Cutting-tool management in computer-integrated manufacturing

The problem of cutting tool management has been brought to the forefront with the emergence of computer-integrated manufacturing (CIM) and, in particular, flexible manufacturing systems (FMSs). The financial and operational ramifications of effective tool management has spurred considerable research in this area during the past decade and many researchers are proposing sound solutions to various facets of this broad-ranging and difficult problem. This paper identifies critical areas of research for the development of tool management systems in CIM. To develop a framework for this, the paper examines and categorizes work in academia and in industry on the management of cutting-tools in CIM and describes some key implementations, particularly in the metal-cutting industry. The solution of manufacturing problems generally demands an eclectic approach, and for this reason, we have tried to taxonomize, describe, and critique the various research thrusts in an attempt to provide a synthesis of use in more unified approaches.     

Superoxide Production by Plant Homologues of the gp91phox NADPH Oxidase. Modulation of Activity by Calcium and by Tobacco Mosaic Virus Infection

Genes encoding homologs of the gp91(phox) subunit of the plasma membrane NADPH oxidase complex have been identified in plants and are hypothesized to be a source of reactive oxygen species during defense responses. However, the direct involvement of the gene products in superoxide (O(2)(-)) production has yet to be shown. A novel activity gel assay based on protein fractionation in native or sodium dodecyl sulfate (SDS)-denaturing polyacrylamide gels was developed. In native polyacrylamide gel electrophoresis, one or two major O(2)(-)-producing formazan bands were detected in tomato (Lycopersicum esculentum Mill. cv Moneymaker) and tobacco (Nicotiana tabacum var. Samsun, NN) plasma membranes, respectively. Denaturing fractionation of tomato and tobacco plasma membrane in SDS-polyacrylamide gel electrophoresis, followed by regeneration of the in-gel activity, revealed NADPH-dependent O(2)(-)-producing formazan bands of 106-, 103-, and 80- to 75-kD molecular masses. The SDS and native activity bands were dependent on NADPH and completely inhibited by diphenylene iodonium or CuZn- O(2)(-) dismutase, indicating that the formazan precipitates were due to reduction by O(2)(-) radicals catalyzed by an NADPH-dependent flavin containing enzyme. The source of the plasma membrane activity bands was confirmed by their cross-reaction with antibody prepared from the C terminus of the tomato gp91(phox) homolog. Membrane extracts as well as the in-gel NADPH oxidase activities were stimulated in the presence of Ca(2+). In addition, the relative activity of the gp91(phox) homolog was enhanced in the plasma membrane of tobacco mosaic virus-infected leaves. Thus, in contrast to the mammalian gp91(phox), the plant homolog can produce O(2)(-) in the absence of additional cytosolic components and is stimulated directly by Ca(2+).     

Effect of oil emulsion sprays on parasitoids of the black parlatoria, Parlatoria ziziphi, in grapefruit

The black parlatoria, Parlatoria ziziphi, a common pest of citrus in the tropics and subtropics, has become the most important citrus pest in Upper Egypt. Spray oils may be a relatively safe alternative to harmful synthetic insecticides. However, the effect of spray oils on black parlatoria and associated parasitoids is unknown. Field studies were conducted in Giza, Egypt to assess the effect of two experimental spray oils on P. ziziphi and three associated parasitoid species on grapefruit (Citrus paradisi). Triona oil was more effective than Shecrona oil and reduced scale populations by up to 99% 75 days after application. The parasitoid Encarsia citrina was not affected significantly by either spray oil. Triona oil was slightly harmful to the other primary parasitoid, Habrolepis aspidioti and reduced parasitism rate by Marietta leopardina. However, because the latter species is a hyperparasitoid, the reduction in its number by Triona was beneficial. Triona application is therefore highly effective in controlling the black parlatoria and it reduced the rate of hyperparasitism by M. leopardina. The oils had only a minor negative impact and only on the less important primary parasitoid in the system.     

Sensitization of resting T cells to autologous natural-killer-cell-mediated lysis by phytohemagglutinin

Natural killer (NK) cells are non-T, non-B cell lymphocytes that lyse a variety of tumor and virus-infected cells. In this study, we demonstrated that phytohemagglutinin (PHA) rendered resistant autologous T cells extremely sensitive to natural-killer(NK)-cell-mediated lysis. The sensitization was very rapid and concentration-dependent (0.01–1 μg/ml); 62% and 95% of autologous T cells were lysed by interleukin-2-activated NK cells 5 min and 18 h respectively after treatment with PHA (1 μg/ml). The maximal decrease in the level of MHC class I molecules observed on T cells was 22%. Induction of susceptibility to NK-mediated lysis was correlated with the expression of activation markers on T cells treated for relatively long intervals (more than 18 h) with high concentrations of PHA (more than 0.1 μg/ml). Sensitization of T cells required RNA and protein synthesis, although DNA synthesis was not essential. We propose that this unique system is suitable for studying the mechanisms involved in recognition and killing of target cells by NK cells. Received: 11 February 1999 / Accepted: 28 July 1999     

The nitric oxide donor sodium nitroprusside requires the 18?kDa Translocator Protein to induce cell death

Various studies have shown that several lethal agents induce cell death via the mitochondrial 18 kDa Translocator Protein (TSPO). In this study we tested the possibility that nitric oxide (NO) is the signaling component inducing the TSPO to initiate cell death process. Cell viability assays included Trypan blue uptake, propidium iodide uptake, lactate dehydrogenase release, and DNA fragmentation. These assays showed that application of the specific TSPO ligand PK 11195 reduced these parameters for the lethal effects of the NO donor sodium nitroprusside (SNP) by 41, 27, 40, and 42 %, respectively. TSPO silencing by siRNA also reduced the measured lethal effects of SNP by 50 % for all of these four assays. With 2,3-bis[2-methoxy-4-nitro-5-sulphophenyl]-2H-tetrazolium-5-carboxyanilide (XTT) changes in metabolic activity were detected. PK 11195 and TSPO knockdown fully prevented the reductions in XTT signal otherwise induced by SNP. Collapse of the mitochondrial membrane potential was studied with the aid of JC-1 (5,5',6,6'-tetrachloro-1,1',3,3'-tetraethyl-benzimidazolylcarbocyanine chloride). PK 11195 and TSPO knockdown reduced, respectively by 36 and 100 %, the incidence of collapse of the mitochondrial membrane potential otherwise induced by SNP. 10-N-Nonyl-Acridine Orange (NAO) was used to detect mitochondrial reactive oxygen species generation due to SNP. PK 11195 and TSPO knockdown reduced this effect of SNP by 65 and 100 %, respectively. SNP did not affect TSPO protein expression and binding characteristics, and also did not cause TSPO S-nitrosylation. However, β-actin and various other proteins (not further defined) were S-nitrosylated. In conclusion, TSPO is required for the lethal and metabolic effects of the NO donor SNP, but TSPO itself is not S-nitrosylated.