Presence Of Tryptophan Research Articles

Conformational Transitions in Yeast Chorismate Mutase Important for Allosteric Regulation as Identified by Nuclear Magnetic Resonance Spectroscopy

Proteins fluctuate between different conformations in solution, and these conformational fluctuations can be important for protein function and allosteric regulation. The chorismate mutase from Saccharomyces cerevisiae (ScCM), a key enzyme in the biosynthesis of aromatic amino acids, is allosterically activated and inhibited by tryptophan and tyrosine, respectively. It was initially proposed that in the absence of effector, ScCM fluctuates between activated R and inhibited T conformations according to the Monod-Wyman-Changeux (MWC) model, although a more complex regulation pattern was later suggested by mutagenesis and kinetic data. Here we used NMR relaxation dispersion experiments to understand the conformational fluctuations on the microsecond-to-millisecond timescale that occur in ScCM. In the absence of allosteric effectors, ScCM did not exclusively exchange between T and R conformations, suggesting that the two-state MWC model is insufficient to explain conformational dynamics. Addition of tyrosine led to the quenching of much of the motion on this timescale, while new motions were identified in the presence of tryptophan. These new motions are consistent with conformational fluctuations into an alternative conformation that may be important for enzyme activity.

A new endophytic fungus CJAN1179 isolated from the Cholistan desert promotes lateral root growth in Arabidopsis and produces IAA through tryptophan-dependent pathway

Fungi, important for growth of plants in arid lands, are expected to be involved in novel biochemical activities during fungal–plant interactions. We isolated 150 fungi associated with rhizosphere and root endosphere of two perennial grasses, Cymbopogon jwarancusa and Panicum antidotale, from Cholistan desert. The isolates were screened for their impact on plant growth and development using Arabidopsis thaliana (Col-0) as a model system. A root-endophytic fungus CJAN1179 from C. jwarancusa showed the highest plant growth-promoting effects. The most remarkable was enhanced number of lateral roots (3.1-fold). CJAN1179 produced indole-3-acetic acid (IAA) particularly in the presence of tryptophan. ITS sequence and phylogenetic analysis characterisation suggested the fungus to be a new species within Sordariomycetidae. CJAN1179 appears to promote plant growth by secreting IAA using tryptophan as a precursor. This fungus can be further explored for its suitability to promote growth of commercially important crops, particularly in arid regions.

Native Rhizospheric and Endophytic Fungi as Sustainable Sources of Plant Growth Promoting Traits to Improve Wheat Growth under Low Nitrogen Input.

Wheat crops require effective nitrogen fertilization to produce high yields. Only half of chemical N2 fertilizers are absorbed into plants while the rest remains in the soil, causing environmental problems. Fungi could maximize nitrogen absorption, and from an environmental and biodiversity point of view, there is an urgent necessity for bioprospecting native fungi associated with wild plants growing in harsh environments, e.g., St. Katherine Protectorate (SKP) in the arid Sinai. Recovered taxa, either endophytic and/or rhizospheric, were screened for their plant growth-promoting (PGP) traits. Eighteen fungal isolates (15 rhizospheric and 3 endophytic) belonging to anamorphic ascomycetes were recovered from 9 different wild plants, and their PGP traits (indole-3-acetic acid [IAA] production, phosphate solubilization, siderophore production, and hydrolytic enzyme production) were measured. Rhizospheric isolate NGB-WS14 (Chaetosphaeronema achilleae) produced high levels of IAA (119.1 μg mL−1) in the presence of tryptophan, while NGB-WS 8 (Acrophialophora levis) produced high IAA levels (42.4 μg mL−1) in the absence of tryptophan. The highest phosphate-solubilizing activity (181.9 μg mL−1) was recorded by NGB-WFS2 (Penicillium chrysogenum). Endophytic isolate NGB-WFE16 (Fusarium petersiae) exhibited a high percentage level of Siderophore Unit (96.5% SU). All isolates showed variability in the secretion of extracellular hydrolytic enzymes. Remarkably, all isolates had antagonistic activity (55.6% to 87.3% suppression of pathogen growth) against the pathogenic taxon Alternaria alternata (SCUF00001378) in the dual-assay results. Out of the 18 isolates, 4 rhizospheric and 1 endophytic isolate showed significant increases in shoot dry weight and shoot nitrogen and chlorophyll content of wheat plants subjected to low inputs of chemical nitrogen (N) fertilizers (50% reduction) compared with the non-inoculated control in a pot experiment. Potent taxa were subjected to sequencing for molecular confirmation of phenotypic identification. The retrieved ITS sequences in this study have been deposited in GenBank under accession numbers from LC642736 to LC642740. This study considered the first report of endophytic fungi of Cheilanthes vellea, a wild plant with PGPF which improves wheat growth. These results recommend using PGPF as inoculants to alleviate low nitrogen fertilization.

Surface Modification of Cu Nanoparticles Coated Commercial Titanium in the Presence of Tryptophan: Comprehensive Electrochemical and Spectroscopic Investigations

Surface Modification of Cu Nanoparticles Coated Commercial Titanium in the Presence of Tryptophan: Comprehensive Electrochemical and Spectroscopic Investigations

Tryptophan Ameliorates Barrier Integrity and Alleviates the Inflammatory Response to Enterotoxigenic Escherichia coli K88 Through the CaSR/Rac1/PLC-γ1 Signaling Pathway in Porcine Intestinal Epithelial Cells.

BackgroundImpaired intestinal barrier integrity plays a crucial role in the development of many diseases such as obesity, inflammatory bowel disease, and type 2 diabetes. Thus, protecting the intestinal barrier from pathological disruption is of great significance. Tryptophan can increase gut barrier integrity, enhance intestinal absorption, and decrease intestinal inflammation. However, the mechanism of tryptophan in decreasing intestinal barrier damage and inflammatory response remains largely unknown. The objective of this study was to test the hypothesis that tryptophan can enhance intestinal epithelial barrier integrity and decrease inflammatory response mediated by the calcium-sensing receptor (CaSR)/Ras-related C3 botulinum toxin substrate 1 (Rac1)/phospholipase Cγ1 (PLC-γ1) signaling pathway.MethodsIPEC-J2 cells were treated with or without enterotoxigenic Escherichia coli (ETEC) K88 in the absence or presence of tryptophan, CaSR inhibitor (NPS-2143), wild-type CaSR overexpression (pcDNA3.1-CaSR-WT), Rac1-siRNA, and PLC-γ1-siRNA.ResultsThe results showed that ETEC K88 decreased the protein concentration of occludin, zonula occludens-1 (ZO-1), claudin-1, CaSR, total Rac1, Rho family member 1 of porcine GTP-binding protein (GTP-rac1), phosphorylated phospholipase Cγ1 (p-PLC-γ1), and inositol triphosphate (IP3); suppressed the transepithelial electrical resistance (TEER); and enhanced the permeability of FITC-dextran compared with the control group. Compared with the control group, 0.7 mM tryptophan increased the protein concentration of CaSR, total Rac1, GTP-rac1, p-PLC-γ1, ZO-1, claudin-1, occludin, and IP3; elevated the TEER; and decreased the permeability of FITC-dextran and contents of interleukin-8 (IL-8) and TNF-α. However, 0.7 mM tryptophan+ETEC K88 reversed the effects induced by 0.7 mM tryptophan alone. Rac1-siRNA+tryptophan+ETEC K88 or PLC-γ1-siRNA+tryptophan+ETEC K88 reduced the TEER, increased the permeability of FITC-dextran, and improved the contents of IL-8 and TNF-α compared with tryptophan+ETEC K88. NPS2143+tryptophan+ETEC K88 decreased the TEER and the protein concentration of CaSR, total Rac1, GTP-rac1, p-PLC-γ1, ZO-1, claudin-1, occludin, and IP3; increased the permeability of FITC-dextran; and improved the contents of IL-8 and TNF-α compared with tryptophan+ETEC K88. pcDNA3.1-CaSR-WT+Rac1-siRNA+ETEC K88 and pcDNA3.1-CaSR-WT+PLC-γ1-siRNA+ETEC K88 decreased the TEER and enhanced the permeability in porcine intestine epithelial cells compared with pcDNA3.1-CaSR-WT+ETEC K88.ConclusionTryptophan can improve intestinal epithelial barrier integrity and decrease inflammatory response through the CaSR/Rac1/PLC-γ1 signaling pathway.

Bacillus siamensis CNE6- a multifaceted plant growth promoting endophyte of Cicer arietinum L. having broad spectrum antifungal activities and host colonizing potential

Exploration of endophytic bacteria with multiple plant growth promoting (PGP) attributes is considered as an eco-friendly and cost-effective alternative to agricultural chemicals for increasing crop productivity. In the present endeavor, healthy chickpea plants (Cicer arietinum L.) collected from district Birbhum, West Bengal, India were subjected for the isolation of endophytic bacteria having multifarious PGP properties. One potent endophytic Gram positive bacterial strain CNE6 was isolated from the nodule of chickpea and was identified as Bacillus siamensis based on 16S rDNA sequence homologies. The isolate showed a number of PGP properties like phosphate solubilization, IAA production, nitrogen fixation, hydroxamate type of siderophore production and ACC deaminase activities. The isolate CNE6 produced 33.27 ± 2.16 μg/mL of IAA in the presence of tryptophan. Production of IAA was also confirmed by HPLC analysis and it was found effective for inducing lateral root branching in chickpea. In addition, the isolate displayed significant antagonistic activity against a number of plant pathogenic fungi when tested by dual culture overlay and agar well diffusion assay. 50 % cell free supernatant of CNE6 was found effective for 60–80 % inhibition of radial growth of pathogenic fungi tested. Scanning electron microscopic observation revealed massive degradation of pathogenic fungal mycelia by the antifungal metabolites of CNE6. LC–MS analysis of bacterial lipopeptides suggested the production of antifungal antibiotics like surfactin, fengycin and iturin by the isolate. The presence of genes encoding antifungal lipopeptides was also confirmed by PCR amplification using specific primers. Green fluorescent protein (GFP) tagging of CNE6 using broad host range plasmid vector (pDSK-GFPuv) followed by colonization study indicated very good host colonization potential of the isolate and its probable movement through xylem vessels. Enhanced shoot and root length and chlorophyll content upon treatment with CNE6 as observed in in vivo pot experiments also supported the positive role of the endophytic isolate on overall development and growth of the chickpea plants. This is the first report of Bacillus siamensis as an endophyte of Cicer arietinum L. which can be successfully applied for improving the productivity of this crop plant.

Oryzicola mucosus gen. nov., sp. nov., a novel slime producing bacterium belonging to the family Phyllobacteriaceae isolated from the rhizosphere of rice plants.

A novel Gram-stain negative, asporogenous, slimy, rod-shaped, non-motile bacterium ROOL2T was isolated from the root samples collected from a rice field located in Ilsan, South Korea. Phylogenetic analysis of the 16S rRNA sequence showed 96.5% similarity to Tianweitania sediminis Z8T followed by species of genera Mesorhizobium (96.4-95.6%), Aquabacterium (95.9-95.7%), Rhizobium (95.8%) and Ochrobactrum (95.6%). Strain ROOL2T grew optimally at 30°C in the presence of 1-6% (w/v) NaCl and at pH 7.5. The major respiratory quinone was ubiquinone-10 and the major cellular fatty acids were C18:1ω7c, summed feature 4 (comprising iso-C17:1 I and/or anteiso-C17:1 B) and summed feature 8 (comprising C18:1ω6c and/or C18:1ω7c). The polar lipid profile consisted of diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylcholine, phosphatidylmethylethanolamine, phosphatidylglycerol, one unidentified aminolipid and two unidentified lipids. The assembled draft genome of strain ROOL2T had 28 contigs with N50 value of 656,326 nt, total length of 4,894,583bp and a DNA G + C content of 61.5%. The average amino acid identity (AAI) values of strain ROOL2T against the genomes of related members belonging to the same family were below 68% and the ANI and dDDH values between the strain ROOL2T and the type strains of phylogenetically related species were 61.8-76.3% and 19.4-21.1%, respectively. Strain ROOL2T only produces carotenoid-type pigment when grown on LB agar and slime on R2A agar. In the presence of tryptophan, strain ROOL2T produced indole acetic acid (IAA), a phytohormone in plant growth and development. Gene clusters for indole-3-glycerol phosphatase and tryptophan synthase were found in the genome of strain ROOL2T. The genotypic and phenotypic characteristics indicated that strain ROOL2T represents a novel genus belonging the family Phyllobacteriaceae, for which the name Oryzicola mucosusgen. nov., sp. nov. is proposed. The type strain is ROOL2T (KCTC 82711T = NBRC 114717T).

Tryptophan as a Safe Compound in Topical Ophthalmic Medications: In Vitro and In Vivo Studies

ABSTRACT Background To evaluate the effects of tryptophan (TRP) on normal human corneal and conjunctival epithelium in vitro and the re-epithelization of corneal erosion in rabbits. Materials and methods Corneal epithelial cell (10.014 pRSV-T) and conjunctival epithelial cell (HC0597) cultures were used. The cellular metabolism, viability, secretion of IL-1β, IL-6, IL-10, cytoskeleton organization, transwell migration were determined. Cells were incubated in the presence of TRP at 1–100 μM. After corneal de-epithelization rabbits received TRP drops (100 μM), 5 times a day. Results TRP increased conjunctival epithelium metabolism at 50 μM and increased the viability of corneal epithelium at 100 μM. TRP (10 μM) enhanced the production of IL-6 by the corneal epithelium and had no effect on IL-1β and IL-10. Conclusions TRP had no influence on the cellular cytoskeleton but induced a significant pseudopodia projection in both epithelia. TRP did not influence corneal re-epithelization in vivo. TRP was not toxic for corneal and conjunctival epithelia.

Application of a Modified Carbon Paste Electrode Using Core–Shell Magnetic Nanoparticle and Modifier for Simultaneous Determination of Norepinephrine, Acetaminophen and Tryptophan

The current study was conducted to synthesize 2-(4-ferrocenyl-[1,2,3]triazol-1-yl)-1-(naphthalen-2-yl) ethanone (2FTNE) as a mediator and magnetic core–shell manganese ferrite nanoparticles (CMNP) as a nanoparticle for construction of a modified carbon paste electrode (CPE). The electrochemical behavior of norepinephrine (NEP) was assessed using cyclic voltammetry and its determination was done by using differential pulse voltammetry (DPV) in the presence of tryptophan (TRP) and acetaminophen (AC). The 2FTNECMNP-modified CPE (2FTNECMNPPE) in comparison with bare CPE and CMNP modified CPE exhibited high electro-catalytic activity to the NEP oxidation. Linearity of the oxidation peak current with concentration of NEP was maintained between 0.075–60 μM (R2 = 0.9995). Limit of detection for NEP was obtained 0.016 μM on the basis of three times of standard deviation (3Sb) of blank. High selectivity, proper stability and suitable reproducibility are some advantages of the 2FTNECMNPPE that was successful in the measurement of NEP, AC and TRP in NEP ampoule, acetaminophen tablet and urine samples.

An indigo-producing plant, Polygonum tinctorium, possesses a flavin-containing monooxygenase capable of oxidizing indole

Polygonum tinctorium (P. tinctorium) is an indigo plant that is cultivated for a specific metabolite that it produces i.e., indoxyl β-D-glucoside (indican). In this study, flavin-containing monooxygenase (PtFMO) from P. tinctorium was cloned. When recombinant PtFMO was expressed in E. coli in the presence of tryptophan, indigo production was observed. Furthermore, we measured the activity of PtFMO using the membrane fraction from E. coli and found that it could produce indigo using indole as a substrate. The co-expression of PtFMO with indoxyl β-D-glucoside synthase (PtIGS), which catalyzes the glucosylation of indoxyl, brought about the formation of indican in E. coli. The results showed that indican was synthesized by sequential reactions of PtFMO and PtIGS. In three-week-old P. tinctorium specimens, the first leaves demonstrated higher levels of PtFMO expression than the subsequent leaves. This result coincided with that of our prior study on PtIGS expression level.Our study provides evidence that PtFMO might contribute to indican biosynthesis.

Induction of Auxins Synthesis by Rhodococcus erythropolis IMV Ac-5017 with the Addition of Tryptophan to the Cultivation Medium

The ability of surfactant producers to synthesize phytohormones expands the scope of their practical application and provides prospects for the development of microbial preparations with growth-stimulating properties. The possibility to intensify the phytohormone-stimulants synthesis by bacterial strains increases the efficiency of such preparations. Aim. The aim is to research the possibility of extracellular auxin synthesis induction in the presence of tryptophan in the cultivation medium of surfactant producer Rhodococcus erythropolis IMV Ac-5017 and establish the optimal concentration of tryptophan and time of introduction into the medium to ensure maximum synthesis of auxins. Methods. Biochemical, microbiological, biotechnological. Cultivation was performed in the liquid mineral medium using ethanol and waste sunflower oil as substrates. Tryptophan was added to the medium as a 1% solution in an amount of 200 or 300 mg/l at the beginning of the cultivation process or at the end of the exponential growth phase. Phytohormones were isolated by triple extraction with organic solvents from the culture broth supernatant after surfactant extraction. Preliminary purification and concentration of phytohormones was performed by thin layer chromatography. Qualitative and quantitative determination of auxins was performed using high performance liquid chromatography. Results. It was found that regardless of the concentration and time of tryptophan introduction to the culture medium of R. erythropolis IMV Ac-5017 with both substrates, a significant increase (by two to three orders of magnitude) was observed in the amount of synthesized auxins compared to tryptophan-free medium. The highest concentration of auxins (5552–5634 μg/l) was achieved by adding 300 mg/l of tryptophan into the culture medium of R. erythropolis IMV Ac-5017 with ethanol, while without the precursor their amount was only 143 μg/l. In contrast to the cultivation of the strain on culture medium with ethanol, where the synthesis of auxins did not depend on the time of tryptophan introduction, R. erythropolis IMV Ac-5017 formed the maximum amount of auxins when 300 mg/l tryptophan was added to the culture medium with waste oil at the end of the exponential growth phase (2398 μg/l compared to 9.8 μg/l on the medium without tryptophan). As auxin compounds were identified: indole-3-acetic acid, indole-3-carboxylic acid and indole-3-butyric acid. However, the highest amount of indole-3-acetic acid was synthesized, the precursor of which is tryptophan. The synthesis of this auxin (the most common plant auxin) in the presence of 300 mg/l of tryptophan increased more than 40 times on ethanol medium and more than 700 times on medium with waste oil. Induction of auxin synthesis by strain R. erythropolis IMV Ac-5017 correlated with the activity of tryptophan transaminase: when cultured on ethanol without tryptophan, it was 138 nmol·min-1·mg-1 of protein, while cultured in the presence of precursor it was increased by 5.2 times (up to 714 nmol·min-1·mg-1 of protein). The obtained results suggest that indole-3-acetic acid biosynthesis by the strain IMV Ac-5017 occurs due to the formation of indole-3-pyruvate. Conclusions. Thus, it was established the possibility of increasing by two or three orders the amount of synthesized auxins in the case of low concentrations of tryptophan introducing to the culture medium of R. erythropolis IMV Ac-5017 not only with ethanol but also with industrial waste (waste oil). The obtained results can be considered as promising for use of exometabolites of R. erythropolis IMV Ac-5017 with growth-stimulating properties in crop production.

Highly sensitive platform utilizing poly(l-methionine) layered carbon nanotube paste sensor for the determination of voltaren

The contemporary study describes the poly(l-methionine) modified carbon nanotube based platform for the enhanced sensitive determination of Voltaren (VTN). The quantitative assessment of this clinically and environmentally important anti-inflammatory drug is of great concern. The distinct voltammetric approaches namely cyclic voltammetry and differential pulse voltammetry were functionalized for the electrochemical investigation of VTN in the solution of phosphate buffer having pH 7.0. The surface features of the proposed electrodes were consummated by Field emission scanning electron microscopy (FE-SEM) and Electron impedance spectroscopy (EIS) data. The fabricated electrode demonstrates enhanced electro-catalytic behaviour towards the redox response of VTN with the diminution of over potential as equated to unmodified electrode. The proposed electrode was successfully used for the selective determination of VTN in the presence of Tryptophan (TRP). The various parameters feigning the enhancement in analytical signal such as number of polymerization cycles, preconcentration time, sweep rate, electrolyte pH were also studied. Under the optimum experimental circumstances VTN presents a linearity in the concentration range of 2 μM to 50 μM and the detection limit was evaluated to be 0.10 μM. The pertinence of the constructed electrode was examined by the analysis of VTN in pharmaceutical formulation.

Effects of electrolytes and fractionated dissolved organic matter on selective adsorption of pharmaceuticals on terephthalic acid-based metal-organic frameworks

In this study, we investigated the synergetic effects of coexisting electrolytes and dissolved organic matter (DOM) on Carbamazepine (CBZ) and Ciprofloxacin (CIP) adsorption on the 1D flexible structure of MIL-53(Al) and 3D rigid structure of UiO-66(Zr). The effects of electrolytes on the adsorption of CBZ and CIP on 1D flexible framework of MIL-53(Al) were more significant than those observed from the 3D framework of UiO-66(Zr). The presence of sulfate, nitrate, and phosphate anions indicates high potential to promote the adsorption of CBZ and CIP onto MIL-53(Al) and UiO-66(Zr) because of the decrease of solubility and strengthening of electrostatic interactions by substitution of oxo-anions at the metal complex node via covalent bonding. The lower hydration energy of the potassium ion enhanced CBZ adsorption on MIL-53(Al), while the higher hydration energy of calcium and magnesium ions reduced the adsorption capacity of CBZ and CIP on MIL-53(Al) and UiO-66(Zr). CBZ interacted with fractionated humic acid better than CIP. High-density carboxylic and aromatic functional groups on humic acid ensured that only humic acid larger than 1KDa was adsorbed by MIL-53(Al). Tryptophan-like and humic acid-like DOM were both detected in real hospital effluent, and their effects on CIP and CBZ adsorption onto MIL-53(Al) were investigated. The presence of tryptophan did not affect CBZ adsorption on MIL-53(Al) (except when coexisting with calcium ions). Conversely, tryptophan interfered with CIP adsorption. The presence of humic acid lower than 1KDa promoted the adsorption of CBZ and CIP by increasing the breathing effect of MIL-53(Al)'s 1D flexible framework. The presence of humic acid with molecular size greater than 1KDa enhanced both CBZ and CIP adsorption via a multilayer adsorption mechanism.

Exemplifying rhizobacteria for growth stimulation and disease suppression in finger millet

Of 111 rhizobacteria isolated from finger millet, 30 isolates exhibiting antagonism against Pyricularia grisea (22.22–44.44%) and Rhizoctonia solani (22.22–38.89%) were selected for functional characterization and in vitro interaction with pathogens. Appraisal of rhizobacteria for antimetabolites revealed HCN production by 3, ammonia production by all (0.80–4.39 µmol/ml) and H2S production by 5 isolates, while all produced siderophore (25.89–93.96%), 20 salicylic acid (3.12–54.46 µg/ml), 19 tested positive for glucanase, 17 for protease and 12 for amylase production. Culture filtrate of all the isolates inhibited growth of Rhizoctonia solani (23.33–81.11%) and Pyricularia grisea (19.35–53.22%). Role of thermostable metabolites in antagonism was observed with 21 isolates against Rhizoctonia solani (11.11–50.0%) and 24 against Pyricularia grisea (8.33–46.66%). Volatile antimetabolites of all the isolates retarded and inhibited growth of Pyricularia grisea (5.88–84.71%) and Rhizoctonia solani (5.5–83.33%), besides affecting mycelial quality and sclerotiation in Rhizoctonia solani. Metabolic extracts of 9 antagonists in ethyl acetate restricted the growth of Pyricularia grisea (8.88–20.80%) and of 10 inhibited Rhizoctonia solani (10.12–23.30%). Enlightening the involvement of bacterial growth regulators in plant growth stimulation, all isolates tested positive for IAA production (1.9–28.8 µg/ml in absence and 9.9–45.7 µg/ml in presence of tryptophan), 19 secreted ACC deaminase and 19 solubilized phosphate, while only 5 exhibited Zn-solubilization potential. Increase in plant height, root length, their fresh weight and chlorophyll content was recorded with seed priming under glasshouse condition.

Structural, compositional and spectral investigation of prawn exoskeleton nanocomposite: UV protection from mycosporine-like amino acids

The present work explores the use of marine resourced prawn exoskeleton/shell as a new class of naturally occurring composite containing UV absorbing proteins. Mycosporine-like amino acids with a central aromatic ring in the exoskeleton/shell of naturally occurring prawns (Fenneropenaeus Indicus) offer excellent UV protection. The architecture of shell composite constitutes a matrix of chitin-proteins with distinct reinforcements such as spherical calcites (CaCO3), microscopic proteins, and traces of hydroxides/oxides of magnesium. The presence of tryptophan, phenylalanine, and tyrosine, forming the basic building blocks of mycosporines, is confirmed by structural, compositional, and microscopic studies on prawn shells. The UV spectroscopic signatures at 290 and 320 nm provides strong evidence for the highest UV absorption. UV absorption attributes to the presence of mycosporine-like amino acids. Hence, the current exploration of naturally occurring prawn shells directs towards an additive-free sunscreen filter without the generation of detrimental free radicals.

IAA production of indigenous isolate of plant growth promoting rhizobacteria in the presence of tryptophan

The plant growth-promoting rhizobacteria (PGPRBs) is an interesting way to promote increased vegetable production. Here, we aimed to isolate, identify, and characterize PGPRBs by using biochemical tests, sequencing of 16S ribossomal DNA, in vitro and screening for indoleacetic acid production. The isolates were identified through VITEK® 2 Compact equipment, which is an automated system. We identified microorganisms such as Alcaligenes faecalis sp. faecalis, Pseudomonas putida, Proteus vulgaris, Providencia rettgeri, Serratia marcescens e Myroides sp. by performing vitek 2 biochemical tests. The analysis of sequencing data for 16S ribossomal DNA of the isolated bacteria showed presence of A. faecalis, Myroides sp., P. putida, P. vulgaris, Providencia sp. and Serratia sp. The in vitro screening of all isolated bacteria showed production of indoleacetic acid under presence of tryptophan, highlighting that higher concentrations were produced by Providencia sp. and Myroides sp. The rhizobacteria studied here have shown the potential to be used in the development of new products for plant growth-promoting.

A Simple Spectrophotometric Method for Determination of Glyoxylic Acid in Its Synthesis Mixture.

A new simple and reliable spectrophotometric method is described to determine glyoxylic acid in its synthesis reaction mixture containing oxalic acid, glycolic acid, acetic acid, glyoxal, and ethylene glycol by means of a modified Hopkins–Cole reaction between glyoxylic acid and tryptophan in presence of ferric chloride and concentrated sulphuric acid. The linear range of glyoxylic acid concentration is 0–0.028 M. The limits of detection (LOD) and quantitation (LOQ) are 0.0019 M and 0.00577 M, respectively. The LOD, LOQ, standard deviation, relative standard deviation, and recovery ratio of the proposed method are comparable with a selected HPLC reference method. Both methods displayed same precision and credibility. Reaction stoichiometry between tryptophan and glyoxylic acid is assumed to be 2 : 3. Reaction mechanism has been postulated based on identified molar ratios of reactants. Glyoxal gave a negative test with tryptophan although it is a dialdehyde.

Electrochemical Sensing of Levodopa in Presence of Tryptophan Using Modified Graphite Screen Printed Electrode with Magnetic Core-Shell Fe3O4@SiO2/GR Nanocomposite

In the present paper, Fe3O4@SiO2/GO nanocomposite was synthesized and used to modify a graphite screen-printed electrode. This modified electrode was used to determine levodopa in the presence of tryptophan. Differential pulse voltammetry data showed that the obtained anodic peak currents were linearly dependent on levodopa concentrations in a range of 0.5–800.0 µM, with the detection limit of 0.09 µM. This novel sensor has several advantages such as rapid response, high stability, reproducibility, and high sensitivity. In addition, this proposed sensor was used to determine levodopa and tryptophan in human blood serum and urine samples.

Sulfur and nitrogen co-doped graphene quantum dot-assisted chemiluminescence for sensitive detection of tryptophan and mercury (II).

A simple one-step thermal treatment to prepare strong fluorescent sulfur and nitrogen co-doped graphene quantum dots (SN-GQD) using citric acid and l-cysteine as precursors was developed. The ultra-weak chemiluminescence (CL) from the reaction of hydrogen peroxide (H2 O2 ) and periodate (IO4 - ) was significantly enhanced by SN-GQD in acidic medium. The enhanced CL was induced by excited-state SN-GQD (SN-GQD*), which was produced from the transfer energy of (O2 )2 * and 1 O2 to SN-GQD and recombination of oxidant-injected holes and electrons in SN-GQD. In the presence of tryptophan (Trp), the CL intensity of the SN-GQD-H2 O2 -KIO4 system was greatly diminished. This finding was used to design a novel method for determination of Trp in the linear range 0.6-20.0 μM, with a limit of detection (LOD) of 58.0 nM. Furthermore, Hg2+ was detectable in the range 0.1-9.0 μM with a LOD of 64.0 nM, based on its marked enhancement of the SN-GQD-H2 O2 -KIO4 CL system. The proposed method was successfully applied to detect Trp in milk and human plasma samples and Hg2+ in drinking water samples, with recoveries in the range 95.7-107.0%.

An Innovative Design of an Efficient Layered Electrochemical Sensor for Determination of Tyrosine and Tryptophan in the Presence of Interfering Compounds in Biological Fluids

The aromatic amino acids tyrosine (TY) and tryptophan (TP) are important as precursors of catecholamines and 5-hydroxytryptamine. An innovative strategy was proposed in preparation of a novel layered sensor based on layer-by-layer modification of a glassy carbon electrode surface (GC) with graphene (RGO), ionic liquid crystal (ILC), multi-walled carbon nanotubes (CNT) and Fe–Zn nano-alloy (GC/RGO/ILC/CNT/Fe–Zn). The conductive layered electrode offered good sensitivities and low detection limit values for determination of tyrosine (TY) and tryptophan (TP) due to the synergistic impact of its components. A major problem expected during electrochemical assays of TY or TP in human biological fluids is overlap of their current responses with ascorbic acid (AA) and uric acid (UA) compounds when using the unmodified electrodes. Thus, the proposed sensor resolved this problem and exhibited excellent electrocatalytic activity towards determination of TY or TP in presence of AA and UA in human serum with low detection limit values 5.1 nM, 86 nM, 2.6 nM for TY, AA and UA and 3.8 nM, 91 nM, 2.9 nM for TP, AA and UA, respectively. Moreover, the proposed sensor displayed good sensitivity towards simultaneous determination of dopamine (DA) and serotonin (ST) with TY or TP. Recovery tests of TY and TP compounds were successful.