ABSTRACT
The present study demonstrates biopolymer production by in situ bio-based dimerization of fatty acids by microorganism isolated from marine sediments. Microbial isolate grown in Zobell medium in the presence of triglycerides for the period of 24-240 h at 37 degrees C, hydrolyze the applied triglycerides and sequentially dimerized the hydrolyzed products and subsequently polymerized and transformed to a biopolymer having appreciable adhesive properties. Physical (nature, odour, stickyness and tensile strength), chemical (instrumentation) and biochemical (cell free broth) methods of analyses carried out provided the hypotheses involved in the formation of the product as well as the nature of the product formed. Results revealed, lipolytic enzymes released during initial period of growth and the biosurfactant production during later period, respectively, hydrolyze the applied triglycerides and initiate the dimerization and further accelerated when the incubation period extended. The existence and the non-existence of in situ hydrolysis of various triglycerides followed by dimerization and polymerization and the mechanism of transformation of triglycerides to biopolymer are discussed in detail.
Subject(s)
Biopolymers/chemistry , Biopolymers/metabolism , Fatty Acids/metabolism , Geologic Sediments/microbiology , Surface-Active Agents/chemistry , Surface-Active Agents/metabolism , Triglycerides/metabolism , Dimerization , Fatty Acids/chemistry , Hydrolysis , Tensile Strength , Triglycerides/chemistry , ViscosityABSTRACT
The present study emphasizes the effect of unspent tannins on liver, kidney and heart of albino rats. Oral administration of unspent tannins at three different concentrations was made for a period of seven days. Carbon tetrachloride served as positive control. Tissues were removed carefully followed by sacrifice and were subjected to sectioning and H&E staining. Histopathological examination of the sections showed, major tissue damage with the highest concentration of tannins (1500mg/kg body weight) irrespective of their nature and source, followed by moderate damage with the 1000mg/kgbw and zero damage with 500mg/kgbw. However, complete damage was observed with the tissues of positive control group. Lipid peroxidase assay using post-mitochondrial supernatant of liver, kidney and heart showed appreciable levels of malondialdehyde release at higher concentrations of tannins.
