Influence of fruit variety, harvest technique, quality sorting, and storage on the native microflora of unpasteurized apple cider

Apple variety, harvest, quality sorting, and storage practices were assessed to determine their impact on the microflora of unpasteurized cider. Seven apple varieties were harvested from the tree or the ground. The apples were used fresh or were stored at 0 to 4 degrees C for < or = 5 months and were pressed with or without quality selection. Cider yield, pH, Brix value, and titratable acidity were measured. Apples, postpressing apple pomace, and cider samples were analyzed for aerobic bacteria, yeasts, and molds. Aerobic bacterial plate counts (APCs) of ciders from fresh ground-picked apples (4.89 log CFU/ml) were higher than those of ciders made from fresh, tree-picked apples (3.45 log CFU/ml). Quality sorting further reduced the average APC to 2.88 log CFU/ml. Differences among all three treatment groups were significant (P < 0.0001). Apple and pomace microbial concentrations revealed harvest and postharvest treatment-dependent differences similar to those found in cider. There were significant differences in APC among apple varieties (P = 0.0001). Lower counts were associated with varieties exhibiting higher Brix values and higher titratable acidity. Differences in APC for stored and fresh apples used for cider production were not significant (P > 0.05). Yeast and mold counts revealed relationships similar to those for APCs. The relationship between initial microbial load found on incoming fruit and final cider microbial population was curvilinear, with the weakest correlations for the lowest apple microflora concentrations. The lack of linearity suggests that processing equipment contributed to cider contamination. Tree-picked quality fruit should be used for unpasteurized cider production, and careful manufacturing practices at cider plants can impact both safety and quality of the final product.     

Tracing Listeria monocytogenes isolates from cold-smoked salmon and its processing environment in Iceland using pulsed-field gel electrophoresis

Listeria spp. and Listeria monocytogenes contamination of cold-smoked salmon (n=125) and its processing environment (n=522) were evaluated during surveys conducted in 1997-1998 and 2001 as well as in samples of final products analysed in 2001. The overall frequencies of Listeria spp. and L. monocytogenes in samples from all sources were 15.1% and 11.3%, respectively, but the incidence of L. monocytogenes in cold-smoked salmon final products was only 4%. A total of 201 L. monocytogenes isolates were characterised by Pulsed-Field Gel Electrophoresis (PFGE) in order to trace L. monocytogenes contamination in the processing plants. The combination of AscI and ApaI macrorestriction patterns yielded 24 different pulsotypes in 6 plants. One pulsotype observed by AscI restriction digestion comprised 148 of the 167 typed isolates from two processing plants. Two other pulsotypes predominated in samples from raw material, processing environments and final products. The results indicate that raw material, floors, and drains are potential sources of the L. monocytogenes found on cold-smoked salmon products. This highlights the need to readdress the design and cleaning of processing plants and equipment, and staff behavior. Hindering the introduction into and spread of the organism through the processing environment is necessary to avoid jeopardizing safety of the final product.     

Efficient H-NMR Quantitation and Investigation of N-Acetyl-d-glucosamine (GlcNAc) and N,N'-Diacetylchitobiose (GlcNAc)(2) from Chitin

A quantitative determination method of N-acetyl-d-glucosamine (GlcNAc) and N,N'-diacetylchitobiose (GlcNAc)(2) is proposed using a proton nuclear magnetic resonance experiment. N-acetyl groups of GlcNAc and (GlcNAc)(2) are chosen as target signals, and the deconvolution technique is used to determine the concentration of the corresponding compound. Compared to the HPLC method, (1)H-NMR spectroscopy is simple and fast. The method can be used for the analysis of chitin hydrolyzed products with real-time analysis, and for quantifying the content of products using internal standards without calibration curves. This method can be used to quickly evaluate chitinase activity. The temperature dependence of (1)H-NMR spectra (VT-NMR) is studied to monitor the chemical shift variation of acetyl peak. The acetyl groups of products are involved in intramolecular H-bonding with the OH group on anomeric sites. The rotation of the acetyl group is closely related to the intramolecular hydrogen bonding pattern, as suggested by the theoretical data (molecular modeling).     

Combined pharmacophore modeling, docking, and 3D-QSAR studies of PLK1 inhibitors

Polo-like kinase 1, an important enzyme with diverse biological actions in cell mitosis, is a promising target for developing novel anticancer drugs. A combined molecular docking, structure-based pharmacophore modeling and three-dimensional quantitative structure-activity relationship (3D-QSAR) study was performed on a set of 4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline derivatives as PLK1 inhibitors. The common substructure, molecular docking and pharmacophore-based alignment were used to develop different 3D-QSAR models. The comparative molecular field analysis (CoMFA) and comparative molecule similarity indices analysis (CoMSIA) models gave statistically significant results. These models showed good q(2) and r(2) (pred) values and revealed a good response to test set validation. All of the structural insights obtained from the 3D-QSAR contour maps are consistent with the available crystal structure of PLK1. The contour maps obtained from the 3D-QSAR models in combination with the structure based pharmacophore model help to better interpret the structure-activity relationship. These satisfactory results may aid the design of novel PLK1 inhibitors. This is the first report on 3D-QSAR study of PLK1 inhibitors.     

Improvement of the uniformity and dipole ferromagnetism in Co nanodots assemblies on Pb/Si(111) via step tuned dimensionality variation

We fabricated quasi-one-dimensional Co nanochain assemblies and two-dimensional Co nanodot assemblies on Pb/Si(111) substrates by step decoration. The morphology and magnetic properties of these two kinds of Co nanodot assemblies were investigated by in situ scanning tunneling microscopy and magneto-optical Kerr effect measurements. It was found that the steps cannot only improve the uniformity of the Co nanodots, but also increase the critical temperature T(c). Monte Carlo simulation indicates that the ferromagnetism mainly originates from the dipolar interactions and the critical temperature T(c) can be enhanced by introducing an in-plane uniaxial magnetic anisotropy via the step tuned dimensionality variation of the nanodot assemblies.     

Adsorption characteristics of Orange II and Chrysophenine on sludge adsorbent and activated carbon fibers

Sludge adsorbent (SA) and commercial activated carbon fibers (ACFC and ACFT) were applied to Orange II and Chrysophenine (CH) adsorption (BET surface area: ACFC>ACFT>SA). ACFT was primarily in the micropore range, while SA was approximately 500 A (macropore) and 80 A (mesopore). The ACFC pore volume was high in both the mesopore and micropore regions. Measurement of the oxygen surface functional groups of the adsorbents using Boehm's titration method showed a similar distribution on the carbon fibers (mainly in the carbonyl group), while SA was mainly in the carboxyl, lactone and phenolic groups. The SA, ACFC and ACFT adsorption capacities of Orange II (30-80 mg/l) ranged from 83 to 270, 209-438, and 25-185 mg/g at temperatures ranging from 10 to 60 degrees C, respectively. CH concentration ranged from 30 to 80 mg/l, corresponding to SA and ACFC adsorption capacities of 39-191 and 48-374 mg/g over the defined temperature range, from 10 to 60 degrees C. CH adsorption on ACFT was low. The adsorption capacity of Orange II on ACFT was lower than on SA at 10 degrees C, but at higher temperatures the Orange II molecules were transported into the ACFT, producing an adsorption capacity similar to that of SA. Mass transfer increased with temperature, overcoming the adsorption energy barrier. Overall, SA and ACFC were more effective than ACFT.     

Dinoflagellate cysts and hydrographical change in Gullmar Fjord, west coast of Sweden

This high-resolution study of the latest Holocene dinoflagellate cyst record from Gullmar Fjord, on the west coast of Sweden, provides evidence for the recognition of two major dinoflagellate communities within the fjord over the last 85 years. These communities may have their origins with the history of cultural eutrophication within the region, but are more likely to be associated with the wider phenomenon of the North Atlantic Oscillation and/or the complex hydrographical response of the fjord to various changing climatic environments between 1915 and 1999. The changing dinoflagellate cyst populations are compared in detail with the many hydrographical parameters available from this well studied fjord with its long instrumental records. Indeed the dinoflagellate cysts fail to demonstrate a convincing ongoing eutrophication record for the fjord but do show a major change in the cyst assemblages at about 1969/1970 at a time when the NAO was changing from a negative phase to the present-day positive phase. Gullmar Fjord is important in the history of dinoflagellate cyst studies, being the site of the 1954 study by Erdtman in which viable cysts, produced within the phytoplankton, were first documented within the water column.     

一种新型的共轴叠加复合涡旋光束

利用束腰半径不同、拓扑电荷数不相等的两束拉盖 尔高斯涡旋光束共轴叠加,产生了一种新型的复合涡旋光束。研究了束腰半径大小对光束分 布的影响以及复合涡旋光束的空间传播特性。结果表明,通过 改变其中一束拉盖尔高斯涡旋光束的束腰半径可以控制复合涡旋光束的明暗花瓣与光束中心 间距离; 复合涡旋光束在空间传播过程中表现出衍射展宽和古伊旋转等特性。基于反射式空间光调制 器(SLM)的 光电实验验证了上述结果。本文研究对深入理解复合涡旋光束的形成、分布特征以及其空间 传播特性等提供了一定的理论和实验依据。