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1.
弓剑 《饲料研究》2012,(10):19-21
反刍动物乳肉产品是人类摄取共轭亚油酸(CLA)的主要来源,但反刍动物乳肉产品中CLA的含量较低,CLA及CLA在乳腺和脂肪组织中的合成前体十八碳单烯酸是不饱和脂肪酸瘤胃生物氢化的中间产物,深入了解不饱和脂肪酸的瘤胃生物氢化过程和代谢途径有助于通过瘤胃调控有针对性地提高反刍动物肉奶产品中CLA的含量.综述不同瘤胃微生物对脂肪酸的生物氢化作用及主要的不饱和脂肪酸在生物氢化过程中的中间代谢产物,为进一步调控反刍动物乳肉脂肪酸组成提供依据.  相似文献   

2.
瘤胃脂肪酸代谢研究进展   总被引:4,自引:0,他引:4  
本文综述了瘤胃微生物对脂肪酸的代谢机理,重点讨论了不饱和脂肪酸的氢化、共轭脂肪酸的形成、微生物脂类的合成以及影响不饱和脂肪酸生物氢化的因素。  相似文献   

3.
脂肪酸的生成与瘤胃发酵参数、生物氢化以及瘤胃微生物等因素密切相关。植物多酚可以调节反刍动物生产性能,提高氮的利用率,调节脂肪酸氢化,影响瘤胃微生物活性及数量。文章综述了植物多酚对反刍动物瘤胃脂肪酸氢化及微生物组成影响的研究进展,为植物多酚在对反刍动物瘤胃脂肪酸氢化及微生物组成影响的研究及应用提供参考。  相似文献   

4.
脂肪酸是反刍动物重要的营养物质。一方面,脂肪酸对于反刍动物瘤胃微生物生长具有抑制作用,尤其是不饱和脂肪酸的抑制作用更明显;另一方面,瘤胃微生物群落能够通过生物氢化作用将不饱和脂肪酸氢化为饱和脂肪酸。本文针对饲粮脂肪酸与瘤胃微生物之间的相互作用进行了综述,涉及的研究方法包括体外培养法以及动物试验研究,结合分子生物学技术方法,为通过饲粮脂肪调控瘤胃微生物群落或结构提供新思路。  相似文献   

5.
偶数链和支链脂肪酸在动物产品中的沉积很大程度上依赖于微生物对脂肪酸的作用.而反刍动物瘤胃营养的特殊性决定了日粮脂肪在摄入后不久便在微生物脂解酶的作用下迅速水解释放出游离脂肪酸,瘤胃微生物利用饲料发酵过程产生的氢将不饱和脂肪酸进行生物氢化,生成饱和脂肪酸,直接影响了动物产品中脂肪酸(特别是不饱和脂肪酸)的含量.  相似文献   

6.
瘤胃挥发性脂肪酸的作用及影响因素   总被引:7,自引:0,他引:7  
瘤胃挥发性脂肪酸与反刍动物瘤胃营养以及瘤胃微生物有着密切的关系。反刍动物瘤胃对养分的消化吸收以及微生物动力学可产生大量的挥发性脂肪酸,其主要作用为供能和维持瘤胃环境。本文综述了瘤胃挥发性脂肪酸(VFA)的作用、影响其产生和组成的因素以及其对反刍动物的影响。  相似文献   

7.
奶牛瘤胃脂肪酸代谢研究进展   总被引:1,自引:0,他引:1  
本文综述了脂肪酸在奶牛瘤胃和小肠内的消化代谢机理,重点讨论了不饱和脂肪酸在瘤胃的脂解、氢化、微生物脂类的合成及影响因素。  相似文献   

8.
反刍动物肌肉脂肪酸营养调控研究进展   总被引:1,自引:0,他引:1  
文章在概述脂肪酸及其营养功能的基础上,讨论了脂肪酸在反刍动物体内的合成与代谢,包括脂肪酸在瘤胃的水解和氢化、在细胞内的脱氢反应及其脂肪酸在瘤胃的合成等,并从饲养方式的改变、添加脂肪等角度讨论了肌肉脂肪酸的营养调控等问题,试图为调控反刍动物肌肉脂肪酸的组成提供理论依据。  相似文献   

9.
作者综述了2009年在ADSA-ASAS大会和CNKI、PubMed等数据库中外源添加剂(离子载体、酶制剂、植物提取物、饲用微生物)对瘤胃发酵调控的相关文献39篇。离子载体如莫能菌素主要通过促进瘤胃丙酸的产生,抑制生物氢化菌,促进长链脂肪酸在瘤胃内发生不完全氢化等瘤胃调控作用,从而缓解反刍动物的能量负平衡,减少甲烷排放,降低乳中脂肪含量。酶制剂(包括纤溶酶和淀粉酶等)在饲喂前加入日粮中能够免受瘤胃蛋白酶的降解,并保持酶活性,促进饲料的消化。植物提取物中皂角甙通过抑制原虫生长降低甲烷的排放,动物长期采食富含单宁的植物可产生单宁耐受菌,并且单宁的植物提取物可影响瘤胃的生物氢化作用,植物精油对瘤胃的调控作用包括减少淀粉和蛋白的降解,以及通过对某种瘤胃微生物的选择性作用抑制氨氮的降解。饲用微生物(主要有酵母菌、乳酸菌、芽孢杆菌等)能增加营养物质消化率,改变瘤胃发酵模式,增加瘤胃微生物菌群,但其益生效果与泌乳阶段、日粮类型、环境条件有关。  相似文献   

10.
反刍动物肌内脂肪及脂肪酸调控研究进展   总被引:1,自引:0,他引:1  
脂肪作为食物中必不可少的养分,它不仅可以提供能量,还可以提供必需脂肪酸。脂肪的硬度、贮存稳定性受肌内脂肪及脂肪酸组成等影响,进而影响脂肪的营养价值、风味以及食用品质,而脂肪酸组成受动物种类、品种、性别和日粮等因素影响。反刍动物由于瘤胃氢化作用导致其脂肪酸饱和程度和异构程度高于单胃动物,从而使其肌内脂肪以及脂肪酸组成不同,导致其肉品质以及风味都不同。本文旨在综述反刍动物肌内脂肪及其脂肪酸构成调控的研究进展。  相似文献   

11.
An experiment was conducted to study disappearance of C14 to C18 fatty acids, lag times and biohydrogenation (BH) rates of C18 fatty acids of ground soya bean and canola seeds in situ. Three ruminally fistulated Dallagh sheep were used to determine ruminal BH of unsaturated fatty acids (UFAs). Differences in the disappearance of fatty acids through the bags and lag times were observed between the oilseeds. We saw that the longer the incubation time of the oilseeds in the rumen, the lower the content of C18:2 and C18:3. Significantly higher lag times for both C18:2 and C18:3 were observed in ground canola compared to ground soya bean. BH rates of C18:2 and C18:3 fatty acids in soya bean were three times higher than those of canola. These results suggest that the fatty acid profile of fat source can affect the BH of UFAs by rumen micro‐organisms. So that UFAs of canola had higher ability to escape from ruminal BH. It seems that fatty acid profile of ruminant products is more affected by canola seed compared to soya bean seed.  相似文献   

12.
Four ruminally and duodenally cannulated Hampshire wethers were used in a 4 x 4 Latin square experiment to determine whether linoleoyl methionine and calcium linoleate would increase duodenal flow of unsaturated fatty acids (C18:2 + cis C18:1). All animals received the same basal diet plus a treatment enclosed in gelatin capsules that were placed directly in the rumen. Of the four experimental treatments, one was a control (empty capsules) and three were 5 g of fatty acid equivalent as either free linoleic acid, calcium linoleate, or linoleoyl methionine. Linoleoyl methionine had the lowest ruminal disappearance of C18:2 + cis C18:1. Ruminal loss of unsaturated fatty acids from each supplement exclusive of feed unsaturated fatty acids was 69.8, 92.9, and 94.6% for linoleoyl methionine, free linoleic acid, and calcium linoleate, respectively. Duodenal flow of methionine also was higher for linoleoyl methionine than for control, free linoleic acid, or calcium linoleate (2.5, 1.7, 2.0, and 2.5 g/d, respectively). Plasma linoleic acid was higher for linoleoyl methionine than for control or free linoleic acid but was not different from calcium linoleate (22.0, 17.8, 18.9, and 20.2% of total fatty acids, respectively). Plasma methionine levels were not different among treatments. Intestinal disappearance of unsaturated fatty acids did not differ among treatments. Linoleoyl methionine resisted ruminal biohydrogenation and was digested normally in the intestine. Calcium linoleate did not escape biohydrogenation by ruminal bacteria.  相似文献   

13.
Recent advances in chromatographic identification of CLA isomers, combined with interest in their possible properties in promoting human health (e.g., cancer prevention, decreased atherosclerosis, improved immune response) and animal performance (e.g., body composition, regulation of milk fat synthesis, milk production), has renewed interest in biohydrogenation and its regulation in the rumen. Conventional pathways of biohydrogenation traditionally ignored minor fatty acid intermediates, which led to the persistence of oversimplified pathways over the decades. Recent work is now being directed toward accounting for all possible trans-18:1 and CLA products formed, including the discovery of novel bioactive intermediates. Modern microbial genetics and molecular phylogenetic techniques for identifying and classifying microorganisms by their small-subunit rRNA gene sequences have advanced knowledge of the role and contribution of specific microbial species in the process of biohydrogenation. With new insights into the pathways of biohydrogenation now available, several attempts have been made at modeling the pathway to predict ruminal flows of unsaturated fatty acids and biohydrogenation intermediates across a range of ruminal conditions. After a brief historical account of major past accomplishments documenting biohydrogenation, this review summarizes recent advances in 4 major areas of biohydrogenation: the microorganisms involved, identification of intermediates, the biochemistry of key enzymes, and the development and testing of mathematical models to predict biohydrogenation outcomes.  相似文献   

14.
Our objectives were to evaluate ruminal fermentation patterns, apparent ruminal biohydrogenation, and site and extent of nutrient disappearance in cattle fed supplemental cracked safflower seeds differing in 18 C fatty acid profile. Nine Angus x Gelbvieh heifers (641 +/- 9.6 kg) fitted with ruminal and duodenal cannulas were used in a triplicated 3 x 3 Latin square. Cattle were fed (OM basis) 9.1 kg of bromegrass hay and either 1) 1.8 kg of corn and 0.20 kg of soybean meal (Control); 2) 0.13 kg of soybean meal and 1.5 kg of cracked high-linoleate (67.2% 18:2) safflower seeds (Linoleate); or 3) 1.5 kg of cracked high-oleate (72.7% 18:1) safflower seeds (Oleate). Safflower seed supplements were formulated to provide similar quantities of N and TDN and 5% dietary fat. Single degree of freedom orthogonal contrasts (Control vs. Linoleate and Oleate; Linoleate vs. Oleate) were used to evaluate treatment effects. True ruminal OM and ruminal NDF disappearances (percentage of intake) were greater (P < or =0.02) for Control than Linoleate and Oleate. True ruminal N degradability (% of intake) was not different (P = 0.38) among treatments. Apparent ruminal biohydrogenation of dietary 18:2 was greatest (Linoleate vs. Oleate, P < 0.001) for Linoleate, whereas biohydrogenation of dietary 18:1 was greatest (Linoleate vs. Oleate, P = 0.02) for Oleate. Duodenal flow of 18:0 was least (P < 0.001) for Control but did not differ (P = 0.92) between Oleate and Linoleate. Total flow of unsaturated fatty acid to the duodenum was greatest (P < 0.001) in cattle fed safflower seeds, and was greater with Linoleate (P < 0.001) than with Oleate. Duodenal flow of 18:1 and 18:2 increased (P < 0.001) in Oleate and Linoleate, respectively. Duodenal flow of 18:1trans-11 was greater (P < 0.001) in cattle fed safflower seeds and in Linoleate than in Oleate. Postruminal disappearance of saturated fatty acids was greatest (P < 0.001) for Control; however, postruminal disappearance of total unsaturated fatty acids was greater (P = 0.002) for Linoleate vs. Oleate. Supplemental high-linoleate or high-oleate safflower seeds to cattle fed forage-based diets may negatively affect ruminal OM and fiber disappearance but not N disappearance. Provision of supplemental fat in the form of safflower seeds that are high in linoleic acid increased intestinal supply and postruminal disappearance of unsaturated fatty acids, indicating that the fatty acids apparently available for metabolism are affected by dietary fat source.  相似文献   

15.
Dietary supplementation of stearidonic acid (SDA; 18:4n-3) has been considered a possible strategy to increase n-3 unsaturated fatty acid content in ruminant products; however, little is known about its metabolism in the rumen. In vitro batch incubations were carried out with bovine ruminal digesta to investigate the metabolism of SDA and its biohydrogenation products. Incubation mixtures (4.5 mL) that contained 0 (control), 0.25, 0.50, 0.75, 1.00, 1.25, or 1.50 mg of SDA supplemented to 33 mg (DM basis) of commercial total mixed ration based on corn silage, for dairy cows, were incubated for 72 h at 39°C. The content of most fatty acids in whole freeze-dried cultures was affected by SDA supplementation. Branched-chain fatty acids decreased linearly (P < 0.01), and odd-chain fatty acids decreased quadratically (P < 0.01), particularly from 1.00 mg of SDA and above, whereas most C18 fatty acids increased linearly or quadratically (P ≤ 0.04). Stearidonic acid concentrations at 72 h of incubation were very small (<0.6% of total fatty acids and ≤0.9% of added SDA) in all treatments. The apparent biohydrogenation of SDA was extensive, but it was not affected by SDA concentration (P > 0.05). Biohydrogenation followed a pattern similar to that of other C18 unsaturated fatty acids up to 1.00 mg of SDA. Stearic acid (18:0) and vaccenic acid (18:1 trans-11) were the major fatty acids formed, with the latter increasing 9-fold in the 1.00 mg of SDA treatment. At greater inclusion rates, 18:0 and 18:1 trans isomers decreased (P ≤ 0.03), accompanied by increases in unidentified 18:3 and 18:4 isomers (P = 0.02), suggesting that the biohydrogenation pathway was inhibited. The present results clearly indicate that SDA was metabolized extensively, with numerous 18:4 and 18:3 products formed en route to further conversion to 18:2, 18:1 isomers, and 18:0.  相似文献   

16.
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.  相似文献   

17.
Five nonlactating Holstein cows (average weight 574 kg) with cannulas in the rumen and duodenum were fed five total mixed diets at 2.14% (DM) of BW for seven 2-wk periods to estimate the ruminal degradation of protein and fatty acids in whole cottonseed (WCS) and extruded soybeans (ESB). Lanthanum was used as an indigestible marker. Ruminal propionic acid (molar proportion) was larger and butyric acid was smaller for WCS diets than for control or ESB diets. Total VFA (mM) and acetic acid (molar proportion) were similar for all diets. Duodenal flow of nonammonia nitrogen (N) was 13% higher for ESB diets than for WCS diets, but was similar for the control and diets with WCS. The percentage of intake protein that was undegraded was 19% higher for ESB diets than for WCS diets. Ruminal and total apparent digestibilities of ADF were not reduced by the addition of oil seed. In conclusion, the protein from ESB was less degraded in the rumen of cows than protein from WCS. The addition of ESB at 12.7% (DM) or WCS at 25.3% of the diet did not reduce the apparent digestibility of fiber. The unsaturated fatty acids in WCS were not protected from ruminal biohydrogenation, presumably due to mastication of the seed coat.  相似文献   

18.
Three Holstein heifers and one nonlactating cow, fitted with ruminal and duodenal cannulas, were arranged in a 4 x 4 Latin square design to determine the effects of degree of fat saturation on ruminal neutral detergent fiber digestion and microbial protein synthesis and to determine whether changes in the efficiency of microbial protein synthesis were related to protozoal populations in the rumen. Corn silage-based diets contained no added fat or 4.85% of diet dry matter as partially hydrogenated tallow, tallow, or animal-vegetable fat. Iodine values of fat sources were 12.8, 50.6, and 109.7 for partially hydrogenated tallow, tallow, and animal-vegetable fat, respectively. Cattle were fed every 2 h and consumed 1.5% of body weight as dry matter daily. Ruminal neutral detergent fiber digestibility was decreased by added fat but was not affected by increasing iodine value. Flows of microbial N and non-NH3-nonmicrobial N to the duodenum were not affected by treatment. Ruminal protozoa concentration decreased linearly as the iodine value of fats increased. The efficiency of microbial protein synthesis was increased and protozoa concentrations tended to decrease when fat was fed. Decreased ruminal protozoa concentration may have decreased intraruminal N recycling. Biohydrogenation of added fat may result in a low ruminal concentration of unsaturated fatty acids when cows are fed frequently, reducing the negative effects of unsaturated fat sources on ruminal neutral detergent fiber digestibility. Protozoa were inhibited by unsaturated fat, but it is not clear if biohydrogenation and frequent feeding lessened inhibition.  相似文献   

19.
脂肪是牛奶中受日粮影响最大的成分。奶牛饲喂高精料日粮或高不饱和油脂均在一定程度上导致乳脂降低综合症的发生,进而影响牛奶加工产品。截至目前,乳脂降低症的主要生物学机制是乳脂合成底物不足以及瘤胃氢化时产生的反式脂肪酸或其它特殊脂肪酸产物抑制了乳腺脂肪酸合成途径所致。作者仅就后者生物氢化理论的研究进展进行综述,力图为相关科技工作者提供一定的参考。  相似文献   

20.
In vitro anaerobic incubations were used to determine the effect of different oils (LO-linseed, SO-sunflower, FO-fish oil) on trans fatty acid production in rumen fluid and to test if combining of monensin (MON) with the oils affects the interactions on trans fatty acid concentrations in mixed cultures of ruminal microorganisms. Two different sources of rumen fluid were used; the inoculum from the sheep fed hay and barley (80:20%)--the inoculum A and the inoculum from the sheep fed alfalfa and barley (80:20 %)--the inoculum B. The analyses showed that inoculum B contained more short chain fatty acids (SCFA), medium chain fatty acids (MCFA) and saturated fatty acids (SFA) than inoculum A. In contrast, inoculum A contained more unsaturated fatty acids (UFA) than inoculum B. The results show, that the oils affected the biohydrogenation of fatty acids (FA) by increasing the concentration of C18:0 (3-7 times) and trans C18:1 isomers (2-9 times). The concentration of two main intermediates of FA biohydrogenation-- cis 9, trans 11 C18:2 (CLA) and trans 11C18:1 (TVA) were increased with the oils, but FO was more efficient than other plant oils on CLA and TVA production.The monensin treatment had similar effect on FA metabolism as the oil treatment in comparison to unincubated control. The interactions of monensin treatment with the oils were characterized with decrease (LO+MON, SO+MON) or increase (FO+MON) of the proportions of C18:0 and trans C18:1 isomers in comparison to oil treatment.The highest concentrations of two main isomers--CLA,TVA were found in the samples containing fish oil and monensin. In conclusion, fish oil treatment and monensin with fish oil treatment was more efficient than other plant oils in the effect on trans fatty acid production (mainly CLA and TVA) in fermentation fluid in vitro.  相似文献   

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