d'Enfert C, Fontaine T
Laboratoire des Aspergillus, Institut Pasteur, Paris, France.
Mol Microbiol. 1997 Apr;24(1):203-16. doi: 10.1046/j.1365-2958.1997.3131693.x.
Aspergillus nidulans conidiospores contain high levels of the non-reducing disaccharide trehalose. We show that upon induction of conidiospore germination, the trehalose pool is rapidly degraded and a glycerol pool is transiently accumulated. A trehalase with an acidic pH optimum was purified from conidiospores. Characterization of the treA gene encoding this trehalase shows that it is homologous to Saccharomyces cerevisiae vacuolar acid trehalase, the product of the ATH1 gene, and to two related proteins of unknown function identified in Mycobacterium tuberculosis and Mycobacterium leprae. A. nidulans mutants that lack acid trehalase activity were constructed by gene replacement at the treA locus. Analysis of these mutants suggests that the treA gene product is localized in the conidiospore wall, is required for growth on trehalose as a carbon source, and is not involved in the mobilization of the intracellular pool of trehalose. Therefore, it is proposed that a cytoplasmic regulatory trehalase is controlling this latter process.
构巢曲霉分生孢子含有高水平的非还原性二糖海藻糖。我们发现,在诱导分生孢子萌发时,海藻糖池迅速降解,甘油池短暂积累。从分生孢子中纯化出一种最适pH为酸性的海藻糖酶。对编码该海藻糖酶的treA基因的表征表明,它与酿酒酵母液泡酸性海藻糖酶(ATH1基因的产物)以及在结核分枝杆菌和麻风分枝杆菌中鉴定出的两种功能未知的相关蛋白同源。通过在treA位点进行基因替换构建了缺乏酸性海藻糖酶活性的构巢曲霉突变体。对这些突变体的分析表明,treA基因产物定位于分生孢子壁,是利用海藻糖作为碳源生长所必需的,且不参与细胞内海藻糖池的动员。因此,有人提出一种细胞质调节性海藻糖酶控制着后一过程。