Effects of antibacterial drugs on the total cholesterol balance of cholesterol-fed mice

Mice were fed a diet containing 1.5% cholesterol, and the total cholesterol balance and the distribution of the consumed sterol among excreta, liver, and carcass were determined, using experimental periods of 9–14 days. It was observed that an average of approximately 12% of the cholesterol was either destroyed or chemically modified. When, however, 1% sulfasuxidine and 0.04% streptomycin were added to the diet, all the sterol “put in” was recovered, within the limits of error of the method. These results were tentatively interpreted to indicate that under the conditions of these experiments, microorganisms of the intestine were primarily responsible for the destruction or modification of the consumed sterol, as observed in the absence of antibacterial drugs.     

Über den Gehalt an auxin- und gibberellinähnlichen Stoffen bei jarowisierten und nicht jarowisierten Embryonen von Sommer- und Winterweizen

V jarovisovaných a nejarovisovaných obilkách jedné ozimé a jedné jarní odr?dy p?enice byly chromatograficky stanoveny látky typu auxin? a giberelin?. Chromatogramy byly vyhodnoceny pomocí biologických test?. U ozimé odr?dy jsme nena?li rozdíly v rozlo?ení r?stových látek mezi jarovisovanou a nejarovisovanou variantou. U jarní odr?dy jsme rozdíly na?li. Na základě výsledk? soudíme, ?e rozdíly mezi oběma variantami jarní odr?dy byly zp?sobeny nespecifickým p?sobením nízké teploty a ?e proces jarovisace není kausálně spjat se změnami hladiny r?stových látek.     

3-Hydroxyanthranilic acid metabolism. IV. Spectrophotometric evidence for the formation of an intermediate

Evidence has been presented for the formation of an intermediate compound in the metabolism of 3-hydroxyanthranilic acid to quinolinic acid by 3-hydroxyanthranilase from rat liver preparations. The production of the intermediate was demonstrated by spectrophotometric analyses and quinolinic acid measurements of incubation mixtures in which small amounts of acetone powder extracts of rat liver were used as the enzyme source. The calculated extinction coefficient of the compound was more than double that of the substrate or of the final product, quinolinic acid.The intermediate was shown to be an oxidation product of 3-hydroxyanthranilate as indicated by Thunberg experiments. The data obtained indicate that the intermediate may be a quinone-type compound.