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After invasion of red blood cells, malaria matures within the cell by degrading hemoglobin avidly. For enormous protein breakdown in trophozoite stage, many efficient and ordered proteolysis networks have been postulated and exploited. In this study, a potential interaction of a 60-kDa Plasmodium falciparum (Pf)-heat shock protein (Hsp60) and Pf-calpain, a cysteine protease, was explored. Pf-infected RBC was isolated and the endogenous Pf-Hsp60 and Pf-calpain were determined by western blot analysis and similar antigenicity of GroEL and Pf-Hsp60 was determined with anti-Pf-Hsp60. Potential interaction of Pf-calpain and Pf-Hsp60 was determined by immunoprecipitation and immunofluorescence assay. Mizoribine, a well-known inhibitor of Hsp60, attenuated both Pf-calpain enzyme activity as well as P. falciparum growth. The presented data suggest that the Pf-Hsp60 may function on Pf-calpain in a part of networks during malaria growth. 相似文献
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Aifang Yang Chunmei He Kewei Zhang 《In vitro cellular & developmental biology. Plant》2006,42(3):215-219
Summary This study was carried out to evaluate the effects of purine synthesis inhibitor mizoribine, purine and pyrimidine synthesis
inhibitors azaserine and acivicin, and surfactant Silwet L-77 on Agrobacterium-mediated transformation efficiency of embryogenic calluses from maize elite inbred lines Qi 319 and Ye 515. After transformation
and three rounds of selection on 2.8 μM chlorsulfuron, resistant calluses were obtained subsequently, and morphologically normal plantlets were regenerated from
80 to 90% of the resistant calluses treated with the compounds. There were no obvious discrepancies between the frequencies
of plantlet regeneration and the ratio of PCR positive plantlets of calluses treated with different compounds. Results of
PCR assay with primers for betA showed that 40.2% (103/256) of the regenerated plantlets were positive. The percentage of resistant calluses was 2–3-fold
higher than the control after being treated with 0.19–0.27 mM mizoribine. The most suitable concentration of azaserin was 0.36 mM, which gave a 4-fold increase in the percentage of resistant calluses. Acivicin at 0.28–0.84 mM yielded a 3–5-fold increase in the percentage of resistant calluses, which is significantly better than the control. When
the calluses were treated with 0.01 or 0.02% Silwet L-77, the percentages of resistant calluses were 34.89 and 25.60%, respectively.
We concluded that purine synthesis inhibitors, purine and pyrimidine synthesis inhibitor and the surfactant Silwet L-77 at
optimal concentrations significantly improved the Agrobacterium-mediated transformation of maize calluses. 相似文献
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为考察金属离子和氨基酸对Eupenicillium sp.E-UN41菌体生长及其产生的次级代谢产物咪唑立宾(MZ)的生物合成影响,在培养基中添加了无机盐和氨基酸.结果表明在发酵培养基中添加适量的镁、钠、锰、钾、钙等金属离子可提高咪唑立宾产量5%~15%,添加1.0%L-组氨酸,MZ产量提高94%.添加适宜的L-天门冬氨酸和L-甘氨酸对产MZ亦有促进作用,而L-精氨酸明显抑制Eupenicillium sp.E-UN41生物合成MZ.本研究为咪唑立宾发酵的产业化奠定了基础. 相似文献
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Tomokazu Nagao Reina Kusunoki Chiaki Iwamura Shigeto Kobayashi Wako Yumura Yosuke Kameoka Toshinori Nakayama Kazuo Suzuki 《Microbiology and immunology》2013,57(9):640-650
Myeloperoxidase‐specific anti‐neutrophil cytoplasmic antibody (MPO–ANCA) is associated with rapidly progressive glomerulonephritis (RPGN) and glomerular crescent formation. Pathogenic factors in RPGN were analyzed by using SCG/Kj mice, which spontaneously develop MPO–ANCA‐associated RPGN. The serum concentration of soluble IL‐6R was determined by using ELISA and those of another 23 cytokines and chemokines by Bio‐Plex analysis. Sections of frozen kidney tissue were examined by fluorescence microscopy and the CD3+B220+ T cell subset in the spleen determined by a flow cytometry. Concentrations of IL‐6 and monocyte chemotactic protein‐1 were significantly correlated with the percentages of crescent formation. Anti‐IL‐6R antibody, which has been effective in patients with rheumatoid arthritis, was administered to SCG/Kj mice to elucidate the role of IL‐6 in the development of RPGN. MPO–ANCA titers decreased after administration of anti‐IL‐6R antibody, but not titers of mizoribine, which is effective in Kawasaki disease model mice. These results suggest that IL‐6‐mediated signaling is involved in the production of MPO–ANCA. 相似文献
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