Fatty Acid Metabolism - What is Life HOME

Lipids and amino acids can also be used as energy sources, but they enter the main pathways at different points. has a functional methylmalonyl-CoA epimerase (racemase) that is involved in propionyl-CoA metabolism for the degradation of branched amino acids and odd-chain fatty acids (). Fatty acid moieties of lipids are broken down by -oxidation into acetyl-CoA (which in turn can enter the TCA cycle). -oxidation occurs in the mitochondrial matrix and also yields reduced electron carriers. Peroxisomal -oxidation of long-chain fatty acids is not linked directly to energy metabolism because the reduced electron carrier is directly oxidized by molecular oxygen (yielding hydrogen peroxide). Amino acids can be broken down via distinct pathways and their carbon skeletons can be metabolized in the TCA cycle.

Fatty Acid Bio Synthesis | Biosynthesis | Metabolism

May 1, 2002. Synthesis of Unsaturated Fatty Acids Linoleic Acid. Walter J. Gensler. Reactions of the Hydrocarbon Chain of Fatty Acids. H. J. Harwood. A second unique step in unsaturated fatty acid biosynthesis. Earlier studies 12 of the fab 13 mutants have yielded the fol- lowing information. a Synthesis of.


Biosynthesis of unsaturated fatty acids

Biosynthesis of Saturated Fatty acids Notes

The search for a chemically defined medium that would support sustained population growth of led to the formulation of a mixture, designated EM1, which was based on the amino acid ratios found in (). This medium was later modified by ) and called Maintenance Medium (CbMM). This medium contained a total of 53 components consisting of minerals, glucose, amino acids, vitamins, growth factors and precursors for nucleic acid synthesis (adjusted to pH 5.9 with KOH). Maintenance Medium (CeMM) has the same basal composition, but contains either more glucose or potassium acetate for energy (; ). This basal medium, which can be replaced by 3% soy peptone and 3% yeast extract, must be further supplemented with sterol and a heme source.


What are the precusors of the biosynthesis of fatty acids?

The lipid portion of the endotoxin, lipid A, is chemically distinct from allother lipids in biological membranes and consists of characteristic 3-hydroxyfatty acids, primarily with carbon chain lengths from 10 to 18, attached tohydroxyl and amino groups of a disaccharide backbone. It has been proposedthat 3-hydroxy fatty acid quantification may be employed as biomarkers ofendotoxins and Gram-negative bacterial community in atmospheric aerosols ().

Fatty Acids :biosynthesis + Report

Free-living nematodes have the ability to synthesize saturated and unsaturated fatty acids (), and they typically store energy as lipids. Recently, it was found that most lipid species in (triglycerides, phospholipids, sphingolipids, etc.) are composed of fatty acids directly absorbed from the bacterial food source (C. Perez and M. Van Gilst, personal communication). Up to 35% of the dry body mass of is lipid, and triacyl glyceride fat stores (~40-55% of total lipids) are the major energy storage molecules (; ; see ). Carbohydrate stores consist primarily of glycogen (3.3% of the dry body mass, ), but significant amounts of trehalose and glucose are also present (; ). Interestingly, O-GlcNac transferase (OGT) modulates the relative use of these macronutrient storage molecules. OGT knockout mutants have a 3-fold elevation of trehalose levels and glycogen stores with a concomitant 3-fold decrease in triglyceride levels (). ) observed that the species rapidly metabolized glycogen when starved. Dauer larvae rely on their lipid reserves for long-term survival ().

Biosynthesis of Fatty Acids & Eicosanoids | …

The dauer stage is an alternative third stage larva that is formed under unfavorable conditions, and is specialized for survival and dispersal (see ). Since dauers do not feed, they must metabolize stored macronutrients, mainly lipids, but also glycogen and trehalose, and suppress energy-consuming metabolic activities. This is indeed the case; dauers consume less oxygen when compared to other juvenile stages (; ; ) and produce less heat (), consistent with an overall reduction of metabolic rate. This appears to be caused by the reduced activities of the enzymes involved in the glycolytic, gluconeogenic, TCA cycle and oxidative phosphorylation pathways in dauers, relative to those of adults (). Micro-array and SAGE analyses of dauer larvae versus recovered dauers or mixed stage populations suggested that the transcription of enzymes involved in the -oxidation of fatty acids, glycolysis, glyoxylate and gluconeogenesis pathways was enhanced, indicating that triglycerides were being converted into sugars (; ; ; ; ). The flux of metabolites through the glyoxylate cyle is relatively more important in the dauer, although this shift is mainly due to a substantial decrease of the carbon flux through the TCA cycle rather than an increased flux through the glyoxylate cycle (). Phosphoenolpyruvate-carboxykinase (PEPCK) levels are relatively high in the dauer, indicating that gluconeogenesis is elevated, but glycogen re-synthesis is apparently suppressed, as indicated by the relatively low activity of fructose 1,6-bisphosphatase (). Thus, the high level of PEPCK activity in dauers is more likely to be associated with the fixation of CO2 into phosphoenolpyruvate to form oxaloacetate, which can be converted to malate and used in other pathways, thereby providing a useful anaplerotic mechanism for the starving dauer larva. The conversion of lipids into sugars may also be required for transportation of energy from lipid-containing cells (intestine and epidermis) into other tissues (muscle, neurons) (). Since the genome does not contain a functional glucose-6-phosphatase, it is assumed that trehalose, rather than glucose is used as a transport sugar () ().