A facile approach to the isolation of proteins in Ferula asafoetida and their enzyme stabilizing, anti-microbial and anti-oxidant activity.

The objective of the present study was to identify the proteome pattern, isolate and study the functions of selective proteins from Ferula asafoetida root exudate using chromatographic techniques. The root exudate proteins were fractionated using ion-exchange and gel filtration chromatography. A range of bioactive protein fractions were then separated in sufficient quantity which is the focus of this study. Based on studies, here we report three main proteins with molecular weights 14kDa, 27kDa, and 39kDa. The biological and pharmacological activities of both purified and unpurified proteins obtained were extensively studied to understand their significance. The study revelaed that 27kDa protein interestingly stabilized trypsin activity in 24h of time and retained about 64% of the enzyme activity. Analyses confirmed 40°C and pH 8.0 are the optimum temperature and pH respectively. The 39kDa protein remarkably increased the activity of chymotrypsin and the 14kDa protein showed anti-bacterial activity against Pseudomonas aeruginosa. Invariably all of the three purified proteins showed enhanced anti-oxidant activity. In conclusion, results here obtained suggested that the primary metabolites (proteins) in asafoetida are mainly responsible for its versatile biological and pharmacological activities.

A versatile chitosan/ZnO nanocomposite with enhanced antimicrobial properties.

Porous chitosan membrane was fabricated by casting method using silica particles. Simultaneously nano ZnO was synthesized by green-synthesis method using tung ting oolong tea extract. Chitosan membrane was combined with nano ZnO in order to increase its antimicrobial activity. Through observations obtained from various techniques such as XRD, SEM, FT-IR, UV-visible and fluorescence emission analyses, chitosan was seen to be able to incorporate nano ZnO in the nanocomposite membrane. A blue shift (from 360 to 335 nm) was observed in the UV-visible spectrum of nanocomposite and fluorescence emission intensity of nanocomposite was considerably lower than that of nano ZnO. Gram negative organism Klebsiella planticola (MTCC2727) and Gram positive organism Bacillus substilis (MTCC3053) were used to test the antibacterial and antifouling activities of newly synthesized nanocomposite chitosan/ZnO membrane. The nanocomposite chitosan/ZnO membrane promisingly inhibited the bacterial growth when compared with as-synthesized chitosan. Gram negative K. planticola (MTCC2727) was comparatively more susceptible for inhibition than that of Gram positive Bacillus substilis (MTCC3053). In conclusion, nanocomposite obtained in this study showed enhanced antibacterial and antifouling activities. We believed that the enhanced physical properties of nanocomposite achieved by incorporating nano ZnO in the chitosan matrix could be beneficial in various applications.