Oxalate Synthesis Research Articles

Kukoamine A alleviates nephrolithiasis by inhibiting endogenous oxalate synthesis via the IL-6/JAK/STAT3/DAO signaling pathway

BackgroundThe recurrent nature and socioeconomic burden of nephrolithiasis demand effective treatments. Delineating the crosstalk between inflammatory processes and the endogenous oxalate metabolism pathway, which underpins nephrolithiasis pathogenesis, is essential for advancing treatment strategies. PurposeWe aim to screen therapeutic Chinese herbal remedies and their bioactive constituents for kidney stone treatment using a fruit fly model, followed by efficacy and mechanism validation in a rodent nephrolithiasis model as well as in vitro human cell culture model. Study design and methodsWe developed a fruit fly model to screen for efficient traditional Chinese medicine herbs and their active compounds for kidney stone treatment. Candidate active compounds from efficient herbs were separated and identified by solid-phase chromatography coupled with LC-MS analysis. Fruit fly genetic tools were employed to manipulate the expression of related genes to explore the therapeutic mechanisms of the Lycii Cortex and kukoamine A (KuA). To confirm the therapeutic effects and mechanisms of KuA for mammalian nephrolithiasis, mouse model of glyoxylate-induced kidney stone and human renal tubular cells were used. The therapeutic role of kukoamine A in nephrolithiasis was evaluated by assessing tubular injury, crystal deposition, and adhesion. The level of expression and phosphorylation in cells and mice was assessed using RT-qPCR and western blot. ResultsOur findings indicate that Lycii Cortex potently inhibits calcium oxalate stone formation via activation of the JNK/Upd3/JAK/STAT signaling cascade, resulting in diminished endogenous oxalate synthesis by downregulating D-amino acid oxidase (DAO) gene expression, predominantly in fruit fly Malpighian tube stellate cells. KuA was identified as the principal bioactive constituent mediating these effects. Both mouse models and human cell assays confirmed KuA's efficacy in preventing calcium oxalate nephrolithiasis in mammals, through hepatic JAK/STAT3 pathway activation and upregulation of IL-6, culminating in reduced urinary crystal deposition. ConclusionOur research underscores the potential of kukoamine A as a lead compound in treating nephrolithiasis and reveals the interplay between the IL-6/JAK/STAT3 inflammatory pathway and endogenous oxalate metabolism in nephrolithiasis pathogenesis. Additionally, it highlights the utility of the fruit fly model as a powerful tool for deciphering the therapeutic mechanisms of traditional Chinese herbs.

Offline constrained reinforcement learning for batch-to-batch optimization of cobalt oxalate synthesis process

The cobalt oxalate synthesis, a batch process, plays a crucial role in the refinement of cobalt metal. The mean particle size of cobalt oxalate is a critical indicator that reflects product quality. However, excessive ammonium oxalate solution flow can heighten waste disposal costs in the production process. To address these issues, we propose a novel offline reinforcement learning (RL) algorithm that guarantees compliance with constraints in the cobalt oxalate synthesis process, utilizing exclusively static datasets. This method employs cost critic networks to assess costs, transforming the constrained optimization problem into an unconstrained one by introducing Lagrangian multipliers. We use exponential moving average (EMA) to optimize the update of proportional integral derivative (PID) control multipliers, reduce overshoot and oscillation in the control process, and thus improve the overall stability of the system. Furthermore, to optimize algorithm performance, a deep residual network (DResNet) is integrated into the policy network. Experimental results indicate that the algorithm’s optimization policy performs significantly better under constraints.

Nitrogen reduces calcium availability by promoting oxalate biosynthesis in apple leaves.

N and Ca are essential nutrients for apple growth and development. Studies have found that Ca content was not low under high N conditions but was poorly available. However, the underlying physiological mechanism through which N regulates Ca availability remains unclear. In this study, apple plants were supplied with N and Ca to analyse the content, in situ distribution, and forms of Ca using noninvasive micro-test technique, electron probe microanalysis, Fourier transform infrared spectroscopy, and transcriptome analysis. A potential interaction was observed between N and Ca in apple leaves. The application of high N and Ca concentration led to a CaOx content of 12.51g/kg, representing 93.54% of the total Ca in the apple leaves. Electron probe microanalysis revealed that Ca deposited in the phloem primarily existed as CaOx rhombus-shaped crystals. Additionally, high N positively regulated oxalate accumulation in the leaves, increasing it by 40.79 times compared with low N concentration. Specifically, N induced oxalate synthesis in apple leaves by upregulating the MdICL, MdOXAC, and MdMDH genes, while simultaneously inhibiting degradation through downregulation of the MdAAE3 gene. Transcriptome and correlation analyses further confirmed oxaloacetate as the precursor for the synthesis of CaOx crystals in the apple leaves, which were produced via the 'photosynthesis/glycolysis -oxaloacetate -oxalate -CaOx' pathway. WGCNA identified potential regulators of the CaOx biosynthesis pathway triggered by N. Overall, the results provide insights into the regulation of Ca availability by N in apple leaves and support the development of Ca efficient cultivation technique.

Promising Natural Approach: Caesalpinia bonduc Seed Extracts for Calcium Oxalate Urolithiasis in Rats

Background: It is essential to identify a therapy for hyperoxaluria that specifically focuses on reducing oxalate excretion since current therapies for urolithiasis have drawbacks. It is noteworthy to observe that the seeds of Caesalpinia bonduc (Family: Caesalpiniaceae) have been historically used by several Indian tribes for the purpose of treating renal diseases. Purpose: The primary purpose of this study was to assess the efficacy of C. bonduc seed extracts as therapeutic agents in rats with experimentally generated calcium oxalate urolithiasis. Methodology: The experimental animals were given 0.75% of ethylene glycol orally for fourteen consecutive days in order to produce calcium oxalate lithiasis. C. bonduc seed extracts, 400 mg/kg of body weight in aqueous and ethanolic forms, were administered in the same way for a further 14 days in succession. The standard antiurolithiatic medicine used was cystone, administered at a dose of 750 mg/kg of body weight. The research primarily examined the quantification of serum biochemical markers and the elimination of salt constituents from urine and renal deposits, which were shown to be challenging. Results: Ethylene glycol administered orally caused hyperoxaluria and augmented calcium, phosphate, and oxalate excretion in the kidneys. Nevertheless, the administration of C. bonduc seed extracts effectively decreased the elevated levels of oxalate in the urine, showing an inhibitory effect on the synthesis of oxalate inside the human body. The renal accumulation of components that cause stone formation in rats with calculogenic conditions decreased considerably after the administration of curative treatments with aqueous and ethanolic extracts. Discussion and Conclusion: Based on the findings, it has been shown that C. bonduc seeds have lithontriptic action, which deserves further investigation as a potential remedy for urolithiasis. Further research is necessary to elucidate the specific phytoconstituents present in seeds that are responsible for their antiurolithiatic activity.

Synthesis and Application of Oxalate–Phosphate–Amine Metal–Organic Framework Fertilizers in Calcareous Soils: Analysis of Nitrogen, Phosphorus, and Grain Yield in Triticum aestivum L.

Synthesis and Application of Oxalate–Phosphate–Amine Metal–Organic Framework Fertilizers in Calcareous Soils: Analysis of Nitrogen, Phosphorus, and Grain Yield in Triticum aestivum L.

Recovery of Ni-Co-Mn Oxides from End-of-Life Lithium-Ion Batteries for the Application of a Negative Temperature Coefficient Sensor

This study demonstrates the current advancements in battery management systems (BMSs), emphasizing the need for precise temperature monitoring within battery packs to enhance safety and performance through efficient thermal management. The increased demand for lithium-ion batteries (LIBs) has driven the development of temperature sensors with improved accuracy and stability. In particular, Ni-Co-Mn-based spinel oxides are commonly used due to their stable negative temperature coefficient (NTC) behavior. However, challenges arise in manufacturing due to the high cost and uncertain supply of critical cathode components (e.g., Co, Ni, and Mn) for LIBs. This research focuses on developing spinel-type (Ni0.6Co0.4Mn2)O4 using recycled Ni-Co-Mn oxides obtained from end-of-life (EOL) LIBs, demonstrating temperature resistance behavior suitable for temperature sensing. The oxides are prepared through hydrometallurgy, oxalate synthesis, and post-heat treatment. Successful integration into spinel-type NTC thermistors suggests broader applications in various industrial fields. A systematic investigation into the synthesis and characterization of recovered Ni-Co-Mn oxides from EOL LIB cathode materials (Li(Ni0.33Co0.33Mn0.33)O2) is presented for NTC thermistor application. Thermogravimetric analysis-derivative thermogravimetry (TGA-DTG) identifies the optimal post-heat treatment temperature. The X-ray diffraction (XRD) patterns confirm a cubic spinel structure of the Ni-Co-Mn oxides, supported by scanning electron microscope (SEM) images showing a uniform microstructure. Also, energy dispersive X-ray spectroscopy (EDS) mapping confirms homogeneous element distribution. Recovered oxide pellets from the sintering process exhibit a single spinel structure, with X-ray photoelectron spectroscopy (XPS) analysis revealing changes in the valence states for Ni and Mn. Resistivity measurements demonstrate semiconductive behavior, which shows a B value (3376.92 K) suitable for NTC thermistor applications. This study contributes valuable insights to black powder recycling from EOL LIBs and its potential in temperature-sensitive electronic devices.

Metabolic diversity analysis and genome wide assessment of oxalate accumulation in the leaves of rice (Oryza sativa) cultivars.

Soluble oxalate accumulates in rice leaves, and it causes mineral deficiency and urinary syndrome in livestock that consume the leaves. In our previous study, we found that the oxalate content was higher in the leaves of Koshihikari (japonica type cultivar) than in those of Takanari (indica type cultivar). This difference was seen even when the two cultivars were grown under a high CO2 concentration, which inhibits oxalate synthesis via photorespiration, suggesting that the difference resulted from genetic factors rather than environmental factors. To clarify whether genetic factors affect the oxalate content of rice leaves, we measured the contents of oxalate and oxalate-related organic acids in the leaves of various rice cultivars the Rice Core Collection (WRC) and Japan Rice Core Collection (JRC) by capillary electrophoresis-mass spectrometry. Results showed that japonica type cultivars tended to accumulate more oxalate than aus or indica type cultivars. Correlation analysis revealed a positive correlation between oxalate accumulation and the citrate content, suggesting that the isocitrate pathway is involved in oxalate accumulation. On the other hand, a genome-wide association study for the oxalate content of the WRC and JRC cultivars did not reveal significant loci directly related to oxalate accumulation. This indicates that the combination of various loci may affect the oxalate contents of rice leaves.

In vivo base editing rescues primary hyperoxaluria type 1 in rats

Primary hyperoxaluria type 1 (PH1) is a childhood-onset autosomal recessive disease, characterized by nephrocalcinosis, multiple recurrent urinary calcium oxalate stones, and a high risk of progressive kidney damage. PH1 is caused by inherent genetic defects of the alanine glyoxylate aminotransferase (AGXT) gene. The invivo repair of disease-causing genes was exceedingly inefficient before the invention of base editors which can efficiently introduce precisely targeted base alterations without double-strand DNA breaks. Adenine base editor (ABE) can precisely convert A·T to G·C with the assistance of specific guide RNA. Here, we demonstrated that systemic delivery of dual adeno-associated virus encoding a split-ABE8e could artificially repair 13% of the pathogenic allele in AgxtQ84X rats, a model of PH1, alleviating the disease phenotype. Specifically, ABE treatment partially restored the expression of alanine-glyoxylate-aminotransferase (AGT), reduced endogenous oxalate synthesis and alleviated calcium oxalate crystal deposition. Western blot and immunohistochemistry confirmed that ABE8e treatment restored AGT protein expression in hepatocytes. Moreover, the precise editing efficiency in the liver remained stable six months after treatment. Thus, our findings provided a prospect of invivo base editing as a personalized and precise medicine for PH1 by directly correcting the mutant Agxt gene.

Dynamic nonlinear soft sensor modelling method using linear slow feature analysis and least squares support vector regression for batch processes

AbstractData‐driven soft sensor models have been extensively utilized in industrial processes. Batch processes are usually employed to manufacture low‐volume and high value‐added products in chemical, materials, and pharmaceutical industries. The most distinctive features of batch process lie in nonlinear, repetition, and slow time varying characteristics. In this paper, a data‐driven soft sensor modelling method based on linear slow feature analysis (LSFA) and least squares support vector regression (LSSVR) is proposed. In this method, LSFA was used to effectively capture the driving force behind the data features that change as slowly as possible. Then, a LSSVR model was constructed between the extracted slow feature variables and quality variables. Finally, a numerical example, industrial penicillin fermentation processes, and cobalt oxalate synthesis process were utilized to confirm the prediction accuracy and model reliability of the proposed approach.

Isolation, Characterization, In-silico and enzyme Inhibition studies of plant Bougainvillea spectabilis against a hyperoxaluria Initiator Glycolate oxidase

Glycolate oxidase has long been thought to be a key player in the formation of oxalate accumulation in the human body. Both the endogenous synthesis of oxalate and clinically identified targets for the therapy of primary hyperoxaluria are affected by this disorder. The role of glycolate oxidase has been investigated in order to provide additional insight into the possible molecular pathways involved. The presence of flavonoids in the ethanolic extract led to the conclusion that it was suitable following phytochemical screening. Column chromatography was used to isolate the active component using the proper solvent system. The structure of the active, separated phytoconstituents was ascertained using a variety of spectral techniques, including FTIR, NMR, and GCMS analysis. Following structure elucidation, glycolate oxidase (PDB: 2RDT) and Quercetin were used as standards in molecular docking investigations. Studies on in- vitro enzyme inhibition were carried out to verify the outcome. Following the investigation of the isolated compound's spectral data, it was determined that the structure might be 4-hydroxy-3-nitro coumarin. Using conventional standard flavonoid Quercetin, additional molecular docking studies were carried out to speculate on the compound's potential mechanism of action. The chemical was discovered to be effective during the inhibition of the target enzyme by occupying the majority of the amino acid active sites. In-vitro enzyme inhibition tests provided additional confirmation for the computational investigations. The isolated compound's significant IC50 value in this study was demonstrated in comparison to standard Quercetin's efficacy. These findings supported the isolated compound's potential mechanism of action, which involves inhibiting the enzyme glycolate oxidase, in terms of its anti-urolithiasis efficacy. The study also provided justification for the compound's potential therapeutic application in urolithiasis.

Efficient cobalt oxalate synthesis process optimization via second‐order modifier adaptation with transfer learning

AbstractThis paper proposes a second‐order modifier adaptation optimization based on the transfer model, which aims to improve the optimization efficiency. Although the traditional modifier adaptation strategy adds a bias to the model to meet the necessary condition of optimality (NCO), approximating only to the first‐order may neglect some key higher‐order information. Making use of as much higher‐order information as possible is an effective way to improve the efficiency of optimization. For this issue, by introducing the second‐order information into the modifier adaptation method to compensate the mismatch of higher‐order information during the optimization, the compensation of the mismatch between model and plant can get accelerated, thus improving the optimization efficiency. To overcome the difficulty of insufficient data for new process modelling, a process transfer model is also used to fit the relationship between manipulated variables and final product quality. The simulation study of the cobalt oxalate synthesis process shows that this strategy has better optimization efficiency.

Rhubarb: A novel model plant to study the conundrum of calcium oxalate synthesis

The study investigated calcium oxalate (CaOx) crystal composition, accumulation, synthesis, and degradation in five rhubarb species from the North-Western Indian Himalayas. Techniques like optical and scanning electron microscopy (SEM), SEM-energy-dispersive X-ray spectroscopy (SEM-EDS), inductively coupled plasma-optical emission spectrometry (ICP-OES), X-ray diffraction spectroscopy (XRD), and real-time (qRT-PCR) expression analysis of strategic genes were used to understand the processes of oxalate synthesis and precipitation. Results showed crystals tend to accumulate around vascular bundles in all species, irrespective of size, indicating a consistent pattern. Crystal synthesis and accumulation were stress-driven, linked to substrate composition, and in planta soluble oxalate and calcium levels, paralleling oxalate precursors. Based on their availability, CaOx crystals precipitated heavy metals mostly associated with its weddellite form. Crystal content correlated positively with mRNA levels of calcium/oxalate/ascorbate-related and stress-responsive genes, and negatively with oxalate oxidation/decarboxylation genes. CaOx crystals were suggested as potential biominerals for addressing heavy metal stress in agriculture.

Insights into kinetics and reaction mechanism of acid-catalyzed transesterification synthesis of diethyl oxalate

The catalytic performance of different acidic catalysts for diethyl oxalate synthesis from the one-step transesterification of dimethyl oxalate and ethanol was evaluated. The effects of different factors (e.g., acidity, electron accepting capacity, cations type and crystalline water) on the catalytic activity of acidic catalysts were investigated respectively. It was proposed and confirmed that the transesterification reaction catalyzed by a Lewis acid (FeCl3) and a Bronsted acid (H2SO4) follows a first-order kinetic reaction process. In addition, the Lewis acid-catalyzed transesterification processes with different ester structures were used to further explore and understand the speculated reaction mechanism. This work enriches the theoretical understanding of acid-catalyzed transesterification reactions and is of great significance for the development of highly active catalysts for diethyl oxalate synthesis, diminishing the industrial production cost of diethyl oxalate, and developing downstream bulk or high-value-added industrial products.

Advanced exergy analysis and optimization of a coal to ethylene glycol (CtEG) process

Coal to ethylene glycol (CtEG) process is criticized for its high energy consumption and poor thermodynamic performance. This process is detailed modeled by dividing it into coal gasification, water gas shift, acid gas removal, dimethyl oxalate synthesis, ethylene glycol synthesis, and ethylene glycol refining units. After comparing and verifying with literature and industrial data, this work conducts a detailed advanced exergy analysis and optimization of the CtEG process. Results show that the exergy efficiency of the CtEG process is only 33.56%, and the coal gasification, dimethyl oxalate synthesis, and ethylene glycol synthesis units have the largest exergy destruction. Furthermore, the exergy destruction of all components in the CtEG process is dominantly endogenous (76.03%) and avoidable (64.62%). The real improvement potential of the CtEG process is 64.62%. A parametric study was then performed to investigate the effect of key parameters on the thermodynamic performance of the CtEG process to reduce its avoidable endogenous and exogenous exergy destruction. After optimization, the exergy efficiency of the improved CtEG process is increased by 12.34%, and the avoidable exergy destruction is reduced by 160.48 MW compared with the reference system. Therefore, the improved CtEG process has better thermodynamic performance than the reference process.

Calcium oxalate crystals, the plant "gemstones": Insights into their synthesis and physiological implications in plants.

From simple algal forms to the most advanced angiosperms, calcium oxalate (CaOx) crystals occur in the majority of taxonomic groups of photosynthetic organisms. Various studies have demonstrated that this biomineralization is not a simple or random event but a genetically regulated coordination between calcium uptake, oxalate synthesis, and sometimes environmental stresses. Certainly, the occurrence of CaOx crystals is old; however, questions related to their genesis, biosynthesis, significance, and genetics exhibit robust evolution. Moreover, their speculated roles in bulk calcium regulation, heavy-metal/oxalate detoxification, light reflectance and photosynthesis, and protection against grazing and herbivory, besides other characteristics, are gaining much interest. So, it is imperative to understand their synthesis and regulation in relation to the ascribed key functions to reconstruct future perspectives in harnessing their potential to achieve nutritious and pest-resistant crops amid anticipated global climatic perturbations. This review critically addresses the basic and evolving concepts of the origin (and recycling), synthesis, significance, regulation, and fate vis-à-vis various functional aspects of CaOx crystals in plants (and soil). Overall, insights and the conceptual future directions present them as potential biominerals to address future climate-driven issues.

Cadmium accumulation in duckweed relates to pH and oxalate synthesis in Cd shock

Cadmium accumulation in duckweed relates to pH and oxalate synthesis in Cd shock

Synthesis of submicron ferrous oxalate from red mud with high Fenton catalytic performance on degradation of methylene blue.

Ferrous oxalate dihydrate (FOD) can be used as a photo-Fenton catalyst with remarkable photo-Fenton catalytic and photocatalytic performances on organic pollutant degradation. Various reduction processes were compared in the current study to synthesize FODs from ferric oxalate solutionutilizing the iron source in alumina waste red mud (RM), including natural light exposure (NL-FOD), UV light irradiation (UV-FOD), and hydroxylamine hydrochloride hydrothermal method (HA-FOD). The FODs were characterized and employed as photo-Fenton catalysts for methylene blue (MB) degradation, and the effects of HA-FOD dosage, H2O2 dosage, MB concentration, and the initial pH were investigated. The results show that HA-FOD has submicron sizes and lower impurity contents with more rapid degradation rates and higher degradation efficiencies compared with the other two FOD products. When using 0.1g/L of each obtained FOD, 50mg/L of MB can be rapidly degraded by HA-FOD by 97.64% within 10min with 20mg/L of H2O2 at pH of 5.0, while NL-FOD and UV-FOD achieve 95.52% in 30min and 96.72% in 15min at the same conditions, respectively. Meanwhile, HA-FOD exhibits strong cyclic stability after two recycling experiments. Scavenger experiments reveal that the predominant reactive oxygen species responsible for MB degradation are hydroxyl radicals. These findings demonstrate that submicron FOD catalyst can be synthesized using hydroxylamine hydrochloride hydrothermal process from ferric oxalate solution with high photo-Fenton degradation efficiency and reduced reaction time for wastewater treatment. The study also provides a new pathway of efficient utilization for RM.

1D Narrow-Bandgap Tin Oxide Materials: Systematic High-Resolution TEM and Raman Analysis.

We demonstrate for the first time the structure identification and narrow-bandgap property of 1D hybridized SnO/SnO2 nanoparticles derived from the calcination of a single-source precursor, i.e., tin(II) oxalate. Systematic Raman analysis together with high-resolution TEM (HR-TEM) measurements of the tin oxide samples were carried out by changing the calcination temperatures. These data revealed the simultaneous formation of 1D SnO/SnO2 in the rod particles that grew in air. It was also found that Sn(II) can be introduced by changing the concentration of Sn(II) salt in the precursor synthesis and the maximum temperature in calcination. Particles measuring 20~30 nm were sintered to produce tin oxide nanorods including tin monoxide, SnO. Photoabsorption properties associated with the formation of the SnO/SnO2 nanocomposites were also investigated. Tauc plots indicate that the obtained tin oxide samples had a lower bandgap of 2.9~3.0 eV originating from SnO in addition to a higher bandgap of around 3.5~3.7 eV commonly observed for SnO2. Such 1D SnOx/SnO2 hybrids via tin oxalate synthesis with this optical property would benefit new materials design for photoenergy conversion systems, such as photocatalysts.

ZnxMg1‐xO Solid Solutions: Efficient Bifunctional Acid‐Base Catalyst for the synthesis of Methyl Ethyl Oxalate from Dimethyl Oxalate and Ethanol

AbstractZnO‐MgO composite catalysts were prepared by the coprecipitation method and used for the synthesis of methyl ethyl oxalate (EMO) from dimethyl oxalate (DMO) and ethanol (EtOH). The results of the SEM, XRD, FT‐IR and XPS confirmed that Zn2+ ions were incorporated into the cubic MgO lattice to form the solid solution structure over ZnO‐MgO composites catalysts with 6–18 mol% ZnO. The ZnO‐MgO composite catalysts with a solid solution structure have a large specific surface area, high medium acidic density, and medium basic density according to the results of N2 adsorption‐desorption, pyridine‐IR (Py‐IR) and NH3/CO2 temperature‐programmed desorption (NH3‐TPD/CO2‐TPD). The ZnxMg1‐xO solid solution with 18 mol% ZnO‐MgO (Zn0.18Mg0.82O) catalyst showed the highest catalytic activity with 71.98 % conversion of DMO and 67.36 % selectivity to EMO (DMO: EtOH molar ratio=1 : 2, reaction time=20 min, reaction temperature=80 °C and catalyst amount=1.5 wt%). The high catalytic activity was attributed to the solid solution structure with high medium acidic density and medium basic density. The conversion of DMO showed a positive linear correlation with the medium acidic density and medium basic density according to the correlation between catalytic activity and acidity‐basicity.

Boosting Efficiency for the Synthesis of Dimethyl Oxalate over Pd/MgAl2O4: Effect of Different Preparation Methods for MgAl2O4 Supports

AbstractHigh active Pd‐based catalyst with low loading capacity for CO oxidative coupling with methyl nitrite (MN) to dimethyl oxalate (DMO) has aroused great interest in the large‐scale production of DMO for the next hydrogenation to bring forth ethylene glycol (EG). Here, spinel composite oxide support, namely MgAl2O4, had been prepared through three different methods: solid combustion method (MAO‐SC), hydrothermal method (MAO‐HT) and co‐precipitation method (MAO‐CP), and further Pd nanoparticles were anchored to the surface of MgAl2O4 through a simple wetness impregnation method. In the CO direct esterification to DMO reaction, the Pd/MAO‐SC catalyst, which used MgAl2O4 support prepared by solid combustion method, exhibited the highest intrinsic activity with Turnover frequency (TOF) value of 2.39 s−1 and DMO weight space‐time yield (956.8 g⋅kgcat−1⋅h−1) with 44.1 % CO conversion and 97.8 % DMO selectivity, and showed negligible attenuation of activity during the process of continuous reaction for 100 h. The characterization results confirmed that abundant oxygen defect sites occurred in MAO‐SC synthesized by combustion method not only can help to anchor the Pd nanoparticles with appropriate size and dispersion, but also can promote the interfacial electron transfer from MgAl2O4 support to Pd nanoparticles, thus significantly enhancing the metal‐support interaction (MSI) and providing more CO bridge‐adsorption sites that is favorable for the CO oxidative coupling with MN to DMO reaction.