Precursor For Synthesis Research Articles

Computational analysis of the deleterious non-synonymous single nucleotide polymorphisms (nsSNPs) in TYR gene impacting human tyrosinase protein and the protein stability.

Tyrosinase, a copper-containing oxidase, plays a vital role in the melanin biosynthesis pathway. Mutations in the tyrosinase gene can disrupt the hydroxylation of tyrosine, leading to decreased production of 3,4-dihydroxyphenylalanine (DOPA). Consequently, this impairs the subsequent formation of dopaquinone, a key precursor in melanin pigment synthesis. This study aimed to identify the deleterious non-synonymous single nucleotide polymorphisms (nsSNPs) within the TYR gene that exert an influence on the human TYR protein. Additionally, we evaluated the impact of 10 FDA-approved drugs on the protein stability of mutated structures, exploring the potential for inhibitory pharmaceutical interventions. Through various bioinformatics tools, we detected 47900 nsSNPs, particularly K142M, I151N, M179R, S184L, L189P, and C321R, which were found to be the most deleterious variants, decreasing the protein stability. These drugs (Sapropterin, Azelaic Acid, Menobenzone, Levodopda, Mequinol, Arbutin, Hexylresorcinol, Artenimol, Alloin and Curcumin) interacted with the binding sites in four mutant models K142M, I151N, M179R, and S184L proving that these ligands directly bind with the active site of mutant tyrosinase protein to inhibit it's working. On the other hand, two mutant models L189P and C321R did not show any binding site residue interaction with any ligands. In conclusion, this in-silico analysis of deleterious nsSNPs in the TYR gene, coupled with the evaluation of ligands/drugs on mutated tyrosinase structures not only advances our understanding of molecular variations but also highlights promising pathways for targeted inhibitory interventions in the intricate network of melanin biosynthesis.

Yeast metabolism adaptation for efficient terpenoids synthesis via isopentenol utilization.

Microbial biosynthesis has become the leading commercial approach for large-scale production of terpenoids, a valuable class of natural products. Enhancing terpenoid production, however, requires complex modifications on the host organism. Recently, a two-step isopentenol utilization (IU) pathway relying solely on ATP as the cofactor has been proposed as an alternative to the mevalonate (MVA) pathway, streamlining the synthesis of the common terpenoid precursors. Herein, we find that isopentenol inhibits energy metabolism, leading to reduced efficiency of the IU pathway in Saccharomyces cerevisiae. To overcome this, we engineer an IU pathway-dependent (IUPD) strain, designed for growth-coupled production. The IUPD strain is compelled to enhance the ATP supply, essential for the IU pathway, and incorporates a high-throughput screening method for enzyme evolution. The refined IU pathway surpasses the MVA pathway in synthesizing complex terpenoids. Our work offers valuable insights into developing growth-coupled strains adapted to efficient natural product synthesis.

Multiple metabolic engineering of Saccharomyces cerevisiae for the production of lycopene

AbstractLycopene is a high‐value‐added tetraterpenoid, which is widely used in cosmetics, medicine, food, and dietary supplements. The intracellular mevalonate pathway of Saccharomyces cerevisiae provides natural precursors for terpenoid product synthesis, so it is an excellent host for the heterologous production of lycopene. In this study, a recombinant strain named L10 with efficient lycopene production capability was constructed through multiple strategies, such as regulating the gene copy number of key enzymes, increasing nicotinamide adenine dinucleotide phosphate supply, and reducing squalene accumulation. Then, considering that intracellular lycopene accumulation can cause cytotoxicity to S. cerevisiae, we attempted to identify a transporter that can efficiently transport lycopene from intracellular to extracellular space. Molecular docking simulations predicted that the ATP‐binding cassette transporter Snq2p may be a potential transporter of lycopene, and its function in promoting lycopene secretion was further determined by overexpression verification. The lycopene secretion titer of the strain L10Z2 overexpressing Snq2p increased to 16.5 times that of the control at the shake‐flask level. After optimizing the galactose regulation system, the intracellular and secreted lycopene production of L11Z2 reached 2113.78 and 26.28 mg/L, respectively, after 150 h fed‐batch culture in a 3‐L bioreactor. This work provides a new research direction for efficient lycopene synthesis in S. cerevisiae cell factory.

Synergistic Regulation of Phase and Nanostructure of Nickel Molybdate for Enhanced Supercapacitor Performance

Nickel molybdate, which has a relatively high theoretical capacity, demonstrates potential for use in supercapacitors. However, its inferior electrical conductivity and cycling stability have led to poor electrochemical performance. Nanostructure engineering of NiMoO4 is an efficient strategy to overcome its performance limitations as an electrode. Here, a facile approach is reported for the precise phase regulation and nanostructure of NiMoO4 by manipulating the synthesis parameters, including duration, precursor selection, and urea concentration. The electrochemical properties of the electrode materials are also investigated. It is interesting to note that the β-NiMoO4 nanosheets show a decent specific capacity of 332.8 C/g at 1 A/g, surpassing the 252.6 C/g of the α-NiMoO4 nanorods. Furthermore, the supercapacitor device constructed with β-NiMoO4 and reduced graphene oxide hydrogel (rGH) electrodes achieves an acceptable energy density of 36.1 Wh kg−1, while retaining 70.2% after 5000 cycles.

The Fabrication of ZIF-L Derived Zns/Mos2@NC Anode Materials for Remarkable Lithium-Ion Storage.

The enhancement of electrochemical performance in lithium-ion batteries can be achieved through the incorporation of MoS2 with carbon materials and various metal sulfides. In this study, a ZnS/MoS2 heterostructure was developed, featuring a two-dimensional nitrogen-doped carbon nanosheet (NC) backbone. The synthesis of ZnMoZIF-L precursors was accomplished by introducing a Mo source in a 1 : 1 molar ratio during the ZIF-L synthesis process. Following high-temperature carbonization and vulcanization treatment, ZnS/MoS2@NC composite materials were successfully synthesized. Compared to the unvulcanized ZnO/MoO3@NC and MoS2 samples, the ZnS/MoS2@NC composite exhibits remarkable lithium storage performance. At a current density of 500 mA g-1, the initial reversible capacity capacity is still as high as 1674 mAh g-1. Furthermore, this composite material demonstrates optimal rate capabilities and a significant contribution to pseudocapacitance. The nitrogen-doped carbon framework effectively mitigates volume changes, while the heterostructural design provides more active sites for lithium-ions, thereby enhancing lithium storage performance.

Different nitrogen conditions regulating extracellular polymeric substances and erosion resistance of sewer sediment: Mechanism of microbial metabolism and molecular response

Nitrogen biotransformation plays a vital role in the metabolism of microbial communities in sewers. Extracellular polymeric substances (EPS) secreted by microbial communities can form gel-like sewer sediments, causing clogging of the sewer. However, knowledge on the effects of varying nitrogen conditions on the erosion resistance of sewer sediments and EPS produced by sewer microorganisms is limited. In this study, two typical organic/inorganic nitrogen ratios of sewage were reproduced in simulated sewer reactors, i.e., 3/7 (R1 group) and 7/3 (R2 group). Higher organic nitrogen (ON) concentrations were found to increase the critical erosion shear stress by 26.43%; this was ascribed to increased particle diameter, weakened electrostatic repulsion of sediments and stimulated EPS secretion in the R2 group. The protein and polysaccharide contents of the R2 group were 48.84% and 34.25% higher than those of the R1 group, respectively, which was supported by increased gene abundances for aromatic amino acid synthesis, general secretory pathways of protein, and synthesis of precursors and polysaccharides. Tightly-bound EPS in R2 group exhibited increased contents of hydrophobic protein secondary structures and intermolecular hydrogen bonds, thereby promoting the formation of gel-like sediment structures with enhanced erosion resistance. However, the microbial diversity and the abundance of key genes involved in EPS generation and secretion (e.g., tyrB, yajC, secB, gumF, and gumH) obviously decreased in the R1 group. Moreover, high ON concentrations increased microbial diversity and enhanced microbial glycolysis, tricarboxylic acid cycle and ammonium assimilation. This study reveals the formation mechanisms of EPS in sewer sediments under different nitrogen conditions and their effects on sediment erosion resistance, which contributed to improved sewer system operation and sewer sediment control.

From molecular precursors to ultra-high temperature ceramics: A novel synthesis of hafnium carbonitride nanoceramics

Hafnium carbonitride (HfCxN1–x) ceramics have drawn considerable interest due to their exceptional mechanical and thermophysical properties. Herein, we report a novel single-source precursor with Hf–N bonds as the main chain and fabricate HfCxN1–x ceramics after pyrolysis of the precursor. The synthesis, ceramic conversion, and microstructural evolution of the single-source precursor as well as the derived HfCxN1–x ceramics treated under various atmospheres were investigated. The results indicate that in an argon atmosphere, the nitrogen content within HfCxN1–x decreases with rising temperature. While under a nitrogen atmosphere, the high concentration of N2 facilitates the rapid conversion of HfO2 to Hf7O8N4, which subsequently promotes the transformation of the HfCxN1–x solid solution ceramics. During this process, there is also an inhibitory effect of N2 on the tendency of HfN into HfC. Moreover, the desired chemical composition of HfCxN1–x can be regulated by adjusting the N2 concentration in the heat treatment atmosphere. The present work proposes a novel strategy for the single-source precursor-derived carbonitride ceramics and provides a deep understanding of the preparation and property modulation of HfCxN1–x ceramics.

INVESTIGATION OF STRUCTURAL FEATURES OF ASPHALTENES USED FOR CARBON MATERIALS SYNTHESIS BY ARC PLASMA TREATMENT

This study presents analysis of asphaltenes isolated from two crude oils: naphthenic-aromatic biodegraded oil and paraffin-naphthenic oil, which have been used as precursors for carbon materials synthesis. The aim of this study is to investigate the interrelationship between the initial structure of asphaltene and the properties of carbon materials. Based on number of spectroscopic and other data, it can be found out that the asphaltenes from napthenic-aromatic biodegraded oil contain less paraffin and more cyclic fragments (aromatic and aliphatic), that are larger and more densely stacked. The asphaltenes of paraffin-naphthenic oil contain a larger number of labile bonds and heteroatoms. Both the asphaltenes contain sulfur enclosed in thiophene and sulfide fragments, nitrogen and oxygen, which are incorporated in different units with different thermal stability. Carbon materials are obtained from both asphaltenes via plasma of an electric arc discharge. The asphaltenes undergo graphitization as a result of plasma treatment, the general trend is an elimination of functional groups and N, S, O. The yields of the carbon materials are almost equal for two studied asphaltenes, giving graphite-like materials as the major product in both cases. The carbon material obtained from the napthenic-aromatic asphaltenes is less thermally stable, the yield of nano-structures and nanofibers are higher compared to the asphaltenes from paraffinic oil, with trace metals remaining during the synthesis process. The carbon material from paraffin-naphthenic oil is amorphous with low heteroatoms content.

Unsaturated organosilanes: synthesis, transformations and applications

The urgency of improving the efficiency of known methods and developing new ones for the synthesis of unsaturated silanes is caused by the need to obtain useful compounds, including biologically active ones, on their basis. This review considers methods for the preparation of unsaturated silanes, their transformations and prospects for their use as precursors in organic and organoelement synthesis. A large number of substituted organosilicon products are given, including those capable of further functionalization and the formation of heterocycles, including silaheterocycles. <br> The bibliography includes 205 references.

Transcriptomics-guided rational engineering in Bacillus licheniformis for enhancing poly-γ-glutamic acid biosynthesis using untreated molasses

The utilization of non-food raw materials for microbial synthesis of poly-γ-glutamic acid (γ-PGA) presents a promising alternative to conventional food-based biosynthesis. However, the complex carbon source and composition of molasses, a prevalent non-food raw material, may impose constraints on its conversion and utilization by microorganisms. This study aimed to enhance the capacity of Bacillus licheniformis to convert untreated molasses into γ-PGA through transcriptomic analysis to guide metabolic modifications. Initial results from the transcriptomic analysis indicated that the strain utilizing molasses exhibited decreased expression of genes associated with substrate utilization (Module 1) and by-product synthesis (Module 2), while upregulating genes related to precursor synthesis (Module 3). Furthermore, we performed a knockout of the acetolactate synthase (AlsS) to reduce the synthesis of metabolic by-products and a knockout of the global regulator (CcpA) to alleviate carbon catabolite repression (CCR) and then promote substrate utilization. Ultimately, following the tandem overexpression of precursor supplying key genes, the titer of γ-PGA reached 48.26 g/L with a productivity of 1.15 g/L/h, using untreated molasses as the sole carbon source, which was 3.12-fold of the starting strain. These findings offer significant insights into the cost-effective synthesis of γ-PGA by bioconversion of untreated molasses during fermentation.

Interplay of CDKs and Cyclins with glycolytic regulatory enzymes PFK and PK.

In plants, as in all eukaryotes, the cell cycle is regulated by the heterodimer formed by cyclins (Cycs) and cyclin-dependent kinases (CDKs), that phosphorylate serine/threonine residues in target proteins. The extensive involvement of these heterodimers in nuclear cell cycle-related processes has been demonstrated. However, recent findings have linked Cyc-CDK complexes to the regulation of cytosolic processes, including various metabolic pathways, suggesting close coordination between the cell cycle and catabolic/anabolic processes to maintain cellular energy homeostasis.This study extends the analysis of Cyc-CDK complex regulation in maize to two key regulators of glycolysis: phosphofructose kinase (PFK) and pyruvate kinase (PK). Both are cytosolic enzymes, highly regulated positively and negatively by different metabolites, showing a similar activation pattern in their homotetrameric form and low activity when as dimers/monomers. Each enzyme exhibits two putative minimal phosphorylation motives for Cyc-CDKs, conserved in some plant species and in four (PFK) and three (PK) isoforms in maize. This work demonstrates that both enzymes are active with fluctuating levels of activity along maize germination; also, that they associate with different maize Cycs and CDKs as demonstrated by pull-down assays, as well as their in vitro phosphorylation by recombinant CycD;2-CDKA or CycD2;2-CDKB complexes. Additionally, the inhibition of PFK and PK activity following phosphorylation by active Cycs-CDKB complexes obtained by immunoprecipitation from imbibed embryonic axis protein extracts suggests a narrow and negative regulation of glycolysis as the cell cycle progresses. A decreased carbon flow through this pathway is proposed to divert carbon from sugars towards the oxidative pentose phosphate pathway, thereby promoting de novo nucleic acid synthesis precursors to stimulate cell cycle progression.

PlsX and PlsY: Additional roles beyond glycerophospholipid synthesis in Gram-negative bacteria.

The unique asymmetry of the Gram-negative outer membrane, with glycerophospholipids (GPLs) in the inner leaflet and lipopolysaccharide (LPS) in the outer leaflet, works to resist external stressors and prevent the entry of toxic compounds. Thus, GPL and LPS synthesis must be tightly controlled to maintain the integrity of this essential structure. We sought to decipher why organisms like Escherichia coli possess two redundant pathways-PlsB and PlsX/Y-for synthesis of the GPL precursor lysophosphatidic acid (LPA). LPA is then converted by PlsC to the universal precursor for GPL synthesis, phosphatidic acid (PA). PlsB and PlsC are essential in E. coli, indicating they serve as the major pathway for PA synthesis. While loss of PlsX or PlsY individually has little consequence on the cell, the absence of both was lethal. To understand the synthetic lethality of this seemingly redundant PlsX/Y pathway, we performed a suppressor screen. Suppressor analysis indicated that ∆plsXY requires increased levels of glycerol-3-phosphate (G3P), a GPL precursor. In agreement, ∆plsXY required supplementation with G3P for survival. Furthermore, loss of PlsX dysregulated fatty acid synthesis, resulting in increased long-chain fatty acids. We show that although PlsX/Y together contribute to PA synthesis, they also contribute to the regulation of overall membrane biogenesis. Thus, synthetic lethality of ∆plsXY is multifactorial, suggesting that PlsX/Y has been maintained as a redundant system to fine-tune the synthesis of major lipids and promote cell envelope homeostasis.IMPORTANCEGram-negative bacteria must maintain optimal ratios of glycerophospholipids and lipopolysaccharide within the cell envelope for viability. Maintenance of proper outer membrane asymmetry allows for resistance to toxins and antibiotics. Here, we describe additional roles of PlsX and PlsY in Escherichia coli beyond lysophosphatidic acid synthesis, a key precursor of all glycerophospholipids. These findings suggest that PlsX and PlsY also play a larger role in impacting homeostasis of lipid synthesis.

Multi-Omics Analysis of Exogenous Potassium (K+)’s Role in Alleviating Trehalose Effects Under NaCl Stress in Tamarix ramosissima

Salt stress significantly impacts plant growth, and Tamarix ramosissima Ledeb is utilized for afforestation in China’s saline–alkali regions. Trehalose, an osmoregulatory compound, enhances plant tolerance to salt stress by stabilizing cell membranes and regulating oxidative states and ion distribution. However, its role in mitigating NaCl-induced damage in Tamarix species remains understudied. In this study, root samples of T. ramosissima were exposed to NaCl stress with exogenous K+ at 0 h, 48 h, and 168 h. Analyses revealed that soluble sugar content increased over time, especially in the 200 mM NaCl + 10 mM KCl treatment at 168 h. Transcriptome sequencing identified 19 trehalose-related genes involved in metabolic and sucrose pathways, with Unigene0015746 notably enhancing D-Glucose 6-phosphate accumulation, a key precursor for trehalose synthesis. This gene emerged as a crucial candidate for further research. The transcriptome data were validated using qRT-PCR. Overall, the study elucidates the molecular mechanisms of trehalose-related genes in T. ramosissima under salt stress with exogenous K+, providing valuable genetic resources for breeding salt-tolerant tree species.

Synthesis of Monodisperse and Discrete Ultra-High Nickel LiNi0.97Co0.02Mn0.01O2 Octahedral Single Crystals via Single Crystal Intermediates for Li-Ion Batteries.

Micrometer-sized single crystal cathodes have garnered significant interest as promising cathode materials for lithium-ion batteries due to their ability to reduce surface area exposure to electrolytes and suppress side reactions, thereby enhancing electrochemical performance. One of the challenging issues with single crystal cathode materials is synthesizing monodisperse and discrete single crystals rather than agglomerated quasi-single crystals. However, conventional solid-state synthesis of most single crystals results in severe agglomeration and cation mixing, as it requires high temperatures to promote particle growth to several micrometers. In this study, a novel morphology-conserving reaction strategy that employs octahedron single crystal intermediates is introduced to synthesize discrete, monodisperse LiNi0.97Co0.02Mn0.01O2 octahedron single crystals. This scalable and cost-effective approach involves using rock-salt Ni0.97Co0.02Mn0.01O1+x octahedrons as single crystal intermediates, which are transformed in unreactive unary lithium salt melts (LiCl and Li2SO4) from spherical Ni0.97Co0.02Mn0.01(OH)2 obtained via coprecipitation. These intermediates are then subjected to a stoichiometric amount of Li precursor in a conventional solid-state synthesis to produce layered LiNi0.97Co0.02Mn0.01O2. This process is a morphology-conserving lithiation reaction, leading to the formation of discrete and monodisperse LiNi0.97Co0.02Mn0.01O2 octahedron single crystals. The resultant LiNi0.97Co0.02Mn0.01O2 single crystals demonstrate superior electrochemical performance, including stable capacity retention over 150 cycles, which surpasses that of typical quasi-single crystals produced through conventional methods. This is attributed to negligible crack formation during cycling, in contrast to significant cracking observed in conventional quasi-single crystals. This implies that single-crystal forms are preferred over agglomerated quasi-single crystal forms for enhancing cycle performance. These findings provide valuable insights into the industrial synthesis of discrete and monodisperse ultrahigh-nickel oxide cathode materials.

Polyoxometalate Derived Materials as Laccase‐Mimic Nanozyme and Reduction Catalyst for p‐Nitrophenol Remediation in Water

Abstractp‐Nitrophenol (PNP), a highly toxic water pollutant, poses significant risks to human health and the environment. For detecting PNP, a colorimetric method utilizing a nanozyme that mimics laccase activity presents a viable approach. In this study, PV14@MIL‐88A, a robust nanozyme with superior laccase‐mimic capabilities, was synthesized by incorporating Na7H2[PV14O42] (PV14) into MIL‐88A, a metal‐organic framework (MOF). This nanozyme demonstrates optimal laccase‐mimicking activity, enabling effective PNP detection via colorimetry and digital image colorimetry using smartphones. Theoretical analyses suggest that the outstanding laccase‐mimic activity of PV14@MIL‐88A is derived from the optimized d‐band center in PV14. Upon calcination with dicyandiamide (DCDA), PV14@MIL‐88A transforms into Fe2O3/VO2@NCNF. In the presence of NaBH4, Fe2O3/VO2@NCNF facilitates the conversion of PNP to p‐aminophenol (PAP), an essential precursor in paracetamol synthesis. The interaction between Fe2O3 and VO2 in Fe2O3/VO2@NCNF enhances adsorption and subsequent reduction of PNP. The saturation magnetization of Fe2O3/VO2@NCNF reaches 25 emu g−1, which supports efficient magnetic separation in the reduction process. This study not only advances an effective method for PNP detection but also facilitates its transformation from a hazardous pollutant into a valuable chemical precursor.

Single Source Precursor Path to 2D Materials: A Case Study of Solution‐Processed Molybdenum‐Rich MoSe2‐x Ultrathin Nanosheets

AbstractTwo‐dimensional Molybdenum diselenide is a versatile and promising material used for a wide range of applications and its synthesis in high quality and yield is currently the subject of intense research. Low temperature solution phase synthesis of nanomaterials using designed molecular precursors enjoys tremendous advantages over traditional high‐temperature solid‐state synthesis. However, molecular precursor chemistry of molybdenum selenide nanomaterials is almost non‐existent. We report here synthesis and structural characterization of new molybdenum molecular precursors with selenoether and selenourea ligands, which due to their easy synthesis, desired Mo/Se composition and moderate processing properties, are highly promising as single source precursors for the scale‐up production of 2D molybdenum diselenide materials. This is demonstrated by the solution‐phase decomposition of the Mo‐selenourea precursor which produced Mo‐rich MoSe2‐x ultrathin nanosheets (NSs) in good yield. These NSs were characterized by Inductively Coupled Plasma Optical Emission Spectroscopy (ICP‐OES), Powder X‐ray diffraction (XRD), Raman spectroscopy, Fourier Transform Infrared Spectroscopy (FT‐IR), Thermogravimetric analysis (TGA), Transmission electron microscopy (TEM) and X‐ray photoelectron spectroscopy (XPS) studies.

Juvenile-related tolerance to papaya sticky disease (PSD): proteomic, ultrastructural, and physiological events.

The proteomic analysis of PMeV-complex-infected C. papaya unveiled proteins undergoing modulation during the plant's development. The infection notably impacted processes related to photosynthesis and cell wall dynamics. The development of Papaya Sticky Disease (PSD), caused by the papaya meleira virus complex (PMeV-complex), occurs only after the juvenile/adult transition of Carica papaya plants, indicating the presence of tolerance mechanisms during the juvenile development phase. In this study, we quantified 1609 leaf proteins of C. papaya using a label-free strategy. A total of 345 differentially accumulated proteins were identified-38 at 3months (juvenile), 130 at 4months (juvenile/adult transition), 160 at 7months (fruit development), and 17 at 9months (fruit harvesting)-indicating modulation of biological processes at each developmental phase, primarily related to photosynthesis and cell wall remodeling. Infected 3- and 4-mpg C. papaya exhibited an accumulation of photosynthetic proteins, and chlorophyll fluorescence results suggested enhanced energy flux efficiency in photosystems II and I in these plants. Additionally, 3 and 4-mpg plants showed a reduction in cell wall-degrading enzymes, followed by an accumulation of proteins involved in the synthesis of wall precursors during the 7 and 9-mpg phases. These findings, along with ultrastructural data on laticifers, indicate that C. papaya struggles to maintain the integrity of laticifer walls, ultimately failing to do so after the 4-mpg phase, leading to latex exudation. This supports initiatives for the genetic improvement of C. papaya to enhance resistance against the PMeV-complex.

Roles of Exogenous 5-Aminolevulinic Acid and Dihydroporphyrin Iron in Chlorophyll Precursor Synthesis and Chlorophyll-Related Enzyme Activities in Wheat Under Different Light Intensities

Aminolevulinic acid (5-ALA) and dihydroporphyrin iron chelates (DHFe) play roles in plant growth regulation under normal and stressful conditions. However, definitive data on their roles in regulating chlorophyll synthesis in wheat are lacking. In this study, the optimal concentrations for foliar-spray application of 5-ALA and DHFe to promote wheat seedling growth and leaf chlorophyll content were assessed. The optimal concentrations of 5-ALA or DHFe (50 mg/L and 0.01 mg/L, respectively) were applied as foliar sprays to seedlings of wheat ‘Bainong 4199’ (high light efficient) and ‘Zhoumai No. 18’ (average light efficient) under different light intensities. Chlorophyll precursor contents and activities of three chlorophyll synthesis-related enzymes were altered, and the combined application of 5-ALA and DHFe more strongly increased the leaf chlorophyll content. 5-ALA significantly increased the contents of the chlorophyll precursors porphobilinogen, uroporphyrinogen III, protoporphyrin IX, and magnesium-protoporphyrin IX, and the activities of 5-amino-ketovalerate dehydratase and uroporphyrinogen III synthase. DHFe resulted in an increase in chlorophyll content but a significant decrease in chlorophyllase activity and protochlorophyllide content. 5-ALA promoted the synthesis of chlorophyll precursors by regulating the activities of 5-amino-ketovalerate dehydratase and uroporphyrinogen III synthase. DHFe decreased chlorophyllase activity, thereby slowing chlorophyll degradation and increasing the chlorophyll content.

Characterizing nano-indentation and microstructural properties of mine tailings-based geopolymers

The mining industry's extraction processes produce vast amounts of waste, including mine tailings (MT), traditionally stored in large ponds, causing significant environmental harm due to a lack of effective recycling methods. This research explores the potential of converting MT into a resource i.e., precursors in geopolymer synthesis. By analyzing the physicochemical and mineralogical properties of MT, the study formulates four geopolymer composites, substituting up to 30 wt% MT for fly ash. The composites' mechanical and microstructural properties show a contribution of MT in the stability of the matrix. Compressive strength of 59 MPa when incorporating 30 wt% MT, along with water absorption, microstructural analysis, and environmental impact assessments, support the hypothesis that the matrix is improved. Nano-indentation techniques further evaluated the nanomechanical properties, such as Young's modulus and fracture toughness. The findings reveal that geopolymers with 30 wt% MT exhibits up to 130 % increased strength. This research highlights the potential for innovative, eco-friendly solutions in waste management and material production, contributing to sustainable mining practices and advancing the field of geopolymer technology.

Essential role of proline synthesis and the one-carbon metabolism pathways for systemic virulence of Streptococcus pneumoniae.

Virulence screens have indicated potential roles during Streptococcus pneumoniae infection for the one-carbon metabolism pathway component Fhs and proline synthesis mediated by ProABC. To define how these metabolic pathways affect S. pneumoniae virulence, we have investigated the phenotypes, transcription, and metabolic profiles of Δfhs and ΔproABC mutants. S. pneumoniae capsular serotype 6B BHN418 Δfhs and ΔproABC mutant strains had strongly reduced virulence in mouse sepsis and pneumonia models but could colonize the nasopharynx. Both mutant strains grew normally in complete media but had markedly impaired growth in chemically defined medium, human serum, and human cerebrospinal fluid. The BHN418 ΔproABC strain also had impaired growth under conditions of osmotic and oxidative stress. The virulence role of proABC was strain specific, as the D39 ΔproABC strain could still cause septicemia and grow in serum. Compared to culture in broth, in serum, the BHN418 Δfhs and ΔproABC strains showed considerable derangement in global gene transcription that affected multiple but different metabolic pathways for each mutant strain. Metabolic data suggested that Δfhs had an impaired stringent response, and when cultured in sera, BHN418 Δfhs and ΔproABC were under increased oxidative stress and had altered lipid profiles. Loss of proABC also affected carbohydrate metabolism and the accumulation of peptidoglycan synthesis precursors in the BHN418 but not the D39 background, linking this phenotype to the conditional virulence phenotype. These data identify the S. pneumoniae metabolic functions affected by S. pneumoniae one-carbon metabolism and proline biosynthesis, and the role of these genetic loci for establishing systemic infection.IMPORTANCERapid adaptation to grow within the physiological conditions found in the host environment is an essential but poorly understood virulence requirement for systemic pathogens such as Streptococcus pneumoniae. We have now demonstrated an essential role for the one-carbon metabolism pathway and a conditional role depending on strain background for proline biosynthesis for S. pneumoniae growth in serum or cerebrospinal fluid, and therefore for systemic virulence. RNAseq and metabolomic data demonstrated that the loss of one-carbon metabolism or proline biosynthesis has profound but differing effects on S. pneumoniae metabolism in human serum, identifying the metabolic processes dependent on each pathway during systemic infection. These data provide a more detailed understanding of the adaptations required by systemic bacterial pathogens in order to cause infection and demonstrate that the requirement for some of these adaptations varies between strains from the same species and could therefore underpin strain variations in virulence potential.