Thioglycolic Acid Research Articles

Modification of sodium aluminum silicate hydrate by thioglycolic acid as a new composite capable of removing and preconcentrating Pb(II), Cu(II), and Zn(II) ions from food and water samples

In this paper, sodium aluminum silicate hydrate was synthesized using rice husk as a silicon source and scrap aluminum cans as an aluminum source. Afterward, with the aid of microwave heating, a composite of sodium aluminum silicate hydrate and (3-aminopropyl)trimethoxysilane was facilely synthesized then modified by thioglycolic acid to produce a new composite. Besides, characterization of the synthesized composite was carried out using XRD, FT-IR, TEM, CHN elemental analyzer, nitrogen gas sorption analyzer, and SEM. The XRD pattern of the produced composite shows that there is a halo at 2θ = 25.0°, which means that there is a crystalline structure that is combined with an amorphous background. The SEM and TEM studies indicate that the synthesized composite has a structure similar to cotton. The synthesized composite was utilized for the efficient removal and preconcentration of Pb(II), Cu(II), and Zn(II) ions from food and water samples prior to determination by flame atomic absorption spectrometry. The produced composite has a maximum adsorption capacity of 185.53, 168.92, and 125.94 mg/g for Pb(II), Cu(II), and Zn(II) ions, respectively. The recovery findings demonstrate that the process is accurate, adaptable, and resulted in quantitative separation (greater than95 percent). Furthermore, the % RSD was less than 3.5 percent, indicating good reproducibility. The Langmuir isotherm and pseudo-second-order model fit the experimental results well. The thermodynamic studies established that the adsorption process is spontaneous, chemical, and exothermic. The produced composite was successfully regenerated and used multiple times to remove the metal ions under investigation from aqueous solutions.

Glutathione-Hemin/Hematin Adduct Formation to Disintegrate Cytotoxic Oxidant Hemin/Hematin in Human K562 Cells and Red Blood Cells' Hemolysates: Impact of Glutathione on the Hemolytic Disorders and Homeostasis.

Hemin, an oxidized form of heme, acts as potent oxidant to regulate glutathione (GSH) content in pro-erythroid K562 nucleated cells, via activation of the KEAP1/NRF2 defensive signaling pathway. Moreover, GSH, as an essential metabolite, is involved in the regulation of cell-redox homeostasis and proposed to scavenge cytotoxic free heme, which is released from hemoglobin of damaged red blood cells (RBCs) during different hemolytic disorders. In the present study, we aimed to uncover the molecular mechanism by which GSH inhibits hemin-induced cytotoxicity (HIC) by affecting hemin’s structural integrity in K562 cells and in RBC hemolysates. GSH, along with other thiols (cysteine, thioglycolic acid, and mercaptoethanol) altered the spectrum of hemin, while each of them co-added with hemin in cultures of K562 cells prevented HIC and growth arrest and markedly reduced the intracellular level of hemin. In addition, GSH endogenous levels served as a barrier to HIC in K562 cells, as shown by the depletion in GSH. LC-MS/MS analysis of the in vitro reaction between hemin and GSH revealed at least five different isomers of GSH–hemin adducts, as well as hydroxy derivatives as reaction products, which are characterized by unique mass spectra (MS). The latter allowed the detection of adducts in human RBC hemolysates. Based on these findings, we proposed a molecular mechanism via which GSH prevents HIC and structurally disintegrates heme. An analogous reaction was observed in RBC hemolysates via direct inter-reaction between hematin (ferric and hydroxide heme) released from hemoglobin and GSH. Overall, GSH–hematin adducts could be considered as novel entities of the human metabolome of RBCs in hemolytic disorders.

Synthesis and Characterization of Polymer-anchored Ni(II) Complex

Polystyrene-3-aldehydosalicylate (PSCH2-FSal) reacts with o-aminophenol in presence of DMF and forms PS-FSal-OAP (A). A reacts with mercaptoacetic acid and converts into PS-FSal-OAP-THZ (B) as a result of cyclization. B reacts with nickel(II) acetate salt and forms [PSCH2– FSal-OAP-THZ.Ni(OAc)(DMF)3]. The coordination compound has been characterized by various studies like: FTIR, diffused reflectance spectral studies and magnetic moment measurements. B behaves like a bidentate (OS donor) ligand in this compound. The acetate group shows its monodenticity in this compound. [PSCH2–FSal-OAP-THZ.Ni(OAc)(DMF)3] exhibits an octahedral structure.

Multicomponent Molecular Systems Based on Porphyrins, 1,3,5-Triazine and Carboranes: Synthesis and Characterization.

2,4,6-Trichloro-1,3,5-triazine (cyanuric chloride) is an excellent coupling reagent for the preparation of highly structured multifunctional molecules. Three component systems based on porphyrin, cyanuric chloride and carborane clusters were prepared by a one-pot stepwise amination of cyanuric chloride with 5-(4-aminophenyl)-10,15,20-triphenylporphyrin, followed by replacement of the remaining chlorine atoms with carborane S- or N-nucleophiles. Some variants of 1,3,5-triazine derivatives containing porphyrin, carborane and residues of biologically active compounds such as maleimide, glycine methyl ester as well as thioglycolic acid, mercaptoethanol and hexafluoroisopropanol were also prepared. A careful control of the reaction temperature during the substitution reactions will allow the synthesis of desired compounds in a good to high yields. The structures of synthesized compounds were determined with UV-vis, IR, 1H NMR, 11B NMR, MALDI-TOF or LC-MS spectroscopic data. The dark and photocytotoxicity as well as intracellular localization and photoinduced cell death for compounds 8, 9, 17, 18 and 24 were evaluated.

SYNTHESIS OF SOME NEWER THIAZOLIDINONYL QUINAZOLINONES AND AZETIDINONYL QUINAZOLINONES AS POTENT ANTI-INFLAMMATORY AGENTS

3-Substitutedphenyl-2-bromomethyl-6-substituted quinazolin-4(3H)-ones (7-10) were treated with hydrazine hydrate to give 3-substitutedphenyl-2-hydrazinomethyl-6-substituted quinazolin-4(3H)-ones (11-14). Compounds 11-14 were condensed with various aldehydes to afford 2-substitutedbenzylidene hydrazinomethyl-3-substitutedphenyl-6-substituted quinazolin-4(3H)-ones (15-22). Cycloaddition of compounds 15-22 with thioglycolic acid and triethylamine / chloroacetyl chloride yielded 2-[(4’-oxo-2’ -substitutedphenyl-thiazolidin-3’-yl)-aminomethyl]-3-substitutedphenyl-6-substituted quinazolin-4(3H)- ones (23-30) and 2-[(4’-oxo-3’-chloro-2’-substitutedphenylazetidin-1’-yl)-aminomethyl]-3- substitutedphenyl-6-substituted quinazolin-4(3H)-ones (31-38), respectively. The structures of these compounds have been elucidated by elemental (C, H, N) and spectral (IR, 1H-NMR) analysis. All the above mentioned compounds were evaluated for their anti-inflammatory activity, ulcerogenic activity and acute toxicity study. Compound 27 was found to be most potent amongst all the newly synthesized compounds. This compound also exhibits less ulcerogenic activity and ALD50 is >2000 mg kg-1 p.o.

Assessment of Acute Oral Toxicity of Thiolated Gum Ghatti in Rats

Various drug delivery systems were developed using a modified form of gum ghatti. Modifying gum ghatti using thioglycolic acid improves its mucoadhesive property, and hence, it is a suitable approach for the fabrication and development of controlled drug delivery systems. In accordance with regulatory guidelines, namely, the Organization for Economic Co-operation and Development’s (OECD) 423 guidelines, an acute oral dose toxicity study was performed to examine the toxicological effects of gum ghattiin an animal (Wistar rat) after a single oral dose administration of pure gum ghatti and thiolated gum ghatti. Orally administered pure and thiolated gum ghatti do not reveal any considerable change in the behavioral pattern, food intake, body weight, hematology, or clinical symptoms of treated animals. Furthermore, histopathological studies showed no pathological mutations in the vital organs of Wistar rats after the oral administration of single doses of both types of gumghatti (i.e., 300 mg/kg and 2000 mg/kg body weight). Whole blood clotting studies showed the low absorbance value of the modified gum (thiolated gum ghatti) in contrast to the pure gum and control, hence demonstrating its excellent clotting capability. The aforementioned toxicological study suggested that the oral administration of a single dose of pure and thiolated gum ghatti did not produce any toxicological effects in Wistar rats. Consequently, it could be a suitable and safe candidate for formulating various drug delivery systems.

Thiol-Ene Reaction of Heparin Allyl Ester, Heparin 4-Vinylbenzyl Ester and Enoxaparin

Heparin allyl ester and heparin 4-vinylbenzyl ester were prepared and examined for their potential for thiol-ene reaction using both free radical initiators and photochemistry. While both undergo reaction with mercaptoacetic acid, the allyl ester adduct proved to be somewhat more labile. Several more examples of adducts from heparin 4-vinylbenzyl ester are reported. Similar reactions on enoxaparin, where the reaction site is solely at the non-reducing end of the molecule, are also reported. These reactions may show promise as a strategy in the development of drug conjugates.

Reliable strategy of sensitive fluorescent nanoprobe for sensing silver nanoparticles using specific carbon dots derived from mercaptoacetic acid and melamine

Nitrogen and sulfur element co-decorated carbon nanodots (N,S-CDs) were synthesized by solid state hydrothermal method utilizing mercaptoacetic acid and melamine as the precursors. The obtained N,S-CDs had wonderful optical and chemical stability. The experimental results demonstrated that silver nanoparticles (AgNPs) could noticeably quench the fluorescence of N,S-CDs. The quenching of fluorescence signal from the presence of AgNPs may be attributed to inner filter effect. The crafted nanoprobe for sensing AgNPs was endowed with some specialties such as simplicity, excellent selectivity and sensitivity, environmental friendliness and low cost. The probe exhibited specific linearity from 0.024 to 1.77 nM, and was endowed a good limit of detection down to 0.022 nM. The experimental results demonstrated that the built probe could be an efficient tool for AgNPs detection and had a prospective application, and also provided a new direction for establishing innovative method for determining and monitoring pollutants from nanoparticles.

Effective Removal of Manure/Mud Balls from Cattle Hides using Thioglycolate Salt Containing Formulations

The effective removal of hardened manure/mud balls from cattle hides remains a challenge for the livestock industry. Hardened manure/mud balls must be removed to minimize the risk of microbial meat contamination and hide quality deterioration. To overcome this challenge, we developed thioglycolic acid and its sodium, potassium and ammonium salts containing formulations. In this study, the developed four formulations were compared based on their efficacy in removing adobe type mud/manure balls from the hides in short time. Hide pieces containing hardened manure/mud balls were soaked in the formulations for 5 minutes followed by gentle brushing to remove the debris. The firmly attached mud/manure balls were removed completely from the hide pieces soaked in sodium, potassium and ammonium thioglycolate containing formulations. However, thioglycolic acid containing formulation did not show that much efficacy and the debris remained attached in the hide pieces soaked in water which was used as a control. Moreover, naturally onboard aerobic bacteria count was significantly reduced along with the mud/manure balls removal from hide pieces. After treatment, the hide pieces were processed into crust shoe leather for quality check analysis including mechanical properties, leather surface analysis and general appearance. The crust leathers made from hide pieces treated with the formulation exhibited similar quality to that made from the control. The implementation of this inventive formulations in slaughterhouses or leather industry will drastically reduce the time consuming and labor-intensive operations currently employed to remove firmly attached debris from cattle hide surface.

Caveolae-dependent endocytosis mediates the cellular uptake of CdTe quantum dots in ovarian cancer cell lines.

Quantum dots (QDs) are semiconductor nanocrystals that are widely used in biology due to their good optical properties. QDs, especially cadmium-based QDs, play an important role in the diagnosis and treatment of cancer due to their intrinsic fluorescence. The aim of the present study was the evaluation of the cellular uptake mechanisms of CdTe QDs in ovarian cancer cell lines. In this study, we used CdTe QDs coated with thioglycolic acid. The ovarian cancer cell lines SKOV3 and OVCAR3 were treated with different concentrations of QDs, triamterene, chlorpromazine, and nystatin, and cell viability was evaluated through the MTT test. To find the way of cellular uptake of CdTe QDs, we used the MTT test and interfering compounds in endocytic pathways. Intrinsic fluorescence and cellular internalization of CdTe QDs were assessed using flow cytometry and fluorescence microscopy imaging. The viability of CdTe QDs-treated cells dose-dependently decreased in comparison to untreated cells. To evaluate the cellular uptake pathways of CdTe QDs, in most cases, a significant difference was observed when the cells were pretreated with nystatin. The results of flow cytometry showed the cellular uptake of CdTe QDs was dose- and time-dependent. Nystatin had a measurable effect on the cellular uptake of CdTe QDs. This finding suggests that caveola-mediated endocytosis has a large portion on the internalization of CdTe QDs. According to the results of this study, CdTe QDs may have potential applications in cancer research and diagnosis.

Improving enzymatic saccharification of corn stover via thioglycolic acid-mediated Fenton pretreatment

Fenton pretreatment is known as a green and mild approach, but it is usually time-consuming and inefficient in promoting lignocellulose enzymatic hydrolysis. Here we demonstrate that thioglycolic acid (TA) significantly accelerates Fenton pretreatment (FP) of corn stover (CS) and improves enzymatic hydrolysis of cellulose and xylan. The results showed that the reducing sugar yield of CS reached 77.0% with TA-assisted FP in only 16 h, while it was only 34.1% and 38.0% with FP alone in 16 h and 72 h, respectively. Via examination of the changes of composition, physical and chemical characteristics of CS before and after pretreatment, it was found that TA-assisted FP greatly improved the removal of hemicellulose and lignin, resulting in increment of the pore volume, pore size and cellulose exposure of CS substrate, which together promoted the enzymatic saccharification of CS.

Ligand-Decomposition assistant formation of CdS/TiO2 hybrid nanostructure with enhanced photocatalytic activity

CdS decorated anatase TiO 2 without capping ligands between them was constructed by the reaction of amorphous TiO 2 sphere modified by thioglycolic acid with Cd 2+ during the heating process (95 °C) directly. We have confirmed that the crystallization of amorphous TiO 2 and the formation of CdS particles are driven by the decomposition of thioglycolic acid. Moreover, the dissociation of thioglycolic acid also avoids the influence of ligand on the charge transfer between TiO 2 and CdS which is beneficial to improving the photocatalytic activity. Benefiting from this fabrication strategy, the photocatalytic activity of the obtained photocatalysts presents the enhanced activity in the wastewater treatment under visible light irradiation compared to conventionally prepared photocatalysts with the ligand. • CdS/TiO 2 composites without capping ligands was fabricated. • The absence of ligand is beneficial to the transient photocurrent response of CdS/TiO 2 . • The crystallization of amorphous TiO 2 and the formation of CdS particles are driven by the decomposition of thioglycolic acid. • The different interactions between original TiO 2 and metal ions can influence the morphology of sulfide/TiO 2 composites.

Development of Novel S-Protective Thiolated-Based Mucoadhesive Tablets for Repaglinide: Pharmacokinetic Study.

Mucoadhesive polymers have an essential role in drug localization and target-specific actions in oral delivery systems. The current work aims to develop and characterize a new mucoadhesive polysaccharide polymer (thiolated xanthan gum-TXG and S-Protected thiolated xanthan gum-STX) that was further utilized for the preparation of repaglinide mucoadhesive tablets. The thiolation of xanthan gum was carried out by ester formation through the reaction of the hydroxyl group of xanthan gum and the carboxyl group of thioglycolic acid. Synthesis of TXG was optimized using central composite design, and TXG prepared using 5.303 moles/L of TGA and 6.075 g/L of xanthan gum can accomplish the prerequisites of the optimized formulation. Consequently, TXG was further combined with aromatic 2-mercapto-nicotinic acid to synthesize STX. TXG and STX were further studied for Fourier-transform infrared spectroscopy, rheological investigations, and Ellman’s assay (to quantify the number of thiol/disulfide groups). A substantial rise in the viscosity of STX might be due to increased interactions of macromolecules liable for improving the mucosal adhesion strength of thiolated gum. STX was proven safe with the support of cytotoxic study data. Mucoadhesive formulations of repaglinide-containing STX showed the highest ex vivo mucoadhesion strength (12.78 g-RSX-1 and 17.57 g- RSX-2) and residence time (>16 h). The improved cross-linkage and cohesive nature of the matrix in the thiolated and S-protected thiolated formulations was responsible for the controlled release of repaglinide over 16 h. The pharmacokinetic study revealed the greater AUC (area under the curve) and long half-life with the RSX-2 formulation, confirming that formulations based on S-protected thiomers can be favorable drug systems for enhancing the bioavailability of low-solubility drugs.

Kinetics and Mechanism of Oxidation of Some Thioacids by Tripropylammonium Chlorochromate

Oxidation of thioglycollic, thiolactic and thiomalic acids by 2-tripropylammonium chlorochromate (TPACC) in dimethylsulphoxide (DMSO) leads to the formation of disulphide dimmers. The reaction is first order in TPACC. Michaelies-Menten type of kinetics is observed with respect to the thioacids. Reaction failed to induce the polymerisation of acrylonitrile. The reaction is catalysed by hydrogen ions. The hydrogen ion dependence has taken the form kobs = a + b [H+]. The oxidation of thiolactic acid has been studied in nineteen different organic solvents. The solvent effect has been analysed by using Kamlet’s and Swain’s multiparametric equations. A mechanism involving the formation of a thioester and its decomposition in slow step has been proposed.

Effect of cobalt doping on the photocatalytic performance of AgInS2 for organic pollutant degradation and hydrogen production

In this work, AgInS2 (AIS) and cobalt (Co) doped AgInS2 (Co-AIS) are prepared by low-temperature liquid phase method using thioglycolic acid (TGA) as the stabilizing agent. The crystal structure, surface elements, binding energy, particle morphology, and optical properties of AIS and Co-AIS are analyzed by XRD, XPS, SEM, TEM, UV-Vis-DRS, and PL. Rhodamine B (RhB) and 4-nitrophenol (4-NP) are used as the model pollutants for evaluating the photocatalytic activities of AIS and Co-AIS. The optimal doping ratio of CoːIn is found to be 10.7:6.3. And, under this optimal ratio, Co-AIS can degrade 95 % of RhB in 1.5 h or 76 % of 4-NP in 2.5 h, respectively. The photocatalytic mechanism is proposed based on the active species trapping experiment, EPR technique, optical properties characterization, and the flat-band potential determination. Moreover, the photocatalytic water splitting performance of Co-AISs with or without the modification of the multi-walled carbon nanotubes (MWCNTs) are investigated, and remarkable hydrogen production is achieved. This research will open a new gateway to synthesizing AgInS2-based materials and exploring their photocatalytic activities.

Preparation of Wool-g-Glycidyl Methacrylate with a Constructed –SH Groups/Ammonium Persulfate Redox System and Characterization

To explore suitable synthesis parameters of efficient graft copolymerization on wool, the disulfide bonds in wool chains were reduced to sulfhydryl groups by the treatment of thioglycolic acid to wool, and then wool-g-poly(glycidyl methacrylate) was prepared by graft copolymerization of wool with glycidyl methacrylate by building a redox system between sulfhydryl groups and ammonium persulfate. The wool-g-poly(glycidyl methacrylate) was characterized by the analyses of Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric and x-ray diffraction. Influences of molar concentrations of monomer and initiator as well as reaction temperature on grafting ratios were investigated. The experimental results showed that the sulfhydryl groups/ammonium persulfate redox system built could effectively initiate graft polymerization of lipophilic glycidyl methacrylate on the wool surface in an aqueous medium. The suitable process parameters of graft copolymerization were: 0.6 mmol/L molar concentration of glycidyl methacrylate, 3.0 mmol/L molar concentration of ammonium persulfate, and reaction temperature of 50 ℃. At the suitable parameters, the grafting ratio of wool-g-poly(glycidyl methacrylate) showed a maximum value of 195.8 %, indicating an efficient graft copolymerization was achieved. The copolymerization could reduce the degree of crystallinity of wool. The wool-g-poly(glycidyl methacrylate) had higher thermal stability than raw wool at a temperature of below 406 ℃ by performing the thermogravimetric analysis. Based on the results, we successfully built new sulfhydryl groups on the wool/ammonium persulfate redox system, prepared the wool-g-poly(glycidyl methacrylate), and this work will lay an important foundation for the application of wool-g-poly(glycidyl methacrylate) in the textile field.

Thioester deprotection using a biomimetic NCL approach.

The reversibility of the thiol-thioester linkage has been broadly employed in many fields of biochemistry (lipid synthesis) and chemistry (dynamic combinatorial chemistry and material science). When the transthioesterification is followed by a S-to-N acyl transfer to give an amide bond, it is called Native Chemical Ligation (NCL), a high-yield chemoselective process used for peptide synthesis. Recently, we described thioglycolic acid (TGA) as a useful reagent for thioester deprotection both in solution and anchored to a solid-support under mild conditions. Inspired by NCL, in this work, we extended this approach and explored the use of 2-aminothiols for the deprotection of thiols bearing an acyl group. The best results were obtained using cysteamine or L-cysteine in an aqueous buffer pH 8 at room temperature for 30 min. The described approach was useful for S-acetyl, S-butyryl, and S-benzoyl heterocycles deprotection with yields up to 84%. Employing this methodology, we prepared six new analogs 2 of mercaptomethyl bisthiazolidine 1, a useful inhibitor of a wide-range of Metallo-β-Lactamases (MBLs). Compared with the previous methodologies (TGA polymer supported and TGA in solution), the biomimetic deprotection herein described presents better performance with higher yields, shorter reaction times, less time-consuming operations, easier setup, and lower costs.

A novel photoelectrochemical immunosensor based on TiO2@Bi2WO6 hollow microspheres and Ag2S for sensitive detection of SARS-COV-2 nucleocapsid protein

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-COV-2) is a cluster of β coronaviruses. The 2019 coronavirus disease (COVID-19) caused by SARS-COV-2 is emerging as a global pandemic. Thus, early diagnosis of SARS-COV-2 is essential to prevent severe outbreaks of the disease. In this experiment, a novel label-free photoelectrochemical (PEC) immunosensor was obtained based on silver sulfide (Ag2S) sensitized titanium dioxide@bismuth tungstate (TiO2@Bi2WO6) nanocomposite for quantitative detection of SARS-COV-2 nucleocapsid protein. The constructed TiO2@Bi2WO6 hollow microspheres had large specific surface area and could produce high photocurrent intensity under visible light illumination. Ag2S was in-situ grown on the surface of thioglycolic acid (TGA) modified TiO2@Bi2WO6. In particular, TiO2@Bi2WO6 and Ag2S formed a good energy level match, which could effectively enhance the photocurrent conversion efficiency and strength the photocurrent response. Ascorbic acid (AA) acted as an effective electron donor to effectively eliminate photogenerated holes. Under optimal experimental conditions, the constructed immunosensor presented a supersensitive response to SARS-COV-2 nucleocapsid protein, with a desirable linear relationship ranged from 0.001 to 50 ng/mL for nucleocapsid protein and a lower detection limit of 0.38 pg/mL. The fabricated sensor exhibited a wide linear range, excellent selectivity, specificity and stability, which provided a valuable referential idea for the detection of SARS-COV-2.

Dihydroxyquingdainone Induces Apoptosis in Leukaemia and Lymphoma Cells via the Mitochondrial Pathway in a Bcl-2- and Caspase-3-Dependent Manner and Overcomes Resistance to Cytostatic Drugs In Vitro.

Isatis tinctoria and its indigo dyes have already provided highly active anti-leukaemic lead compounds, with the focus mainly being on indirubin, whereas indigo itself is inactive. There are many more indigoids to find in this plant extract, for example, quingdainone, an indigoid derived from tryptanthrin. We present here a new synthesis of hitherto neglected substituted quingdainones, which is very necessary due to their poor solubility behaviour, and a structure-dependent anti-leukaemic activity study of a number of compounds. Substituted α-phenylaminoacrylic acid was synthesised by hydrogen sulfide extrusion from an analogue mercaptoacetic acid, available from the condensation of rhodanin and a substituted tryptanthrin. It is shown that just improving water solubility does not increase anti-leukaemic activity, since a quingdainone carboxylic acid is inactive compared to dihydroxyquingdainone. The most effective compound, dihydroxyquingdainone with an AC50 of 7.5 µmole, is further characterised, revealing its ability to overcome multidrug resistance in leukaemia cells (Nalm-6/BeKa) with p-glycoprotein expression.

Endophytic Bacillus subtilis SR22 Triggers Defense Responses in Tomato against Rhizoctonia Root Rot.

Rhizoctonia root rot is one of the most destructive diseases of tomato and other crops. The biocontrol of plant diseases using endophytic bacteria has gained significant attention due to their distinct advantages compared with the free-living ones, as well as their new unexplored and unique properties. Endophytic Bacillus subtilis SR22 represents a promising and more effective biocontrol and growth-promoting agent for tomato plants than the free-living agents, being an ecofriendly and sustainable tool in modern agriculture. In this study, the direct antagonistic activity of B. subtilis SR22 was investigated against Rhizoctonia solani in vitro. The biocontrol activity of B. subtilis SR22 against Rhizoctonia root rot of tomato was also investigated. Effects on the level of the transcriptional expression of defense-related genes, biochemical responses, and the vegetative growth of tomato plants were also studied. The dual culture test showed 51% inhibition in the mycelial growth of R. solani due to B. subtilis SR22, indicating its potent antagonistic behavior. Using a GC-MS analysis, twenty bioactive compounds were detected to be produced by B. subtilis SR22, including chlorogenic acid, pyrrolo [1,2-a]pyrazine-1,4-dione, hexahydro, propyl thioglycolic acid, phthalic acid, and 2,3-butanediol. Under greenhouse conditions, the application of B. subtilis SR22 led to a reduction (up to 51%) in Rhizoctonia root rot of tomato. Furthermore, an upregulation in the expression of the responsive factor JERF3 (10.9-fold) and the defense-related genes POD (9.1-fold) and PR1 (4.5-fold) in tomato plants was recorded due to the application of B. subtilis SR22. In addition, this treatment enhanced the total phenolic content (76.8%) and activity of the antioxidant enzymes POD (56%) and PPO (29.2%) in tomato roots, indicating its resistance-inducing effect on tomato plants. Moreover, this treatment enhanced most of the evaluated growth parameters in tomato plants (up to 35%). We can conclude that B. subtilis SR22 is a promising biocontrol agent and growth promoter in tomato plants against Rhizoctonia root rot. An evaluation of the formulation and field application of this bio-agent is necessary in future studies.