Departamento de Biologia Celular, Universidade de Brasília, 70910-900 DF, Brazil.
Microbiol Res. 2010;165(1):75-81. doi: 10.1016/j.micres.2008.08.002. Epub 2008 Sep 18.
The regulation of the gene encoding the extracellular exo-beta-1,3-glucanase (tag83) produced by the mycoparasite Trichoderma asperellum was studied. Enzyme activity was detected in all carbon sources, but the highest levels were found when starch and purified cell walls from Rhizoctonia solani were used. These results are supported by the appearance of one strong band with enzyme activity in non-denaturing PAGE. Experiments using RT-PCR showed that exo-beta-1,3-glucanase induction in T. asperellum occurred at the transcriptional level. We used RT-PCR and real-time PCR analysis to examine the expression of tag83 gene during in vivo assay of T. asperellum against R. solani. We showed that the expression of tag83 is significantly increased by the presence of R. solani.
研究了产朊假丝酵母(Trichoderma asperellum)所产生的胞外外-β-1,3-葡聚糖酶(tag83)基因的调控。在所有碳源中都检测到了酶活性,但当使用淀粉和立枯丝核菌的纯化细胞壁时,酶活性达到最高水平。这些结果得到了非变性 PAGE 中出现一条具有酶活性的强带的支持。使用 RT-PCR 的实验表明,产朊假丝酵母中的外-β-1,3-葡聚糖酶诱导发生在转录水平。我们使用 RT-PCR 和实时 PCR 分析来检查 tag83 基因在产朊假丝酵母对抗立枯丝核菌的体内试验中的表达。我们表明,tag83 的表达在立枯丝核菌存在时显著增加。