Total C18 Research Articles

지방급원 형태와 수준에 따른 연속배양장치 내 반추위 발효성상, 지방산의 수소첨가 현상 및 Conjugated Linoleic Acid 생산에 미치는 영향 연구

본 연구는 사료 내 농후사료의 비율을 높임으로서 불포화 지방산의 반추위 내 by-pass율의 향상 가능성을 조사하고, 아마종실과 전지대두 급여 시 CLA 생산을 상호 비교하기 위하여 연속배양장치를 이용하여 수행하였다. 지방 급원에 따른 발효 성상의 차이는 보이지 않았다. 한편 사료 내 농후사료 비율이 높은 (80%) 처리구는 농후사료 비율이 낮은 (40%) 처리구와 비교하여 pH는 감소하였으나, 암모니아, 총 휘발성 지방산, acetate, butyrate 및 valerate 농도가 증가되었다. 지방급원 (전지대두 vs 아마종실)과 사료 내 농후사료 비율은 organic matter (OM), total nitrogen, neutral detergent fiber (NDF) 및 acid detergent fiber (ADF)의 소화율에 영향을 끼치지 않았다. 반면에 전지대두는 아마종실과 비교하여 trans C18:1, C18:2 n-6 및 C18:3 n-3 유출율은 증가시켰다. 지방 급원에 의한 CLA flow는 영향을 받지 않았으나 사료 내 농후사료 비율이 높을 때와 전지대두와 아마종실의 함량이 높았을 때는 증가되었다. 수소 첨가현상은 C18:1 n-9 와 C18:2 n-6에서 지방 급원에 의하여 영향을 받지 않았으나, 아마종실 처리구에서는 C18:3 n-3 과 총 C18 불포화지방산의 수소 첨가현상이 전지대두 처리구와 비교하여 높은 비율로 발생했다. 한편 사료 내 농후사료 비율이 높을 때 처리구에서 C18:2 n-6, C18:3 n-3 및 총 C18 불포화 지방산의 수소 첨가현상은 농후사료 저 처리구와 비교하여 감소되었다. This experiment employed a rumen simulated continuous culture system to examine the possibility of improving the rumen bypass of polyunsaturated fatty acids (PUFA) by using a high proportion of concentrate in the feed, and compared soya and linseed in terms of conjugated linoleic acid (CLA) production. No effect of type of fat source was observed on ruminal fermentation. A high proportion of concentrate (80%) in the feed decreased (P<0.001) vessel pH but increased (P<0.01) ammonia nitrogen, total VFA, acetate, butyrate and valerate concentrations compared with a low proportion (40%). Fat sources (soya vs. linseed) and concentrate ratio in the feed did not affect digestibilities of organic matter (OM), total nitrogen, neutral detergent fiber (NDF) and acid detergent fiber (ADF). Soya increased the flows of trans C18:1, C18:2 n-6 and C18:3 n-3 compared with linseed. The difference in fat source alone did not affect the flow of CLA but this was increased when high levels of soya and linseed were associated with a high proportion of concentrate in the feed. There was no effect of fat source on biohydrogenation of C18:1 n-9 and C18:2 n-6, but biohydrogenation of C18:3 n-3 and total C18 PUFA was higher with the linseed than with the soya treatment. A high proportion of concentrate decreased biohydrogenation of C18:2 n-6, C18:3 n-3 and total C18 PUFA compared with a low proportion.

Effect of dietary fish oil on biohydrogenation of fatty acids and milk fatty acid content in cows

AbstractMechanisms underlying milk fat conjugated linoleic acid (CLA) responses to supplements of fish oil were investigated using five lactating cows each fitted with a rumen cannula in a simple experiment consisting of two consecutive 14-day experimental periods. During the first period cows were offered 18 kg dry matter (DM) per day of a basal (B) diet formulated from grass silage and a cereal based-concentrate (0·6 : 0·4; forage : concentrate ratio, on a DM basis) followed by the same diet supplemented with 250 g fish oil per day (FO) in the second period. The flow of non-esterified fatty acids leaving the rumen was measured using the omasal sampling technique in combination with a triple indigestible marker method based on Li-Co-EDTA, Yb-acetate and Cr-mordanted straw. Fish oil decreased DM intake and milk yield, but had no effect on milk constituent content. Milk fat trans-11 C18:1, total trans-C18 : 1, cis-9 trans-11 CLA, total CLA, C18 : 2(n-6) and total C18 : 2content were increased in response to fish oil from 1·80, 4·51, 0·39, 0·56, 0·90 and 1·41 to 9·39, 14·39, 1·66, 1·85, 1·25 and 4·00 g/100 g total fatty acids, respectively. Increases in the cis-9, trans-11 isomer accounted for proportionately 0·89 of the CLA response to fish oil. Furthermore, fish oil decreased the flow of C18 : 0(283 and 47 g/day for B and FO, respectively) and increased that of trans-C18 : 1fatty acids entering the omasal canal (38 and 182 g/day). Omasal flows of trans-C18 : 1acids with double bonds in positions from delta-4 to -15 inclusive were enhanced, but the effects were isomer dependent and primarily associated with an increase in trans-11 C18 : 1 leaving the rumen (17·1 and 121·1 g/day for B and FO, respectively). Fish oil had no effect on total (4·36 and 3·50 g/day) or cis-9, trans-11 CLA (2·86 and 2·08 g/day) entering the omasal canal. Flows of cis-9, trans-11 CLA were lower than the secretion of this isomer in milk. Comparison with the transfer of the trans-9, trans-11 isomer synthesized in the rumen suggested that proportionately 0·66 and 0·97 of cis-9, trans-11 CLA was derived from endogenous conversion of trans-11 C18 : 1in the mammary gland for B and FO, respectively. It is concluded that fish oil enhances milk fat cis-9, trans-11 CLA content in response to increased supply of trans-11 C18:1that arises from an inhibition of trans-C18 : 1reduction in the rumen.

Evaluation of fatty acids as biomarkers for a natural plankton community. A field study of a spring bloom and a post-bloom period off West Greenland

An investigation of the fatty acid composition of a natural arctic plankton community was carried out over two fishing banks located between 63°N and 65°N off the West Greenland coast. Samples for fatty acid analyses, species determination and biomass assessments of the plankton community were taken at the depth of fluorescence maximum. High biomass and diatom dominance during the spring bloom and low biomass and flagellate dominance in the post-bloom period were reflected by the fatty acid profiles. The total amount of fatty acid ranged from 55 to 132 µg l–1 during the spring bloom and from 1 to 5 µg l–1 during the post bloom. Analysis of the fatty acids showed that when the plankton was dominated by diatoms of the genera Thalassiosira and Chaetoceros, the proportions of C16:1(n-7) and C20:5(n-3) were correspondingly high. C18s, and particularly C18:1(n-9), were more abundant when the plankton was dominated by small autotrophic flagellates, primarily haptophytes. We found a good positive correlation between the common diatom marker, C16:1(n-7)/C16:0, and the biomass percentage of diatoms (r=0.742, P<0.001), as well as between the biomass percentage of flagellates and total C18 fatty acids (r=0.739, P<0.001). This supports the use of these specific fatty acids and fatty acid ratios as general biomarkers of the plankton community. However, the fatty acids are not specific enough to sufficiently characterise the composition of the plankton community, and microscopical support is needed to verify observed trends.

Fatty acid composition of muscle and fat tissues of Omani Jebel Akhdar goats of different sexes and weights

This paper describes the fatty acid (FA) composition of muscle and fat tissue in Omani Jebel Akhdar buck, wether and does slaughtered at 11, 18 or 28 kg body weight (BW). The fat percentage in dry matter (DM) of the subcutaneous and kidney fats ranged between 85 and 98% and that of muscle ranged between 17 and 21%. Subcutaneous fat tended to have lower DM than kidney fat. Palmitic (C16:0), stearic (C18:0) and oleic (C18:1) acids comprised the largest proportions of FA in the muscle tissue (approximately 80%) with oleic acid being the most abundant. Ninety-one percent of the total FA were contributed by the C16 and C18 fatty acids being 31.6 and 58.5%, respectively. C19 and C20 were not detected in the muscle tissue. The essential FA, C20:2, C20:3 and C20:4 contributing about 1%. Muscle tissue of the Jebel Akhdar goat contained an average 51.3% and 48.7% of saturated (SFA) and unsaturated fatty acids (UFA), respectively. Polyunsaturated FA (PUFA) constituted about 5% and monounsaturated (MFA) 43.5% of the total FA. Subcutaneous fat contained more total FA (68.08%) than kidney fat (48.14%) in the whole tissue. Kidney fat contained higher percentages of C16 and C18 but less C:18:1 than subcutaneous fat. The proportions of SFA to UFA was high in both fat depots with the SFA being much higher in the kidney than subcutaneous fats. C16, C18 and C:18:1c acids comprised 64.2 and 78% and C16s and C18s made up 81 and 85% of total FA in subcutaneous and kidney fats, respectively. In both subcutaneous and kidney fats, there was a trend of increasing values of DM and fat percentage with intact males having the lowest and females the highest values. Males had higher levels of C15, C18:2 and C18:3 but lower levels of C17, C18 and total C16, C18 and C18:1 in muscle tissue. Intact males had higher levels of C10, 12, 15 FA but lower C16:1 and C16+18+18:1 than others in subcutaneous fat. Intact males had a similar trend for C12 and 14 but lower SFA and higher UFA in kidney fat. There was a trend of increasing DM and fat% in dry matter with increasing body weight. C10, 12 and 14 of the kidney fat decreased with increasing slaughter weight. There was a trend of the two C16 FA decreasing and the four C18 increasing with BW in the kidney fat. This resulted in proportions of the total C16 and C18 FA increasing from 81.8 to 86.8%. These findings confirm those of other studies on goat meat quality that, as judged by fatty acid composition it is not inferior to that of meats from other farm animals.

Genetic Variation of Palmitate and Oil Content in a Winter Oilseed Rape Doubled Haploid Population Segregating for Oleate Content

Increasing the oil content and reducing the content of saturated fatty acids in seed oil are important breeding goals for rapeseed (Brassica napus L.). The objective of the study was to investigate the influence of a major change in oleate content on the palmitate and oil content. An oilseed rape doubled haploid (DH) population (n = 60) segregating for one major gene mutation, that increases the oleate content in the seed oil by 11%, was used in a field experiment in five environments. Subdividing the DH lines into normal and high oleate classes showed that the mutation caused a significant reduction in the saturated fatty acids palmitate and stearate and of the ratio of total C16 to total C18 fatty acids (C16/C18). The high oleate class had a significantly increased oil content and an identical protein content, compared with the normal oleate class. Both oleate classes showed a significant negative correlation for oleate and palmitate and a significant positive correlation for oleate and oil content, and oil content was negatively correlated with palmitate. The results show that the high oleate mutation has a pleiotropic effect on palmitate and oil content. The β‐ketoacyl‐acyl carrier protein (ACP) synthase II (KAS II) activity reflected by the C16/C18 ratio has been used to explain this effect. Results indicated that palmitate content can be reduced either by recurrent selection for increased oleate content or continued selection for high oil content.

Genetic Variation of Palmitate and Oil Content in a Winter Oilseed Rape Doubled Haploid Population Segregating for Oleate Content

Increasing the oil content and reducing the content of saturated fatty acids in seed oil are important breeding goals for rapeseed (Brassica napus L.). The objective of the study was to investigate the influence of a major change in oleate content on the palmitate and oil content. An oilseed rape doubled haploid (DH) population (n = 60) segregating for one major gene mutation, that increases the oleate content in the seed oil by 11%, was used in a field experiment in five environments. Subdividing the DH lines into normal and high oleate classes showed that the mutation caused a significant reduction in the saturated fatty acids palmitate and stearate and of the ratio of total C16 to total C18 fatty acids (C16/C18). The high oleate class had a significantly increased oil content and an identical protein content, compared with the normal oleate class. Both oleate classes showed a significant negative correlation for oleate and palmitate and a significant positive correlation for oleate and oil content, and oil content was negatively correlated with palmitate. The results show that the high oleate mutation has a pleiotropic effect on palmitate and oil content. The β-ketoacyl-acyl carrier protein (ACP) synthase II (KAS II) activity reflected by the C16/C18 ratio has been used to explain this effect. Results indicated that palmitate content can be reduced either by recurrent selection for increased oleate content or continued selection for high oil content.

Changes in fatty acid composition in plant tissues expressing a mammalian delta9 desaturase.

Plant tissues expressing a mammalian stearoyl-CoA delta9 desaturase were reported to accumulate delta9 hexadecenoic acid (16:1), normally very minor in most plant tissues. The transgenic plants were thoroughly analyzed for alterations of individual lipids in different subcellular sites. Western blot analysis indicated that the animal desaturase was targeted to the microsomes. The delta9 16:1 was incorporated into both the sn-1 and sn-2 positions of all the major membrane lipids tested, indicating that the endoplasmic reticulum acyltransferases do not exclude unsaturated C16 fatty acids from the sn-2 position. In addition to increases in monounsaturated and decreases in saturated fatty acids, accumulation of 16:1 was accompanied by a reduction in 18:3 in all the lipids tested except phosphatidylglycerol, and increases in 18:2 in phospholipids. Total C16 fatty acid content in the galactolipids of the transgenics was significantly higher than that in the control, but those in the phospholipids were unchanged. In transgenics, delta11 18:1 was detected in the sn-1 position of the lipids tested except phosphatidylinositol and phosphatidylserine. Introduction of the animal desaturase, controlled by a seed-specific phaseolin promoter, into soybean somatic embryo resulted in a significant reduction in saturated fatty acids. Such effects were greater in cotyledons than hypocotyl-radicles. This study demonstrated that the animal desaturase can be used to decrease the levels of saturated fatty acids in a crop plant.

Effects of saturation and esterification of fat sources on site and extent of digestion in steers: digestion of fatty acids, triglycerides, and energy.

Five steers (mean BW 526 kg) fitted with ruminal, duodenal, and ileal cannulas were used in a 5 x 6 Youden square design with 14-d periods. Diets contained chopped alfalfa hay, corn silage, and concentrate (25:35:40, DM basis). Treatments were 1) control (no added fat); 2) tallow (T), iodine value (IV) = 51.5; 3) partially hydrogenated tallow (PHT), IV = 30.7; 4) hydrogenated tallow (HT), IV = 6.9; 5) blend (1: 1) of HT and hydrogenated free fatty acids (HTHFA), IV = 9.0; and 6) hydrogenated free fatty acids (HFA), IV = 11.2. Fats replaced cornstarch in the control diet to supply 5% added fatty acids. Intake was restricted to 90% of ad libitum; DMI was similar among diets (mean 9 kg/d). Total fatty acid intake averaged 170, 500, 506, 525, 489, and 491 g/d for treatments 1 to 6, respectively. Flows of total C16, total C18, and total fatty acids to the duodenum were increased by supplemental fat; flows of total C18 and total fatty acids were greater than their intake for all treatments. Flow of total fatty acids associated with ruminal bacteria accounted for 50 and 17% of the total duodenal fatty acid flow for the control and fat-supplemented diets, respectively. Digestibility of total fatty acids entering the small intestine (74, 71, 62, 39, 53, and 63% for treatments 1 to 6, respectively) was greater for the control diet than for fat-supplemented diets and decreased as either saturation (T < PHT < HT) or esterification (HFA < HTHFA < HT) increased. Digestibilities of fatty acids in the total tract followed similar patterns. Ruminal lipolysis of dietary triglycerides decreased linearly as the degree of saturation of fat sources increased. Small intestinal disappearance of triglycerides (89, 75, 51, 44, 64, and 73% of duodenal flow for treatments 1 to 6, respectively) decreased linearly as either saturation or esterification increased. Flows and digestion of gross energy followed patterns similar to those for fatty acids and triglycerides. Resistance to ruminal and small intestinal lipolysis is a major factor contributing to the poor digestibility of highly saturated triglycerides.

Analysis of C18:1cis and trans fatty acid isomers by the combination of gas‐liquid chromatography of 4,4‐dimethyloxazoline derivatives and methyl esters

AbstractTrans fatty acids in foods are usually analyzed by gas‐liquid chromatography (GLC) of fatty acid methyl esters (FAME). However, this method may produce erroneously low values because of insufficient separation between cis and trans isomers. Separation can be optimized by preceding silver‐ion thin‐layer chromatography (Ag‐TLC), but this is laborious. We have developed an efficient method for the separation of 18‐carbon trans fatty acid isomers by combining GLC of FAME with GLC of fatty acid 4,4‐dimethyloxazoline (DMOX) derivatives. We validated this method against conventional GLC of FAME, with and without preceding Ag‐TLC. Fatty acid isomers were identified by comparison with standards, based on retention times and mass spectrometry. Analysis of DMOX derivatives allowed the 13t, 14t, and 15t isomers to be separated from the cis isomers. The combination of the GLC analyses of FAME and DMOX derivatives gave results comparable with those obtained by GLC of FAME after preceding Ag‐TLC, while saving about 100 h of manpower per 25 samples. It allowed the identification and quantitation of 11 trans and 8 cis isomers and resulted in 25% higher values for total C18:1trans, compared with the analysis of FAME alone. The combination of DMOX and FAME analyses, as applied to the analysis of 14 foods that contained ruminant fat and partially hydrogenated vegetable and fish oils, indicated that the most common isomers were 11t in ruminant fats, 9t in partially hydrogenated fish fats, and either 9t or 10t in partially hydrogenated vegetable fats. The combination of GLC analyses of FAME and DMOX derivatives of fatty acids improves the quantitation of 18‐carbon fatty acid isomers and may replace the laborious and time‐consuming Ag‐TLC.

Effects of Postruminal Protein on Fatty Acid Digestibility in Dairy Cows

Eight ruminally cannulated Holstein cows (four multiparous and four primiparous) were used in a replicated 4×4 Latin square with an extra period to determine the effects of postruminal protein on fatty acid digestibility. Samples were collected during the last 4 d of each 14-d period. Total mixed rations were composed of 41% alfalfa haylage, 42% corn silage, 12% concentrate based on corn, and 5% tallow. Cows were fed at 90% of ad libitum intake. Treatments were abomasal infusion of guar gum or guar gum plus urea, corn gluten meal, or blood meal in 12L of water. The basal ration contained 12% crude protein (CP), and infusion of N sources increased CP to approximately 14%. Dry matter intake was similar for cows on all treatments. Milk, 3.5% fat-corrected milk, milk protein, and milk fat yields increased for cows receiving postruminal CP. Postruminal CP did not affect milk fat and protein percentages. Dry matter, organic matter, and CP digestibilities were greater in cows receiving postruminal CP. Total fatty acid and total C18 fatty acid digestibilities were not affected by treatment. Total C16 fatty acid and C18:0 fatty acid digestibilities were greater for cows receiving nonprotein N than for those receiving true protein.

Fatty Acid Flow to the Duodenum and in Milk from Cows Fed Diets that Contained Fat and Nicotinic Acid

Four cows fitted with ruminal and duodenal cannulas were used in a 4×4 Latin square design; treatments were arranged in a 2×2 factorial. Treatments were 1) low fat diet, no nicotinic acid; 2) low fat diet, 12 g/d of nicotinic acid; 3) high fat diet, no nicotinic acid; and 4) high fat diet, 12 g/d of nicotinic acid. Cows were fed for ad libitum intake diets consisting of 35% alfalfa silage, 15% corn silage, and either 50% low fat concentrate or 40% high fat concentrate (tallow supplied 6.25% of concentrate) and 10% whole raw soybeans (dry matter basis). Intake of gross energy (104 Mcal/d) was not different among treatments. Ruminal and postruminal digestibility of energy was not altered by fat or nicotinic acid. Fatty acid intake and flow to the duodenum were increased by fat but were not affected by nicotinic acid. For all diets, flows to the duodenum of C16:0, C18:0, total C18, and total fatty acids increased, and flows of C16:1, C18:1, C18:2, and C18:3 decreased, compared with their intakes. Biohydrogenation of unsaturated C18 was decreased by fat but was not affected by nicotinic acid. Digestibilities of C18:0, C18:1, C18:2, C18:3, and total fatty acids that flowed to the duodenum were decreased by fat but were not affected by nicotinic acid. The yield of C18:0 in milk was increased, and yields of C6:0 to C16:0 fatty acids were decreased, by fat, but yields were not affected by nicotinic acid.

Effects of Chain Length and Unsaturation of Fatty Acid Mixtures Infused into the Abomasum of Lactating Dairy Cows

Six cows were utilized in a 6×6 Latin square design with 21-d periods to determine effects of the postruminal profile of fatty acids on dry matter (DM) intake, milk yield and composition, nutrient digestibilities, and plasma metabolites. Treatments were abomasal infusions of 1) control [168 g/d of meat solubles (carrier for fatty acids) plus 10.6 g/d of Tween 80® (emulsifier)], 2) control plus 450 g/d of mostly saturated fatty acids, 3) control plus 450 g/d of palm oil fatty acids low in linoleic acid, 4) control plus 450 g/d of palm oil fatty acids, 5) control plus 450 g/d of soybean oil fatty acids, and 6) control plus 450 g/d of soybean oil fatty acids high in palmitic acid. Treatments 2, 3, 4, and 6 contained similar ratios of C16 to C18 fatty acids. Infusion of soybean oil fatty acids or soybean oil fatty acids high in palmitic acid decreased intakes of DM, organic matter, crude protein, acid detergent fiber, neutral detergent fiber, gross energy, and total fatty acids and tended to decrease yields of milk and fat-corrected milk compared with the infusion of mostly saturated fatty acids. Infusion of palm oil fatty acids low in linoleic acid or palm oil fatty acids decreased milk fat percentage compared with other treatments. Ruminal characteristics and apparent digestibilities of DM, organic matter, crude protein, acid detergent fiber, neutral detergent fiber, energy, total fatty acids, and total C18 fatty acids were not different. Infusion of fatty acids increased concentrations of cholesterol in plasma. The amount of unsaturated fatty acids passing into the small intestine may influence responses of dairy cows to supplemental fat.

Rumen fermentation, nutrient flow to the duodenum and digestibility in bulls fed calcium soaps of rapeseed fatty acids and soya bean meal coated with calcium soaps

Three Polish Friesian bulls fitted with rumen and duodenal canulas were used in a 3 × 3 Latin square experiment to study the effect of Ca soaps of rapeseed fatty acids (CSRFA) on rumen fermentation, nutrient and fatty acid (FA) flow to the duodenum, and to investigate in vivo the possibility of using CSRFA as a means of protecting soya bean meal protein against degradation in the rumen. Treatments were (1) control, no fat (2) CSRFA, at 2% of dietary DM and (3) SBM protein coated with CSRFA (CSRFA:SBM, 1:1, wt/wt), at 4% of dietary DM. The animals were fed isonitrogenous diets, containing 45% meadow hay, 10% fodder beet and 45% concentrate mixture on a DM basis. Intake was limited to 80 g DM d −1 kg −0.75. There were no treatment effects on rumen fermentation, rumen liquid turnover rate or volume, suggesting that CSRFA were inert in the rumen. A slight decrease in ammonia concentration in the rumen fluid from the CSRFA:SBM diet and the degradability data do not confirm the protection of SBM protein by CSRFA. Treatments did not affect apparent OM digestibility in the rumen, total N and NAN (non-ammonia nitrogen) flow into the duodenum or microbial protein synthesis. However, rumen degradability of protein was increased by feeding CSRFA. Feeding CSRFA significantly increased the duodenal flows of C18:0, C18:1 and total FA, but when expressed as a percentage of intake, there were no significant treatment differences. The average duodenal flow of total FA was 81.7% of intake. Extents of biohydrogenation of unsaturated FA were decreased in diets containing CSRFA. Estimated net biohydrogenation of C18:2, C18:3 and total unsaturated C18 FA of CSRFA was 43.3, 60.4 and 59.4%, respectively. Postrumen and total tract digestibility of total and individual FA were not different between treatments

Effect of Nigericin, Monensin, and Tetronasin on Biohydrogenation in Continuous Flow-Through Ruminal Fermenters

Four ionophores differing in cation selectivity were compared for their effect on microbial fermentation and biohydrogenation by ruminal bacteria in continuous culture. Monensin and nigericin are monovalent antiporters with selective binding affinities for Na+ and K+, respectively. Tetronasin is a divalent antiporter that binds preferentially with Ca2+ or Mg2+. Valinomycin is a monovalent uniporter and does not exchange K+ for H+. Steady-state concentrations of 2μg/ml of monensin, nigericin, tetronasin, or valinomycin were maintained by constant infusion into fermenters. Molar percentages of acetate were lower, and those of propionate were higher, in the presence of monensin, nigericin, and tetronasin; all three ionophores also decreased CH4 production. Concentrations of valinomycin as high as 8μg/ml had no effect on volatile fatty acids or CH4 production.Monensin, nigericin, and tetronasin inhibited the rate of biohydrogenation of linoleic acid. Continuous infusion of C18:2n-6 at a steady-state concentration of 314μg/ml into fermenters receiving monensin, nigericin, or tetronasin resulted in lower amounts of stearic acid and higher amounts of oleic acid. Ionophores increased total C18:2 conjugated acids mainly because of an increase in the cis-9, trans-11-C18:2 isomer. If reflected in milk fat, ionophore-induced changes in ruminal lipids could enhance the nutritional qualities of milk.

Utilization of Supplemental Triglycerides or Free Fatty Acids by Calves from 4 to 10 Weeks of Age

Our objectives were 1) to determine the effects of increased availability of 2-monoglycerides from triglyceride digestion on absorption of free fatty acids (FFA) and utilization of nutrients by calves of weaning age and 2) to determine whether absorption of FFA increased with age. Thirty-two male Holstein calves were fed milk replacer until d 28 of age and then were assigned to one of four treatments: 1) control, 80 g/d of whey protein concentrate in 2L of water; 2) control plus 120 g/d of lard triglycerides; 3) control plus 90 g/d of lard triglycerides plus 30 g/d of lard FFA (low FFA); and 4) control plus 60 g/d of triglycerides plus 60 g/d of lard FFA (high FFA). Treatments were fed by nipple pail twice daily to maintain closure of the esophageal groove. Intake of calf starter (available continuously) was decreased by supplemental fats and tended to be lower for calves fed high FFA than for those fed low FFA. Digestibilities of total C18 fatty acids and total fatty acids were lower for calves fed triglycerides than for calves fed FFA, but digestibilities were not affected by age. Energy digestibility was greater for fat treatments than for controls and was greater for FFA treatments than for triglycerides, but intakes of digestible energy and metabolizable energy did not differ. Absorbed N was greater for calves on the control treatment than for those on the fat treatments, but retained N and average daily gain did not differ. Digestibility of fatty acids was greater for calves fed mixtures of triglycerides and FFA than for those fed triglycerides alone, but digestibility did not change during wk 6 to 10 of age.

Study of the Competitive Binding of TBA and CP Ions on C18 Surface

Abstract The adsorption behavior of tetrabutylammonium (TBA) and cetylpyridinium (CP) cations was studied on Hypersil 5-ODS sorbent. After establishing that CP has about 5-fold stronger affinity to the C18 surface than the structurally different, symmetric, spherical molecule of TBA, the adsorption from their common solution was also examined. The data of “competitive binding” seem to show that TBA should have certain selective binding sites on the C18 surface from which it can not be displaced by the CP, even in the case where the latter is present in a 4-fold excess in the mobile phase. The maximal coverage was found to be 52.9%(CP) and 12%(TBA), i.e., every second C18 group is covered by CP cations and only l/8th of C18 groups may interact with TBA. The accessible, proton releasing silanol content, related to the total C18 content of the column, was found to be very low.

Isomeric distribution and rapid determination of trans‐octadecenoic acids in German brands of partially hydrogenated edible fats

AbstractThe determination of trans fatty acids (TFA), in particular trans‐octadecenoic acids, in edible fats is of current interest, since just in the last years a variety of negative physiological effects has been related to TFA. A main source of C18:1 trans fatty acids are partially hydrogenated fats. Besides the total content of trans‐octadecenoic acids, their isomeric distribution seems to be even more important, as fats of different origin, e.g. partially hydrogenated fats and ruminant fats, possibly show different physiological properties. In this study, 46 margarines and 16 shortenings and cooking fats, purchased in August of 1994, were analyzed for trans‐octadecenoic acid isomers by a two‐step method (Ag‐TLC/HRGC). The mean relative isomeric distributions (g/100 g TFA) of both groups determined with a 100 m‐column were comparable, with Δ9 and Δ10 being the main isomers. By repeated analysis of 15 brands between August of 1994 and January of 1996, the mean total C18:1 TFA content was found to have decreased in these margarines (n = 8) from 9.58% to 4.62% but not in shortenings/cooking fats (n = 7; 11.62% to 11.92%). The relative isomeric distribution was not affected in both groups. To avoid the problem of overlaps between cis‐and trans‐C18:1 isomers with GC analysis, formulae for the rapid determination of total C18:1 TFA contents in margarines and shortenings/cooking fats from direct GC data were statistically derived. Thus, applying these formulae and considering the mean relative distributions, absolute contents of all individual isomers of trans‐octadecenoic acids can rapidly be determined from direct GC.

Lipid and Fatty Acid Contents in Red Tides from Tropical Fish Ponds of the Coastal Water of South China Sea

Microplanktonic red tide blooms (dominated by dinoflagellates) were observed in brackish water fish ponds of Terengganu between March 1992 to January 1993. The first short-lived bloom (2-3 days) occurred in October 1992 while the second long-lived bloom (6-7 days) occurred in January 1993. The dominant dinoflagellate species comprised of Peridinium quinquecorne (> 90% total cell count) with considerable proportion of Protoperidinium excentricum. Ciliophora consisting of Tintinopsis sp. and Favella sp. were also present during the bloom period. The total ash, chlorophyll, phaeopigment, lipid and fatty acid content of the microplankton were studied. Considerable amounts (6-11% of the total fatty acid) of the polyunsaturated fatty acid 18:3w3 (linolenic acid) were present in the microplankton. However, high amounts of 20:5w3 (eicosapentanoic acid) and 22:6w3 (docosahexaenoic acid) were present with variable but usually high amounts of 22:4w6 and 22:5w6 acids. The latter microplankton bloom contained higher amounts of 20:5w3 and 22:6w3 acids than the earlier bloom. Lipid content were three to five times higher than chlorophyll a. There was an increase with successive day after bloom outbreak in the relative proportion of total C18, C20, and C22 fatty acid components. The algae microplankton contained the w3-polyunsaturated fatty acids (PUFAs) probably needed for the growth and survival rate of grazing pond animals.

Site of Digestion and Milk Production by Cows Fed Fats Differing in Saturation, Esterification, and Chain Length1,2

Four cannulated cows in a 4 × 4 Latin square design were used to study the effects of supplemental dietary fatty acids from roasted soybeans combined with tallow or partially hydrogenated fats, varying in esterification and fatty acid chain length, on nutrient digestion and lactation performance. Diets were formulated to contain (DM basis) 48% forage in addition to 1.5% fatty acids from roasted soybeans and 2.5% fatty acids from tallow, partially hydrogenated tallow triglycerides, partially hydrogenated tallow fatty acids, or a blend of 30% tallow and 70% hydrogenated fatty acids that were rich in palmitic acid. Apparent total tract digestibilities of OM, N, and NDF were similar among diets. Supplemental fat as fatty acids, compared with triglycerides, increased digestibilities of total fatty acids and C18:1 in the small intestine, perhaps indicating that lipolysis was rate-limiting. Fatty acids also increased milk fat percentage and efficiency of 4% FCM production. Although intake of C16 fatty acids was higher for cows fed the fat rich in palmitic acid than for those fed the tallow fatty acids, total duodenal flows of C16 fatty acids were similar, and digestibility in the small intestine was unaffected. Dry matter intake, 4% FCM production, and milk protein percentage were similar among treatments.

Optimized analysis oftrans-octadecenoic acids in edible fats

Trans fatty acids (TFA) in edible fats are of interest, since they are suspected to influence serum lipid levels. Thus, to estimate the atherogenic potency of edible fats a precise analytical method for the determination of TFA is required. The present study does not only aim at the quantitative analysis of total C18:1 TFA, but also at the determination of the isomeric pattern oftrans-octadecenoic acids in different fats.