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[Display omitted] • Oleaginous yeast offers sustainable solution to energy scarcity, waste mitigation. • Metabolic pathways coupling waste degradation and lipid synthesis are portrayed. • Biodiesel derived from oleaginous yeast grown in waste, meets fuel standards. • Omics approaches are robust tool to advance the waste bioconversion into lipids. The escalating challenge of waste disposal and the potential threat to global energy supply have sparked renewed interest in repurposing waste materials for the production of sustainable and renewable fuels. In line with this objective, there has been a growing focus on biodiesel production from oleaginous yeast through the valorization of waste. While numerous reports have been published on this subject, only a limited number of studies provide a comprehensive overview of recent advancements. To address this gap and the economic viability challenges associated with yeast-derived biodiesel production, the present review aims to highlight the opportunities offered by various recalcitrant wastes as a renewable feedstock for oleaginous yeast cultivation. The review also delves into extensive knowledge about the metabolic pathways that facilitate the conversion of different recalcitrant wastes into single-cell oil (SCO), which has not been extensively covered in a single platform before. Moreover, the most promising species of oleaginous yeast are described, taking into consideration economic aspects and the sustainability of the overall process. Furthermore, the review emphasizes the application of omics techniques to advance waste bioconversion into lipids for the purpose of commercialization. In summary, this study contributes to expanding our current understanding of the topic and facilitates the future upscaling and commercialization of biodiesel derived from oleaginous yeasts. [ABSTRACT FROM AUTHOR]

Minimal natural resistance in guar against Alternaria cyamopsidis blight or leaf spots requires the need to develop improved cultivars with high level of resistance. In this study, we report the silencing of AcCHS7 gene with pSilentCHS7-2 and pARTCHS7 constructs in Alternaria pathogen and guar plants of HG 2–20 variety, respectively. The down-regulation of AcCHS7 delays the disease progression in guar by damaging the hyphae, reducing mycelium growth and conidiation in Alternaria. Hence, this study demonstrates the role of host induced post-transcriptional gene silencing of AcCHS7 as an effective approach to increase the guar productivity by developing resistance against Alternaria cyamopsidis. • Alternaria cyamopsidis causes leaf spot disease in guar which results in yield loss. • AcCHS7 silencing reduce sporulation and mycelium growth in Alternaria cyamopsidis. • The disease progression in transgenic guar plants got delayed by 7-8 weeks. • Survival rate of transgenics was 70% compared to wild plants on fungal infection. [ABSTRACT FROM AUTHOR]

Candida tropicalis is an opportunistic human pathogen with an ability to cause superficial as well as systemic infections in immunocompromised patients. The formation of biofilm by C. tropicalis can cause dreadful and persistent infections which are difficult to treat due to acquired resistance. Presently, available anti-Candida drugs exhibit a high frequency of resistance, low specificity and toxicity at a higher dosage. In addition, the discovery of natural or synthetic anti-Candida drugs is slow paced and often does not pass clinical trials. Citral, a monoterpene aldehyde, has shown effective antimicrobial activities against various microorganisms. However, only few studies have elaborated the action of citral against the biofilm of C. tropicalis. In the present work, the aim was to study the fungicidal effect, differential expression of proteome and changes in extracellular matrix in response to the sub-lethal concentration (16 µg/mL) of citral. The administration of citral on C. tropicalis biofilm leads to a fungicidal effect. Furthermore, the differential expression of proteome has revealed twenty-five proteins in C. tropicalis biofilm, which were differentially expressed in the presence of citral. Among these, amino acid biosynthesis (Met6p, Gln1p, Pha2p); nucleotide biosynthesis (Xpt1p); carbohydrate metabolism (Eno1p, Fba1p, Gpm1p); sterol biosynthesis (Mvd1p/Erg19p, Hem13p); energy metabolism (Dnm1p, Coa1p, Ndk1p, Atp2p, Atp4p, Hts1p); oxidative stress (Hda2p, Gre22p, Tsa1p, Pst2p, Sod2p) and biofilm-specific (Adh1p, Ape1p, Gsp1p) proteins were identified. The overexpression of oxidative stress–related proteins indicates the response of biofilm cell to combating oxidative stress during citral treatment. Moreover, the upregulation of Adh1p is of particular interest because it subsidizes the biofilm inhibition through ethanol production as a cellular response. The augmented expression of Mvd1p/Erg19p signifies the effect of citral on ergosterol biosynthesis. The presence of citral has also shown an increment in hexosamine and ergosterol component in extracellular matrix of C. tropicalis biofilm. Hence, it is indicated that the cellular response towards citral acts through multifactorial processes. This study will further help in the interpretation of the effect of citral on C. tropicalis biofilm and development of novel antifungal agents against these potential protein targets. [ABSTRACT FROM AUTHOR]

• Development and validation of visible light-activatable nitrosyl complexes of ruthenium under the illumination of low intensity light. • Reduced myoglobin has been delivered using light-triggered NO. • The Griess experiment was used to examine the visible-light triggered NO. • Antibacterial activity examined under the exposure of visible light. • This kind of NO complexes may immediately release NO to targets located at a certain spot. In this article, a chloro-bridged dinuclear ruthenium complex Ru-(a) has been synthesized, which was employed for the synthesis of a photolabile NO liberating complex Ru-(b). A newly synthesized tridentate ligand 2-methyl-6-((2-phenyl-2-(pyridin-2-yl)hydrazineylidene)methyl)pyridine with three N-atoms as donating site was used to synthesize the complex Ru-(a). The molecular structure of Ru-(a) was investigated by single-crystal X-ray crystallography and, in solution was characterized by or ESI mass spectrometry. Several spectroscopic techniques were used for the characterization of the ligand as well as complexes. To understand the electronic structure of Ru-(a) and Ru-(b) , DFT computations were utilized. By the utilization of visible light, photo-liberation experiments were examined. The amount of NO released during the photodissociation experiment was measured using the Griess reagent assay technique. The photodissociated NO was fruitfully transported to reduced myoglobin (Mb). The antibacterial activity against Escherichia coli was carried out with 31.2 μg/mL concentration of Ru-(b). In the final results, we detected considerable antibacterial activity against E. coli and showed >99 % inhibition of the bacterial cells after 120 min of the experiment on exposure to visible light. These investigations proposed that Ru-(b) could be employed to treat several topical deliveries of NO for treating various topical and bacterial infections. [Display omitted] [ABSTRACT FROM AUTHOR]

Fusarium oxysporum f. sp. lycopersici is a soil-borne phytopathogenic species which causes vascular wilt disease in the Solanum lycopersicum (tomato). Due to the continuous competition for zinc usage by Fusarium and its host during infection makes zinc-binding proteins a hotspot for focused investigation. Zinc-binding effector proteins are pivotal during the infection process, working in conjunction with other essential proteins crucial for its biological activities. This work aims at identifying and analysing zinc-binding proteins and zinc-binding proteins effector candidates of Fusarium. We have identified three hundred forty-six putative zinc-binding proteins; among these proteins, we got two hundred and thirty zinc-binding proteins effector candidates. The functional annotation, subcellular localization, and Gene Ontology analysis of these putative zinc-binding proteins revealed their probable role in wide range of cellular and biological processes such as metabolism, gene expression, gene expression regulation, protein biosynthesis, protein folding, cell signalling, DNA repair, and RNA processing. Sixteen proteins were found to be putatively secretory in nature. Eleven of these were putative zinc-binding protein effector candidates may be involved in pathogen–host interaction during infection. The information obtained here may enhance our understanding to design, screen, and apply the zinc-metal ion-based antifungal agents to protect the S. lycopersicum and control the vascular wilt caused by F. oxysporum. [ABSTRACT FROM AUTHOR]

Occurrence of non-canonical G-quadruplex (G4) DNA structures in the genome have been recognized as key factors in gene regulation and several other cellular processes. The mosR and ndhA genes involved in pathways of oxidation sensing regulation and ATP generation, respectively, make Mycobacterium tuberculosis (Mtb) bacteria responsible for oxidative stress inside host macrophage cells. Circular Dichroism spectra demonstrate stable hybrid G4 DNA conformations of mosR/ndhA DNA sequences. Real-time binding of mitoxantrone to G4 DNA with an affinity constant ~105–107 M−1, leads to hypochromism with a red shift of ~18 nm, followed by hyperchromism in the absorption spectra. The corresponding fluorescence is quenched with a red shift ~15 nm followed by an increase in intensity. A change in conformation of the G4 DNA accompanies the formation of multiple stoichiometric complexes with a dual binding mode. The external binding of mitoxantrone with a partial stacking with G-quartets and/or groove binding induces significant thermal stabilization, ~20–29 °C in ndhA/mosR G4 DNA. The interaction leads to a two/four-fold downregulation of transcriptomes of mosR/ndhA genes apart from the suppression of DNA replication by Taq polymerase enzyme, establishing the role of mitoxantrone in targeting G4 DNA, as an alternate strategy for effective anti-tuberculosis action in view of deadly multi-drug resistant tuberculosis disease causing bacterial strains t that arise from existing therapeutic treatments. [ABSTRACT FROM AUTHOR]

According to current research, anti-cancer anthraquinones impact telomere disruption and may interact with G-quadruplex DNA that triggers signaling to apoptosis. The present study represents the biophysical investigation of oxidative stress, late apoptosis, and induced senescence among cancer cells after binding laboratory synthesized piperidine-based anthraquinone derivatives, 2, 6- Bis [(3-piperidino)acetamido)]anthracene-9,10-dione (N 1P) and 2, 6-Bis [piperidino)propionamido]anthracene-9,10-dione (N 2P), with G-quadruplex DNA. We employed biophysical approaches to explore the interaction of synthetic anthraquinone derivatives with quadruplex DNA sequences to influence biological activities in the presence of K+ and Na+ cations. The binding affinity for N 2P and N 1P are K b = 5.8 × 106 M−1 and K b = 1.0 × 106 M−1, respectively, leading to hypo-/hyper-chromism with 5–7 nm red shift and significant fluorescence quenching and changes in ellipticity resulting in external binding of both the ligands to G-quadruplex DNA. Ligand binding induced enhancement of thermostability of G4 DNA is greater in Na+ environment (Δ T m = 34 °C) as compared to that in K+ environment (Δ T m = 21 °C), thereby restricting telomerase binding access to telomeres. Microscopic images of treated cells indicated cellular shape, nuclear condensation, and fragmentation alterations. The findings pave the path for therapeutic research, given the great potential of modifying anthraquinone substituent groups towards improved efficacy, ROS generation, and G-quadruplex DNA selectivity. [Display omitted] • Real time binding of 2, 6 anthraquinone derivatives to human telomeric DNA by SPR. • Absorption, fluorescence and circular dichroism depict external groove binding. • Ligand-binding induced thermal stabilization up to ∼36 °C observed by DSC/CD. • ROS generation significantly triggered late apoptosis under effect of ligands. • Cancer cell cytotoxicity and nuclear condensation in treated cells by ligands. [ABSTRACT FROM AUTHOR]

Renewable biofuels, such as biodiesel, bioethanol, and biobutanol, serve as long-term solutions to fossil fuel depletion. A sustainable approach feedstock for their production is plant biomass, which is degraded to sugars with the aid of microbes-derived enzymes, followed by microbial conversion of those sugars to biofuels. Considering their global demand, additional efforts have been made for their large-scale production, which is ultimately leading breakthrough research in biomass energy. Metagenomics is a powerful tool allowing for functional gene analysis and new enzyme discovery. Thus, the present article summarizes the revolutionary advances of metagenomics in the biofuel industry and enlightens the importance of unexplored habitats for novel gene or enzyme mining. Moreover, it also accentuates metagenomics potentials to explore uncultivable microbiomes as well as enzymes associated with them. [ABSTRACT FROM AUTHOR]

Development of efficient wastewater treatment technologies along with circular economic approaches are the most imperative biotechnological attention presently. Thus, to add more value in this process, current study accessed a novel oleaginous yeast strain, R. glutinis ISO A1 for its biodegrading potential in sewage wastewater encompassing toxic formulations. To achieve improved performance light irradiance of various intensities (50 lux–150 lux) was applied during the cultivation period as an abiotic stress factor. All irradiances significantly stimulated nutrient removal efficiency of R. glutinis and improved growth rate but intracellular accumulation of carotenoids was found slightly inhibited. Boosted lipogenesis (lipid content ⁓40.66%) along with phenomenal reduction in COD (88.33 ± 1.88%), nitrate (73.2 ± 3.95%) and phosphate (85.1 ± 2.97%) was monitored with an optimum exposure condition at 100 lux. Cultures illuminated with light (50 lux–150 lux) also showed excellent tolerance for multiple heavy metals (Zn, Cd, Cr) and exhibited their complete removal. Further, analysis of fatty acid methyl esters (FAME) presented an increase in saturated fatty acids that reveal modulations in R. glutinis 's membrane fluidity against stress generated due to the light exposure. Besides, estimated biodiesel properties of obtained FAME complying European and American fuel standards. These findings shed new light on the factors affecting wastewater bioremediation and successfully established a photo-induced biological treatment system in an oleaginous yeast for the very first time with an addition to successive lipid enhancement. [ABSTRACT FROM AUTHOR]

Algae-based wastewater bioremediation offers a cost-effective method for sustainably treating wastewater while simultaneously addressing global water scarcity and pollution. This study highlights the benefits of treating primary-treated (PTW) and secondary-treated (STW) paper-pulp industrial wastewaters using the microalga Tetradesmus obliquus (Turpin) Kützing. A batch culture study revealed that 50 % secondary treated wastewater can increase the biomass yield 1.8 fold to 2.51 g L−1 in 15 days with a corresponding lipid yield of 390.2 mg L−1. Upscaling this work in 200 L open raceway ponds with 50 % STW as the growth medium showed areal biomass and lipid productivities of 26.80 and 3.90 g m−2 day−1, respectively, in 15 days at 20 cm culture depth. This translates to a projected high annual biomass productivity of approximately 85.0 tons hectare−1 year−1 based on datasets spanning two consecutive years. Bioremediation efficiencies of 80.0 %, 91.51 %, and 92.10 % were achieved for COD, TOC, and NH 4 + respectively. Biodiesel produced showed a large percentage of saturated and monounsaturated fatty acids (∼90 %) and its fuel properties complied with the global biodiesel standards. This study thus shows that using paper-pulp industrial wastewater for algal growth offers a sustainable solution for energy generation and wastewater treatment, with significant implications for environmental sustainability. [ABSTRACT FROM AUTHOR]

Algae-based wastewater bioremediation offers a cost-effective method for sustainably treating wastewater while simultaneously addressing global water scarcity and pollution. This study highlights the benefits of treating primary-treated (PTW) and secondary-treated (STW) paper-pulp industrial wastewaters using the microalga Tetradesmus obliquus (Turpin) Kützing. A batch culture study revealed that 50 % secondary treated wastewater can increase the biomass yield 1.8 fold to 2.51 g L−1 in 15 days with a corresponding lipid yield of 390.2 mg L−1. Upscaling this work in 200 L open raceway ponds with 50 % STW as the growth medium showed areal biomass and lipid productivities of 26.80 and 3.90 g m−2 day−1, respectively, in 15 days at 20 cm culture depth. This translates to a projected high annual biomass productivity of approximately 85.0 tons hectare−1 year−1 based on datasets spanning two consecutive years. Bioremediation efficiencies of 80.0 %, 91.51 %, and 92.10 % were achieved for COD, TOC, and NH 4 + respectively. Biodiesel produced showed a large percentage of saturated and monounsaturated fatty acids (∼90 %) and its fuel properties complied with the global biodiesel standards. This study thus shows that using paper-pulp industrial wastewater for algal growth offers a sustainable solution for energy generation and wastewater treatment, with significant implications for environmental sustainability. [ABSTRACT FROM AUTHOR]

Plastic materials, particularly polyethylene, are the potential source of environmental pollution. In the present study, a fungal strain was isolated from plastic waste dumpsites capable of adhering to high-density polyethylene (HDPE) surface. The fungal strain was identified as Aspergillus niger (ITCC no. 6052). A visible increase in the growth of the fungi was observed on the surface of the polyethylene when cultured in minimal medium at 30°C and 120 rpm, for 1 month. Approximately 3.44% reduction (gravimetrically) in mass and 61% reduction in tensile strength of polyethylene was observed after 1 month of incubation with fungal isolate. Scanning electron microscope analysis showed hyphael penetration and cracks on the surface of polyethylene. A thick network of fungal hyphae forming a biofilm was also observed on the surface of the plastic pieces. The efficient biofilm formation on polyethylene surface by Aspergillus niger (ITCC no. 6052) is attributed to its high cell surface hydrophobicity. This study indicated that Aspergillus niger (ITCC no. 6052) has ability to degrade thermally oxidized polyethylene. [ABSTRACT FROM AUTHOR]

Abstract: Arabinogalactanl protein (AGP) a highly water-soluble glyco-conjugate from groundnut (Arachis hypogaea L.) seedling was isolated and purified by precipitation with β-glucosyl Yariv reagent. Quantification of AGP was done by gel diffusion assay. Purified AGP was conjugated to amphotericin-B (AmB) by Schiff base reaction at pH 11.0, with aim to prepare a water-injectable lesser toxic AGP–AmB conjugate without affecting AmB antifungal potential. The AGP–AmB conjugate antifungal activity was assayed by serial broth dilution and disc method against several Candida albicans clinical isolates. Both AmB and AGP–AmB showed similar MICs and MFCs activities, indicating that AGP do not reduced the antifungal activity of AmB. However, the in vitro and in vivo toxicity assays revealed that AGP–AmB conjugate was lesser toxic than AmB, as high MTD (45mg/kg body weight) was observed. It is suggested that AGP could be a potent carrier in AmB formulation, which may result in effective treatment of fungal infections. [Copyright &y& Elsevier]

Oral squamous cell carcinoma (OSCC) is highly predominant in India due to excessive use of tobacco. Here we investigated Long INterpersed Element 1 (LINE or L1) retrotransposon activity in OSCC samples in the same population. There are almost 500,000 copies of L1 occupied around 30% of the human genome. Although most of them are inactive, around 150–200 copies are actively jumping in a human genome. L1 encodes two proteins designated as ORF1p and ORF2p and expression of both proteins are critical for the process of retrotransposition. Here we have analyzed L1 ORF1p expression in a small cohort (n = 15) of paired cancer-normal tissues obtained from operated oral cancer patients. Immunohistochemistry (IHC) with the human ORF1 antibody showed the presence of ORF1p in almost 60% cancer samples, and few of them also showed aberrant p53 expression. Investigating L1 promoter methylation status, showed certain trends towards hypomethylation of the L1 promoter in cancer tissues compared to its normal counterpart. Our data raise the possibility that L1ORF1p expression might have some role in the onset and progression of this particular type of cancer. [ABSTRACT FROM AUTHOR]

• Identification of full length CtMYC gene from guar leaves. • This TF showed tissue specific expression and over expressed during drought stress. • CtMYC gene was cloned, expressed, and purified. • Conformational changes showed binding ability of this protein with DNA. • Glu, Arg and His, DNA binding residues were also conserved in structure alignment. The MYC transcription factor (TF) has a variety of roles in abiotic stress responses of plants. In the present work, MYC TF named CtMYC (Cymopsis tetragonoloba) from guar plant, which is induced by drought stress, was identified. The mature leaves of guar were employed to detect the full-length CtMYC TF on the 8th day of drought stress. The CtMYC gene showed tissue-specific expression and up regulated under drought stress conditions as compared to the control and maximum expression was observed in mature leaves. Additionally, CtMYC TF was cloned and expressed in E. coli Rosetta cells and CtMYC protein was purified. The circular dichroism (CD) analysis revealed the presence of helical content and beta sheets and in the presence of genomic DNA the conformational changes were observed in secondary structure, which showed DNA binding potential of CtMYC. These results were analyzed by CD and fluorescence studies. In silico studies reveal the presence of conserved bHLH domain and DNA-binding amino acid residues His, Glu and Arg in CtMYC. This is first report on CtMYC TF with DNA binding potential that is responsive to drought. This study provides the structure and characterization of CtMYC TF and DNA binding ability in drought tolerance mechanism in guar. [ABSTRACT FROM AUTHOR]

[Display omitted] • R. glutinis ISO A1 augmented 45% lipid content in 25% ASW. • Yeast remodels its neutral sugars to cope up with high salinity. • Rise in SOD, GR and APX activities assisted salinity tolerance in cells. • De-fatted yeast biomass was evaluated as feedstock for thermochemical conversion. In the present study, a marine red yeast Rhodotorula glutinis ISO A1 cultivated under combinations of artificial seawater (ASW) and sewage wastewater (SWW) has been subjected to detailed mechanistic investigations via physiological and biochemical analysis to dissect the pathway of halotolerance behavior and carbon flux channelization towards enhanced lipid synthesis. Amid all tested groups (25–100% ASW), cells grown in 25% ASW yielded ∼ 1.4-fold higher lipid yield than glucose synthetic medium (GSM) and revealed metabolic rewiring of cells to channelize carbon pools for producing neutral lipids of vehicular quality. Detailed carbohydrate profiling showed enhanced glycerol, trehalose, mannose, and xylitol/arabitol under saline stress, suggesting the interplay of these metabolites to impart tolerance against osmotic imbalance. Further, the strengthened enzymatic activity (glutathione reductase, superoxide dismutase, ascorbate peroxidase) and non-enzymatic metabolites (betaine, proline) highlighted the active yeast defence network to counter altered redox state arise due to high salinity. The stress-induced responses also constituted substantial variations in membrane fluidity and production of biodiesel-quality lipids. Further findings like low thermal degradation temperature (at ∼ 265°C) and high chitin (can be converted into chitosan) entity in yeast de-oiled biomass primarily derived from yeast cells grown under contaminated environment; sea and sewage wastewater, signified its potential utilization for chitosan recovery, a commercially important product. Conclusively, this study elucidated a competent model of yeast-based biorefinery approach integrating seawater-wastewater utilization and simultaneous production of biodiesel and value-added products vital for a sustainable and circular bioeconomy. [ABSTRACT FROM AUTHOR]

Candida tropicalis is an emerging non-albicans Candida species which is pathogenic to the immune-compromised humans, especially in tropical countries, including India. The acquired resistance of Candida species towards antifungal therapies is of major concern. Moreover, limited efficacy and dosage constraint of synthetic drugs have indicated the prerequisite of finding new and natural drugs for treatment. In the present study, we have compared the influence of citral and thymol on C. tropicalis and its biofilm along with expression levels of certain antifungal tolerance genes. The antifungal and anti-biofilm activities of the both were studied using 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide sodium salt (XTT) reduction assay, field emission scanning electron microscope (FE-SEM) and confocal laser scanning microscope (CLSM) and real-time reverse transcription polymerase chain reaction (RT-PCR) analysis. Citral and thymol have damaged the cells with distorted surface and less viability. Quantitative real-time PCR analysis showed augmented expression of the cell membrane biosynthesis genes including ERG11/CYT450 against citral and the cell wall related tolerance genes involving CNB1 against thymol thus, depicting their differential mode of actions. [ABSTRACT FROM AUTHOR]

The first committed step of the shikimate pathway is catalyzed by a metalloenzyme 3-deoxy- d -arabino-heptulosonate-7-phosphate synthase (DAH7PS), which exhibits vulnerability to the oxidative stress. DAH7PS undergoes inactivation in multiple ways in the presence of redox metal, H 2 O 2 , and superoxide. The molecular mechanism and susceptibility of its inactivation might differ in different organisms and are presently unclear. In the present work, we have cloned, expressed and purified a DAH7PS from Providencia alcalifaciens (PaDAH7PS). The oligomeric state and effect of redox metal treatment on its stability were analyzed through the size exclusion chromatography. The FTIR, MALDI-TOF/TOF-MS studies revealed that methionine residues were modified to methionine sulfoxide in PaDAH7PS. During oxidation, PaDAH7PS is altered into partially folded protein and unfolded states as determined by CD and Fluorescence studies. A significant loss in enzymatic activity of PaDAH7PS was determined and the formation of amorphous aggregates was visualized using AFM imaging and also confirmed by ThT binding based assay. This is the first report where we have shown a hexameric DAH7PS and the methionine residues of PaDAH7PS get oxidize in the presence of oxidative stress. The partially folded and unfolded oligomeric states with high β-content of PaDAH7PS might be the critical precursors for aggregation. [ABSTRACT FROM AUTHOR]

Therapeutic effectiveness of biogenically synthesized Woodfordia fruticosa nano-gold particles (WfAuNPs) has been claimed in this study which prevents microbial adhesion and enhanced wound healing potential on Wistar albino rats. The synthesized WfAuNPs were characterized using several biophysical techniques such as UV–Visible Spectroscopy (UV–vis), X-Ray Diffraction (XRD), Dynamic Light Scattering (DLS), Zeta Potential, Fourier Transform Infrared Spectroscopy (FTIR), Field Emission Scanning Electron Microscopy (FE-SEM), Atomic Force Microscopy (AFM) and High Resolution Transmission Electron Microscopy (HR-TEM) analysis. The synthesized WfAuNPs in the size range of 10–20 nm were used to develop 1% Carbopol® 934 based nano gold formulation (WfAuNPs-Carbopol® 934). The WfAuNPs-Carbopol® 934 nanoformulation was evaluated using viscosity and spreadability measurements. The wound healing potential of WfAuNPs-Carbopol® 934 monitored up to 12 days was confirmed by performing wound contraction (%), epithelialization, and histopathological studies done in vivo on Wistar albino rats. The hydroxyproline content was also measured in the re-epithelized skin for quantification of collagen content. The effects of WfAuNPs on microbial adhesion leading to biofilm formation were evaluated against Candida albicans and Cryptococcus neoformans fungal strains. The respective Minimum Inhibitory Concentration (MIC 80 ), Biofilm Inhibitory Concentration (BIC 80 ) and Biofilm Eradication Concentration (BEC 80 ) values of C. albicans was found to be 16, 32, 256 μg/ml respectively while for C. neoformans it was recorded to be 32, 64, 256 μg/ml respectively. Data obtained, confirmed the effectiveness in preventing microbial adhesion and wound healing potential of the WfAuNPs as compared to current marketed formulations. [ABSTRACT FROM AUTHOR]

Biofortification of bread wheat by the transfer of useful variability of high grain Fe and Zn from Aegilops kotschyi through induced homoeologous pairing is the most feasible approach to alleviate micronutrient malnutrition worldwide. Deficiency of chromosome 5B in interspecific hybrids allows homoeologous pairing and recombination of chromosomes of wheat with those of the related species. The interspecific hybrid plants without 5B chromosome showed much higher chromosome pairing than did the plants with 5B. The F plants without 5B chromosome were selected and repeatedly backcrossed with wheat cultivar PBW343. The chromosome number of BCF plants ranged from 43 to 60 with several univalents and multivalents. Molecular markers and GISH analysis confirmed the introgression of U/S chromosomes of Ae. kotschyi and their fragments in wheat. The BCF plants showed up to 125 % increase in Fe and 158 % increase in Zn compared to PBW343 with Lr24 and Yr36. Induced homoeologous pairing in the absence of 5B was found to be an effective approach for transfer of useful variability for enhanced grain Fe and Zn content for biofortification of wheat for high grain micronutrient content. [ABSTRACT FROM AUTHOR]

Simple sequence repeat (SSR) markers are highly efficient for genetic mapping and molecular breeding in crop plants. Chromosomes 7S and 7U of related non-progenitorAegilopsspecies possess superior genetic systems for high grain iron and zinc content. This study was undertaken to conduct a comprehensive analysis of transferability and polymorphism among group-7 anchored SSR markers of bread wheat (Triticum aestivumL.) toAegilopsspecies for wheat improvement. The study revealed 77% transferability of group 7-specific SSR markers of bread wheat to 7U/7S chromosomes ofAegilopsspecies. More than 80% of the 7D specific markers were found to be transferable with a high level of polymorphism. The transferability to 7S and 7U genome suggested higher similarity between bread wheat genome(s) and S genome as compared with U genome ofAegilopsspecies. These polymorphic markers are highly informative, robust and cost-effective for molecular breeding and could be further utilized for identification of introgression/transfer(s) of 7S/7U chromosomal fragments in bread wheat genome through wide hybridization. [ABSTRACT FROM AUTHOR]

PurposeTo transfer the 2S chromosomal fragment(s) ofAegilops kotschyi(2Sk) into the bread wheat genome which could lead to the biofortification of wheat with high grain iron and zinc content. Materials and methodsWheat-Ae. kotschyi2A/2Sksubstitution lines with high grain iron and zinc content were used to transfer the gene/loci for high grain Fe and Zn content into wheat using seed irradiation approach. ResultsBread wheat plants derived from 40 krad-irradiated seeds showed the presence of univalents and multivalents during meiotic metaphase-I. Genomic in situ hybridization analysis of seed irradiation hybrid F2seedlings showed several terminal and interstitial signals indicated the introgression ofAe. kotschyichromosome segments. This proves the efficacy of seed radiation hybrid approach in gene transfer experiments. All the radiation-treated hybrid plants with high grain Fe and Zn content were analyzed with wheat group 2 chromosome-specific polymorphic simple sequence repeat markers to identify the introgression of small alien chromosome fragment(s). ConclusionRadiation-induced hybrids showed more than 65% increase in grain iron and 54% increase in Zn contents with better harvest index than the elite wheat cultivar WL711 indicating effective and compensating translocations of 2Skfragments into wheat genome. [ABSTRACT FROM AUTHOR]

The first quarter of the 21st century has remarkably been characterized by a multitude of challenges confronting human society as a whole in terms of several outbreaks of infectious viral diseases, such as the 2003 severe acute respiratory syndrome (SARS), China; the 2009 influenza H1N1, Mexico; the 2012 Middle East respiratory syndrome (MERS), Saudi Arabia; and the ongoing coronavirus disease 19 (COVID-19), China. COVID-19, caused by SARS-CoV-2, reportedly broke out in December 2019, Wuhan, the capital of China's Hubei province, and continues unabated, leading to considerable devastation and death worldwide. The most common target organ of SARS-CoV-2 is the lungs, especially the bronchial and alveolar epithelial cells, culminating in acute respiratory distress syndrome (ARDS) in severe patients. Nevertheless, other tissues and organs are also known to be critically affected following infection, thereby complicating the overall aetiology and prognosis. Excluding H1N1, the SARS-CoV (also referred as SARS-CoV-1), MERS, and SARS-CoV-2 are collectively referred to as coronaviruses, and taxonomically placed under the realm Riboviria, order Nidovirales, suborder Cornidovirineae, family Coronaviridae, subfamily Orthocoronavirinae, genus Betacoronavirus, and subgenus Sarbecovirus. As of 23 September 2021, the ongoing SARS-CoV-2 pandemic has globally resulted in around 229 million and 4.7 million reported infections and deaths, respectively, apart from causing huge psychosomatic debilitation, academic loss, and deep economic recession. Such an unprecedented pandemic has compelled researchers, especially epidemiologists and immunologists, to search for SARS-CoV-2-associated potential immunogenic molecules to develop a vaccine as an immediate prophylactic measure. Amongst multiple structural and non-structural proteins, the homotrimeric spike (S) glycoprotein has been empirically found as the most suitable candidate for vaccine development owing to its immense immunogenic potential, which makes it capable of eliciting both humoral and cell-mediated immune responses. As a consequence, it has become possible to design appropriate, safe, and effective vaccines, apart from related therapeutic agents, to reduce both morbidity and mortality. As of 23 September 2021, four vaccines, namely, Comirnaty, COVID-19 vaccine Janssen, Spikevax, and Vaxzevria, have received the European Medicines Agency's (EMA) approval, and around thirty are under the phase three clinical trial with emergency authorization by the vaccine-developing country-specific National Regulatory Authority (NRA). In addition, 100–150 vaccines are under various phases of pre-clinical and clinical trials. The mainstay of global vaccination is to introduce herd immunity, which would protect the majority of the population, including immunocompromised individuals, from infection and disease. Here, we primarily discuss category-wise vaccine development, their respective advantages and disadvantages, associated efficiency and potential safety aspects, antigenicity of SARS-CoV-2 structural proteins and immune responses to them along with the emergence of SARS-CoV-2 VOC, and the urgent need of achieving herd immunity to contain the pandemic. [ABSTRACT FROM AUTHOR]

[Display omitted] • Eucalyptol/β-cyclodextrin loaded nanofibers fabricated using electrospinning. • Antibiofilm activity of eucalyptol enhanced due to its encapsulation in nanofibers. • These nanofibers could be used as an antifungal agent in future. Fungal infections pose a serious threat to humankind due to the toxicity of conventional antifungal therapy and continuous emerging incidence of multidrug resistance. Essential oils fascinated researchers because of their broad antimicrobial activity and minimal cytotoxicity. However, hydrophobic, volatile and low water solubility of essential oils hinder their applications in pharmaceutical industries. Therefore, in this study we have loaded eucalyptol/ β-cyclodextrin inclusion complex to gellan/polyvinyl alcohol nanofibers (EPNF) to eradicate Candida albicans and Candida glabrata biofilms. The electrospun nanofibers characterized by various physicochemical techniques and it was observed that EPNF possess highly hydrophilic surface property that facilitate rapid drug release. EPNF inhibited approximately 70% biofilm of C. albicans and C. glabrata. Time kill results depicted that eucalyptol (EPTL) encapsulation in the nanofibers prolonged its antifungal activity than the pure EPTL. Electron microscopy studies revealed that EPNF disrupted the cell surface of Candida. Collectively the current study suggested nanofiber encapsulation enhanced antibiofilm activity of eucalyptol and these nanoscale systems can serve as an alternative therapeutic strategy to treat fungal infections. Further, the developed nanofibrous materials can be applied as cost effective coating agent for biomedical implants. [ABSTRACT FROM AUTHOR]

A T-DNA insertional mutant OsPE of rice gives twin and triplet seedlings in up to 20 % of the seeds. Detailed cytological and histological analysis of OsPE indicated normal male and female gametogenesis in the OsPE mutant. Confocal laser scanning microscopic (CLSM) analysis of the developing seeds of OsPE showed multiple embryo development in up to 60 % of the ovules. The multiple embryos, mostly twins and triplets, and rarely quadruplets, developed through sequential cleavage from a single zygotic embryo in each ovule. The reduced number of multiple seedlings compared with multiple embryos observed in CLSM study may be attributed to their inability to develop further due to competition in a single embryo sac. Key message Multiple seedlings in the OsPE mutant are due to sequential proliferation and cleavage of the zygotic embryos. The nucellar tissue was not involved in multiple embryo development. [ABSTRACT FROM AUTHOR]

Coronavirus disease 19 (COVID-19) is caused by an enveloped, positive-sense, single-stranded RNA virus, referred to as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which belongs to the realm Riboviria, order Nidovirales, family Coronaviridae, genus Betacoronavirus and the species Severe acute respiratory syndrome-related coronavirus. This viral disease is characterized by a myriad of varying symptoms, such as pyrexia, cough, hemoptysis, dyspnoea, diarrhea, muscle soreness, dysosmia, lymphopenia and dysgeusia amongst others. The virus mainly infects humans, various other mammals, avian species and some other companion livestock. SARS-CoV-2 cellular entry is primarily accomplished by molecular interaction between the virus's spike (S) protein and the host cell surface receptor, angiotensin-converting enzyme 2 (ACE2), although other host cell-associated receptors/factors, such as neuropilin 1 (NRP-1) and neuropilin 2 (NRP-2), C-type lectin receptors (CLRs), as well as proteases such as TMPRSS2 (transmembrane serine protease 2) and furin, might also play a crucial role in infection, tropism, pathogenesis and clinical outcome. Furthermore, several structural and non-structural proteins of the virus themselves are very critical in determining the clinical outcome following infection. Considering such critical role(s) of the abovementioned host cell receptors, associated proteases/factors and virus structural/non-structural proteins (NSPs), it may be quite prudent to therapeutically target them through a multipronged clinical regimen to combat the disease. [ABSTRACT FROM AUTHOR]

Psoriasis is an inflammatory skin disease with complex pathogenesis and multiple etiological factors. Besides the essential role of autoreactive T cells and constellation of cytokines, the discovery of IL-23/Th17 axis as a central signaling pathway has unraveled the mechanism of accelerated inflammation in psoriasis. This has provided insights into psoriasis pathogenesis and revolutionized the development of effective biological therapies. Moreover, genome-wide association studies have identified several candidate genes and susceptibility loci associated with this disease. Although involvement of cellular innate and adaptive immune responses and dysregulation of immune cells have been implicated in psoriasis initiation and maintenance, there is still a lack of unifying mechanism for understanding the pathogenesis of this disease. Emerging evidence suggests that psoriasis is a high-mortality disease with additional burden of comorbidities, which adversely affects the treatment response and overall quality of life of patients. Furthermore, changing trends of psoriasis-associated comorbidities and shared patterns of genetic susceptibility, risk factors and pathophysiological mechanisms manifest psoriasis as a multifactorial systemic disease. This review highlights the recent progress in understanding the crucial role of different immune cells, proinflammatory cytokines and microRNAs in psoriasis pathogenesis. In addition, we comprehensively discuss the involvement of various complex signaling pathways and their interplay with immune cell markers to comprehend the underlying pathophysiological mechanism, which may lead to exploration of new therapeutic targets and development of novel treatment strategies to reduce the disastrous nature of psoriasis and associated comorbidities. • Psoriasis is a momentous health challenge affecting more than 125 million people globally. • IL-23/Th17 axis provided insights into immunological interactions and cytokines constellation in psoriasis. • Despite the role of immune responses and dysregulated immune cells, psoriasis lacks a unifying mechanism of pathogenesis. • Multifactorial pathophysiology and additional comorbidities present psoriasis as a systemic disease. • Understanding the interplay of complex signaling pathways in psoriasis-related comorbidities is important. [ABSTRACT FROM AUTHOR]

Background: Harnessing the halotolerant characteristics of microalgae provides a viable alternative for sustainable biomass and triacylglyceride (TAG) production. Scenedesmus sp. IITRIND2 is a fast growing fresh water microalga that has the capability to thrive in high saline environments. To understand the microalga's adaptability, we studied its physiological and metabolic flexibility by studying differential protein, metabolite and lipid expression profiles using metabolomics, proteomics, real-time polymerase chain reaction, and lipidomics under high salinity conditions. Results: On exposure to salinity, the microalga rewired its cellular reserves and ultrastructure, restricted the ions channels, and modulated its surface potential along with secretion of extrapolysaccharide to maintain homeostasis and resolve the cellular damage. The algal-omics studies suggested a well-organized salinity-driven metabolic adjustment by the microalga starting from increasing the negatively charged lipids, up regulation of proline and sugars accumulation, followed by direction of carbon and energy flux towards TAG synthesis. Furthermore, the omics studies indicated both de-novo and lipid cycling pathways at work for increasing the overall TAG accumulation inside the microalgal cells. Conclusion: The salt response observed here is unique and is different from the well-known halotolerant microalga; Dunaliella salina, implying diversity in algal response with species. Based on the integrated algal-omics studies, four potential genetic targets belonging to two different metabolic pathways (salt tolerance and lipid production) were identified, which can be further tested in non-halotolerant algal strains. [ABSTRACT FROM AUTHOR]