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Aspergillus fumigatus catalases: cloning of an Aspergillus nidulans catalase B homologue and evidence for at least three catalases

机译:aspergillus fumigatus催化剂:克隆曲霉属植物植物植物过症酶B同源物和至少三种过渡酶的同源物和证据

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摘要

The presence of catalases in the water soluble fractions of three Aspergillus fumigatus strains was investigated using nondenaturing and denaturing polyacrylamide gel electrophoresis and Western analysis. Using non-denaturing polyacrylamide gel electrophoresis and staining for catalase activity, three separate catalases were identified. An A. fumigatus catalase gene (catB) was cloned from genomic DNA using the Aspergillus niger catR gene as a probe. Polyclonal antibodies were raised to a glutathione S-transferase-CatB fusion product expressed in Escherichia coli. Western analysis indicated that, under denaturing conditions, the polyclonal antibody recognised a 90-kDa band and under non-denaturing conditions, two separate bands were identified. These results indicate that A. fumigatus in addition to CatB, produces at least two other catalases, one of which is similar in size to CatB. The polyclonal antibody was also used to observe catalase expression in mice, experimentally infected with A. fumigatus. Staining was observed heterogeneously throughout the fungal hyphae. This result indicates that catalase is produced by A. fumigatus during invasive aspergillosis.
机译:使用NondeNatuping和变性聚丙烯酰胺凝胶电泳和Western分析,研究了三种曲霉菌菌株的水溶性级分的过度酶的存在。使用非变性聚丙烯酰胺凝胶电泳和用于过氧化氢酶活性的染色,鉴定了三种单独的过失酶。使用Aspergillus Niger Catr基因作为探针,从基因组DNA克隆A.Fumigatus过氧化氢酶基因(CATB)。将多克隆抗体升高到大肠杆菌中表达的谷胱甘肽S-转移酶-CATB融合产物。 Western分析表明,在变性条件下,多克隆抗体识别90kDa带,并且在非变性条件下,鉴定了两个单独的条带。这些结果表明A.Fumigatus除CATB之外,还产生至少另外两个还原酶,其中一个也与CATB相似。多克隆抗体也用于观察小鼠的过氧化氢酶表达,实验地用A. fumigatus感染。在整个真菌菌丝中异质地观察到染色。该结果表明,在侵袭性曲柄中的A. fumigatus产生过氧化氢酶。

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    T Takasuka;

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  • 年度 1999
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  • 原文格式 PDF
  • 正文语种 eng
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