Synthesis, Spectral Characterization, and Antiproliferative Studies of Mixed Ligand Titanium Complexes of Adamantylamine

Titanium complexes have been synthesized by the reaction between titanium tetrachloride (TiCl4), respective bidentate ligand [4,4′ -dimethoxy-2,2′ -bipyridine (bpome), 6,6′-dimethyl-2,2′-bipyridine (dpme), 1,2-diaminocyclohexane (dach), 1,10-phenanthroline (phen), and benzoylacetone (bzac)], and adamantylamine (ada) in 1 : 2 : 2 molar ratios, respectively. The structure of synthesized complexes was confirmed using elemental analysis, FTIR, UV-visible, 1H NMR, and mass spectrometry techniques. The nanocrystalline nature of complexes was confirmed by powder XRD study. The complexes were evaluated for cytotoxic potential in HeLa (cervical), C6 (glioma), and CHO (Chinese hamster ovarian) cell lines. The complex E was found to be more effective cytotoxic agent against HeLa cell line with an IC50 value of 4.06 µM. Furthermore, the effect of synthesized complexes was studied on different stages of the cell cycle in CHO cells. All complexes exhibited the dose dependent increase in cytotoxicity. The results have shown an increase in sub-G0 population with increase in concentration which is an indicative measure of apoptosis

Standardization of packaging material, storage durations and chemical treatments on vase life of soft shield fern Polystichum squarrosum (D. Don)

Polystichum species, native to warm-temperate and montane-tropical environments (including some alpine regions), are terrestrial or rock-dwelling ferns. These plants exhibit dark green, leather-like, and lustrous fronds, which are highly valued in floral arrangements due to their aesthetic elegance and longevity. Polystichum squarrosum is not being cultivated commercially but collected from forests for its use as cut green in the florist industry. Hence the collected material should be handled carefully to utilize every frond. Therefore, the present study aimed to develop suitable post-harvest handling procedures for this valued cut green. A Completely Randomized Design (CRD) Factorial layout with 19 treatment modules (M0 to M18) was employed. Treatment modules included packaging material as poly mesh net bags and packing materials as corrugated fiberboard boxes , two storage durations (3 and 6 days) and chemical treatments [glycerol (4%) and Benzyl adenine (25mg L-1)]. Results revealed that spraying cut fronds with 4% glycerol, wrapping them in cellophane sheets and storing them for three days (M9) resulted in significant improvements in appearance, weight change, vase life and water uptake. Fronds from Season-II (March-April 2020) exhibited excellent performance over Season-I (August-September 2019). The interaction between M9 and Season-II further enhanced the postharvest parameters. The combination of glycerol treatment and cellophane wrapping for three-day storage proved most effective in preserving the quality of cut fronds.

Comparative In Vitro

The binding of TiCl2(dpme)2 (1), (dpme = 6,6′-dimethyl-2,2′-bipyridine), Ti(ada)2(bzac)2 (2), (ada = adamantylamine; bzac = benzoylacetone), and TiCl2(bzac)(bpme) (3), (bpme = 4,4′-dimethyl-2,2′-bipyrdine) with calf thymus (ct) DNA has been studied by UV-visible spectroscopy, thermal denaturation, and circular dichroism spectroscopy. In UV-visible study complexes 1, 2, and 3 showed red, blue, and red shifts, respectively, upon the addition of ct-DNA along with a significant hyperchromism. The intrinsic binding constants (Kb) calculated from UV-visible absorption studies were 2.3 × 103 M−1, 3.3 × 103 M−1 and, 7.1 × 103 M−1 for complexes 1, 2, and 3, respectively. The change in melting temperature (ΔTm) was calculated to be 2-3°C for each complex. Circular dichroism (CD) study showed blue shift for complex 2 and red shift for complexes 1 and 3 along with rise in molecular ellipticity upon the addition of complexes. Results suggest a binding mode of complex 2 different than 1 and 3

SISALv2: A comprehensive speleothem isotope database with multiple age-depth models

Characterizing the temporal uncertainty in palaeoclimate records is crucial for analysing past climate change, correlating climate events between records, assessing climate periodicities, identifying potential triggers and evaluating climate model simulations. The first global compilation of speleothem isotope records by the SISAL (Speleothem Isotope Synthesis and Analysis) working group showed that age model uncertainties are not systematically reported in the published literature, and these are only available for a limited number of records (ca. 15 %, n = 107=691). To improve the usefulness of the SISAL database, we have (i) improved the database's spatiooral coverage and (ii) created new chronologies using seven different approaches for age depth modelling. We have applied these alternative chronologies to the records from the first version of the SISAL database (SISALv1) and to new records compiled since the release of SISALv1. This paper documents the necessary changes in the structure of the SISAL database to accommodate the inclusion of the new age models and their uncertainties as well as the expansion of the database to include new records and the qualitycontrol measures applied. This paper also documents the age depth model approaches used to calculate the new chronologies. The updated version of the SISAL database (SISALv2) contains isotopic data from 691 speleothem records from 294 cave sites and new age depth models, including age depth temporal uncertainties for 512 speleothems. SISALv2 is available at https://doi.org/10.17864/1947.256 (Comas-Bru et al., 2020a). © 2020 Author(s)

Nano-Biotechnology for Bacteria Identification and Potent Anti-bacterial Properties: A Review of Current State of the Art

Sepsis is a critical disease caused by the abrupt increase of bacteria in human blood, which subsequently causes a cytokine storm. Early identification of bacteria is critical to treating a patient with proper antibiotics to avoid sepsis. However, conventional culture-based identification takes a long time. Polymerase chain reaction (PCR) is not so successful because of the complexity and similarity in the genome sequence of some bacterial species, making it difficult to design primers and thus less suitable for rapid bacterial identification. To address these issues, several new technologies have been developed. Recent advances in nanotechnology have shown great potential for fast and accurate bacterial identification. The most promising strategy in nanotechnology involves the use of nanoparticles, which has led to the advancement of highly specific and sensitive biosensors capable of detecting and identifying bacteria even at low concentrations in very little time. The primary drawback of conventional antibiotics is the potential for antimicrobial resistance, which can lead to the development of superbacteria, making them difficult to treat. The incorporation of diverse nanomaterials and designs of nanomaterials has been utilized to kill bacteria efficiently. Nanomaterials with distinct physicochemical properties, such as optical and magnetic properties, including plasmonic and magnetic nanoparticles, have been extensively studied for their potential to efficiently kill bacteria. In this review, we are emphasizing the recent advances in nano-biotechnologies for bacterial identification and anti-bacterial properties. The basic principles of new technologies, as well as their future challenges, have been discussed

Glycoconjugates coated gold nanorods based novel biosensor for optical detection and photothermal ablation of food borne bacteria

Foodborne bacterial species have been identified as the major cause in most of the severe pathogen related diseases. Conventional methods like plating and enzyme-linked immunosorbent assay (ELISA) are time overriding and laborious. Fast detection of bacterial species in food is a proximate obligation to guarantee food safety. Nanotechnology has emerged as a great field in case of rapid detection of pathogens in recent years. In the present work, gold nanorods, (AuNRs) based sensor was developed for swift and sensitive detection of foodborne bacteria. AuNRs has good electro-optical properties due to its Near-Infrared (NIR) absorption and scattering in surface plasmon resonance (SPR) wavelength regions. By exploiting the sugar based adhesion properties of bacteria, the sugar capped AuNRs can be used as potential nanobiosensor to detect the food borne bacteria. Polyethylene glycol (PEG) coated AuNRs were covalently functionalized with different types of amine terminated sugar using EDC coupling reaction. The sensitivity of synthesized nanobiosensor was probed by lectin binding assay and also with food borne bacteria (Escherichia coli) by using spectrophotometric and microscopic techniques. Pseudomonas aeruginosa was also used to probe the specificity of our synthesized biosensor through lectin-sugar interaction. Due to the specific interaction of sugar coated probe with foodborne bacteria, our nanoprobe has shown significant and selective photoablation of targeted bacteria. This nanorod based nanobiosensor can be an ideal candidate for optical detection and ablation of foodborne bacteria

A Comprehensive Review on Role of Plant Tissue Culture in Ornamental Crops: Cultivation Factors, Applications and Future Aspects

Ornamental plants are grown largely for their artistic value, floriculturists must prioritize the proliferation and improvement of quality traits, as well as the production of unique diversity. Micropropagation, clonal reliability and conservation are all crucial factors to consider. Application of in vitro techniques in ornamental plant such as in vitro embryo rescue, somatic hybridization, in vitro pollination and in vitro ploidy manipulation but to enhance, techniques like as embryo rescue and somatic hybridization are commonly employed. The creation of synthetic seed allows for season-independent seed producing and long-term seed preservation. Many factors influence ornamental plant tissue culture, including plant genotype, explants type, and the physical environment (light, temperature, humidity, and CO2), in addition to medium composition and growth regulators. We compiled and reviewed an overall update on cultivation factors, application procedures in ornamental plant tissue culture, in vitro plant enhancement approaches and future prospects in this study

An Assessment of Growth Media Enrichment on Lipid Metabolome and the Concurrent Phenotypic Properties of <i>Candida albicans</i>

<div><p>A critical question among the researchers working on fungal lipid biology is whether the use of an enriched growth medium can affect the lipid composition of a cell and, therefore, contribute to the observed phenotypes. One presumption is that enriched medias, such as YPD (yeast extract, peptone and dextrose), are likely to contain lipids, which may homogenize with the yeast lipids and play a role in masking the actual differences in the observed phenotypes or lead to an altered phenotype altogether. To address this issue, we compared the lipids of <i>Candida albicans</i>, our fungus of interest, grown in YPD or in a defined media such as YNB (yeast nitrogen base). Mass spectrometry-based lipid analyses showed differences in the levels of phospholipids, including phosphatidylinositol, phosphatidylglycerol, lyso-phospholipids; sphingolipids, such as mannosyldiinositolphosphorylceramide; and sterols, such as ergostatetraenol. Significant differences were observed in 70 lipid species between the cells grown in the two media, but the two growth conditions did not affect the morphological characteristics of <i>C. albicans</i>. The lipid profiles of the YNB- and YPD-grown <i>C. albicans</i> cells did vary, but these differences did not influence their response to the majority of the tested agents. Rather, the observed differences could be attributed to the slow growth rate of the <i>Candida</i> cells in YNB compared to YPD. Notably, the altered lipid changes between the two media did impact the susceptibility to some drugs. This data provided evidence that changes in media can lead to certain lipid alterations, which may affect specific pathways but, in general, do not affect the majority of the phenotypic properties of <i>C. albicans</i>. It was determined that either YNB or YPD may be suitable for the growth and lipid analysis of <i>C. albicans</i>, depending upon the experimental requirements, but additional precautions are necessary when correlating the phenotypes with the lipids.</p></div

Effect of cell wall perturbing agents and protein biosynthesis inhibitors on <i>C. albicans</i> cells grown in YPD or YNB.

<p>A) CW. B) CR. C) TX-100. D) SDS. E) CYCLO. Values are means ± SEM (n = 4). YPD and YNB control datasets are same for the subfigures A–E.</p