans-10 pathway of biohydrogenation. So the objective of this study was to investigate the effects of live yeasts (Saccharomyces cerevisiae) on the biohydrogenation in the rumen of dairy cows receiving a high concentrate diet without added fat. Three ruminally fistulated lactating dairy cows were given three diets based on corn silage (control, control plus 0.5g/d or control plus 5.0g/d of Saccharomyces cerevisiae NCYC SC47), according to a Latin square design. Ruminal contents were sampled and liquid and solid phases were separated with a 0.25mm metal sieve. Fatty acids profiles were obtained by gas chromatography. The two doses of yeast resulted in similar effects. Live yeast significantly decreased myristic and stearic acids proportions, and significantly increased oleic and linoleic acids proportions by 16 and 32% in the liquid and the solid phases, respectively. No significant effect was observed for other biohydrogenation intermediates, but the cis9,trans11-C18:2 tended (P = 0.154) to increase with the addition of yeasts, whereas trans10-C18:1 numerically decreased (P = 0.225). These results suggested that live yeasts affect microbial activity, lowering the extent of biohydrogenation without shifting toward the trans-10 isomers pathway

    In Vitro Versus in Situ Ruminal Biohydrogenation of Unsaturated Fatty Acids from a Raw or Extruded Mixture of Ground Canola Seed/Canola Meal

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    Raw or extruded blends of ground canola seeds and canola meal were used to compare in vitro and in situ lag times and rates of disappearance due to ruminal biohydrogenation of unsaturated fatty acids. The in situ study resulted in higher lag times for biohydrogenation for polyunsaturated fatty acids and lower rates of biohydrogenation of unsaturated fatty acids than the in vitro study, so the in situ biohydrogenation of polyunsaturated fatty acids was not complete at 24 h of incubation. With both methods, rates of biohydrogenation of polyunsaturated fatty acids were higher than for cis-9C18:1. Extrusion did not affect the rate of biohydrogenation of cis-9C18:1, but resulted in higher rates of biohydrogenation of polyunsaturated fatty acids with higher proportions of trans intermediates of biohydrogenation at 4 h of incubation in vitro and at 8 h of incubation in situ. These results suggest that extrusion affects the isomerization of polyunsaturated fatty acids, rather than the hydrogenation steps. In conclusion, in vitro and in situ methods can both show differences of ruminal metabolism of unsaturated fatty acids due to processing, but the methods provide very different estimates of the rates of disappearance due to biohydrogenation

    In situ ruminal biohydrogenation of fatty acids from extruded soybeans: effects of dietary adaptation and of mixing with lecithin or wheat straw

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    Kinetics and intermediates of biohydrogenation of fatty acids were investigated in situ using extruded soybeans, a blend of extruded soybeans and lecithin (99:1), or a blend of extruded soybeans plus wheat straw (66:34). Two dry dairy cows received successively a diet with added palmitic acid and a diet with added extruded soybeans, and assays were completed after a 3-week adaptation to each diet. Adaptation of the cows to dietary polyunsaturated fatty acids suppressed the lag time before the beginning of biohydrogenation. Adaptation of cows, and mixing straw with soybeans, increased the rate of biohydrogenation of C18:2 and C18:3, resulting in less C18:2 and C18:3, and more trans C18:1 and C18:0 in the in situ bags. Lecithin did not affect the kinetics of biohydrogenation or the profile of fatty acids in the in situ bags. Differences in the rate of biohydrogenation, and profile of residual fatty acids in the bags were observed between the two cows. Even with a mixture of soybeans and straw in cows receiving dietary polyunsaturated fatty acids, biohydrogenation was slower and resulted in higher proportions of trans-C18:1 than expected from results of literature in vivo. Resultsshow that the biohydrogenation in situ is slow, highly dependent on experimental conditions, and that the use of several cows, adapted to the test fat source before the assay is initiated, is necessary in order to obtain a reliable estimate of kinetics parameters

    In situ evaluation of the ruminal and intestinal degradability of extruded whole horsebeans

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