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Effect of protein-protected fat on ruminal and total nutrient digestibility of sheep diets.

Experiments were conducted to determine the effects of supplementing chopped ryegrass hay with 0, 5, 10, or 20% fat coated with ruminal bypass protein (Prolip on ruminal digestion by cows and nutrient digestibility by sheep. Ruminal disappearances of DM, ADF, and NDF were measured by the in sacco technique using a cannulated cow. Degradation of DM, ADF, and NDF was not affected by protected fat supplementation at the 5, 10, or 20% level during the first 16 h in the rumen. In addition, supplementation with Prolip did not influence in vitro fermentation characteristics such as pH and VFA patterns. A digestibility experiment with six mature sheep in a switch-back design showed no decrease in feed intake or other undesired effects between unsupplemented (basal) and Prolip-supplemented diets. Whatever the diet fed to sheep, fiber digestibility was similar; however, DM and nitrogen digestibilities were significantly higher relative to the basal diet when ryegrass hay was substituted at 20% (64.2 vs 59.0% and 74.1 vs 71.1%, respectively). Ether extract digestion was enhanced by increasing level of Prolip; the corresponding values were 48.0, 64.9, 74.6, and 84.6% at 0, 5, 10, or 20% Prolip. Likewise, Prolip supplementation at the 10 or 20% level augmented digestibility of energy (62.7 or 65.9 vs 59.2%). Nitrogen and energy retentions were improved due to the decreases in fecal and(or) urinary excretion(s).

Animal Feed↗

Effects of brown midrib 3 mutation in corn silage on productivity of dairy cows fed two concentrations of dietary neutral detergent fiber: 2. Chewing activities.

The effects of digestibility of corn silage neutral detergent fiber (NDF) and dietary NDF content on chewing activities were evaluated with eight multiparous high producing dairy cows in a duplicated 4 x 4 Latin square design with 21-d periods. Experimental diets contained corn silage from a brown midrib (bm3) hybrid or its isogenic normal control at two concentrations of dietary NDF (29 and 38%). The NDF digestibility estimated by 30-h in vitro fermentation was higher for bm3 corn silage by 9.4 units (55.9 vs. 46.5%). Feeding behavior of animals and ruminal pH were monitored continuously for 4 d in each period by a computerized data acquisition system. Ruminal digesta were evacuated twice per period to determine the ruminal NDF pool and its turnover rate. There was no effect of NDF digestibility on total chewing time either per day or per kilogram of NDF intake, or on ruminating time either per day or per kilogram of NDF intake. Although bm3 treatments increased the turnover rate of NDF in the rumen, they increased dry matter intake and had no effect on ruminal NDF pool size. Total chewing time and ruminating time per day were related positively to NDF intake and ruminal NDF pool size, but were not related to ruminal turnover rate of NDF. These results provide no evidence that enhanced NDF digestibility decreases the physical effectiveness of NDF of corn silage.

Animals↗

Enhanced intake and production of cows offered ensiled alfalfa with higher neutral detergent fiber digestibility.

The objective of this study was to determine the effect of forage fiber digestibility as part of a total mixed diet on intake and production of cows with intakes that were likely limited by rumen fill, using treatments that were not confounded by fiber source, concentrate, or ratio of forage to concentrate. Two alfalfa silages with similar NDF concentrations (40%) but different NDF digestibilities (40 vs. 45% after 24 h of in vitro fermentation) were harvested, mixed with concentrate to achieve diets containing 35% NDF, and offered to 12 multiparous cows (13 DIM) in a two-period balanced crossover design. Samples taken during silage feeding revealed that diets differed in both NDF digestibility (3 percentage units) and NDF content (1.8 percentage units), making interpretation of results difficult. Nonetheless, milk production (36.3 vs. 38.2 kg/d) and DMI (19.4 vs. 20.4 kg/d) were significantly higher with the higher NDF digestibility diet. Apparent in vivo DM and NDF digestibilities, total rumen VFA after feeding, and molar percentage of propionate were also higher with this diet. Equal NDF intake between diets suggested that higher DMI was due to the lower NDF content in the more digestible NDF diet. Higher NDF digestibility might also increase DMI; further experimentation is necessary with larger unconfounded differences in fiber digestibility at the time of feeding.

Animals↗

Effect of coating whole cottonseed on performance of lactating dairy cows.

Thirty-six lactating Jersey cows were used in a randomized block design to determine the effect of coating whole fuzzy cottonseed to improve handling characteristics on intake, milk yield, apparent digestibility of nutrients, and blood gossypol concentrations. Treatments included whole cottonseed at 15% of dietary dry matter either as whole cottonseed, whole cottonseed coated with 5% gelatinized corn starch, or whole cottonseed coated with 5% corn starch plus 10% maltodextrin sugar. Dry matter intake, milk yield, percentage of milk protein and lactose, and yield of milk components were not different among treatments; however, the percentage of milk fat was depressed when maltodextrin sugar was included in the coating. When in vitro fermentations of mixed ruminal microorganism were conducted, final pH was lower and concentrations of total fatty acids, propionate, and L-lactate were higher for whole cottonseed coated with starch and sugar compared with uncoated cottonseed. Nutrient intake was similar among treatments, but the apparent digestibility of acid and neutral detergent fiber was reduced when coated cottonseed were fed. Total plasma gossypol concentration was higher for the cottonseed coated with starch compared with cottonseed coated with starch and sugar, but the difference was not of biological significance. Results of this study indicate that coating whole cottonseed with starch does not alter its palatability or nutrient value for supporting milk yield, but a reduction in fiber digestibility was observed. Inclusion of 10% maltodextrin sugar in the coating altered ruminal fermentation and resulted in a depressed percentage of milk fat.

Animal Feed↗

Adaptation of rate of organic acid production of hindgut bacteria to chronic intake of galactooligosaccharide in the rat.

We studied the adaptational effect of galactooligosaccharide (GOS) on the concentration of organic acids in cecal content, fecal water content and organic acid production from GOS in cultures with the cecal inocula of rats fed GOS for 1, 2, 7 or 21 d. The fecal water content of rats fed GOS for 1 d was higher than that of the controls. The concentration of each organic acid in the cecal contents was affected by diet, not by the time of adaptation. In in vitro fermentation, lactic acid was produced by rapidly and remained in the cultures with homogenates of rats fed GOS for 1 d. Acetic acid in the cultures of the GOS-diet rats' cecal homogenates was produced more rapidly than that of the controls on days 2, 7 and 21 of adaptation. Propionic acid was produced more rapidly in the GOS homogenate cultures than in that of the controls on day 2. Butyric acid in the cultures from the GOS-fed rats was produced more rapidly than that of the controls on days 2 and 21. These results suggest that the time period of GOS feeding influenced the production rate of each organic acid, and the changes varied among acids.

Animals↗

[Features of lipid peroxidation in brain and liver tissues from aging rats under stress].

The lipid peroxidation (LPO) level between in the adult and old rats brain and liver was determined as to be essentially undiffering. Stress activated the LPO independence the age of animals and tissues investigated. The concentration changes of LPO products testify to it. In the adult rats under the stress capability of tissues to induction in vitro ferment and ascorbat-depending LPO, in comparison with the control, decreases, at old--does not change in the brain and considerably grows in the liver. Stress is accompanied by an oppression of Na, K-ATP-ase PM activity of hepatocytes, more expressed in the old animals.

Aging↗

Patulin production by Penicillium granulatum and inhibition of ruminal flora.

The maximum patulin production by Penicillium granulatum was obtained during the 16th day of culture at 26 degrees C (2.9 g/L) on liquid Czapek medium (+ 8 p. 1000 glucose), followed by 32 degrees C after 24 days and 20 degrees C after 32 days. At 26 degrees C patulin production was maximum before the greatest rate of sporulation when the pH of the medium was about 4. Toxin production was studied by anaerobic culture for 75 days and then the cultures were exposed to ambient air. P. granulatum did not produce its toxin under anaerobic conditions. An in vitro fermentation model with rumen liquor was used, and within 4 hr acetic acid production declined and dose-dependent protein synthesis was inhibited with 20, 100, and 300 microgram patulin/mL rumen liquid.

Animals↗

Jimson weed seed toxicity in cattle.

A subacute experiment was undertaken for 14 days. The results obtained from these studies suggest that: 1) unless a highly Jimson weed seed contaminated feed is ingested (greater than 0.09% of body weight) or force fed, death should be a rare consequence of Jimson weed seed contamination; 2) Jimson weed seed toxicity in cattle as a result of feed contamination appears a self-limiting problem (rumen atony and anorexia prevent further intoxication until the blood levels of alkaloids are reduced to allow normal ruminant intestinal function); 3) cattle may exhibit signs of atropine toxicity at contamination levels of 881 seed/kg of feed or higher; 4) rumen fluid from heifers fed diet containing 4,408 Jimson weed seed had the greatest VFA concentration change from day 0 to 7; 5) in vitro fermentation of diets resulted in no difference in IVDMD values, but VFA concentration values tended to increase with increased concentrations of Jimson weed seed in the diet.

Alkaloids↗

Microbial fermentation of rice straw: nutritive composition and in vitro digestibility of the fermentation products.

Rice straw was fermented with Cellulomonas sp. and Alcaligenes faecalis. Microbial cells and undigested residue, as well as chemically treated (NaOH or NH4OH) and untreated straws, were analyzed for nutrient composition and in vitro digestibility. In a typical fermentation, 75% of the rice straw substrate was digested, and 18.6% of the total substrate weight that disappeared was recovered as microbial protein. The microbial cell fraction was 37% protein and 5% crude fiber; the residue was 12% protein and 45% crude fiber. The microbial protein amino acid profile was similar to alfalfa, except for less cysteins. The microbial cells had more thiamine and less niacin than Torula yeast. In vitro digestibility of the microbial protein was 41.2 to 55%, that of cellulose was 52%.

Actinomycetales↗

Colonic fermentation capacity in vitro: development during weaning in breast-fed infants is slower for complex carbohydrates than for sugars.

Fresh feces from 27 healthy infants-12 breastfed (complete, exclusive breast-feeding), 7 in early weaning (partial, high breast-feeding), and 8 in late weaning (partial, low breast-feeding)-were cultured with simple and complex carbohydrates in vitro to test the hypothesis that colonic fermentation capacity for carbohydrates increases during weaning. Infants in all three groups were able to ferment sugars, with no significant differences in median total short-chain fatty acid (SCFA) concentrations (mmol/L): preweaning, 56.4(range: 0-77.6); early weaning 68.5(range: 57.9-98.8); late weaning, 61.3(range: 28.6-120.4) for glucose. Preweaned infants were less able to ferment oligosaccharides and complex carbohydrates than were weaned infants (P < 0.05). Ability to ferment raftilose was higher in early weaning; median total SCFA concentrations (mmol/L) were as follows: preweaning 31.0 (range: 3.6-48.9), early weaning 57.1 (range: 2.5-70.6), late weaning 68.6 (range: 22.0-113.4) (P < 0.05). Ability to ferment complex carbohydrates did not develop until late weaning; median total SCFA concentrations for guar gum (mmol/L) were as follows: preweaning 6.4 (range: 0.1-57.3), early weaning 18.4 (range: 0.0-40.5), late weaning 45.4 (range: 15.6-62.1) (P < 0.05, preweaning and early weaning compared with late weaning). Development of the ability to ferment complex carbohydrate was slow. Cultures of feces from preweaned infants produced eight times more SCFAs with glucose than with complex carbohydrates, at early weaning there was a threefold difference and by late weaning the difference was only 25%, but this was still only 42% of the SCFAs produced by cultures of adult feces. These data suggest that for the complex carbohydrates tested, colonic fermentation is likely to contribute only a small proportion of daily energy needs of weaning infants.

Breast Feeding↗

Screening for the effects of natural plant extracts at different pH on in vitro rumen microbial fermentation of a high-concentrate diet for beef cattle.

Six natural plant extracts and three secondary plant metabolites were tested at five doses (0, 0.3, 3, 30, and 300 mg/L) and two different pH (7.0 and 5.5) in a duplicate 9 x 5 x 2 factorial arrangement of treatments to determine their effects on in vitro microbial fermentation using ruminal fluid from heifers fed a high-concentrate finishing diet. Treatments were extracts of garlic (GAR), cinnamon (CIN), yucca (YUC), anise (ANI), oregano (ORE), and capsicum (CAP) and pure cinnamaldehyde (CDH), anethole (ATL), and eugenol (EUG). Each treatment was tested in triplicate and in two periods. Fifty milliliters of a 1:1 ruminal fluid-to-buffer solution were introduced into polypropylene tubes supplied with 0.5 g of DM of a 10:90 forage:concentrate diet (15.4% CP, 16.0% NDF; DM basis) and incubated for 24 h at 39 degrees C. Samples were collected for ammonia N and VFA concentrations. The decrease in pH from 7.0 to 5.5 resulted in lower (P < 0.05) total VFA, ammonia N, branched-chain VFA concentration, acetate proportion, and acetate:propionate, and in a higher (P < 0.05) propionate proportion. The interaction between pH and doses was significant for all measurements, except for ATL and CDH for butyrate, ATL and EUG for acetate:propionate ratio, and ORE for ammonia N concentration. The high dose of all plant extracts decreased (P < 0.05) total VFA concentrations. When pH was 7.0, ATL, GAR, CAP, and CDH decreased (P < 0.05) total VFA concentration, and ANI, ORE, CIN, CAP, and CDH increased (P < 0.05) the acetate:propionate. The CIN, GAR, CAP, CDH, ORE, and YUC decreased (P < 0.05), and EUG, ANI, and ATL increased (P < 0.05) ammonia N concentration. The effects of plant extracts on the fermentation profile when pH was 7.0 were not favorable for beef production. In contrast, when pH was 5.5, total VFA concentration did not change (ATL, ANI, ORE, and CIN) or increased (P < 0.05) (EUG, GAR, CAP, CDH, and YUC), and the acetate:propionate (ORE, GAR, CAP, CDH, and YUC) decreased (P < 0.05), which would be favorable for beef production. Ammonia N (ATL, ANI, CIN, GAR, CAP, and CDH) and branched-chain VFA (ATL, EUG, ANI, ORE, CAP, and CDH) concentrations also were decreased (P < 0.05), suggesting that deamination was inhibited. Results indicate that the effects of plant extracts on ruminal fermentation in beef cattle diets may differ depending on ruminal pH. When pH was 5.5, GAR, CAP, YUC, and CDH altered ruminal microbial fermentation in favor of propionate, which is more energetically efficient.

Ammonia↗

Effect of inoculation rate of selected strains of lactic acid bacteria on fermentation and in vitro digestibility of grass-legume forage.

Grass-legume forage was used to evaluate the effect of inoculation rate of selected strains of lactic acid bacteria on fermentation and in vitro digestibility during 57 d of ensiling. Chopped forage (DM = 28%) was ensiled in 4 to 6-kg quantities and treated as: 1) control, 10(3) epiphytic lactic acid bacteria; 2) 10(5) added lactic acid bacteria; and 3) 10(6) added lactic bacteria/g of wet forage. Samples were obtained for analyses on d 0, 1, 2, 3, 6, 10, 14, 29, and 57 of fermentation. Treated silages were observed to have: 1) greater quantities of lactic acid bacteria, 2) a greater proportion of homofermentative lactic acid bacteria, and 3) lactic acid bacteria with greater biological activity. Addition of each amount of lactic acid bacteria: 1) increased the rate of utilization of water-soluble carbohydrate and decline in pH, 2) limited the formation of NH3 N, and 3) increased the in vitro digestibility of DM and ADF. No differences were observed in the lactic acid content of the silages after 57 d of fermentation.

Ammonia↗

The impact of fermentation and in vitro digestion on the formation of angiotensin-I-converting enzyme inhibitory activity from pea and whey protein.

Pea and whey protein were fermented by Lactobacillus helveticus and Saccharomyces cerevisiae in monoculture and in combination at 28 and 37 degrees C in order to release angiotensin-I-converting enzyme (ACE) inhibitory peptides. The fermentation products were subjected to in vitro gastrointestinal digestion, and the digests of nonfermented samples served as controls. After fermentation, the ACE inhibitory activity (%) increased by 18 to 30% for all treatments, except for the fermentations of whey protein with Saccharomyces cerevisiae at 28 degrees C, where no significant change was observed. After digestion, however, both fermented and nonfermented samples reached maximum ACE inhibitory activity. The whey digests tended to have lower (50%) inhibitory concentrations (IC50; 0.14 to 0.07 mg/ml), hence, higher ACE inhibitory activity, than the pea digests (0.23 to 0.11 mg/ml). The nonfermented whey protein digest showed the highest ACE inhibitory activity of all. For pea protein, the nonfermented sample had the lowest IC50 value. These results suggest that in vitro gastrointestinal digestion was the predominant factor controlling the formation of ACE inhibitory activity, hence, indicating its importance in the bioavailability of ACE inhibitory peptides.

Angiotensin-Converting Enzyme Inhibitors↗

Effects of laidlomycin propionate and monensin on the in vitro mixed ruminal microorganism fermentation.

The objective of this study was to compare the effects of laidlomycin propionate and monensin on the in vitro fermentation of ground corn, Trypticase, or alfalfa hay by mixed ruminal microorganisms. Ruminal fluid was collected from two steers fed 9.27 kg DM of a high-concentrate (62.2% ground corn and 17.4% cottonseed hulls) diet per day and composited. In the first study, no ionophore was included in the diet; the diet in the second study contained 11.1 g of laidlomycin propionate per ton of feed. The animals were allowed an adjustment period of 14 d for each dietary treatment before samples were collected. When ruminal fluid from unadapted animals was used, both monensin and laidlomycin propionate decreased (P<.05) CH4 concentration and the acetate:propionate ratio with ground corn and alfalfa hay. Monensin reduced (P<.05) in vitro dry matter disappearance of alfalfa and increased (P<.05) final pH in the ground corn and alfalfa hay fermentations. Both laidlomycin propionate and monensin decreased (P<.05) concentrations of acetate, propionate, isobutyrate, isovalerate, CH4, and NH3 in Trypticase fermentations. When ruminal fluid from adapted animals was used, both ionophores still reduced the concentrations of most fermentation products. However, there was generally less inhibition compared with fermentations inoculated with unadapted mixed ruminal microorganisms. In the presence of 5 mM maltose, mixed ruminal bacteria produced high concentrations (10 to 11 mM) of lactate, and addition of both ionophores to these fermentations was effective in reducing (P<.05) lactate production. In conclusion, laidlomycin propionate alters the mixed ruminal microorganism fermentation in a manner similar to monensin, but, at the concentrations used in this study, monensin seemed to be a more potent inhibitor.

Animal Feed↗

Preventing in vitro lactate accumulation in ruminal fermentations by inoculation with Megasphaera elsdenii.

In vitro fermentations containing a mixed culture of ruminal bacteria (ruminal fluid from a hay-fed steer), buffer, and primarily rapidly degradable substrates (starch, glucose, cellulose, cellobiose, and trypticase) were inoculated with an overnight culture of Megasphaera elsdenii B159. Triplicate flasks were either uninoculated or inoculated to obtain a final concentration of 8.7 x 10(5) and 8.7 x 10(6) colony forming units of M. elsdenii per milliliter of culture fluid. Inoculation with M. elsdenii prevented an accumulation of lactic acid and excessive drop in pH. Lactate peaked at more than 40 mM in untreated cultures. In cultures inoculated with a low dose of M. elsdenii, lactate concentration peaked at approximately 25 mM at 5 h of fermentation but decreased rapidly to less than 5 mM by 7 h of fermentation. With the addition of the high dose of M. elsdenii, lactate was never greater than 2 mM (P < .05) throughout fermentation. Cultures treated with M. elsdenii had greater amounts (P < .05) of isobutyrate, butyrate, isovalerate, and valerate than untreated cultures. After 24 h of fermentation, one-half of the culture fluid was transferred to an equal volume of fresh buffer with substrate but was not inoculated with further quantities of M. elsdenii. Six hours after transfer, cultures that had been originally treated with M. elsdenii had lower (P < .05) amounts of lactate than untreated cultures. Inoculation with M. elsdenii has potential to prevent lactate accumulation in diets containing readily fermentable carbohydrates.

Animals↗

Estimation of the fermentability of dietary fibre in vitro: a European interlaboratory study.

Five European laboratories tested a simple in vitro batch system for dietary fibre fermentation studies. The inoculum was composed of fresh human faeces mixed with a carbonate-phosphate buffer complex supplemented with trace elements and urea. Five dietary fibre sources (cellulose, sugarbeet fibre, soyabean fibre, maize bran and pectin) were used by each laboratory on three occasions to determine pH, residual non-starch polysaccharides (NSP) and short-chain fatty acid production during fermentation. Cellulose and maize bran degradabilities were very low (7.2(SE 10.8) and 6.2 (SE 9.1)% respectively after 24 h), whereas pectin and soyabean fibre were highly degraded (97.4 (SE 4.4) and 91.1 (SE 3.4)% respectively after 24 h). Sugarbeet fibre exhibited an intermediate level of degradability (59.5 (SE 14.9)%). Short-chain fatty acid production was closely related to NSP degradation (r 0.99). Although each variable was ranked similarly by all laboratories, some differences occurred with respect to absolute values. However, the adaptation of donors to the experimental substrates was not an influential factor. Interlaboratory differences could be reduced either by adding less substrate during incubations or using less-diluted inocula. In vitro fermentations with inocula made from human faeces and from rat caecal contents gave similar results. There was a close correspondence between the data obtained in the present experiment and those previously published in in vivo studies in the rat using the same fibres. The in vitro batch system tested during the present study provides a rapid means of obtaining quantitative estimates of the fermentation and the estimation of the energy content of new sources of dietary fibre.

Animals↗

Taurocholic acid adsorption during non-starch polysaccharide fermentation: an in vitro study.

The association of radiolabelled taurocholic acid with the solid fraction of a faecal fermentation mixture was measured. A human faecal inoculum was incubated with [24-14C]taurocholic acid and several non-starch polysaccharide sources (pectin, wheat bran, ispaghula (Plantago ovata) husk and seed), glucose or a substrate-free control. Portions of fermentation mixture were taken at 0, 3, 6, 21 and 24 h and centrifuged to acquire a supernatant fraction and a pellet containing the fermentation residue. 14C was measured in supernatant fractions and pellets at all time points. Volatile fatty acids (VFA) were measured at 0 and 24 h to confirm bacterial growth. Radioactivity in the pellet increased over time for all substrates. Glucose resulted in the greatest incorporation of taurocholic acid into the pellet, followed by pectin. At 24 h the proportion of the total radioactivity found in the pellet was 92% for glucose, 79% for pectin, 60% for wheat bran, 59% for ispaghula seed, 53% for ispaghula husk and 26% for the control (mean of duplicates). Glucose and pectin produced the greatest quantity of VFA at 24 h. VFA production was highly correlated with radioactivity in the pellet (r0.976, P < 0.005). These results suggest that the bile acid binding capacity of a faecal culture mixture may be strongly influenced by the fermentability of the available substrate and hence related to bacterial metabolic activity.

Adsorption↗

Effect of various types of fermentation on in vitro protein and starch digestibility of differently processed pearl millet.

Pearl millet (Pennisetum typhoideum) grains were fermented with Lactobacilli and yeast alone, in combination and with natural flora at 30 degrees C for 48 h after giving various processing treatments viz, fine and coarse grinding, soaking, debranning, dry heat treatment, germination and autoclaving after adding of water. Fermentation was carried out with Lactobacillus acidophilus and Rhodotorula isolated from naturally fermented pearl millet and Lactobacillus acidophilus, Candida utilis and natural fermentation using freshly ground pearl millet flour as inoculum. All the processing treatments except coarse grinding improved the protein and starch digestibility. Autoclaving enhanced the digestibilities of processed samples which was further improved by different types of fermentation, the maximum being in case of germinated and naturally fermented pearl millet. A combination of Lactobacilli and yeast was more effective in increasing the protein as well as starch digestibility as compared to pure culture fermentation.

Fermentation↗