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Antimicrobial potential of Citrus medica var. sarcodactylis (Siebold ex Hoola van Nooten) Swingle and Limonia acidissima L. fruits and leaves extracts CMF, CML, LAF and LAL, respectively were evaluated. Gas chromatography–mass spectrometry (GC-MS) analysis for lipoidal matters revealed a high percentage of non-oxygenated compounds. Phytol was the major in LAL. Palmitic and linoleic acid were the major in CML and LAL, respectively. Rutin and P-hydroxy benzoic acid were the main compounds identified by High-performance liquid chromatography (HPLC) analysis. The antibacterial and antifungal activities of the plants extract were determined by the well diffusion method. Antimicrobial investigation for different successive fractions of active methanol extracts of CML, LAL, LAF and CMF showed the highest activity (CML), whereas the petroleum ether (CML PE) and MeOH (CML) fractions exhibit a significant antifungal activity against Candida albicans minimum inhibitory concentration (MIC) 12 and 15 µg/mL, respectively. The antifungal activity prevailed by C. medica leaves may be attributed to its polyphenolics (rutin, chlorogenic and rosmarinic acid) in addition to phenylated hydrocarbon. [ABSTRACT FROM AUTHOR]

Leonotis nepetifolia (L.) R. Br. (Lamiaceae) is a naturalised medicinal plant in Brazil known as 'cordão-de-frade', being used in folk medicine for the treatment of a variety of conditions such as infections and inflammations. L. nepetifolia leaf and flower essential oils were isolated by hydrodistillation, and their compounds were identified by GC-MS analysis. The leaf essential oil major constituents were germacrene D (31.5%), and β-caryophyllene (19.2%), while in flower essential oil the main constituents were β-elemene (31.2%), and germacrene D (12.1%). The essential oils were investigated against a broad spectrum of bacteria and fungi using the microdilution method, exhibiting MIC50 values of 3.93–250 µg mL−1. Both oils showed excellent antifungal properties, which is a very important finding since most fungi have shown increased resistance to known antifungal agents. According to these results, the essential oils of L. nepetifolia are promising sources of new antimicrobial agents, especially for yeast. [ABSTRACT FROM AUTHOR]

Ticks are responsible for transmitting of pathogenic microorganisms during their feeding process on the hosts. They also cause significant losses in livestock production and, in many cases, the death of infected animals. In recent decades, many efforts have been carried out to combat ticks by using natural compounds. The present study aimed to evaluate the acaricidal effect of the hydroalcoholic extract of honey bee propolis against Haemaphysalis spp. in vitro. The acaricidal activities of the propolis were considered at concentrations of 25, 50, and 100 mg/ml and negative and positive controls (distilled water and Cypermethrin) following 10, 30, and 60 minutes of exposure. In this experiment the spraying and contact methods were used, and all tests were repeated twice. The chemical composition of propolis was identification by Gas Chromatography-Mass Spectrometry (GC–MS). Data were analyzed using GraphPad Prism software version 5.0. According to the results, propolis had an acaricidal effect; however, this effect was more potent in the spraying. The propolis showed a 100% mortality rate at 100 mg/ml concentrations after 60 min exposure. GC-MS investigation showed that Heptanone (48.65%) was the main ingredient of propolis. The results indicated that the hydroalcoholic propolis extract carry potent acaricidal ingredients and might afford new natural acaricidal compounds for the control of Haemaphysalis spp. [ABSTRACT FROM AUTHOR]

The quality of oysters is reflected by volatile organic components. To rapidly assess the freshness level of oysters and elucidate the changes in flavor substances during storage, the volatile compounds of oysters stored at 4, 12, 20, and 28 °C over varying durations were analyzed using GC-MS and an electronic nose. Data from both GC-MS and electronic nose analyses revealed that alcohols, acids, and aldehydes are the primary contributors to the rancidity of oysters. Notably, the relative and absolute contents of Cis-2-(2-Pentenyl) furan and other heterocyclic compounds exhibited an upward trend. This observation suggests the potential for developing a simpler test for oyster freshness based on these compounds. Linear Discriminant Analysis (LDA) demonstrated superior performance compared to Principal Component Analysis (PCA) in differentiating oyster samples at various storage times. At 4 °C, the classification accuracy of the optimal support vector machine (SVM) and random forest (RF) models exceeded 90%. At 12 °C, 20 °C, and 28 °C, the classification accuracy of the best SVM and RF models surpassed 95%. Pearson correlation analysis of the concentrations of various volatile compounds and characteristic markers with the sensor response values indicated that the selected sensors were more aligned with the volatiles emitted by oysters. Consequently, the volatile compounds in oysters during storage can be predicted based on the response information from the sensors in the detection system. This study also demonstrates that the detection system serves as a viable alternative to GC-MS for evaluating oysters of varying freshness grades. [ABSTRACT FROM AUTHOR]

In this study antimicrobial linen-cotton jacquard textiles were manufactured using green chemistry methods. The functionalization of the fabrics was executed by impregnating chitosan microencapsulated bio-based oils from angelica (Angelica archangelica L.) (AAC) and marsh Labrador tea (Rhododendron tomentosum Harmaja) (MLTC) obtained with pilot scale supercritical carbon dioxide extraction. The chemical compositions of the extracts of angelica and marsh Labrador tea were analyzed by a combination of gas chromatography and mass spectrometry. The antimicrobial activities of the extracts, AAC and MLTC microcapsules, and the microencapsulated textiles (AAC and MLTC textiles) were analyzed against gram-positive Staphylococcus aureus and gram-negative Escherichia coli bacteria, dimorphic yeast Candida albicans and filamentous mold Aspergillus brasiliensis. The AAC textile proved 40% inhibition against S. aureus, whereas the MLTC textile demonstrated 43.8% and 51.7% inhibition against both S. aureus and E. coli, respectively. Although the chitosan shell material itself indicated mild activity against both bacterial strains, the extracts increased the antibacterial activities in microencapsulated textiles. In addition, the antifungal impact of the MLTC textile was demonstrated against A. brasiliensis. According to the Fourier transform infrared spectroscopy with attenuated total reflection and field emission scanning electron microscopy analyses, covalent bonding between the microcapsules and textile fibers was established with citric acid as a cross-linker. The antimicrobial activity was also shown to persist in the MLTC textiles after six domestic washing cycles. [ABSTRACT FROM AUTHOR]

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Multiple sclerosis (MS) is a neurodegenerative and inflammatory disease of the central nervous system (CNS) that leads to a loss of myelin. There are three main types of MS: relapsing-remitting MS (RRMS) and primary and secondary progressive disease (PPMS, SPMS). The differentiation in the pathogenesis of these two latter courses is still unclear. The underlying mechanisms of MS are yet to be elucidated, and the treatment relies on immune-modifying agents. Recently, lipidomics and metabolomics studies using human biofluids, mainly plasma and cerebrospinal fluid (CSF), have suggested an important role of lipids and metabolites in the pathophysiology of MS. In this review, the results from studies on metabolomics and lipidomics analyses performed on biological samples of MS patients and MS-like animal models are presented and analyzed. Based on the collected findings, the biochemical pathways in human and animal cohorts involved were investigated and biological mechanisms and the potential role they have in MS are discussed. Limitations and challenges of metabolomics and lipidomics approaches are presented while concluding that metabolomics and lipidomics may provide a more holistic approach and provide biomarkers for early diagnosis of MS disease. [ABSTRACT FROM AUTHOR]

Background: Clear cell renal cell carcinoma (ccRCC) comprises the majority, approximately 70–80%, of renal cancer cases and often remains asymptomatic until incidentally detected during unrelated abdominal imaging or at advanced stages. Currently, standardized screening tests for renal cancer are lacking, which presents challenges in disease management and improving patient outcomes. This study aimed to identify ccRCC-specific volatile organic compounds (VOCs) in the urine of ccRCC-positive patients and develop a urinary VOC-based diagnostic model. Methods: This study involved 233 pretreatment ccRCC patients and 43 healthy individuals. VOC analysis utilized stir-bar sorptive extraction coupled with thermal desorption gas chromatography/mass spectrometry (SBSE-TD-GC/MS). A ccRCC diagnostic model was established via logistic regression, trained on 163 ccRCC cases versus 31 controls, and validated with 70 ccRCC cases versus 12 controls, resulting in a ccRCC diagnostic model involving 24 VOC markers. Results: The findings demonstrated promising diagnostic efficacy, with an Area Under the Curve (AUC) of 0.94, 86% sensitivity, and 92% specificity. Conclusions: This study highlights the feasibility of using urine as a reliable biospecimen for identifying VOC biomarkers in ccRCC. While further validation in larger cohorts is necessary, this study's capability to differentiate between ccRCC and control groups, despite sample size limitations, holds significant promise. [ABSTRACT FROM AUTHOR]

Matrix solid-phase dispersion using a humate-based magnetic sorbent is proposed as an efficient method for the concentration of bisphenol A from fish muscular and hepatic tissue samples followed by the chromatography-mass spectrometry determination of an analyte prederivatized with acetic anhydride. Under the optimum concentration conditions (the stirring time is 10 min and the sorbent weight is 0.05 g), the recovery of bisphenol A upon single sorption reaches 85%. The percentage desorption exceeds 99% (the eluate is methanol, the time is 3 min, and the volume is 1 mL). The maximum enrichment factor is 718. The limit of the detection of bisphenol A is 0.15 μg/kg (on a dry basis) for muscular tissue and 0.25 μg/kg for liver. [ABSTRACT FROM AUTHOR]

An innovative SPME head space GC–MS method, in cooling mode, using a fully automated routine, was developed to detect 2-phenyl-2-propanol, a representative urinary metabolite of cumene. Following an acid hydrolysis and derivatization step with lowered quantities of reagents, acetic anhydride and pyridine, a 30 μm polydimethylsiloxane SPME fiber was used to sample derivatized 2-phenyl-2-propanol, such as benzenemethanol,α,α-dimethyl-acetate, from the headspace. Performances of the method, optimized through experimental design, provide an LOD of 0.034 mg/L and an LOQ 0.10 mg/L, with a short sampling time necessary per sample. The method, developed on standard solutions, will be applied to both occupationally exposed and non-exposed populations. [ABSTRACT FROM AUTHOR]

Medicinal fungi Phellinus igniarius exhibited hypoglycemic effects; however, the protective mechanisms of P. igniarius on type 2 diabetes are not yet fully understood. Herein, the anti‐diabetic effect of P. igniarius was investigated via gas chromatography–mass spectrometry (GC/MS)‐based metabolome analysis. The rats were divided into normal group; model group; positive group; and groups treated with low, medium, and high dose of P. igniarius. After the treatments, a significant decrease in blood glucose concentration was observed. The levels of total cholesterol and triglyceride were dramatically decreased, whereas the level of insulin was increased. Multivariate statistical analysis revealed 31 differential endogenous metabolites between model group and normal group. A total of 14, 28, and 31 biomarkers were identified for low, medium, and high dose of P. igniarius treated groups, respectively. Twenty‐one of the biomarkers were validated by using standard substances. The linear correlation coefficients ranged from 0.9990 to 1.0000. The methodology exhibited good repeatability, recoveries, and stability. The major intervened metabolic pathways covered glyoxylate and dicarboxylic acid metabolism; alanine, aspartate, and glutamate metabolism; and glycine, serine, and threonine metabolism. Our metabolome analysis has provided insights into the underlying mechanism of P. igniarius on type 2 diabetes. [ABSTRACT FROM AUTHOR]

Simple Summary: Natural products offer significant potential in the fight against parasitic diseases. Coccidiosis is a disease caused by the Eimeria genus of parasites that infect many animals all over the world. The development of resistance to anticoccidial medications has refocused attention on finding new compounds for alternative therapeutic approaches. The purpose of this study was to determine the efficacy of Holothuria polii extract (HpE) in treating eimeriosis in mice. The results indicated that animals treated with 200 mg/kg of HpE showed a significant decrease in oocyst count and higher expression of the MUC2 gene. In conclusion, HpE functions as an anticoccidial substance. Eimeria is a parasite that causes coccidiosis in a variety of animals, leading to nutritional imbalances, issues with food digestion and absorption, low weight, and intestinal inflammation of varying degrees in its hosts. Anticoccidial medication resistance has become a significant obstacle to disease control efforts, leading to a renewed focus on discovering novel chemicals for alternative therapeutic approaches. The purpose of this study was to determine the efficacy of Holothuria polii extract (HpE) in treating eimeriosis in mice. Five groups of mice were studied, with E. papillata sporulated oocysts (1 × 103) used to infect three groups experimentally. The first group was treated with 200 mg/kg of HpE, the second group with Amprolium (120 mg/kg), and the third group was left untreated as a control. The fourth and fifth groups were uninfected, with one of them treated with 200 mg/kg of HpE and the other used as a negative control. The results revealed that HpE has 10 phytochemical compounds according to GC-MS analysis. Treatment with HpE resulted in a substantial decrease in oocyst output in feces. Also, the parasitic stages showed morphometric alterations, with reductions in the measurements compared with the infected, untreated mice. Moreover, expression of the mucin gene (MUC2) was higher in treated mice compared to infected ones, with significant increases in goblet cell numbers, which provided additional evidence for the activity of HpE as an anticoccidial product. In conclusion, there are a wide variety of natural products and many have been employed in folk medicine for treating a range of parasitic diseases. [ABSTRACT FROM AUTHOR]

Indian people have belief in medicinal plants for their various ailments from fever to cancer without knowing the chemical nature. This research work will pave a new way to understand important active chemical components in medicinal plants have been used in long term for human diseases. Recent high mortality rate in India by non-communicable diseases were identified and chosen one of the important diseases (cardiovascular diseases). The second step to identify widely used medicinal plant and may be practiced by medical practioners for chosen human disease. The medicinal plant was collected and identified with the help of botanists and then shade-dried plant species used to prepare the extracts for identifying secondary metabolites and anti-oxidant (biomolecules have medicinal property) with different polar solvents. The extracts were used to identify the secondary metabolites and anti-oxidant with the help of GC-MS, FTIR and UV-Visible Spectrophotometer with standard biomolecule estimation procedure. The valuable medicinally active chemical components of selected plant species were identified and concluded the value with the help of standard biochemical experiments through qualitative and quantitatively especially antioxidant by DPPH Assay. The identified compounds were: terpenoids, steroids, alkaloids, flavonoids and polyphenols. [ABSTRACT FROM AUTHOR]

The morphological characters of Southeast Asia's indigenous Peperomia species are very similar, especially in their flower structures. The flowers are simple, hermaphrodite and lack a perianth. Therefore, many species are hard to distinguish using morphological characters alone. Here, we apply chemometric data for species identification and classification, gathered using multiwavelength detection combined with the colour scale High-Performance Thin-Layer Chromatography (HPTLC) fingerprinting procedure and chemical compounds determined by Gas Chromatography–Mass Spectrometry (GC-MS). Fourteen taxa were investigated using hexane, ethyl acetate and ethanol solvent extractions. Principal component analysis (PCA) and hierarchical cluster analysis (HCA) were used with the colour scale fingerprints to classify the Peperomia species. The PCA and HCA using the chromatogram profile from hexane divided the taxa into six groups compared to the profile from ethyl acetate and ethanol, which each detected seven groups. The chromatogram from the combined dataset of all three solvents can differentiate all the species. The GC-MS data detected a total of 40 compounds from the hexane extract, and these differed among Peperomia species. This approach based on HPTLC fingerprinting and GC-MS analysis can therefore be used as a tool for authentication and identification studies of Peperomia species. [ABSTRACT FROM AUTHOR]

Main conclusion: New findings are presented for Chaerophyllum coloratum L. on the volatile composition of the essential oil, based on data of hydrosol and fresh plant material, light and electron microscopy of leaves, and cytotoxic and antiviral activity. The widespread Apiaceae family includes many well-known and economically important plants that are cultivated as food or spices. Many produce essential oils and are generally a source of secondary metabolites and compounds that have numerous applications in daily life. In this study, the chemical composition of volatile organic compounds (VOCs), ultrastructure and biological activity of the Mediterranean endemic species Cheaerophyllum coloratum L. are investigated, as literature data for this plant species are generally very scarce. The essential oil and hydrosol were extracted from the air-dried leaves by hydrodistillation and the chemical composition of both extracts was analysed by GC–MS in conjunction with headspace solid-phase microextraction (HS-SPME) of VOCs from the hydrosol and the fresh plant material. In the composition of the essential oil, the oxygenated sesquiterpenes spathulenol and caryophyllene oxide were the most abundant components. In the fresh plant material, non-oxygenated sesquiterpenes dominated, with β-caryophyllene and germacrene D being the main components. The hydrosol was dominated by monoterpenes, with the oxygenated monoterpene p-cymen-8-ol being the most abundant. Light and electron micrographs of the leaf of C. coloratum show secretory structures, and we hypothesize that glandular leaf trichomes, secretory epidermal cells and secretory canals are involved in the production of volatiles and their secretion on the leaf surface. Since the biological potential of C. coloratum is poorly investigated, we tested its cytotoxic activity on cancer and healthy cell lines and its antiviral activity on plants infected with tobacco mosiac virus (TMV). Our results dealing with the composition, ultrastructure and biological activity show that C. coloratum represent a hidden valuable plant species with a potential for future research. [ABSTRACT FROM AUTHOR]

The present study investigated the phytochemical constituents and antimicrobial effects of aqueous methanolic extract of Haloxylon salicornicum against some phytopathogenic bacterial and fungal strains. The selected bacterial strains were Pectobacterium carotovorum, Pectobacterium atrosepticum, Ralstonia solanacearum, and Streptomyces scabiei, while fungal strains were Fusarium oxysporum, Botrytis cinerea, and Rhizoctonia solani. The extract demonstrated significant efficacy against P. atrosepticum and P. carotovorum at a concentration of 1,000 µg/mL, resulting in inhibition zones measuring 12.3 and 11 mm, respectively. Furthermore, the extract demonstrated considerable effectiveness against fungal strains, achieving an impressive fungal growth suppression rate of 68.8% against R. solani at a concentration of 5,000 µg/mL. The high-performance liquid chromatography analysis identified nine notable phenolic compounds and six common flavonoid compounds in the extract. The identified phenolic compounds in the highest quantities were gallic acid (6427.5 µg/g), vanillin (1145.4 µg/g), chlorogenic acid (498.1 µg/g), and syringic acid (322.5 µg/g). Apigenin (1155.9 µg/g), daidzein (460.9 µg/g), quercetin (382.7 µg/g), and naringenin (160.4 µg/g) exhibited the most significant concentrations of flavonoid compounds. Gas chromatography–mass spectrometry analysis revealed that n-hexadecanoic acid (53.7%), 9-octadecenoic acid (26.9%), 9,12-octadecadienoic acid (Z,Z) (8.67%), palmitic acid, and TMS derivative (4.36%) were the predominant compounds in the extract. Consequently, the H. salicornicum aqueous methanolic extract could be used for the first time as an environmentally safe antimicrobial pesticide agent against plant pathogens to reduce the excessive use of chemical pesticides.

The goal of the present investigation was to demonstrate the antibacterial activity of different solvent extracts (methanol, ethanol, cold aqueous and hot aqueous) of Crassocephalum crepidioides against ATCC bacterial cultures of Staphylococcus aureus, Escherichia coli, Methicillin resistant Staphylococcus aureus, Pseudomonas aeruginosa and its antioxidant potential. Furthermore, the chemical constituents present in the extract was perused by Gas chromatography-mass spectroscopy (GC-MS), along with in vitro cytotoxicity assessment. All the extracts were shown to be sensitive against S. aureus, MRSA and P. aeruginosa except for the ethanolic extract which was resistant to P. aeruginosa. Of all the extracts, hot aqueous extract found to be the most effective. It was found that Minimum inhibitory concentration (MIC) value of hot aqueous extract against S. aureus, MRSA and P. aeruginosa were 5 mg/mL, 5 mg/mL and 40 mg/mL, respectively. DPPH results showed that C. crepidioides leaf extract has potent antioxidant activity with IC50 value of 57.9 µg/mL. 22 compounds were detected in hot aqueous extract through Gas chromatography-mass spectroscopy. The results of the cytotoxicity evaluation displayed that the IC50 value of the hot aqueous extract of C. crepidioides on Vero cell lines was 292 µg/mL. This study concludes that C. crepidioides leaf extract is non-toxic, has various bioactive components and strong antibacterial and antioxidant activities, thus making it a promising therapeutic agent for various biomedical applications.

Abstract Cannabis flower scent is one of the key characteristics of the cannabis plant. The diverse scents impact user experiences and offer medicinal benefits. These scents originate from volatile compounds, particularly terpenes and terpenoids. This study characterized the volatile profile of 19 different dried cannabis flowers using gas chromatography-mass spectrometry coupled with headspace-solid phase microextraction (HS-SPME-GC-MS). A total of 75 compounds were identified, including alcohols, aldehydes, benzenes, esters, ketone, monoterpenes, monoterpenoids, sesquiterpenes, and sesquiterpenoids. Cluster analysis was able to group the 19 cannabis cultivars into five clusters based on volatile chemotypes using chemometric techniques of hierarchical cluster analysis (HCA) and principal component analysis (PCA). Potential discriminant markers of each cultivar were then analyzed using a supervised partial least squares discriminant analysis (PLS-DA) verified through Variable Importance in Projection values (VIP), identifying twenty discriminant markers. In addition, the correlations among 75 volatile compounds were also obtained. The findings of this study provide a valuable database of single cannabis cultivars, useful for identifying individual strains and verifying their quality. Clustering the cultivars by volatile chemotype can be used for the classification of cannabis in the market. The results of this study are expected to be a starting point for further cannabis breeding programs to expand knowledge of this plant. Furthermore, the proposed method is applicable to other aroma plants in the future.

Phytochemical analysis of Artemisia herba-alba Asso (Asteraceae) species has been carried out using fourier-transform infrared spectroscopy (FT-IR) technique and gas chromatography–mass spectrometry (GC-MS) analyses. FT-IR spectra of the aerial parts (buds AB, leaves AL and flowers AF) of A. herba-alba powder revealed the presence of 12 peaks, of which 11 common peaks characteristics of the three A. herba-alba studied aerial parts. Whereas, the peak of 1632 cm-1 [(assigned to Alkenyl C=C stretch-Olefinic (alkene) group)] was observed in AB and AF aerial parts and not in AL. As for GC-MS analysis, data revealed 12 & 10 chemical compounds classes in A. herba-alba buds extracts of which, Bicyclic monoterpenoids (37.026 & 49.022%) was presented as a major compound in methanolic and ethanolic buds extracts, respectively. Whereas, 17 & 14 chemical compounds classes were detected in A. herba-alba leaves extracts, of which, Fatty acid amides (28.687 & 25.687%) was presented as a major compound in methanolic and ethanolic leaves extracts, respectively. While, 16 & 11 chemical compounds classes were detected in A. herba-alba flowers extracts, of which Fatty acid amides (25.623 & 23.295%) was presented as a major compound in methanolic and ethanolic flowers extracts, respectively. These bioactive materials make this species as a good candidates for different pharmaceutical and medicine academic researches and applications.

This study elucidated the optimization conditions, GC-MS analysis conditions, total antioxidant activity, and components closely related to antioxidant activity for supercritical extraction of active ingredients in Huoluo Xiaoling Dan (HLXLD). The yield, octyl acetate content, and total antioxidant activity of HLXLD under different conditions were obtained through orthogonal experiments, and the optimal supercritical extraction conditions were determined to be 45°C, 25 MPa, and 4 h. The supercritical extract was subjected to GC-MS analysis and matched with the WILEY and NIST databases, resulting in the qualitative identification of 37 chemical components with a matching degree above 60. The similarity evaluation system of traditional Chinese medicine fingerprint was used to evaluate all orthogonal experimental samples, with a similarity ranging from 0.522 to 0.989. Thirteen common characteristic peaks were selected, and the quantification of these peaks was performed using peak area normalization method. The combination of the content of common characteristic peaks in different samples and their total antioxidant activity was analyzed using multivariate statistical methods such as principal component analysis and multiple regression equation. It was found that five components, F3, F2, F5, F7 and F12, among the common characteristic peaks were closely related to antioxidant activity.

This study involved the exploration of hydro-distilled essential oil (EsO) from the aerial parts of Cordia dichotoma fruits, stems, seeds and leaves via gas chromatography‒mass spectrometry. Approximately 33 volatile components were detected throughout the study. Almost 27 and 23 compounds (comprising 64.83% and 31.55%, respectively, of the total components) were detected in the fruits and stems, whereas 25 compounds (57.12% of the total components) were detected in the seeds, and 25 compounds (52.48% of the total components) were found in the leaves. The main components of the fruit oil were Nonanal (5.77%), Oleic acid (4.30%), β-Damascenone (4.12%), 3, 4-Dehydro-β-ionone (4.06%), Methyl jasmonate (3.32%), Sabinene (3.31%), Phytol (3.22%) and Vitispirane (3.11%). From stem oil, the major components were Nonanal (6.52%), Nonadecane (3.22%) and 2, 3-Octanedione (2.16%). Whereas, the major components of the seed oils were Nonanal (12.14%), Oleic acid (5.13%), Dihydroactindiolide (3.35%), 2-Methoxy-4-vinylphenol (3.18%), Dodecanoic acid (3.16%) and Methyl jasmonate (3.11%). Similarly, the major components of the leaf oils were 2, 4-di-t-Butylphenol (10.25%), 3-Methylnonane (4.73%), 2-Undecanol (4.64%), 3, 4-Dehydro-β-ionone (3.52%) and Nonanal (3.16%). These EsO were used for antibacterial activity against two bacteria i.e. E. coli (G-ve) and the S. aureus (G+ve) by disc diffusion method to determine the MIC (minimum inhibitory concentration) and MBC (maximum bactericidal concentration). However, among the four parts of C. dichotoma, fruit and seed EsO were highly effective against E. coli (MIC and MBC were 125 μg/mL, 1000 μg/mL respectively) compared to S. aureus (MICs of 250 and 500 μg/mL with an MBC of 1000 μg/mL)

Objective: To evaluate the cardioprotective effect of bioassay-guided isolated fractions of Cleome viscosa methanolic extract in streptozotocin-induced diabetic rats. Methods: Total phenolics, flavonoids, and in vitro antioxidant activities of the methanolic extract of Cleome viscosa were evaluated. The FD-40 fraction from this extract was further evaluated for antihyperglycemic efficacy (insulin and HbA1c), antioxidant activity, and cardioprotective effects (creatine kinase-MB, lactate dehydrogenase, and histopathology) in streptozotocin-induced diabetic rats. In silico studies were also conducted to assess the bioactivity of FD-40. Results: Cleome viscosa methanolic extract exhibited the highest antioxidant activity in DPPH, ABTS, H2O2, and FRAP assays compared to other extracts. Treatment with FD-40 (40 mg/kg b.w.) isolated from this extract normalized blood glucose, insulin, HbA1c, creatine kinase-MB, and lactate dehydrogenase levels in diabetic rats. It also significantly reduced oxidative stress by increasing antioxidant enzymes, decreasing lipid peroxidation as well as restoring the levels of ascorbic acid and glutathione. Histological study demonstrated that FD-40 treatment improved cardiac structure in diabetic rats. Molecular docking analysis revealed that phytocompounds from FD-40 had strong binding affinities with cardiac markers and oxidative enzymes. Hexose (5TMS) demonstrated greater binding affinity with xanthine oxidase and lactate dehydrogenase. Conclusions: FD-40 of Cleome viscosa methanolic extract exhibits significant cardioprotective effects in diabetic rats by regulating cardiac markers and reducing oxidative stress. The underlying mechanisms need to be elucidated in the future.

The oral cavity is home to a large and diversified microbial flora, which plays an important role in the genesis of multiple diseases, including tooth decay. Indeed, tooth decay is the most common ailment in the world, with almost everyone having experienced it at least once in their lifetime. Examining plants used in traditional medicine is one of the research approaches used to discover novel, potent antibacterial chemicals with a broad spectrum of action, as present antibacterials have significant drawbacks. This study aims to examine the chemical composition of Algerian clove Syzygium aromaticum using GC-MS and to evaluate the antibacterial activity of the methanol extract against bacteria isolated from dental caries caused by Streptococcus spp. and Lactobacillus spp. The results show a strong extraction yield of 29.7%, with high amounts of polyphenols and flavonoids calculated at 178.82 mg GAEQ/g and 24.13 mg QEQ/g. The principal chemical elements of S. aromaticum peel methanol extract were identified as eugenol (61.23%) and eugenol acetate (26.45%) based on mass spectrum data and retention times. The methanol extract has a significant antibacterial effect against tested strains, with MICs ranging from 111.37 to 445.5 mg/mL. Higher concentrations of polyphenols resulted in a significant increase in inhibition zone diameter against S1 (r2 = 0.94, p < 0.001), L3 (r2 = 0.94, p < 0.001), L5 (r2 = 0.93, p < 0.001), and L9 (r2 = 0.96, p < 0.001).

Plant extracts with insecticidal properties are promising alternatives to conventional insecticides, which may pose risks to human health and the environment in pest management. In the current study, the methanolic extract of Acokanthera oblongifolia (Hochst.) Benth & Hook.f. ex B.D.Jacks. was characterized using high-performance liquid and gas-mass spectrometry chromatography. High-performance liquid chromatography analysis identified 14 polyphenols, the highest of which is chlorogenic acid (65637.79 µg/g), followed by naringenin and pyrocatechol at 2022.98 and 1509.11 µg/g, respectively. However, quercetin, gallic acid, ferulic acid, rutin, and kaempferol showed moderate quantities. The gas chromatography–mass spectrometry analysis identified the major polysaccharide, inositol (15.52%), followed by squalene and triterpene (11.02%) out of 35 polysaccharides. The major fatty acids, 11-octadecenoic acid, methyl ester, and methyl 9-cis, 11-trans-octadecadienoate, were 9.06 and 6.30%, respectively. The crude extract and chlorfluazuron 5% EC at LC15 were evaluated for the life table and biological aspects of S. littoralis (Boisd.) neonates after 48 h under laboratory conditions compared to the control. The toxicity of the LC15 at 48 h of chlorfluazuron 5% EC (0.31 mg/L) excelled the extract (178.95 mg/L) on the neonates. Life span tests showed that the larval longevity of the extract and chlorfluazuron colonies were 27.34 and 30 days, respectively. The control colony completed its life span at 38.66 days, whereas the extract colony ended at the pupae stage at 33.67 days. Biological aspects showed that the tested compounds decreased pupation percentages and weight. Pupae malformations caused by the extract (80.56%) outperformed chlorfluazuron (33.33%). The adult emergency decreased by the extract (0.33%), and no emergency was observed in chlorfluazuron colony. Ultimately, A. oblongifolia extract demonstrated significant life table elongations and developmental impairment, which may suggest potential and eco-friendly use for its prospective commercial preparations in controlling S. littoralis alternatively to chlorfluazuron 5% EC.

Abstract Marjoram (Origanum majorana L.), also known as “sweet marjoram” or “sweet oregano” is a Mediterranean herbaceous perennial herb cultivated in Egypt and widely consumed as an herbal supplement for treatment of several ailments. The main goal of this study was to assess volatiles’ variation in marjoram samples collected from two different widely consumed commercial products using two different extraction techniques viz. head space solid phase microextraction (HS-SPME) and petroleum ether using gas chromatography mass spectrometry (GC-MS) analysis and multivariate data analysis. A total of 20 major aroma compounds were identified in samples extracted with HS-SPME found enriched in monoterpene hydrocarbons and oxygenated compounds. The major volatiles included β-phellandrene (20.1 and 14.2%), γ-terpinene (13.4 and 11.7%), 2-bornene (12.3 and 11.5%), p-cymene (9.8 and 4.6%) terpenen-4-ol (16.4 and 7.5%), sabinene hydrate (16.02 and 8.8%) and terpineol (4.2 and 3.2%) in MR and MI, respectively. Compared with HS-SPME, 51 aroma compounds were identified in marjoram samples extracted with petroleum ether, found more enriched in aliphatic hydrocarbons (42.8 and 73.8%) in MR and MI, respectively. While a higher identification score was observed in the case of solvent extraction, SPME appeared to be more selective in the recovery of oxygenated terpenes to account more for marjoram aroma. Multivariate data analysis using principal component analysis (PCA) revealed distinct discrimination between volatile composition of both marjoram samples. The total phenolic and flavonoid contents in marjoram samples were at (111.9, 109.1 µg GA/mg) and (18.3, 19.5 µg rutin eq/mg) in MR and MI, respectively. Stronger antioxidant effects were observed in MR and MI samples with IC50 at 45.5 and 56.8 µg/mL respectively compared to IC50 6.57 µg/mL for Trolox as assayed using DPPH assay. Moderate anti-bacterial effect was observed in MR and MI samples and expressed as a zone of inhibition mostly against Bacillus subtilis (16.03 and 15.9 mm), B. cereus (12.9 and 13.7 mm), Enterococcus faecalis (14.03 and 13.97 mm), and Enterobacter cloacae (11.6 and 11.6 mm) respectively.

旨在为植物油中甘油二酯的检测与分析提供技术参考，以亚麻籽甘油二酯油为检测样品，经两级固相萃取纯化后采用气相色谱-质谱联用法（GC-MS）对亚麻籽甘油二酯油中的甘油二酯进行分析，根据甘油二酯的特征离子碎片分析甘油二酯的组成，通过总离子流色谱（TIC）图及提取离子色谱（EIC）图对异构体进行研究，并与高效液相色谱法（HPLC）进行对比。结果表明：亚麻籽甘油二酯油经两次固相萃取后可以得到纯度较高的甘油二酯，Rxi-65TG气相色谱柱的分离效果优于DB-5ms的；特征离子碎片分析结果和EIC表明亚麻籽甘油二酯油中共含有20种甘油二酯，主要为1-亚油酸-3-亚麻酸甘油二酯（21.36%）、1，3-二亚麻酸甘油二酯（16.57%）和1-油酸-3-亚麻酸甘油二酯（15.75%）；相较于HPLC，GC-MS可以实现甘油二酯的准确定性与定量，且峰分离度优于HPLC。综上，GC-MS可用于植物油中甘油二酯的组成分析。Aiming to provide technical reference for the detection and analysis of diacylglycerol in vegetable oils, the diacylglycerol in flaxseed diacylglycerol oil was analysed by gas chromatography-mass spectrometry (GC-MS) after purification by two stage solid phase extraction using flaxseed diacylglycerol oil as the test sample, the composition of the diacylglycerol was analysed based on the characteristic ionic fragments of the diacylglycerol, the composition of the diacylglycerol was analysed through the total ion current chromatogram (TIC) and the extracted ion chromatogram (EIC) for the study of isomers and compared with the high performance liquid chromatography (HPLC) method for the determination of diacylglycerol. The results showed that high purity diacylglycerol could be obtained after two stage solid phase extraction of the flaxseed diacylglycerol oil, and the separation effect of the Rxi-65TG GC column was better than that of the DB-5ms. The results of the characteristic ionic fragmentation analysis and the EIC indicated that the flaxseed diacylglycerol oil contained a total of 20 kinds of diacylglycerols, which mainly consisted of 1-linoleic-3-linolenic acid diacylglycerol(21.36%), 1, 3-di-linolenic acid diacylglycerol(16.57%) and 1-oleic acid-3-linolenic acid diacylglycerol (15.75%). Compared with HPLC, GC-MS could achieve accurate characterization and quantification of diacylglycerol, and the peak separation was better than that of HPLC. In conclusion, GC-MS can be used for the analysis of the composition of diacylglycerol in vegetable oils.

Introduction: Alpinia galanga (L.) Willd is a rhizomatous, recurrent herb used to treat numerous diseases, including cancer. This study examines the efficiency of the different parts of A. galanga for their phytochemical, antioxidant, and anti-cancer properties. Methods: The powdered leaf, stem, and rhizome of A. galanga were extracted using hexane, ethyl acetate and methanol; the phytochemical compositions of the extracts were characterized using high performance liquid chromatography (HPLC) and gas chromatography-mass spectroscopy (GC-MS). Their antioxidant potentials were evaluated using different assays, including 2,2-Diphenyl-1picrylhydrazil (DPPH), 2-Azino-bis-3-ethylbenzothiazoline-6-sulphonic acid (ABTS), Superoxide anion (O2-), Hydroxyl radical (OH), and Phosphomolybdenum assays. The in vitro anticancer activity was studied using the 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay. Comet assay was used to determine the level of DNA damage. Inductions of morphological alterations were studied using the AO/Et-Br dual staining method. The ELISA kits were used to measure caspase activities. Results: The cytotoxicity results showed that the various extracts had inhibitory and cytotoxic effects on cancer cell lines. The leaf hexane (LH) extract of A. galanga induced DNA damage with prominent increased tail length and tail moment followed by the induction of apoptotic cells and up-regulation of the caspase activities. HPLC and GC-MS analysis allowed the identification of bioactive compounds, recognized as apoptotic inducers in human cancer cells by activating caspase-dependent pathways. Conclusion: This work reports for the first time the effect of LH extract of A. galanga in triggering apoptosis in A-549 and HeLa cells through the upregulation of caspase-8 and caspase-3 activities.

为了快速检测食用植物油中的16种多环芳烃（PAHs)，以氨基化多壁碳纳米管（NH2-MWCNTs）作为样品前处理的吸附剂，采用分散固相萃取（d-SPE）/气相色谱-质谱联用（GC-MS）同时测定食用植物油中的16种PAHs。通过单因素实验对样品前处理条件（吸附剂用量、吸附时间、洗脱剂类型及用量、洗脱时间）进行了优化，对所建立的方法进行了方法学考察，并与已有检测方法进行了对比分析，同时采用所建立的方法对实际样品进行了测定。结果表明：样品前处理最优条件为吸附剂用量15 mg(样品食用植物油质量1.0 g)、吸附时间1 min、洗脱剂甲苯、洗脱剂用量500 μL、洗脱时间5 min；16种PAHs在1～200 μg/kg范围内线性关系良好，方法的检出限在0.05～043 μg/kg之间，定量限在0.17～1.42 μg/kg，加标回收率和相对标准偏差分别为70.67%～10183%和1.34%～9.32%；与已有前处理方法相比，d-SPE高效、简便，且最大程度地减少了有机溶剂的消耗；6种市售食用植物油中苯并\[a\]芘含量均小于2 μg/kg。综上，所建立的方法适用于食用植物油中16种PAHs的测定。To rapidly detect 16 polycyclic aromatic hydrocarbons (PAHs) in edible vegetable oil, the aminated multi-walled carbon nanotubes (NH2-MWCNTs) were used as adsorbents for sample pretreatment, and the dispersion solid phase extraction (d-SPE) with GC-MS method was developed for the simultaneous determination of 16 PAHs in edible vegetable oil samples. The sample pretreatment conditions (the adsorbent dosage, adsorption time, the type and amount of eluent, elution time) were optimized by single factor experiments, and the methodology of the established detection method was investigated and compared with existing methods. Meanwhile, actual samples were detected using the established method. The results showed that the optimal conditions for sample pretreatment were as follows: adsorbent dosage 15 mg (for 1.0 g edible vegetable oil sample), adsorption time 1 min, toluene as the eluent, eluent dosage 500 μL, elution time 5 min. The 16 PAHs showed good linear relationship in the range of 1-200 μg/kg, and the detection limits of the method ranged from 0.05 μg/kg to 0.43 μg/kg, with quantitative limits between 0.17 μg/kg and 1.42 μg/kg. The spiked recovery rate and relative standard deviation were 70.67%-101.83% and 1.34%-9.32%, respectively. Compared to existing pretreament methods, d-SPE is efficient, simple and minimizes the consumption of organic solvents. The content of benzo \[a\] pyrene in 6 commercial edible vegetable oils was less than 2 μg/kg. In summary, the established method is suitable for the determination of 16 PAHs in edible vegetable oil.

Euphorbia dracunculoides Lam. possesses significant biological potential due to its rich bioactive compounds. To enhance this potential, zinc oxide nanoparticles (ZnO NPs) were synthesized using the methanolic extract of E. dracunculoides, exploiting ZnO NPs’ superior physiochemical properties and bioavailability. The synthesis of ZnO NPs was confirmed through UV–Vis spectroscopy (with an absorption maximum at 368 nm), X-ray diffraction (crystalline nature), Fourier transform infrared spectroscopy (functional groups involved in Zn²⁺ reduction), scanning electron microscopy (rod-shaped and triangular morphologies, average size 79 nm), and EDX (presence of Zn and O). The ED-ZnO NPs exhibited dose-dependent cytotoxicity against U87 cells (IC50: 229.51 µg·mL−1) and anti-leishmanial activity against Leishmania tropica promastigotes (IC50: 9.11 µg·mL−1). Additionally, in vivo studies demonstrated significant antihyperlipidemic effects, with decreased cholesterol, triglyceride, and low-density lipoprotein levels, and increased high-density lipoprotein levels. ED-ZnO NPs also normalized alkaline phosphatase, alanine transaminase, aspartate transaminase, total bilirubin, creatinine, urea, and glucose levels compared to controls. Overall, ED-ZnO NPs effectively enhance the bioactive compounds’ efficacy in treating various disorders.

Abubakr A Hammad,1,2 Abdelgadir A Abdelgadir,2,3 Sitelbanat Yassin,4 Abdulrahim A Alzain,5 Elhadi M Ahmed2,3 1Department of Pharmacognosy, Faculty of Pharmacy, Omdurman Islamic University, Omdurman, Sudan; 2Department of Pharmacognosy, Faculty of Pharmacy, University of Gezira, Wad Madani, Sudan; 3Medicinal and Aromatic Plants Research Center, Faculty of Pharmacy, University of Gezira, Wad Madani, Sudan; 4Department of Pharmaceutics, Faculty of Pharmacy, University of Gezira, Wad Madani, Sudan; 5Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Gezira, Wad Madani, SudanCorrespondence: Abubakr A Hammad, Email abubakr.hammad7@gmail.comIntroduction: Antimicrobial resistance is a critical global issue, and medicinal plants, as a key source of therapeutic agents, offer potential solutions by offering new antibacterial agents. Acacia polyacantha tree, known as Al Kakamout in Sudan, is a significant source of Gum Arabic and has been traditionally used to treat bacterial diseases. This study aimed to investigate a hydro-ethanol extract of Kakamout stem bark through GC-MS analysis, evaluate its antibacterial activity against two standard bacterial strains, and conduct molecular docking and ADME studies.Methods: The stem bark of the plant was extracted by maceration using a hydro-ethanol solvent and analyzed via GC-MS. The antibacterial activity of the extract was evaluated against Staphylococcus aureus ATCC 25923 and Pseudomonas aeruginosa ATCC 27853 using the well diffusion method. The identified compounds were studied in silico to investigate their binding affinities with the target bacterial proteins. The ADMET properties were predicted for the top scoring compounds.Results: GC-MS analysis revealed the presence of 11 compounds, with the major ones being dopamine, N, N-dimethyl-, dimethyl ether (43.76%), 4-O-methylmannose (23.27%), sucrose (8.09%), 1,4,7-triazacyclononane, 1-benzoyl- (5.41%), and lupeol, trifluoroacetate (5.24%). The extract demonstrated significant effectiveness against both bacterial strains, even at a low concentration of 50 mg/mL. Molecular docking showed that compounds 1, 3, 4, and 6 had the best docking scores with enoyl-acyl carrier protein reductase (FabI) (PDB ID: 3GR6) from S. aureus (− 6.142, − 10.843, − 6.218 and − 7.14 Kcal/mol). Similarly, compounds 1– 6 exhibited favorable binding energies with LasR-TP4 complex (PDB ID: 3JPU) from P. aeruginosa (− 10.025, − 9.127, − 8.623, − 7.092, − 7.722, and − 6.019 Kcal/mol).Conclusion: This study provides the first GC-MS analysis of Acacia polyacantha stem bark, identifying potential antibacterial compounds. Molecular docking and ADMET predictions suggest several promising compounds for further investigation as antibacterial agents.Keywords: Acacia polyacantha, antibacterial, GC-MS, ADME, molecular docking

To analyze the metabolic differences in Wangdu peppers, this study employed high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) to detect chemical components and perform non-targeted metabolomics analysis on five different varieties of Wangdu peppers: Yan Jiao (YJ), La Yan (LY), Guo Ta (GT), Yan Jiao 110 (YJA), and Re La (RL). Machine learning was used to classify and identify the differential metabolites screened. First, HPLC was used to measure the content of capsaicin, dihydrocapsaicin, and Vitamin C (VC) in the five pepper varieties. Then, GC-MS was used for non-targeted metabolite analysis of the five peppers. Principal component analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA) were employed to identify differential metabolites and metabolic pathways. Machine learning methods were used to identify the different pepper varieties based on the differential metabolites. In the five pepper varieties, Re La had the highest content of capsaicin and dihydrocapsaicin, at 533.897±62.187 μg/g and 264.526±28.532 μg/g, respectively. Yan Jiao had the highest VC content at 146.9±0.029 mg/100 g. OPLS-DA identified 16 differential metabolites, including organic acids such as quinic acid and aconitic acid, which were higher in Yan Jiao, D-sorbitol, which was highest in La Yan, citric acid, D-fructose, D-mannose, and lactic acid, which were most enriched in Guo Ta, D-tagatose and amino acids, which were highest in Yan Jiao 110, and glucose and inositol, which were most abundant in Re La. KEGG pathway enrichment analysis indicated that the differential metabolic pathways mainly included galactose metabolism, fructose and mannose metabolism, the citric acid cycle, starch and sucrose metabolism, glyoxylate and dicarboxylate metabolism, and pyruvate metabolism. Finally, three machine learning methods—random forest (RF), XGBoost, and backpropagation (BP) neural networks were used to classify and validate the differential metabolites of the five pepper varieties. The established classification models achieved accuracies of 100%, 92.9%, and 78.6%, respectively, demonstrating their utility in identifying pepper varieties. These results would provide fundamental data for the quality evaluation, variety improvement, and comprehensive utilization of Wangdu peppers.

Abstract [Objective] This study aims to explore the flowering characteristics and flower fragrance components and their release patterns of Rhus chinensis, so as to provide a basis for further development and utilization of floral fragrance of R. chinensis. [Methods] Scanning electron microscope was used to observe pollen morphology. Headspace-solid phase microextraction (HS-SPME) and gas chromatography-mass spectrometry (GC-MS) techniques were used to analyze the main floral scent components in different flowering stages and daily change pattern. [Results] A total of 92 floral substances (29 terpenes, 19 aldehydes, 15 esters, 14 alcohols, 5 ketones, 4 olefins, 2 aromatic hydrocarbons, and 1 each of phenols, alkanes, acids, and others) were detected in different flowering periods. Its relative content was increased and then decreased, reaching a maximum (3.60 μg/g) at the full-flowering stage, with significant differences among the flowering stages. A total of 84 floral aroma substances were detected during full flowering stage. The release showed a parabolic daily variation trend, which was higher during the day than at night and reached the maximum at 18:00 (4.80 μg/g), and then continued to decrease and reached the lowest at 6:00, with 2.58 μg/g. Terpenes were the main floral substances of R. chinensis, with a relative content of about 70% of the total floral components. [Conclusion] R. chinensis is rich in floral components, with a clear diurnal rhythm. Terpenes are its main floral substances.

BACKGROUND: Spearmint and peppermint teas are widely consumed around the world for their flavor and therapeutic properties. Dynamic headspace sampling (HS) coupled to gas chromatography/mass spectrometry (GC–MS) with principal component analysis (PCA) of 'fingerprint' volatile profiles were used to investigate 27 spearmint and peppermint teas. Additionally, comparisons between mint teas were undertaken with an electronic nose (enose). RESULTS: Twenty compounds, all previously known in the literature, were identified using HS–GC–MS. PCA found distinct differences between the fingerprint volatile profiles of spearmint, peppermint and spearmint/peppermint combination teas. HS–GC–MS analysis performed with an achiral column allowed faster processing time and yielded tighter clustering of PCA tea groups than the analysis which used a chiral column. Two spearmint outliers were detected. One showed a high degree of variation in volatile composition and a second wholly overlapped with the peppermint PCA grouping. Enose analysis separated all treatments with no overlaps. CONCLUSION: Characterizing the volatile fingerprints of mint teas is critical to quality control for this valuable agricultural product. The results of this study show that fingerprint volatile profiles and enose analysis of mint teas are distinctive and could be used to rapidly identify unknown samples. With specific volatile profiles identified for each tea, samples could be tested in the laboratory, or potentially on a farm or along the supply chain, to confirm the provenance and authenticity of mint food or beverage commodities. © 2024 Society of Chemical Industry. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA. [ABSTRACT FROM AUTHOR]

BACKGROUND: 'Xynisteri' is considered as the reference white grape cultivar in Cyprus with remarkable adaptation to adverse edaphoclimatic conditions and appreciable oenological properties that renders it as an appropriate cultivar for studies within a global context due to climate change. To this aim, two distinct non‐irrigated plots with different climatic conditions, soil properties and levels of rainfall were selected; Koilani [KO, altitude 800 m, 76% calcium carbonate (CaCO3) content, pH 7.97, average temperature: 16.5 °C, rainfall: 229 mm] and Kyperounda (KY, altitude 1200 m, CaCO3‐free soil, pH 6.47, average temperature: 14.9 °C, rainfall: 658 mm). An array of physiological, biochemical and qualitative indices during successive developmental stages (BBCH 75–89) were determined. During the advanced on‐vine developmental stages (BBCH 85–89), the aromatic profile of grapes was assessed with the employment of gas chromatography–mass spectrometry (GC–MS). Such analysis was complemented with non‐destructive chemometric analyses. RESULTS: Berry ripening process substantially differed on the examined plots; BBCH 89 stage reached at 267 and 303 Julian days for KO and KY, respectively. Results indicated that berry weight, soluble solids content (SSC) and α‐amino nitrogen were higher in KO than in KY, with exception made for ammonium nitrogen content. A total of 75 compounds, including aliphatic alcohols, benzenic compounds, phenols, vanillins, monoterpenes and C13‐norisoprenoids were identified and quantified. The variations of mesoclimatic conditions affected the volatile organic compound (VOC) profiles at the fully‐ripe stage, showing a considerable rise in glycosylated aroma compounds, especially monoterpenes and benzenic compounds. In particular, the higher amount of glycosylated aroma compounds were obtained in KY berries up to mid‐ripe, whereas KO showed higher glycosylated aroma compounds at fully‐ripe stage. Results reported herein indicate that aroma profile of 'Xynisteri' grapes varied substantially in the examined terroirs. Interestingly, the limited rainfall in KΟ non‐irrigated vine did not compromise qualitative and aromatic properties of berries. CONCLUSIONS: The present study aimed at dissecting the impact of terroir on bush‐trained, non‐irrigated grapevines of a cultivar appropriate for extreme climate change scenarios. The volatilome fingerprint was highly variable among the examined plots; such results can be further exploited at vinification level towards production of single vineyard premium end products. © 2024 The Author(s). Journal of the Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

BACKGROUND: Genetic breeding is essential to develop grapevine genotypes adapted to warm climates and resistant to pathogens. Traditionally cultivated Vitis vinifera is susceptible to biotic and abiotic stresses. Winemakers and consumers, however, perceive wines from non‐vinifera or hybrid cultivars as inferior. In this study, sensory analyses and comprehensive metabolite profiling by targeted and untargeted approaches were used to investigate the oenological potential of wines from grapes of genotypes developed throughout four breeding cycles to improve climate adaptation, sugar contents and berry color. RESULTS: Novel genotypes had higher yields and the wines exhibited increased contents of polyphenols, including anthocyanins. Volatile monoterpenes in the wines decreased throughout breeding cycles in the absence of selective pressure. Polyphenol contents were higher in intermediate wines, with hydroxytyrosol contents reaching up to three times reported values. Mouthfeel attributes astringency, leafy taste, flavor and body, and persistency showed significant correlation with untargeted features. Supervised model‐based analyses of the metabolome effectively discriminate wines from distinct genetic origins. CONCLUSION: Taken together, the results demonstrate the potential of novel grapevine genotypes to a more sustainable viticulture and quality wine production in warm climates. Comprehensive metabolite profiling of the wines reveals that genotype clustering is dependent on the chemical class and that traits not submitted to selective pressure are also altered by breeding. Supervised multivariate models were effective to predict the genetic origin of the wines based on the metabolic profile, indicating the potential of the technique to identify biomarkers for wines from sustainable genotypes. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

The translocation of broomcorn millet (Panicum miliaceum) is an enticing subject of archaeological investigation. While the species was rapidly dispersed across Eurasia during prehistory, its adoption appears to have been inconsistent, with evidence for its sudden and gradual adoption, as well as its rejection, observed within and between contemporary communities and cultures. The translocation of P. miliaceum may be better understood through the identification of its role and significance as a foodstuff among past populations. This study employs molecular investigation and bulk and compound-specific isotope analysis to study organic residues produced during culinary activities at Bruszczewo, Poland, during the Early Bronze Age (EBA) and Late Bronze Age / Early Iron Age (LBA/EIA). The analysis of ceramic-absorbed and charred 'foodcrust' residues enabled a comprehensive examination of vessel use-life and the production of individual meals. This study strongly suggests that P. miliaceum was not present at Bruszczewo during the EBA, conforming to its established translocation chronology, while highlighting its extensive use during the LBA/EIA. The cereal was incorporated into a variety of culinary activities, constituting both a minor and major ingredient of many meals, while being absent in others. Finally, the observation of apparently unrestricted use of P. miliaceum at Bruszczewo provided further insight into the role and significance of this cereal relative to contemporary LBA/EIA evidence for its use across the region. [ABSTRACT FROM AUTHOR]

The pesticide transportation to deeper soil layers can result in groundwater contamination and, consequently, environmental issues. In this research, our objective was to investigate transport efficiency of indoxacaarb using three different soils to understand the leaching potential. The leaching experiments were performed using a 0.01 M calcium chloride solution over five consecutive days. Leachates (water) and soil samples were collected and the residues of indoxacarb were analyzed using gas chromatography mass spectrometry. The method’s accuracy was validated by conducting recovery experiments at levels ranging from 0.01 to 0.1 µg/g. The results showed that 82.67 to 84.00%, 80.67 to 82.70% and 76.68 to 78.70% of the indoxacarb applied was retained in the topsoil layer (0–10 cm) for acid, alkali and neutral soil, respectively. Its low leaching behavior, as evidenced by its retention in the topsoil layer and absence in the leachate, contributes to its limited mobility within the soil profile. The study suggests that indoxacarb has no potential for contaminating groundwater and the soil environment through leaching processes. [ABSTRACT FROM AUTHOR]

The present study appraised the inhibitory role of ethanol (PDEE) and ethyl acetate (PDEAE) extracts of Phoenix dactylifera L. against three molecularly identified fungi: Fusarium oxysporum, Botrytis cinerea, and Rhizoctonia solani. HPLC analysis revealed that gallic acid was the major phenolic compound in both extracts: (PDEE: 1721.90 μg/g) and (PDEAE: 101.53 μg/g). The major flavonoids in PDEE are rutin, kaempferol, and quercetin, whereas PDEAE contains kaempferol, naringenin, and quercetin. The GC-MS showed 11-octadecenoic acid methyl ester (26.25%) is the highest compound in PDEE, while diisooctyl phthalate (18.82%) is the most important compound in PDEAE. At 50 μg/mL, the inhibition percentage of PDEAE initiated the highest growth inhibition of F. oxysporum (49.63%) and R. solani (71.43%). Meanwhile, PDEE at 200 μg/mL initiated an inhibition value of 77.78% for B. cinerea. As a result, PDEAE is considered more effective than PDEE in controlling the growth of selected isolates.

Abstract Collective behaviors of social insects are often regulated by pheromones. In subterranean termites, some workers forage for and exploit decaying wood for new food resources while forming tunnels from their nest. Colonizing new food resources requires workers to build and disinfect tunnels and chambers inside the nest and ingest decaying wood; therefore subterranean termite colonies should have mechanisms to establish and maintain groups of workers to perform these functions. Recently, an aggregation pheromone was identified in workers of the termite Reticulitermes speratus, which induces quick attraction of nestmate workers and prolonged aggregation to the site of attraction. In this study, we extended this work to another species of Reticulitermes and identified a worker aggregation pheromone in the termite R. virginicus. GC–MS analysis and bioassays demonstrated that this pheromone consists of 3-octanone, 3-octanol, and palmitic acid and shows a colony-specific, dose-dependent attractant response but not an arrestant response. Furthermore, these pheromone components were most likely emitted from the surface of the body. This suggests that aggregation pheromone composition and function differ significantly among termite species, even within the same genus. This study advances our understanding of the regulatory mechanisms of termite aggregation behavior.

Background: Lactobacillus plantarum can produce many secondary metabolites, some of which have antibacterial effects. This study aimed to explore the main antimicrobial metabolites of Lactobacillus plantarum LPZN19. Results: The results of antibacterial activity after fermentation for different durations showed that the metabolites from the LPZN19 cell-free supernatant (LCFS) after 24 h had the strongest antibacterial activity, which was confirmed by the highest contents of organic acids and fatty acids in the LCFS after 24 h. Lactic acid, phenyllactic acid, malic acid, aspartic acid, dodecanoic acid and propionic acid were the main differentially abundant metabolites. LCFS was separated by semi-preparative liquid chromatography to obtain 4 antibacterial parts, mainly organic acids such as lactic acid, glycolic acid, and citric acid, and fatty acids such as stearic acid, palmitic acid, and octanoic acid. In addition, fatty glycerides and amino acids with antimicrobial activity were included. Conclusions: Our findings indicate that the main antimicrobial metabolites of L. plantarum LPZN19 include organic acids, fatty acids, fatty glycerides and some amino acids with antimicrobial activity, which not only clarifies the main antimicrobial metabolites of L. plantarum LPZN19 but also provides an effective method for rapid screening of antimicrobial substances.How to cite: Wang Y, Xu Y. Analysis and identification of the main antimicrobial metabolites of Lactobacillus plantarum LPZN19. Electron J Biotechnol 2024;71. https://doi.org/10.1016/j.ejbt.2024.05.005.

Chemicals and antibiotics are serious problems that cause the resistance of bacteria and the persistence of chemical residues in food. These chemical products affect human health and promote diseases. Therefore, the use of natural resources, especially plants, appears as an alternative to avoid the harmful impacts of such products. Plant active substances such as essential oils, alkaloids and phenols are of great interest to scientists and have been studied for their biological activities. Essential oils (Eos) from the stems of Santolina africana were extracted by hydrodistillation and analyzed by Gaz Chromatography/ Mass Spectrometry (GC-MS). The antioxidant activity of crude extracts and Eos was evaluated by the DPPH assay and the antibacterial activity was evaluated by the disc diffusion method and the broth microdilution method against Gram-positive strains (Bacillus subtilis, Staphylococcus aureus) and Gram-negative strains (Escherichia coli, Salmonella paratyphi, and Pseudomonas aeruginosa). S.africana Eos from Morocco and Tunisia were found to be rich in artemisia ketone (35.4% and 44.3%, respectively), santolina alcohol (16.2%and 3.2%, respectively) and isoborneol (6.1% and 26.6%, respectively). Methanol extracts were rich in phenolic and flavonoids contents and showed the highest DPPH radical scavenging activity. Results exhibited the sensitivity of the strains to essential oils from S. africana especially against Gram-positive bacteria. This current research will provide new information about this plant that can be used as a natural antioxidant and antibacterial for industrial purposes.

The aim of the entry was to write a substantial contribution that analyses and compares the biological pollution of indoor air, the possibilities of its assessment and the control methods. In addition, the aim of our entry was to review journals covering both commercial and residential buildings. By analysing the above topics from the existing articles, one can have the impression that air pollution is one of the most important problems that need to be solved in the modern world. Adequate air quality is important for maintaining human health, affects the health of ecosystems, including animals, and determines crop production. With the development of civilisation, the quality of air in the atmosphere and indoors is constantly deteriorating. Indoor air pollution can be divided into physical (e.g., noise, inadequate lighting, ionising radiation), chemical (e.g., tobacco smoke, household products) and microbiological (bacteria, viruses, fungi and products of their metabolism) factors. Each of these factors can have a negative impact on a person’s health or cause premature death. The entry deals with indoor air pollution, focussing on biological pollutants. It compares different methods available and describes the method of sampling to analyse indoor air pollution and ways to reduce it.

Abstract Indian mustard (Brassica juncea; Brassicaceae) is an edible, oilseeds-yielding crop widely consumed as a food spice owing to its richness in nutrients with several health benefits. The current study aims to dissect the B. juncea metabolome heterogeneity among its different organs including leaf, stem, flower, and seed. Moreover, assessing the metabolome differences between two different varieties RH-725 and RH-761 grown at the same conditions. Gas chromatography-mass spectrometry (GC–MS) post-silylation was used to dissect the composition of nutrient metabolites coupled to multivariate data analysis. Variation in sulphur aglycones was measured using headspace-solid phase-microextraction HS-SPME coupled to GC–MS. A total of 101 nutrient metabolites were identified with the abundance of sugars represented by monosaccharides in all organs, except for seeds which were enriched in disaccharides (sucrose). α-Linolenic acid was detected as a marker fatty acid in leaf from RH-725 at 12.5 µg/mg. Malic acid was detected as a significant variant metabolite between the two varieties as detected in the leaf from the RH-725 variety at ca. 128.2 µg/mg compared to traces in RH-761. 7 Volatile sulphur compounds were detected at comparable levels in RH-725 and RH-761, with 3-butenyl isothiocyanate was the most abundant at 0.8–2 ng/mg.

Abstract Mosquitoes, one of the deadliest animals on the planet, cause millions of fatalities each year by transmitting several human illnesses. Synthetic pesticides were previously used to prevent the spread of diseases by mosquitoes, which was effective in protecting humans but caused serious human health problems, environmental damage, and developed mosquito pesticide resistance. This research focuses on exploring new, more effective, safer, and environmentally friendly compounds to improve mosquito vector management. Phytochemicals are possible biological agents for controlling pests and many are target-specific, rapidly biodegradable, and eco-friendly. The potential of extracts of Lantana camara, Melia azedarach, Nerium oleander, Ricinus communis, and Withania somnifera against 3rd instar Culex pipiens (Common house mosquito) larvae was evaluated. Methanol extracts had more toxic effects against Cx. pipiens larvae (95–100%, 24 h post-treatment) than aqueous extracts (63–91%, 24 h post-treatment). The methanol extracts of Nerium oleander (LC50 = 158.92 ppm) and Ricinus communis (LC50 = 175.04 ppm) were very effective at killing mosquito larvae, 24 h after treatment. N. oleander (LC50 = 373.29 ppm) showed high efficacy in aqueous plant extracts. Among the different extracts of the five plants screened, the methanol extract of R. communis recorded the highest ovicidal activity of 5% at 800 ppm concentration. Total developmental duration and growth index were highly affected by R. communis and M. azedarach methanol extracts. In field tests it was clear that plant extracts decreased mosquito larval density, especially when mixed with mosquito Bti briquette, with stability up to seven days for N. oleander. GC–MS results showed that the methanol extract had a higher number of chemical compounds, particularly with more terpene compounds. A high-performance liquid chromatography (HPLC) technique was used to detect the existence of non-volatile polyphenols and flavonoids. All five methanol extracts showed high concentrations of active ingredients such as gallic acid, chlorogenic acid (more than 100 μg/ml) and the rosmarinic acid was also found in all the five extracts in addition to 17 active polyphenols and flavonoids presented at moderate to low concentrations. Molecular modeling of 18 active ingredients detected by the HPLC were performed to the vicinity of one of the fatty acid binding proteins of lm-FABP (PDB code: 2FLJ). Rutin, Caffeic acid, coumaric acid and rosmarinic acid which presented densely in R. communis and N. oleander showed multiple and stable intermolecular hydrogen bonding and π–π stacking interactions. The inhibition ability of the fatty acid binding protein, FABP4, was evaluated with remarkable receptor inhibition evident, especially with R. communis and N. oleander having inhibitory concentrations of IC50 = 0.425 and 0.599 µg/mL, respectively. The active phytochemical compounds in the plants suggest promising larvicidal and ovicidal activity, and have potential as a safe and effective alternative to synthetic insecticides.

Abstract Ethnomedicinal plants are thought to have better prospects of harboring endophytes that produce natural products with pharmacological activities. This study aimed to investigate the antiplasmodial and anticancer properties of secondary metabolites of endophytic fungi from three medicinal plants. The endophytic fungi included Lasiodiplodia theobromae isolated from Cola acuminata, Curvularia lunata Bv4 isolated from Bambusa vulgaris, and Curvularia lunata Eg7 isolated from Elaeis guineensis. The identification of the fungi was based on the internal transcribed spacer (ITS-rDNA) sequence. The fungi were subjected to solid-state fermentation and the secondary metabolites were extracted with ethyl acetate. In vitro antiplasmodial screening of extracts was performed using the SYBR green I-based fluorescence assay on the chloroquine-resistant Plasmodium falciparum strain DD2. The cytotoxicity of the extracts on human red blood cells and Jurkat (leukemia) cells was assessed using the tetrazolium-based colorimetric MTT assay. Gas chromatography-mass spectrometry (GC–MS) analysis was used to identify the constituents of the fungal extracts. The extract of L. theobromae showed the best antiplasmodial activity against chloroquine-resistant P. falciparum (IC50 = 5.4 µg/mL) and was not harmful to erythrocytes (CC50 > 100 µg/mL). All three fungal extracts showed a weak cytotoxic effect against Jukart cell lines (CC50 > 100 µg/mL). GC–MS analysis of the three endophytic fungal extracts revealed the presence of forty major bioactive compounds, including: oxalic acid, isobutyl nonyl ester, 2,4-di-tert-butylphenol, and hexadecanoic acid, among others. The endophytic fungi from the medicinal plants in this study were promising sources of bioactive compounds that could be further evaluated as novel drugs for the treatment of malaria caused by P. falciparum-resistant strains.

Sol LeWitt, a pioneer of conceptual art, created during his career over 1350 wall drawings, including the Wall Drawing #736 (1993) at the Center for Contemporary Art Luigi Pecci in Prato (Prato, Italy). The painting, executed by Andrea Marescalchi and Antony Sansotta under LeWitt’s instructions, features a grid of coloured rectangles obtained by overlapping different layers of inks. During a 2021 restoration by the Wall Paintings and Stuccoes Department of the Opificio delle Pietre Dure (Firenze, Italy), an in-depth investigation of the composition and the materials used by LeWitt’s assistants in producing Wall Drawing #736 was performed. A multi-analytical approach entailing Raman spectroscopy, high-performance liquid chromatography coupled to diode array and high-resolution mass spectrometry, gas chromatography–mass spectrometry (GC–MS), and pyrolysis coupled with GC–MS was applied. Our results revealed the use of animal glue, shellac resin, paraffin wax, linseed oil, and various organic pigments. The binder in the preparation layer was identified as poly(vinyl acetate), while poly(n-butyl methacrylate) was determined as a fixative. This research provided valuable insights into LeWitt’s techniques. The acquired knowledge on the paint technique is highly relevant in supporting conservators in restoration and consolidating the many wall drawings produced exploiting the same technique all over the world.

Abstract Background The present study aims to enhance the wound healing potential of the seed oil (SO) of Lagenaria siceraria (Egyptian cultivar) via the preparation of SO-loaded binary nanoethosomal (SO-BNE) gels. SO-BNEs were prepared using 23 factorial design, characterized for vesicle size, zeta potential, polydispersity index, linoleic and oleic acid EE% for ensuring improved skin permeability. The L. siceraria SO, optimized SO-BNE gels (0.5% and 5%) and Mebo® were topically applied in full-thickness wounded rat model twice daily for 10 days. Results In the SO-BNE gel groups, the normal appearance of the skin architecture and structure of the dermis was revealed. In addition, the levels of NRF2, TGF-β1 and FOXO1, collagen type I, SMA-α and MIP2 were significantly elevated. The wound healing potential of SO-BNE gels was proposed to be via suppression of oxidative stress and stimulation of skin regeneration biomarkers. Furthermore, the SO screening through GC/MS unveiled high percentages of unsaturated fatty acids. SO was also found to be nontoxic to human skin fibroblast cells; enhanced viability and migration rates at concentration of 50 g/mL by 99.76% and 75.9%, respectively. Conclusion These findings demonstrate that the Lagenaria siceraria SO-loaded BNE gels represent a promising delivery for wound healing with enhanced release and bioavailability.