Acetylation Research Articles

Regioselective Deacetylation in Nucleosides and Derivatives.

Nucleoside analogues are a promising class of natural compounds in the pharmaceutical industry, and many antiviral, antibacterial and anticancer drugs have been created through structural modification of nucleosides scaffold. Acyl protecting groups, especially the acetyl group, play an important role in the protection of hydroxy groups in nucleoside synthesis and modification; consequently, numerous methodologies have been put forth for the acetylation of free nucleosides. However, for nucleosides that contain different O- and N-based functionalities, selective deprotection of the acetyl group(s) in nucleosides has been studied little, despite its practical significance in simplifying the preparation of partially or differentially substituted nucleoside intermediates. In this mini-review, recent approaches for regioselective deacetylation in acetylated nucleosides and their analogues are summarized and evaluated. Different regioselectivities (primary ester, secondary ester, full de-O-acetylation, and de-N-acetylation) are summarized and discussed in each section.

Assessing N-terminal acetylation status of cellular proteins via an antibody specific for acetylated methionine

N-terminal acetylation is being recognized as a factor affecting protein lifetime and proteostasis. It is a modification where an acetyl group is added to the N-terminus of proteins, and this occurs in 80 % of the human proteome. N-terminal acetylation is catalyzed by enzymes called N-terminal acetyltransferases (NATs). The various NATs acetylate different N-terminal amino acids, and methionine is a known target for some of the NATs. Currently, the acetylation status of most proteins can only be assessed with a limited number of methods, including mass spectrometry, which although powerful and robust, remains laborious and can only survey a fraction of the proteome. We here present testing of an antibody that was developed to specifically recognize Nt-acetylated methionine-starting proteins. We have used dot blots with synthetic acetylated and non-acetylated peptides in addition to protein analysis of lysates from NAT knockout cell lines to assess the specificity and application of this anti-Nt-acetylated methionine antibody (anti-NtAc-Met). Our results demonstrate that this antibody is indeed NtAc-specific and further show that it has selectivity for some subtypes of methionine-starting N-termini, specifically potential substrates of the NatC, NatE and NatF enzymes. We propose that this antibody may be a powerful tool to identify NAT substrates or to analyse changes in N-terminal acetylation for specific cellular proteins of interest.

Эксплуатационные характеристики древесно-полимерных композитов на основе ацетилированного древесного наполнителя

The demand for composite materials is growing every year. In this regard, the competitiveness of a particular product is determined primarily by the price-quality ratio. The most rational option for the production of wood-filled composites is using the materials with the increased performance characteristics. To date, it is the performance characteristics of modern composite materials that are the most significant, not only for final consumers, but also for manufacturers. In this regard, to improve performance characteristics in the production of wood-filled composites, various methods of pre-treatment of wood are used – thermal modification, acetylation, furfulation, ultra-high-frequency processing, alkali treatment, the use of various additives, etc. A promising way to improve the physical and mechanical properties of wood-filled materials is acetylation, whose mechanism consists in the formation of acetyl groups in wood during processing. To reduce production costs and the cost of the final product, it is possible to use a cheaper precursor (for example, icy acetic acid instead of acetic anhydride) with the possibility of intensifying the impregnation process. This article presents the results of obtaining wood-filled composites based on acetylated birch wood flour with its various proportions in the composition. The effect of introducing acetylated wood filler into the composition on the performance properties of composites (abradability, frost-resistance, flexural strength) has been evaluated in comparison with control samples made from untreated birch wood flour. The effect of acetylation with glacial acetic acid on the structure of birch wood flour has been characterized using Fourier-transform infrared spectroscopy. The IR-spectra of the control and acetylated samples contain absorption bands belonging to the corresponding groups of cellulose and lignin of hardwoods. The abradability and frost-resistance coefficients for a wood-filled composite based on acetylated birch wood flour are on average 1.5–2 times lower for all compositions compared to control samples. The results of the research allow us to conclude that acetylation of wood flour as a method of pre-treatment of the filler in order to improve the performance characteristics of the final product is promising for implementation in the production of wood-filled materials.

Enhancing cellulose acetate biodegradability in cigarette filters: an in-depth analysis of thermal alkaline pretreatment, microbial dynamics, and breakdown pathway prediction

BackgroundThe demand for bioplastics has increased exponentially as they have emerged as alternatives to petrochemical plastics. However, there is a substantial lack of knowledge regarding bioplastic degradation. This study developed a novel pretreatment method to improve the accessibility of a bioplastic substrate for biodegradation. In this study, cellulose acetate, a bioplastic found in the world’s most littered waste, e.g. cigarette filters, was selected as a potential substrate. Before anaerobic digestion, three thermal alkaline pretreatments: TA 30 °C, TA 90 °C, and TA 121 °C, were used to evaluate their effects on the chemical alterations of cellulose acetate.ResultThe ester groups in cellulose acetate were significantly reduced by the TA 30 °C pretreatment, as seen by a decrease in C = O stretching vibrations and shortening of C − O stretches (1,270 ∼ 1,210 cm− 1), indicating effective removal of acetyl groups. This pretreatment significantly enhanced cellulose acetate biodegradability to a maximum of 91%, surpassing the previously reported cellulose acetate degradation. Methane production increased to 695.0 ± 4 mL/g of volatile solid after TA 30 °C pretreatment, indicating enhanced cellulose acetate accessibility to microorganisms, which resulted in superior biogas production compared to the control (306.0 ± 10 mL/g of volatile solid). Diverse microbes in the anaerobic digestion system included hydrolytic (AB240379_g, Acetomicrobium, FN436103_g, etc.), fermentative, and volatile fatty acids degrading bacteria (JF417922_g, AB274492_g, Coprothermobacter, etc.), with Methanobacterium and Methanothermobacter being the sole hydrogenotrophic methanogens in the anaerobic digestion system. Additionally, an attempt to predict the pathway for the effective degradation of cellulose acetate from the microbial community in different pretreatment conditions.ConclusionsTo the best of our knowledge, this is the first study to estimate the maximum cellulose acetate degradation rate, with a simple and cost-effective pretreatment procedure. This approach holds promise for mitigating the environmental impact of cellulose acetate of cigarette filters and presents a sustainable and economically viable waste management strategy.

Fabrication of Fully Positively Charged Layer-by-Layer Polyelectrolyte Nanofilms with pH-Dependent Swelling Properties.

Nanofilms fabricated by layer-by-layer (LbL) assembly from polyelectrolytes (PEs) are important materials for various applications. However, PE films cannot retain the charges along the polymer chains during fabrication, resulting in a low charge density. In this study, the preparation of LbL nanofilms with preserved positive charges via a controllable and efficient approach was achieved. To fabricate fully positively charged (FPC) LbL nanofilms, a polycation, poly-l-lysine, was partially grafted with azide and alkyne groups. Through copper-catalyzed azide-alkyne cycloaddition and the LbL procedure, nanofilms were fabricated with all of the individual layers covalently bonded, improving the pH stability of the nanofilms. Because the resulting nanofilms had a high charge density with positive charges both inside and on the surface, they showed unique pH-dependent swelling properties and adsorption of negatively charged molecules compared with those of traditional polyelectrolyte LbL nanofilms. This kind of FPC nanofilm has great potential for use in sensors, diagnostics, and filter nanomaterials in the biomedical and environmental fields.

Enzyme-instructed intramitochondrial polymerization for enhanced anticancer treatment without the development of drug-resistance

Intracellular polymerization in living cells motivated chemists to generate polymeric structures with a multitude of possibilities to interact with biomacromolecules. However, out-of-control of the intracellular chemical reactions would be an obstacle restricting its application, providing the toxicity of non-targeted cells. Here, we reported intracellular thioesterase-mediated polymerization for selectively occurring polymerization using disulfide bonds in cancer cells. The acetylated monomers did not form disulfide bonds even under an oxidative environment, but they could polymerize into the polymeric structure after cleavage of acetyl groups only when encountered activity of thioesterase enzyme. Furthermore, acetylated monomers could be self-assembled with doxorubicin, providing doxorubicin loaded micelles for efficient intracellular delivery of drug and monomers. Since thioesterase enzymes were overexpressed in cancer cells specifically, the micelles were disrupted under activity of the enzyme and the polymerization could occur selectively in the cancer mitochondria. The resulting polymeric structures disrupted the mitochondrial membrane, thus activating the cellular death of cancer cells with high selectivity. This strategy selectively targets diverse cancer cells involving drug-resistant cells over normal cells. Moreover, the mitochondria targeting strategy overcomes the development of drug resistance even with repeated treatment. This approach provides a way for selective intracellular polymerization with desirable anticancer treatment.

New click chemistry scheme towards improvement of filler/polymer crosslinking in bio-based polymer composites

ABSTRACT The current study aims to develop a cutting-edge methodology to enhance compatibility between natural fiber and polymeric matrix in bio-composites. To achieve this, an innovative approach for grafting an azide functional group (Az) onto the surface of polypropylene (PP) was successfully developed and confirmed. The Az group contributed to enhancing the interfacial interaction between the polymer matrix and the bio-filler through chemical crosslinking. Crosslinking is achieved through an innovative and efficient chemical process known as click chemistry. In particular, a click reaction is established between the functionalized PP with an azide group and functionalized natural filler with an alkyne group. The effectiveness of the proposed technique is verified using Fourier Transform Infrared (FTIR) spectroscopy, X-ray Photoelectron Spectroscopy (XPS), Thermo-Gravimetric Analysis (TGA), and Scanning Electron Microscopy (SEM). The resulting bio-composite exhibits higher mechanical properties, better thermal stability, and improved biocompatibility compared to conventional materials. Specifically, the maximum tensile strength was achieved at 10% DPP loading, showing a 22% increase over the base material (DPP/PP) and a 7% increase over neat PP. A more significant enhancement was observed in Young’s modulus results across all samples. Therefore, the established method is beneficial for polymer modification, promoting the production of high-performance bio-composite materials.

Optimizing cellulose acetate microbead formation through premixed membrane emulsification: Unraveling critical parameters

This study explores the fabrication of cellulose acetate microbeads using the premix membrane emulsification technique and their subsequent conversion to cellulose microbeads through deacetylation, emphasizing the need for environmentally friendly alternatives to conventional synthetic microbeads. By systematically investigating critical processing parameters such as oil-to-water phase ratio, cellulose acetate concentration, dispersion solvent, drying temperature, and flux rate, we optimized the conditions for producing uniform and well-dispersed microbeads. The optimal oil-to-water phase ratio was identified at 6:1, with higher concentrations of cellulose acetate yielding better dispersion and reduced bead size. The flux rate significantly influenced the morphology of the microbeads, with lower rates favoring spherical shapes. Non-polar solvents like hexane were found to enhance bead dispersion, whereas the drying temperature showed no significant impact. The successful transformation from cellulose acetate to cellulose microbeads was confirmed by FT-IR spectroscopy, demonstrating the removal of acetyl groups and indicating complete deacetylation. Our findings provide valuable insights into the production of cellulose-based microbeads, offering a sustainable alternative for various industrial and environmental applications.

New Derivatives of Modified Starch for Food Technology.

The food industry extensively uses chemically modified starches and their hydrolysates, which is mainly due to their emulsification ability. Therefore, it becomes inevitable to develop new starch derivatives, including modified starch hydrolysates, and effective preparation methods to meet the increasing demands of producers, consumers, and technology. This study comprehensively researches the physical, chemical, and functional properties (such as the water-binding capacity, swelling power, solubility, and fat absorption capacity) of chemically modified biopolymers and their enzymatic hydrolysis products. We utilized oxidized and acetylated potato and waxy-corn starches with varying degrees of substitution by carboxyl and acetyl groups in our research. The process of enzymatic hydrolysis was performed in a recirculated membrane reactor (CRMR). Our findings indicated that the physicochemical properties of starch derivatives and their hydrolysates depended on the biological origin of the biopolymer and the type and degree of modification. However, the presence of carboxyl groups in the modified starch molecules is critical and affects the rheological properties and water-binding capacity of the starch preparations. For example, in the case of waxy-corn starch preparations with a lower content of carboxyl groups (i.e., derivatives with a low degree of oxidation), the water-binding capacity (WBC) increases when compared to native starch. The highest WBC value of 206.3% was noted for the doubly modified waxy-corn starch with an oxidation degree of 0.2% and an acetylation degree of 2.5%, while native waxy-corn starch shows a WBC of 161.4%. In contrast, it was observed that preparations with a higher content of carboxyl groups, i.e., derivatives with an oxidation degree of 2.5%, show a lower swelling power compared to native waxy starch.

Deletion of myeloid HDAC3 promotes efferocytosis to ameliorate retinal ischemic injury

Ischemia-induced retinopathy is a hallmark finding of common visual disorders including diabetic retinopathy (DR) and central retinal artery and vein occlusions. Treatments for ischemic retinopathies fail to improve clinical outcomes and the design of new therapies will depend on understanding the underlying disease mechanisms. Histone deacetylases (HDACs) are an enzyme class that removes acetyl groups from histone and non-histone proteins, thereby regulating gene expression and protein function. HDACs have been implicated in retinal neurovascular injury in preclinical studies in which nonspecific HDAC inhibitors mitigated retinal injury. Histone deacetylase 3 (HDAC3) is a class I histone deacetylase isoform that plays a central role in the macrophage inflammatory response. We recently reported that myeloid cells upregulate HDAC3 in a mouse model of retinal ischemia-reperfusion (IR) injury. However, whether this cellular event is an essential contributor to retinal IR injury is unknown. In this study, we explored the role of myeloid HDAC3 in ischemia-induced retinal neurovascular injury by subjecting myeloid-specific HDAC3 knockout (M-HDAC3 KO) and floxed control mice to retinal IR. The M-HDAC3 KO mice were protected from retinal IR injury as shown by the preservation of inner retinal neurons, vascular integrity, and retinal thickness. Electroretinography confirmed that this neurovascular protection translated to improved retinal function. The retinas of M-HDAC3 KO mice also showed less proliferation and infiltration of myeloid cells after injury. Interestingly, myeloid cells lacking HDAC3 more avidly engulfed apoptotic cells in vitro and after retinal IR injury in vivo compared to wild-type myeloid cells, suggesting that HDAC3 hinders the reparative phagocytosis of dead cells, a process known as efferocytosis. Further mechanistic studies indicated that although HDAC3 KO macrophages upregulate the reparative enzyme arginase 1 (A1) that enhances efferocytosis, the inhibitory effect of HDAC3 on efferocytosis is not solely dependent on A1. Finally, treatment of wild-type mice with the HDAC3 inhibitor RGFP966 ameliorated the retinal neurodegeneration and thinning caused by IR injury. Collectively, our data show that HDAC3 deletion enhances macrophage-mediated efferocytosis and protects against retinal IR injury, suggesting that inhibiting myeloid HDAC3 holds promise as a novel therapeutic strategy for preserving retinal integrity after ischemic insult.

Hydrolysis of Babool wood biomass using carbocation scavengers assisted ionic liquid pretreatment for the production of sugars and furfurals

The present study highlights the performance of carbocation scavengers for the pretreatment of hardwood biomass followed by the production of bio-based products. The behaviour of different carbocation scavengers namely; 2-Napthol, 4 Hydroxybenzoic acid, Vanillic acid, Catechol, Hydroquinone, Resorcinol and Phenol and their mitigating effect on the rate of hydrolysis was explored under different operating conditions. All the carbocation scavengers show significant changes in the crystallinity index leading to distinct morphological and physiochemical changes in the biomass structure. Results revealed that the addition of carbocation scavengers not only reduces the inhibitory effect of structured lignin but also enhances the accessibility of cellulose and hemicellulose and facilitates the production of sugars and 5-Hydroxymethyl Furfural. Maximum 5-HMF yield was observed using 2-Napthol at an optimised concentration of 2 wt% (1.5 mL) at 190 °C in 60 min. Further, to evaluate the effect of acetyl groups, biomass deacetylation was also performed. The highest deacetylation effect was observed at 170 °C and showed ∼73% and ∼94% reduction in the holocellulosic content in 60 min. The proposed study develops a sustainable and viable route to suppress the inhibitory effect of lignin with the utilization of carbocation scavengers and enhances biomass digestibility that favours the production of bio-based chemicals.

Valorization of Lignocellulose with One-Step Acidified Monophasic Phenoxyethanol Fractionation.

Effective fractionation of lignocelluosic biomass and subsequent valorization of all three major components under mild conditions were achieved. Pretreatment with acidified monophasic phenoxyethanol (EPH) efficiently removed 92.6 % lignin and 80 % xylan from poplar at 110 °C in 60 min, yielding high-value EPH-xyloside, EPH-modified lignin (EPHL), and a solid residue nearly purely composed of carbohydrates. After removing the grafted acetyl groups using 1 % NaOH at 50 °C, the highest enzymatic digestibility reached 92.3 %. EPHL could be recovered in high yield and purity with an uncondensed structure, while xylose was converted to EPH-xyloside, a potential precursor in biomedical industries. Additionally, the acidified monophasic EPH solvent could effectively fractionate biomass from species other than hardwood, achieving over 70 % delignification from recalcitrant pinewood under the same mild conditions, demonstrating the high potential of monophasic EPH pretreatment.

Crystal structures of four thio-glycosides involving carbamimido-thio-ate groups.

The compounds 2',3',4',6'-tetra-O-acetyl-β-d-gluco-pyranosyl N'-cyano-N-phenyl-carbamimido-thio-ate (C22H25N3O9S, 5a), 2',3',4',6'-tetra-O-acetyl-β-d-galacto-pyranosyl N'-cyano-N-phenyl-carbamimido-thio-ate, (C22H25N3O9S, 5b), 2',3',4',6'-tetra-O-acetyl-β-d-galacto-pyranosyl N'-cyano-N-methyl-carbamimido-thio-ate (C17H23N3O9S, 5c), and 2',3',4',6'-tetra-O-acetyl-β-d-galacto-pyranosyl N'-cyano-N-p-tolyl-carbamimido-thio-ate (C23H27N3O9S, 5d) all crystallize in P212121 with Z = 4. For all four structures, the configuration across the central (formal) C=N(CN) double bond of the carbamimido-thio-ate group is Z. The torsion angles C5-O1-C1-S (standard sugar numbering) are all close to 180°, confirming the β position of the substituent. Compound 5b involves an intra-molecular hydrogen bond N-H⋯O1; in 5c this contact is the weaker branch of a three-centre inter-action, whereas in 5a and 5d the H⋯O distances are much longer and do not represent significant inter-actions. The C-N bond lengths at the central carbon atom of the carbamimido-thio-ate group are almost equal. All C-O-C=O torsion angles of the acetyl groups correspond to a synperiplanar geometry, but otherwise all four mol-ecules display a high degree of conformational flexibility, with many widely differing torsion angles for equivalent groups. In the crystal packing, 5a, 5c and 5d form layer structures involving the classical hydrogen bond N-H⋯Ncyano and a variety of 'weak' hydrogen bonds C-H⋯O or C-H⋯S. The packing of 5b is almost featureless and involves a large number of borderline 'weak' hydrogen bonds. In an appendix, a potted history of wavelength preferences for structure determination is presented and it is recommended that, even for small organic crystals in non-centrosymmetric space groups, the use of Mo radiation should be considered.

Effects of konjac glucomannan with different degrees of deacetylation on the properties and structure of wheat gluten protein

The properties and structure of gluten protein with different deacetylation degrees of konjac glucomannan (KGM) were investigated, in an attempt to improve the quality of gluten protein in flour products. Results showed that deacetylated KGM (DKGM) could improve the textural properties and enhance the thermal stability of gluten protein. DKGM increased the water holding capacity and shortened the T2 relaxation time of gluten after removing some acetyl groups. As the deacetylation degree increased, the hardness and adhesiveness of gluten gels gradually increased, while the springiness decreased. In addition, the presence of DKGM promoted the conversion from free sulfhydryl to disulfide bonds and increased the β-sheet content in gluten protein. The low-deacetylation KGM decreased the surface hydrophobicity and fluorescence intensity of gluten protein, and the microstructures of gluten gels became more compact. Compared with gluten protein-KGM complex gel, the degradation temperature of gluten protein-DKGM complex gels was observed to increase by >3 °C. Overall, the low-deacetylation KGM was beneficial for improving the physicochemical properties and maintaining the network structure of gluten protein. This study provides valuable references and practical insights to improve gluten quality in the flour industry.

Bacterial protein acetylation: mechanisms, functions, and methods for study.

Lysine acetylation is an evolutionarily conserved protein modification that changes protein functions and plays an essential role in many cellular processes, such as central metabolism, transcriptional regulation, chemotaxis, and pathogen virulence. It can alter DNA binding, enzymatic activity, protein-protein interactions, protein stability, or protein localization. In prokaryotes, lysine acetylation occurs non-enzymatically and by the action of lysine acetyltransferases (KAT). In enzymatic acetylation, KAT transfers the acetyl group from acetyl-CoA (AcCoA) to the lysine side chain. In contrast, acetyl phosphate (AcP) is the acetyl donor of chemical acetylation. Regardless of the acetylation type, the removal of acetyl groups from acetyl lysines occurs only enzymatically by lysine deacetylases (KDAC). KATs are grouped into three main superfamilies based on their catalytic domain sequences and biochemical characteristics of catalysis. Specifically, members of the GNAT are found in eukaryotes and prokaryotes and have a core structural domain architecture. These enzymes can acetylate small molecules, metabolites, peptides, and proteins. This review presents current knowledge of acetylation mechanisms and functional implications in bacterial metabolism, pathogenicity, stress response, translation, and the emerging topic of protein acetylation in the gut microbiome. Additionally, the methods used to elucidate the biological significance of acetylation in bacteria, such as relative quantification and stoichiometry quantification, and the genetic code expansion tool (CGE), are reviewed.

High internal phase Pickering emulsions via complexation of cellulose nanofibrils and nanochitin: Enhanced interfacial adsorption and structured aqueous network

High internal phase emulsion is a novel emulsion type for a range of applications, while its preparation is limited by low stability and the selection of proper emulsifiers. Herein, an edible sunflower oil-in-water high internal phase Pickering emulsion (HIPPE) stabilized by complexation of cellulose nanofibrils (CNF) and nanochitin (NCh) is prepared using a two-step method. The stabilization capacity of the CNF/NCh complexes stems from restricted coalescence, droplet breakage, and coarsening upon HIPPE formation, showing the minimal droplet size at 80 μm. This is the result of a dual stabilization mechanism including: enhanced adsorption of the complexes at the oil-water interfaces by existence of the acetyl groups in the complexes and structuring the aqueous phase to form networking structures within HIPPEs. The CNF/NCh complex suspensions exhibit tolerance to changes in pH (3–5) and salinity (0–500 mM), showing capability of forming and stabilizing HIPPEs with minimal alteration to droplet size and morphology. The complex-stabilized HIPPEs remain stability after at least 2-year storage at ambient condition. Overall, complexation of CNF and NCh greatly extend the conditions on forming highly stable, tuneable HIPPEs, offering potential on engineering applications relevant to clean-label, green foodstuffs.

Production of chitosan from Aspergillus niger and quantitative evaluation of the process using adapted analytical tools

The chitosan production process from fishery waste is already established in industrial scale, whereby fungal chitosan is produced in lower amounts. Since fungal chitosan could be isolated from under-valorized vegan streams while exhibiting slightly different characteristics, it has also potential for other applications. Within this publication, we focus on the chitosan production from Aspergillus niger. This study provides a detailed determination of the biomass composition, adapting and comparing different analytical tools, with special focus on the chitin and chitosan content. The major content of the dried biomass is composed of glucans (48.6 ± 1.4%), followed by proteins with an amount of 22.2 ± 0.7%. Chitin and chitosan provide 16.0 ± 0.8% of the biomass. Within our chitosan production studies, we compared the effect of different process strategies including steps as deproteinization (DP), acid extraction (AE), deacetylation (DA), as well as purification. Initially, we obtained poor values (lower than 73.6%) for the chitosan purity. A direct DA step followed by purification resulted in a chitosan purity of up to 89.6%, a recovery of 30.5% and a yield with regard to the biomass of 5.5%. The DA degree of the resulting chitosan is similar to chitosan derived from fishery waste, whereas the molecular weight is lower. The results achieved so far are consistent with the literature, extending beyond, the data emphasized that a chitosan production from residual fungal biomass after fermentation is suitable by direct DA and purification. However, further adaption is necessary so that other matrix compounds could be also obtained.

MECHANISM OF DEPROTONATION OF THE AMINO GROUP OF GLUTAMATE UPON BINDING TO N-ACETYLGLUTAMATE SYNTHASE

Gcn5-related N-acetyltransferases catalyze the transfer of an acetyl group to a primary amino group of a wide class of substrates. Protonation of the amino group upon binding to the enzyme is necessary to activate the nucleophilic attack on the substrate. The process of glutamate binding to N-acetylglutamate synthase is considered using molecular modeling and quantum chemistry methods. It has been shown that deprotonation of the primary amino group of glutamate occurs upon binding to the active site of the enzyme with the participation of the side chain of the aspartate residue.

Simple Synthesis of Cellulose Triacetate from HVS Paper Waste and Its Application for Optode

The optode membrane is a membrane that can identify ions in an aqueous solution. One of the most widely used optode membranes is cellulose triacetate based. Cellulose triacetate (CTA) has the characteristics of hydrophobic, transparent, elastic, and affordable. There are sources of cellulose triacetate that can be utilized and waste paper is one of them. Waste paper is extracted to obtain the cellulose, then by acetylization reaction to produce cellulose triacetate. The resultant cellulose triacetate has a degree of substitution (DS) of 2.89 and an acetyl group percentage (% AG) of 43.64. The standard and synthesized CTA optode membrane are tested for performance with various parameters, ie optimum pH, optimum immersion time, working range, limit of detection (LOD), and limit of quantification (LOQ). The standard CTA optode membranes and synthesized worked at pH 3 and 4 with optimum immersion time for 15 min, respectively. The optode produced a linear response in detecting Cr(VI) ion in the concentration range of 0.02-1 mg/L for standard CTA with an R2 of 0.9726 and 1-25 mg/L for synthesized CTA with an R2 of 0.9764, The limit of detection (LOD) and limit of quantitation (LOQ) were 0.0015 mg/L and 0.0051 mg/L for standard CTA, while 0.0224 mg/L and 0.0749 mg/L for synthesis CTA respectively. Since both optode membranes' performance test results are adequate, the synthesis results of CTA optode membranes can be employed as one source of cellulose triacetate.

Tunable hydrophobicity and biodegradability of acetylated lignin/polyester fibrous mat for water/oil separation

ABSTRACT The development of eco-friendly and biodegradable biopolymer composites has become increasingly important. In this study, acetylated lignin (ACL) was synthesized, and its potential as an effective additive for biodegradable polymers was investigated. ACL was synthesized through a one-step acetylation process in which hydroxyl groups of lignin were substituted with acetyl groups. ACL exhibited enhanced molecular weight and thermal stability, along with improved solubility in organic solvents compared to unmodified kraft lignin (KL). Hydrophobic ACL was uniformly dispersed in a mixture of a polycaprolactone (PCL) polymer and organic solvent, leading to the successful fabrication of a fibrous mat using electrospinning. The ACL/PCL fibrous mat demonstrated enhanced mechanical strength and hydrophobicity, notably indicating a substantially high-water contact angle of 143.3 ± 1.4°. Subsequently, it was utilized as a water/oil separator, showing a separation efficiency exceeding 90% for oil within a short time, effectively addressing water/oil emulsions. Biodegradability results demonstrated enhanced hydrolysis degradation efficiency with the incorporation of ACL into PCL fibers. Consequently, this study proposes a feasible approach to enhance the efficacy of ACL as a biodegradable polymer additive, while presenting promising opportunities for membrane applications targeting water/oil separation.