Effects of saponins, quercetin, eugenol, and cinnamaldehyde on fatty acid biohydrogenation of forage polyunsaturated fatty acids in dual-flow continuous culture fermenters

Four different plant secondary metabolites were screened for their effect on rumen biohydrogenation of forage long-chain fatty acids, using dual-flow continuous culture fermenters. Treatments were as follows: control (no additive), positive control (12 mg/L of monensin), and plant extracts (500 and 1,000 mg/L of triterpene saponin; 250 and 500 mg/L of quercetin; 250 mg/L of eugenol; 500 mg/L of cinnamaldehyde). Monensin increased propionate, decreased acetate and butyrate proportions, and inhibited the complete biohydrogenation of fatty acids resulting in the accumulation of intermediates of the biohydrogenation process (C18:2 trans-11, cis-15 rather than C18:1 trans-11). Cinnamaldehyde decreased total VFA concentration and proportions of odd and branched-chain fatty acids in total fat effluent. Apparent biohydrogenation of C18:2n-6 and C18:3n-3 was also less, and a shift from the major known biohydrogenation pathway to a secondary pathway of C18:2n-6 was observed, as evidenced by an accumulation of C18:1 trans-10 and trans-10, cis-12 CLA. Quercetin (500 mg/L) increased total VFA concentration, but no shifts in the pathways or extent of biohydrogenation were observed. Eugenol resulted in the accumulation of C18:1 trans-15 and C18:1 cis-15, end products of an alternative biohydrogenation pathway of C18:3n-3. Triterpene saponins did not affect the fermentation pattern, the biohydrogenation pathways, or the extent of biohydrogenation. At the doses tested in this study, we could only show a direct relation between changes in the rumen fatty acid metabolism and the presence of cinnamaldehyde but not for eugenol, quercetin, or triterpene saponins.     

Evaluation of rumen fatty acid hydrogenation intermediates and differences in bacterial communities after feeding wheat- or corn-based dried distillers grains to feedlot cattle

The effect of partially replacing rolled barley (86.6% of control diet) with 20% wheat dried distillers grains plus solubles (DDGS), 40% wheat DDGS, 20% corn DDGS, or 40% corn DDGS (dietary DM basis) on rumen fluid fatty acid (FA) composition and some rumen bacterial communities was evaluated using 100 steers (20 per treatment). Wheat DDGS increased the 11t- to 10t-18:1 ratio (P < 0.05) in rumen fluid and there was evidence that the conversion of trans-18:1 to 18:0 was reduced in the control and wheat DDGS diets but not in the corn DDGS diet. Bacterial community profiles obtained using denaturing gradient gel electrophoresis and evaluated by Pearson correlation similarity matrices were not consistent for diet and, therefore, these could not be linked to different specific rumen FA. This inconsistency may be related to the nature of diets fed (dominant effect of barley), limited change in dietary composition as the result of DDGS inclusion, large animal-to-animal variation, and possibly additional stress as a result of transport just before slaughter. Ruminal densities of a key fiber-digesting bacteria specie that produces 11t-18:1 from linoleic and linolenic acids (Butyrivibrio fibrisolvens), and a lactate producer originally thought responsible for production of 10t,12c-18:2 (Megasphaera elsdenii) were not influenced by diet (P > 0.05).     

Effect of linseed oil and fish oil alone or as an equal mixture on ruminal fatty acid metabolism in growing steers fed maize silage-based diets

Because of the potential benefits to human health, there is interest in increasing 18:3n-3, 20:5n-3, 22:6n-6, and cis-9,trans-11 CLA in ruminant foods. Four Aberdeen Angus steers (406 ± 8.2 kg of BW) fitted with ruminal and duodenal cannulas were used in a 4 × 4 Latin square experiment with 21-d periods to examine the potential of fish oil (FO) and linseed oil (LO) in the diet to increase ruminal outflow of trans-11 18:1 and total n-3 PUFA in growing cattle. Treatments consisted of a control diet (60:40; forage:concentrate ratio, on a DM basis, respectively) based on maize silage, or the same basal ration containing 30 g/kg of DM of FO, LO, or a mixture (1:1, wt/wt) of FO and LO (LFO). Diets were offered as total mixed rations and fed at a rate of 85 g of DM/(kg of BW(0.75)/d). Oils had no effect (P = 0.52) on DMI. Linseed oil had no effect (P > 0.05) on ruminal pH or VFA concentrations, whereas FO shifted rumen fermentation toward propionate at the expense of acetate. Compared with the control, LO increased (P < 0.05) 18:0, cis 18:1 (Δ9, 12-15), trans 18:1 (Δ4-9, 11-16), trans 18:2, geometric isomers of 9,11, 11,13, and 13,15 CLA, trans-8,cis-10 CLA, trans-10,trans-12 CLA, trans-12,trans-14 CLA, and 18:3n-3 flow at the duodenum. Inclusion of FO in the diet resulted in greater (P < 0.05) flows of cis-9 16:1, trans 16:1 (Δ6-13), cis 18:1 (Δ9, 11, and 13), trans 18:1 (Δ6-15), trans 18:2, 20:5n-3, 22:5n-3, and 22:6n-3, and decreased (P < 0.001) 18:0 at the duodenum relative to the control. For most fatty acids at the duodenum, responses to LFO were intermediate of FO and LO. However, LFO resulted in greater (P = 0.04) flows of total trans 18:1 than LO and increased (P < 0.01) trans-6 16:1 and trans-12 18:1 at the duodenum compared with FO or LO. Biohydrogenation of cis-9 18:1 and 18:2n-6 in the rumen was independent of treatment, but both FO and LO increased (P < 0.001) the extent of 18:3n-3 biohydrogenation compared with the control. Ruminal 18:3n-3 biohydrogenation was greater (P < 0.001) for LO and LFO than FO, whereas biohydrogenation of 20:5n-3 and 22:6n-3 in the rumen was marginally less (P = 0.05) for LFO than FO. In conclusion, LO and FO at 30 g/kg of DM altered the biohydrogenation of unsaturated fatty acids in the rumen, causing an increase in the flow of specific intermediates at the duodenum, but the potential of these oils fed alone or as a mixture to increase n-3 PUFA at the duodenum in cattle appears limited.     

酵母发酵饲料对瘤胃菌群数量及多样性的影响

本试验研究日粮中添加酵母发酵饲料对蒙古绵羊瘤胃菌群数量及多样性的影响.选用10只安装永久性瘤胃瘘管且体重约40 kg的14月龄蒙古羯羊,分为对照组和试验组,每组各5只.对照组饲喂基础日粮,试验组饲喂基础日粮+酵母发酵饲料(13.37％).预试期15 d,正试期5 d.于正试期晨饲后0、3、6、9、12 h依次采集瘤胃液...     

不同精粗比颗粒饲料对断奶公犊牛瘤胃发酵参数和微生物的影响

本试验旨在研究不同精粗比颗粒饲料对中国荷斯坦断奶公犊牛瘤胃微生物蛋白、发酵参数和微生物数量的影响。选用12头3月龄大的中国荷斯坦断奶公犊牛,按照日龄相近(103.92±1.5 d)、体重相似(121.25±4.12 kg)的原则随机分成4组,每组3头,分别饲喂精粗比为75∶25(Ⅰ)、70∶30(Ⅱ)、65∶35(Ⅲ)、60∶40(Ⅳ)的4种全价颗粒饲料。预试期14 d,正试期56 d。测定犊牛瘤胃微生物蛋白、发酵参数和微生物数量。结果表明,处理组Ⅳ的总挥发性脂肪酸和乙酸浓度最低,且显著低于处理组Ⅰ(P<0.05);处理组Ⅳ的丁酸浓度最高,且显著高于处理组Ⅰ、Ⅲ(P<0.05);处理组Ⅲ的乙酸/丙酸最大,且显著大于处理组Ⅳ(P<0.05)。处理组Ⅳ的白色瘤胃球菌、溶纤维丁酸弧菌和真菌的相对表达量最高,且显著高于其他各处理组(P<0.05);处理组Ⅲ的黄色瘤胃球菌的相对表达量最高,且显著高于其他各处理组(P<0.05)。综上所述,高精料全价颗粒饲料虽然能提高犊牛瘤胃总挥发性脂肪酸和乙酸的水平,但会抑制瘤胃纤维降解菌和厌氧真菌的生长。     

不同长链脂肪酸组合对体外瘤胃细菌发酵和群体结构的影响

本试验旨在研究不同长链脂肪酸组合对体外培养瘤胃细菌发酵和群体结构的影响。以3头瘤胃瘘管奶牛提供瘤胃液,对照(A)组底物含5%脂肪酸钙,试验组培养底物中硬脂酸、油酸、亚油酸和亚麻酸的含量分别为1.5%、1.0%、0.5%和1.5%(B组),1.5%、1.0%、1.5%和1.0%(C组),1.0%、1.5%、1.5%和0.5%(D组)以及1.5%、0.5%、0.5%和1.0%(E组)。在培养后0、3、6、12、18、24 h采集培养液,测定p H、氨氮浓度和瘤胃细菌含量。结果表明:1)培养液p H在组间的差异不显著(P0.05);C组的培养液氨氮浓度显著高于B、D组(P0.05)。2)除白色瘤胃球菌,其他菌属含量在组间存在显著差异(P0.05)。其中琥珀酸拟杆菌、生黄瘤胃球菌、蛋白溶解梭菌和嗜淀粉瘤胃杆菌含量在B组较高;C组溶纤维丁酸弧菌、埃氏巨球菌、降解淀粉瘤胃球菌以及瘤胃总细菌含量显著高于其他各组(P0.05)。培养液埃氏巨球菌含量最高,为优势菌。综合得出,脂肪酸组合对瘤胃总细菌和大部分细菌种属含量有显著影响,这与发酵模式有关。     

Effects of incremental amounts of fish oil on trans fatty acids and Butyrivibrio bacteria in continuous culture fermenters

Previous studies have shown that adding fish oil (FO) to ruminant animal diets increased vaccenic acid (VA; t11 C18:1) accumulation in the rumen. Therefore, the objective of this study was to evaluate the effect of dietary FO amounts on selected strains of rumen bacteria involved in biohydrogenation. A single‐flow continuous culture system consisting of four fermenters was used in a 4 × 4 Latin square design with four 9 days consecutive periods. Treatment diets were as follows: (i) control diet (53:47 forage to concentrate; CON), (ii) control plus FO at 0.5% (DM basis; FOL), (iii) control plus FO at 2% (DM basis; FOM) and (iv) control plus FO at 3.5% (DM basis; FOH). Fermenters were fed treatment diets three times daily at 120 g/day. Samples were collected from each fermenter on day 9 of each period at 1.5, 3 and 6 h post‐morning feeding and then composited into one sample per fermenter. Increasing dietary FO amounts resulted in a linear decrease in acetate and isobutyrate concentrations and a linear decrease in acetate‐to‐propionate ratio. Propionate, butyrate, valerate and isovalerate concentrations were not affected by FO supplementation. Concentrations of C18:0 in fermenters linearly decreased, while concentrations of t10 C18:1 and VA linearly increased as dietary FO amounts increased. The concentrations of c9t11 and t10c12 conjugated linoleic acid were not affected by FO supplementation. The DNA abundance for Butyrivibrio fibrisolvens, Butyrivibrio vaccenic acid subgroup, Butyrivibrio stearic acid subgroup and Butyrivibrio proteoclasticus linearly decreased as dietary FO amounts increased. In conclusion, FO effects on trans fatty acid accumulation in the rumen may be explained in part by FO influence on Butyrivibrio group.     

Effects of dietary concentrate level and chromium-methionine supplementation on ruminal fermentation,and ruminal bacterial and fatty acid composition in Tan lambs北大核心CSCD

This study evaluated the effects of dietary concentrate level and chromium methionine(Cr-Met)supplementation on ruminal fermentation and fatty acid composition, and ruminal bacteria abundance in Tan lambs. Forty male Tan lambs [(21.00±1.23) kg body weight, 5 months of age] were randomly assigned to four treatment groups with 10 lambs in each treatment. The treatments were: a low-concentrate (LC) diet (concentrate:forage, 35:65) without Cr-Met supplementation; a high-concentrate (HC) diet (concentrate:forage, 55:45) without Cr-Met supplementation; groups fed the HC diet with 0.75 or 1.50 g·d-1·lamb-1 Cr-Met (HCM and HCH, respectively). Ruminal fluid was collected on day 65 with an oral stomach tube about 3 h after the morning feed and samples used for fermentation analysis, fatty acid composition determination and bacterial DNA extraction. It was found that: 1) Ruminal pH, acetate proportion and acetate:propionate were greater (P<0.05) with the LC diet whereas microbial crude protein, propionate and valerate proportions were greater (P<0.05) with the HC diet. The acetate:propionate was greater (P<0.05) in the HCM group than in the HC group. 2) For the HC diet, the DNA abundances of Butyrivibrio fibrisolvens vaccenic acid subgroup (Butyrivibrio VA) and Ruminococcus flavefaciens were decreased (P<0.05), compared with the LC diet, whereas the DNA abundance of Anaerovibrio lipolytica was increased (P<0.05). For lambs fed the HC diet, DNA abundances of B. fibrisolvens stearic acid subgroup, Butyrivibrio VA, Butyrivibrio proteoclasticus, and A. lipolytica showed a linear decrease (P<0.05) with increasing Cr-Met supplementation level; However, the DNA abundance of R. flavefaciens showed a linear increase (P<0.05). 3) Compared with the LC group, the concentrations of t11 C18:1, trans C18:1, c9t11 CLA, t10c12 CLA, C18:2n6, and C18:3n3 were decreased by the HC diet without Cr-Met supplementation whereas the concentration of C18:0 was increased. There was a linear increase in t11 C18:1 and trans C18:1 with increasing Cr-Met supplementation level in lambs fed the HC diet. The results suggest that the HC diet inhibited the growth of ruminal bacteria involved in the ruminal biohydrogenation process, and the addition of Cr-Met had a potentially positive effect on conjugated linoleic acid (CLA) synthesis in body tissue. © 2022, Editorial Office of Acta Prataculturae Sinica. All rights reserved.     

Sainfoin (Onobrychis viciifolia) silage in dairy cow rations reduces ruminal biohydrogenation and increases transfer efficiencies of unsaturated fatty acids from feed to milk

The effects of replacing grass silage by sainfoin silage in a total mixed ration (TMR) based diet on fatty acid (FA) reticular inflow and milk FA profile of dairy cows was investigated. The experiment followed a crossover design with 2 dietary treatments. The control diet consisted of grass silage, corn silage, concentrate and linseed. In the sainfoin diet, half of the grass silage was replaced by a sainfoin silage. Six rumen cannulated lactating multiparous dairy cows with a metabolic body weight of 132.5 ± 3.6 kg BW^0.75, 214 ± 72 d in milk and an average milk production of 23.1 ± 2.8 kg/d were used in the experiment. Cows were paired based on parity and milk production. Within pairs, cows were randomly assigned to either the control diet or the sainfoin diet for 2 experimental periods (29 d per period). In each period, the first 21 d, cows were housed individually in tie-stalls for adaptation, then next 4 d cows were housed individually in climate-controlled respiration chambers to measure CH₄. During the last 4 d, cows were housed individually in tie stalls to measure milk FA profile and determine FA reticular inflow using the reticular sampling technique with Cr-ethylenediaminetetraacetic acid disodium salt dihydrate (EDTA) and Yb-acetate used as digesta flow markers. Although the dietary C18:3n-3 intake was lower (P = 0.025) in the sainfoin diet group, the mono-unsaturated FA reticular inflow was greater (P = 0.042) in cows fed the sainfoin diet. The reticular inflow of trans-9, trans-12-C18:2 and cis-12, trans-10 C18:2 was greater (P ≤ 0.024) in the sainfoin diet group. The cows fed sainfoin diet had a lower (P ≤ 0.038) apparent ruminal biohydrogenation of cis-9-C18:1 and C18:3n-3, compared to the cows fed the control diet. The sainfoin diet group had greater (P ≤ 0.018) C18:3n-3 and cis-9, cis-12-C18:2 proportions in the milk FA profile compared to the control diet group. Transfer efficiencies from feed to milk of C18:2, C18:3n-3 and unsaturated FA were greater (P ≤ 0.0179) for the sainfoin diet. Based on the results, it could be concluded that replacing grass silage by sainfoin silage in dairy cow rations reduces ruminal C18:3n-3 biohydrogenation and improves milk FA profile.     

The effect of dietary Chlorella vulgaris supplementation on micro‐organism community,enzyme activities and fatty acid profile in the rumen liquid of goats

Microalgae might be considered as an alternative source of fat and/or protein for ruminant's diets. However, changes in populations of ruminal micro‐organisms associated with biohydrogenation process, methane and ammonia production in response to microalgae dietary supplementation have not been well characterized. Thus, 16 cross‐bred goats were divided into two groups. Each goat of both groups was fed individually with alfalfa hay and concentrates separately. The concentrates of the control group had no microalgae while those of the treated group were supplemented with 10 g lyophilized Chlorella vulgaris/kg concentrate (chlor). On the 30th experimental day, samples of rumen fluid were collected for microbial DNA extraction, fatty acid profile and enzyme activity analyses. The results showed that the chlor diet compared with the control increased significantly the populations of Methanosphaera stadtmanae, Methanobrevibacter ruminantium and Methanogens bacteria and protozoa in the rumen of goats. A significant reduction in the cellulase activity and in the abundance of Ruminococcus albus, and a significant increase in the protease activity and in the abundance of Clostridium sticklandii in the rumen liquid of goats fed with the chlor diet, compared with the control, were found. Chlorella vulgaris supplementation promoted the formation of trans C_18:1, trans‐11 C_18:1 and monounsaturated fatty acids (MUFA), while the proportions of C_18:0 and long‐chain fatty acids (LCFA) reduced significantly in the rumen liquid of goats. This shift in ruminal biohydrogenation pathway was accompanied by a significant increase in Butyrivibrio fibrisolvens trans C_18:1‐producing bacteria. In conclusion, the supplementation of diets with microalgae needs further investigation because it enhances the populations of methane‐producing bacteria and protozoa.     

不同亚油酸水平培养基对溶纤维丁酸弧菌脂肪酸合成的影响

为探究亚油酸对反刍动物瘤胃中溶纤维丁酸弧菌脂肪酸合成的影响，试验用不同水平亚油酸培养基进行溶纤维丁酸弧菌体外厌氧培养试验，分光光度计测定菌液D_{600 nm}值达到1.0时，在培养基中添加亚油酸，使试验1组（对照）、2、3及4组培养基亚油的浓度分别为0、2.5、5.0及7.5 mg/100 mL，培养24 h后收集菌液检测35种脂肪酸含量。结果显示，细菌代谢相关的C8：0、C11：0、C14：0、C15：0、C17：0、C17：1、C18：1（n-9） C、C18：2（n-6） C、C18：3（n-6）、C20：0、C20：2、C20：3（n-3）、C20：3（n-6）、C20：5（n-3）、C21：0、C22：0、C22：2、C22：1（n-9）及C22：6（n-3）脂肪酸随着培养基中亚油酸浓度的提高无显著变化（P>0.05）；培养基中添加亚油酸使C10：0、C12：0、C16：0、C18：0、C20：4（n-6）、C23：0、C24：1合成量显著减少（P<0.05）；而C15：1及C18：3（n-3）合成量在2.5 mg/100 mL亚油酸组显著增加（P<0.05）；C14：1在对照组中合成量最高，在添加亚油酸的试验组中，随着亚油酸含量增加而增加；C24：0在7.5 mg/100 mL亚油酸组合成量最高。综上所述，亚油酸对于溶纤维丁酸弧菌合成脂肪酸有一定影响作用，可抑制C10：0、C12：0、C16：0、C18：0、C23：0、C14：1、C20：4（n-6）等脂肪酸的合成，C15：1、C16：1、C18：3（n-3）含量增加，但超过一定量时合成量会减少。     

Palm oil protects α-linolenic acid from rumen biohydrogenation and muscle oxidation in cashmere goat kids

Background: In ruminants, dietary C18:3 n-3 can be lost through biohydrogenation in the rumen; and C18:3 n-3 that by-passes the rumen still can be lost through oxidation in muscle, theoretically reducing the deposition of C18:3 n-3,the substrate for synthesis of poly-unsaturated fatty acids(n-3 LCPUFA) in muscle. In vitro studies have shown that rumen hydrogenation of C18:3 n-3 is reduced by supplementation with palm oil(rich in cis-9 C18:1). In addition, in hepatocytes, studies with neonatal rats have shown that cis-9 C18:1 inhibits the oxidation of C18:3 n-3. It therefore seems likely that palm oil could reduce both rumen biohydrogenation of C18:3 n-3 and muscle oxidation of C18:3 n-3. The present experiment tested whether the addition of palm oil to a linseed oil supplement for goat kids would prevent the losses of C18:3 n-3 and thus improve the FA composition in two muscles, Longissimus dorsi and Biceps femoris. To investigate the processes involved, we studied the rumen bacterial communities and measured the mRNA expression of genes related to lipid metabolism in Longissimus dorsi. Sixty 4-month-old castrated male Albas white cashmere kids were randomly allocated among three dietary treatments. All three diets contained the same ingredients in the same proportions, but differed in their fat additives: palm oil(PMO), linseed oil(LSO) or mixed oil(MIX; 2 parts linseed oil plus 1 part palm oil on a weight basis).Results: Compared with the LSO diet, the MIX diet decreased the relative abuandance of Pseudobutyrivibrio, a bacterial species that is positively related to the proportional loss rate of dietary C18:3 n-3 and that has been reported to generate the ATP required for biohydrogenation(reflecting a decrease in the abundance of rumen bacteria that hydrogenate C18:3 n-3 in MIX kids). In muscle, the MIX diet increased concentrations of C18:3 n-3, C20:5 n-3, C22:6 n-3,and n-3 LCPUFA, and thus decreased the n-6/n-3 ratio; decreased the mRNA expression of CPT1β(a gene associated with fatty acid oxidation) and increased the mRNA expression of FADS1 and FADS2(genes associated with n-3 LCPUFA synthesis), compared with the LSO diet. Interestingly, compared to Longissimus dorsi, Biceps femoris had greater concentrations of PUFA, greater ratios of unsaturated fatty acids/saturated fatty acids(U/S), and poly-unsaturated fatty acids/saturated fatty acids(P/S), but a lesser concentration of saturated fatty acids(SFA).Conclusions: In cashmere goat kids, a combination of linseed and palm oils in the diet increases the muscle concentration of n-3 LCPUFA, apparently by decreasing the relative abundance of rumen bacteria that are positively related to the proportional loss rate of dietary C18:3 n-3, by inhibiting m RNA expression of genes related to C18:3 n-3 oxidation in muscle, and by up-regulating m RNA expression of genes related to n-3 LCPUFA synthesis in muscle,especially in Longissimus dorsi.     

Concentrations of conjugated linoleic acid (cis-9, trans-11-octadecadienoic acid) are not increased in tissue lipids of cattle fed a high-concentrate diet supplemented with soybean oil

Conjugated linoleic acid (CLA), a mixture of isomers of linoleic acid, has many beneficial effects, including decreased tumor growth in animal cancer models. The cis-9, trans-11 isomer of CLA (CLA9,11) can be formed in the rumen as an intermediate in biohydrogenation of linoleic acid. Recent data, however, indicate that tissue desaturation of trans-fatty acids is an important source of CLA9,11 in milk. Our objective was to determine whether supplementing a high-corn diet with soybean oil (SBO; a source of linoleic acid) would increase concentrations of CLA in ruminal contents and tissue lipids. Four ruminally cannulated steers were utilized in a Latin square design with 28-d periods. A control diet (80% cracked corn, 2.0% corn steep liquor, 8.0% ground corn cobs, and 10% supplement [soybean meal, ground shelled corn, minerals, and vitamins]) was supplemented with 2.5, 5.0, or 7.5% (DM basis) SBO. Supplemental SBO did not affect ruminal pH or concentrations of the major VFA. The proportion and amount (mg FA/g DM ruminal contents) of CLA9,11 were not increased by increasing dietary SBO. However, the proportion and amount of the trans-10, cis-12 CLA isomer (CLA10,12) in ruminal contents increased linearly (P < 0.006) as dietary SBO increased. Trans-18:1 isomers in ruminal contents increased linearly (P < 0.02) as dietary SBO increased. The proportion of CLA10,12 was correlated positively (P < 0.001) with proportions of trans-C 18:1 isomers in ruminal contents. Conversely, CLA9,11 was correlated negatively (P < 0.05) with the proportions of trans-18:1 in ruminal contents. The same high-corn diet, supplemented with 0 or 5% SBO, was fed to 20 Angus-Wagyu heifers for 102 d in a randomized complete block design to determine the effect of added SBO on tissue deposition of CLA. Supplemental SBO did not affect feed intake, gain:feed, or carcass quality. Tissue samples were obtained from the hindquarter, loin, forequarter, liver, large and small intestine, and subcutaneous, mesenteric, and perirenal adipose depots. The concentration of CLA9,11 was greatest in subcutaneous adipose tissue but was not affected in any tissue by SBO. Supplementing high-corn diets with SBO does not increase CLA9,11 concentrations in tissues of fattening heifers. Research is needed to identify regulatory factors for pathways of biohydrogenation that lead to increased concentrations of CLA10,12 in ruminal contents when high-oil, high-concentrate diets are fed.     

DAP-decarboxylase activity and lysine production by rumen bacteria.

The last step of pathway of lysine biosynthesis by rumen bacteria was tested. The first measurements of DAP-decarboxylase activity and of lysine production by Megasphera elsdenii, Selenomonas ruminantium, Clostridium spp., Butyrivibrio fibrisolvens and Bacteroides succinogenes as well as the first attempts to increase the lysine production by ruminal streptococci by mutation are described. The highest values were measured in Selenomonas ruminantium (DAP-decarboxylase activity = 146 micrograms DAP.min-1.mg-1 protein and lysine production was 390 micrograms.mg-1 protein) and the lowest values were ascertained in Butyrivibrio fibrisolvens (DAP-decarboxylase activity = 27 micrograms DAP.min-1.mg-1 protein and lysine production was 32 micrograms.mg-1 protein). DAP-decarboxylase activity was increased by mutation especially in Streptococcus bovis, the lysine production in both of tested ruminal streptococci. The potential use of lysine-excreting mutants in calves in future is suggested.     

Comparison of alternative beef production systems based on forage finishing or grain-forage diets with or without growth promotants: 2. Meat quality, fatty acid composition, and overall palatability

Five beef cattle management regimens were evaluated for their effect on meat quality, fatty acid composition, and overall palatability of the longis-simus dorsi (LD) muscle in Angus cross steers. A 98-d growing phase was conducted using grass silage with or without supplementation of growth promotants (Revalor G and Rumensin) or soybean meal. Dietary treatments in the finishing phase were developed with or without supplementation of growth promotants based on exclusive feeding of forages with no grain supplementation, or the feeding of grain:forage (70:30) diets. Growth promotants increased (P < 0.01) shear force and tended (P = 0.06) to increase toughness of the LD muscle due to limited postmortem proteolytic activity (lower myofibrillar fragmentation index value; P = 0.02). Grain feeding increased DM and intramuscular fat content (P = 0.03 and P = 0.05, respectively) in the LD but decreased the sensory panel tenderness score (P = 0.01). Growth promotants increased (P 相似文献   

埃氏巨型球菌及其乙酸生成关键酶基因缺失工程菌体外代谢特性的初步研究

埃氏巨型球菌是奶牛瘤胃中的一种优势菌。本研究运用瘤胃微生态理论,结合埃氏巨型球菌能利用乳酸发酵产生丙酸的特点,初步研究埃氏巨型球菌(H6)及其乙酸生成关键酶基因缺失工程菌(TnH6)体外发酵特性。经健康羊瘤胃液体外连续培养结果表明,埃氏巨型球菌及其乙酸生成关键酶基因缺失工程菌均能利用乳酸生成VFA,发酵生成的VFA以丙酸为主,发酵类型倾向于丙酸型,但工程菌生成乙酸的能力明显降低,尽管丙酸生成能力有所下降,但显著降低了乙酸与丙酸的比例,从而为调控瘤胃乳酸发酵和利用H6、TnH6防治奶牛亚临床性瘤胃乳酸酸中毒提供了理论和试验基础。     

The biohydrogenation of linoleamide in vitro and its effects on linoleic acid concentration in duodenal contents of sheep

Previous studies showed that oleamide was protected from ruminal biohydrogenation and increased 18:1(n-9) concentration in milk when fed to lactating dairy cows. To appraise whether this protection extended to linoleamide, a rumen in vitro experiment was conducted to determine biohydrogenation of linoleamide followed by two sheep experiments to evaluate whether linoleamide could increase 18:2 (n-6) concentration in duodenal contents. Treatments for the in vitro and sheep studies consisted of three diets containing no added lipid (control), linoleic acid, or linoleamide. Lipids were added at 10% (DM basis) of the in vitro substrate (ground grass hay). The three substrates were incubated with mixed ruminal microbes in triplicate, and 5 mL of culture contents was taken at 0, 24, and 48 h for analysis of 18:2 (n-6) concentration by gas chromatography. The concentrations of 18:2 (n-6) (corrected for 18:2 (n-6) in the control cultures) at 0, 24, and 48 h were 2.51, 0.38, and 0.11 mg/5 mL for the linoleic acid cultures compared to 2.10, 1.35, and 1.08 mg/5 mL for the linoleamide cultures. Compared to linoleic acid, the cultures containing linoleamide had higher 18:1 (n-9) and lower concentrations of biohydrogenation products including trans-18:1 and 18:0. Three sheep with duodenal cannulas were fed the three diets in two separate 3 x 3 Latin squares each with 2-wk periods. The two squares only differed in the amount of added lipid (1.5 vs 5% of the ration DM). When the lipids were added at 1.5% of the ration DM, they had little effect on duodenal 18:2 (n-6) concentration (2.8, 3.6, and 4.3 mg/g DM for the control, linoleic acid, and linoleamide treatments, respectively). At 5% of the ration DM, both lipid supplements increased duodenal 18:2 (n-6) concentration over the control diet with a greater response observed for linoleamide (2.5, 12.2, and 16.8 mg/g DM for the control, linoleic acid, and linoleamide treatments, respectively). This study demonstrates reduced biohydrogenation of linoleamide based on its ability to maintain a higher concentration of 18:2 (n-6) in ruminal cultures and in duodenal contents of sheep compared to free linoleic acid.     

Effect of feeding high-temperature, microtime-treated diets with different lipid sources on conjugated linoleic acid formation in finishing Hanwoo steers

The present study was conducted to examine the effects of different plant oils or plant oil mixtures and high-temperature, microtime processing (HTMT) on the CLA content in Hanwoo steers. Experiment 1, consisting of 3 in vitro trials, was conducted to determine how the biohydrogenation of C18 fatty acids and CLA production were affected by fat sources (tallow, soybean oil, linseed oil, or mixtures of soybean oil and linseed oil) or HTMT treatment in the rumen fluid. The results showed that HTMT was capable of protecting unsaturated fatty acids from biohydrogenation by ruminal bacteria. The HTMT-treated diet containing 4% linseed oil (LU) and a supplement containing 2% linseed oil and 1% soybean oil treated with HTMT + 1% soybean oil (L(2)S(1)U+S(1)) produced an increased quantity of trans-11 C18:1 and cis-9, trans-11 CLA, and a reduced quantity of trans-10, cis-12 CLA. Based on these results, in vivo studies (Exp. 2) were conducted with LU and L(2)S(1)U+S(1). These 2 treatments increased the content of cis-9, trans-11 CLA in LM compared with the control diet. The content of trans-10, cis-12 CLA in subcutaneous fat was also increased in the L(2)S(1)U+S(1) treatment compared with other treatments. The subcutaneous fat thickness in the LU treatment was decreased compared with the L(2)S(1)U+S(1) treatment. The LU treatment significantly decreased fatty acid synthase expression but simultaneously increased leptin expression. In this report, we showed that diets containing LU and L(2)S(1)U+S(1) were capable of increasing CLA in the intramuscular fat of beef.     

Effects of induced subacute ruminal acidosis on milk fat content and milk fatty acid profile

Two lactating dairy cows fitted with a rumen cannula received successively diets containing 0%, 20%, 34% and again 0% of wheat on a dry matter basis. After 5, 10 and 11 days, ruminal pH was measured between 8:00 and 16:00 hours, and milk was analysed for fat content and fatty acid profile. Diets with 20% and 34% wheat induced a marginal and a severe subacute ruminal acidosis respectively. After 11 days, diets with wheat strongly reduced the milk yield and milk fat content, increased the proportions of C8:0 to C13:0 even- or odd-chain fatty acids, C18:2 n-6 and C18:3 n-3 fatty acids but decreased the proportions of C18:0 and cis-9 C18:1 fatty acids. Wheat also increased the proportions of trans-5 to trans-10 C18:1, the latter exhibiting a 10-fold increase with 34% of wheat compared with value during the initial 0% wheat period. There was also an increase of trans-10, cis-12 C18:2 fatty acid and a decrease of trans-11 to trans-16 C18:1 fatty acids. The evolution during adaptation or after return to a 0% wheat diet was rapid for pH but much slower for the fatty acid profile. The mean ruminal pH was closely related to milk fat content, the proportion of odd-chain fatty acids (linear relationship) and the ratio of trans-10 C18:1/trans-11 C18:1 (nonlinear relationship). Such changes in fatty acid profile suggested a possible use for non-invasive diagnosis of subacute ruminal acidosis.