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Silver nanoparticles (AgNPs) synthesized through biological methods have emerged as a difficult alternative to traditional chemical synthesis due to their increased biocompatibility and environmental attainability. In this study, we investigated the stability and various biological activities of AgNPs synthesized using Bacillus flexus BAgNPs. The solidification of the nanoparticles was monitored for one month using UV-Vis spectroscopy, which revealed consistent surface plasmon resonance (SPR) peaks around 430-450 nm, indicating sustained nanoparticle integrity. The synthesized B-AgNPs proved significant antifungal, antibacterial, and antioxidant activities. The antifungal efficacy was evaluated against multiple strains of Alternaria solani with B-AgNPs showing superior inhibition compared to standard antifungal drugs. Even at low concentrations, the nanoparticles demonstrated powerful inhibitory effects on Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. Results indicate that B-AgNPs exhibit antioxidant activity also approximate to that of DPPH, particularly at higher concentrations (50 ppm), where the scavenging activity of B-AgNPs is nearly the same as that of DPPH. These findings indicate that B-AgNPs synthesized using B. flexus possess important potential uses in agriculture and biomedicine, with superior stability and biological activity compared to conven- [ABSTRACT FROM AUTHOR]

Silver nanoparticles (AgNPs) synthesized through biological methods have emerged as a difficult alternative to traditional chemical synthesis due to their increased biocompatibility and environmental attainability. In this study, we investigated the stability and various biological activities of AgNPs synthesized using Bacillus flexus B-AgNPs. The solidification of the nanoparticles was monitored for one month using UV-Vis spectroscopy, which revealed consistent surface plasmon resonance (SPR) peaks around 430-450 nm, indicating sustained nanoparticle integrity. The synthesized B-AgNPs proved significant antifungal, antibacterial, and antioxidant activities. The antifungal efficacy was evaluated against multiple strains of Alternaria solani with B-AgNPs showing superior inhibition compared to standard antifungal drugs. Even at low concentrations, the nanoparticles demonstrated powerful inhibitory effects on Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. Results indicate that B-AgNPs exhibit antioxidant activity also approximate to that of DPPH, particularly at higher concentrations (50 ppm), where the scavenging activity of B-AgNPs is nearly the same as that of DPPH. These findings indicate that B-AgNPs synthesized using B. flexus possess important potential uses in agriculture and biomedicine, with superior stability and biological activity compared to conventional methods.

In order to study the chemical constituents from Chloranthus henryi and their antitumor activities in vitro. The chemical constituents of ethyl acetate fraction, extracted with 95% ethanol from C. henryi were isolated and purified by silica gel column chromatography, reversed phase column chromatography, Sephadex LH-20 column chromatography and preparation liquid chromatography, and their structures were identified by the physicochemical properties, spectral data combined with relevant literatures. The cytotoxic activities of these compounds were evaluated by MTT method. The results were as follows: (1) Twelve compounds were isolated and identified as pipercyclobutanamide C (1), chololactone A (2), sarcanolide B (3), oxacol A (4), chloramultiol D (5), chlorasessilifol B (6), chlorajaponol (7), tianmushanol (8), spicachlorantins B (9), spicachlorantins A (10), serrachlorin A (11), chloramultiols A (12). Among them, Compound 1 was identified as a new compound, and except for Compound 8, all the other compounds were isolated from the C. henryi for the first time. (2) The cytotoxic activity test results showed that only compounds 2 and 7 had good inhibitory effects on HeLa cells in vitro, while the other compounds showed no inhibition effects. The IC50 of the two compounds were (4.50±0.27) μmol·L-1 and (4.25±0.08) μmol·L-1 respectively. In conclusion, the study enriches the chemical constituents of C. henryi, and provides a reference for the further exploration and utilization of this Chloranthus herb plants.

Arnica montana (AM), which belongs to the daisy family Asteraceae, has a longstanding traditional use in Europe and North America for pain and inflammation treatment. This study investigates the inhibitory effects of ‘Arnica montana extract hydrogel patch (AHP)’ on Carrageenan-induced paw edema and hot plate-induced pain models. AHP exhibited transdermal permeability without the occurrence of issues like crystal precipitation. This study employed two animal model assessments using AHP, in comparison with Arnicare Gel (AG), to evaluate anti-inflammatory and pain relief effects. AHP treatment for 2 days showed a decrease in paw edema thickness in mice as compared to vehicle or AG groups; Carrageenan-induced swelling increased maximally at 1 h with the AHP group demonstrating a higher reduction. Thus, the AHP group exhibited a lower ratio of right/left paw thickness and a superior reduction in swelling, supportive of its ability to diminish edema. A histological analysis showed that AHP treatment reduced inflammatory cell infiltration. Consistently, the mRNA levels of inflammatory markers (tnfa, il1b, and il6) were decreased to a greater extent than the AG group. Particularly, tnfa inhibition was better in the AHP group, and the levels of il1b and il6 transcripts showed ~80% and 40% lower. Likewise, AHP reduced pain scores in a hot plate-induced rat model, although AG failed to do so. Together, these results demonstrate that AHP has long-lasting inhibitory effects on fluid effusion and edema formation, the production of inflammatory mediators, and pain-sensation, supporting its anti-inflammatory and pain-relieving pharmacological effects.

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The dynamical behaviors of an epidemic model based on the susceptible–infected–susceptible (SIS) model are investigated. The Beddington–DeAngelis functional response is used for the infection rate to present the dependence of the transmission of the infection on the ratio of both susceptible and infected populations. A Caputo fractional derivative is applied to show the existence of memory in nature affects population dynamics. The disease-free and endemic equilibrium points are obtained as the equilibrium points that describe the condition when the population is free from the disease or the disease exists in the population throughout time. The existence, uniqueness, non-negativity, and boundedness are proven which state the biological validity of the mathematical model. The local and global stability of each equilibrium point is studied including the basic reproduction number and its influence on the dynamical behaviors. Some numerical simulations are portrayed to explore more about the dynamics of the model which are relevant to the analytical findings. The partial rank correlation coefficient is presented to investigate the dominant parameter with respect to the basic reproduction number and the density of susceptible and infected populations. The parameter continuations are demonstrated to show the impact of infection rate and the inhibitory effect which lead to the occurrence of forward bifurcations. The memory effect is also demonstrated numerically to show the changes in convergence rate due to the changes in memory strength.

Copyright of Jurnal Fitopatologi Indonesia is the property of IPB University and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Cocoa is an economically valuable plantation commodity, but its cultivation often faces a significant challenge, which is caused by the Phytophthora palmivora. Phylloplane yeast has an important role in protecting plant surfaces from pathogen infection. The aim of the study was to assess the diversity of phylloplane yeasts found on cocoa fruits, and determine them as biological control agents for P. palmivora. The metode include isolating yeasts from young, old and rotten cocoa pods and testing them as antagonists against P. palmivora. The findings of this study yielded eight yeast isolates that were significant in inhibiting the growth of P. palmivora. These isolates spanned across six genera, including Debaryomyces sp., Metschnikowia sp., Zygosaccharomyces sp., Candida sp., Wickerhamomyces sp., and Cryptococcus sp. Candida sp.2 and Wickerhamomyces sp. as particularly promising species species that had a consistently resistant level of inhibitory effect, achieved percentage inhibition of 36.26% (10.8 mm) and 34.44% (9.6 mm), respectively.

Acacia nilotica, (Fabaceae), is valued for its medicinal properties. We examine the antiproliferative properties of the aqueous fruit extract of A. nilotica. Aqueous extract from Acacia has been associated with potential anticancer effects in fruits and vegetables through screening, antiproliferative, and molecular docking evaluation. Phytochemical screening reveals the presence of alkaloids, saponins, tannins, flavonoids, steroids, and carbohydrates. The extracts showed significant antiproliferative effects at eight concentrations (8–50 mg mL–1) examined in comparison to the standard (methotrexate). When compared to Sorghum bicolor seed radicles treated with methotrexate at 48, 72, and 96 h, 50 mg mL–1 extract significantly inhibited the generation of seed radicals, with potent inhibitions of 87.06, 83.48, and 81.45%. Analysis of molecular docking results showed that [(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl]3,4,5-trihydroxybenzoate (D21), (5R,9R,10R,13S,14S,17S)-17-[(2S,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one (D28) and [(2R,3S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl] 3,4,5-trihydroxybenzoate (D29) have strong tendency to inhibit dihydrofolate reductase (1VDR), capase-9 (6J15) and Mycobacterium tuberculosis (Mtb) (6J17) better than methotrexate and azacitidine, known antiproliferative drugs. These findings support the use of A. nilotica in traditional medicine for the treatment of tuberculosis and cancer.

Tobacco (Nicotiana tabaccum L.) is an agricultural commodity in Indonesia, with production reaching 261.40 thousand tonnes in 2020. Tobacco leaves contain flavonoids and alkaloids, which are helpful as antibacterial, antifungal, and anti-insect agents. This study aimed to optimize the extraction process of tobacco leaves as an antibacterial agent. The factors used were material-to-solvent ratio (w/v) and extraction time. The microwave-assisted extraction (MAE) was used, with the response surface methodology (RSM) for data processing. This study showed that thematerial-to-solvent ratio and extraction time significantly affected the total flavonoid value, the extract inhibitory activity against S. mutans bacteria, and the extract yield. However, no significant effect was observed on the extract’s pH. The highest total flavonoid value, inhibitory activity, and pH were obtained from the treatment with a ratio of 1:2172 (w/v) and 6 minutes extraction time, giving an average value of 524.67 mg EQ/g, 22.4 mm, and 5.6, respectively. The highest yield of 4.61% was obtained from the treatment with a ratio of 1:5 (w/v) and 6 minutes extraction time. The optimal solution for the tobacco leaves extraction process was obtained from material-to-solvent ratio of 1: 2.6 (w/v) and 7 minutes of extraction time, giving the total flavonoids, inhibitory activity, pH, and yield of 428.4 mg EQ/g, 20.7 mm, 5.8, and 3.1%, respectively.

Copyright of Industrial Water Treatment is the property of CNOOC Tianjin Chemical Research & Design Institute and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

(1) Background: This study summarizes the findings of two studies investigating the inhibitory effects of Pseudomonas aeruginosa strains from clinical and environmental sources against gram-positive and gram-negative bacteria and fungi. The studies also analyzed the correlation between enzyme production and inhibitory effects to gain insights into the antimicrobial capabilities of P. aeruginosa strains; (2) Methods: Both studies employed similar methodologies, including the use of disk diffusion and well diffusion methods to assess the inhibitory effects of P. aeruginosa strains against target pathogens. Enzyme production was analyzed through various biochemical assays to determine the diversity and frequencies of enzyme secretion among the strains; (3) Results: A comparative analysis of enzyme production in P. aeruginosa strains from clinical sources revealed significant variations in enzyme production, with hemolysin and protease being the most commonly produced enzymes. Gelatinase production showed lower rates, whereas chondroitinase and hyaluronidase were absent or occurred less frequently. In contrast, a comparative analysis of enzyme production in environmental isolates showed different patterns, indicating adaptation to environmental conditions. Pyocyanin production was absent in all environmental isolates. The inhibitory effects against gram-positive and gram-negative bacteria varied among different P. aeruginosa strains, with strain-specific variations observed. Limited inhibitory effects were observed against fungi, primarily toward gram-positive bacteria; (4) Conclusions: The findings highlight the strain-specific nature of inhibitory effects and enzyme production in P. aeruginosa strains. The correlation between enzyme production and inhibitory effects against gram-positive bacteria suggest a potential role of specific enzymes, such as hemolysin and protease, in the antimicrobial activity. The complexity of the relationship between enzyme production and the inhibition of different pathogens requires further investigation. The results emphasize the potential of P. aeruginosa strains as sources for antimicrobial strategies, particularly against gram-positive bacteria. Future research should focus on understanding the mechanisms underlying these inhibitory effects and exploring their therapeutic applications. [ABSTRACT FROM AUTHOR]

In this study, a Bayesian network (BN)-based inhibition model is developed for the rainstorm–landslide–debris flow (R-L-D) disaster chain in the mountainous area of the Greater Bay Area (GBA), China, using the historical disaster data. Twelve nodes are selected for the inhibition model, which are classified into four types, including Hazardous Factor, Response Operation, Disaster Evolution, and Disaster Result. By combining the proposed inhibition with the scenario analysis method, the probabilities of the BN nodes under different rainfall scenarios are analyzed, and then the inhibitory effects of the environmental geological conditions and rescue speed on the R-L-D disaster chain under the most unfavorable rainfall scenario are investigated. On this basis, an inhibition framework consisting of the early warning, inhibition, and measures layers is proposed for the R-L-D disaster chain. The results reveal that under the most unfavorable rainfall scenarios, where the rainfall intensity is greater than 100 mm/d and the rainfall duration is greater than 24 h, the probability of landslides and debris flow is 0.930 and 0.665, respectively. Improving the environmental geological conditions such as slope, lithology and geological structure can greatly inhibit the occurrence of the R-L-D disaster chain. Moreover, the improvement of geological structure conditions is the most significant, and reduces the probability of landslides and debris flow by 0.684 and 0.430, respectively, as well as reducing the probability of death and direct economic loss by 0.411 and 0.619, respectively. Similarly, increasing the rescue speed leads to a reduction in the probability of death and direct economic loss by 0.201 and 0.355, respectively. This study can provide theoretical and practical insights into the prevention and inhibition of the R-L-D disaster chain. [ABSTRACT FROM AUTHOR]

To study the inhibitory effects of Enterococcus faecalis Z096 on the biofilm and quorum sensing (QS) system of Vibrio parahaemolyticus, the competition, elimination and exclusion were performed to simulate the interaction between Z096 and V. parahaemolyticus in microbial communities. In addition, the effects of Z096 extract (Z096-E) on V. parahaemolyticus biofilm formation, mature biofilm elimination, cell surface hydrophobicity, auto-aggregation, QS signal molecule AI-2 activity, motility ability (swarming and swimming), extracellular polysaccharide and protein synthesis were further explored. The results showed that Z096 could significantly reduce the number of V. parahaemolyticus cells in plankton and biofilm by competition, elimination and exclusion, and interfere with the adhesion of V. parahaemolyticus on the carrier surface. Moreover, Z096-E could significantly inhibit biofilm formation and effectively eliminate the mature biofilm of V. parahaemolyticus. When treated with 1.6 mg/mL of Z096-E for 12 h, the biofilm inhibition rate was 70.43%, and the metabolic activity decreased by 84.15%; When the mature biofilm of V. parahaemolyticus was treated with 12.8 mg/mL of Z096-E for 4 h, the biofilm removing rate was 58.21%, and the metabolic activity decreased by 69.84%. The swarming and swimming ability, cell surface hydrophobicity and auto-aggregation, extracellular polysaccharide and protein synthesis of V. parahaemolyticus were inhibited by 1.6 mg/mL of Z096-E by 47.26%, 53.56%, 63.37%, 89.38%, 77.65% and 51.91%, respectively, and the inhibitory effect was dose-dependent. In addition, Z096-E weakened the activity of QS signal molecule AI-2 of V. parahaemolyticus, indicating that Z096-E was an AI-2 quorum sensing inhibitor, which could affect the physiological characteristics of V. parahaemolyticus by interfering with the QS system. Therefore, we found one strain of lactic acid bacteria (LAB) that could inhibit V. parahaemolyticus biofilm, and the Z096-E could be used as a novel LAB-based biological agent to prevent and control V. parahaemolyticus biofilm. This study would be of positive significance to eliminate V. parahaemolyticus biofilm pollution and develop novel antibacterial agents.

Simple Summary: Osteosarcoma is the most prevalent orthotopic bone tumor. Due to its high metastatic properties, it has become the leading cause of cancer death worldwide. At this time, there is no effective treatment for osteosarcoma. Hence, we aimed to investigate the efficacy of ononin on osteosarcoma cell migration, invasion, and the underlying mechanisms. The dose-dependent manners of ononin treatment increased the expression of apoptosis and inhibition of cell proliferation in MG-63 and U2OS osteosarcoma cell lines through the EGFR-Erk1/2 signaling pathways. For consistency, we used the MG-63-xenograft mice model to confirm the in vivo anti-tumorigenic and anti-migratory efficacy of ononin. These findings suggest that ononin could be a potentially effective agent against the metastasis of osteosarcoma. Osteosarcoma is a common malignancy of the bone. Due to its high metastatic properties, osteosarcoma becomes the leading cause of cancer death worldwide. Ononin is an isoflavone glycoside known to have various pharmacological properties, including antioxidant and anti-inflammatory activities. In the present study, we aimed to investigate the efficacy of ononin on osteosarcoma cell migration, invasion, and the underlying mechanisms. The in vitro anti-tumorigenic and anti-migratory properties of ononin were determined by MTT, colony formation, invasion, and migration in MG-63 and U2OS osteosarcoma cell lines. The results were compared with the standard chemotherapeutic drug, doxorubicin (DOX), as a positive control. The dose-dependent manners of ononin treatment increased the expression of apoptosis and inhibition of cell proliferation through the EGFR-Erk1/2 signaling pathways. Additionally, ononin significantly inhibited the invasion and migration of human osteosarcoma cells. For consistency, we used the MG-63-xenograft mice model to confirm the in vivo anti-tumorigenic and anti-migratory efficacy of ononin by inhibiting the protein expressions of EGFR-Erk1/2 and MMP2/9. According to the histological study, ononin had no adverse effect on the liver and kidney. Overall, our findings suggested that ononin could be a potentially effective agent against the development and metastasis of osteosarcoma. [ABSTRACT FROM AUTHOR]

Cladophora members are present in seawater and freshwater ecosystems worldwide. Their growth poses a serious threat to water environment, fisheries, production and living. In order to explore safe and ecological treatment methods, the inhibitory effects and oxidative damages (48 and 96 h) in Cladophora sp. (Cladophoraceae) exposed to 0–0.30 g L−1 berberine were investigated. Results showed that the LC 50 of berberine to Cladophora was 0.147 g L−1 and 0.063 g L−1 at 48 h and 96 h, respectively. Malondialdehyde and total protein contents first increased and then decreased sharply with increasing exposure concentrations of berberine. The Cladophora cells accelerated protein synthesis when their cell membranes were subjected to oxidative damage. Superoxide dismutase activity was down-regulated slightly after exposure to low berberine concentration (0.05 g L−1) and strongly when the Cladophora cells suffered from great oxidative damage. Total antioxidant capacity (T-AOC) first decreased sharply and then increased with increasing exposure concentrations of berberine. The decrease in T-AOC indicated the enzymatic antioxidants were continuously inhibited with increasing exposure concentrations of berberine. The increase in T-AOC indicated the secretion of non-enzymatic antioxidants was continuously strengthened with increasing exposure concentrations of berberine. Cladophora DNA also underwent oxidative damage due to berberine. Low concentrations of berberine activated its repair mechanisms, but high concentrations could cause irreparable damage. Therefore, these results suggested that berberine could inhibit the growth of Cladophora by oxidative damage, and Cladophora responded physiologically to this stress accordingly.

Introduction: Nowadays, the widespread use of antimicrobial peptides as a natural preservative due to the side effects of synthetic preservatives (cancers and liver damages in medicines and foods) has received much attention. Materials and methods: In the present study, five antibacterial peptides including Nisin A of Lactococcus lactis, melitin of Apis mellifera, copsin from Coprinopsis cinerea, Terpene of Erythrolobus australicus, and thionin from Arabidopsis thaliana were studied using bioinformatics analysis. Results: The results showed that these peptides (peptides studied in eukaryotics and prokaryotics) had cytoplasmic targeting and the studied peptides were not protected in different organisms. There was a variation in the number of α helixes and β sheets among the studied peptides. The results of the phylogenetic tree by Mega5 showed that besides Apis mellifera, four other species were located in the same cluster. The domains were different in the five studied species, but all domains had antibacterial properties. These peptides showed a wide range of physicochemical properties. The substitution template, substitution model, and D-Tajima sequence of the studied peptides showed that Apis mellifera was isolated from other species during evolution. Three-dimensional (3-D) modeling of peptides by the homology modeling method and Swiss Model database showed that the three-dimensional structure of terpene and thionin had high quality. Using peptidecutter and allermatch websites, it was found that nisin A, melitin, copsine, terpene, and thionin were not allergenic. To determine the minimum lethal concentration and minimum inhibitory concentration, the disk diffusion method was used. The highest inhibition of nisin of Lactococcus Lactis was obtained in Staphylococcus aureus and Escherichia coli by disk diffusion. Blank discs were 19, 23 mm, 5, and 1 mm, respectively. Discussion and conclusion: The results showed that nisin can be used as a natural preservative to delay food spoilage against gram-positive bacteria.

(1) Background: This study summarizes the findings of two studies investigating the inhibitory effects of Pseudomonas aeruginosa strains from clinical and environmental sources against gram-positive and gram-negative bacteria and fungi. The studies also analyzed the correlation between enzyme production and inhibitory effects to gain insights into the antimicrobial capabilities of P. aeruginosa strains; (2) Methods: Both studies employed similar methodologies, including the use of disk diffusion and well diffusion methods to assess the inhibitory effects of P. aeruginosa strains against target pathogens. Enzyme production was analyzed through various biochemical assays to determine the diversity and frequencies of enzyme secretion among the strains; (3) Results: A comparative analysis of enzyme production in P. aeruginosa strains from clinical sources revealed significant variations in enzyme production, with hemolysin and protease being the most commonly produced enzymes. Gelatinase production showed lower rates, whereas chondroitinase and hyaluronidase were absent or occurred less frequently. In contrast, a comparative analysis of enzyme production in environmental isolates showed different patterns, indicating adaptation to environmental conditions. Pyocyanin production was absent in all environmental isolates. The inhibitory effects against gram-positive and gram-negative bacteria varied among different P. aeruginosa strains, with strain-specific variations observed. Limited inhibitory effects were observed against fungi, primarily toward gram-positive bacteria; (4) Conclusions: The findings highlight the strain-specific nature of inhibitory effects and enzyme production in P. aeruginosa strains. The correlation between enzyme production and inhibitory effects against gram-positive bacteria suggest a potential role of specific enzymes, such as hemolysin and protease, in the antimicrobial activity. The complexity of the relationship between enzyme production and the inhibition of different pathogens requires further investigation. The results emphasize the potential of P. aeruginosa strains as sources for antimicrobial strategies, particularly against gram-positive bacteria. Future research should focus on understanding the mechanisms underlying these inhibitory effects and exploring their therapeutic applications.

Xian-Ling-Gu-Bao (XLGB) capsule, a well-known traditional Chinese medicine prescription, is widely used for the treatment of osteoporosis. It could significantly increase the levels of estrogen in ovariectomized rats and mice. However, this working mechanism has not been well elucidated. Considering that UDP-glucuronosyltransferase (UGT) enzymes are the important enzymes that inactivate and regulate estrogen activity in vivo, this study aimed to identify the bioactive compounds from XLGB against the glucuronidation of estrogens. First, thirty compounds were considered as candidate bioactive compounds based on our previous studies including pharmacological evaluation, chemical profiles, and metabolic profiles. Second, the characteristics of estrogen glucuronidation by uridine diphosphate glucuronic acid (UDPGA)-supplemented human liver microsomes (HLM), human intestine microsomes (HIM), and expressed UGT enzymes were determined, and the incubation systems of their key UGT enzymes were optimized. Then, inhibitory effects and mechanisms of XLGB and its main compounds toward the key UGT isozymes were further investigated. As a result, estrogen underwent efficient glucuronidation by HLM and HIM. UGT1A10, 1A1, and 2B7 were mainly responsible for the glucuronidation of estrone, ß-estradiol, and estriol, respectively. For E1 and E2, UGT1A10 and 1A1 tended to mediate estrogen-3-O-glucuronidation, while UGT2B7 preferred catalyzing estrogen-16-O-glucuronidation. Furthermore, the incubation system for active UGT isoforms was optimized including Tris-HCl buffer, detergents, MgCl2 concentration, ß-glucuronidase inhibitors, UDPGA concentration, protein concentration, and incubation time. Based on optimal incubation conditions, eleven, nine, and nine compounds were identified as the potent inhibitors for UGT1A10, 1A1, and 2B7, respectively (IC50 < 4.97 µM and Ki < 3.35 µM). Among them, six compounds (bavachin, isobavachin, isobavachalcone, neobavaisoflavone, corylifol A, and icariside II) simultaneously demonstrated potent inhibitory effects against these three active enzymes. Prenylated flavanols from Epimedium brevicornu Maxim., prenylated flavonoids from Psoralea corylifolia L., and salvianolic acids from Salvia miltiorrhiza Bge. were characterized as the most important and effective compounds. The identification of potent natural inhibitors of XLGB against the glucuronidation of estrogen laid an important foundation for the pharmacodynamic material basis. [ABSTRACT FROM AUTHOR]

Abstract Drought is one of the most damaging abiotic stress that hinder plant growth and development. The present study aimed to determine the effects of various Ca/Mg quotients under polyethylene glycol (PEG)–induced osmotic stress on growth, uptake and translocation of Ca and Mg in Avena sativa (L). Plants were grown in nutrient solution supplemented with three different Ca/Mg molar quotients (0.18, 2, and 4). After 30 days plants were exposed to two different PEG (Polyethylene glycol) concentrations (0.6 MPa & 0.2 MPa) for 8 days, and solutions were renewed after 4 days. A solution containing Ca and Mg nutrients has mitigated the negative impact caused via osmotic stress on relative growth rate (RGR), absolute growth rate (AGR), crop growth rate (CGR), leaf area ratio (LAR), Leaf index ratio (LAI), root-shoot ratio (RSR), water use efficiency (WUE) and net assimilation rate (NAR). In addition, it adversely affected germination parameters, including final emergence percentage (FEP), mean germination time (MGT), Timson germination Index (TGI), germination rate index (GRI) and percent field capacity (%FC), of oat (Avena sativa L.). Mg and Ca in shoot and root and Ca translocation factor decreased with increasing Ca in solution, while Mg translocation factor increased with increasing Ca in nutrient solution. In this work, the combined effects of various Ca/Mg quotients and osmotic stress produced by polyethylene glycol (PEG) in different concentrations (0.6 MPa, 0.2 MPa) on the growth and element uptake of Avena sativa L. are examined. As a result, the Ca/Mg Quotient may naturally combat the moderate drought stress experienced by field crops.

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Background & Aims: The increasing rate of vancomycin resistant Staphylococcus aureus (VRSA) with biofilm formation may become a new threat to humans. In such cases, finding an effective treatment strategy such as using Nanotechnology (Nano- drugs) to deal with these types of infections may be promising. This study aimed to investigate the inhibitory effects of silver nanoparticles (SNPs) on biofilm formation of VRSAs. Materials and Methods: Clinical S. aureus isolates were identified to the species level by conventional methods, and their identities were later confirmed by PCR. Following the determination of susceptibility patterns of the isolates; all the screened S.aureus isolates have been assessed regarding their susceptibility to vancomycin. Detection of vanA gene and determination of minimum inhibitory concentrations (MICs) of VRSAs were carried out using PCR and Etest methods, respectively. The biofilm production was assessed on all VRSA isolates in the presence/absence of SNPs using micro-titer plate method. Results: In total, 11 (6.21%) VRSAs were identified among 177 S. aureus clinical isolates. These isolates were included in the biofilm production assay. All of the VRSAs were multidrug resistance and biofilm producers. The inhibitory effect of SNPs in concentration of 250 µg/ml on biofilm formation of VRSA isolates was significant (Pv = 0.01). Conclusion: Based on our findings, SNPs can prevent biofilm formation of VRSAs and applying of these nanoparticles may prohibit from the persistence and colonization of such resistant isolates.

This paper aims to explore the effect and mechanism of rising housing prices on residents' physical and mental health. Using data from the China Family Panel Studies from 2014 to 2018, we investigate the impact and mechanism of rising housing prices on the mental and physical health of urban residents through multiple grouping regression and analysis of variance. The study finds that overall, rising housing prices have a positive effect on residents' mental health but a negative effect on physical health, and those who do not own a house show the greatest adverse effect. The impact of rising housing prices on health is mainly reflected in three aspects: the wealth effect, cost effect, and comprehensive environmental expectation effect. Of these, the wealth effect and comprehensive environmental expectation effect play a role in promoting residents' health, whereas the cost effect has a strong inhibitory effect. This paper also analyzes how house prices impact health and finds that having health insurance reduces residents' active health behavior, thus affecting their physical and mental health levels, which has a positive effect on uninsured residents.

Among popular artisanal dairy products, kariesh cheese, Laban Rayeb and yoghurt are occupying advanced rank in the human consumers` interest in Egypt. The current study included the microbiological investigations of 25 each of such products primarily to isolate and discriminate staphylococci and different lactobacillus strains and secondly to search for some of this lactobacillus to be considered as a probiotic. via investigating several characteristics including, their ability to resist and survive gastrointestinal tract conditions represented in gastric acidity (pH 2.5-3) and duodenal bile acids, and at the same time, having safety or non-pathogenicity, which principally includes non-harboring of antibiotic resistance (AR) patterns or virulence factors. Finally, the isolated lactobacillus strains were tested as inhibitors for some pathogenic bacteria such as Staphylococcus aureus and E. coli.

A new eudesmane sesquiterpenoid (1), named sapleudesone, together with four known analogs (2-5) were isolated from the aerial parts of Salvia plebeia. The structure of compound 1 was established by NMR and HRESIMS data, and the absolute configuration of 1 was determined by comparing the experimental ECD spectrum with the calculated ECD spectra. The known compounds were identified to be salplebeone A (2), linderolide I (3), chlorantene D (4), and chlomultin B (5), respectively, by comparing the NMR data and specific rotations with reported data. All five compounds were tested for the inhibitory effects against NO production in LPS-activated RAW 264.7 macrophages. As a result, compound 2 exhibited weak inhibitory effects with an IC50 value of 42.3 ± 1.4 μM. [ABSTRACT FROM AUTHOR]

Copyright of Biological Journal of Microorganism is the property of University of Isfahan and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The etiology of diarrhea-predominant irritable bowel syndrome (IBS-D) is complicated and closely related to neurotransmission in the gastrointestinal (GI) tract. Developing new strategies for treating this disease is a major challenge for IBS-D research. Berberine hydrochloride (BBH), the derivative of berberine, is a herbal constituent used to treat IBS. Previous studies have shown that BBH has potential anti-inflammatory, antibacterial, analgesic, and antidiarrheal effects and a wide range of biological activities, especially in regulating the release of some neurotransmitters. A modified IBS-D rat model induced by chronic restraint stress was used in all experiments to study the effects of BBH on the GI tract. This study measured the abdominal withdrawal reflex (AWR) response to graded colorectal distention (CRD; 20, 40, 60, and 80 mmHg) and observed the fecal areas of stress-induced IBS-D model. Experiments were conducted using organ bath techniques, which were performed in vitro using strips of colonic longitudinal smooth muscle. Inhibitory and excitatory neurotransmitter agents were added to each organ bath to observe contractile responses on the strips and the treatment effect exerted by BBH. The IBS-D rat model was successfully induced by chronic restraint stress, which resulted in an increased defecation frequency and visceral hypersensitivity similar to that of humans. BBH could reduce 4-h fecal areas and AWR response to CRD in IBS-D. The stress-induced IBS-D model showed upregulated colonic mRNA expression levels of 5-hydroxytryptamine-3A receptor and downregulated expression levels of neuronal nitric oxide synthase. Meanwhile, BBH could reverse this outcome. The responses of substances that regulate the contraction induced by related neurotransmission in the longitudinal smooth muscle of IBS-D colon (including the agonist of acetylcholine, carbachol; NOS inhibitor, L-NAME; and P2Y1 receptor antagonist, MRS2500) can be inhibited by BBH. In summary, BBH promotes defecation frequency and visceral hypersensitivity in IBS-D and exerts inhibitory effects on contractile responses in colonic longitudinal smooth muscle. Thus, BBH may represent a new therapeutic approach for treating IBS-D.

The etiology of diarrhea-predominant irritable bowel syndrome (IBS-D) is complicated and closely related to neurotransmission in the gastrointestinal (GI) tract. Developing new strategies for treating this disease is a major challenge for IBS-D research. Berberine hydrochloride (BBH), the derivative of berberine, is a herbal constituent used to treat IBS. Previous studies have shown that BBH has potential anti-inflammatory, antibacterial, analgesic, and antidiarrheal effects and a wide range of biological activities, especially in regulating the release of some neurotransmitters. A modified IBS-D rat model induced by chronic restraint stress was used in all experiments to study the effects of BBH on the GI tract. This study measured the abdominal withdrawal reflex (AWR) response to graded colorectal distention (CRD; 20, 40, 60, and 80 mmHg) and observed the fecal areas of stress-induced IBS-D model. Experiments were conducted using organ bath techniques, which were performed in vitro using strips of colonic longitudinal smooth muscle. Inhibitory and excitatory neurotransmitter agents were added to each organ bath to observe contractile responses on the strips and the treatment effect exerted by BBH. The IBS-D rat model was successfully induced by chronic restraint stress, which resulted in an increased defecation frequency and visceral hypersensitivity similar to that of humans. BBH could reduce 4-h fecal areas and AWR response to CRD in IBS-D. The stress-induced IBS-D model showed upregulated colonic mRNA expression levels of 5-hydroxytryptamine-3A receptor and downregulated expression levels of neuronal nitric oxide synthase. Meanwhile, BBH could reverse this outcome. The responses of substances that regulate the contraction induced by related neurotransmission in the longitudinal smooth muscle of IBS-D colon (including the agonist of acetylcholine, carbachol; NOS inhibitor, L-NAME; and P2Y1 receptor antagonist, MRS2500) can be inhibited by BBH. In summary, BBH promotes defecation frequency and visceral hypersensitivity in IBS-D and exerts inhibitory effects on contractile responses in colonic longitudinal smooth muscle. Thus, BBH may represent a new therapeutic approach for treating IBS-D. [ABSTRACT FROM AUTHOR]

Old textiles are important elements of thecultural heritage. As a result of their composition mostly of natural elements old textiles are extremely prone to physical and chemical degradation due to fungal action. The treatments usually applied for the cleaning of heritage textiles target the use of synthetic fungicides, which are potentially harmful to both human health and the environment. Numerous studies highlight as an alternative to the use of conventional antifungals, the employment of essential oils and plant extracts, which are environmentally friendly and which have no adverse effects on human health. Against this background the present study aims to test six essential oils (Lavandula angustifolia, Citrus limon, Mentha piperita, Marjoram, Melaleuca alternifolia, Origanum vulgare) to establish their inhibitory effects against fungi identified on an old piece of traditional Romanian clothing from Maramureş. For the study, the types of fungi present on the objects was determined primarily through the open plates technique and microscopic identification. After identification, the essential oils were applied to the delimited surfaces, and their effects observed up to 32 days after application. The results show that these essential oils have a strong inhibitory effect on such fungal genera as Penicillinum sp., Cladosporium sp., Aspergillus spp., Candida guillermondii, Botrys sp., Mucor sp., having no observable side-effects on the physical properties of the materials concerned. The antimicrobial effects that essential oils and plant extracts have in the short term must be tested in future to ensure the enhanced preservation of heritage textiles and the health integrity of the restorers and visitors who view them in museums, collections or exhibitions. [ABSTRACT FROM AUTHOR]

In this work, inhibitory effects of naringenine (NAR) on cytochrome P450 (CYP450) were investigated by recording different types of electrochemical data including electrochemical impedance spectroscopy (EIS), differential pulse voltammetry (DPV), linear sweep voltammetry (LSV), cyclic voltammetry (CV) and normal pulse voltammetry (NPV). First of all, direct analysis of the electrochemical data helped us to obtain some information about binding of NAR to CYP450 and then, electrochemical data were hard-modeled by EQUISPEC, SPECFIT, SQUAD and REACTLAB to compute binding constant of the NAR to CYP450. Then, DPV, LSV, CV and NPV data were row-wise augmented into a data matrix and analyzed by MCR-ALS to obtain more information about binding of NAR to CYP450. Further investigation of the binding of NAR to CYP450 was investigated by molecular docking and these results were compatible with experimental results. On the whole, our study confirmed a strongly binding of NAR to CYP450 which justified inhibitory effects of NAR to CYP450. Finally, our study was expanded to develop a novel electroanalytical method for determination of the CYP450 based on inhibiting of CYP450 by NAR. Statement: All the sections of this work have been performed by Dr. Ali R. Jalalvand.

Fosil yakıt kaynaklarının hızla tüketilmesi ve enerji ihtiyacının karşılanmasında dışa bağımlılık kaygısı, alternatif yakıt araştırmalarına yol açmıştır. Transesterifikasyon yoluyla bitkisel yağ ve hayvansal yağ gibi birçok yenilenebilir kaynağından elde edilebilen biyodizel, otomobiller için, özellikle çevre dostu olmak için en çekici alternatif yakıttır. Ancak bazı eksiler de var. Biyodizelde su ve serbest yağ asitleri varlığı onu petrol türevi dizelden daha korozif yapar ve bu istenmeyen bir özelliktir. Biyodizel ile temastan kaynaklanan korozyon hem metal parçaların ömrünü azaltır hem de yakıt özelliklerini kötüleştirir ve bu nedenle motor performansını olumsuz olarak etkiler. Bu nedenle, biyodizelin korozif özellikleri, motor bileşenlerinin uzun süreli dayanıklılığı için çok önemlidir. Bu çalışmada, farklı biyodizel yakıtlarıyla farklı sıcaklıklarda farklı dönemler için önceki çalışmaların test sonuçlarını değerlendirerek ve karşılaştırarak biyodizel ve harmanların motor parçaları üzerindeki korozif etkileri araştırılmıştır. Katkı maddeleri kullanarak biyodizelin korozif etkilerini önlemek veya azaltmak için düzeltici önlemler de ele alınmaktadır.

Rapid depletion of fossil fuel resources as well as concerns for foreign dependence in meeting energy needs have led researches for alternative fuels. Biodiesel, which can be obtained from many renewable resources such as vegetable oil and animal fat through transesterification, is the most attractive alternative fuel for cars, especially for being environmentally friendly. However, there are some cons, too. The presence of water and free fatty acids in the biodiesel makes it more corrosive than petrol-diesel, and this is an undesired feature. Corrosion induced by contact with biodiesel both reduces the life of metal parts and deteriorates the fuel properties, hence adversely affects engine performance. Therefore, the corrosive characteristics of biodiesel are very important for long term durability of engine components. In this study, we tried to investigate the corrosive effects of biodiesel and blends on engine parts by evaluating and comparing test results from earlier studies for different periods at different temperatures with different biodiesel fuels. Remedial measures to inhibit or mitigate corrosive effects of biodiesel by using additives are also tackled.

This study assesses the potential of antibiotics-producing Pseudomonas chlororaphis strains to increase potato yield and to inhibit the mycelial growth of phytopathogenic fungi Fusarium oxysporum (Fo) isolated from potato. P. chlororaphis subsp. aurantiaca strain Q16 (PchlQ16) caused the highest growth inhibition (67.07%) of FoA2 isolate in vitro. In field trials the effect of PchlQ16 was measured as the number of stems, number and weight of tubers and a total potato yield of the Rudolph potato variety. Application of P. chlororaphis and the number of treatments exhibited a significant effect on the yield. Two treatments of PchlQ16 increased the total yield of tubers from 4.9% to 33.05%, while four treatments from 9.3% to 92.35%, compared to the control. Based on our field results we can recommend a frequent application of PchlQ16 (4 times) during potato growth season. The results of our in vitro experiment support these findings as the bacterial strain suppressed growth of F. oxysporum. In this investigation PchlQ16 was confirmed as an effective growth promoting agent in potato production and can be highly effective in prevention of F. oxysporum infection.

To study the inhibitory effects of Chaetomium globosum strain FS-01 against Alternaria panax, Sclerotinia schinseng, Botrytis cinerea, Rhizoctonia solani and Fusarium solani of ginseng pathogens, mycelia, fermentation broth and conidia suspension were tested in laboratory. The results showed that Chaetomium globosum FS-01 had certain inhibitory effects against five kinds of ginseng pathogens by confront culture. Among them, the highest inhibition rate to mycelia growth of Alternaria panax, reached 30.80%, followed by Rhizoctonia solani, Sclerotinia schinseng, Fusarium solani and Botrytis cinerea; On the PDA plate mixed with Chaetomium globosum FS-01 fermentation broth, the highest inhibition rate to mycelia growth of Botrytis cinerea, reached 82.09%, followed by Sclerotinia schinseng, Alternaria panax, Rhizoctonia solani and Fusarium solani; On the PDA plate mixed with Chaetomium globosum FS-01 conidia suspension, the highest inhibition rate to mycelia growth of Alternaria panax, reached 83.72%, followed by Botrytis cinerea, Rhizoctonia solani, Sclerotinia schinseng and Fusarium solani. Endophytic fungi FS-01 strain had a significant inhibitory effects, it could be utilized as a biological control resource inhibiting ginseng pathogens. [ABSTRACT FROM AUTHOR]

Copyright of Food Research & Development is the property of Food Research & Development Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Protein glycosylation is an effective way to enhance the properties of proteins in food systems. However, the negative effects of glycosylation, such as generation of advanced glycation end products (AGEs), have received less attention; these effects are closely related to the occurrence of various chronic metabolic diseases. In this study, a perilla seed meal protein (PSMP)-fructose/dextran (DEX)-caffeic acid (CA) ternary emulsifying system was constructed. Then, AGEs formation and emulsifying properties were characterized, and the optimal emulsifying system for β-carotene (BC) delivery was investigated. The resulting complex was examined using a high-performance liquid chromatography (HPLC)-ultraviolet (UV) detector, ultra-HPLC-tandem mass spectrometry (UHPLC-MS/MS) system, and nanoparticle size analyzer. The results indicated that CA conjugated with glycosylated PSMP significantly reduced the formation of fructosamine (13.5%), methylglyoxal (33.26%), N ε -carboxymethyl lysine, and N ε -carboxyethyl lysine (>80%). Compared with other conjugates, the PSMP-DEX-CA ternary conjugate showed the lowest AGEs content, smaller particle size, better emulsifying active index, lower polydispersity index, and acceptable ζ-potential. The emulsifying system constructed using abovementioned ternary conjugate revealed better UV and thermal stability in BC delivery, which slowed BC degradation. This study provides a novel approach for constructing a low AGEs emulsion system to deliver BC via PSMP with different modifications. [Display omitted] • PSMP-dextran-caffeic acid (CA) ternary conjugate was firstly constructed. • More than 80% of CML and CEL were inhibited by caffeic acid in ternary conjugate. • Smaller particle size and lower PDI were observed in the ternary conjugate emulsion. • Ternary conjugate emulsion holds high UV and thermal stability for BC delivery. [ABSTRACT FROM AUTHOR]

Mangroves are considered one of the most productive ecosystems worldwide, providing multiple environmental goods and services; however, in recent years, there have been modifications and deterioration in the structure and function of these ecosystems, caused by various natural events and anthropic activities, such as the construction of roads, wastewater discharge, unsustainable livestock, and agricultural practices, as well as the impact of chemicals, such as heavy metals, oil spills, and the use of herbicides. In this research, phytotoxic effects on seedlings of Rhizophora mangle were evaluated at an exposure of five dilutions w/v (5%, 10%, 25%, 50%, and 100%) of the commercial presentation of 2,4-dichlorophenoxyacetic acid (2,4-D). Propagules grown in a greenhouse under local tidal regimes were used, so the growth of stem diameter, height, biomass production in root, leaves, and stems, as well as the concentration of chlorophyll a of the exposed seedlings were measured. The comparison of these parameters in seedlings with only seawater presented significant differences (p ≤ 0.05) and inhibitory effects on growth (diameter), the stem concentration of chlorophyll a, and the production of biomass of leaves, stems, and roots. The inhibitory effect of exposure to 2,4-D on chlorophyll production and root biomass is highlighted, with an average decrease of 45% relative to the control. The sensitivity of the Rhizophora mangle seedlings to the applied concentrations of herbicide evidence the inhibitory effects on the morphological variables of biomass production and chlorophyll a production in mangrove leaves.

Post-harvest diseases of mango reduce fruit quality and cause severe yield losses with completely unmarketable fruits. The most common diseases of mangos are anthracnose (Colletotrichum gloeosporioides). In this study, the antibacterial activities of essential oils from Artemisia scoparia, Artemisia lavandulaefolia, and Artemisia annua against C. gloeosporioides were tested. The results showed that the essential oil of A. scoparia was more effective by the agar diffusion method; the EC50 value was 9.32 µL/mL. The inhibition rate was 100%, at a concentration of 10 μL/mL, through the spore germination method. The morphological changes of the mycelium were observed by scanning electron microscopy (SEM), the mycelia treated with essential oils showed shrinking, deformity, fracture, and dryness through SEM. A. scoparia essential oil was inoculated in vivo and subjected to paroxysm testing under natural conditions. A. scoparia had significantly inhibitory activity, and the inhibition rate was 66.23% in vivo inoculation tests after 10 days. The inhibition rate was 92.06% in the paroxysm test under natural conditions after 15 days. Finally, A. acoparia essential oil was analyzed by gas chromatography-mass spectrometry. The main compounds were 2-ethenyl-Naphthalene (23.5%), 2,4-pentadiynyl-Benzene (11.8%), 1,2-dimethoxy-4-(2-propenyl)-Benzene (10.0%), β-Pinene (8.0%), and 1-methyl-4-(1-methylethyl)-1,4-Cyclohexadiene (6.3%). The results have revealed the potential use of A. scoparia essential oil against post-harvest fungal pathogens C. gloeosporioides.

UDP-glucuronosyltransferase 1A1 (UGT1A1) plays a key role in detoxification of many potentially harmful compounds and drugs. UGT1A1 inhibition may bring risks of drug–drug interactions (DDIs), hyperbilirubinemia and drug-induced liver injury. This study aimed to investigate and compare the inhibitory effects of icotinib and erlotinib against UGT1A1, as well as to evaluate their potential DDI risks via UGT1A1 inhibition. The results demonstrated that both icotinib and erlotinib are UGT1A1 inhibitors, but the inhibitory effect of icotinib on UGT1A1 is weaker than that of erlotinib. The IC50 values of icotinib and erlotinib against UGT1A1-mediated NCHN-O-glucuronidation in human liver microsomes (HLMs) were 5.15 and 0.68 μmol/L, respectively. Inhibition kinetic analyses demonstrated that both icotinib and erlotinib were non-competitive inhibitors against UGT1A1-mediated glucuronidation of NCHN in HLMs, with the Ki values of 8.55 and 1.23 μmol/L, respectively. Furthermore, their potential DDI risks via UGT1A1 inhibition were quantitatively predicted by the ratio of the areas under the concentration–time curve (AUC) of NCHN. These findings are helpful for the medicinal chemists to design and develop next generation tyrosine kinase inhibitors with improved safety, as well as to guide reasonable applications of icotinib and erlotinib in clinic, especially for avoiding their potential DDI risks via UGT1A1 inhibition.

LAMP has received great interest and is widely utilized in life sciences for nucleic acid analysis. To monitor a real-time LAMP assay, a fluorescence DNA dye is an indispensable component and therefore the selection of a suitable dye for real-time LAMP is a need. To aid this selection, we investigated the inhibition effects of twenty-three DNA dyes on real-time LAMP. Threshold time (Tt) values of each real-time LAMP were determined and used as an indicator of the inhibition effect. Based on the inhibition effects, the dyes were classified into four groups: (1) non-inhibition effect, (2) medium inhibition effect, (3) high inhibition effect, and (4) very high inhibition effect. The signal to noise ratio (SNR) and the limit of detection (LOD) of the dyes in groups 1, 2, and 3 were further investigated, and possible inhibition mechanisms of the DNA dyes on the real-time LAMP are suggested and discussed. Furthermore, a comparison of SYTO 9 in different LAMP reactions and different systems is presented. Of the 23 dyes tested, SYTO 9, SYTO 82, SYTO 16, SYTO 13, and Miami Yellow were the best dyes with no inhibitory effect, low LOD and high SNR in the real-time LAMP reactions. The present classification of the dyes will simplify the selection of fluorescence dye for real-time LAMP assays in point of care setting.

Old textiles are important elements of thecultural heritage. As a result of their composition mostly of natural elements old textiles are extremely prone to physical and chemical degradation due to fungal action. The treatments usually applied for the cleaning of heritage textiles target the use of synthetic fungicides, which are potentially harmful to both human health and the environment. Numerous studies highlight as an alternative to the use of conventional antifungals, the employment of essential oils and plant extracts, which are environmentally friendly and which have no adverse effects on human health. Against this background the present study aims to test six essential oils (Lavandula angustifolia, Citrus limon, Mentha piperita, Marjoram, Melaleuca alternifolia, Origanum vulgare) to establish their inhibitory effects against fungi identified on an old piece of traditional Romanian clothing from Maramureş. For the study, the types of fungi present on the objects was determined primarily through the open plates technique and microscopic identification. After identification, the essential oils were applied to the delimited surfaces, and their effects observed up to 32 days after application. The results show that these essential oils have a strong inhibitory effect on such fungal genera as Penicillinum sp., Cladosporium sp., Aspergillus spp., Candida guillermondii, Botrys sp., Mucor sp., having no observable side-effects on the physical properties of the materials concerned. The antimicrobial effects that essential oils and plant extracts have in the short term must be tested in future to ensure the enhanced preservation of heritage textiles and the health integrity of the restorers and visitors who view them in museums, collections or exhibitions.

LAMP has received great interest and is widely utilized in life sciences for nucleic acid analysis. To monitor a real-time LAMP assay, a fluorescence DNA dye is an indispensable component and therefore the selection of a suitable dye for real-time LAMP is a need. To aid this selection, we investigated the inhibition effects of twenty-three DNA dyes on real-time LAMP. Threshold time (Tt) values of each real-time LAMP were determined and used as an indicator of the inhibition effect. Based on the inhibition effects, the dyes were classified into four groups: (1) non-inhibition effect, (2) medium inhibition effect, (3) high inhibition effect, and (4) very high inhibition effect. The signal to noise ratio (SNR) and the limit of detection (LOD) of the dyes in groups 1, 2, and 3 were further investigated, and possible inhibition mechanisms of the DNA dyes on the real-time LAMP are suggested and discussed. Furthermore, a comparison of SYTO 9 in different LAMP reactions and different systems is presented. Of the 23 dyes tested, SYTO 9, SYTO 82, SYTO 16, SYTO 13, and Miami Yellow were the best dyes with no inhibitory effect, low LOD and high SNR in the real-time LAMP reactions. The present classification of the dyes will simplify the selection of fluorescence dye for real-time LAMP assays in point of care setting. [ABSTRACT FROM AUTHOR]

Endometrial cancer is the most common malignant tumors of gynecologic neoplasms in Western society. In recent years, the incidence of endometrial cancer has increased, and it has become the third most common female gynecological cancer (after ovarian and cervical cancer) in Taiwan. Adlay (Coix lachryma-jobi L. var. Ma-yuen Stapf.) has been demonstrated to have bioactive polyphenols, flavonoids, phytosterols, and essential nutrients for health benefits, including anticancer effects in humans. However, little is known about the effect of adlay seeds on endometrial cancer. Our study aimed to investigate the potential growth inhibitory effects of several adlay seed fractions, including ethyl acetate (ATE-EA) and its bioactive constituents, separately on endometrial cancer cells—HEC-1A (phosphatase and tensin homolog-positive) and RL95-2 (phosphatase and tensin homolog-negative)—and identify related active ingredients. In addition, the potential active fractions and the phytochemical compounds were elucidated. The results demonstrate superior activity of ATE-EA with significant in vitro cell proliferation inhibitory capacity, particularly its C.D.E.F-subfraction. Moreover, HPLC- and GC/FID-based quantification of ATE-EA subfractions showed that phenolic compounds (caffeic acid, protocatechuic acid, and p-hydroxybenzaldehyde), flavonoids, steroids, and fatty acid compounds exert anti-proliferative effects in the cell model. Finally, it was shown that cell growth and cell cycle arrest most significantly occurred in the in G1 or G2/M phase under ATE-EA treatment. Collectively, our results demonstrate an antiproliferative effect of ATE-EA on endometrial cancer cells that suggest a positive health outcome for women from consumption of these compounds.

The present work deals with the study of chemical synthesis of Schiff base ligand, (L) derived from 5-amino-4H-1,2,4-triazole-3-thiol and 3-hydroxy-4-methoxy benzaldehyde and its Cu(II), Co(II), Mn(II), Zn(II) and Ni(II) complexes in 2:1 stoichiometric ratio (2L:M). The structures of all the synthesized compounds were analyzed using FTIR, UV–Visible, MS, 1H NMR, 13C NMR and thermo gravimetric methods. Further, the ligand (L) and its metal complexes were screened for in vitro antibacterial activity against nine food pathogens and their potential activity were qualitatively and quantitatively assessed by the presence/absence for zone of inhibition and minimum inhibitory concentration (MIC) values. The standard antibiotic drug amoxicillin was used as positive control. Impregnated paper discs containing only DMSO used as negative control did not show zone of inhibition. The free radical scavenging ability of test samples were assessed by employing a series of in vitro assays viz., DPPH, ABTS and Superoxide, where Butylated hydroxyl anisole (BHA) was used as a positive control. We have also tested in vitro Inhibitory effects on yeast α-glucosidase and α-amylase using acarbose as a positive control.

Objective: To investigate the antibacterial activities of green vegetables (pennywort, mint, garlic, parsley and celery) against four common enteric bacteria [Salmonella enterica (ATCC 25957) (S. enterica), Shigella flexneri (ATCC 12022) (S. flexneri), Escherichia coli (ATCC 43889) (E. coli) and Enterobacter cloacae (ATCC 13047) (E. cloacae)] as an alternative medicine for controlling food borne diarrhea disease and the synergistic effect of green vegetables against those bacteria. Methods: Five common vegetables (pennywort, mint, garlic, parsley and celery) were purchased and extracted. The antimicrobial activities of these extracts were tested against four common enteric bacteria (S. enterica, S. flexneri, E. coli and E. cloacae). Ten different concentrations of the extracts (from 640 to 1.25 mg/mL) were prepared and used for the study. The minimal inhibitory concentration (MIC) was determined by the broth dilution method. The antimicrobial activities were assessed by using both well diffusion and disc diffusion methods. Results: Garlic extract showed excellent inhibitory effects on all enteric bacteria. Other plants (parsley, celery, mint and pennywort) were not effective against enteric bacteria. The MIC of garlic against S. flexneri and E. cloacae was 40 mg/mL. The MIC of S. enterica and E. coli were 20 and 10 mg/mL, respectively. The performance of the well diffusion method was better than that of the disc diffusion method with clear and sharp inhibition zones of tested bacteria against plant extracts. Conclusions: Garlic had excellent antimicrobial effects against enteric bacteria and was recommended to be given to patients with gastroenteritis. The other vegetables (pennywort, mint, parsley and celery) showed no inhibitory effects on enteric bacteria but still can be used for its richness in vitamins and fibers. The performance of the well diffusion method was better than that of the disc diffusion method in detecting the antibacterial effects of green vegetables.

Rapid depletion of fossil fuel resources as well as concerns for foreign dependence in meeting energy needs have led researches for alternative fuels. Biodiesel, which can be obtained from many renewable resources such as vegetable oil and animal fat through transesterification, is the most attractive alternative fuel for cars, especially for being environmentally friendly. However, there are some cons, too. The presence of water and free fatty acids in the biodiesel makes it more corrosive than petrol-diesel, and this is an undesired feature. Corrosion induced by contact with biodiesel both reduces the life of metal parts and deteriorates the fuel properties, hence adversely affects engine performance. Therefore, the corrosive characteristics of biodiesel are very important for long term durability of engine components. In this study, we tried to investigate the corrosive effects of biodiesel and blends on engine parts by evaluating and comparing test results from earlier studies for different periods at different temperatures with different biodiesel fuels. Remedial measures to inhibit or mitigate corrosive effects of biodiesel by using additives are also tackled. [ABSTRACT FROM AUTHOR]