TL;DR: In this paper, dendrochenlical and foliar biocllemical markers indicate perturbations in biological processes in healthy red spruce trees across the northeastern USA.
Abstract: Dendrochemical and biochemical markers link stress in apparently healthy red spruce trees (Picea rubeits) to acidic deposition. Acidic deposition to spruce forests of the northeastern USA increased sharply during the 1960s. Previous reports related visible damage of trees at high elevations to root and soil processes. In this report, dendrochenlical and foliar biocllemical markers indicate perturbations in biological processes in healthy red spruce trees across the northeastern USA. Previous research on the dendrochemistry of red spruce ste~nwood indicated that under uniform environmental conditions, stemwood concentrations of Ca and Mg decreased with increasing radial distance from the pith. For nine forest locations, frequency analysis shows that 28 and 52% of samples of red spruce stemwood formed in the 1960s are enriched in Ca and Mg, respectively, relative to wood formed prior to and after the 1960s. This enrich~nent in trees tllroughont the northeastern USA may be interpretable as a signal of increased availability of essential cations in forest soils. Such a temporary increase in the availability of Ca and Mg could be caused by cation mobilization, a consequence of increased acidic deposition. During cation mobilization, essential Ca and Mg as well as potentially harnlful Al become more available for interaction with binding sites in the soil and absorbing roots. As conditions which favor cation nlobilization continue, Ca and Mg can be leached or displaced from the soil. A nleasure of the interaction between Ca and Al is the AUCa binding ratio (molar charge ratio of exchangeable Al to exchangeable Ca). As the AUCa binding ratio in the root zone increased from 0.3 to 1.9, the foliar concentration of the biochen~ical stress marker putrescine also increased from 45 to 145 nm g-.'. The correlation of the pntrescine concentration to the AUCa binding ratio (adj. r" 0.68, P < 0.027) suggests that foliar stress may be linked to soil chenlistry. the mobilization of harmful A1 in high elevation watersheds of the northeastern USA was associated with the atmospheric deposition of nitric and sulfuric acid (Cronan and Schofield, 1979). This mobilization of A1 was described as a possible cause for the deterioration of forest canopies, and death of red spruce trees in these same watersheds (Hertel, 1988).
TL;DR: In inhibition studies, inhibition studies showed that LnqQ and AucA have different antimicrobial potency against the Gram-positive strains tested, suggesting that sequence disparities play a crucial role in their mechanisms of action.
Abstract: Lacticin Q (LnqQ) and aureocin A53 (AucA) are leaderless bacteriocins from Lactococcus lactis QU5 and Staphylococcus aureus A53, respectively. These bacteriocins are characterized by the absence of an N-terminal leader sequence and are active against a broad range of Gram-positive bacteria. LnqQ and AucA consist of 53 and 51 amino acids, respectively, and have 47% identical sequences. In this study, their three-dimensional structures were elucidated using solution nuclear magnetic resonance and were shown to consist of four α-helices that assume a very similar compact, globular overall fold (root-mean-square deviation of 1.7 A) with a highly cationic surface and a hydrophobic core. The structures of LnqQ and AucA resemble the shorter two-component leaderless bacteriocins, enterocins 7A and 7B, despite having low levels of sequence identity. Homology modeling revealed that the observed structural motif may be shared among leaderless bacteriocins with broad-spectrum activity against Gram-positive organisms. The elucidated structures of LnqQ and AucA also exhibit some resemblance to circular bacteriocins. Despite their similar overall fold, inhibition studies showed that LnqQ and AucA have different antimicrobial potency against the Gram-positive strains tested, suggesting that sequence disparities play a crucial role in their mechanisms of action.
TL;DR: Both functionals were found to perform very well in reproducing experimental D(0) ( composite function), IE, and molecular parameters, and theoretical calculations were carried out for these species by density functional theory methods used in conjunction with Stuttgart relativistic effective core potentials.
Abstract: The intermetallic molecules AuBe and AuCa were identified by means of the Knudsen-Effusion Mass Spectrometry technique in the high-temperature vapors produced by vaporizing Au-Be-Ca alloys of proper composition. The gaseous equilibria AuBe(g)+Au(g)=Au2(g)+Be(g) and AuCa(g)+Au(g)=Au2(g)+Ca(g) were studied in the temperature ranges 1720–1841 K and 1669–1841 K, respectively, by monitoring the partial pressures of all the species involved. The equilibrium data were analyzed by the third-law method, obtaining for the first time the dissociation energy D0∘ of the two intermetallic species: D0∘(AuBe)=234.0±4.0 kJ/mol; D0∘(AuCa)=246.7±4.0 kJ/mol. These values are significantly higher than the recently published D0∘ of the species AuMg (175.4±2.7 kJ/mol). Furthermore, the ionization energies (IE) of AuBe, AuMg, and AuCa were obtained by measuring the electron impact ionization efficiency curves, IE(AuBe)=7.5±0.3 eV, IE(AuMg)=6.7±0.3 eV, and IE(AuCa)=5.5±0.3 eV. Theoretical calculations were also carried out for th...