Nicotinamide Adenine Dinucleotide Hydrogen Research Articles

THE IMPACT OF WINTER SWIMMING ON FUNCTIONAL MICROVASCULAR CHANGES

Objective: Microcirculation plays an important role in the development of cardiovascular control. Therefore, the aim of our study was to investigate the impact of winter swimming on functional changes in cutaneous microcirculation Flow-mediated skin fluorescence (FMSF) is a novel and non-invasive technique assessing microvascular function based on the measurements of nicotinamide adenine dinucleotide hydrogen (NADH) fluorescence intensity in the epidermis and post occlusive reactive hyperemia test. NADH intensity changes in response to blockage and release of blood flow in the brachial artery, which corresponds to microvascular function. Design and method: FMSF examinations were performed before and after the winter swimming period lasting from November 2022 to April 2023 in 37 subjects (mean age 46±4,0 years, 65% women). The mean frequency of winter swimming activity was 1,3 times per week. We analysed the following variables: the ischemic response (IRmax and IRindex) – the ratio of relative to baseline maximal increase in fluorescence intensity during cuff occlusion and the hyperaemic response after cuff release (HRmax and HRindex). Flowmotion, measured at baseline (FM) and at reperfusion (FM(R)), reflects flow oscillations. Normoxia oscillatory index (NOI) represents the proportion of endothelial and neurogenic blood flow oscillations in relation to all oscillations detected in low frequency range. The hypoxia sensitivity (HS), measured during reperfusion, reflects the intensity of flowmotion related to myogenic oscillations. Results: The statistical analysis revealed following results according to the winter swimming: Conclusions: Increase in microvascular oscillations denoted by NOI and HS suggests a beneficial impact of winter swimming on cutaneous microcirculation. Improvement in microcirculation performance may partly explain lowering of cardiovascular risk in regular winter swimmers.

Development of superoxide dismutase based visual and spectrophotometric method for rapid differentiation of fresh and frozen-thawed buffalo meat

Study aimed to develop biomarker-based assay for rapid detection of fresh and frozen-thawed buffalo meat in the supply chain. The method is based on development of a solvent system and identification of suitable substrate and developer for screening of biomarkers. For the confirmation column chromatography, gel electrophoresis and Western Blotting were carried out. Validation was done by intra- and inter-day validation, storability study, and determination of thermal history. Best results were shown with pH 8.0 Tris-HCl; extraction buffer, 205 µM nicotinamide adenine dinucleotide hydrogen; substrate, 184 µM Nitroblue tetrazolium, and 1.9 µM phenazine methosulfate; developer. The thermal history ranged from 0.14 to 0.17 during storage at −20 °C. The intra- and inter-day assay precision (CV %) ranged from 5.3 to 6.5 %; in chilled and 14.1 – 9.2 % in frozen-thawed samples. The study confirmed SOD as a viable biomarker. Developed method using SOD has significant potential for rapidly differentiating chilled or frozen-thawed meat.

Regulation of organic acid and hydrogen production by NADH/NAD+ ratio in Synechocystis sp. PCC 6803.

Cyanobacteria serve as useful hosts in the production of substances to support a low-carbon society. Specifically, the unicellular cyanobacterium Synechocystis sp. PCC 6803 (Synechocystis 6803) can produce organic acids, such as acetate, lactate, and succinate, as well as hydrogen, under dark, anaerobic conditions. The efficient production of these compounds appears to be closely linked to the regulation of intracellular redox balance. Notably, alterations in intracellular redox balance have been believed to influence the production of organic acids and hydrogen. To achieve these alterations, genetic manipulations involved overexpressing malate dehydrogenase (MDH), knocking out d-lactate dehydrogenase (DDH), or knocking out acetate kinase (AK), which subsequently modified the quantities and ratios of organic acids and hydrogen under dark, anaerobic conditions. Furthermore, the mutants generated displayed changes in the oxidation of reducing powers and the nicotinamide adenine dinucleotide hydrogen (NADH)/NAD+ ratio when compared to the parental wild-type strain. These findings strongly suggest that intracellular redox balance, especially the NADH/NAD+ ratio, plays a pivotal role in the production of organic acids and hydrogen in Synechocystis 6803.

Reduction of Cr(VI) by planktonic cells and biofilm of Acinetobacter sp. (ADHR1) isolated from electroplating wastewater

In this research it was possible to analyze the capacity of Acinetobacter sp. (ADHR1) bacteria to reduce chromium (VI). Bacteria isolated from residual effluents from automobile chrome plating processes auto parts were identified by phenotypiic and genotypic methods. ADHR1 was able to 100% reduce Cr(VI) to Cr(III), resulting in: 100–500 mg / L of Cr(VI) in a lapse of time between 18 to 24 h; likewise, it was possible to show the reduction process in concentrations of 2000 mg / L which was 73% as a result. In addition to this, it was also possible to show that planktonic cells had a greater capacity to reduce hexavalent chromium compared to biofilm cells. The ChrR gene was amplified by PCR confirming the presence of the chromate reductase enzyme. The reduction in chromium was attributed to the presence of the nicotinamide adenine dinucleotide hydrogen (NADH) dependent enzyme chromate reductase in the cytosolic fraction and in the membrane associated fraction. In conclusion, Acinetobacter sp. (ADHR1) used in the study showed great potential to reduce different concentrations of Cr(VI). This research represents a truly eco-friendly alternative in the removal of sites contaminated by metals, knowing the Acinetobacter sp. (ADHR1) has the ability to reduce Cr(VI).

Phenyllactic acid maintains the storage quality of ‘Zaosu’ pears by regulating respiration and energy metabolism

Respiration and energy metabolism are intricately linked to the quality and senescence of fruit after harvest. This investigation was carried out to examine alternations in quality parameters, respiration, and energy metabolism of ‘Zaosu’ pears subsequent to phenyllactic acid immersion. Results demonstrated that phenyllactic acid treatment led to a reduction in L* , a* , b* values, ΔE, and mass loss. Additionally, it maintained ascorbic acid, reducing sugar, soluble sugar, soluble solids, and chlorophyll contents; delayed the decrease in flesh firmness and titratable acidity of pears. The activities and gene expressions of glucose-6-phosphate dehydrogenase, glucose phosphate isomerase, hexokinase, nicotinamide adenine dinucleotide kinase, cytochrome C oxidase, and succinate dehydrogenasepears in pears were enhanced by phenyllactic acid. Moreover, phenyllactic acid promoted PbPK, PbAOX, PbH+-ATPase, and PbCa2+-ATPase expressions, while inhibiting malate dehydrogenase activity and the expressions of PbPFK and PbMDH in pears. Phenyllactic acid also led to a decrease in the levels of nicotinamide adenine dinucleotide hydrogen and nicotinamide adenine dinucleotide, while causing an increase in the levels of nicotinamide adenine dinucleotide phosphate hydrogen and nicotinamide adenine dinucleotide phosphate within the fruit. Collectively, postharvest phenyllactic acid treatment can effectively preserve the storage quality of ‘Zaosu’ pears by regulating the activity and gene expression of the key enzymes involved in respiration and energy metabolism.

Regulation of Embden-Meyerhof-Parnas (EMP) Pathway and Tricarboxylic Acid (TCA) Cycle Concerning Aberrant Chilling Injury Behavior in Postharvest Papaya (Carica papaya L.).

Postharvest abnormal chilling injury (CI) behavior in papaya (Carica papaya L.) fruit is a rare phenomenon that may be associated with respiratory metabolism. This study thus aimed to investigate the impacts of storage temperatures (1 and 6 °C) on the respiratory metabolism of postharvest papaya and its impact on CI development. Results demonstrated that 1 °C storage reduced the activities of hexokinase (HK), phosphofructokinase (PFK), pyruvate kinase (PK), citrate synthase (CS), and α-ketoglutarate dehydrogenase (α-KGDH) and regulated the expression of corresponding enzymes in the Embden-Meyerhof-Parnas (EMP) pathway and tricarboxylic acid (TCA) cycle compared with 6 °C storage, resulting in a lower respiration rate of the EMP-TCA pathway and mitigating the development of CI. Meanwhile, lower contents of nicotinamide adenine dinucleotide (hydrogen) (NAD(H)) were observed in papaya fruit stored at 1 °C. Notably, papaya fruit stored at 1 °C maintained higher activity and transcriptional levels of SDH and IDH during the whole storage period. These findings suggest that 1 °C storage reduced the respiration rate of the EMP-TCA pathway by reducing the expression level and activity of related enzymes, which is conducive to the reduction of respiration substrate consumption and finally alleviating the occurrence of CI.

Mechanisms of biochar-mediated promotion of acidogenic fermentation in waste activated sludge and propionic acid production pathways

The conversion of organic matter in waste activated sludge (WAS) into high value-added chemicals of volatile fatty acids (VFAs) has become a focus of attention worldwide. However, the conversion of WAS to a certain acid among VFAs is difficult. Herein, for the first time, biochar was used to promote sludge solubilization, hydrolysis and acidogenic fermentation for the production of propionic acid. The results illustrated that biochar (prepared at 450 °C, containing environmental persistent free radicals (EPFRs) of 15.91 × 1015 spins/g) stimulated sludge solubilization, hydrolysis and VFAs production, enhancing sludge cell lysis rate, VFAs production, propionic acid ratio, protease, α-glucosidase and nicotinamide adenine dinucleotide hydrogen (NADH)/nicotinamide adenine dinucleotide (NAD+) ratio by 10.53 %, 107.42 %, 17.52 %, 68 %, 32 % and 76.10 % respectively, compared with those observed in the control group without biochar addition. And once the EPFRs were shielded, they decreased. The signal of EPFRs decreased from 15.91 × 1015 spins/g to 15.20 × 1015 spins/g on day 2 and 8.50 × 1015 spins/g on day 4. The EPFRs contained in the biochar played an important role in the intermediary function and interfered with the bacterial metabolic pathways. Metagenomics sequencing also revealed that biochar EPFRs promoted the sludge acidogenic fermentation to produce propionic acid ([EC:7.1.1.2]) and partly inhibited acetic acid production ([EC:1.2.1.3]). This study reveals that biochar could promote sludge solubilization, hydrolysis and promote propionic acid production, which could be used as a new strategy for acid production in the future.

Identification of peripheral vascular function measures and circulating biomarkers of mitochondrial function in patients with mitochondrial disease.

The development of pharmacological therapies for mitochondrial diseases is hampered by the lack of tissue-level and circulating biomarkers reflecting effects of compounds on endothelial and mitochondrial function. This phase 0 study aimed to identify biomarkers differentiating between patients with mitochondrial disease and healthy volunteers (HVs). In this cross-sectional case-control study, eight participants with mitochondrial disease and eight HVs matched on age, sex, and body mass index underwent study assessments consisting of blood collection for evaluation of plasma and serum biomarkers, mitochondrial function in peripheral blood mononuclear cells (PBMCs), and an array of imaging methods for assessment of (micro)circulation. Plasma biomarkers GDF-15, IL-6, NT-proBNP, and cTNI were significantly elevated in patients compared to HVs, as were several clinical chemistry and hematology markers. No differences between groups were found for mitochondrial membrane potential, mitochondrial reactive oxygen production, oxygen consumption rate, or extracellular acidification rate in PBMCs. Imaging revealed significantly higher nicotinamide-adenine-dinucleotide-hydrogen (NADH) content in skin as well as reduced passive leg movement-induced hyperemia in patients. This study confirmed results of earlier studies regarding plasma biomarkers in mitochondrial disease and identified several imaging techniques that could detect functional differences at the tissue level between participants with mitochondrial disease and HVs. However, assays of mitochondrial function in PBMCs did not show differences between participants with mitochondrial disease and HVs, possibly reflecting compensatory mechanisms and heterogeneity in mutational load. In future clinical trials, using a mix of imaging and blood-based biomarkers may be advisable, as well as combining these with an in vivo challenge to disturb homeostasis.

FTIR microspectroscopy and multivariate analysis facilitate identification of dynamic changes in epithelial-to-mesenchymal transition induced by TGF-β in prostate cancer cells.

The standard diagnosis of prostate cancer is accomplished by the identification of cytomorphological deviations in biopsied tissues while immunohistochemistry is used to resolve the equivocal cases. Accumulating evidence favors the concept that epithelial-to-mesenchymal transition (EMT) is a stochastic process composed of multiple intermediate states instead of a single binary switch. Despite its significant role in promoting cancer aggressiveness, the current tissue-based risk stratification tools do not include any of the EMT phenotypes as a metric. As a proof-of-concept, the present study analyzes the temporal progression of EMT in transforming growth factor-beta (TGF-β) treated PC3 cells encompassing multifarious characteristics such as morphology, migration and invasion, gene expression, biochemical fingerprint, and metabolic activity. Our multimodal approach reinstates EMT plasticity in TGF-β treated PC3 cells. Further, it highlights that mesenchymal transition is accompanied by discernible changes in cellular morphometry and molecular signatures particularly in the range of 1800-1600 cm-1 and 3100-2800 cm-1 of Fourier-transformed infrared (FTIR) spectra signifying Amide III and lipid, respectively. Investigation of attenuated total reflectance (ATR)-FTIR spectra of extracted lipids from PC3 cell populations undergoing EMT identifies changes in stretching vibration at FTIR peaks at 2852, 2870, 2920, 2931, 2954, and 3010 cm-1 characteristics of fatty acids and cholesterol. Chemometric analysis of these spectra indicates that the level of unsaturation and acyl chain length of fatty acid coregister with differential epithelial/mesenchymal states of TGF-β treated PC3 cells. Observed changes in lipids also correlate with cellular nicotinamide adenine dinucleotide hydrogen (NADH) and flavin adenine dinucleotide dihydrogen (FADH2) levels and mitochondrial oxygen consumption rate. In summary, our study establishes that morphological and phenotypic traits of epithelial/mesenchymal variants of PC3 cells concur with their respective biochemical and metabolic properties. It also underscores that spectroscopic histopathology has a definitive potential to refine the diagnosis of prostate cancer reckoning its molecular and biochemical heterogeneities.

Differentiating between fresh and frozen-thawed fish fillets by muscle fibre permeability measurement

There is no comprehensive method for differentiating between fresh and frozen-thawed fish fillets. This is an ongoing problem, particularly in relation to regulations. In this study, we showed the relevance of using the properties of mitochondria to discriminate fresh fish fillets from frozen-thawed fish fillets. The use of red muscle fibres of Gilthead sea bream allowed us to leave mitochondria in their physiological environment and to avoid possible alterations of mitochondrial membranes during isolation steps. The impact of freezing on fillets was evaluated by measuring the permeability of fibres and mitochondrial membranes to nicotinamide adenine dinucleotide + hydrogen (NADH). NADH permeability of fresh fillet fibres stored at 4 °C was compared to the permeability of fibres extracted from frozen-thawed fillets. Two approaches were used to measure permeability changes: a spectrophotometric method that measured consumption of NADH by complex I, and an oxygraphic approach that measured stimulation of O2 consumption by NADH. Fibres from frozen-thawed fillets were more permeable to NADH and were less sensitive to the permeabilizer alamethicin. The sensitivity of this method allowed us to clearly detect red muscle fibres from frozen-thawed fish versus fresh fish fillets.

Enzyme histochemical characterization of orbital glands in fetuses of Indian buffalo (Bubalus bubalis).

The orbital glands, viz. lacrimal gland, superficial and deep gland of third eyelid (LG, SGT and HG), are important for normal eye functions. These glands have different functions in various animals. The information about the enzyme histochemical nature of prenatal orbital glands in Indian buffalo seems to be unavailable. Therefore, the study was planned on orbital glands of six full term recently died fetuses from animals with dystocia. The frozen sections of all these glands were subjected to standard localization protocols for Alkaline Phosphatase (AKPase), Glucose 6 phosphatase (G-6-Pase), Lactate dehydrogenase (LDH), Succinate dehydrogenase (SDH), Glucose 6 phosphate dehydrogenase (G-6-PD), Nicotinamide Adenine Dinucleotide Hydrogen Diaphorase (NADHD), Nicotinamide Adenine Dinucleotide Phosphate Hydrogen diaphorase (NADPHD), Dihydroxy phenylalanine oxidase (DOPA-O), Tyrosinase, non-specific esterase (NSE) and Carbonic anhydrase (CAse). The results revealed a mixed spectrum of reaction for the above enzymes in LG, SGT and HG which ranged from moderate (for LDH in SGT) to intense (for most of the enzymes in all three glands). However, DOPA-O, Tyrosinase and CAse did not show any reaction. From the present study, it can be postulated that the orbital glands of fetus have a high activity of metabolism as it has many developmental and functional activities which were mediated with the higher activity of the enzymes involved.

UiO-66-Mediated Light-Driven Regeneration of Intracellular NADH in Clostridium tyrobutyricum to Strengthen Butyrate Production

With the increasing depletion of petroleum and fossil resources, the development of green, low-carbon recycling systems has become the main goal for achieving carbon neutrality. Biohybrid photosynthesis systems have been confirmed to reduce carbon loss and promote microbial metabolism to achieve high yields of chemicals. Here, we used UiO-66, an excellent photocatalyst, to increase the intracellular pool of reduced nicotinamide adenine dinucleotide hydrogen (NADH) for butyrate production in Clostridium tyrobutyricum. The NADH/NAD+ ratio increased by 62% in the UiO-66 and C. tyrobutyricum hybrid system compared to the other groups under illumination, which resulted in a 25% increase in butyrate production (11.71 ± 0.16 vs 9.36 ± 0.14 g/L). The system improved the utilization rate of carbon sources and reduced carbon loss. Proteomic analysis also revealed that UiO-66 enhanced the intracellular NADH supply under illumination, leading to an increase in butyrate production. Thus, this system provides an outstanding strategy for improving the conversion of organic carbon into useful chemicals that helps to achieve energy savings and reduce emissions.

Hydrogen sulfide alleviates chilling injury by modulating respiration and energy metabolisms in cold-stored peach fruit

The respiration and energy metabolisms of refrigerated peach fruit and their relationship to chilling injury (CI) treated with hydrogen sulfide (H2S) were investigated. Results showed that H2S treatment reduced the activities of hexokinase (HK), phosphor-glucose isomerase (PGI), phosphofructokinase (PFK) and pyruvate kinase (PK), and the contents of glucose, pyruvate and nicotinamide adenine dinucleotide (hydrogen) (NAD(H)) in the Embden-Meyerhof-Parnas (EMP) and tricarboxylic acid (TCA)-cycle compared to control and hypotaurine (HT, H2S scavenger) treatment, resulting in a lower respiration rate. Meanwhile, H2S treatment increased the activities of NADK, glucose-6-phosphate dehydrogenase (G6PDH) and 6-phosphogluconate dehydrogenase (6PGDH) and NADP(H) contents in the pentose phosphate pathway (PPP), while HT showed the opposite results. Moreover, H2S treatment induced the higher activities of adenosine triphosphatases (ATPases), succinic dehydrogenase (SDH) and cytochrome C oxidase (CCO) along with enhanced levels of ATP and energy charge, whereas HT suppressed energy generation, which increased cell membrane permeability and malondialdehyde content. Therefore, results suggested that H2S could maintain the integrity of the membrane structure by inhibiting the respiration and substance consumption in EMP pathway, increasing the proportion of PPP and energy supply to alleviate CI in peaches.

Molecular Docking of the Inhibitory Activities of Selected Phytochemicals in Artemisia Afra Against NADH-Ubiquinone Oxidoreductase of Plasmodium Falciparum (PfNDH2)

Nicotinamide Adenine Dinucleotide Hydrogen (NADH)-ubiquinone oxidoreductase in Plasmodium falciparum (PfNDH2) constitute a feasible target for anti-malarial drug discovery. This work aims at investigating the inhibitory activities of selected phytochemicals in Artemisia Afra against NADH-Ubiquinone Oxidoreductase of Plasmodium Falciparum. 50 phytochemicals were selected based on structural stability. Quantum mechanical Density Functional Theory (DFT) studies with B3LYP at 6-311G* level was done on pfNDH2 as the apoprotein control. Pharmacokinetic ADMET profiling, bioactivity assessment, physicochemical studies, molecular docking was used to study the PfNDH2 inhibiting activities of the 50 compounds from Artemisia afra. Out of these 50 phytochemicals, 2,4,6-Triphenyl-1,3 dioxane (2,4,6 TPD), chamazulene, aromadendrene, 1-epi-bBicyclosesquiphellandrene (1-EBSP) and cis-muurola-3,5-diene (CM3,5D) passed the physicochemical properties of the Lipinski rule of 5, binding mode, molecular interaction and ADMET calculations. These five compounds also showed high binding affinity of -8.9 kJ/mol, -7.7kJ/mol, -7.3kJ/mol, -7.1kJ/mol and -7.1kJ/mol at the binding pores of PfNDH2 respectively. The reactivity of these compounds was also investigated by the electron donating and accepting activities of the compounds using Density Functional Theory calculated Higher Occupied Molecular Orbital, Lower Unoccupied Molecular Orbital energy and HOMO/LUMO energy gap revealed the stability of the compounds due to the low energy gap values obtained. The values obtained showed that aromadendrene and chamazulene were potential inhibitors of PfNDH2 and were the most potent and therefore, recommended for therapeutic efficacy investigation.

Catalytically Active Metal-Organic Frameworks Elicit Robust Immune Response to Combination Chemodynamic and Checkpoint Blockade Immunotherapy.

Chemodynamic therapy (CDT) strategies rely on the generation of reactive oxygen species (ROS) to kill tumor cells, with hydroxyl radicals (•OH) serving as the key mediators of cytotoxicity in this setting. However, the efficacy of CDT approaches is often hampered by the properties of the tumor microenvironment (TME) and associated limitations to the Fenton reaction that constrains ROS generation. As such, there is a pressing need for the design of new nanoplatforms capable of improving CDT outcomes. In this study, an Fc-based metal-organic framework (MOF) vitamin k3 (Vk3)-loaded cascade catalytic nanoplatform (Vk3@Co-Fc) was developed. This platform was capable of undergoing TME-responsive degradation without impacting normal cells. After its release, Vk3 was processed by nicotinamide adenine dinucleotide hydrogen phosphate (NAD(P)H) quinone oxidoreductase-1 (NQO1), which is highly expressed in tumor cells, thereby yielding large quantities of H2O2 that in turn interact with Fe ions via the Fenton reaction to facilitate in situ cytotoxic •OH production. This process leads to immunogenic cell death (ICD) of the tumor, which then promotes dendritic cell maturation and ultimately increases T cell infiltration into the tumor site. When this nanoplatform was combined with programmed death 1 (PD-1) checkpoint blockade approaches, it was sufficient to enhance tumor-associated immune responses in breast cancer as evidenced by increases in the frequencies of CD45+ leukocytes and CD8+ cytotoxic T lymphocytes, thereby inhibiting tumor metastasis to the lungs and improving murine survival outcomes. Together, this Vk3@Co-Fc cascading catalytic nanoplatform enables potent cancer immunotherapy for breast cancer regression and metastasis prevention.

Highly Selective Nitrogen-Doped Graphene Quantum Dots/Eriochrome Cyanine Composite Photocatalyst for NADH Regeneration and Coupling of Benzylamine in Aerobic Condition under Solar Light

Photocatalysis is an ecofriendly and sustainable pathway for utilizing solar energy to convert organic molecules. In this context, using solar light responsive graphene-based materials for C–N bond activation and coenzyme regeneration (nicotinamide adenine dinucleotide hydrogen; NADH) is one of the utmost important and challenging tasks in this century. Herein, we report the synthesis of nitrogen-doped graphene quantum dots (NGQDs)-eriochrome cyanine (EC) solar light active highly efficient “NGQDs@EC” composite photocatalyst for the conversion of 4-chloro benzylamine into 4-chloro benzylamine, accompanied by the regeneration of NADH from NAD+, respectively. The NGQDs@EC composite photocatalyst system is utilized in a highly efficient and stereospecific solar light responsive manner, leading to the conversion of imine (98.5%) and NADH regeneration (55%) in comparison to NGQDs. The present research work highlights the improvements in the use of NGQDs@EC composite photocatalyst for stereospecific NADH regeneration and conversion of imine under solar light.

A profitable function ofCeriporia lacerataHG2011 on nodulation and biological nitrogen fixation of green bean (Phaseolus vulgaris L.)

Green bean (Phaseolus vulgaris L.) is a popular vegetable worldwide. The use of beneficial fungi is a simple and effective way to improve the biological nitrogen fixation (BNF) of this leguminous vegetable. A micro-plot was conducted to investigate the enhancement of BNF using 15N natural abundance technology and agronomic performances of green bean caused by wood-rot fungus Ceriporia lacerata HG2011. The results showed the soil for frequently growing green bean featured abundant native rhizobia, and newly inoculated rhizobia may have to compete with them in nodulation and only highly competitive rhizobia can succeed. The addition of C. lacerata HG2011 to the soil increased the population of ammonia oxidizers, nitrifiers, and phosphorus (P)-mobilizing microbes in rhizosphere, accelerated nitrification and P mobilization, creating a favorable soil environment with high P and low ammonia for BNF. Green bean received C. lacerata HG2011 had higher dehydrogenase activity in roots and higher nodulation rate and large nodules. These phenomena implied abundant supplies of adenosine triphosphate, nicotinamide adenine dinucleotide hydrogen, or nicotinamide adenine dinucleotide phosphate hydrogen for BNF in the roots, a large proportion of N2 fixation tissues, and a greater sink for receiving photosynthates. As a result, C. lacerata HG2011 considerably increased the percentage of N derived from the atmosphere, BNF, and plant nutrient uptake (including N, P, and potassium), leading to 15.58%-28.51% of biomass increasment and 9.82%-17.03% of peapod yield increasment along with quality improvement compared with non-fungal application. C. lacerata HG2011 increased the nodulation and BNF of green bean, accelerated the nutrient uptake (NPK) and therefore improved the yield and peapod quality of green bean. The study demonstrates that C. lacerata HG2011 could be used as a biofertilizer for BNF improvement of legumes.

NDUFA4 promotes cell proliferation by enhancing oxidative phosphorylation in pancreatic adenocarcinoma.

Pancreatic adenocarcinoma (PAAD) is the third leading cause of cancer-related deaths, with a 5-year relative survival rate of 6%. Hence, novel therapeutic targets need to be urgently explored for PAAD. Recently, oxidative phosphorylation (OXPHOS) has been identified to contribute to the development of PAAD. Nicotinamide adenine dinucleotide + hydrogen (NADH) dehydrogenase (ubiquinone) 1 alpha subcomplex 4 (NDUFA4) is known to affect the mitochondrial respiration pathway. However, the function of NDUFA4 in PAAD remains unclear. In this study, NDUFA4 expression was examined in samples from patients with PAAD using real-time polymerase chain reaction and immunohistochemical staining. Furthermore, cell proliferation and cell cycle were analyzed using Cell Counting Kit-8 assay and flow cytometry. A xenograft tumor model derived from a PAAD cell line was developed to validate the in vitro findings. NDUFA4 was observed to be upregulated in the PAAD samples, and high levels were associated with a poor survival rate. NDUFA4 knockdown reduced cell proliferation by inducing G1 arrest in SW1990 cells. Mechanistically, NDUFA4 knockdown decreased the oxygen consumption rate, cellular adenosine triphosphate level, mitochondrial complex IV activity, and protein levels of COX6C and COX5B, which indicated the suppression of OXPHOS. In contrast, NDUFA4 overexpression exerted the opposite effects. Finally, NDUFA4 knockdown significantly inhibited the growth of the xenograft tumor derived from the SW1990 cell line in vivo. Therefore, NDUFA4 contributes to PAAD proliferation by enhancing OXPHOS.

Nicotinamide adenine dinucleotide hydrogen regeneration in a microbial electrosynthesis system by Enterobacter aerogenes

Costly cofactors such as nicotinamide adenine dinucleotide hydrogen (NADH) are essential to have high activity in many redox enzymatic processes. Cofactor regeneration methods have been suggested to improve the economic aspects of the system. Here, we introduce a microbial electrosynthesis process to regenerate NADH in a two-chamber set-up with Enterobacter aerogenes biofilm as the bio-cathode. The effects of several important factors on the regeneration efficiency were studied and the highest NADH regeneration yield was achieved equal to 65 % at the potential of −1.5 V and the initial NAD+ concentration of 1 mM after 8 h of operation. The regenerated cofactor was highly enzymatically active (93 ± 4 %) which was a great merit of the process. Studying the kinetics of regeneration revealed that the electron transfer rate to the biofilm was the limiting factor. We tried to remove the limitation through co-culturing Pseudomonas aeruginosa and producing more electrochemical active compounds in the biofilm. Although, this modification was not effective for the regeneration yield, it showed that the external potential implicitly influenced the regeneration process by changing the internal microbial cell metabolic fluxes. Finally, it can be concluded that the microbial electrosynthesis is a promising green process for NADH regeneration.

A Case of a 23-Year-Old Male With Leber Hereditary Optic Neuropathy With a Rare Mutation

Mitochondrial DNA(mtDNA) is responsible for encoding 13 subunits of the respiratory chain. These subunits are crucial in providing reducing equivalents for the energy-intensive intracellular processes. Leber hereditary optic neuropathy (LHON) is a mitochondrial illness that causes carcinogenesis due to oxidative stress and painless loss of central vision as a result of selective degradation of retinal ganglion cells as well as their axons. We present a case of a 23-year-old male patient who was diagnosed with subacute LHON. The mutation in our patient was found in a less commonly mutated exon sequence of MT-NDL4, which codes for NADH (nicotinamide adenine dinucleotidehydrogen, reduced) dehydrogenase subunit 4L. The MT-ND4L exon is located immediately upstream of the MTD4 exon on the human mtDNA. The take-home message is to always perform a comprehensive mitochondrial genome analysis for identifying rare mutations when LHON is suspected.