Activity Of Benzaldehyde Research Articles

Hydrodeoxygenation of Anisole and Benzaldehyde Over Bifunctional CoMo/USY Catalyst

Hydrodeoxygenation (HDO) of anisole and Benzaldehyde over bifunctional zeolite USY (ultra-stable Y) supported CoMo catalysts has been studied. The catalyst consisted of metals that Co and Mo were loaded at three different sequences; Co loaded first (Co-Mo/USY), Mo loaded first (Mo-Co/USY), and simultaneously loaded (CoMo/USY). The experiments were conducted in a flow reactor within a temperature of 350 °C for an hour. The oxygen-free products from the HDO process were benzene and toluene compounds. CoMo/USY catalyst exhibited the best catalytic activity of anisole towards the total production of aromatic hydrocarbons yield by 9.17%. It was also found that Mo-Co/USY catalyst exhibited the best catalytic activity of Benzaldehyde with aromatic hydrocarbons yield by 10.46%.

Volatile organic compounds produced by Lysinibacillus sp. FJAT-4748 possess antifungal activity against Colletotrichum acutatum

ABSTRACTFJAT-4748 is a bacterial strain isolated from forest soil samples taken from Dongba Valley, Lijiang, Kunming, Yunnan Province, PR China. This strain was identified as Lysinibacillus sp. based on a 16S rRNA gene sequence analysis. FJAT-4748 has been shown to possess antifungal activity against different fungi, including Colletotrichum acutatum, Aspergillus niger, Fusarium solani, Fusarium moniliforme and Fusarium oxysporum. The results of the present study indicate that this antifungal activity results from volatile organic compounds (VOCs) produced by this strain. The observed inhibition rates of VOCs from FJAT-4748 against these fungi were 100%, 100%, 37.20%, 18.94% and 7.64%, respectively. GC-MS analysis identified 24 VOCs from FJAT-4748, which included different categories of compounds, such as aldehydes, ketones, alcohols, aromatic hydrocarbons and alkanes. Of these 24 VOCs, the most abundant compound was 2-ethyl-1-hexanol, which constituted 36.24% of the total VOCs based on the relative peak area. In the in vitro C. acutatum mycelial growth assay, 2-ethyl-1-hexanol exhibited the strongest activity, with an inhibitory rate of 100% using 10 µL/plate of this VOC. The activity of benzaldehyde was lower. 2-decanone showed the weakest activity among the compounds tested. The inhibitory activity of an artificial mixture of three VOCs against the C. acutatum increased with the amount of artificial mixture used. The inhibition rate reached 100% using 30 µL/plate of this artificial mixture in the plate test. Taken together, these results show that the antifungal VOCs produced by Lysinibacillus sp. FJAT-4748 are potentially useful as agents for controlling anthracnose caused by Colletotrichum acutatum.

Substituent Effects on Electrophilic Catalysis by the Carbonyl Group: Anatomy of the Rate Acceleration for PLP-Catalyzed Deprotonation of Glycine

First-order rate constants, determined by (1)H NMR, are reported for deuterium exchange between solvent D(2)O and the α-amino carbon of glycine in the presence of increasing concentrations of carbonyl compounds (acetone, benzaldehyde, and salicylaldehyde) and at different pD and buffer concentrations. These rate data were combined with (1)H NMR data that define the position of the equilibrium for formation of imines/iminium ions from addition of glycine to the respective carbonyl compounds, to give second-order rate constants k(DO) for deprotonation of α-imino carbon by DO(-). The assumption that these second-order rate constants lie on linear structure-reactivity correlations between log k(OL) and pK(a) was made in estimating the following pK(a)'s for deprotonation of α-imino carbon: pK(a) = 22, glycine-acetone iminium ion; pK(a) = 27, glycine-benzaldehyde imine; pK(a) ≈ 23, glycine-benzaldehyde iminium ion; and, pK(a) = 25, glycine-salicylaldehyde iminium ion. The much lower pK(a) of 17 [Toth, K.; Richard, J. P. J. Am. Chem. Soc. 2007, 129, 3013-3021] for carbon deprotonation of the adduct between 5'-deoxypyridoxal (DPL) and glycine shows that the strongly electron-withdrawing pyridinium ion is unique in driving the extended delocalization of negative charge from the α-iminium to the α-pyridinium carbon. This favors carbanion protonation at the α-pyridinium carbon, and catalysis of the 1,3-aza-allylic isomerization reaction that is a step in enzyme-catalyzed transamination reactions. An analysis of the effect of incremental changes in structure on the activity of benzaldehyde in catalysis of deprotonation of glycine shows the carbonyl group electrophile, the 2-O(-) ring substituent and the cation pyridinium nitrogen of DPL each make a significant contribution to the catalytic activity of this cofactor analogue. The extraordinary activity of DPL in catalysis of deprotonation of α-amino carbon results from the summation of these three smaller effects.

The Effect of Plant Compounds from Whisky Cask on Horse Liver Alcohol Dehydrogenase Activity

Aged whisky contains many plant derived compounds from oak wood cask, and the color of whisky gradually changes to deep amber. More than 500 kinds of compounds are known as minor components in aged whisky. The taste of whisky becomes smooth with aging, and we can sober up feeling good. However, detail effect of these plant derived components from whisky cask on alcohol metabolism has not been clarified. In this experiment, we investigated the relation between the structure of components and the rate of ethanol oxidation reaction by using 26 kinds of plant derived components from oak wood cask and its derivatives. All the compounds which we used have a benzene ring as a basic frame, and have a hydroxyl group, an aldehyde group, and a carboxyl group further. All 26 compounds from oak wood cask and its derivatives used in this experiment were inhibited the ethanol oxidation. Interestingly, the relative activity of compound with an aldehyde group (Benzaldehyde and its derivatives) inhibited most strongly to be 30~40%. However, the relative activity of Benzaldehyde with one hydroxyl group had about 70% of relative activity and it had only one hydroxyl group, it clarified that the inhibition effect becomes weaker. The inhibition effect of compounds with calboxyl group (Benzoic acid and its derivatives) was weak and showed 90% of re lative activity. However, in contrast to the case of Benzaldehyde, the inhabitation effect of Benzoic acid only with one hydroxyl group becomes strong. From these results, it is clarified that many compounds from oak wood cask inhibite the ethanol oxidation. But the mechanism of inhabitation is complex and the additivity of the functional group contribution is not applied simply.

Aldehyde dehydrogenase activities in hepatocyte nodules and hepatocellular carcinomas from Wistar rats.

The activities of aldehyde dehydrogenases using benzaldehyde and propionaldehyde as substrates and NADP and NAD as coenzymes were determined in normal liver, hepatocyte nodules and hepatocellular carcinomas from male Wistar rats. Hepatocyte nodules were produced by intermittent exposure of rats to 0.05% 2-acetylaminofluorene or by initiation with diethylnitrosamine followed by selection using 2 weeks of dietary exposure to 0.02% 2-acetylaminofluorene and partial hepatectomy. The activities of propionaldehyde:NAD and benzaldehyde:NADP aldehyde dehydrogenases were increased in hepatocyte nodules of all types as well as in most hepatocellular carcinomas. The most prominent elevation of enzyme activity was found in the cytosol of persistent hepatocyte nodules (35-60 times) and some hepatocellular carcinomas (92 times) using benzaldehyde and NADP. The benzaldehyde:NADP aldehyde dehydrogenase activity varied considerably between different nodules suggesting the existence of a subpopulation of hepatocyte nodules with very high enzymatic activities. The activity of propionaldehyde:NAD aldehyde dehydrogenase activity as well as of gamma-glutamyltransferase did not show substantial internodular variations. The activity of benzaldehyde:NADP aldehyde dehydrogenase in individual carcinomas investigated in these experiments varied extensively. The data did not support the idea that all hepatomas had been developed from pre-neoplastic nodules with very high activity of this enzyme.