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1.
An in vitro trial was conducted to investigate the effect of different inoculum sources (buffalo vs. cattle) on rumen fermentation and degradability. Incubations were carried out using rumen fluid obtained from buffalo or cattle fed the same diet [60% grass hay and 40% concentrate; 18 kg dry matter (DM)/day]. The fermentation kinetics of eight feeds commonly used in ruminant nutrition (alfalfa hay, barley meal, beet pulp, corn meal and silage, ryegrass hay and silage and soya bean meal s.e.) were studied with the in vitro gas production technique and rumen fermentation parameters (substrate disappearance, pH and volatile fatty acids production) were determined after 120 h of incubation. The linear relationship indicates that the microbial metabolic pathways of the two inocula for all the substrates were qualitatively similar, albeit often quantitatively different. In this in vitro study, a significant influence of rumen inoculum (buffalo vs. cow) on fermentation and degradability of the examined substrates was found. The differences in buffalo and cattle rumen fermentation can be explained with a different microbial activity of the two ruminant species, because of different amount of microbial population or microbial population constituted by different species of bacteria and protozoa.  相似文献   

2.
Efficient red deer supplementary feeding depends on estimations of the nutritive value of offered feeds, frequently estimated with the use of equations derived from domestic ruminants. The aim of this study was to compare the 24‐hour in vitro true dry matter degradability (ivTD24), in vitro gas production (GP) kinetic parameters, GP in 24 hr of incubation (GAS24) and short‐chain fatty acid (SCFA) and microbial biomass (MBS) produced after 24‐hour incubation of feeds in inoculum prepared from sheep and red deer rumen fluid. Eleven feeds, frequently consumed by red deer in Slovenia, which occur either naturally (two fresh grasses, chestnut fruits and common and sessile oak acorns) or are fed as winter supplemental feeds (two grass hays, two grass silages, apple pomace, fresh sugar beetroot), were investigated. The in vitro GP kinetic parameters, GAS24 and ivTD24, did not differ between animal species. Amounts of SCFAs were greater (p < 0.05) when feeds were incubated in sheep inoculum, while molar proportions of acetic and propionic acids did not differ. Molar proportions of butyric acid produced during incubation of high fibre feeds did not differ between animal species, but were higher (p < 0.05) when feeds high in starch or sugar were incubated in red deer inoculum. Greater production of SCFA by sheep rumen microbes suggests better coverage of host animal with energy precursors, while greater production of MBS by red deer rumen microbes suggests better coverage of host animal with protein. Results also suggest that rumens of sheep and red deer are inhabited by different microbial communities, which did not affect the extent of in vitro GP and degradation of feeds used in the present experiment. However, the possibility exists that the divergent nutrient use could be a consequence of different priming by different feeds of the donor animal diets.  相似文献   

3.
We used DNA probes to study dietary effects on the prokaryotic population in the rumen. Procedures used to isolate and quantify prokaryotic 16S ribosomal RNA (rRNA) from the rumen using universal and species-specific DNA probes were evaluated. In this experiment, three ruminally fistulated steers were fed orchard-grass hay, and ruminal digesta were collected at 0, 3, and 9 h after offering hay (0800). Samples of ruminal digesta were taken from the interior portion of the digesta mat and from the fluid below the mat in the dorsal rumen. Freezing (-65 degrees C) and blending samples both increased (P less than .07) the yield of 16S rRNA from ruminal digesta. Extraction of prokaryotic rRNA was greater (P less than .04) when phenol buffered with sodium acetate was used than when it was buffered with hydroxymethyl-amino-methane. Prokaryotic 16S rRNA concentration of the fluid phase was similar (P greater than .10) at 0, 3, and 9 h after offering hay. Prokaryotic 16S rRNA concentration of the mat phase increased up to the 9 h after feeding. The proportion of Fibrobacter succinogenes remained constant in both digesta phases at all times measured. From these data we concluded that DNA probes can be used to monitor bacterial population shifts in the rumen.  相似文献   

4.
The effects of rumen fluid on the content of zearalenone in animal fodder   总被引：2，自引：0，他引：2  
The object of the study was to clarify whether rumination has a bearing on the decomposition of zearalenone in the metabolism of the toxin or not. The experiment was performed using rumen fluid in vitro. Rumen fluid samples containing various amounts of zearalenone were incubated in a carbon dioxide atmosphere at 38 degrees C for two days. The zearalenone content was determined by liquid chromatography after 0, 4, 24 and 48 hours incubation periods. The incubation of 4 hours decreased the toxin content by 11%, that of 24 h by 29% and that of 48 h by 37.5% on average. These results indicate that the quantity of zearalenone and the quality of rumen fluid have effects on the ratio of the toxin decomposed.  相似文献   

5.
采用瘤胃体外发酵技术评定了不同化学处理对稻草体外发酵特性的影响。试验以3头装有永久性瘤胃瘘管的荷斯坦奶牛为瘤胃液供体,用复合碱、氨及尿素处理稻草后,称量1 g样品于含有10 mL瘤胃液和90 mL培养基的39℃发酵瓶内体外发酵,分别于24,48,72,96 h冰浴终止发酵,测定产气量、发酵液中挥发性脂肪酸、氨态氮及微生物蛋白浓度。结果表明,化学处理提高了稻草发酵的产气量、挥发性脂肪酸、氨态氮以及微生物蛋白浓度。其中复合碱处理组的发酵速度最快,累计产气量、干物质消失率和挥发性脂肪酸浓度最高,显著高于其他各组,其次为尿素处理组和氨化处理组,对照组最低;尿素处理组的pH、氨态氮浓度和微生物蛋白含量最高,显著高于其他各组,氨化处理组和碱化处理组次之,对照组最低。化学处理提高了稻草的体外降解率,其中复合碱化处理的效果最好。  相似文献   

6.
The objective of the present experiment was to determine the effects of addition of silicate minerals, zeolite (Z), bentonite (B), kaolin (K), granite (G) on the rumen fermentation parameters, total gas, methane, total and individual volatile fatty acids (VFA) and hydrogen recovery in rumen fluid inoculum from sheep. Different materials (0.25 g) meadow hay (MH), wheat straw (WS), barley (BA) and amorphous cellulose (AC) were used as substrates. Silicate minerals (0.1 g) were added to the fermentation bottles containing substrates and rumen fluid inoculum and incubated for 72 h in vitro. The gas production technique simulates fermentation in the rumen was used to determine fermentation parameters. The total gas production was significantly higher compared to control for MH plus B (MHB), MH plus G (MHG), WS plus Z (WSZ), WS plus B (WSB), WS plus K (WSK), WS plus G (WSG), AC plus B (ACB), AC plus G (ACG), BA plus Z (BAZ), BA plus B (BAB), BA plus K (BAK), BA plus granite (BAG). Significant differences of the methane production were found between the controls, WSG, BAB and BAK. The total VFA concentration was increased in ACG (83.1 mM). The acetate: propionate (A:P) ratio of the control and additives ranged between 3.1 and 3.6 for MH, 2.7 and 3.5 for WS, 1.6 and 1.8 for AC and 2.3 and 2.9 for BA. It was concluded that the silicate minerals had no appreciable effect on the methane production, however, they support the microbial metabolism by influencing (bentonite, granite) and slightly influencing (zeolite, kaolin) the rumen fermentation.  相似文献   

7.
The effects of non‐starch‐polysaccharide‐degrading enzymes, added to a maize silage‐ and grass silage‐based total mixed ration (TMR) at least 14 h before feeding, on the rumen bacterial population were investigated. Six non‐lactating Holstein Friesian cows were allocated to three treatment groups using a duplicate 3 × 3 Latin square design with three 31‐day periods (29 days of adaptation and 2 days of sampling). Treatments were control TMR [69% forage and 31% concentrates on a dry matter (DM) basis] or TMR with 13.8 or 27.7 ml/kg of feed DM of Roxazyme G2 liquid with activities (U/ml enzyme preparation) of xylanase 260 000, β‐glucanase 180 000 and cellulase 8000 (DSM Nutritional Products, Basel, Switzerland). The concentrations of 16S rDNA of Anaerovibrio lipolytica, Fibrobacter succinogenes, Prevotella ruminicola, Ruminococcus flavefaciens, Selenomonas ruminantium and Treponema bryantii, and their relative percentage of total bacteria in rumen samples obtained before feeding and 3 and 7 h after feeding and from two rumen fractions were determined using real‐time PCR. Sampling time had only little influence, but bacterial numbers and the composition of the population differed between the transition layer between rumen fluid and the fibre mat (fraction A) and the rumen fluid (fraction B) highlighting the importance to standardize sampling. The 16S rDNA copies of total bacteria and the six bacterial species as well as the population composition were mainly unaffected by the high levels of exogenous enzymes supplemented at all sampling times and in both rumen fractions. Occasionally, the percentages of the non‐fibrolytic species P. ruminicola and A. lipolytica changed in response to enzyme supplementation. Some increases in the potential degradability of the diet and decreases in lag time which occurred collaterally indicate that other factors than changes in numbers of non‐particle‐associated bacteria are mainly responsible for the effects of exogenous enzymes.  相似文献   

8.
This study describes the results of ultrasonographic examination of the rumen in 30 healthy Saanen goats. A linear or convex transducer with a variable frequency of 5 to 13 MHz was used to scan standing, non-sedated goats. The location and size of the rumen, the distance between the wall of the rumen and abdominal wall and the appearance and size of the gas, fibre mat and fluid layers of the ruminal contents were assessed. The rumen was seen as a large organ medial to the left abdominal wall. The wall of the rumen appeared as a thick echogenic line. The longitudinal groove was seen as an echogenic notch, which divided the rumen into the dorsal and ventral sacs. The rumen could be visualized from the 9th to 12th intercostal space (ICS) and flank on the left side in all the goats. The rumen was largest in the 12th ICS at 41.6 ± 5.13 cm and smallest in the 8th ICS at 11.3 ± 4.29 cm. The dorsal sac of the rumen was largest in the left cranial flank (17.4 ± 4.43 cm) and the ventral sac was largest in the 12th ICS on the left (29.1 ± 6.03 cm). In the cranial left flank, the rumen was situated immediately adjacent to the abdominal wall in all the goats. The spleen was located between the rumen and abdominal wall in the 8th to 12 th ICS in many of the goats. The gas, fibre mat and fluid layers of the ruminal contents could be visualized in all the goats. The gas layer was 9.9 ± 3.05 cm, the fibre mat layer 16.0 ± 4.55 cm and the fluid layer 12.2 ± 5.57 cm.  相似文献   

9.
The comparative in vitro sulphoreduction of the (+) and (-) enantiomers of albendazole sulphoxide (ABZSO) and oxfendazole (OFZ) by ruminal fluid obtained from sheep and cattle, was investigated, under anaerobic conditions, in this study. Ruminal fluid samples were obtained from Holstein steers fitted with a permanent rumen fistula and from Corriedale lambs via an oesophageal tube. Albendazole sulphoxide, incubated as either the racemic (rac) mixture or as each individual enantiomeric form, was extensively sulphoreduced to form albendazole (ABZ) by ruminal fluid from both species. The concentrations of ABZ formed at different incubation times were between 55 and 158% greater after the incubation of cattle ruminal fluid with (+) ABZSO, compared with that produced when (-) ABZSO was the incubated substrate. Similarly, the concentrations of ABZ were 1.3--3.0-fold higher when (+) ABZSO was incubated with sheep ruminal fluid. Significantly higher rates of depletion were observed for the (+) enantiomeric form when ABZSO was incubated with ruminal fluid from both species. The rates of ABZ formation from both ABZSO enantiomeric forms were significantly higher in sheep compared with cattle ruminal fluid. Fenbendazole (FBZ) was the metabolite formed after the incubation of the racemic form of OFZ with ruminal fluid obtained from both species. The metabolic profile of both OFZ enantiomers followed a similar pattern to that observed for ABZSO enantiomers. A bi-directional chiral inversion of one enantiomer into its antipode was observed. The (+) enantiomer appeared in the incubation medium when (-) ABZSO was the incubated substrate, and also the (-) antipode was detected after (+) ABZSO incubation with ruminal fluid obtained from both species. The results reported here demonstrate an enantioselective ruminal sulphoreduction of ABZSO and OFZ (substrate enantioselectivity). These findings contribute to interpret the chiral behaviour of benzimidazole-sulphoxide anthelmintics.  相似文献   

10.
本试验旨在研究断奶前后犊牛在不同固液比例饲喂模式下营养物质代谢及其瘤胃发酵的异同,从而探索基于不同饲喂模式下的犊牛断奶方式。试验选用7日龄荷斯坦公犊牛36头,随机分成3组,每组12头,各组采用相同原料组成、相同营养成分的代乳粉和颗粒料。在总干物质饲喂量保持一致的情况下,改变固液饲料饲喂比例,形成3种饲喂模式组:高液体饲料比例(HL)组,28~56日龄内,颗粒料∶代乳粉保持在1∶2,56日龄断奶;对照(LS)组28~56日龄内,颗粒料∶代乳粉从1∶2逐步降低到1∶1,56日龄断奶;高固体饲料比例(HS)组,28~42日龄内,颗粒料∶代乳粉从1∶2逐步降低至1∶0,并于42日龄断奶。试验期77 d。分别于犊牛28、42、56和84日龄采集瘤胃液,35和63日龄进行断奶前后消化代谢试验。结果表明:断奶前,与HS组相比,HL、LS组犊牛总能代谢率相对较高,但差异不显著(P0.05);断奶后,HS组消化能代谢率、氮利用率及氮的生物学价值较HL组显著提高(P0.05)。与HL组相比,HS组84日龄瘤胃液微生物蛋白含量显著提高(P0.05)。3组间瘤胃液氨态氮浓度无显著差异(P0.05)。84日龄时,HS组犊牛瘤胃液总挥发性脂肪酸浓度和丁酸比例显著高于HL组(P0.05),各组间丙酸、戊酸比例无显著差异(P0.05)。综上可得,适量增加固体饲料饲喂比例有助于改善断奶前后犊牛瘤胃发酵环境,促进瘤胃微生物蛋白的合成,提高断奶后犊牛饲粮能量代谢率、氮的生物学价值及氮利用率;采用高固体饲料饲喂模式,犊牛在42日龄固体饲料采食量达到1.0 kg/d时实施断奶具有一定优势。  相似文献   

11.
不同来源肽对培养液中瘤胃细菌蛋白产量的影响   总被引：12，自引：1，他引：12  
试验研究了大豆肽、玉米肽和瘤胃液肽对培养液中瘤胃细菌蛋白产量的影响。结果表明:培养液中氨基氮含量越高,细菌生长速度越快,菌体蛋白氮产量显著增加(P<0 01或P<0 05)。培养初期(0～6h),细菌生长快,菌体蛋白氮产量也显著增加(P<0 01或P<0 05);培养后期(6～24h),细菌生长缓慢,菌体蛋白氮产量处于平稳期(P>0 05)。对于不同来源肽来说,瘤胃液肽和大豆肽对细菌生长的促进作用要明显好于玉米肽(P<0 05)。结果表明:瘤胃细菌生长需要肽营养,肽可能是细菌生长的限制性因素之一。  相似文献   

12.
Fermentation characteristics of wheat, rye, maize and triticale starches by mixed micro-organisms from the sheep rumen were determined in an in vitro experiment. Starch was incubated with ruminal fluid for 2, 4, 6, 8, 10 and 12 h and various fermentation variables were determined. The rates of fermentation of the starches were not different (p > 0.05) from each other except for 2 and 4 h of incubation. Likewise, net ammonia production, sugar utilization, microbial biomass and the efficiency of microbial protein synthesis did not differ between the starches (p > 0.05). The proportions of sugar utilized were similar between the starches and approximately 75% of the starches were fermented during the 12-h incubation. The 12-h net concentrations of individual and total volatile fatty acids (VFA) were affected (p < 0.05) by the type of starch. The concentrations of acetate, propionate and butyrate and that of total VFA from wheat, maize and triticale incubations were higher (p < 0.05) than those from rye incubation. The results suggest that the type of starch subject to investigation had no measurable effects on fermentation variables determined in this study except for individual and total VFA concentrations.  相似文献   

13.
A three-phase laboratory procedure suitable for predicting protein degradability in the rumen and digestibility of undegraded protein is reported. In the first phase the feed was incubated with starch and buffered rumen fluid. In the incubation mixture the viability of protease-active bacteria was checked by anaerobic culturing, whereas changes in protease activity were monitored by azocasein degradation. In the second and third phase rumen undegradable protein (UDP) was digested with pepsin and pancreatin, respectively. The measurements showed that 63.2, 5.2 and 4.7% of the crude protein of green lucerne was decomposed by rumen fluid, pepsin and pancreatin, respectively. Degradability of the crude protein of extracted sunflower meal was 68.3, 17.7 and 5.5% in the three phases, respectively. Repeated determination yielded crude protein degradabilities of 66.7, 27.1 and 5.1% for the three phases, respectively.  相似文献   

14.
本试验通过体外培养法,研究在不同精粗比饲粮中添加维生素B12对体外瘤胃发酵和微生物酶活力的影响。试验采用3×3双因子试验设计,即3个底物精粗比(玉米∶羊草=35∶65、50∶50和65∶35)和3个维生素B12添加量(0、40和90 ng/mL)。体外试验用瘤胃液取自3只安装有永久性瘤胃瘘管的湖羊。体外培养24 h后测定体外瘤胃发酵参数和微生物酶活力。结果显示:1)随着底物精粗比和维生素B12添加量的提高,体外培养24 h的产气量、潜在产气量和有机物消化率极显著地增加(P<0.01),且维生素B12添加量与上述指标存在线性剂量效应(P<0.01)。2)当底物精粗比为50∶50和65∶35时,添加维生素B12显著提高了发酵液中氨态氮、微生物蛋白、总挥发性脂肪酸、乙酸和丙酸浓度(P<0.05),但对丁酸浓度和乙酸/丙酸无显著影响(P>0.05)。3)当底物精粗比为35∶65和50∶50时,添加40 ng/mL维生素B12使发酵液中羧甲基纤维素酶、木聚糖酶活力显著提高(P<0.05);当精粗比为65∶35时,添加90 ng/mL维生素B12使发酵液中羧甲基纤维素酶、木聚糖酶活力显著提高(P<0.05)。结果提示,底物精粗比和维生素B12添加量影响体外瘤胃发酵。添加维生素B12可增加瘤胃微生物酶的活力,从而提高有机物消化率以及微生物蛋白和总挥发性脂肪酸的产量。当底物精粗比(玉米∶羊草)较高(50∶50和65∶35)时,维生素B12的添加效果更明显,并且具有剂量依赖效应。  相似文献   

15.
The objective of this experiment was to investigate the possibility of estimating the outflow of nutrients and microbial protein from the rumen based on sampling reticular contents as an alternative to duodenal sampling. Microbial protein flow estimates were also compared with a third method based on sampling of ruminal contents. Reticular and duodenal digesta and ruminal contents were recovered from 4 cows used in a 4 x 4 Latin square design experiment, in which the ruminal effects of 4 exogenous enzyme preparations were studied. Large and small particulate and fluid markers were used to estimate digesta flow in a triple-marker model; 15N was used as a microbial marker. Reticular and duodenal digesta were segregated into small and large particles (SP and LP, respectively) and a fluid phase, and ruminal digesta was segregated into particulate and fluid phases. Compared with digesta recovered at the duodenum, reticular digesta had lower OM and greater NDF contents. The proportion of microbial N was notably greater in the fluid phase of reticular digesta. Ruminal outflow of DM and OM was greater (by 17 and 28%) and that of NDF was lower (by 14%) when estimated from duodenal compared with reticular samples. There was no difference in the estimated flow of starch and nonammonia and microbial N between the reticular and duodenal techniques. Microbial N flow estimated based on ruminal sampling was similar to those based on duodenal and reticular sampling. The ruminal method, however, grossly overestimated flow of DM, OM, and NDF. This study supports the concept that microbial protein outflow from the rumen can be measured based on sampling of ruminal or reticular digesta. The reticular sampling technique can also provide reliable estimates for ruminal digestibility of OM, N, and fiber fractions. These findings need to be confirmed in experiments with basal diets varying in structure and forage-to-concentrate ratios.  相似文献   

16.
The in vitro incubation technique of Zhao and Lebzien (2000; Arch. Anim. Nutr. 53, 293-302) was used for the estimation of utilizable amino acids (uAA) (sum of amino acids from undegraded feed protein and microbial protein, when N is not limiting) of feeds for ruminants. The rumen fluid from a cow fed only with hay (Expt. 1) and that from a sheep fed with a mixed ration (Expt. 2) was compared with respect to estimation of uAA. In Expt. 1, 30 feeds and feed mixtures were tested and in Expt. 2, 33 feeds and feed mixtures were tested. A close linear relationship was found between the utilizable crude protein (uCP=undegraded feed protein + microbial protein) (X, g/kg) calculated from in vivo experiments and the uAA (Y, g/kg) estimated from in vitro incubations both in Expt. 1: y= 0.95 x-1.39, r2=0.85, p<0.001,n=30; and in Expt. 2: Y=0.85X-6.67,r2= 0.85,p<0.001,n=33. Statistical analysis indicates that there was a significant regressive relationship between uAA determined with the rumen fluid of a sheep (X, g/kg) and uAA determined with the rumen fluid of a cow (Y, g/kg): Y=1.06X+12.4,r2= 0.80,p<0.001,n=27. The results indicate that the in vitro incubation technique of Zhao and Lebzien (2000) can be used for the estimation of uAA of feeds for ruminants. As a rumen-fistulated cow is more expensive than a rumen-fistulated sheep, it is suggested to use a sheep fed a mixed ration as the donor of rumen fluid for the estimation of uAA of feeds with in vitro incubation. Further experiments should be performed to standardize the method and to test the most valid length of the incubation period.  相似文献   

17.
In two experiments the influence of the treatment of samples, the sampling time and the composition of the rations on the RNA: N ratio in the rumen microbes was checked. Experiment I proved that freezing (-21 degrees C), thawing and freeze-drying of isolated bacteria and protozoa from the rumen fluid and from the duodenal content did not result in a change of the RNA content and the RNA-N: total N relation. If, however, the rumen fluid is stored deep-frozen before the isolation of the bacteria the N content in the DM of the bacteria decreases by 17% and that of RNA by 30%. This results in a change of the RNA: N relation of 16%. In conclusion, the bacteria are to be isolated immediately after rumen fluid sampling. Isolated bacteria can be stored deep-frozen before RNA determination and then freeze-dried. Experiment II showed that the RNA content of the rumen protozoa varies according to the period after feeding. The RNA: N relation was 0.50, 0.92, 0.70 and 0.58 on average 0, 3, 6 and 8 h after feeding, in which the 3rd hour after feeding can obviously be considered the time of increased microbial activity. The conclusion from this variation is that more than one isolation of microbes must be carried out in the course of the day in order to achieve representative samples. These statements apply to easily and not easily fermentable protein as N source in the feed. It could also be proved that no essential variation is to be expected in the RNA: N relation in the microbes isolated from the rumen fluid in the range of 8-21% crude protein in the DM of the ration (roughage: concentrate = 55: 45). On average the rumen microbes contained 1.7 g RNA-N/16 g N, essential differences between bacteria and protozoa could not be ascertained. From the slight variation of the RNA-N: N relation in the isolated bacteria from various cows one can conclude that there is no need to isolate the microbes of each individual animal.  相似文献   

18.
In this study, the relative contribution of different microbial groups to ruminal metabolism was investigated for different diets. The rumen microbial cultures included whole rumen fluid, fungi + protozoa, bacteria + protozoa, protozoa and bacteria + fungi and were established by physical and chemical methods. Gas production, short‐chain fatty acid (SCFA) and ammonium production were measured at 24 hr in in vitro incubations using the Hohenheim gas test (HGT) procedure. Seven donor animal diets with different concentrate‐to‐roughage ratios (C:R: 10:90, 30:70, 50:50, 70:30, 70:30BC (BC = NaHCO3), 90:10 and 90:10BC) and five HGT diets (C:R: 10:90, 30:70, 50:50, 70:30 and 90:10) were formulated. Incubations in the HGT were always based on inoculum from sheep diets with the respective C:R ratio. Gas and ammonium production increased (p < 0.001) as a result of a gradual increase in concentrate proportion of the diets. In general, SCFA production followed the same trend. Whole rumen fluid and bacteria + fungi produced approximately 50% higher gas volume than protozoa and fungi + protozoa fractions, whereas gas production with bacteria + protozoa was at an intermediate level. Coculture of protozoa either with bacteria or with fungi produced more ammonium. Populations without bacteria were characterized by a particularly high acetate/propionate ratio. Although an interaction between microbial group and diet was observed for several variables, no clear direction could be established. Manipulating rumen fluid by selectively suppressing specific rumen microbial groups may be a helpful tool in elucidating their role in nutrient degradation and turnover in vitro.  相似文献   

19.
植物乳杆菌在瘤胃内发酵产共轭亚油酸的体外研究   总被引：1，自引：0，他引：1  
在体外研究植物乳杆菌(Lactobacillus plantarum)ANCLA 01发酵添加葵花籽油的瘤胃液,达到提高共轭亚油酸(CLA)产量的目的。结果表明:油脂的添加可以提高发酵液CLA产量,在3%的接种量和4mg/mL的油脂添加量条件下,过滤除菌瘤胃液组CLA的产量显著高于其他试验组(P<0.05)。在灭菌瘤胃液组,植物乳酸菌的生长良好,但CLA的产量低于过滤瘤胃液组。  相似文献   

20.
本研究旨在分析不同处理凤仙花(Impatiens balsamina)对瘤胃微生物体外产甲烷( CH4)及发酵特性的影响.试验采集装有永久性瘤胃瘘管牛瘤胃液,以稻草粉、玉米粉和黄豆粉为人工饲料,通过体外培养法研究了凤仙花水浸提液、乙醇浸提液和固体粉剂3种处理方式不同添加量(0.5％、1.0％和2.5％)对气体产生以及瘤胃发酵参数pH、氨态氮(NH3-N)和微生物蛋白质(MCP)的影响.结果表明,凤仙花固体粉剂累积产气量最高,平均比对照提高了56.8％,乙醇浸提液和水浸提液分别平均比对照提高了24.7％和14.1％;凤仙花明显提高CO2含量,降低CH4和pH,且添加量越大,效果越明显,2.5％固体粉剂完全抑制CH4生成.凤仙花明显提高MCP含量,降低NH3-N含量,其中固体粉剂效果最显著,水浸提液效果最差.固体粉剂3个添加量使MCP含量分别比对照提高了84.9％、139.7％和199.7％ (P ＜0.05),NH3-N含量分别比对照降低了41.1％、52.2％和55.4％ (P＜0.05).结果提示,体外培养条件下,凤仙花明显降低CH4生成、提高CO2生成,并促进NH3-N向MCP转化,且固体粉剂处理效果最好.  相似文献   

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