Preparation of spread oils meeting U.S. Food and Drug Administration Labeling requirements for trans fatty acids via pressure-controlled hydrogenation

On July 11, 2003, the U.S. Food and Drug Administration (FDA) announced final regulations for trans fatty acid (TFA) labeling. By January 1, 2006, the TFA content of foods must be labeled as a separate line on the Nutrition Facts label. Products containing <0.5 g of TFA/14 g serving may be declared as zero. This paper describes technologies allowing compliance with TFA labeling requirements. Soybean oil was hydrogenated in a 2-L vessel at temperatures ranging from 120 to 170 degrees C at a hydrogen pressure of 200 psi. A commercial nickel-supported catalyst (25% Ni) was used at 0.02% Ni by weight of oil. The hydrogenated oils were characterized for fatty acid composition, solid fat content, and melting point. Compared to commercially processed soybean oil basestocks that typically contain approximately 40% TFA, those obtained at lower temperatures and higher pressures contain >56% less TFA. Basestocks prepared in the laboratory when blended with liquid soybean oil will yield spread oils meeting FDA labeling requirements for zero TFA, that is, <0.5 g of TFA/serving.     

Resistance to ascochyta blights of cool season food legumes

Ascochyta blights are the most important diseases of cool season food legumes (peas, lentils, chickpeas, and faba beans) and are found in nearly all production regions. Despite having the same common disease name, the pathogen species differ for each of the crops. These diseases cause serious yield losses under favourable cool and humid conditions. Planting resistant cultivars is often the first choice and most economical means in managing the diseases. Therefore breeding for resistance to ascochyta blights has been an important objective of many cool season food legume research programmes. Systematic screening of germplasm collections at international research centres and other national research programmes have identified useful resistance sources that have been used successfully to breed resistant or tolerant cultivars. Genetic studies have revealed inheritance patterns of the resistance genes. Genetic linkage analyses and QTL mapping have identified molecular markers that could be useful for marker-assisted selection and gene pyramiding. In general, research towards developing resistance to ascochyta blights in cool season food legume faces mainly two limitations: the lack of availability of efficient resistance sources and the lack of a good understanding of the variability of the pathogen populations. Research efforts to alleviate these limitations should be pursued. Given that modern technologies of marker development and genomics are available, further advances in deploying resistance to manage ascochyta blights in this group of legume crops will depend on concerted efforts in developing accurate screening procedures with adequate knowledge of pathogen variability and identification of additional sources of resistance.     

根系限制对番茄幼苗生长、根系呼吸、ATPase和PPase活性的影响

 采用营养液水培的方式, 研究了根系限制处理对番茄幼苗生长、根系呼吸、质膜和液泡膜上相关酶以及根尖细胞超微结构的影响。结果表明, 在处理初期, 根系限制促进了番茄幼苗根系细胞色素途径呼吸而抑制了交替途径呼吸; 而在后期, 根系限制处理显著地抑制了番茄植株的生长, 对根系的生长抑制更为明显, 且抑制过程伴随着根系总呼吸、细胞色素途径呼吸的降低。此外, 根系限制显著抑制了质膜H⁺ -ATPase, 液泡膜H⁺-ATPase和H⁺ -PPase的活性并导致根尖细胞核的解体。     

The toxicities of some analogues of dieldrin,endosulfan and isobenzan to bloodsucking diptera,especially tsetse flies

The dieldrin analogue, 1, 8, 9, 10, 11, 11-hexachloro-4, 5-exo-epoxy-2, 3-7, 6-endo-tricyclo-[6.2.1.0^{2, 7}]undec-9-ene (HEOM), and the isomeric 3, 4-exo-epoxy-and 3, 6-endo-epoxy compounds (HCE and ODA, respectively), incorporating structural modifications of the non-chlorinated ring system, were tested against adult mosquitoes (mainly Anopheles stephensi List.), tsetse flies (mainly Glossina austeni Newst.) and stable flies, Stomoxys calcitrans (L.). The order of toxicity was ODA > HCE > HEOM. In further tests of residual activity against A. stephensi, ODA was better than HCE but neither was sufficiently persistent to be a promising mosquito toxicant. Analogues of dieldrin (HEOD), endosulfan and isobenzan with reduced numbers of chlorine atoms were tested against G. austeni. In the pentachloro-analogues of dieldrin and α-endosulfan, the anti-bridge chlorine was more important than the syn-chlorine for toxicity. The general effect of reductive dechlorination was to reduce toxicity, but the effect was small for some endosulfan analogues and in one case there was an increase in toxicity. In the main, toxicities of the endosulfan analogues compared favourably with those of the dieldrin analogues. However, toxicity fell drastically following replacement of the second ethylenic chlorine in isobenzan. The effect of these structural changes on toxicity evidently varied from one series to another and was influenced in an unpredictable manner by the rest of the molecule.     

Contagious equine metritis: Antibody response of experimentally infected pony mares

Intrauterine inoculation of pony mares with the bacterium that is the causative agent of contagious equine metritis (CEM) resulted in clinical disease. A humoral immune response could be detected by agglutination and complement fixation (CF), and in some cases precipitating antibody was found by immunodiffusion tests. Agglutinating antibody was the most reliable serological indicator of overt infection and was detected in 8 of 28 mares after initial intrauterine inoculation of 3–4 × 10⁵ bacteria. Seventy percent of mares given a second inoculation and all mares given a third inoculation of 3–4 × 10⁵ bacteria produced detectable agglutinating antibody. Only two of five mares given the third inoculation developed detectable complement-fixing antibody. Only one mare showed evidence of reinfection after a second or third intrauterine inoculation. All of the mares given a single intrauterine inoculum of ≥ 8 × 10⁸ bacteria produced agglutinating antibody 10 to 30 days postinoculation (DPI) and 86% gave a positive CF test 10 to 20 DPI. Only mares with an agglutination titer of 320 or more produced precipitating antibody. Sera were considered positive in agglutination tests if they were reactive at a dilution of greater than 4 and positive in CF tests if they were reactive at a dilution of 4 or greater.Pony serum frozen at ?70°C was anticomplementary (AC). Treatment at 56°C abolished AC activity and revealed enhancing or procomplementary activity with guinea pig complement. Procomplementary activity could be abolished by treatment of heated pony serum with formaldehyde, which increased CF titers ≥ threefold in weakly reactive sera.     

Quick estimation of dieldrin in fresh cotton-leaf samples

Hexane was the most convenient extraction solvent. Consistent recoveries of 80% dieldrin were obtained after cold grinding with 10 mi hexane/g of leaf for 5 min. After filtering, solutions did not require a “clean-up” before g.l.c. analysis, provided they were not concentrated further. Radioactive dieldrin in such extracts could be directly counted with a simple scintillation apparatus if pre-treated with acidified potassium permanganate solution to eliminate the colour-quenching effect and stored in the dark for 24 h to allow phosphorescence from some leaf materials to decay. Extractions using other solvents would need a “clean-up” procedure before g.l.c. analysis, but radioactive dieldrin in hexane-isopropanol extracts could be quickly estimated by simple scintillation counting after decolorisation with sodium hypochlorite and storage in the dark for 24 h.     

Recombinant single-chain canine interleukin 12 induces interferon gamma mRNA expression in peripheral blood mononuclear cells of dogs with visceral leishmaniasis

Canine visceral leishmaniasis poses important concerns for public health and veterinary medicine in many areas of the world. Resistance to it seems to be associated with cellular specific immune responses of the so-called Th1 type. Interleukin-12 (IL-12) is one of the most potent inducers of Th1 type of immune responses to co-administered antigens. Herein, the cloning of canine IL-12, as a single-chain fusion protein (sccaIL-12), and its expression in biologically active form in COS-7 cells is reported. Supernatants from these cells stimulated the expression of comparable amounts of interferon gamma mRNA in peripheral blood mononuclear cells from dogs with natural visceral leishmaniasis. In addition, after stimulation with sccaIL-12, there was no difference between interferon gamma mRNA expressions in peripheral blood mononuclear cells of dogs with visceral leishmaniasis and from normal healthy control animals.     

The effects of dietary n-3 vs. n-6 fatty acids on ex-vivo LTB4 generation by canine neutrophils

Dietary n-3 polyunsaturated fatty acids are widely used for amelioration of inflammatory skin disease in dogs. In this study, a diet containing two different sources of n-3 polyunsaturated fatty acid–triglyceride (from menhaden oil) and concentrated ethyl esters–was fed to one group of six purpose-bred dogs, while an isocaloric isonitrogenous diet with corn oil (n-6 polyunsaturated fatty acids) was fed to another group of eight purpose-bred dogs for six weeks. Peripheral blood neutrophils, isolated at week–1 (baseline), week 2 and week 6, were stimulated with calcium ionophore A23187 and the amount of leukotriene B₄ produced was determined via reversed-phase high performance liquid chromatography. Analysis of variance of log-transformed data revealed a significant effect for diet ( P  = 0.005) at six weeks, with dogs fed the high n-3 polyunsaturated fatty acid diet having significantly less mean ex vivo neutrophil leukotriene B₄ production than dogs fed the high n-6 polyunsaturated fatty acid diet. Further studies on the clinical usefulness of n-3 polyunsaturated fatty acid ethyl esters are warranted.