Green Chemo-Prevention: An Integrated Review Between Agriculture and Medicine

The isothiocyanate's chemoprevention properties are reported to be present in cruciferous veggies through a variety of mechanisms. Sulforaphane, a phytochemical found in green leafy vegetables, has shown promise in the prevention and treatment of several cancers, including those of the prostate, breast, colon, skin, urinary bladder, and oral cavities. These malignancies include those that affect these organs. This substance is naturally present in broccoli sprouts, kale, cabbage, cauliflower, and garden cress. Broccoli should be a regular part of your diet because it contains a variety of bioactive substances such as vitamins, polyphenols, sulfides, glucosinolates, and antioxidants. Sulforaphane may be used as an inexpensive replacement or dietary supplement for chemo preventive therapy, according to the findings of epidemiological and experimental studies. Phase 2 detoxification enzymes like glutathione transferases, epoxide hydrolase, NAD(P)H: quinone reductase, and glucuronosyltransferases, as well as epoxide hydrolase and epoxide hydrolase, are produced when the body is stimulated. This is a useful tactic for preventing cancer and fending off the harm that electrophiles and reactive oxygen species can cause. Isothiocyanates are widely distributed in the Cruciferae family and Brassica genus of food plants, which include both broccoli and cauliflower. The most typical form of these substances is glucosinolate precursors. Sulforaphane and 4-methylsulfinylbutyl isothiocyanate, two of these isothiocyanates, are particularly powerful inducers of phase 2 enzymes. It is feasible to successfully extract glucosinolates and isothiocyanates from plants by homogenizing them at a temperature of around 50 degrees Celsius in a solution of equal parts dimethyl sulfoxide, dimethylformamide, and acetonitrile. This method avoids the hydrolysis of glucosinolates by myrosinase.   It's interesting to note that glucoraphanin, the precursor to sulforaphane, is 10–100 times more abundant in 3-day-old sprouts of various cruciferous vegetables, including broccoli and cauliflower than it is in fully grown veggies. Dimethylbenz(a)anthracene-treated rats displayed notable reductions in mammary tumor occurrence, quantity, and rate of growth when fed extracts from 3-day-old broccoli sprouts. These extracts' primary enzyme-inducing components were either glucoraphanin or sulforaphane. As a result, crucifer sprouts might provide an equivalent amount of cancer prevention to eating far larger quantities of the same mature vegetable species

Fluorescence Up-Conversion Studies of [2,2′-Bipyridyl]-3,3′-diol in Octyl-β‑d‑glucoside and Other Micellar Aggregates

In this present work, excited state double proton transfer dynamics (ESIDPT) of 2,2′-bipyridyl-3,3′-diol (BP­(OH)₂) molecules has been probed in a nontoxic, biocompatible sugar surfactant assembly, namely, octyl-β-d-glucoside (OBG) micelle with the help of steady state and fluorescence up-conversion techniques. Moreover, the ultrafast double proton transfer dynamics in conventional micelles (SDS, CTAB) and bile salts aggregates have been probed and compared. Interestingly, in all these supramolecular aggregates, the ESIDPT dynamics is found to follow sequential pathway; however, the time-scale of proton transfer dynamics varies from 11 to 30 ps. This difference in proton transfer time scale in different supramolecular aggregates has been explained in terms of accessibility of water molecules in the vicinity of probe

Topological Influence of Lyotropic Liquid Crystalline Systems on Excited-State Proton Transfer Dynamics

In the present work, we have investigated the excited-state proton transfer (ESPT) dynamics inside lipid-based reverse hexagonal (H_II), gyroid Ia3d, and diamond Pn3m LLC phases. Polarized light microscopy (PLM) and small-angle X-ray scattering (SAXS) techniques have been employed for the characterization of LLC systems. Time-resolved fluorescence results reveal the retarded ESPT dynamics inside liquid crystalline systems compared to bulk water, and it follows the order H_II < Ia3d < Pn3m < H₂O. The slower solvation, hampered “Grotthuss” proton transfer process, and most importantly, topological influence, of the LLC systems are believed to be mainly responsible for the slower and different extent of ESPT dynamics. Interestingly, recombination dynamics is found to be faster with respect to bulk water and it follows the order H₂O < Pn3m < Ia3d < H_II. Faster recombination dynamics arises due to lower dielectric constant and different channel diameters of these LLC systems. However, the dissociation dynamics is found to be slower than bulk water and it follows the order H_II < Ia3d < Pn3m < H₂O. Differences in critical packing parameter of LLC systems are believed to be the governing factors for the slower dissociation dynamics in these liquid crystalline systems

Ultrafast Fluorescence Dynamics of Highly Stable Copper Nanoclusters Synthesized inside the Aqueous Nanopool of Reverse Micelles

Herein, we have reported a new strategy for the synthesis of highly stable fluorescent copper nanoclusters (CuNCs) with l-cysteine (Cys) as a protecting ligand within the water nanopool of reverse micelles (RMs). In the present work, efforts are also given to address the origin of excitation-dependent fluorescence spectral shift of CuNCs. From our experiments, we have elucidated that the broad fluorescence from CuNCs in RMs consists of two spectrally overlapped bands corresponding to the metal-core and surface states of CuNCs. The intrinsic emission of CuNCs distributed in shorter wavelength regions (<470 nm) is mainly originated from the metal core. On the other hand, the extrinsic fluorescence band (>470 nm) is caused by surface states and consists of a much broader emission because of the presence of numerous surface states. The trapping of excited electrons in the various surface states leads to the emission in the longer wavelength regions and is believed to be responsible for excitation-dependent emission of CuNCs in RMs. Excited state dynamics, which controls the optical properties of CuNCs, have also been investigated by time-correlated single photon counting (TCSPC) and femtosecond fluorescence upconversion techniques. Femtosecond fluorescence upconversion and TCPSC decay profiles of CuNCs comprise of multitude of lifetime components spanning from <1 ps to few nanosecond timescales. We have rationalized the dynamics on the basis of several competing deactivation pathways and a broad distribution of radiative electron–hole recombination dynamics originating from core and surface states

A Highly Efficient UV–Vis–NIR Active Ln³⁺-Doped BiPO₄/BiVO₄ Nanocomposite for Photocatalysis Application

In this Article, we report the synthesis of Ln³⁺ (Yb³⁺, Tm³⁺)-doped BiPO₄/BiVO₄ nanocomposite photocatalyst that shows efficient photocatalytic activity under UV–visible–near-infrared (UV–vis–NIR) illumination. Incorporation of upconverting Ln³⁺ ion pairs in BiPO₄ nanocrystals resulted in strong emission in the visible region upon excitation with a NIR laser (980 nm). A composite of BiPO₄ nanocrystals and vanadate was prepared by the addition of vanadate source to BiPO₄ nanocrystals. In the nanocomposite, the strong blue emission from Tm³⁺ ions via upconversion is nonradiatively transferred to BiVO₄, resulting in the production of excitons. This in turn generates reactive oxygen species and efficiently degrades methylene blue dye in aqueous medium. The nanocomposite also shows high photocatalytic activity both under the visible region (0.010 min^–1) and under the full solar spectrum (0.047 min^–1). The results suggest that the photocatalytic activity of the nanocomposite under both NIR as well as full solar irradiation is better compared to other reported nanocomposite photocatalysts. The choice of BiPO₄ as the matrix for Ln³⁺ ions has been discussed in detail, as it plays an important role in the superior NIR photocatalytic activity of the nanocomposite photocatalyst

Emergence of slip-ideal-slip behavior in tip-links serve as force filters of sound in hearing

Abstract Tip-links in the inner ear convey force from sound and trigger mechanotransduction. Here, we present evidence that tip-links (collectively as heterotetrameric complexes of cadherins) function as force filters during mechanotransduction. Our force-clamp experiments reveal that the tip-link complexes show slip-ideal-slip bond dynamics. At low forces, the lifetime of the tip-link complex drops monotonically, indicating slip-bond dynamics. The ideal bond, rare in nature, is seen in an intermediate force regime where the survival of the complex remains constant over a wide range. At large forces, tip-links follow a slip bond and dissociate entirely to cut-off force transmission. In contrast, the individual tip-links (heterodimers) display slip-catch-slip bonds to the applied forces. While with a phenotypic mutant, we showed the importance of the slip-catch-slip bonds in uninterrupted hearing, our coarse-grained Langevin dynamics simulations demonstrated that the slip-ideal-slip bonds emerge as a collective feature from the slip-catch-slip bonds of individual tip-links

Measurement report: An assessment of the impact of a nationwide lockdown on air pollution – a remote sensing perspective over India

These Python codes are developed for studying the air pollution study over the Indian region under the stick lockdown in connection with the COVID-19 Pandemic. The study carried out on satellite-based NO2, CO, and AOD. All codes are described properly for users to use easily

Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection

Curcumin has been transformed to racemic curcuminoids via an azomethine ylide cycloaddition reaction using isatin/ acenaphthoquinone and proline as the reagents. The products were characterized by extensive 1D/2D NMR analysis and single-crystal X-ray crystallographic studies. The enantiomers of one racemic product were separated by HPLC on a Chiralcel OD-H column and were indeed confirmed by the CD spectra of the separated enantiomers

Fungal-Based Remediation in the Treatment of Anthropogenic Activities and Pharmaceutical-Pollutant-Contaminated Wastewater

Pharmaceutical personal care products (PPCPs) have increased in consumption due to the worldwide post-pandemic situation, marking them as chemical and pathogenic pollutants in significantly higher concentrations than ever in the ecosystem. Considering the inexplicable levels of these chemical residues discharged into the environment, concerns have been raised regarding their probable ecotoxicity to marine and terrestrial life. A further concern is the potential for developing and spreading antibiotic-resistant microorganisms and genes in aquatic ecosystems due to antibiotic exposure. Hence, knowing how these compounds impact aquatic ecosystem functioning is imperative, and thus is a critical area of research. The ecological risk analysis of PPCPs in aquatic ecosystems has been carried out using various strategies. Previous studies have reported numerous approaches for eliminating these PPCPs, including conventional treatment methods, activated sludge processes, generated wetlands, biological remediation, sequencing batch reactors, phytoremediation, and membrane bioreactors. In terms of green biotechnology approaches, the current research aims to discover effective procedures for removing PPCPs and their emerging resources as pollutants. Therefore, this review focuses on the over-extensive utilization of PPCPs and their emergent sources responsible for the contamination and environmental threat for future wastewater purposes. Further, as fungi and their enzymes and derivatives can remove pharmaceuticals and personal care products from wastewater through oxidation and several processes, they have attracted the attention of the scientific community due to their ability to remove PPCPs as pollutants and their status as emerging resources in wastewater. This review examines the fundamental approach and progress of the bioremediation of pharmaceutical- and personal-care-contaminated wastewater using fungal-based systems. It also discusses mechanistic approaches through hybridizing cultures and other biological systems with fungal strains, current technologies, and prospects for future research on PPCPs in wastewater treatment

The intertwining of Zn-finger motifs and abiotic stress tolerance in plants: Current status and future prospects

Environmental stresses such as drought, high salinity, and low temperature can adversely modulate the field crop’s ability by altering the morphological, physiological, and biochemical processes of the plants. It is estimated that about 50% + of the productivity of several crops is limited due to various types of abiotic stresses either presence alone or in combination (s). However, there are two ways plants can survive against these abiotic stresses; a) through management practices and b) through adaptive mechanisms to tolerate plants. These adaptive mechanisms of tolerant plants are mostly linked to their signalling transduction pathway, triggering the action of plant transcription factors and controlling the expression of various stress-regulated genes. In recent times, several studies found that Zn-finger motifs have a significant function during abiotic stress response in plants. In the first report, a wide range of Zn-binding motifs has been recognized and termed Zn-fingers. Since the zinc finger motifs regulate the function of stress-responsive genes. The Zn-finger was first reported as a repeated Zn-binding motif, comprising conserved cysteine (Cys) and histidine (His) ligands, in Xenopus laevis oocytes as a transcription factor (TF) IIIA (or TFIIIA). In the proteins where Zn2+ is mainly attached to amino acid residues and thus espousing a tetrahedral coordination geometry. The physical nature of Zn-proteins, defining the attraction of Zn-proteins for Zn2+, is crucial for having an in-depth knowledge of how a Zn2+ facilitates their characteristic function and how proteins control its mobility (intra and intercellular) as well as cellular availability. The current review summarized the concept, importance and mechanisms of Zn-finger motifs during abiotic stress response in plants