scholarly journals Long-Chain Saturated Fatty Acids, Palmitic and Stearic Acids, Enhance the Repair of Photosystem II

2020 ◽  
Vol 21 (20) ◽  
pp. 7509
Author(s):  
Haruhiko Jimbo ◽  
Kensuke Takagi ◽  
Takashi Hirashima ◽  
Yoshitaka Nishiyama ◽  
Hajime Wada

Free fatty acids (FFA) generated in cyanobacterial cells can be utilized for the biodiesel that is required for our sustainable future. The combination of FFA and strong light induces severe photoinhibition of photosystem II (PSII), which suppresses the production of FFA in cyanobacterial cells. In the present study, we examined the effects of exogenously added FFA on the photoinhibition of PSII in Synechocystis sp. PCC 6803. The addition of lauric acid (12:0) to cells accelerated the photoinhibition of PSII by inhibiting the repair of PSII and the de novo synthesis of D1. α-Linolenic acid (18:3) affected both the repair of and photodamage to PSII. Surprisingly, palmitic (16:0) and stearic acids (18:0) enhanced the repair of PSII by accelerating the de novo synthesis of D1 with the mitigation of the photoinhibition of PSII. Our results show chemical potential of FFA in the regulation of PSII without genetic manipulation.

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 Blood was withdrawn at the end of these times for the determination of deuterium enrichment, and the animals were killed to isolate the various tissues for lipid extraction for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.


2004 ◽  
Vol 82 (1) ◽  
pp. 22-29 ◽  
Author(s):  
R Menéndez ◽  
R Más ◽  
J Pérez ◽  
R M González ◽  
S Jiménez

D-003 is a mixture of very long chain saturated fatty acids (VLCSFA) purified from sugar cane wax with cholesterol-lowering effects proven in animal models and healthy volunteers. D-003 inhibits cholesterol biosynthesis through the regulation of HMG-CoA reductase activity. Rabbits fed diets enriched with casein develop endogenous hypercholesterolemia (EH), making them a very useful model for determining the mechanism of action of drugs affecting lipids. We examined whether D-003 prevented EH. Rabbits were fed a casein diet for 4 weeks, administered simultaneously with D-003 (5, 50, and 100 mg·kg–1·day–1). As expected, nontreated rabbits became hipercholesterolemic; however, as early as 15 days following administration, the treated group (50 and 100 mg·kg–1·day–1) had significantly decreased total cholesterol and low-density lipoprotein cholesterol (LDL-C). Triglycerides were not affected; however, at study completion, HDL-C levels significantly increased at all the doses assayed. D-003 inhibited de novo synthesis of cholesterol, since the incorporation of 3H2O into sterols in the liver and proximal small bowel was significantly depressed. Also, D-003 significantly raised the rate of removal of [125I]-LDL from serum and significantly elevated [125I]-LDL binding activity to liver homogenates. Taken together, these results show that the efficacy of D-003 in reducing casein-derived hypercholesteromeia could involve, at least partially, an inhibition of hepatic cholesterol bio synthesis, which may elicit a decreased cholesterol concentration in hepatocytes, preventing the loss of hepatic LDL receptors induced by casein administration. However, since casein-induced hypercholesterolemia is also a consequence of a stimulation of cholesterol absorption in the lumen and an increase of the output of cholesterol associated with LDL, the effect of D-003 on cholesterol absorption and LDL synthesis by the liver should be investigated.Key words: D-003, very long chain saturated fatty acids, casein-fed rabbits, LDL-C, cholesterol biosynthesis, LDL clearance, LDL receptor.


2013 ◽  
Vol 5 (3) ◽  
pp. 270-274 ◽  
Author(s):  
Anamaria COZMA ◽  
Doina MIERE ◽  
Lorena FILIP ◽  
Sanda ANDREI ◽  
Roxana BANC ◽  
...  

Milk fat and its fatty acid profile are important determinants of the technological, sensorial, and nutritional properties of milk and dairy products. The two major processes contributing to the presence of fatty acids in ruminant milk are the mammary lipogenesis and the lipid metabolism in the rumen. Among fatty acids, 4:0 to 12:0, almost all 14:0 and about a half of 16:0 in milk fat derive from de novo synthesis within the mammary gland. De novo synthesis utilizes as precursors acetate and butyrate produced through carbohydrates ruminal fermentation and involves acetyl-CoA carboxylase and fatty acid synthetase as key enzymes. The rest of 16:0 and all of the long-chain fatty acids derive from mammary uptake of circulating lipoproteins and nonesterified fatty acids that originate from digestive absorption of lipids and body fat mobilization. Further, long-chain fatty acids as well as medium-chain fatty acids entering the mammary gland can be desaturated via Δ-9 desaturase, an enzyme that acts by adding a cis-9-double bond on the fatty acid chain. Moreover, ruminal biohydrogenation of dietary unsaturated fatty acids results in the formation of numerous fatty acids available for incorporation into milk fat. Ruminal biohydrogenation is performed by rumen microbial population as a means of protection against the toxic effects of polyunsaturated fatty acids. Within the rumen microorganisms, bacteria are principally responsible for ruminal biohydrogenation when compared to protozoa and anaerobic fungi.


2021 ◽  
Vol 22 (19) ◽  
pp. 10432
Author(s):  
Haruhiko Jimbo ◽  
Koki Yuasa ◽  
Kensuke Takagi ◽  
Takashi Hirashima ◽  
Sumie Keta ◽  
...  

Free fatty acids (FFAs) are generated by the reaction of lipases with membrane lipids. Generated polyunsaturated fatty acids (PUFAs) containing more than two double bonds have toxic effects in photosynthetic organisms. In the present study, we examined the effect of exogenous FFAs in the growth medium on the activity of photosystem II (PSII) under strong light in the cyanobacterium Synechocystis sp. PCC 6803 (Synechocystis). PUFAs but not monounsaturated fatty acids accelerated the rate of photodamage to PSII by inactivating electron transfer at the oxygen-evolving complex. Moreover, supplemented PUFAs were specifically incorporated into the sn-2 position of phosphatidylglycerol (PG), which usually contains C16 fatty acids at the sn-2 position in Synechocystis cells. The disruption of the gene for an acyl-ACP synthetase reduced the effect of PUFAs on the photoinhibition of PSII. Thus, the specific incorporation of PUFAs into PG molecules requires acyl-ACP synthetase and leads to an unstable PSII, thereby accelerating photodamage to PSII. Our results are a breakthrough into elucidating the molecular mechanism of the toxicity of PUFAs to photosynthetic organisms.


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.  


2020 ◽  
Author(s):  
Kelli L. VanDussen ◽  
Lisa J. Funkhouser-Jones ◽  
Marianna E. Akey ◽  
Deborah A. Schaefer ◽  
Kevin Ackman ◽  
...  

AbstractThe protozoan parasite Cryptosporidium is a leading cause of diarrheal disease in those with compromised or under-developed immune systems, particularly infants and toddlers in resource-poor localities. As an enteric pathogen, Cryptosporidium invades the apical surface of intestinal epithelial cells, where it resides in close proximity to metabolites in the intestinal lumen. However, the effect of gut metabolites on susceptibility to Cryptosporidium infection remains largely unstudied. Here, we first identified which gut metabolites are prevalent in neonatal mice when they are most susceptible to Cryptosporidium parvum infection, and then tested the isolated effects of these metabolites on C. parvum invasion and growth. Our findings demonstrate that medium or long-chain saturated fatty acids inhibit C. parvum growth, while long-chain unsaturated fatty acids enhance C. parvum invasion. The influence of these two classes of metabolites on C. parvum infection likely reflects the streamlined metabolism in C. parvum, which is unable to synthesize fatty acids. Hence, gut metabolites, either from diet or produced by the microbiota, play an important role in the early susceptibility to cryptosporidiosis seen in young animals.ImportanceCryptosporidium occupies a unique intracellular niche that exposes the parasite to both host cell contents and the intestinal lumen, including metabolites from the diet and produced by the microbiota. Both dietary and microbial products change over the course of early development, and could contribute to the changes seen in susceptibility to cryptosporidiosis in humans and mice. Consistent with this model, we show that the immature gut metabolome influenced growth of C. parvum in vitro and may increase susceptibility to infection in young mice. Interestingly, metabolites that significantly altered parasite growth were fatty acids, a class of molecules that Cryptosporidium is unable to synthesize de novo. The enhancing effects of polyunsaturated fatty acids and the inhibitory effects of saturated fatty acids provide further insight into reliance on fatty acid salvage and metabolism of this enteric parasite.


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.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Weng Sheng Kong ◽  
Naohiro Tsuyama ◽  
Hiroko Inoue ◽  
Yun Guo ◽  
Sho Mokuda ◽  
...  

AbstractBreastfeeding influences the immune system development in infants and may even affect various immunological responses later in life. Breast milk provides a rich source of early nutrition for infant growth and development. However, the presence of certain compounds in breast milk, related to an unhealthy lifestyle or the diet of lactating mothers, may negatively impact infants. Based on a cohort study of atopic dermatitis (AD), we find the presence of damage-associated molecular patterns (DAMPs) activity in the mother’s milk. By non-targeted metabolomic analysis, we identify the long-chain saturated fatty acids (LCSFA) as a biomarker DAMPs (+) breast milk samples. Similarly, a mouse model in which breastfed offspring are fed milk high in LCSFA show AD onset later in life. We prove that LCSFA are a type of damage-associated molecular patterns, which initiate a series of inflammatory events in the gut involving type 3 innate lymphoid cells (ILC3s). A remarkable increase in inflammatory ILC3s is observed in the gut, and the migration of these ILC3s to the skin may be potential triggers of AD. Gene expression analysis of ILC3s isolated from the gut reveal upregulation of genes that increase ILC3s and chemokines/chemokine receptors, which may play a role in ILC migration to the skin. Even in the absence of adaptive immunity, Rag1 knockout mice fed a high-LCSFA milk diet develop eczema, accompanied by increased gut ILC3s. We also present that gut microbiota of AD-prone PA milk-fed mice is different from non-AD OA/ND milk-fed mice. Here, we propose that early exposure to LCSFAs in infants may affect the balance of intestinal innate immunity, inducing a highly inflammatory environment with the proliferation of ILC3s and production of interleukin-17 and interleukin-22, these factors may be potential triggers or worsening factors of AD.


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.


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