COMPARATIVE STUDY ON HYDROLYTIC ENZYMES PRODUCED BY DIFFERENT MORPHOLOGICAL FORMS OF CANDIDA ALBICANS

In recent years, the incidence of fungal infections has been rising all over the world. The ability of Candida albicans to switch from yeast to hyphal growth is essential for its virulence. The aim of this comparative study was to biotype and characterize phospholipase, proteinase, phosphatase and haemolytic activities of yeast and hyphal forms of Candida albicans. The hyphal form of Candida albicans secrets high quantity of hydrolytic enzymes than yeast form, which helps in its virulence. These results suggest that pathogenic fungi produce larger amount of inducible hydrolytic enzymes than non-pathogenic fungi. In this investigation, plate methods were used to determine the phospholipase, proteinase and haemolytic activities and spectrophotometric method was employed for testing acid phosphatase activity

Synthesis and Biological Assessment of Carbazole Linked Pyrazole Schiff bases and Diarylthiourea Derivatives

In this study, (E)-9-ethyl-N-((1,3-diphenyl-1H-pyrazol-4-ylmethylene)-9H-carbazol-3-amine (3a–f) and 1-(9-ethyl-9H-carbazol-6-yl)-3-phenylthiourea (5a–f) derivatives were synthesized and their in vitro antimicrobial and antimalarial activities were evaluated. The structures of the synthesized compounds were elucidated and confirmed by using IR, 1H NMR, 13C NMR, and mass spectra. This work is licensed under a Creative Commons Attribution 4.0 International License

Photo-Induced Cytotoxicity and Anti-Metastatic Activity of Ruthenium(II)-Polypyridyl Complexes Functionalized with Tyrosine or Tryptophan

The synergistic effect of oxygen, light, and photosensitizer (PS) has found applications in medicine for the treatment of cancer through photodynamic therapy (PDT). Induction of apoptosis to cancerous cells will prevent tumor metastasis that spreads cancer cells to the neighboring organs/tissues. Herein, we report the two apoptotic Ru(II)–polypyridyl complexes that are functionalized with pendant amino acid moieties tyrosine (1) and tryptophan (2), respectively. These two water soluble complexes were found to interact strongly (K1a = (1.18 ± 0.28) × 105 M−1 and K2a = (1.57 ± 0.77) × 105 M−1) with CT-DNA. Isothermal titration calorimetry (ITC) studies revealed that these complexes bind to CT-DNA through an entropically driven process. Both the complexes showed photo-induced cytotoxicity and exhibit apoptotic activity under photo-irradiation conditions. The comet assay indicated that these complexes can damage cellular DNA, which is attributed to the significant build-up of 1O2 level even on irradiation with low intensity light (10 J cm−2, λRange 450–480 nm). This photoinduced DNA damage and apoptosis in A549 cells was induced by reactive oxygen species (ROS) and occurred through up-regulation of apoptotic marker caspase-3. Control experiments under dark conditions revealed an insignificant cytotoxicity towards these cells for two photosensitive molecules