ABSTRACT
Besides a known Coumarin derivative, Scopoletin, the iridoids gardenoside was isolated for the first time from an Ipomoea species, namely Ipomoea reniformis (Convolvulaceae). Its structure was established on the basis of its spectroscopic data.
ABSTRACT
Adulteration of automotive fuels, especially, gasoline with cheaper fuels is widespread throughout south Asia. Some adulterants decrease the performance and life of the engine and increase the emission of harmful pollutants causing environmental and health problems. The present investigation is carried out to study the exhaust emissions from a single cylinder spark ignition (SI) engine with kerosene blended gasoline with different versions of the engine, such as conventional engine and catalytic coated engine with different proportions of the kerosene ranging from 0% to 40% by volume in steps of 10% in the kerosene-gasoline blend. The catalytic coated engine used in the study has copper coating of thickness 400 microns on piston and inner surface of the cylinder head. The pollutants in the exhaust, carbon monoxide (CO) and unburnt hydrocarbons (UBHC) are measured with Netel Chromatograph CO and HC analyzer at peak load operation of the engine. The engine is provided with catalytic converter with sponge iron as a catalyst to control the pollutants from the exhaust of the engine. An air injection is also provided to the catalytic converter to further reduce the pollutants. The pollutants found to increase drastically with adulterated gasoline. Copper-coated engine with catalytic converter significantly reduced pollutants, when compared to conventional engine.
Subject(s)
Air Pollutants/analysis , Carbon Monoxide/analysis , Gasoline , Hydrocarbons/analysis , Kerosene , Vehicle Emissions/analysisABSTRACT
Mismatches in DNA occur either due to replication error or during recombination between homologous but non-identical DNA sequences or due to chemical modification of bases. The mismatch in DNA, if not repaired, result in high spontaneous mutation frequency. The repair has to be in the newly synthesized strand of the DNA molecule, otherwise the error will be fixed permanently. Three distinct mechanisms have been proposed for the repair of mismatches in DNA in prokaryotic cells and gene functions involved in these repair processes have been identified. The methyl-directed DNA mismatch repair has been examined in Vibrio cholerae, a highly pathogenic gram negative bacterium and the causative agent of the diarrhoeal disease cholera. The DNA adenine methyltransferase encoding gene (dam) of this organism which is involved in strand discrimination during the repair process has been cloned and the complete nucleotide sequence has been determined. Vibrio cholerae dam gene codes for a 21·5 kDa protein and can substitute for the Escherichia coli enzyme. Overproduction of Vibrio cholerae Dam protein is neither hypermutable nor lethal both in Escherichia coli and Vibrio cholerae. While Escherichia coli dam mutants are sensitive to 2-aminopurine, Vibrio cholerae 2-aminopurine sensitive mutants have been isolated with intact GATC methylation activity. The mutator genes mutS and mutL involved in the recognition of mismatch have been cloned, nucleotide sequence determined and their products characterized. Mutants of mutS and mutL of Vibrio cholerae have been isolated and show high rate of spontaneous mutation frequency. The mutU gene of Vibrio cholerae, the product of which is a DNA helicase II, codes for a 70 kDa protein. The deduced amino acid sequence of the mutU gene hs all the consensus helicase motifs. The DNA cytosine methyltransferase encoding gene (dam) of Vibrio cholerae has also been cloned. The dcm gene codes for a 53 kDa protein. This gene product might be involved in very short patch (VSP) repair of DNA mismatches. The vsr gene which is directly involved in VSP repair process codes for a 23 kDa protein. Using these information, the status of DNA mismatch repair in Vibrio cholerae will be discussed.