Construction and Building Materials, Journal Year: 2024, Volume and Issue: 456, P. 139280 - 139280
Published: Nov. 24, 2024
Language: Английский
Construction and Building Materials, Journal Year: 2024, Volume and Issue: 456, P. 139280 - 139280
Published: Nov. 24, 2024
Language: Английский
Journal of the Indian Chemical Society, Journal Year: 2025, Volume and Issue: unknown, P. 101592 - 101592
Published: Jan. 1, 2025
Language: Английский
Citations
2Journal of Basic Microbiology, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 2, 2025
ABSTRACT Soil ecosystems consist of diverse microbial communities with great potential for ecological and biotechnological applications. These encounter various abiotic stresses, which expedite the activation transient overexpression heat shock proteins (HSPs). In present study, a soil bacterium was isolated identified as Bacillus licheniformis strain PSK.A1, its growth parameters were optimized before exposing it to heat, salt, pH, antibiotic stress conditions. Comparative protein expression analyzed using SDS‐PAGE, stabilization via aggregation assays, survival through single spot dilution colony‐counting methods under The pre‐treatment short dosage showed endured overall tolerance lethal conditions, evidenced by moderately enhanced total soluble intracellular content, better stabilization, comparatively over‐expressed HSPs, relatively cell survival. findings highlighted that cells grown optimal conditions more susceptible environments than stressed cells, their linked 20 distinct HSPs 17–91 kD. insights offer developing strategies enhance resilience applications including bacterial bioprocessing, bio‐remediation, infectious disease management.
Language: Английский
Citations
2Food and Humanity, Journal Year: 2024, Volume and Issue: 3, P. 100366 - 100366
Published: July 27, 2024
Language: Английский
Citations
15The Microbe, Journal Year: 2024, Volume and Issue: 4, P. 100151 - 100151
Published: Aug. 24, 2024
Language: Английский
Citations
8International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: 306, P. 141780 - 141780
Published: March 5, 2025
Language: Английский
Citations
1Pathogens, Journal Year: 2025, Volume and Issue: 14(1), P. 32 - 32
Published: Jan. 5, 2025
The path to survival for pathogenic organisms is not straightforward. Pathogens require a set of enzymes tissue damage generation and obtain nourishment, as well toolbox full alternatives bypass host defense mechanisms. Our group has shown that the parasitic protist Entamoeba histolytica encodes 14 sphingomyelinases (SMases); one them (acid sphingomyelinase 6, aSMase6) involved in repairing membrane exhibits hemolytic activity. enzymatic characterization aSMase6 been be activated by magnesium ions but zinc, human aSMase, strongly inhibited cobalt. However, no structural data are available enzyme. In this work, bioinformatic analyses showed aSMases diverse enzymes, evolutionarily related hemolysins derived from bacteria, similar overall structure parasitic, free-living protists mammalian enzymes. AlphaFold3 models predicted occupancy cobalt active site Cavity blind docking substrate pushed outward when bound instead ions. Additionally, E. loop absent rest aSMases, suggesting it may activity, demonstrated experimentally using recombinant proteins aSMase4 aSMase6. Trichomonas vaginalis show putative transmembrane domain seem functionally different histolytica. This work provides insight into future biochemical can mechanistic features sphingomyelinases, ultimately rendering these potential therapeutic targets.
Language: Английский
Citations
0Published: Jan. 1, 2025
Language: Английский
Citations
0International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(4), P. 1724 - 1724
Published: Feb. 18, 2025
The rise in multidrug-resistant bacteria highlights the critical need for novel antibiotics. This study explores clovibactin-like compounds as potential therapeutic agents targeting lipid II, a crucial component bacterial cell wall synthesis, using silico techniques. A total of 2624 clovibactin analogs were sourced from PubChem database and screened ProTox 3.0 software based on their ADME-Tox properties, prioritizing candidates with favorable pharmacokinetic profiles minimal toxicity. Molecular docking protocols then employed to assess binding interactions selected II. Our analysis identified Compound 22 particularly promising candidate, exhibiting strong affinity, stable complex formation, high selectivity target. Binding energy analysis, conducted via molecular dynamics simulations, revealed highly negative value -25.50 kcal/mol 22, surpassing that underscoring its efficacy. In addition, was prioritized due exceptional affinity II suggesting lower likelihood adverse effects. These characteristics position candidate further pharmacological development. While our computational results are encouraging, experimental validation is essential confirm efficacy safety these compounds. not only advances understanding but also contributes ongoing efforts combat antimicrobial resistance through innovative antibiotic
Language: Английский
Citations
0International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 142651 - 142651
Published: March 1, 2025
Language: Английский
Citations
0ChemistrySelect, Journal Year: 2025, Volume and Issue: 10(14)
Published: April 1, 2025
Abstract Diabetes is a complex metabolic disorder characterized by oxidative stress and chronic inflammation, necessitating the development of multifunctional therapeutic agents. This study evaluates in vitro silico antihyperglycemic, antioxidant, anti‐inflammatory activities four 3‐(4,5‐diaryl‐1 H ‐imidazol‐2‐yl)quinoline‐2‐amine derivatives (a–d) . Among them, compound (a) exhibited strong antihyperglycemic activity, with significant α‐amylase inhibition (IC 50 = 132.55 ± 4.12 µg/mL) enhanced glucose uptake yeast cells 126.32 3.48 µg/mL). Compound (d) showed superior antioxidant 42–44 properties. Molecular docking against PPAR‐γ confirmed binding interactions for all compounds, showing collectively better affinity (−10 kcal/mol −11.1 kcal/mol). Further, molecular dynamics normal mode analysis validated its stability functional potential. The ADMET predictions suggested favorable pharmacokinetics, especially compounds (b) findings suggest that has potential as lead molecule treatment moderate also shows promise, albeit slightly lower bioactivity. Despite these promising findings, none tested outperformed efficacy standard drugs any assays, indicating need further structural optimization to enhance their
Language: Английский
Citations
0