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81.
Fatty acid hydroperoxide lyase (HPOL), an enzyme of the octadecanoid pathway that forms carbon-6 aldehydes such as n-hexanal or (Z)-3-hexenal, was cloned from Arabidopsis thaliana as a full-length cDNA. The HPOL activity obtained by expressing the cDNA in Escherichia coli formed n-hexanal from linoleic acid 13-hydroperoxide, whereas linoleic acid 9-hydroperoxide was not a substrate for the enzyme. The HPOL mRNA is expressed at low level in leaves; however, its accumulation can be found in the inflorescence. Wounding or methyl jasmonate treatments increase the mRNA level in leaves. These results indicate that the HPOL gene is up-regulated in leaves in response to wounding and that the enzyme may be an active component of the octadecanoid defense response. 相似文献
82.
Immune gene therapy of experimental mouse brain tumor with adenovirus-mediated gene transfer of murine interleukin-4 总被引:1,自引:0,他引:1
Yoshikawa K Kajiwara K Ideguchi M Uchida T Ito H 《Cancer immunology, immunotherapy : CII》2000,49(1):23-33
We examined the antitumor activity of replication-deficient adenoviral vectors carrying the murine interleukin-4 (IL-4) gene
(AdCIL4) using a syngeneic brain tumor model in mice. Mice implanted with malignant astrocytoma cells infected with AdCIL4
survived significantly longer than those in the control groups. Immunocytochemical analysis of the tumors showed that AdCIL4
caused the strong up-regulation of MHC class II antigen expression by the tumor cells and macrophages, and consequent infiltration
by CD8+ T lymphocytes. This study demonstrates the efficacy of IL-4 gene transfection mediated by adenoviral vectors for intracerebral
tumor and characterizes the immunoreaction caused by AdCIL4.
Received: 27 August 1999 / Accepted: 12 November 1999 相似文献
83.
84.
Genes encoding an alpha-oxygenase, in Nicotiana tabacum and Arabidopsis thaliana, have been recently isolated. However, the reaction mechanism of the enzyme has not so far been elucidated. In this study, a cDNA encoding the fatty acid alpha-oxygenase gene in rice plants was isolated. The deduced amino acid sequence showed high similarity (63.6%) to that of N. tabacum. The gene was cloned into an expression vector system, pQE-30, and expressed in Escherichia coli as a host cell. Palmitic acid as a substrate was incubated with the lysate of the cells, and the products were analysed by HPLC. A compound formed predominantly by the recombinant enzyme was shown to be n-pentadecanal. By incubating the mixture at 0 degrees C, 2-hydroperoxypalmitic acid was detected as a primary product and little formation of n-pentadecanal was detected. Furthermore, uptake of molecular oxygen was observed with an oxygen electrode. This indicated that the gene in rice plants encodes the alpha-oxygenase. 相似文献
85.
86.
Fatty acid hydroperoxide lyase in tomato fruits: cloning and properties of a recombinant enzyme expressed in Escherichia coli 总被引:2,自引:0,他引:2
Matsui K Miyahara C Wilkinson J Hiatt B Knauf V Kajiwara T 《Bioscience, biotechnology, and biochemistry》2000,64(6):1189-1196
Fatty acid hydroperoxide lyase (HPL) is a member of a novel subfamily of cytochrome P450 and catalyzes a cleavage reaction of fatty acid hydroperoxides to form short-chain aldehydes and oxo-acids. A cDNA encoding tomato fruit HPL (LeHPL) was obtained. An active LeHPL was expressed in E. coli and purified. It showed highest activity against the 13-hydroperoxide of linolenic acid, followed by that of linoleic acid. 9-Hydroperoxides were poor substrates. The absorption spectrum of the purified LeHPL in the native form was similar to that of most P450s although a CO-adduct having a lambda max at 450 nm could not be obtained. LeHPL activity is reversibly inhibited by nordihydroguaiaretic acid, while salicylic acid irreversibly inhibited it. LeHPL is kinetically inactivated by fatty acid hydroperoxides, especially 9-hydroperoxides. The inactivation is prevented by inhibitors of LeHPL. Thus, HPL catalytic activity is thought to be essential to its inactivation. During the inactivation, an abolition of the Soret band was evident, indicating that inactivation is caused mainly by degradation of the prosthetic heme in LeHPL. 相似文献
87.
Stability analysis of pathogen-immune interaction dynamics 总被引:2,自引:0,他引:2
The paper considers models of dynamics of infectious disease in vivo from the standpoint of the mathematical analysis of stability. The models describe the interaction of the target cells, the pathogens, and the humoral immune response. The paper mainly focuses on the interior equilibrium, whose components are all positive. If the model ignores the absorption of the pathogens due to infection, the interior equilibrium is always asymptotically stable. On the other hand, if the model does consider it, the interior equilibrium can be unstable and a simple Hopf bifurcation can occur. A sufficient condition that the interior equilibrium is asymptotically stable is obtained. The condition explains that the interior equilibrium is asymptotically stable when experimental parameter values are used for the model. Moreover, the paper considers the models in which uninfected cells are involved in the immune response to pathogens, and are removed by the immune complexes. The effect of the involvement strongly affects the stability of the interior equilibria. The results are shown with the aid of symbolic calculation software. 相似文献
88.
89.
O-Wang J Kajiwara K Kawamura K Kimura M Miyagishima H Koseki H Tagawa M 《Biochemical and biophysical research communications》2002,293(3):1132-1137
The REV3 gene of budding yeast encodes the catalytic subunit of DNA polymerase zeta that carries out translesion DNA synthesis. While REV3-null yeast mutants are viable and exhibit normal growth, Rev3-deficient mice die around midgestation of embryogenesis, which is accompanied by massive apoptosis of cells within the embryo proper. We have investigated whether REV3 is required for the survival of mouse cells and whether the embryonic lethality caused by REV3 deficiency can be rescued by introduction of a Rev3 transgene or by inactivation of p53, the cellular gatekeeper that regulates DNA damage-induced apoptosis. We show that Rev3(-/-) blastocysts were unable to survive and grow in culture but expression of a Rev3 transgene restored their outgrowth. Moreover, Rev3 transgene expression suppressed the apoptosis in E7.5 Rev3(-/-) embryos. The Rev3(-/-) embryonic lethality, however, was not rescued by either Rev3 transgene expression or p53 deficiency. These results reveal an essential role for REV3 in the survival and growth of mammalian cells and suggest that Rev3(-/-) embryonic death occurs in a p53-independent pathway. 相似文献
90.