Compounds Of Type Research Articles

A highly selective and recyclable fluorescent sensor based on a Salamo-Salen-Salamo type ligand for continuous detection of Al3+ and phosphates in drug

In this work, a fluorescence chemical sensor continuous detection Al3+ and phosphates by a Salamo-Salen-Salamo type compound (SL) was employed. The sensor continuously recognized Al3+ and phosphates with good selectivity and fast response time, and a low limit of detection of 0.25 μΜ and 0.96 μM, at the same time accompanied by a naked-eye identification specificity. The detection mechanism of SL towards Al3+ is due to the chelating fluorescence enhancement effect and ICT effect, and continuously towards phosphates is due to the collapse of the SL-Al3+ and coordination interaction between Al3+ and phosphates, by Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, other spectral characterization and DFT calculation as evidence. In addition, the sensor had good recyclability and reusability. The distribution of Al3+ and phosphates in zebrafish cells was effectively monitored by confocal microscopy based on the good biocompatibility and tissue permeability of SL. Furthermore, the feasibility of using sensor SL to detect the content of Al3+ and phosphate ions in certain drugs was quantitatively analyzed through experiments. It was found SL had a good result in practical application.

A highly efficient chemoenzymatic process to produce (R)-6,7-dihydroxygeraniol

The efficient asymmetric dihydroxylation of 6,7-epoxygeraniol was performed using a chemoenzymatic process employing a yeast epoxide hydrolase (EH) resolution stereoinversion step, followed by stereoretentive chemical hydrolysis of the remaining epoxide to produce (6 R)-6,7-dihydroxygeraniol at unprecedented high enantiometic excess (ee) (>97.5%) and high isolated yield (72 mol % overall yield over 5 steps from commercially available geraniol). The enzymatic process was completed within 2 h at 250 g/L substrate loading reaching > 49.5 mass % conversion of the racemic epoxide. The reaction was self-limiting and furnished both the homochiral (6 R)-triol and the residual (6 R)-epoxide at > 99% ee, due to enantio-inversion of the (6S)-epoxide. The (6 R)-epoxide was subsequently chemically hydrolysed, without first needing to separate the epoxide and triol products, to afford the desired (6 R)-triol product in >97.5% ee, at multigram scale. This chemoenzymatic procedure offers an excellent alternative to chemical asymmetric epoxidation or dihydroxylation for the production of enantiopure 6,7-dihydroxygeranyl and 6,7-epoxygeranyl type compounds in general. It exemplifies the benefits of using greener EH bioprocesses to produce such compounds in high ee’s and high isolated yields.

Metal nitrides as electrocatalysts in green ammonia synthesis

Green ammonia is assumed to be an important part of the European hydrogen economy and one of the most important substrates of chemical industry. The future development of its manufacturing processes can be related to the electrocatalytic studies yielding in the development of the catalytic materials that would effectively break the nitrogen-nitrogen bond to successfully drive the N2RR—a process of molecular nitrogen electroreduction to ammonia. Molecular nitrogen is characterized with strong triple bond energies (942 kJ/mol) which leading into large dissociation energy of N2 (9,76 eV) and also large energy barrier of the first step of triple bond dissociation 410 kJ/mol (4,25 eV). Those large energies makes reduction to ammonia an extremely difficult task. Metal nitrides of d and f block became in interest due to their activity in ammonia production from molecular nitrogen and hydrogen. Practically all the transition elements occurs in one of the four types of crystalline structures: regular, regular face cantered, hexagonal and hexagonal close packed. The reactions of these metals with nitrogen (or ammonia) typically yields in nitride compounds of an identical type of crystalline structure as the initial metal. Dealing with single metal systems, their ternary counterparts and metal–metal nitride heterostructures, the presented review shows that nitrides are promising groups of electrocatalytic materials. Being property-prone to their internal structural features such as non-stoichiometry and correlated concentration of nitrogen vacancies, metal nitrides are a good candidate for joined investigations spanned between electrochemistry, inorganic chemistry and material engineering.

Investigation of structural, dielectric, impedance, and conductivity properties of layered perovskites type compound: LiNdSnO4

Investigation of structural, dielectric, impedance, and conductivity properties of layered perovskites type compound: LiNdSnO4

Synthesis and electropolymerization of a selenophene based chemiluminescent monomer and its use in blood detection

A new selenophene based trimeric chemiluminescent compound, namely 5,7-di(selenophen-2-yl)-2,3-dihydrothieno[3,4-d]pyridazine-1,4-dione (S2T-Lum), was synthesized in two steps via electron donor-acceptor-donor approach. Its chemiluminescent reaction with hydrogen peroxide was investigated in an alkaline solution in the presence of various catalysts such as different metal ions, hemin and blood samples and the results were compared with its thiophene analogue (T2T-Lum) and luminol. It was found that S2T-Lum was very sensitive to copper(II) and iron(III) ions, and blood samples. Also, it can be easily concluded that S2T-Lum as a new member of luminol type compounds is a potential candidate for the detection of blood findings in forensic science. Furthermore, S2T-Lum has an irreversible oxidation peak at 1.28 V vs Ag/AgCl, which is responsible from its electropolymerization. S2T-Lum was successfully polymerized electrochemically via potentiodynamic electrolysis without cleavage of its chemiluminescent active appendage. To the best of our knowledge, its corresponding polymer PS2T-Lum film is the first member of selenophene based luminol type electroactive polymers.

Study of minor Sc and Zr additions effect on silicon rich Al–Mg–Si aluminum alloy microstructure during Sc multistage thermal treatment

The study addresses the effect of multistage thermal treatment on microstructure formation of Al–Mg–Si series alloy with scandium and zirconium additions in Mg/Si = 0.3 proportion. Basic alloy AlM–Si without Sc and Zr and them modification AlMg1SiZrSc were cast. AlMgSiScZr alloy multi-stage thermal treatment included the following 4 annealing stages –550 °C 8 h + 440 °C 8 h + 500 °C 0.5 h + 180 °C 5 h. For AlMg1Si alloy it was performed following 550 °C 8 h + 180 °C 5 h practice. AlMgSiScZr microstructure was examined using scanning (SEM) and transmission (TEM) microscopy both in as-cast state and after each stage of thermal treatment, for AlMg1Si – both in as-cast state and after final thermal treatment. Coarse intermetallic particles were examined using SEM, while fine particles were examined using TEM. Besides, microhardness values were measured after various thermal treatment stages. It was found out, that coarse intermetallic compounds of Fe2Mg7Si10Al18 type are formed in both alloys during as-cast structure cooling down with such compounds partial dissolution during further thermal treatment. At the same time particles, that can be attributed either to (AlSi)3ScZr or to AlSc2Si2τ-phase, occur in inter-grain boundary of alloys with scandium-zirconium additions. No traces of scandium solid solution discontinuous decomposition have been identified during ingot cooling down. Thermal treatment during 8 h at 550 °C 8 and 8 h at 440 °C results in formation of the phase, which can represent both AlSc2Si2 and Al5SiZr2. At the same time nanoparticles (AlSi)3ScZr do not form during this thermal treatment stage. Heating to 500 °C during 30 min interval allows complete dissolution of magnesium in supersaturated aluminum solid solution. During the final stage β’’ particles (Mg5Si6), representing the major type, form in both alloys; in these conditions scandium does not produce significant effect on their formation.

Actinomycetota Amycolatopsis nalaikhensis sp. nov. and Amycolatopsis carbonis sp. nov., two novel actinobacteria with antimicrobial activity isolated from a coal mining site in Mongolia.

Two-novel filamentous actinobacteria designated strains 2-2T and 2-15T were isolated from soil of a coal mining site in Mongolia, and their taxonomic positions were determined using a polyphasic approach. Phylogenetic analyses based on 16S rRNA gene sequences showed that each of the strains formed a distinct clade within the genus Amycolatopsis. The 16S rRNA gene sequence similarity analysis showed that both strains were mostly related to Amycolatopsis rhabdoformis NCIMB 14900T with 99.0 and 99.4% sequence similarity, respectively. The genome-based comparison indicated that strain 2-2T shared the highest digital DNA-DNA hybridization value of 35.6% and average nucleotide identity value of 86.9% with Amycolatopsis pretoriensis DSM 44654T, and strain 2-15T shared the corresponding values of 36.5 and 87.9% with A. rhabdoformis NCIMB 14900T, all of which being well below the thresholds for species delineation. The chemotaxonomic properties of both strains were typical of the genus Amycolatopsis. In silico prediction of chemotaxonomic markers was also carried out, and the results were consistent with the chemotaxonomic profiles of the genus. Genome mining for secondary metabolite production in strains 2-2T and 2-15T revealed the presence of 29 and 24 biosynthetic gene clusters involved in the production of polyketide synthase, non-ribosomal peptide synthetase, ribosomally synthesized and post-translationally modified peptides, lanthipeptide, terpenes, siderophore, and a number of other unknown type compounds. Both strains showed broad antifungal activity against several filamentous fungi and also antibacterial activity against methicillin-resistant Staphylococcus aureus and Acinetobacter baumannii. The phenotypic, biochemical, and chemotaxonomic properties indicated that both strains could be clearly distinguished from other species of Amycolatopsis, and thus the names Amycolatopsis nalaikhensis sp. nov. (type strain, 2-2T=KCTC 29695T=JCM 30462T) and Amycolatopsis carbonis (type strain, 2-15T=KCTC 39525T=JCM 30563T) are proposed accordingly.

Generation and modulation of soliton molecules in an all-polarization-maintaining fiber laser mode-locked by NPE

In this paper, we report the experimental observation of multiple soliton molecule forms and modulation results in an all-polarization-maintaining (PM) linear fiber laser mode-locked by nonlinear polarization evolution (NPE). The relationship between the waveplate angle and the reflectivity profile of the structure is analyzed numerically. Experimentally, it was found that the soliton number inside the bound states decreases from 4 solitons to 1 soliton by reducing the pump power. The soliton separation and the spectral shape could be evolved by slightly rotating the angle of the half-wave plate or λ/8-wave plate respectively. In addition to the above soliton molecules with regular triangular autocorrelation envelopes, (2+1)-type and (1+2+1)-type compound bound states are also obtained, and the fine temporal structure inside these soliton complexes are obtained by numerical simulation. The investigated results enrich the nonlinear dynamics of femtosecond mode-locked fiber lasers and lay the foundation for the application of all-PM fiber lasers mode-locked by NPE.

Investigation of structural, dielectric, impedance, and conductivity properties of layered perovskite type compound; NaYSnO4

In this paper, the structural study of NaYSnO4 (NYSO), a layered perovskite ceramic oxide, was done using an X-ray diffractometer (XRD) to identify the phase and determine the composition of NYSO. The microscopic structure of the sample seen by Scanning Electron Microscopy (SEM) was found to be polycrystalline and a mixture of large and small grains, which indicate the anisotropic nature of the sample. A FTIR spectroscopic behaviour of the material was used to identify the formation of different bonds in the material, and the XPS study gives an idea of the binding energy of each element in NYSO. A thorough analysis of the impedance, dielectric constant, dielectric loss, modulus and AC conductivity properties concerning temperature and frequency displays the electronic device characteristics. The complex impedance spectra were studied at temperatures range between 25 and 500˚C and frequency of 100 Hz to 1 MHz range. Nyquist plots reveal the charge conduction mechanism of the grain and well-defined grain boundaries that correspond to the resistive and capacitive phenomena of the material. Furthermore, the activation energy has been estimated to investigate the charge transportation mechanism. This article concludes by discussing future possibilities and scientific challenges in NTCR thermistors using NYSO.

Enhanced electrochemical performances of ternary polypyrrole/MXene/Gum arabic composites as supercapacitors electrode materials

The development of supercapacitor electrodes for high energy storage applications requires the use of ternary composites made of PPy, Mxene, Gum Arabic (PPy/Mxene/GA) these materials are special because they have new characteristics like cyclic stability, and high specific capacitance. The pure PPy, PPy/Mxene and PPy/Mxene/Gum Arabic show the shifting and appearance of new peaks in UV-Visible spectra, which are further supported by the Fourier transform infrared spectroscopy (FT-IR). The appearance of new peaks in X-ray diffraction (XRD) of PPy confirms presence of Mxene and Gum Arabic, which is in agreement with the energy dispersive X-ray (EDX) analysis. The electrochemical techniques such as Cyclic Voltammetry (CV), Galvanostatic Charge Discharge (GCD) and Electrochemical Impedance Spectroscopy (EIS) show that the (PPy/Mxene/GA) ternary composite maintains 94 % of the specific capacitance retention after 2000 cycles and; reaches a maximum specific capacitance of 657.64 F/g at 1 A/g. As compared to Pure PPy and PPy/Mxene composite the PPy/Mxene/GA composite show small intrinsic resistance Rs and charge transfer Rct values 0.11Ω and 6.15Ω respectively. The outstanding electrochemical properties of PPy/Mxene/GA composite are ascribed to the blending of three different type compounds PPy, Mxene and GA and theirs mutual beneficial effects. These findings show that ternary composite material holds great promise for use in these condition involving portable electronic storage devices.

Comparison of 624-type Capillary Columns II

The present paper is the continuation of our "equivalent column" study. 624-type columns were investigated in a capillary gas chromatograph with a flame ionization detector (FID). In the preceding work, we used a homemade test mixture containing mainly acidic type compounds, which we complemented in the current study with additional basic test compounds to give a more precise description of the behaviour of the stationary phases. The columns had the same dimensions (30 m × 0.32 mm × 1.0 μm; length, internal diameter and film thickness, respectively) but were purchased from different manufacturers or the same manufacturer but from different batches. In addition, also their pre-life was different. These circumstances influence the condition of the stationary phase, and therefore their separation ability. These factors imply the necessity of testing the column from time to time. To distinguish between the separation ability of the columns, we compared the chromatograms, the retention times and retention order of the molecules, as well as peak asymmetry factors. Besides these parameters, quantitative determination is also performed based on the results of separation. We used the effective carbon number (ECN) and the limit of quantitation (LoQ) to demonstrate these differences which are caused by the different stationary phase conditions.

NH2(CH3)2CuCl3 Organic-Inorganic Hybrid Perovskite: Consideration to Crystal Structure, Thermodynamics, and Structural Molecular Dynamics.

The crystal structure of NH2(CH3)2CuCl3, an organic-inorganic hybrid perovskite, undergoes a phase transition from triclinic to monoclinic at the phase transition temperature T C of 287 K. We investigated the temperature dependencies of NMR chemical shifts and spin-lattice relaxation time T 1ρ to gain insights into the structural geometry and molecular dynamics during the transition from phase II to phase I at high temperatures. Analysis of the 1H and 13C NMR chemical shifts of the cation revealed a continuous change in the surrounding structural geometry with temperature, without any anomalous changes around T C. The sudden decrease in T 1ρ values from low to high temperatures indicated a significant variation in proton and carbon dynamics at T C, arising from the slowing motion of molecular dynamics across the phase transition. The activation energies E a obtained from the temperature dependence of T 1ρ for 1H and 13C were larger in phase I than in phase II. This suggests that molecular motions in phase II exhibit a higher degree of freedom compared to those in phase I, where they are more constrained. These findings on NH2(CH3)2CuCl3 are presented to enhance its potential applications by elucidating the crystal configuration and structural molecular dynamics of ABX3 type compound.

Preparation and Third‐Order Nonlinear Optical Properties of Novel Axial Fullerenol‐Substituted Phthalocyanines

AbstractThis research presents the optical limiting properties of a novel axially linked D‐A type compound, LaPc‐C60(OH)n, where lanthanide phthalocyanine serves as the donor and fullerenol as the acceptor. The incorporation of fullerenol expands the π‐conjugated system, decreases the aggregation of the phthalocyanine, and significantly increases the solubility of the compound. The establishment of this D‐A system promotes intramolecular electron transfer, effectively improving both the non‐linear optical (NLO) response and optical limiting properties. In addition, homogeneous poly(methyl methacrylate) (PMMA) composite films (LaPc‐C60(OH)n/PMMA) are prepared using a simple solution casting method. Compared to fullerenol or lanthanum phthalocyanine individually, LaPc‐C60(OH)n exhibited a superior NLO response both in solution and in the solid composite film. In particular, LaPc‐C60(OH)n/PMMA demonstrated an increase in the non‐linear absorption coefficient (2050 cm GW−1) and a larger third‐order magnetization (1.84 × 10−8 esu). In addition to exhibiting an excellent NLO response at 532 nm, LaPc‐C60(OH)n also shows significant NLO enhancement at 1064 nm, extending the limiting range into the near‐infrared region. This behavior is attributed to different nonlinear absorption mechanisms and the synergistic effect that arise from the photo‐induced electron transfer process between the fullerenol and LaPc.

Efficient Adsorption of Cr(VI) from Aqueous Solutions Using Composites Modified with Ni/Al LDH and Keggin Type Compounds

Efficient Adsorption of Cr(VI) from Aqueous Solutions Using Composites Modified with Ni/Al LDH and Keggin Type Compounds

How to chew gum: the post-ingestion fate of foliar secondary compounds consumed by a eucalypt herbivore

Herbivorous insects require mechanisms to deal with defence compounds produced by their host plants. Despite an array of secondary compounds associated with defence, eucalypts are hosts to many insect species that readily obtain nutrients also produced by these plants. Gonipterus weevils are foliage-feeding eucalypt specialists as larvae and adults, with a notable characteristic of protecting their eggs with a hardened frass-like substance. The aim of this study was to assess plant, weevil frass and egg capsule chemistry to determine how the weevil eliminates plant secondary metabolites. We hypothesised that noxious compounds would be metabolised prior to elimination and that egg capsules would be composed of frass and additional substances. Weevils were fed on Eucalyptus globulus plants for seven days, with their frass and egg capsules collected daily, and the damaged, first, fully-expanded leaves of the host collected at the end of the assay. Compounds present in each sample were extracted in hexane and analysed by gas chromatography-mass spectrometry. The most abundant compounds in each sample were waxes and terpenoids, and metabolism of 1,8-cineole was evident, with two metabolites that may have semiochemical activity. Comparative analysis revealed significant differences between all samples, with shared compounds varying in relative proportions and exclusive compounds in sample type. These findings contribute to the understanding of Gonipterus physiology and highlight the differences between frass and the cover of egg capsules.

Enhancement of electrochemical stability by molecular cation vacancies of the electrode material CH3NH3NiCl3 for lithium-ion batteries

At present, efforts are being made to find new low-cost materials for photovoltaic, optoelectronic and energy storage applications. In this regard, compounds of the halide perovskite type have been increasingly studied over the past few years. The incorporation of small cations in these compounds and their possible use in rechargeable batteries can be achieved by the electrochemical reversibility technique, where perovskites with large cations are used to obtain a new isostructural compound with smaller cations and large interstitial space or free vacancies for ionic transport. The present work studied the electrochemical reversibility of lithium-ion into CH3NH3NiCl3 (MANiCl3) active material, after the formation of MA+ vacancies or interstitial spaces, taking both experimental and theoretical approaches. The material displayed an anodic behavior and an initial capacity of discharge of ca. 170 mAhg−1 at 0.2C (0.1 mA), a full capacity retention up to the first 25 cycles of charge–discharge, and even reached a retention of up to 80 % of initial capacity at the 80th cycle. First-principles density functional theory calculations show that the shape of the crystal lattice and volume changes of all the different phases involved in the electrochemical process are tiny, at about 3 Å3 per cell. In addition, there are no appreciable elastic contributions to the energy variation during the de-lithiation/lithiation process, indicating that memory effects are not an issue. The calculated formation energies of the lithiated structures and the open circuit voltages are −2.91 eV and 1.33 V for LinMA1-nNiCl3 and −1.41 eV and 2.91 V for Li2nMA1-nNiCl3, respectively. These findings suggest that incorporating one or, at most, to two lithium atoms is favorable for the overall stability and electrochemical performance.

Physicochemical, sugar, and volatile profile characterization of blong song, bidens, coffee, and mint honeys originating from Vietnam

In this study, the pollen analysis, physicochemical and volatile profiles of blong song, bidens, coffee, and mint honeys from Vietnam were analyzed. The primary pollen content was 87.0%, 37.5%, 5.7%, and 2.7% in the blong song, coffee, bidens, and mint honey, respectively. The average values of the physicochemical properties ranged from 9.4 to 33.5 mS m−1 for electrical conductivity, from 9.5 to 19.7 meq kg−1 for free acidity, from <2 to 10.7 DN for diastase activity, from 0 to 44.7 mm Pfund for color, and from 2.9 to 39.2 mg kg−1 for 5-hydroxymethyl-2-furfural (5-HMF) showed statistically significant differences (p < 0.05) among the four types of honey. Principal component analysis (PCA) of sugars revealed that trehalose was typical for blong song honey; melibiose, sucrose, and maltose for bidens honey; and turanose for mint honey. Using headspace solid phase microextraction coupled with gas chromatography-mass spectrometry (HS-SPME/GC-MS) several specific volatile compounds for each honey type were identified: linalool oxide isomers for blong song honey, acetic acid phenylethyl ester for bidens honey, citral, nonanoic acid, α-terpineol, 1-nonanol, and benzeneacetaldehyde for coffee honey and menthol isomers, and isomethyl acetate for mint honey. The results provide comprehensive data on chemometrics, melissopalynological profiles, and volatile compounds analysis for the classification of honey with different floral origins from Vietnam.

Morphological and Chemical Diversity within Japanese Laurencia Complex (Rhodomelaceae, Ceramiales, Rhodophyta).

Seaweeds of the red algal genus Laurencia are distributed worldwide in tropical, subtropical to temperate zones, growing in Japan from Hokkaido to Okinawa. Laurencia is highly difficult to classify morphologically because of a high degree of morphological variation within individual species. Nevertheless, Laurencia investigation is favored by organic chemists as it produces uniquely structured compounds. Halogenated secondary metabolites are considered to be used as chemical markers for chemical systematics (chemotaxonomy) of this troublesome genus. As a "weedy seaweed", Laurencia is not effectively utilized, yet it produces a variety of metabolites and thus, holds good potential for containing compounds with specific activity, especially in aspects of secondary metabolites. In this review, we reported significant morphological features to distinguish species in this genus, and the morphological features, habitat, distribution, and chemical composition that help discriminate Japanese Laurencia species.

Antibacterial, antidiabetic and antioxidant bioevaluation of Calamus leptospadix Griff. and isolation of a flavan type compound

The plant based natural products have always been a rich source of bioactive molecules for drug discovery. The tender shoots of Calamus leptospadix Griff., an edible medicinal plant was extracted using methanol, water and ethanol as three different solvents to study the effect of the extracting solvents and temperature on their antioxidant, antidiabetic and antibacterial properties and total phenolic and flavonoid contents. The antioxidant properties were determined by the 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid (ABTS) and ferric reducing antioxidant power (FRAP) assay. The α-glucosidase inhibitory assay was carried out to determine the antidiabetic potential. The antibacterial properties of the extracts were determined against four strains of bacterial species viz. Bacillus subtilis, Streptococcus pneumoniae, Escherichia coli and Citrobacter freundii using Broth macro dilution method.The methanolic extracts of the plant were found to possess the highest total phenolic and total flavonoid contents. In the antioxidant assays, the cold methanolic extract was found to exhibit the highest DDPH radical scavenging activity and ferric-reducing antioxidant power. In the antidiabetic assay, the extract exhibited better α-glucosidase inhibitory potential than that of the positive control acarbose. It was also found to be effective against both gram-positive and gram-negative strains in the antibacterial assay. A flavan-type compound 4-(5,7-dimethoxychroman-2-yl)phenol was isolated from the most bioactive cold methanolic extract of the plant and characterised from its XRD, 1H and 13C NMR, HRMS and IR data.

Utilizing nutrient type compounds as anti-bacterial compounds: arginine and cysteine inhibit Salmonella survival in egg white.

Because of growing levels of antibiotic resistance, new methods to combat bacteria are needed. We hypothesized that because bacteria evolved to survive in specific environments, the addition of compounds, including nutrient type compounds, to an environment, might result in a modification of that environment that will disrupt bacterial growth or in maladaptive bacterial behavior, i.e., gene expression. As a proof of concept, we focused on the egg white environment and the pathogen Salmonella. Despite egg white's antibacterial nature, Salmonella is able to survive and grow in egg white, and this ability of Salmonella leads to infection of chicks and humans. Here, the 20L-amino-acids were screened for their ability to affect the growth of Salmonella in egg white. L-arginine and L-cysteine were found to reduce growth in egg white in physiologically relevant concentrations. To determine the mechanism behind L-arginine inhibition TnSeq was utilized. TnSeq identified many Salmonella genes required for survival in egg white including genes required for iron import, biotin synthesis, stress responses, cell integrity, and DNA repair. However, a comparison of Salmonella in egg white with and without L-arginine identified only a few differences in the frequency of transposon insertions, including the possible contribution of perturbations in the cell envelope to the inhibition mechanism. Finally, both D-arginine and D-cysteine were found to inhibit Salmonella in egg white. This implied that the effect of arginine and cysteine in egg white is chemical rather than biological, likely on the egg white environment or on the bacterial outer membrane. To conclude, these results show that this approach of addition of compounds, including nutrient type compounds, to an environment can be used to limit bacterial growth. Importantly, these compounds have no inherent anti-bacterial properties, are used as nutrients by animals and bacteria, and only become anti-bacterial in a specific environmental context. Future research screening for the effects of compounds in relevant environments might uncover new ways to reduce pathogen levels in the poultry industry and beyond.