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Novel metaled fatty polyesters were prepared using polytransesterification reactions between dimethyl terephthalate (DMT) and different fatty metaled (Si/Ge) alcohol obtained from the undec-10-en-1-ol. The corresponding yields were excellent and the structure of the polyesters were determined by spectroscopic methods. Considering one hour of polymerization, the polymers exhibited acceptable molecular weights. The thermogravimetric analysis showed that these polyesters were more stable than their corresponding monomers and presented thermal degradation above 400°C. [ABSTRACT FROM AUTHOR]

The combination of surfactants and fatty alcohols leads to the formation of lamellar gel network (LGNs) which are widely used in cosmetic and pharmaceutical industries. Alkyl polyglucosides are known to stabilize oil-in- water emulsions and here, we report their use in combination with fatty alcohol for the stabilization of all-aqueous water-in-water (W/W) emulsions based on dextran-in-poly(ethylene glycol). Two different APGs were used: decyl glucoside and lauryl glucoside. We systematically studied the influence of the concentrations of APGs, and the molar ratio between the APGs and decanol as model fatty alcohol on the size and stability of the aqueous emulsion droplets with time. The self-assembled structure formed by decanol/APGs was characterized by using Small Angle X-ray Scattering and confocal microscopy, and shown to be lamellar in the bulk phase and probably also at the surface of dextran-rich droplets. We also demonstrated that the stabilization of W/W emulsions can be extended to other alkyl polyglucoside and to other fatty alcohols. In addition, we reported the production of a foam using such W/W emulsions as the continuous phase. Our results show that it is possible to stabilized W/W emulsions using LGNs based on different APGs and fatty alcohols, which will undoubtedly expand the use of W/W emulsions for various fields. [ABSTRACT FROM AUTHOR]

To evaluate a potential thermal battery material for thermal energy storage applications, this study prepared a stable organic nano-dispersed PCM (NDPCM) with 1-tetradecanol (TD) with a melting point and latent heat of 37.8 °C and 236.4 J/g, respectively, as base PCM and investigated its thermal properties. The high thermal conductive nano-additives of functionalized multi-walled carbon nanotubes (MWCNT-COOH) with a concentration range of 1 wt% to 5 wt% were infused in the pure PCM. As a result, MWCNT-COOH shows better dispersion stability. The SEM microimage confirms no agglomeration was observed for the prepared NDPCM. The supercooling was reduced from 10.6 °C for the pure TD to 7.7 °C for TD with 5 wt% of MWCNT. The latent heat of the NDPCM with 5 wt% MWCNT-COOH was 212.6 J/g with a 10% reduction compared to pure TD. The reduction in latent heat values is lower than the previously investigated TD composite PCM. The thermal stability study through gravimetric analysis confirms that the decomposition of the NDPCMs initiates at 200 °C, which will not be affected by thermal fluctuation in the system. The sample with 5 wt% of nano-additives had the most excellent thermal conductivity (TC) improvement, 56.2% in the liquid phase, whereas 50% in the solid phase. The reported values are significantly higher compared to the previous thermal conductivity improvement of TD using metallic nanoparticles. The prepared NDPCM shows better thermal properties than the pure PCM and can be a possible material for high-density thermal energy storage applications.

Abstract Efficient conversion of pentose sugars remains a significant barrier to the replacement of petroleum-derived chemicals with plant biomass-derived bioproducts. While the oleaginous yeast Rhodosporidium toruloides (also known as Rhodotorula toruloides) has a relatively robust native metabolism of pentose sugars compared to other wild yeasts, faster assimilation of those sugars will be required for industrial utilization of pentoses. To increase the rate of pentose assimilation in R. toruloides, we leveraged previously reported high-throughput fitness data to identify potential regulators of pentose catabolism. Two genes were selected for further investigation, a putative transcription factor (RTO4_12978, Pnt1) and a homolog of a glucose transceptor involved in carbon catabolite repression (RTO4_11990). Overexpression of Pnt1 increased the specific growth rate approximately twofold early in cultures on xylose and increased the maximum specific growth by 18% while decreasing accumulation of arabitol and xylitol in fast-growing cultures. Improved growth dynamics on xylose translated to a 120% increase in the overall rate of xylose conversion to fatty alcohols in batch culture. Proteomic analysis confirmed that Pnt1 is a major regulator of pentose catabolism in R. toruloides. Deletion of RTO4_11990 increased the growth rate on xylose, but did not relieve carbon catabolite repression in the presence of glucose. Carbon catabolite repression signaling networks remain poorly characterized in R. toruloides and likely comprise a different set of proteins than those mainly characterized in ascomycete fungi.

[Display omitted] Sculpting liquids into different shapes is usually based on the interfacial interactions of functionalized nanoparticles or polymers with specific ligands, leading to exciting material properties due to the combination of the mobility of liquid components with the solid-like characteristic of the arrested liquid/liquid interface. There is an intense interest in novel structured liquids produced from simple compounds with versatile application potentials. Complexes of oppositely charged commercial polyelectrolytes and traditional aliphatic surfactants are good candidates for this goal since they reveal rich structural features and could adsorb at various interfaces. However, they have not been applied yet for structuring liquids. The interfacial interactions and film formation between aqueous sodium poly(styrene) sulfonate solutions (NaPSS) and hexadecylamine (HDA) solutions in various alkanols were investigated by surface tension measurements and ATR-IR spectroscopy. 3D printing experiments also assessed the robustness of the formed films. Arrested fatty alcohol/water interfaces were formed due to the interfacial association of NaPSS, HDA, and alkanol molecules, which also act as cosurfactants in the surface region. These solid films enable the synthesis of temperature-sensitive all-in-liquid constructs and offer alternatives to bulk polyion/mixed surfactant assemblies prepared earlier through numerous synthesis steps. [ABSTRACT FROM AUTHOR]

Fatty alcohols are important products in the chemical industry, given that they are frequently used in the formulation of surfactants and lubricants. In this context, this work describes a catalytic heterogeneous approach for the production of 1-octadecanol (C18OH) from ethyl stearate (ES) using nanosized Ru-supported on tungstated zirconia (W/Zr). The activity and selectivity of this series of catalysts have been studied during the hydrogenation of ES in a batch reactor at 175 °C and PH2 = 40 bar. The so-prepared catalysts were characterized by a sort of characterization techniques (i.e., X-ray diffraction, H2-TPR, etc.), confirming the high dispersion and higher reducibility of Ru nanoparticles on the W/Zr surface (primarily tetragonal zirconia) with respect to pure zirconia. Overall, the catalysts were significantly active. In addition, a strong synergistic effect was revealed between Ru and W species, according to catalytic data. Finally, the reaction sequence towards fatty alcohol has also been elucidated, pointing to the ester hydrogenolysis to the aldehyde and ulterior hydrogenation of the latter as the main route for fatty alcohol formation. [ABSTRACT FROM AUTHOR]

The combination of surfactants and fatty alcohols leads to the formation of lamellar gel network (LGNs) which are widely used in cosmetic and pharmaceutical industries. Alkyl polyglucosides are known to stabilize oil-in-water emulsions and here, we report their use in combination with fatty alcohol for the stabilization of all-aqueous water-in-water (W/W) emulsions based on dextran-in-poly(ethylene glycol). Two different APGs were used: decyl glucoside and lauryl glucoside. We systematically studied the influence of the concentrations of APGs, and the molar ratio between the APGs and decanol as model fatty alcohol on the size and stability of the aqueous emulsion droplets with time. The self-assembled structure formed by decanol/APGs was characterized by using Small Angle X-ray Scattering and confocal microscopy, and shown to be lamellar in the bulk phase and probably also at the surface of dextran-rich droplets. We also demonstrated that the stabilization of W/W emulsions can be extended to other alkyl polyglucoside and to other fatty alcohols. In addition, we reported the production of a foam using such W/W emulsions as the continuous phase. Our results show that it is possible to stabilized W/W emulsions using LGNs based on different APGs and fatty alcohols, which will undoubtedly expand the use of W/W emulsions for various fields.

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Sjögren–Larsson syndrome (SLS) is a rare inherited neurocutaneous disease characterized by ichthyosis, spastic diplegia or tetraplegia, intellectual disability and a distinctive retinopathy. SLS is caused by bi-allelic mutations in ALDH3A2, which codes for fatty aldehyde dehydrogenase (FALDH) and results in abnormal lipid metabolism. The biochemical abnormalities in SLS are not completely known, and the pathogenic mechanisms leading to symptoms are still unclear. To search for pathways that are perturbed in SLS, we performed untargeted metabolomic screening in 20 SLS subjects along with age- and sex-matched controls. Of 823 identified metabolites in plasma, 121 (14.7%) quantitatively differed in the overall SLS cohort from controls; 77 metabolites were decreased and 44 increased. Pathway analysis pointed to disrupted metabolism of sphingolipids, sterols, bile acids, glycogen, purines and certain amino acids such as tryptophan, aspartate and phenylalanine. Random forest analysis identified a unique metabolomic profile that had a predictive accuracy of 100% for discriminating SLS from controls. These results provide new insight into the abnormal biochemical pathways that likely contribute to disease in SLS and may constitute a biomarker panel for diagnosis and future therapeutic studies. [ABSTRACT FROM AUTHOR]

Fatty alcohols (FOHs) are important feedstocks in the chemical industry to produce detergents, cosmetics, and lubricants. Microbial production of FOHs has become an attractive alternative to production in plants and animals due to growing energy demands and environmental concerns. However, inhibition of cell growth caused by intracellular FOH accumulation is one major issue that limits FOH titers in microbial hosts. In addition, identification of FOH-specific exporters remains a challenge and previous studies towards this end are limited. To alleviate the toxicity issue, we exploited nonionic surfactants to promote the export of FOHs in Rhodosporidium toruloides, an oleaginous yeast that is considered an attractive next-generation host for the production of fatty acid-derived chemicals. Our results showed FOH export efficiency was dramatically improved and the growth inhibition was alleviated in the presence of small amounts of tergitol and other surfactants. As a result, FOH titers increase by 4.3-fold at bench scale to 352.6 mg/L. With further process optimization in a 2-L bioreactor, the titer was further increased to 1.6 g/L. The method we show here can potentially be applied to other microbial hosts and may facilitate the commercialization of microbial FOH production.

Abstract Background Construction of efficient microbial cell factories is one of the core steps for establishing green bio-manufacturing processes. However, the complex metabolic regulation makes it challenging in driving the metabolic flux toward the product biosynthesis. Dynamically coupling the biosynthetic pathways with the cellular metabolism at spatial–temporal manner should be helpful for improving the production with alleviating the cellular stresses. Results In this study, we observed the mismatch between fatty alcohol biosynthesis and cellular metabolism, which compromised the fatty alcohol production in Saccharomyces cerevisiae. To enhance the fatty alcohol production, we spatial-temporally regulated fatty alcohol biosynthetic pathway by peroxisomal compartmentalization (spatial) and dynamic regulation of gene expression (temporal). In particular, fatty acid/acyl-CoA responsive promoters were identified by comparative transcriptional analysis, which helped to dynamically regulate the expression of acyl-CoA reductase gene MaFAR1 and improved fatty alcohol biosynthesis by 1.62-fold. Furthermore, enhancing the peroxisomal supply of acyl-CoA and NADPH further improved fatty alcohol production to 282 mg/L, 2.52 times higher than the starting strain. Conclusions This spatial–temporal regulation strategy partially coordinated fatty alcohol biosynthesis with cellular metabolism including peroxisome biogenesis and precursor supply, which should be applied for production of other products in microbes.

Tridodecylborate (TD), tritetradecylborate (TT) and trioctadecylborate (TO) were produced as solid-liquid phase change materials (SL-PCMs) for thermal energy storage (TES) applications via condensation of boric acid and 1-dodecanol, 1-tetradecanol, and 1-octadecanol, respectively. Boron is used for the first time in the production of such synthetic PCMs instead of carbonaceous compounds. Produced fatty boron ether compounds were structurally characterized by using FT-IR and proton and carbon NMR spectroscopy methods as they were thermally characterized by DSC and time/temperature analysis techniques. Melting points of TD, TT, and TO are in the range of 10.1–10.8, 26.9–27.0, and 50.8–51.8°C in the thermal cycling tests, respectively, while solid-liquid phase change melting/crystallization enthalpies of them are 110.4/-112.8, 125.7/-132.3, and 141.8/-149.9 Jg-1, respectively. That is, the produced fatty boron-ethers had different operating temperatures than the fatty alcohols from which they were produced and could produce significant enthalpy values for heat energy storage applications. The increase in chain length caused an increase in enthalpy values as in fatty alcohols. The lack of PCM with similar melting and enthalpy values expands the usage area of synthesized boron-ethers. The thermal stability of fatty boron ether compounds (TD, TT, and TO) were tested by 10 times repeated DSC measurements instead of accelerated thermal cycling and FTIR spectroscopy analysis after these operations. In the surface examinations of boron ethers, original crystal formation was observed, and the loss of appearance above the phase transition temperature indicated amorphous transformation. In addition, it has been proven in the TG investigations that the fatty boron ethers produced can remain intact up to higher temperatures than fatty alcohols. [ABSTRACT FROM AUTHOR]

Lipid biosynthesis plays a vital role in living cells and has been increasingly engineered to overproduce various lipid-based chemicals. However, owing to the tightly constrained and interconnected nature of lipid biosynthesis, both understanding and engineering of lipid metabolism remain challenging, even with the help of mathematical models. Here we report the development of a kinetic metabolic model of lipid metabolism in Saccharomyces cerevisiae that integrates fatty acid biosynthesis, glycerophospholipid metabolism, sphingolipid metabolism, storage lipids, lumped sterol synthesis, and the synthesis and transport of relevant target-chemicals, such as fatty acids and fatty alcohols. The model was trained on lipidomic data of a reference S. cerevisiae strain, single knockout mutants, and lipid overproduction strains reported in literature. The model was used to design mutants for fatty alcohol overproduction and the lipidomic analysis of the resultant mutant strains coupled with model-guided hypothesis led to discovery of a futile cycle in the triacylglycerol biosynthesis pathway. In addition, the model was used to explain successful and unsuccessful mutant designs in metabolic engineering literature. Thus, this kinetic model of lipid metabolism can not only enable the discovery of new phenomenon in lipid metabolism but also the engineering of mutant strains for overproduction of lipids. • Development of a kinetic model of lipid metabolism in Saccharomyces cerevisiae • Discovery of a futile cycle in the triacylglycerol biosynthesis pathway • Rationalization of mutant designs for fatty alcohol overproduction in literature [ABSTRACT FROM AUTHOR]

Background: Construction of efficient microbial cell factories is one of the core steps for establishing green bio-manufacturing processes. However, the complex metabolic regulation makes it challenging in driving the metabolic flux toward the product biosynthesis. Dynamically coupling the biosynthetic pathways with the cellular metabolism at spatial–temporal manner should be helpful for improving the production with alleviating the cellular stresses. Results: In this study, we observed the mismatch between fatty alcohol biosynthesis and cellular metabolism, which compromised the fatty alcohol production in Saccharomyces cerevisiae. To enhance the fatty alcohol production, we spatial-temporally regulated fatty alcohol biosynthetic pathway by peroxisomal compartmentalization (spatial) and dynamic regulation of gene expression (temporal). In particular, fatty acid/acyl-CoA responsive promoters were identified by comparative transcriptional analysis, which helped to dynamically regulate the expression of acyl-CoA reductase gene MaFAR1 and improved fatty alcohol biosynthesis by 1.62-fold. Furthermore, enhancing the peroxisomal supply of acyl-CoA and NADPH further improved fatty alcohol production to 282 mg/L, 2.52 times higher than the starting strain. Conclusions: This spatial–temporal regulation strategy partially coordinated fatty alcohol biosynthesis with cellular metabolism including peroxisome biogenesis and precursor supply, which should be applied for production of other products in microbes. [ABSTRACT FROM AUTHOR]

Cu/SBA-15 and Cu-NbO x /SBA-15 catalysts were prepared and evaluated in the hydrogenation of palmitic acid to palmitic alcohol. A high palmitic alcohol yield of 90.8% was obtained using palmitic acid as feedstock. NbO x has been considered to be crucial for the excellent performance and the synergy between Cu and NbO x was well investigated. The interaction between Cu species and NbO x -containing support was studied by various characterizations, such as powder X-ray diffraction (XRD), transmission electron microscopy (TEM), H 2 -temperature programmed reduction (H 2 -TPR) and X-ray photoelectron spectra (XPS) and Auger electron spectroscopy (AES). The kinetic data for rate determining step were also collected. The synergistic effect of Cu and NbO x to catalytic activity was discussed and the following insights were obtained: i) the NbO x doping led to form abundant Cu species with more electron-deficient, which is beneficial for the production of alcohol; ii) the oxygen affinity of NbO x promotes the adsorption of oxygen-containing group. Finally, the natural product of palm oil was taken as feedstock and an ideal yield 84.2% of palmitic alcohol was harvested. [Display omitted] • A catalyst Cu-NbO x /SBA-15 with uniform and small size Cu species supported on SBA-15 was obtained by introducing NbO x species. • The Cu-NbO x /SBA-15 performed excellently in hydrogenation of palmitic acid to palmitic alcohol, with a yield of 90.8%. • The high-efficiency of Cu-NbO x /SBA-15 is attributed to the synergistic effect between Cu and NbO x species. [ABSTRACT FROM AUTHOR]

Catalytic hydrotreating of fatty acid is respected to produce bio-based chemicals especially oleochemicals that can be applied as a high valuable raw material or intermediate materials for industries. Low-cost Ni/LY char and limonite catalysts can compensate the expensively commercial catalysts. Palmitic acid (PA) was represented as reactant. Chemical compositions of liquid product were analyzed and presented in compound group, carbon number distribution and product selectivity. Catalyst characteristics and liquid product properties were also investigated. BET surface area, pore volume, and pore size of the prepared Ni/LY char catalyst were 308 m2/g, 0.188 cm3/g and 2.43 nm, respectively, and those of limonite catalyst were 95 m2/g, 0.3 cm3/g and 12.59 nm, respectively. Based on the initial 3 MPa H2 at 300 °C, the obtained oleochemicals depended on catalyst type, reaction time and solvent. In case of Ni/LY char catalyst, ester was found in yield of 58.94% that mainly contained with isopropyl palmitate up to 82% of ester, meanwhile product from limonite was principally distributed in alcohol group with 51.84% in which n-pentadecanol was the major compound with 37.05% yield. The products showed the oxygen removal in range of 19.11–65.15 mol% and HHVs were increased to 32.11–34.13 MJ/kg when compared with PA.

Fatty alcohols are important products in the chemical industry, given that they are frequently used in the formulation of surfactants and lubricants. In this context, this work describes a catalytic heterogeneous approach for the production of 1-octadecanol (C18OH) from ethyl stearate (ES) using nanosized Ru-supported on tungstated zirconia (W/Zr). The activity and selectivity of this series of catalysts have been studied during the hydrogenation of ES in a batch reactor at 175 °C and PH2 = 40 bar. The so-prepared catalysts were characterized by a sort of characterization techniques (i.e., X-ray diffraction, H2-TPR, etc.), confirming the high dispersion and higher reducibility of Ru nanoparticles on the W/Zr surface (primarily tetragonal zirconia) with respect to pure zirconia. Overall, the catalysts were significantly active. In addition, a strong synergistic effect was revealed between Ru and W species, according to catalytic data. Finally, the reaction sequence towards fatty alcohol has also been elucidated, pointing to the ester hydrogenolysis to the aldehyde and ulterior hydrogenation of the latter as the main route for fatty alcohol formation.

Palm oil‐based fatty alcohol is a basic oleochemical with many different applications depending on its carbon chain length. The carbon chain distribution using a GC‐flame ionization detector (GC‐FID) is a quality control tool for monitoring the composition of either single or blended fatty alcohol. There is a published GC‐FID method but it requires a derivatization step. The objective of this work is to develop a derivatization‐free method with simple preparation steps. It can be used for routine analysis of the carbon chain distribution to determine the composition of palm‐based fatty alcohol. The GC‐FID method developed used a ZB‐FFAP (60 m × 0.25 mm i.d., 0.25 μm film thickness) consisting of polyethylene glycol bonded nitroterephthalic acid phase for separation of eight types of fatty alcohol with a run time of 40 min. The method showed good validation parameters performance in terms of accuracy (as compared with FAL standards), linearity (R2 > 0.9999) and intraday and intermediate precision (CV < 0.05% for retention time and CV < 1.5% for peak area). Monitoring of commercial FAL from local manufacturers showed that the composition was consistent with the required specifications. [ABSTRACT FROM AUTHOR]

Fatty alcohols are widely used in the fields of food, pharmaceutical and renewable energy and so on, thus biosynthesis of fatty alcohols has attracted wide attention in recent years. However, the concentration of fatty alcohols is still at a low level. In this paper, we constructed an Escherichia coli strain with high yield of fatty alcohols through the combinatorial regulation of three key genes of fabH, fabZ, and far. Firstly, we designed new ribosome-binding sequences (RBS) of fabH and fabZ with 10-fold strengths compared to the original ones by RBS calculator, separately. Secondly, we engineered the starting strain MGL1 by replacing the original RBS with designed ones, which resulted in MGLHS (fabH-RBS1), MGLZS (fabZ-RBS2), and MGLHZS (fabH-RBS1/fabZ-RBS2), respectively. Thirdly, the plasmid pL1 harboring far gene was transferred into above strains to test fatty alcohols production under the induction of different isopropyl-β-D-thiogalactoside concentrations. The results showed that the concentration of fatty alcohols in strains MGLHS-far, MGLZS-far and MGLHZS-far reached 2.75 g/L, 2.54 g/L and 3.82 g/L, respectively, which increased 35%, 25% and 88% than that of the starting strain MGL1-far. The fatty alcohols reached 9.35 g/L in fed batch fermentation with MGLHZS-far, of which the main components were two saturated fatty alcohols (C14:0 and C16:0) and two unsaturated fatty alcohols (C16:1 and C18:1). The results demonstrated that combinatorial regulation of three key genes of fabH, fabZ, and far in E. coli can achieve high-yield production of fatty alcohols. [ABSTRACT FROM AUTHOR]

Triterpenoids and fatty alcohols were identified from the sediments of five mangrove ecosystems (Kunjimangalam, Pazhayangadi, Pappinissery, Thalassery, and Kadalundi) in the northern Kerala coast, India, to illustrate the organic matter sources. Straight chain fatty alcohols in the range C12–32 were detected, and among these the long chain fatty alcohols (C20–32) were exclusively even chained compounds. Branched fatty alcohols (6,10,14-trimethyl-pentadecan-2-ol and 3,7,11,15-tetramethyl-2-hexadecanol) of bacterial origin were detected in a few observations. Twenty triterpenoids were detected from the study region in which 13 of them were sterols. Triterpenoids originated from higher plants such as stigmasterol, campesterol, β-sitosterol, taraxerol, lupeol, germanicol, β-amyrin, α-amyrin, and betulin were identified in the study. Brassicasterol, a diatom marker and dinosterol, a dinoflagellates marker were also detected in the study region. An elevated % composition of dinosterol and dissolved oxygen super-saturation were noticed in Kunjimangalam during pre-monsoon, which may suggest elevated input of algal organic matter in the mangrove system. Cholesterol transformation products such as coprostanol and epi-coprostanol were detected, which indicated the presence of fecal contamination in the sedimentary organic matter. From the ternary diagram, it was recognized that the organic matter contribution from marine algae was feeble as compared to terrestrial input. [ABSTRACT FROM AUTHOR]

Sjögren–Larsson syndrome (SLS) is a rare inherited neurocutaneous disease characterized by ichthyosis, spastic diplegia or tetraplegia, intellectual disability and a distinctive retinopathy. SLS is caused by bi-allelic mutations in ALDH3A2, which codes for fatty aldehyde dehydrogenase (FALDH) and results in abnormal lipid metabolism. The biochemical abnormalities in SLS are not completely known, and the pathogenic mechanisms leading to symptoms are still unclear. To search for pathways that are perturbed in SLS, we performed untargeted metabolomic screening in 20 SLS subjects along with age- and sex-matched controls. Of 823 identified metabolites in plasma, 121 (14.7%) quantitatively differed in the overall SLS cohort from controls; 77 metabolites were decreased and 44 increased. Pathway analysis pointed to disrupted metabolism of sphingolipids, sterols, bile acids, glycogen, purines and certain amino acids such as tryptophan, aspartate and phenylalanine. Random forest analysis identified a unique metabolomic profile that had a predictive accuracy of 100% for discriminating SLS from controls. These results provide new insight into the abnormal biochemical pathways that likely contribute to disease in SLS and may constitute a biomarker panel for diagnosis and future therapeutic studies.

Various lipids (mainly meibum lipids secreted by the meibomian glands) are present in the tear film lipid layer and play important roles in tear stability and the health of the cornea and conjunctiva. Many meibum lipids contain fatty alcohols (FAls) with chain lengths ≥C24, but the fatty acyl‐CoA reductases (FARs) that produce them remain unclear. Here, using cell‐based assays, we found that the two FAR isozymes (FAR1 and FAR2) show different substrate specificities: FAR1 and FAR2 are involved in the production of C16–C18 and ≥C20 FAls, respectively. Next, we generated Far2 knockout (KO) mice and examined their dry eye phenotype and meibum lipid composition. These mice showed a severe dry eye phenotype, characterized by plugged meibomian gland orifices, corneal damage, and tear film instability. The plugging was attributed to an increase in the melting point of the meibum lipids. Liquid chromatography coupled with tandem mass spectrometry revealed that FAl‐containing meibum lipids (wax monoesters and types 1ω, 2α, and 2ω wax diesters) with a hydroxyl group at position 1 were almost completely absent in Far2 KO mice. The levels of di‐unsaturated (O‐acyl)‐ω‐hydroxy fatty acids were higher in Far2 KO mice than in wild type mice, but those of tri‐unsaturated ones were comparable, suggesting the presence of two synthesis pathways for type 1ω wax diesters. These results indicate the importance of FAl‐containing meibum lipids in the formation of a functional tear film lipid layer. In addition, our study provides clues to the molecular mechanism of the biosynthesis of meibum lipids. [ABSTRACT FROM AUTHOR]

[Display omitted] Catalytic hydrotreating of fatty acid is respected to produce bio-based chemicals especially oleochemicals that can be applied as a high valuable raw material or intermediate materials for industries. Low-cost Ni/LY char and limonite catalysts can compensate the expensively commercial catalysts. Palmitic acid (PA) was represented as reactant. Chemical compositions of liquid product were analyzed and presented in compound group, carbon number distribution and product selectivity. Catalyst characteristics and liquid product properties were also investigated. BET surface area, pore volume, and pore size of the prepared Ni/LY char catalyst were 308 m2/g, 0.188 cm3/g and 2.43 nm, respectively, and those of limonite catalyst were 95 m2/g, 0.3 cm3/g and 12.59 nm, respectively. Based on the initial 3 MPa H 2 at 300 °C, the obtained oleochemicals depended on catalyst type, reaction time and solvent. In case of Ni/LY char catalyst, ester was found in yield of 58.94% that mainly contained with isopropyl palmitate up to 82% of ester, meanwhile product from limonite was principally distributed in alcohol group with 51.84% in which n-pentadecanol was the major compound with 37.05% yield. The products showed the oxygen removal in range of 19.11–65.15 mol% and HHVs were increased to 32.11–34.13 MJ/kg when compared with PA. [ABSTRACT FROM AUTHOR]

Evaporation is the main outflow of many water bodies. In hypersaline Lake Urmia (LU), which has experienced significant shrinkage during the last 3 decades, evaporation is the only water outflow. The 15-year daily saline water evaporation pan data collected near the lake indicate that approximately 71% of the annual evaporation occurred from May to September, about 4.15 billion m3/year. To reduce this water loss, three self-assembled layer coatings—fatty alcohols of stearyl and cetyl with stearic acid in hexane solvents, stearyl and cetyl alcohols with stearic acid powder, and stearyl and cetyl alcohols in ethanol solvents—were tested on pools and evaporation pans adjacent to LU in July, when the lake had the highest evaporation rate. Results of 60 h of experiments for each test showed that the coating composed of stearyl and cetyl alcohols with stearic acid in hexane had the best performance and could reduce evaporation by about 52%. This suggests that applying this coating to LU for 5 months/year could reduce the lake evaporation by about 1.5 billion m3 , which is more than the total annual supply of the main river flowing into the lake. A short-term study of Artemia urmiana indicated that the coatings did not have a significant effect on their length and weight. However, long-term side effects on human health and the environment need further investigation. [ABSTRACT FROM AUTHOR]

Sjögren-Larsson syndrome (SLS) is a neurocutaneous disease caused by mutations in ALDH3A2 that result in deficient fatty aldehyde dehydrogenase (FALDH) activity and impaired fatty aldehyde and fatty alcohol oxidation. The pathogenesis of SLS is thought to involve accumulation of long-chain fatty aldehydes and alcohols and/or metabolically-related ether glycerolipids. Fatty aldehydes are particularly toxic molecules that can covalently react with proteins and certain amino-containing lipids such as phosphatidylethanolamine (PE), generating an unusual aldehyde adduct, N-alkyl-PE (NAPE). Using Faldh-deficient Chinese hamster ovary cells (FAA-K1A) as a cellular model for SLS, we investigated the ability of an aldehyde trapping agent, ADX-102 [2-(3-amino-6-chloro-quinolin-2-yl)-propan-2-ol], to mitigate the harmful effects of fatty aldehydes. FAA-K1A cells were protected from octadecanal (C18:0-al) induced cytotoxicity and apoptosis by ADX-102. Metabolism of C18:0-al to fatty alcohol (octadecanol) was also inhibited by ADX-102. FAA-K1A cells accumulated 5-fold more NAPE with C16- and C18-linked N-alkyl chains compared to wild-type cells, but NAPE levels decreased to normal after growth for 4 days with 50 μM ADX-102. Our results suggest that small aldehyde-reactive molecules, such as ADX-102, should be explored as novel therapeutic agents for SLS by preventing aldehyde adduct formation with critical cellular targets and inhibiting fatty aldehyde metabolism to fatty alcohol.

Construction of efficient microbial cell factories always requires assembling biosynthetic pathways and rewiring cellular metabolism with overexpression of multiple genes. Genomic integration is considered to be helpful for stable gene expression in compared with the episomal plasmids. However, the limited availability of suitable loci hinders the extensive metabolic engineering. We here characterized 30 neutral sites in Saccharomyces cerevisiae genome that did not affect cellular fitness by using expression cassettes of green fluorescent protein (eGFP) and fatty acyl-CoA reductase (MaFAR1) with the aid of efficient CRISPR-Cas9 technique. We found that integration of gene expression cassettes to different genome loci resulted a varied GFP signal and fatty alcohol production, which showed that genomic loci could be used for tuning gene expression. The characterized set of neutral sites should be helpful for extensively metabolic engineering of S. cerevisiae for chemical production and other purposes. [ABSTRACT FROM AUTHOR]

Fatty alcohol‐polysorbate 60‐water ternary systems were used as models to represent the continuous phases of the respective semisolid oil‐in‐water emulsions for topical delivery of cosmetic and medicinal agents. The influence of batch variation of polysorbate 60 and fatty alcohol on structure and consistency of these systems was investigated using microscopy, rheology, differential scanning calorimetry and X‐ray scattering techniques. The polysorbate 60 : cetostearyl alcohol mixed emulsifying wax showed swelling in water, that is, the lamellar repeat distance continually augmented from 93 to 125 Å with water percentage 20–90%. Cetostearyl alcohol ternary systems were thicker than cetyl alcohol ones independently of polysorbate 60 batches used. All the ternary systems showed an initial increase in consistency over the first 2 weeks of storage, which was followed by slight changes in consistency (cetostearyl alcohol systems) due to the re‐allocation of polysorbate 60 molecules in the gel network or significant breakdown of structure (cetyl alcohol systems) due to the transformation of swollen α‐lamellar gel phase into β, γ crystals on 25°C storage. With all fatty alcohols, the consistency of polysorbate 60 ternary system was directly dependent upon interlamellar water thickness as governed by the length and distribution of polyoxyethylene groups within polysorbate 60 molecules. In relation with the composition of polysorbate 60 batches used, the consistency of ternary systems was higher when prepared with the polysorbate 60 batch containing a greater amount of sorbitan polyoxyethylene monoesters. It was proposed that the swollen α‐crystalline gel phase could be better formed by sorbitan polyoxyethylene monoesters rather than sorbitan polyoxyethylene diesters. [ABSTRACT FROM AUTHOR]

Context A variety of Acmella oleracea (L.) R.K. Jansen (Asteraceae) is used by the Mizo people of India and Myanmar for intestinal helminthiasis. Objective To perform a chemical analysis of the plant extract using gas chromatography-mass spectrometry (GC-MS) and test the anthelmintic activity on intestinal parasites. Materials and methods An extract of the aerial parts was prepared in hexane and analysed using GC-MS. Survival test was performed in vitro on the cestode, Taenia tetragona, and the nematode, Ascaridia perspicillum. Concentrations of 1.25, 2.5, 5, 10 and 20 mg/mL, prepared in phosphate-buffered saline (PBS) with 1% dimethylsulphoxide (DMSO), were tested. Negative control was maintained in PBS with DMSO, and albendazole was used as a reference drug. Each treatment consisted of six worms and was done until death was confirmed. Scanning electron microscopy was used to describe the structural changes. Results Nineteen compounds were detected. The major compounds were fatty alcohols such as 3,7,11,15-tetramethylhexadec-2-en-1-ol and (9Z)-9-hexadecen-1-ol. Important bioactive compounds including an alkylamide, N-isobutyl-(2E,4Z,8Z,10E)-dodecatetraenamide, and a triterpenoid, lupeol, were also confirmed. The lethal concentration (LC50) of the plant extract was 5128.61 ppm on T. tetragona and 8921.50 ppm on A. perspicillum. Tegumental shrinkage, erosion of microtriches, and distortion of the suckers were observed on the cestode. The nematode showed collapse of the lips and shrunk cuticle. Conclusions Acmella oleracea contains important bioactive compounds, which are responsible for the broad-spectrum anthelmintic activity. Further study on the pharmacology of the compounds is warranted.

SUMMARY: Suberin is a complex hydrophobic polymer of aliphatic and phenolic compounds which controls the movement of gases, water, and solutes and protects plants from environmental stresses and pathogenic infection. The synthesis and regulatory pathways of suberin remain unknown in Brachypodium distachyon. Here we describe the identification of a B. distachyon gene, BdFAR4, encoding a fatty acyl‐coenzyme A reductase (FAR) by a reverse genetic approach, and investigate the molecular relevance of BdFAR4 in the root suberin synthesis of B. distachyon. BdFAR4 is specifically expressed throughout root development. Heterologous expression of BdFAR4 in yeast (Saccharomyces cerevisiae) afforded the production of C20:0 and C22:0 fatty alcohols. The loss‐of‐function knockout of BdFAR4 by CRISPR/Cas9‐mediated gene editing significantly reduced the content of C20:0 and C22:0 fatty alcohols associated with root suberin. In contrast, overexpression of BdFAR4 in B. distachyon and tomato (Solanum lycopersicum) resulted in the accumulation of root suberin‐associated C20:0 and C22:0 fatty alcohols, suggesting that BdFAR4 preferentially accepts C20:0 and C22:0 fatty acyl‐CoAs as substrates. The BdFAR4 protein was localized to the endoplasmic reticulum in Arabidopsis thaliana protoplasts and Nicotiana benthamiana leaf epidermal cells. BdFAR4 transcript levels can be increased by abiotic stresses and abscisic acid treatment. Furthermore, yeast one‐hybrid, dual‐luciferase activity, and electrophoretic mobility shift assays indicated that the R2R3‐MYB transcription factor BdMYB41 directly binds to the promoter of BdFAR4. Taken together, these results imply that BdFAR4 is essential for the production of root suberin‐associated fatty alcohols, especially under stress conditions, and that its activity is transcriptionally regulated by the BdMYB41 transcription factor. [ABSTRACT FROM AUTHOR]

Fatty alcohols (FA-OH) are aliphatic unbranched primary alcohols with a chain of four or more carbon atoms. Besides potential industrial applications, fatty alcohols have important biological functions as well. In nature, fatty alcohols are produced as a part of a mixture of pheromones in several insect species, such as moths, termites, bees, wasps, etc. In addition, FA-OHs have a potential for agricultural applications, for example, they may be used as a suitable substitute for commercial insecticides. The insecticides have several drawbacks associated with their preparation, and they exert a negative impact on the environment. Currently, pheromone components are prepared mainly through the catalytic hydrogenation of plant oils and petrochemicals, which is an unsustainable, ecologically unfriendly, and highly expensive process. The biotechnological production of the pheromone components using engineered microbial strains and through the expression of the enzymes participating in the biosynthesis of these components is a promising approach that ensures ecological sustenance as well. The present study was aimed at evaluating the production of FA-OHs in the oleaginous yeast, Yarrowia lipolytica, with different lengths of fatty-acyl chains by expressing the fatty acyl-CoA reductase (FAR) BlapFAR4 from B. lapidarius, producing C16:0-OH, C16:1Δ9-OH, and lower quantities of both C14:0-OH and C18:1Δ9-OH, and BlucFAR1 from B. lucorum, producing FA-OHs with a chain length of 18–26 carbon atoms, in this yeast. Among the different novel Y. lipolytica strains used in the present study, the best results were obtained with JMY7086, which carried several lipid metabolism modifications and expressed the BlucFAR1 gene under the control of a strong constitutive promoter 8UAS-pTEF. JMY7086 produced only saturated fatty alcohols with chain lengths from 18 to 24 carbon atoms. The highest titer and accumulation achieved were 166.6 mg/L and 15.6 mg/g DCW of fatty alcohols, respectively. Unlike JMY7086, the BlapFAR4-expressing strain JMY7090 produced only 16 carbon atom-long FA-OHs with a titer of 14.6 mg/L.

Concerns about climate change and environmental destruction have led to interest in technologies that can replace fossil fuels and petrochemicals with compounds derived from sustainable sources that have lower environmental impact. Fatty alcohols produced by chemical synthesis from ethylene or by chemical conversion of plant oils have a large range of industrial applications. These chemicals can be synthesized through biological routes but their free forms are produced in trace amounts naturally. This review focuses on how genetic engineering of endogenous fatty acid metabolism and heterologous expression of fatty alcohol producing enzymes have come together resulting in the current state of the field for production of fatty alcohols by microbial cell factories. We provide an overview of endogenous fatty acid synthesis, enzymatic methods of conversion to fatty alcohols and review the research to date on microbial fatty alcohol production. The primary focus is on work performed in the model microorganisms, Escherichia coli and Saccharomyces cerevisiae but advances made with cyanobacteria and oleaginous yeasts are also considered. The limitations to production of fatty alcohols by microbial cell factories are detailed along with consideration to potential research directions that may aid in achieving viable commercial scale production of fatty alcohols from renewable feedstock.

Owing to their high energy density and composition, fatty acid-derived chemicals possess a wide range of applications such as biofuels, biomaterials, and other biochemical, and as a consequence, the global annual demand for products has surpassed 2million tons. With the exhausting petroleum reservoirs and emerging environmental concerns on using petroleum feedstock, it has become indispensable to shift to a renewable-based industry. With the advancement in the field of synthetic biology and metabolic engineering, the use of microbes as factories for the production of fatty acid-derived chemicals is becoming a promising alternative approach for the production of these derivatives. Numerous metabolic approaches have been developed for conditioning the microbes to improve existing or develop new methodologies capable of efficient oleochemical production. However, there still exist several limitations that need to be addressed for the commercial viability of the microbial cell factory production. Though substantial advancement has been made toward successfully producing these fatty acids derived chemicals, a considerable amount of work needs to be done for improving the titers. In the present review, we aim to address the roadblocks impeding the heterologous production, the engineering pathway strategies implemented across the range of microbes in a detailed manner, and the commercial readiness of these molecules of immense application. [ABSTRACT FROM AUTHOR]

To investigate the effect of fatty alcohol oxidase (FA0) gene disruption on Candida tropicalis, FA01 and FA02 genes were knocked out and complemented by homologous recombination.The growth of mutants and the changes of intracellular fatty alcohol oxidase activity were tested, and the ability of cells to synthesize fatty alcohols using alkanes was further evaluated. Strains FTYT(FA011/FA012), 2aT2bT (FA02a/FA026) and F3YT ( FA011/FA012AFA02a/FA026 ) were successfully constructed.All strains performed similar growth pattern to the control strain when using glucose as a carbon source.However, when using re-alkane( C12-C14) as carbon sources, the growth condition of each strain was different.The growth rate of FTYT strain was faster than other strains, and F3YT strain was significantly inhibited,indicating that the disruption of FA01 and FA02 genes impeded the ability of cells to utilize alkanes and affected cell growth. Compared with the parent strain, both the mutant strains of FTYT (F011 /F012) and F3YT (FA011 /FA012FA02a/FA02b) could convert alkane to 1-dodecanol and the latter strain could accumulate 59. 63 mg/L 1-dodecanol in shake flask fermentation level.FA01 and FA02 genes play an important role in the utilization of alkanes in cells and can serve as potential targets for the metabolic engineering of C.tropicalis for fatty alcohols production. [ABSTRACT FROM AUTHOR]

A variety of Acmella oleracea (L.) R.K. Jansen (Asteraceae) is used by the Mizo people of India and Myanmar for intestinal helminthiasis. To perform a chemical analysis of the plant extract using gas chromatography-mass spectrometry (GC-MS) and test the anthelmintic activity on intestinal parasites. An extract of the aerial parts was prepared in hexane and analysed using GC-MS. Survival test was performed in vitro on the cestode, Taenia tetragona, and the nematode, Ascaridia perspicillum. Concentrations of 1.25, 2.5, 5, 10 and 20 mg/mL, prepared in phosphate-buffered saline (PBS) with 1% dimethylsulphoxide (DMSO), were tested. Negative control was maintained in PBS with DMSO, and albendazole was used as a reference drug. Each treatment consisted of six worms and was done until death was confirmed. Scanning electron microscopy was used to describe the structural changes. Nineteen compounds were detected. The major compounds were fatty alcohols such as 3,7,11,15-tetramethylhexadec-2-en-1-ol and (9Z)-9-hexadecen-1-ol. Important bioactive compounds including an alkylamide, N-isobutyl-(2E,4Z,8Z,10E)-dodecatetraenamide, and a triterpenoid, lupeol, were also confirmed. The lethal concentration (LC50) of the plant extract was 5128.61 ppm on T. tetragona and 8921.50 ppm on A. perspicillum. Tegumental shrinkage, erosion of microtriches, and distortion of the suckers were observed on the cestode. The nematode showed collapse of the lips and shrunk cuticle. Acmella oleracea contains important bioactive compounds, which are responsible for the broad-spectrum anthelmintic activity. Further study on the pharmacology of the compounds is warranted. [ABSTRACT FROM AUTHOR]

The heterocysts present in filamentous cyanobacteria such as Anabaena sp. PCC 7120 are known to be regulated by HetN and PatS, the repressors of heterocyst differentiation; therefore, the inactivation of these proteins will result in the formation of multiple heterocysts. To enhance the accumulation of fatty alcohols synthesized in the heterocyst, we introduced mutations of these repressors to increase heterocyst frequency. First, we isolated double mutants of hetN and patS and confirmed that the null mutation of these genes promoted higher frequencies of heterocyst formation and higher accumulation of heterocyst-specific glycolipids (Hgls) compared with its wild type. Next, we combined hetN and patS mutations with an hglT (encoding glycosyltransferase, an enzyme involved in Hgl synthesis) mutation to increase the accumulation of fatty alcohols since knockout mutation of hglT results in accumulation of very long chain fatty alcohol, the precursor of Hgl. We also observed retarded growth, lower chlorophyll content and up to a five-fold decrease in photosynthetic activity of the hetN/patS/hglT triple mutants. In contrast, the triple mutants showed three times higher heterocyst formation frequencies than the hglT single mutant and wild type. The production rate of fatty alcohol in the triple mutants attained a value 1.41 nmol/mL OD730, whereas accumulation of Hgls in the wild type was 0.90 nmol/mL OD730. Aeration of culture improved the accumulation of fatty alcohols in hetN/patS/hglT mutant cells up to 2.97 nmol/mL OD730 compared with cells cultured by rotation. Our study outlines an alternative strategy for fatty alcohol production supported by photosynthesis and nitrogen fixation.

Abstract Background The filamentous fungus Trichoderma reesei, the most widely used cellulase producer, also has promising applications in lignocellulose-based biorefinery: consolidated bioprocessing for the production of high value-added products. However, such applications are thwarted by the time-consuming metabolic engineering processes (design–build–test–learn cycle) for T. reesei, resulted from (i) the spore separation-mediated purification as the multinucleate hyphae, (ii) transformant screening for high expression levels since unavailable of episomal expression system, and (iii) cases of inexpressible heterologous proteins. Results In this study, a GFP-fusion coupled fluorescence-activated cell sorting (FACS) platform was established to speed up the build and test process of the DBTL cycle, by enabling rapid selection for expressible heterologous genes and bypassing both laborious spore separation and transformant screening. Here, the feasibility of flow cytometry in analyzing and sorting T. reesei cells harboring GFP-fused expressible protein was proven, as well as the application of the platform for constitutive promoter strength evaluation. As a proof-of-concept, the platform was employed to construct the first T. reesei strain producing fatty alcohol, resulting in up to 2 mg hexadecanol being produced per gram biomass. Pathway construction was enabled through rapid selection of functional fatty acyl-CoA reductase encoding gene Tafar1 from three candidate genes and strains with high expression level from spore pools. As a result of using this method, the total costed time for the build and test cycle using T. reesei, subsequently, reduced by approx. 75% from 2 months to 2 weeks. Conclusion This study established the GFP-fusion coupling FACS platform and the first filamentous fungal fatty alcohol-producing cell factory, and demonstrated versatile applications of the platform in the metabolic engineering of filamentous fungi, which can be harnessed to potentially advance the application of filamentous fungi in lignocellulose-based biorefinery.

Sjögren-Larsson syndrome is a genetic disease characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene coding for fatty aldehyde dehydrogenase, an enzyme necessary for oxidation of fatty aldehydes and fatty alcohols. We investigated the cutaneous abnormalities in 9 patients with Sjögren-Larsson syndrome to better understand how the enzymatic deficiency results in epidermal dysfunction. Histochemical staining for aldehyde oxidizing activity was profoundly reduced in the epidermis. Colloidal lanthanum perfusion studies showed abnormal movement of tracer into the extracellular spaces of the stratum corneum consistent with a leaky water barrier. The barrier defect could be attributed to the presence of abnormal lamellar bodies, many with disrupted limiting membranes or lacking lamellar contents. Entombed lamellar bodies were present in the cytoplasm of corneocytes suggesting blockade of lamellar body secretion. At the stratum granulosum-stratum corneum interface, non-lamellar material displaced or replaced secreted lamellar membranes, and in the stratum corneum, the number of lamellar bilayers declined and lamellar membrane organization was disrupted by foci of lamellar/non-lamellar phase separation. These studies demonstrate the presence of a permeability barrier abnormality in Sjögren-Larsson syndrome, which localizes to the stratum corneum interstices and can be attributed to abnormalities in lamellar body formation and secretion.

Abstract Background The ideal biofuel should not only be a regenerative fuel from renewable feedstocks, but should also be compatible with the existing fuel distribution infrastructure and with normal car engines. As the so-called drop-in biofuel, the fatty alcohol 1-octanol has been described as a valuable substitute for diesel and jet fuels and has already been produced fermentatively from sugars in small amounts with engineered bacteria via reduction of thioesterase-mediated premature release of octanoic acid from fatty acid synthase or via a reversal of the β-oxidation pathway. Results The previously engineered short-chain acyl-CoA producing yeast Fas1R1834K/Fas2 fatty acid synthase variant was expressed together with carboxylic acid reductase from Mycobacterium marinum and phosphopantetheinyl transferase Sfp from Bacillus subtilis in a Saccharomyces cerevisiae Δfas1 Δfas2 Δfaa2 mutant strain. With the involvement of endogenous thioesterases, alcohol dehydrogenases, and aldehyde reductases, the synthesized octanoyl-CoA was converted to 1-octanol up to a titer of 26.0 mg L−1 in a 72-h fermentation. The additional accumulation of 90 mg L−1 octanoic acid in the medium indicated a bottleneck in 1-octanol production. When octanoic acid was supplied externally to the yeast cells, it could be efficiently converted to 1-octanol indicating that re-uptake of octanoic acid across the plasma membrane is not limiting. Additional overexpression of aldehyde reductase Ahr from Escherichia coli nearly completely prevented accumulation of octanoic acid and increased 1-octanol titers up to 49.5 mg L−1. However, in growth tests concentrations even lower than 50.0 mg L−1 turned out to be inhibitory to yeast growth. In situ extraction in a two-phase fermentation with dodecane as second phase did not improve growth, indicating that 1-octanol acts inhibitive before secretion. Furthermore, 1-octanol production was even reduced, which results from extraction of the intermediate octanoic acid to the organic phase, preventing its re-uptake. Conclusions By providing chain length control via an engineered octanoyl-CoA producing fatty acid synthase, we were able to specifically produce 1-octanol with S. cerevisiae. Before metabolic engineering can be used to further increase product titers and yields, strategies must be developed that cope with the toxic effects of 1-octanol on the yeast cells.

This study reports the in-depth investigation of the thermophysical properties and thermal reliability of caprylic acid-stearyl alcohol (CA-SA) eutectic phase change material (PCM) for cooling applications. The phase diagram of CA-SA showed a eutectic point at a 90:10 molar ratio. The onset melting/freezing temperature and latent heat of fusion of caprylic acid-stearyl alcohol from the differential scanning calorimetry (DSC) were 11.4 °C/11.8 °C and 154.4/150.5 J/g, respectively. The thermal conductivity for the prepared eutectic PCM in the solid phase was 0.267 W/m.K (0 °C), whereas, in the liquid phase, it was 0.165 W/m.K (20 °C). In addition, the maximum relative percentage difference (RPD) marked at the end of 200 thermal cycles was 5.2% for onset melting temperature and 18.9% for phase change enthalpy. The Fourier transform infrared spectroscopy (FT-IR) result shows that the eutectic PCM holds good chemical stability. Corrosion tests showed that caprylic acid-stearyl alcohol could be a potential candidate for cold thermal energy storage applications.

This study focuses on the preparation, thermophysical and rheological characterization of phase change material nanoemulsions as latent functionally thermal fluids. Aqueous dispersions with fine droplets of cetyl alcohol (with a melting temperature at ~321 K) were prepared by means of a solvent-assisted method, combining ultrasonication with non-ionic and anionic emulsifiers. Eicosyl alcohol (melting at ~337 K) and hydrophobic silica nanoparticles were tested as nucleating agents. Droplet size studies through time and after freeze–thaw cycles confirmed the good stability of formulated nanoemulsions. Phase change analyses proved the effectiveness of eicosyl alcohol to reduce subcooling to a few Kelvin. Although phase change material emulsions exhibited thermal conductivities much larger than bulk cetyl alcohol (at least 60% higher when droplets are solid), reductions in this property reached 15% when compared to water. Samples mainly showed desirable Newtonian behavior (or slight shear thinning viscosities) and modifications in density around melting transition were lower than 1.2%. In the case of phase change material nanoemulsions with 8 wt.% content of dispersed phase, enhancements in the energy storage capacity overcome 20% (considering an operational temperature interval of 10 K around solid–liquid phase change). Formulated dispersions also showed good thermal reliability throughout 200 solidification–melting cycles.

Copyright of Al-Mustansiriyah Journal for Pharmaceutical Sciences is the property of Republic of Iraq Ministry of Higher Education & Scientific Research (MOHESR) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of SDU Journal of Engineering Sciences & Design / Mühendislik Bilimleri ve Tasarım Dergisi is the property of Journal of Engineering Sciences & Design and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Fatty alcohols are widely used for various applications and are found in products ranging from detergents to cosmetics and cleaning agents. Currently, over 3 million tonnes of fatty alcohols are produced per year from bio‐based and petroleum‐based feedstocks through chemical conversion and synthetic processes. However, the environmental impact of current fatty alcohol production processes has become a major concern, and several bioprocesses have emerged as alternative methods for synthesis. These biological processes are environmentally friendly due to their metal‐free nature, low consumption of energy, and mild reaction conditions. This review overviews the current status of fatty alcohol production – both chemical and biological approaches. Our focus is on biological synthesis approaches using biocatalysis and metabolic engineering due to their proven efficacy. Potential downstream processing for these bioprocesses is also presented. © 2020 Society of Chemical Industry and John Wiley & Sons, Ltd [ABSTRACT FROM AUTHOR]

Sjögren-Larsson syndrome (SLS) is a rare genetic neurocutaneous disease caused by mutations in ALDH3A2 that results in deficiency of fatty aldehyde dehydrogenase and accumulation of fatty aldehydes and alcohols. The disease is associated with ichthyosis, spasticity, and intellectual disability. Patients exhibit a characteristic retinopathy with macular crystalline inclusions that first appear in early childhood and increase with age. Once formed, the inclusions are thought to be inert and irreversible. We sought to document how the crystalline inclusions change over time. Serial retinal photographs of 4 SLS subjects (9–23 years old) were taken over a period of 1–3 years. Images were compared by visual inspection and analyzed using ImageJ/Fiji software to observe changes. Visual inspection of retinal photographs of SLS subjects taken over time demonstrated distinctive changes in crystalline inclusions. New inclusions were formed and some established inclusions regressed. These changes were conveniently demonstrated with software-based photographic image analysis. We conclude that macular inclusions in SLS are not simply inert deposits, but are dynamic structures that form over time and are subject to remodeling. This conclusion provides new insight into the interplay between the metabolic defect and retinal pathology in SLS, and raises the potential for new therapeutic approaches to reverse some aspects of the maculopathy. [ABSTRACT FROM AUTHOR]

The heterocysts present in filamentous cyanobacteria such as Anabaena sp. PCC 7120 are known to be regulated by HetN and PatS, the repressors of heterocyst differentiation; therefore, the inactivation of these proteins will result in the formation of multiple heterocysts. To enhance the accumulation of fatty alcohols synthesized in the heterocyst, we introduced mutations of these repressors to increase heterocyst frequency. First, we isolated double mutants of hetN and patS and confirmed that the null mutation of these genes promoted higher frequencies of heterocyst formation and higher accumulation of heterocyst-specific glycolipids (Hgls) compared with its wild type. Next, we combined hetN and patS mutations with an hglT (encoding glycosyltransferase, an enzyme involved in Hgl synthesis) mutation to increase the accumulation of fatty alcohols since knockout mutation of hglT results in accumulation of very long chain fatty alcohol, the precursor of Hgl. We also observed retarded growth, lower chlorophyll content and up to a five-fold decrease in photosynthetic activity of the hetN / patS / hglT triple mutants. In contrast, the triple mutants showed three times higher heterocyst formation frequencies than the hglT single mutant and wild type. The production rate of fatty alcohol in the triple mutants attained a value 1.41 nmol/mL OD730, whereas accumulation of Hgls in the wild type was 0.90 nmol/mL OD730. Aeration of culture improved the accumulation of fatty alcohols in hetN / patS / hglT mutant cells up to 2.97 nmol/mL OD730 compared with cells cultured by rotation. Our study outlines an alternative strategy for fatty alcohol production supported by photosynthesis and nitrogen fixation. [ABSTRACT FROM AUTHOR]

In oleogel food systems (based on the mixture between stearic acid and stearyl alcohol) the strong effect of the weight ratio (R) between these two components on the textural and structural properties is well described. The effect of R for other fatty acids and fatty alcohols is less explored. Moreover, they do not show an enhancement of the oleogel properties for specific R. The effect of R on the oleogel properties, for a mixture of fatty acid and fatty alcohol with longer alkyl chains (behenyl alcohol and behenic acid) in sunflower and soybean oils, which are raw materials widely used in cosmetic and pharmaceutical industries, was investigated. We characterized the oleogel properties as a function of R in terms of structuring potential: hardness, oil loss and gel stability. This information was correlated with microstructural data obtained at different length scales by coupling optical microscopy, DSC, SFC, SAXS and WAXS experiments. Our results highlight that R tunes the oleogel properties in a comparable manner to previous results obtained for stearic acid and stearyl alcohol-based oleogels. Two specific R (8:2 and 7:3) close to the 3:1 molecular ratio gave oleogels with both the highest hardness and stability. The morphology and size of the mixed crystals obtained for these R cannot solely explain why they are stronger gels with low oil loss in comparison to the other R. The almost complete crystallization for these two R is one of the key parameters controlling the oleogel properties. As described in the literature, we also suggest that the differences in oleogel properties come from the spatial distribution of the crystalline mass. In this study, we confirm that the effect of the 3:1 molecular ratio in mixed surfactant systems described more than 50 years ago for foams, emulsions and Langmuir monolayers occurs also on the crystallization of mixed fatty alcohol and fatty acid in oils leading to better oleogels properties. [ABSTRACT FROM AUTHOR]