Natural colourants with bio-potential are of great commercial demands as we are moving away from the hazardous and toxic chemical dyes. Bixa orellana L. a representative of Bixaceae is rich in bixin and nor-bixin pigments which could be explored for various applications. In the present study, extraction and characterization of bixin and its associated pigment from the aril of the B. orellana L. seeds were performed using various spectroscopic techniques. Spectroscopic analysis and Gas chromatographic profiling of the pigment were performed to understand the present pigments. Toxicity was evaluated through in silico method. The major component, bixin and nor-bixin were proved to be non-toxic, non-carcinogenic and non-mutagenic through in silico methods. The pigment was found to be a potent antioxidant as well as bactericidal against opportunistic bacteria. It was found that bixin extract was a potential antioxidant and bactericidal agent. Hence it could be used for imparting bactericidal potential for cellulosic materials like papers or textiles in biomedical applications.
相似文献Epilepsy disease is characterized by the neuronal dysfunction or abnormal neuronal activity of the brain which is regulated by astrocytes. These are glial cells and found to be the major regulators of the brain which are guided by the occurrence of adenosine kinase (ADK) enzyme in the central nervous system (CNS). During the normal physiological environment, ADK maintains the level of adenosine in the CNS. Dysfunction of ADK levels results in accumulation of adenosine levels in the CNS that leads to the pathophysiology of the brain such as astrogliosis which is a pathological hallmark of epileptic seizures. Vicine, an alkaloid glycoside in bitter gourd juice (Momordica charantia) is found to be toxic to the human system if the bitter gourd juice is consumed more. This compound inhibits ADK enzyme activity to lead epilepsy and seizure. Here, the toxic effect of vicine targeting ADK using computational predictions was investigated. The 3-dimensional structure of ADK has been constructed using I-Tasser, which has been refined by ModRefiner, GalaxyRefine, and 3D refine and it was endorsed using PROCHECK, ERRAT, and VADAR. 3D structure of the ligand molecule has been obtained from PubChem. Molecular docking has been achieved using AutoDock 4.2 software, from which the outcome showed the effective interaction between vicine and ADK, which attains binding free energy (?G) of ??4.13 kcal/mol. Vicine molecule interacts with the active region ARG 149 of ADK and inhibits the functions of ADK that may cause imbalance in energy homeostasis. Also, pre-ADMET results robustly propose in which vicine possesses toxicity, and meanwhile, from the Ames test, it was shown as mutagenic. Hence, the results from our study suggest that vicine was shown to be toxic that suppresses the ADK activity to undergo pathological conditions in the neuronal junctions to lead epilepsy.
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