scholarly journals Unravelling genetic variation underlying de novo-synthesis of bovine milk fatty acids

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Tim Martin Knutsen ◽  
Hanne Gro Olsen ◽  
Valeria Tafintseva ◽  
Morten Svendsen ◽  
Achim Kohler ◽  
...  
Author(s):  
Magdalena Stolcova ◽  
Dalibor Řehák ◽  
Luděk Bartoň

The aim of this study was to compare the changes in milk composition postpartum, especially ketones and milk fatty acids (FAs), in Holstein and Fleckvieh cows kept under identical management conditions. Milk composite samples were collected from 66 cows during afternoon milking, at weekly intervals from one to eight weeks postpartum, and their components were determined by Fourier transform infrared spectroscopy. The Holstein cows had higher (P < 0.05) concentrations of long-chain FAs (ranging from 6% to 16% in different weeks), monounsaturated FAs (6% to 12%), and C18:1 (5% to 16%), as well as lower (P < 0.05) concentrations of saturated FAs (3% to 8%) and short-chain FAs (7% to 17%) in their milk than the Fleckvieh cows for almost the entire monitored period. These differences can be explained by pronounced lipomobilization, due to a negative energy balance, when mainly long-chain FAs from adipose tissue are incorporated into milk and significantly inhibit the de novo synthesis of FAs in the mammary gland. In conclusion, it can be assumed that breed-related metabolic changes during the first weeks of lactation have a large effect on the milk FA composition. This reflection of the metabolic load changes and lipomobilization in differing milk FA profiles would allow for the use of selected milk FAs to detect energy imbalances and their associated diseases in early lactation cows.  


1997 ◽  
Vol 78 (1) ◽  
pp. S37-S47 ◽  
Author(s):  
R. J. Mansbridge ◽  
J. S. Blake

The predominant fatty acids in milk are the long-chain fatty acids myristic, palmitic and stearic. These saturated fatty acids account for 75 % of the total fatty acids, with a further 21 % occurring as monounsaturated fatty acids of which the most prevalent is oleic acid. Only 4 g/lOO g of the milk fatty acids are polyunsaturated, occurring mainly as linoleic and linolenic acids. All milk fatty acids are derived, almost equally, from either de novo synthesis or directly from preformed fatty acids in the diet. There are four main dietary sources of fatty acids: forages, oilseeds, fish oil and fat supplements. The digestive tract exerts a profound influence on the fate of dietary fatty acids. The short-chain saturated free fatty acids are absorbed through the walls of the rumen or abomasum into the bloodstream. The medium- and longer-chain saturated fatty acids pass into the small intestine, diffuse across the membrane wall where they are incorporated into lipoproteins and enter the bloodstream via the lymphatic system. The majority of unsaturated fatty acids are extensively hydrogenated in the rumen. However, recent work has shown that the levels of certain saturated fatty acids can be reduced and the levels of oleic, linoleic and linolenic fatty acids increased by feeding oilseeds rich in mono- or polyunsaturated fatty acids. In addition, work reported here has confirmed that eicosapentaenoic and docosahexaenoic acids can be transferred to milk when a diet containing fish oil is fed, but the transfer efficiencies are low


2000 ◽  
Vol 25 ◽  
pp. 201-223 ◽  
Author(s):  
J.J. Murphy

AbstractMilk fat consists of approximately 960-980 g of triacylglycerol, 20-25 g of 1,2-diacylglycerol, 10 g of phospholipid, 5g of cholesterol and very small quantities of free fatty acids and monoacylglycerol per kg. There are three stages in milk fat biosynthesis: the accumulation of fatty acids in the mammary cells through de-novo synthesis or absorption from the blood stream, triacylglycerol construction and fat globule assembly and secretion. Fatty acids in mammary secretory cells arise from two sources. Those having between 4 and 14 carbon atoms are synthesised de-novo in the mammary gland whereas those with 18 carbon atoms are of dietary origin and are absorbed from the blood stream. Palmitic acid (16 carbon atoms) is supplied almost equally from the diet and de-novo synthesis. In ruminants the principal sources of carbon for fatty acid synthesis are acetic acid and b-hydroxybutyrate.Alteration of milk fat concentration is achieved by changimore spreadable butter. Monounsaturated fatty acids in the diet have been shown to have beneficial effects on the plasma lipoprotein indicators of coronary heart disease risk. From a human nutrition point of view it could be beneficial to incorporate the long chain omega-3 fatty acids, eicosapentanoic (EPA, C20:5) and docosahexanoic (C22:6) acids, into milk fat. The principal source of these fatty acids is fish oil but research to date indicates that their transfer into milk fat is inefficient. Conjugated linoleic acid (CLA) is a collective term describing one or more positional and geometric isomers of linoleic acid (cis-9, cis-12 C18:2). CLA has been shown to have anticarcinogenic activity, antiatherogenic activity, an ability to reduce the catabolic effects of immune stimulation and an ability to enhance growth promotion and reduce body fat. It is present in ruminant milk and meat as a result of biohydrogenation in the rumen where it is an intermediate. Its concentration in bovine milk fat is influenced by dietary factors such as pasture feeding and supplementation with full fat oilseeds. Two other components of bovine milk fat which have been shown to have anticarcinogenic properties are butyric acid and sphingomyelin and their concentration warrants further study. It is likely that research will continue into means of manipulating both the content and composition of milk fat but ultimately the adoption of any of the strategies in practice is likely to depend on strong economic or consumer imperatives.ng either the level of de-novo synthesis in the mammary gland or the supply of long chain fatty acids in the diet. Dietary factors that affect the supply of acetic acid from the rumen for de-novo synthesis include fibre quantity and quality, forage to concentrate ratio, buffer inclusion, concentrate composition and concentrate feeding frequency. The effects of fat supplements on fat concentration are variable. In general, feeding rumen protected fat increases milk fat concentration whereas moderate amounts of unprotected unsaturated fat tend to decrease it.Most nutritional manipulation has been directed at increasing the proportion of unsaturated fatty acids in milk fat in order to enhance its appeal to the consumer and to produce a softer fat. A more spreadable butter could be produced from such fat thus overcoming a major criticism of conventional butter.If unsaturated fatty acids are fed to ruminants in an unprotected form rumen microbial digestion can be impaired and the unsaturated fatty acids are extensively saturated in the rumen. One strategy to overcome this is to include unsaturated fatty acids in a form protected from microbial digestion in the rumen. This resulted in the production of polyunsaturated milk fat from which a low melting point butter was produced. This product was predisposed to oxidative deterioration. More recently whole oilseeds have been fed to dairy cows. The unsaturated 18-carbon fatty acids in these seeds are hydrogenated in the rumen but the activity of a D-9 desaturase in the mammary gland and to a lesser extent the intestine converts the stearic acid (C18:0) to the monounsaturated fatty acid, oleic acid (C18:1). Milk fat rich in oleic acid is softer than conventional milk fat allowing the manufacture of a more spreadable butter. Monounsaturated fatty acids in the diet have been shown to have beneficial effects on the plasma lipoprotein indicators of coronary heart disease risk.From a human nutrition point of view it could be beneficial to incorporate the long chain omega-3 fatty acids, eicosapentanoic (EPA, C20:5) and docosahexanoic (C22:6) acids, into milk fat. The principal source of these fatty acids is fish oil but research to date indicates that their transfer into milk fat is inefficient. Conjugated linoleic acid (CLA) is a collective term describing one or more positional and geometric isomers of linoleic acid (cis-9, cis-12 C18:2). CLA has been shown to have anticarcinogenic activity, antiatherogenic activity, an ability to reduce the catabolic effects of immune stimulation and an ability to enhance growth promotion and reduce body fat. It is present in ruminant milk and meat as a result of biohydrogenation in the rumen where it is an intermediate. Its concentration in bovine milk fat is influenced by dietary factors such as pasture feeding and supplementation with full fat oilseeds. Two other components of bovine milk fat which have been shown to have anticarcinogenic properties are butyric acid and sphingomyelin and their concentration warrants further study.It is likely that research will continue into means of manipulating both the content and composition of milk fat but ultimately the adoption of any of the strategies in practice is likely to depend on strong economic or consumer imperative.


1995 ◽  
Vol 269 (2) ◽  
pp. E247-E252 ◽  
Author(s):  
H. O. Ajie ◽  
M. J. Connor ◽  
W. N. Lee ◽  
S. Bassilian ◽  
E. A. Bergner ◽  
...  

To determine the contributions of preexisting fatty acid, de novo synthesis, and chain elongation in long-chain fatty acid (LCFA) synthesis, the synthesis of LCFAs, palmitate (16:0), stearate (18:0), arachidate (20:0), behenate (22:0), and lignocerate (24:0), in the epidermis, liver, and spinal cord was determined using deuterated water and mass isotopomer distribution analysis in hairless mice and Sprague-Dawley rats. Animals were given 4% deuterated water for 5 days or 8 wk in their drinking water. Blood was withdrawn at the end of these times for the determination of deuterium enrichment, and the animals were killed to isolate the various tissues for lipid extraction for the determination of the mass isotopomer distributions. The mass isotopomer distributions in LCFA were incompatible with synthesis from a single pool of primer. The synthesis of palmitate, stearate, arachidate, behenate, and lignocerate followed the expected biochemical pathways for the synthesis of LCFAs. On average, three deuterium atoms were incorporated for every addition of an acetyl unit. The isotopomer distribution resulting from chain elongation and de novo synthesis can be described by the linear combination of two binomial distributions. The proportions of preexisting, chain elongation, and de novo-synthesized fatty acids as a percentage of the total fatty acids were determined using multiple linear regression analysis. Fractional synthesis was found to vary, depending on the tissue type and the fatty acid, from 47 to 87%. A substantial fraction (24-40%) of the newly synthesized molecules was derived from chain elongation of unlabeled (recycled) palmitate.


1972 ◽  
Vol 50 (10) ◽  
pp. 1263-1267 ◽  
Author(s):  
K. R. Penner ◽  
J. S. Barlow

The fatty acid composition of newly emerged Ips paraconfusus Lanier shows no sexual dimorphism and is approximately as follows: C14:0, 0.5%; C16:0, 23.0%; C16:1, 6%; C18:0, 3%; C18:1, 55%; C18:2, 9%; C18:3, 2%. Both sexes, but particularly the female, use up fatty acids, particularly the monounsaturated acids, during reproduction. Isotope from 1-14C-acetate injected into newly emerged females appeared in all saturated and monounsaturated fatty acids within 30 min. There was evidence of de novo synthesis of C14:0 and C16:0, chain elongation of C16:0 to C18:0, and desaturation of C16:0 and C18:0 to yield C16:1 and C18:1 respectively.


2014 ◽  
Vol 46 (1) ◽  
pp. 2 ◽  
Author(s):  
Aniek C Bouwman ◽  
Bruno D Valente ◽  
Luc L G Janss ◽  
Henk Bovenhuis ◽  
Guilherme J M Rosa

2016 ◽  
Vol 9 (1) ◽  
Author(s):  
Rafael A. Baraúna ◽  
Diego A. das Graças ◽  
Catarina I. P. Nunes ◽  
Maria P. C. Schneider ◽  
Artur Silva ◽  
...  

1976 ◽  
Vol 54 (6) ◽  
pp. 578-582 ◽  
Author(s):  
Mary Mes-Hartree ◽  
John B. Armstrong

The total lipid content, amount of phospholipid, proportions of major polar and neutral lipid classes, and the overall fatty acid composition were examined in Xenopus laevis embryos. No obvious differences were observed in any of the parameters between fertilization and hatching, or between eggs produced by different females. The average lipid content per egg was 113 μg, 31.6 μg of which was phospholipid. The major phospholipids were phosphatidylcholine and sphingomyelin. The major fatty acids were palmitic and oleic acids, but polyunsaturated fatty acids were also present in substantial amounts. The results suggest that significant de novo synthesis of lipids does not occur until after hatching.


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