In situ density estimation of timber pieces by drilling residue analysis

Density values are essential for the characterization of wood elements in existing structures. A new method for the in-situ density estimation of timber pieces is proposed based on weighting the residue generated by conventional drilling. This research includes the design and development of a residue collector device coupled to a conventional drill and testing on four Spanish coniferous species: Laricio pine, Scots pine, Radiata pine and Maritime pine (Pinus nigra Arn., Pinus sylvestris L., Pinus radiata D. Don. and Pinus pinaster Ait., respectively). For each species, 44 specimens (except Scots pine, with 42) 60?×?90 mm cross-section and 150 mm length (half radial and half tangential orientation) were tested. Specimen density was obtained by mass/volume ratio. Three 8 mm diameter 46.5 mm deep holes were drilled in each specimen using a brad point bit. The drilling residue was weighed and density was calculated as a ratio to bore volume. Although only slightly smaller, residue density statistically differs from average specimen density. But the specimen density can be inferred by the correlation, statistically significant, with residuals drilling density (R²?=?80.7%) and even better with residual drilling mass (R²?=?84.4%).     

Depletion study of enrofloxacin and its metabolite ciprofloxacin in edible tissues and feathers of white leghorn hens by liquid chromatography coupled with tandem mass spectrometry

To ensure delivery of safe foods to consumers, withdrawal times for drugs must be respected according to the maximum residual limits established by regulatory agencies. Because of availability and price, feather meal is currently incorporated into animal feed as a protein source for farm species. Few data are available on residual drugs in feathers from treated animals. A depletion study was performed with laying hens treated intramuscularly with 5% enrofloxacin (Enromic) at 10 mg/kg body weight over 3 days. Thirty-three birds were treated and slaughtered at different times between 6 and 216 h after treatment; and samples of muscle plus skin, liver, kidney, and feathers were collected. High-performance liquid chromatography coupled with a tandem mass spectrometry method was validated before sample analysis to determine the decision limit, detection capability, recovery, and precision. Liver was the edible tissue with the slowest drug depletion. A withdrawal time of 6 days was calculated based on European Union maximum residual limits (100 microg/kg). A withdrawal time of 9 days was calculated based on Japan maximum residual limits (10 microg/kg). Enrofloxacin plus ciprofloxacin concentrations in feathers remained high through all sampling periods. Thus, feathers from treated animals should not be fed to food-producing animals.     

A competitive enzyme-linked immunosorbent assay for detection of bovine milk in ovine and caprine milk and cheese using a monoclonal antibody against bovine beta-casein.

A competitive ELISA (enzyme-linked immunosorbent assay) was performed to detect and quantify bovine milk in ovine and caprine milk and cheese using a monoclonal antibody (AH4 MAb) against bovine beta-casein. Ovine or caprine milk and cheese containing bovine milk were added simultaneously with the AH4 MAb to the wells of a microtiter plate that had been previously sensitized with commercial bovine beta-casein. The bovine caseins in milk or cheese samples compete with the bovine beta-casein bound to the plate for the AH4 MAb binding sites. Further immunorecognition of AH4 MAb bound to the bovine beta-casein immobilized onto the plate was attained with rabbit anti-mouse immunoglobulin conjugated to peroxidase. Subsequent enzymic conversion of the substrate showed clear differences in absorbance values during assay of mixtures of ovine and caprine milk and cheese containing various amounts of bovine milk. The competitive ELISA developed in this work allows the quantitative detection of bovine milk in ovine and caprine milk and cheese samples in the range of 0.5 to 25% of substitution.     

Functionality of enzymes that hydrolyse starch and non-starch polysaccharide in breadmaking

 Nine commercial enzyme preparations and two laboratory-designed mixes with amylase and/or pentosanase/xylanase activity were used to prepare bread samples, and the effects on bread quality and keeping properties were determined. With the doses added, enzymes significantly shortened fermentation time without affecting the pH or the machinability of the doughs. Bread with an improved volume, a greater intensity of aroma and a softer texture was obtained. Loaves had a less intense and characteristic taste and, in some cases, an uneven grain. All enzymes delayed bread firming, but rates varied with each preparation. Factor analysis classified bread samples according to their composition and source. Received:7 November 1996/Revised version: 21 January 1997     

Isolation and characterization of a new dimeric esterase from Lactobacillus sakei 23K

The M_w of a Lactobacillus sakei intracellular esterase, determined by gel filtration, was compared to those obtained from SDS-PAGE or MALDI-TOF, pointing to a dimeric structure. Its N-terminal sequence and peptide mass fingerprint suggest that it is the putative LSA044 protein from L. sakei 23K genome.     

Phenolic compounds and fatty acids in different parts of Vitis labrusca and V. vinifera grapes

trans-Resveratrol, antioxidant activity, phenolic compounds, proximate composition, and fatty-acid composition were quantified in different parts (peel, pulp, and seeds) of four grape varieties: Brazil (Vitis vinifera), Benitaka (V. vinifera), Isabel (Vitis labrusca) and Niagara (V. labrusca). Large concentrations of polyunsaturated fatty acid (18.84 and 9204.27 mg 100 g^− 1), linoleic acid (LA, 18:2n-6), from 5890.87 to 9148.93 mg 100 g^− 1, and alpha-linolenic (LNA, 18:3n-3), from 5.25 to 56.85 mg 100 g^− 1, were found in different parts of the four grape varieties. The lowest concentrations necessary for 50% inhibition of DPPH were (9.26 to 126.91 ??g mL^− 1) in seeds; the pulp did not have antioxidant activity. The total phenolic content varied between 0.04 and 122.35 mg EAG g^− 1; seeds had the highest concentrations (89.83 to 122.35 mg EAG g^− 1), especially in Niagara and Isabel varieties. trans-Resveratrol was detected in peels (1.17 to 12.96 ??g g^− 1) and seeds (2.03 to 2.44 ??g g^− 1) of the four varieties; however, it was absent in the pulp.     

Comparison of different washing treatments for reducing pathogens on orange surfaces and for preventing the transfer of bacterial pathogens to fresh-squeezed orange juice

The objectives of this study were to compare the effectiveness of various washing treatments for reducing Escherichia coli O157:H7, Salmonella sp., and Listeria monocytogenes populations on orange surfaces and to measure the effect of some of these treatments in preventing the transfer of pathogens during juice extraction. Orange surfaces inoculated with L. monocytogenes or a mixture of E. coli O157:H7 and Salmonella Typhimurium were washed by water spray and then sprayed with or dipped in water at 80°C for 1 min, 70% ethanol for 15, 30, or 45 s or 1, 2, or 4 min, 2 or 4% lactic acid solution at 55°C for 15, 30, or 45 s or 1, 2, or 4 min, or 200 mg/liter hypochlorite at pH 6.5 or 10 for 15 s. The surviving populations of these pathogens on the oranges were enumerated after each treatment. In a further stage, the ability of these pathogens to be transferred to the juice during extraction was tested. Juice was obtained from inoculated oranges that were subjected to selected treatments using chlorine, lactic acid, ethanol, and hot water as described above, and then bacterial counts in orange juice were determined. The application of these treatments reduced the populations of pathogens on orange surfaces by 1.9 to >4.9 log, 1.9 to >4.6 log, and 1.4 to 3.1 log cycles for E. coli O157:H7, Salmonella Typhimurium, and L. monocytogenes, respectively. The treatments using hot water or lactic acid showed greater reductions than other treatments. The time, antimicrobial concentration, and form of application affected the bacterial reduction. All treatments resulted in undetectable counts in the juice. Nevertheless, pathogens were recovered by the enrichment-plating method. Treatment of oranges before juice extraction may reduce the risk associated with consuming orange juice.     

Differentiation of milks and cheeses according to species based on the mineral content

Summary The mineral composition of 113 samples of ewes', cows', and goats' milk and 68 samples of different types of pure-milk cheeses made from the milks of these species was analysed. Stepwise discriminant analysis of the milk samples yielded the variables K/Mg, Na/Ca, Zn, Cu/Zn, and Cu/Na as the most useful in differentiating the samples, achieving correct classification in 98.2% of cases. The most useful variables for the cheese samples were Fe/K, Na/Ca, Zn/Cu, Na/Mg, and Zn, which yielded correct classification in 97.1% of cases. The three goat's milk cheeses were successfully distinguished using the variables K/Zn, Fe/Cu, and P.

---

Unterscheidung zwischen verschiedenen Milch- und Käsesorten anhand ihrer Mineralstoff-Zusammensetzung

Zusammenfassung An 113 Milchproben und 68 mit Schafmilch, Kuhmilch und Ziegenmilch hergestellten Käseproben wurde die Mineralstoff-Zusammensetzung analysiert. Die Anwendung der schrittweisen Diskriminatoriusanalyse bei den Milchproben ergab die Auswahl der Veränderlichen K/Mg, Na/Ca, Zn, Cu/Zn und Cu/Na als beste Unterschiedlichkeitsparameter mit einer zu 98,2% einwandfreien Klassifizierung. Die bei Käse ausgewählten Veränderlichen waren Fe/K, Na/Ca, Zn/Cu, Na/Mg und Zn mit einer zu 97,1% einwandfreien Klassifizierung. Die Unterscheidung zwischen den 3 geprüften Ziegenmilch-Käsesorten wurde durch die Veränderlichen K/Zn, Fe/Cu und P ermöglicht.

     

Regulation of proteinases during mouse peri-implantation development: urokinase-type plasminogen activator expression and cross talk with matrix metalloproteinase 9

Trophoblast cells express urokinase-type plasminogen activator (PLAU) and may depend on its activity for endometrial invasion and tissue remodeling during peri-implantation development. However, the developmental regulation, tissue distribution, and function of PLAU are not completely understood. In this study, the expression of PLAU and its regulation by extracellular matrix proteins was examined by RT-PCR, immunocytochemistry, and plasminogen-casein zymography in cultured mouse embryos. There was a progressive increase in Plau mRNA expression in blastocysts cultured on gestation days 4-8. Tissue-type plasminogen activator (55?kDa) and PLAU (a triplet of 40, 37, and 31?kDa) were present in conditioned medium and embryo lysates, and were adsorbed to the culture plate surface. The temporal expression pattern of PLAU, according to semi-quantitative gel zymography, was similar in non-adhering embryos and embryos cultured on fibronectin, laminin, or type IV collagen, although type IV collagen and laminin upregulated Plau mRNA expression. Immunofluorescence revealed PLAU on the surface of the mural trophectoderm and in non-spreading giant trophoblast cells. Exogenous human plasminogen was transformed to plasmin by cultured embryos and activated endogenous matrix metalloproteinase 9 (MMP9). Indeed, the developmental expression profile of MMP9 was similar to that of PLAU. Our data suggest that the intrinsic developmental program predominantly regulates PLAU expression during implantation, and that PLAU could be responsible for activation of MMP9, leading to localized matrix proteolysis as trophoblast invasion commences.