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Paper sludge consists mainly of wet short cellulose fibers that are lost during papermaking and of residual chemicals used in the manufacturing process that remain dissolved in the water. Each ton of paper generates about 40–50 kg of dry sludge, of which 70% is primary sludge. Paper production, which exceeded 400 million tons globally in 2020, generates vast volumes of solid waste. Primary sludge is usually fiber-rich and hence suitable to be recycled back into the papermaking process. However, if the sludge is to be disposed of in landfills, sustainable practices must be developed in order to recover the fibers as they are valuable source for manufacturing high value-added products. This study investigates the valorization of paper sludge discarded by a filter paper manufacturer, with the purpose of producing cellulose acetate films for food packaging. The process involves recovering cellulose fibers from the sludge, purifying them and through acetylation reaction produce cellulose acetate films. FTIR spectra confirmed successful acetylation of fibers and also that acetyl groups reduced the hydrophilicity of cellulose—the contact angle was increased to over 80° from 50° in native cellulose. The films exhibited very good water barrier properties at both 50% and 90% relative humidity (RH), Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. This publication is part of the Project PID2020-114070RB-I00 (CELLECOPROD), funded by MCIN/ AEI/10.13039/501100011033. Elisabet Quintana is a Serra Húnter Fellow. Authors are grateful to PhD student Noemi Huete for kindly providing information about the composition of waste paper sludge, Postprint (published version)

Nucleosomes are the basic compaction unit of chromatin and nucleosome structure and their higher-order assemblies regulate genome accessibility. Many post-translational modifications alter nucleosome dynamics, nucleosome-nucleosome interactions, and ultimately chromatin structure and gene expression. Here, we investigate the role of two post-translational modifications associated with actively transcribed regions, H3K36me3 and H4K5/8/12/16ac, in the contexts of tri-nucleosome arrays that provide a tractable model system for quantitative single-molecule analysis, while enabling us to probe nucleosome-nucleosome interactions. Direct visualization by AFM imaging reveals that H3K36me3 and H4K5/8/12/16ac nucleosomes adopt significantly more open and loose conformations than unmodified nucleosomes. Similarly, magnetic tweezers force spectroscopy shows a reduction in DNA outer turn wrapping and nucleosome-nucleosome interactions for the modified nucleosomes. The results suggest that for H3K36me3 the increased breathing and outer DNA turn unwrapping seen in mononucleosomes propagates to more open conformations in nucleosome arrays. In contrast, the even more open structures of H4K5/8/12/16ac nucleosome arrays do not appear to derive from the dynamics of the constituent mononucleosomes, but are driven by reduced nucleosome-nucleosome interactions, suggesting that stacking interactions can overrule DNA breathing of individual nucleosomes. We anticipate that our methodology will be broadly applicable to reveal the influence of other post-translational modifications and to observe the activity of nucleosome remodelers.

Regular exercise promotes whole-body health and prevents disease, but the underlying molecular mechanisms are incompletely understood1-3. Here, the Molecular Transducers of Physical Activity Consortium4 profiled the temporal transcriptome, proteome, metabolome, lipidome, phosphoproteome, acetylproteome, ubiquitylproteome, epigenome and immunome in whole blood, plasma and 18 solid tissues in male and female Rattus norvegicus over eight weeks of endurance exercise training. The resulting data compendium encompasses 9,466 assays across 19 tissues, 25 molecular platforms and 4 training time points. Thousands of shared and tissue-specific molecular alterations were identified, with sex differences found in multiple tissues. Temporal multi-omic and multi-tissue analyses revealed expansive biological insights into the adaptive responses to endurance training, including widespread regulation of immune, metabolic, stress response and mitochondrial pathways. Many changes were relevant to human health, including non-alcoholic fatty liver disease, inflammatory bowel disease, cardiovascular health and tissue injury and recovery. The data and analyses presented in this study will serve as valuable resources for understanding and exploring the multi-tissue molecular effects of endurance training and are provided in a public repository ( https://motrpac-data.org/ ).

BACKGROUND: Tau is aberrantly acetylated in various neurodegenerative conditions, including Alzheimers disease, frontotemporal lobar degeneration (FTLD), and traumatic brain injury (TBI). Previously, we reported that reducing acetylated tau by pharmacologically inhibiting p300-mediated tau acetylation at lysine 174 reduces tau pathology and improves cognitive function in animal models. METHODS: We investigated the therapeutic efficacy of two different antibodies that specifically target acetylated lysine 174 on tau (ac-tauK174). We treated PS19 mice, which harbor the P301S tauopathy mutation that causes FTLD, with anti-ac-tauK174 and measured effects on tau pathology, neurodegeneration, and neurobehavioral outcomes. Furthermore, PS19 mice received treatment post-TBI to evaluate the ability of the immunotherapy to prevent TBI-induced exacerbation of tauopathy phenotypes. Ac-tauK174 measurements in human plasma following TBI were also collected to establish a link between trauma and acetylated tau levels, and single nuclei RNA-sequencing of post-TBI brain tissues from treated mice provided insights into the molecular mechanisms underlying the observed treatment effects. RESULTS: Anti-ac-tauK174 treatment mitigates neurobehavioral impairment and reduces tau pathology in PS19 mice. Ac-tauK174 increases significantly in human plasma 24 h after TBI, and anti-ac-tauK174 treatment of PS19 mice blocked TBI-induced neurodegeneration and preserved memory functions. Anti-ac-tauK174 treatment rescues alterations of microglial and oligodendrocyte transcriptomic states following TBI in PS19 mice. CONCLUSIONS: The ability of anti-ac-tauK174 treatment to rescue neurobehavioral impairment, reduce tau pathology, and rescue glial responses demonstrates that targeting tau acetylation at K174 is a promising neuroprotective therapeutic approach to human tauopathies resulting from TBI or genetic disease.

Primary familial brain calcification (PFBC) is characterized by calcium deposition in the brain, causing progressive movement disorders, psychiatric symptoms, and cognitive decline. PFBC is a heterogeneous disorder currently linked to variants in six different genes, but most patients remain genetically undiagnosed. Here, we identify biallelic NAA60 variants in ten individuals from seven families with autosomal recessive PFBC. The NAA60 variants lead to loss-of-function with lack of protein N-terminal (Nt)-acetylation activity. We show that the phosphate importer SLC20A2 is a substrate of NAA60 in vitro. In cells, loss of NAA60 caused reduced surface levels of SLC20A2 and a reduction in extracellular phosphate uptake. This study establishes NAA60 as a causal gene for PFBC, provides a possible biochemical explanation of its disease-causing mechanisms and underscores NAA60-mediated Nt-acetylation of transmembrane proteins as a fundamental process for healthy neurobiological functioning.

Biomaterial scaffolds have been used successfully to promote the regenerative repair of small endometrial lesions in small rodents, providing partial restoration of gestational function. The use of rabbits in this study allowed us to investigate a larger endometrial tissue defect and myometrial injury model. A gelatin/polycaprolactone (GT/PCL) gradient-layer biofilm was sutured at the defect to guide the reconstruction of the original tissue structure. Twenty-eight days postimplantation, the uterine cavity had been restored to its original morphology, endometrial growth was accompanied by the formation of glands and blood vessels, and the fragmented myofibers of the uterine smooth muscle had begun to resemble the normal structure of the lagomorph uterine cavity, arranging in a circular luminal pattern and a longitudinal serosal pattern. In addition, the repair site supported both embryonic implantation into the placenta and normal embryonic development. Four-dimensional label-free proteomic analysis identified the cell adhesion molecules, phagosome, ferroptosis, rap1 signaling pathways, hematopoietic cell lineage, complement and coagulation cascades, tricarboxylic acid cycle, carbon metabolism, and hypoxia inducible factor (HIF)-1 signaling pathways as important in the endogenous repair process of uterine tissue injury, and acetylation of protein modification sites upregulated these signaling pathways. Copyright 2024, Mary Ann Liebert, Inc., publishers.

Lysine deacetylase inhibitors (KDACis) are approved drugs for cutaneous T cell lymphoma (CTCL), peripheral T cell lymphoma (PTCL), and multiple myeloma, but many aspects of their cellular mechanism of action (MoA) and substantial toxicity are not well understood. To shed more light on how KDACis elicit cellular responses, we systematically measured dose-dependent changes in acetylation, phosphorylation, and protein expression in response to 21 clinical and pre-clinical KDACis. The resulting 862,000 dose-response curves revealed, for instance, limited cellular specificity of histone deacetylase (HDAC) 1, 2, 3, and 6 inhibitors; strong cross-talk between acetylation and phosphorylation pathways; localization of most drug-responsive acetylation sites to intrinsically disordered regions (IDRs); an underappreciated role of acetylation in protein structure; and a shift in EP300 protein abundance between the cytoplasm and the nucleus. This comprehensive dataset serves as a resource for the investigation of the molecular mechanisms underlying KDACi action in cells and can be interactively explored online in ProteomicsDB., QC 20240703

The chromatin organization and its dynamic remodeling determine its accessibility and sensitivity to DNA damage oxidative stress, the main source of endogenous DNA damage. We studied the role of the VRK1 chromatin kinase in the response to oxidative stress. which alters the nuclear pattern of histone epigenetic modifications and phosphoproteome pathways. The early effect of oxidative stress on chromatin was studied by determining the levels of 8-oxoG lesions and the alteration of the epigenetic modification of histones. Oxidative stress caused an accumulation of 8-oxoG DNA lesions that were increased by VRK1 depletion, causing a significant accumulation of DNA strand breaks detected by labeling free 3′-DNA ends. In addition, oxidative stress altered the pattern of chromatin epigenetic marks and the nuclear phosphoproteome pathways that were impaired by VRK1 depletion. Oxidative stress induced the acetylation of H4K16ac and H3K9 and the loss of H3K4me3. The depletion of VRK1 altered all these modifications induced by oxidative stress and resulted in losses of H4K16ac and H3K9ac and increases in the H3K9me3 and H3K4me3 levels. All these changes were induced by the oxidative stress in the epigenetic pattern of histones and impaired by VRK1 depletion, indicating that VRK1 plays a major role in the functional reorganization of chromatin in the response to oxidative stress. The analysis of the nuclear phosphoproteome in response to oxidative stress detected an enrichment of the phosphorylated proteins associated with the chromosome organization and chromatin remodeling pathways, which were significantly decreased by VRK1 depletion. VRK1 depletion alters the histone epigenetic pattern and nuclear phosphoproteome pathways in response to oxidative stress. The enzymes performing post-translational epigenetic modifications are potential targets in synthetic lethality strategies for cancer therapies.

Transparent Natural Fiber Composite Materials may pose a more environmentally friendly alternative regarding energy efficiency and low CO2 emissions in contrast to traditional composites, exhibiting transparency for future smart building or photovoltaic applications. The present study involved a research effort for the development of a lightweight flax fiber-reinforced composite material, which will exemplify high optical transparency. A detailed focus is conducted, on minimizing light absorption phenomena with delignification methods of flax fibers, eliminating light scattering via a Refractive Index Matching procedure between the reinforcement and the polymer matrix and via fiber modifications which tackle several issues such as enhancing the imperfect interphase between the hydrophilic reinforcement and the hydrophobic matrix, or providing finer polymer impregnation of the fibers. Acetylation, nitric acid, or TEMPO-oxidation treatments that modify the fiber’s nature and morphology are implemented to tackle these obstacles. Transparent Flax Fiber Reinforced Composites of 35-45 % fiber volume fraction were fabricated with wet-lamination and hot press forming techniques, indicating a maximum total light transmittance of approximately 70% (at low thickness) and 56-58% (at high thickness), depending on the fiber modification implemented. Regarding mechanical properties, a maximum specific flexural strength of 153 MPa/(g/(cm3)) and a specific flexural stiffness of 11.95 GPa/(g/(cm3)) was achieved for these materials. The transparent FFCMs showed comparable values of total light transmission correlated to reference materials like GFRPs or other natural fiber-reinforced composite materials, with similar volume fractions, signifying the success of achieving high optical transparency., Materials Science and Engineering

One of the most heavily researched oncoproteins is the MYC oncoprotein and this oncogenic transcription factor can regulate a large fraction of cellular genes. MYC overexpression becomes oncogenic and has been shown to be observed in many types of human cancers. GCN5, a histone acetyltransferase (HAT), can acetylate MYC via the STAGA complex at K323, but MYC can also be acetylated by different HATs. For example, p300, another HAT, can preferentially acetylate MYC at K149 and K158. However, p300-mediated acetylation increases MYC turnover, whereas GCN5-mediated acetylation stabilizes MYC. However, the significance of MYC acetylation and the functions of these three acetylated residues have yet to be elucidated. In vertebrates, there is a paralogous gene called PCAF, which codes for an enzyme much like GCN5. Due to their almost nearly identical sequences, it is thought that PCAF and GCN5 have largely redundant functions. PCAF has been reported to have ubiquitin E3 ligase activity within the N-terminal PCAF homology domain and this domain is highly conserved in GCN5. However, it is unknown whether GCN5 has any intrinsic E3 ligase activity or whether it recruits an E3 ligase for its surprising role in ubiquitination. Here we show that these three main lysine residues of MYC are reversibly acetylated in various immortalized non-tumorigenic and malignant cells. Furthermore, acetylation of MYC at different lysine residues differentially affects its stability in a cell type-dependent manner and all acetylated lysine (AcK) residues are required for anchorage independent growth in vitro. We show that each individual AcK site has gene-specific functions in controlling select MYC-regulated processes and are required for the oncogenic transformation of MYC. In this study, we have also reported that not only can GCN5 directly acetylate MYC at K323, but it can also stimulate MYC ubiquitination in a GCN5-dependent manner. Furthermore, the PCAF homology domain of GCN5, described ear

An increased understanding of how the acceptor site in Gcn5-related N-acetyltransferase (GNAT) enzymes recognizes various substrates provides important clues for GNAT functional annotation and their use as chemical tools. In this study, we explored how the PA3944 enzyme from Pseudomonas aeruginosa recognizes three different acceptor substrates, including aspartame, NANMO, and polymyxin B, and identified acceptor residues that are critical for substrate specificity. To achieve this, we performed a series of molecular docking simulations and tested methods to identify acceptor substrate binding modes that are catalytically relevant. We found that traditional selection of best docking poses by lowest S scores did not reveal acceptor substrate binding modes that were generally close enough to the donor for productive acetylation. Instead, sorting poses based on distance between the acceptor amine nitrogen atom and donor carbonyl carbon atom placed these acceptor substrates near residues that contribute to substrate specificity and catalysis. To assess whether these residues are indeed contributors to substrate specificity, we mutated seven amino acid residues to alanine and determined their kinetic parameters. We identified several residues that improved the apparent affinity and catalytic efficiency of PA3944, especially for NANMO and/or polymyxin B. Additionally, one mutant (R106A) exhibited substrate inhibition toward NANMO, and we propose scenarios for the cause of this inhibition based on additional substrate docking studies with R106A. Ultimately, we propose that this residue is a key gatekeeper between the acceptor and donor sites by restricting and orienting the acceptor substrate within the acceptor site.

Lignin, en av huvudkomponenterna i lignocellulosabiomassa, utgör en stor mängd av sidoströmen från massaindustrin. Lignin är aromatiska makromolekyler som förekommer i rikliga mängder i naturen och uppvisar unika antioxidant-, uv-skyddande, anti-ultravioletta, antikorrosiva och antimikrobiella egenskaper, etc. Ligninbaserade produkter är ännu inte kommersialiserade eftersom de är begränsade av den kemiska heterogeniteten hos lignin som separerats från olika råvaror och producerats i olika industriella processer. Istället förbränns lignin vanligtvis för värme- och elproduktion efter extraktion. Tillvägagångssätt för att bevara värdefulla egenskaper hos lignin och samtidigt övervinna begränsningar har blivit heta ämnen. I detta projekt genomfördes kemiska modifieringar av kraftlignin från olika naturliga råvaror, gran och eukalyptus, där fenolgrupperna ersattes av alkylgrupper med olika kedjelängder (kolnummer 1, 6 och 12). De kemiska strukturerna och de termiska egenskaperna hos kraftlignin studerades med en kombination av analytiska metoder. Egenskaperna hos två typer av tekniska kraftligniner och dess derivat undersöktes även för jämförelse. Resultaten visade att kemiskt modifierat lignin kan vara ett lovande råmaterial för förädlade produkter som till exempel ligninbaserade nanopartiklar., Lignin, one of the major components in lignocellulose biomass, makes up a large amount of sidestream from the pulp industry. As an abundant feedstock of bio- originated aromatic macromolecules, lignin shows unique antioxidant, UV-protective, anticorrosive, and antimicrobial properties, etc. However, limited by the chemical heterogeneity of lignin separated from different bioresources and industrial procedures as well as its recalcitrance as macromolecules, lignin-based products are not yet commercialized, while lignin is commonly burnt for heat or power generation after extraction. Approaches of preserving valuable properties of lignin meanwhile overcoming limitations have become heated topics. In this project, chemical modifications of kraft lignin from different natural bio-origins, spruce and eucalyptus, were conducted, with alkyl groups of various chain lengths (carbon numbers 1, 6 and 12) substituting the phenolic groups. A combination of analytical methods for characterizing the chemical structures and thermal properties of kraft lignin and chemically modified kraft lignin were studied. Meanwhile, the characteristics of two kinds of technical kraft lignin and their derivatives were investigated for comparison. Results highlighted that chemically modified lignin could be a promising material to serve as a feedstock for value-added products such as lignin-based nanoparticles.

Bioplastics that possess characteristics like durability and low cost are desired for versatile applications in industries such as automotive manufacturing, marine transport manufacturing, aerospace applications, and the building industry. The automotive industry is an example of an industry that is now shifting towards a more focused approach addressing the issue concerning sustainability and the development of sustainable material. To achieve a lightweight and sustainable construction, one of the methods used by the automotive original equipment manufacturers is by substituting conventional fossil-based, non-renewable composites, and metallic materials with a bio-based alternative. One of the drawbacks with biobased polymers can be the poor interfacial adhesion, leading to poor mechanical properties when compares to conventional material. The aim of this research is to investigate if a low-cost by-product could be used as a component in a composite matrix material in the automotive industry to reduce the final weight and increase the non-petrochemical material usage of composite material without compromising the thermal and mechanicals properties demanded. In this research, lignin was chemically altered by esterification the functional groups to increase the compatibility with polylactic acid. The esterification was performed with the use of acetic acid anhydride and pyridine. To evaluate and determine the esterification, Fourier transform Infrared Spectroscopy was used. By blending the modified lignin with polylactic acid the intention was to improve the thermomechanical properties and the interfacial linkage between the components. The effects of lignin acetylation on the tensile properties, impact strength, and thermal stability and moisture repellence behaviour were investigated. According to the experimental results the modification of lignin, increased the impact strength for all the blends containing acetylated lignin compares to pristine lignin. The larges

Birch plywood has superior mechanical properties compared with plywood made from most softwood species, which makes it suitable for structural application. Plywood is also more environmentally friendly, cost-efficient, and less prefabrication demanding than steel plates. For a proper design of birch plywood as joint plates in timber-timber connections, the embedment behavior of mechanical connectors into plywood needs to be properly investigated. In this study, the authors performed embedment tests of dowel connectors into birch plywood specimens under five different angles from parallel to perpendicular to the face grain with a step size of 22.5 degrees. Dowel connectors with three different diameters were utilized to study the influence of dowel diameter on embedment strength and stiffness. Besides, test series using self-drilling screws and acetylated birch plywood specimens were conducted to study the effect of both fastener type and acetylation. Moreover, full-hole and half -hole test results were compared. The embedment strengths were calculated analytically according to different term definitions. The test results were then compared with the analytical results based on formulas reported in the literature, e.g., Eurocode 5 and other design standards.

Tuberous sclerosis complex (TSC) is a neurogenetic disorder leading to epilepsy, developmental delay, and neurobehavioral dysfunction. The syndrome is caused by pathogenic variants in TSC1 (coding for hamartin) or TSC2 (coding for tuberin). Recently, we reported a progressive frontotemporal dementia-like clinical syndrome in a patient with a mutation in TSC1, but the neuropathological changes seen in adults with TSC with or without dementia have yet to be systematically explored. Here, we examined neuropathological findings in adults with TSC (n = 11) aged 30-58 years and compared them to age-matched patients with epilepsy unrelated to TSC (n = 9) and non-neurological controls (n = 10). In 3 of 11 subjects with TSC, we observed a neurofibrillary tangle-predominant "TSC tauopathy" not seen in epilepsy or non-neurological controls. This tauopathy was observed in the absence of pathological amyloid beta, TDP-43, or alpha-synuclein deposition. The neurofibrillary tangles in TSC tauopathy showed a unique pattern of post-translational modifications, with apparent differences between TSC1 and TSC2 mutation carriers. Tau acetylation (K274, K343) was prominent in both TSC1 and TSC2, whereas tau phosphorylation at a common phospho-epitope (S202) was observed only in TSC2. TSC tauopathy was observed in selected neocortical, limbic, subcortical, and brainstem sites and showed a 3-repeat greater than 4-repeat tau isoform pattern in both TSC1 and TSC2 mutation carriers, but no tangles were immunolabeled with MC1 or p62 antibodies. The findings suggest that individuals with TSC are at risk for a unique tauopathy in mid-life and that tauopathy pathogenesis may involve TSC1, TSC2, and related molecular pathways.

The evolutionarily conserved cohesin complex mediates sister chromatid cohesion and facilitates mitotic chromosome condensation, DNA repair, and transcription regulation. These biological functions require cohesin's two ATPases, formed by the Smc1p and Smc3p subunits. Cohesin's ATPase activity is stimulated by the Scc2p auxiliary factor. This stimulation is inhibited by Eco1p acetylation of Smc3p at an interface with Scc2p. It was unclear how cohesin's ATPase activity is stimulated by Scc2p or how acetylation inhibits Scc2p, given that the acetylation site is distal to cohesin's ATPase active sites. Here, we identify mutations in budding yeast that suppressed the in vivo defects caused by Smc3p acetyl-mimic and acetyl-defective mutations. We provide compelling evidence that Scc2p activation of cohesin ATPase depends on an interface between Scc2p and a region of Smc1p proximal to cohesin's Smc3p ATPase active site. Furthermore, substitutions at this interface increase or decrease ATPase activity to overcome ATPase modulation by acetyl-mimic and acetyl-null mutations. Using these observations and an existing cryo-EM structure, we propose a model for regulating cohesin ATPase activity. We suggest that Scc2p binding to Smc1p causes the adjacent Smc1p residues and ATP to shift, stimulating Smc3p's ATPase. This stimulatory shift is inhibited through acetylation of the distal Scc2p-Smc3p interface.

Histone acetylation is a pivotal epigenetic modification that controls chromatin structure and regulates gene expression. It plays an essential role in modulating zygotic transcription and cell lineage specification of developing embryos. While the outcomes of many inductive signals have been described to require enzymatic activities of histone acetyltransferases and deacetylases (HDACs), the mechanisms by which HDACs confine the utilization of the zygotic genome remain to be elucidated. Here, we show that histone deacetylase 1 (Hdac1) progressively binds to the zygotic genome from mid-blastula and onward. The recruitment of Hdac1 to the genome at blastula is instructed maternally. Cis-regulatory modules (CRMs) bound by Hdac1 possess epigenetic signatures underlying distinct functions. We highlight a dual function model of Hdac1 where Hdac1 not only represses gene expression by sustaining a histone hypoacetylation state on inactive chromatin, but also maintains gene expression through participating in dynamic histone acetylation-deacetylation cycles on active chromatin. As a result, Hdac1 maintains differential histone acetylation states of bound CRMs between different germ layers and reinforces the transcriptional program underlying cell lineage identities, both in time and space. Taken together, our study reveals a comprehensive role for Hdac1 during early vertebrate embryogenesis.

Due to the recent flourish of modern timber structures, there is an increasing demand for engineered wood products (EWPs). However, outdoor exposure of EWPs often poses a risk of durability-related issues. For load-bearing timber structures, especially those in the outdoor environment, the combination of wood modification by acetylation and concept of EWPs allows manufacturing more durable and stable timber elements. This thesis concerns the angle-dependent in-plane mechanical properties of plywood manufactured from acetylated birch veneers (ABP). Specifically, tensile, compressive, shear and bending tests were conducted at three different load-to-face grain angles, namely from 0° (parallel), 22.5°, to 45°. The test results were compared with ordinary unmodified birch plywood (UBP) concerning stress-strain relationships, failure modes, strength, and elastic properties. Besides, for better understanding the moisture effect on the mechanical properties of both acetylated and unmodified birch plywood, specimens of both type were conditioned in climate chambers under three different environments, with the temperature of 20°C and elevating relative humidity (RH) from 35% to 65% to 95%. In this case, specimens with the load-to-face grain angles of 0°, 45°, and 90° were tested. The influence of both RH and measured moisture contents (MC) on bending strength and stiffness was evaluated. Variations of utilized brittleness terms under different RH conditions and load-face grain angles were also studied. Prediction formulas of mechanical properties with MC were derived by performing linear regressions among test results. The test results reveal that ABP possesses equivalent mechanical properties to UBP specimens. Under relative humidity elevation, acetylated plywood depicts more stable mechanical properties but higher brittleness than untreated specimens., Marknaden för träbaserade byggsystem har expanderat kraftigt under senare år vilket inneburit ökad efterfrågan på förädlade träprodukter, så kallade engineered wood products (EWPs). Utomhusexponering av EWPs innebär dock ofta en risk för beständighetsrelaterade problem. För bärande träkonstruktioner i utomhusmiljö möjliggör kombinationen av trämodifiering genom acetylering och EWP, en tillverkning av träkonstruktionselement med både hög beständighet och hållfasthet. Denna avhandling berör de mekaniska egenskaperna hos plywood tillverkad av acetylerade björkfanér. Specifikt utfördes drag-, tryck-, skjuvnings- och böjtester i förhållande till fibervinkeln hos plywoodens ytfanér vid 0° (parallellt med fiberriktningen), 22,5°, och 45°. Testresultaten jämfördes med kommersiell omodifierad björkplywoods egenskaper avseende spännings- och töjningsförhållanden, orsaker till brott, styrka och styvhet. Dessutom genomfördes liknande tester där prover konditionerats i tre olika klimat för att undersöka inverkan av klimatet på de mekaniska egenskaperna hos både acetylerad och omodifierad björkplywood. Konditioneringen genomfördes i klimatkammare vid en temperatur av 20°C vid 35, 65 respektive 95 % relativ luftfuktighet (RF). I detta fall belastades proverna i förhållande till fibervinkeln hos ytfanéren vid 0°, 45° och 90°. Inverkan av konditioneringen i olika klimat studerades med avseende på böjhållfasthet, styvhet och sprödhet. Testresultaten visar att acetylerad björkplywood har likvärdiga mekaniska egenskaper som omodifierad. Vid förhöjd RF har acetylerad björkplywood mer stabila mekaniska egenskaper jämfört med omodifierad björkplywood. Acetylerad björkplywood är dock sprödare., QC 20230503

Sirtuins and autophagy are well-characterized agents that can promote longevity and protect individual organisms from age-associated diseases like neurodegenerative disorders. In recent years, more and more data has been obtained that discerned potential overlaps and crosstalk between Sirtuin proteins and autophagic activity. This review aims to summarize the advances within the field for each individual Sirtuin in mammalian systems. In brief, most Sirtuins have been implicated in promoting autophagy, with Sirtuin 1 and Sirtuin 6 showing the highest immediate involvement, while Sirtuin 4 and Sirtuin 5 only demonstrate occasional influence. The way Sirtuins regulate autophagy, however, is very diverse, as they have been shown to regulate gene expression of autophagy-associated genes and posttranslational modifications of proteins, with consequences for the activity and cellular localization of these proteins. They have also been shown to determine specific proteins for autophagic degradation. Overall, much data has been accumulated over recent years, yet many open questions remain. Especially although the dynamic between Sirtuin proteins and the immediate regulation of autophagic players like Light Chain 3B has been confirmed, many of these proteins have various orthologues in mammalian systems, and research so far has not exceeded the bona fide components of autophagy., source:https://onlinelibrary.wiley.com/doi/10.1002/jcb.30377

Cancer is a health problem that affects millions of people around the world. Being such a complex disease, not all aspects involved in its development are yet known. One of the cellular mechanisms that have attracted the interest of researchers is acetylation of proteins. This consists of adding acetyl groups to the amino acid chain of proteins. In mitochondrial proteins, this modification has a negative effect leading to impaired mitochondrial function, which induces changes in the cellular machinery that predispose to the onset and development of cancer. Modulation of mitochondrial protein acetylation patterns may be a viable therapeutic approach for the treatment of this disease., El cáncer es un problema de salud que afecta a millones de personas en todo el mundo. Al ser una enfermedad tan compleja, todavía no se conocen todos los aspectos implicados en su desarrollo. Uno de los mecanismos celulares que han atraído el interés de los investigadores es la acetilación de proteínas. Ésta consiste en adicionar grupos acetilo a la cadena de aminoácidos de proteínas. En proteínas mitocondriales, esta modificación tiene un efecto negativo que conduce a un funcionamiento deficiente de las mitocondrias, las cuales inducen cambios en la maquinaria celular que predisponen la aparición y el desarrollo del cáncer. La modulación de los patrones de acetilación de proteínas mitocondriales puede ser un enfoque terapéutico viable para el tratamiento de esta enfermedad.

The global production of paper was more than 400 million tons in 2020, and about 40–50 kg of dry sludge/ton paper produced was generated. The management of this huge volume of solid waste material has become a serious problem for paper industry and an environmental challenge. Sustainable practices, alternative to disposal by landfilling, must be developed. The present work studied the potential of reusing sludge waste from paper manufacturer with the purpose to produce cellulose acetate films., Peer Reviewed, Objectius de Desenvolupament Sostenible::9 - Indústria, Innovació i Infraestructura, Objectius de Desenvolupament Sostenible::13 - Acció per al Clima, Objectius de Desenvolupament Sostenible::12 - Producció i Consum Responsables, Postprint (published version)

In 2010, the WHO recommended an increase in the daily doses of first-line anti-tuberculosis medicines in children. We aim to characterize the pharmacokinetics of the once-daily isoniazid (INH) dose at 10 mg/kg of body weight in infants <6 months of age. We performed a multicenter pharmacokinetic study in Spain. The N-acetyltransferase 2 gene was analyzed to determine the acetylation status. Samples were analyzed using a validated UPLC-UV assay. A non-compartmental pharmacokinetic analysis was performed. Twenty-three pharmacokinetic profiles were performed in 20 infants (8 females) at a median (IQR) age of 19.0 (12.6-23.3) weeks. The acetylator statuses were homozygous fast (n = 1), heterozygous intermediate (n = 12), and homozygous slow (n = 7). INH median (IQR) Cmax and AUC0-24h values were 4.8 (3.7-6.7) mg/L and 23.5 (13.4-36.7) h*mg/L and the adult targets (>3 mg/L and 11.6-26.3 h*mg/L) were not reached in three and five cases, respectively. The age at assessment or acetylator status had no impact on Cmax values, but a larger INH AUC0-24h (p = 0.025) and trends towards a longer half-life (p = 0.055) and slower clearance (p = 0.070) were observed in homozygous slow acetylators. Treatment was well tolerated; mildly elevated alanine aminotransferase levels were observed in three cases. In our series of young infants receiving isoniazid, no major safety concerns were raised, and the target adult levels were reached in most patients.

The MYC oncogenic transcription factor is acetylated by the p300 and GCN5 histone acetyltransferases. The significance of MYC acetylation and the functions of specific acetylated lysine (AcK) residues have remained unclear. Here, we show that the major p300-acetylated K148(149) and K157(158) sites in human (or mouse) MYC and the main GCN5-acetylated K323 residue are reversibly acetylated in various malignant and nonmalignant cells. Oncogenic overexpression of MYC enhances its acetylation and alters the regulation of site-specific acetylation by proteasome and deacetylase inhibitors. Acetylation of MYC at different K residues differentially affects its stability in a cell type-dependent manner. Lysine-to-arginine substitutions indicate that although none of the AcK residues is required for MYC stimulation of adherent cell proliferation, individual AcK sites have gene-specific functions controlling select MYC-regulated processes in cell adhesion, contact inhibition, apoptosis, and/or metabolism and are required for the malignant cell transformation activity of MYC. Each AcK site is required for anchorage-independent growth of MYC-overexpressing cells in vitro, and both the AcK148(149) and AcK157(158) residues are also important for the tumorigenic activity of MYC transformed cells in vivo. The MYC AcK site-specific signaling pathways identified may offer new avenues for selective therapeutic targeting of MYC oncogenic activities.

BackgroundEnhancers are essential in defining cell fates through the control of cell-type-specific gene expression. Enhancer activation is a multi-step process involving chromatin remodelers and histone modifiers including the monomethylation of H3K4 (H3K4me1) by MLL3 (KMT2C) and MLL4 (KMT2D). MLL3/4 are thought to be critical for enhancer activation and cognate gene expression including through the recruitment of acetyltransferases for H3K27.ResultsHere we test this model by evaluating the impact of MLL3/4 loss on chromatin and transcription during early differentiation of mouse embryonic stem cells. We find that MLL3/4 activity is required at most if not all sites that gain or lose H3K4me1 but is largely dispensable at sites that remain stably methylated during this transition. This requirement extends to H3K27 acetylation (H3K27ac) at most transitional sites. However, many sites gain H3K27ac independent of MLL3/4 or H3K4me1 including enhancers regulating key factors in early differentiation. Furthermore, despite the failure to gain active histone marks at thousands of enhancers, transcriptional activation of nearby genes is largely unaffected, thus uncoupling the regulation of these chromatin events from transcriptional changes during this transition. These data challenge current models of enhancer activation and imply distinct mechanisms between stable and dynamically changing enhancers.ConclusionsCollectively, our study highlights gaps in knowledge about the steps and epistatic relationships of enzymes necessary for enhancer activation and cognate gene transcription.

Skeletal muscle is more resilient to ischemia-reperfusion injury than other organs. Tissue specific post-translational modifications of cytochrome c (Cytc) are involved in ischemia-reperfusion injury by regulating mitochondrial respiration and apoptosis. Here, we describe an acetylation site of Cytc, lysine 39 (K39), which was mapped in ischemic porcine skeletal muscle and removed by sirtuin5 in vitro. Using purified protein and cellular double knockout models, we show that K39 acetylation and acetylmimetic K39Q replacement increases cytochrome c oxidase (COX) activity and ROS scavenging while inhibiting apoptosis via decreased binding to Apaf-1, caspase cleavage and activity, and cardiolipin peroxidase activity. These results are discussed with X-ray crystallography structures of K39 acetylated (1.50 Å) and acetylmimetic K39Q Cytc (1.36 Å) and NMR dynamics. We propose that K39 acetylation is an adaptive response that controls electron transport chain flux, allowing skeletal muscle to meet heightened energy demand while simultaneously providing the tissue with robust resilience to ischemia-reperfusion injury.

[Background]: Dynamic chromatin remodeling is associated with changes in the epigenetic pattern of histone acetylations and methylations required for processes based on dynamic chromatin remodeling and implicated in different nuclear functions. These histone epigenetic modifications need to be coordinated, a role that may be mediated by chromatin kinases such as VRK1, which phosphorylates histones H3 and H2A., [Methods]: The effect of VRK1 depletion and VRK1 inhibitor, VRK-IN-1, on the acetylation and methylation of histone H3 in K4, K9 and K27 was determined under different conditions, arrested or proliferating cells, in A549 lung adenocarcinoma and U2OS osteosarcoma cells., [Results]: Chromatin organization is determined by the phosphorylation pattern of histones mediated by different types of enzymes. We have studied how the VRK1 chromatin kinase can alter the epigenetic posttranslational modifications of histones by using siRNA, a specific inhibitor of this kinase (VRK-IN-1), and of histone acetyl and methyl transferases, as well as histone deacetylase and demethylase. Loss of VRK1 implicated a switch in the state of H3K9 posttranslational modifications. VRK1 depletion/inhibition causes a loss of H3K9 acetylation and facilitates its methylation. This effect is similar to that of the KAT inhibitor C646, and to KDM inhibitors as iadademstat (ORY-1001) or JMJD2 inhibitor. Alternatively, HDAC inhibitors (selisistat, panobinostat, vorinostat) and KMT inhibitors (tazemetostat, chaetocin) have the opposite effect of VRK1 depletion or inhibition, and cause increase of H3K9ac and a decrease of H3K9me3. VRK1 stably interacts with members of these four enzyme families. However, VRK1 can only play a role on these epigenetic modifications by indirect mechanisms in which these epigenetic enzymes are likely targets to be regulated and coordinated by VRK1, [Conclusions]: The chromatin kinase VRK1 regulates the epigenetic patterns of histone H3 acetylation and methylation in lysines 4, 9 and 27. VRK1 is a master regulator of chromatin organization associated with its specific functions, such as transcription or DNA repair.

[Background]: Dynamic chromatin remodeling is associated with changes in the epigenetic pattern of histone acetylations and methylations required for processes based on dynamic chromatin remodeling and implicated in different nuclear functions. These histone epigenetic modifications need to be coordinated, a role that may be mediated by chromatin kinases such as VRK1, which phosphorylates histones H3 and H2A., [Methods]: The effect of VRK1 depletion and VRK1 inhibitor, VRK-IN-1, on the acetylation and methylation of histone H3 in K4, K9 and K27 was determined under different conditions, arrested or proliferating cells, in A549 lung adenocarcinoma and U2OS osteosarcoma cells., [Results]: Chromatin organization is determined by the phosphorylation pattern of histones mediated by different types of enzymes. We have studied how the VRK1 chromatin kinase can alter the epigenetic posttranslational modifications of histones by using siRNA, a specific inhibitor of this kinase (VRK-IN-1), and of histone acetyl and methyl transferases, as well as histone deacetylase and demethylase. Loss of VRK1 implicated a switch in the state of H3K9 posttranslational modifications. VRK1 depletion/inhibition causes a loss of H3K9 acetylation and facilitates its methylation. This effect is similar to that of the KAT inhibitor C646, and to KDM inhibitors as iadademstat (ORY-1001) or JMJD2 inhibitor. Alternatively, HDAC inhibitors (selisistat, panobinostat, vorinostat) and KMT inhibitors (tazemetostat, chaetocin) have the opposite effect of VRK1 depletion or inhibition, and cause increase of H3K9ac and a decrease of H3K9me3. VRK1 stably interacts with members of these four enzyme families. However, VRK1 can only play a role on these epigenetic modifications by indirect mechanisms in which these epigenetic enzymes are likely targets to be regulated and coordinated by VRK1., [Conclusions]: The chromatin kinase VRK1 regulates the epigenetic patterns of histone H3 acetylation and methylation in lysines 4, 9 and 27. VRK1 is a master regulator of chromatin organization associated with its specific functions, such as transcription or DNA repair.

The accessibility of DNA to different cellular functions requires a dynamic regulation of chromatin organization that is mediated by different epigenetic modifications, which regulate chromatin accessibility and degree of compaction. These epigenetic modifications, particularly the acetylation of histone H4 in lysine 14 (H4K16ac), determine the degree of chromatin accessibility to different nuclear functions, as well as to DNA damage drugs. H4K16ac is regulated by the balance between two alternative histone modifications, acetylation and deacetylation, which are mediated by acetylases and deacetylases. Tip60/KAT5 acetylates, and SIRT2 deacetylates histone H4K16. However, the balance between these two epigenetic enzymes is unknown. VRK1 regulates the level of H4K16 acetylation by activating Tip60. We have shown that the VRK1 and SIRT2 are able to form a stable protein complex. For this work, we used in vitro interaction, pull-down and in vitro kinase assays. In cells, their interaction and colocalization were detected by immunoprecipitation and immunofluorescence. The kinase activity of VRK1 is inhibited by a direct interaction of its N-terminal kinase domain with SIRT2 in vitro. This interaction causes a loss of H4K16ac similarly to the effect of a novel VRK1 inhibitor (VRK-IN-1) or VRK1 depletion. The use of specific SIRT2 inhibitors in lung adenocarcinoma cells induces H4K16ac, contrary to the novel VRK-IN-1 inhibitor, which prevents H4K16ac and a correct DNA damage response. Therefore, the inhibition of SIRT2 can cooperate with VRK1 in the accessibility of drugs to chromatin in response to DNA damage caused by doxorubicin.

Nucleosomes are the basic units of chromatin and critical for storage and expression of eukaryotic genomes. Chromatin accessibility and gene readout are heavily regulated by epigenetic marks, in which post-translational modifications of histones play a key role. However, the mode of action and the structural implications at the single-molecule level of nucleosomes is still poorly understood. Here we apply a high-throughput atomic force microscopy imaging and analysis pipeline to investigate the conformational landscape of the nucleosome variants three additional methyl groups at lysine 36 of histone H3 (H3K36me3), phosphorylation of H3 histones at serine 10 (H3S10phos), and acetylation of H4 histones at lysines 5, 8, 12, and 16 (H4K5/8/12/16ac). Our data set of more than 25,000 nucleosomes reveals nucleosomal unwrapping steps corresponding to 5-bp DNA. We find that H3K36me3 nucleosomes unwrap significantly more than wild-type nucleosomes and additionally unwrap stochastically from both sides, similar to centromere protein A (CENP-A) nucleosomes and in contrast to the highly anticooperative unwrapping of wild-type nucleosomes. Nucleosomes with H3S10phos or H4K5/8/12/16ac modifications show unwrapping populations similar to wild-type nucleosomes and also retain the same level of anticooperativity. Our findings help to put the mode of action of these modifications into context. Although H3K36me3 likely acts partially by directly affecting nucleosome structure on the single-molecule level, H3S10phos and H4K5/8/12/16ac must predominantly act through higher-order processes. Our analysis pipeline is readily applicable to other nucleosome variants and will facilitate future high-resolution studies of the conformational landscape of nucleoprotein complexes.

The wood-water interactions of modified beech wood (Fagus sylvatica L.) were studied. Specimens were thermally modified at 180 (TM1), 200 (TM2) and 220 degrees C (TM3), acetylated (Acet), and melamine formaldehyde (MF) resin (Mel) modified. Afterwards, the water vapour characteristics, i.e. water vapour sorption isotherms, equilibrium moisture content (EMC), dimensional stability of specimens conditioned at 30, 65 and 90% RH and liquid water characteristics, i.e. water absorption, maximum moisture content (MC), leachability and swelling kinetics, were determined and the results compared with reference (Ref) specimens. From the results, it is evident that the scale of wood-water interactions was highly dependent on the thermal modification temperature and type of chemical modification. The water vapour isotherms of thermally modified wood decreased, whereas more severe treatment exhibited more distinct reduction. The EMC values of the Mel and TM1 specimens decreased only at high RH, whereas the most significant decrease, within the whole range of observation, was found in the Acet group. The maximum MC reduction was achieved by acetylation. As a consequence of swelling reduction, dimensional stability expressed as anti-swelling efficiency (ASE) was considerably improved. A relatively high initial linear-phase swelling rate was found for the Ref specimens, whereas modified wood exhibited comparatively slow and gradual swelling.

Gaseous acetic acid is formed under conditions of storage of historic paper objects. Its presence not only promotes hydrolytic cleavage of cellulose, but also causes acetylation of the cellulosic material to very small degree. The acetylation reaction proceeds under ambient conditions and without catalyst. Different analytical methods were used to prove the presence of organic acetates on cellulosic paper matrices. DESI-MS in combination with 2H-isotopic labeling showed the presence of sugar fragments with different acetylation patterns. A method based on Zemplen saponification was applied and worked also in the presence of a large excess of acetic acid and/or inorganic acetates. The acetylation effect was quantified for model papers and original, naturally aged paper samples. While cellulose acetylation was clearly proven to be another general pathway of paper aging, further studies of this acetylation phenomenon are needed with regard to conservational aspects and suitable paper storage conditions.

Histone lactylation and acetylation compete for epigenetic modification of lysines and mark the levels of lactates and acetyl-CoA. Whether pyruvate is committed to lactate or acetyl-CoA generation as the outlet of glycolysis determines cell fate towards malignancy or not. Taking control over the glycolytic switch as marked by lactylation suggests novel therapeutic opportunities against cancers.

Mitochondrial transcription factor A (TFAM) plays important roles in mitochondrial DNA compaction, transcription initiation, and in the regulation of processes like transcription and replication processivity. It is possible that TFAM is locally regulated within the mitochondrial matrix via such mechanisms as phosphorylation by protein kinase A and nonenzymatic acetylation by acetyl-CoA. Here, we demonstrate that DNA-bound TFAM is less susceptible to these modifications. We confirmed using EMSAs that phosphorylated or acetylated TFAM compacted circular double-stranded DNA just as well as unmodified TFAM and provide an in-depth analysis of acetylated sites on TFAM. We show that both modifications of TFAM increase the processivity of mitochondrial RNA polymerase during transcription through TFAM-imposed barriers on DNA, but that TFAM bearing either modification retains its full activity in transcription initiation. We conclude that TFAM phosphorylation by protein kinase A and nonenzymatic acetylation by acetyl-CoA are unlikely to occur at the mitochondrial DNA and that modified free TFAM retains its vital functionalities like compaction and transcription initiation while enhancing transcription processivity.

The outstanding mechanical properties of birch plywood make it promising to be applied for structural purposes. However, the poor durability of birch against biodeterioration limits its outdoor uses. Chemical modification, e.g., acetylation, is one of the potent ways to mitigate the durability issues. Embedment strength is one of the main parameters that affect the strength of timber connection. This paper reveals the embedment behavior of both acetylated and unmodified birch plywood. Specifically, embedment tests are conducted on acetylated and unmodified birch plywood at three different angles, i.e., 0° (parallel), 45°, and 90°(perpendicular) to the face grain. The test results show that the embedment stiffness and strength of acetylated birch plywood exhibit slight angle-dependence, while for the unmodified specimens the influence of the load-to-face grain angle on the embedment stiffness and strength is less pronounced. Moreover, acetylated birch plywood specimens show higher embedment strength than unmodified ones at all angles to the face grain, which could be attributed to the enhanced density and reduced moisture content induced by the acetylation process. Lastly, the characteristic embedment strength predicted by using the formula in Eurocode 5 is compared with the one derived from the test results., QC 20220603

Heart failure, mostly associated with cardiac hypertrophy, is a major cause of illness and death. Oxidative stress causes accumulation of reactive oxygen species (ROS), leading to mitochondrial dysfunction, suggesting that mitochondria-targeted therapies could be effective in this context. The purpose of this work was to determine whether mitochondria-targeted therapies could improve cardiac hypertrophy induced by mitochondrial ROS. We used neonatal (NCMs) and adult (ACMs) rat cardiomyocytes hypertrophied by isoproterenol (Iso) to induce mitochondrial ROS. A decreased interaction between sirtuin 3 and superoxide dismutase 2 (SOD2) induced SOD2 acetylation on lysine 68 and inactivation, leading to mitochondrial oxidative stress and dysfunction and hypertrophy after 24 h of Iso treatment. To counteract these mechanisms, we evaluated the impact of the mitochondria-targeted antioxidant mitoquinone (MitoQ). MitoQ decreased mitochondrial ROS and hypertrophy in Iso-treated NCMs and ACMs but altered mitochondrial structure and function by decreasing mitochondrial respiration and mitophagy. The same decrease in mitophagy was found in human cardiomyocytes but not in fibroblasts, suggesting a cardiomyocyte-specific deleterious effect of MitoQ. Our data showed the importance of mitochondrial oxidative stress in the development of cardiomyocyte hypertrophy. We observed that targeting mitochondria by MitoQ in cardiomyocytes impaired the metabolism through defective mitophagy, leading to accumulation of deficient mitochondria.

The effect of prolonged ultraviolet (UV) irradiation on the performance of superhydrophobized birch and acetylated birch wood was investigated. The surface modification of the wood was based on a newly developed method using silicone nanofilaments. The combination of surface modification and acetylation of wood showed good wetting resistance also after 600 h of UV exposure, with water contact angles greater than 140° and water uptake 30 times lower by weight than that of the non-surface-modified wood as determined by multicycle Wilhelmy plate measurements. Scanning electron microscopy images revealed that the silicone nanofilaments can still be observed on the wood samples after UV irradiation. The surface-modified wood samples exhibited significant color change after UV exposure. FTIR spectra showed that lignin was degraded on both the non-surface-modified wood surfaces and the wood surface-modified with the silicone nanofilaments.

Background: High doses of doxorubicin put cancer patients at risk for developing dilated cardiomyopathy. Previously, we showed that doxorubicin treatment decreases SIRT3 (sirtuin 3), the main mitochondrial deacetylase and increases protein acetylation in rat cardiomyocytes. Here, we hypothesize that SIRT3 expression can attenuate doxorubicin induced dilated cardiomyopathy in vivo by preventing the acetylation of mitochondrial proteins. Methods: Nontransgenic, M3-SIRT3 (truncated SIRT3; short isoform), and M1-SIRT3 (full-length SIRT3; mitochondrial localized) transgenic mice were treated with doxorubicin for 4 weeks (8 mg/kg body weight per week). Echocardiography was performed to assess cardiac structure and function and validated by immunohistochemistry and immunofluorescence (n=4-10). Mass spectrometry was performed on cardiac mitochondrial peptides in saline (n=6) and doxorubicin (n=5) treated hearts. Validation was performed in doxorubicin treated primary rat and human induced stem cell derived cardiomyocytes transduced with adenoviruses for M3-SIRT3 and M1-SIRT3 and deacetylase deficient mutants (n=4-10). Results: Echocardiography revealed that M3-SIRT3 transgenic mice were partially resistant to doxorubicin induced changes to cardiac structure and function whereas M1-SIRT3 expression prevented cardiac remodeling and dysfunction. In doxorubicin hearts, 37 unique acetylation sites on mitochondrial proteins were altered. Pathway analysis revealed these proteins are involved in energy production, fatty acid metabolism, and oxidative stress resistance. Increased M1-SIRT3 expression in primary rat and human cardiomyocytes attenuated doxorubicin-induced superoxide formation, whereas deacetylase deficient mutants were unable to prevent oxidative stress. Conclusions: Doxorubicin reduced SIRT3 expression and markedly affected the cardiac mitochondrial acetylome. Increased M1-SIRT3 expression in vivo prevented doxorubicin-induced cardiac dysfunction, suggesting that SIRT, QC 20220530

Cellulose acetate (CA) is subjected to different aqueous environments (e.g., lake water, seawater, artificial seawater) under controlled laboratory conditions to investigate the degradation potential in natural water systems. The main changes in the CA films are detected during the first months of the 12-month study. Approximately 5% and 10% weight losses are observed during the first month of aging at RT and at 60 °C, respectively. The temperature effect is rather negligible and the weight loss also does not significantly increase on prolonged aging. A quantitative high-performance liquid chromatography analysis shows that this weight loss is mainly caused by deacetylation and depending on the aging conditions, 10–30% of the acetate groups are lost during the first 1–3 months of aging. Fourier transform infrared and nuclear magnetic resonance analyses further support this. It is well established that a high degree of substitution (DS) is the bottleneck for biodegradation of CA and a significantly higher biodegradation rate has been demonstrated for CA materials with degree of substitution, DS<2, compared to those with DS>2. The degree of deacetylation observed here is enough to decrease the DS to below 2, which can therefore have a significant effect on the subsequent biodegradation., QC 20230615