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首页> 外文期刊>Canadian journal of microbiology >Molecular characterization and expression profile of pectin-lyase-encoding genes from Penicillium griseoroseum.
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Molecular characterization and expression profile of pectin-lyase-encoding genes from Penicillium griseoroseum.

机译:青霉青霉的果胶裂解酶编码基因的分子表征和表达谱。

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Penicillium griseoroseum has been studied by our group because of its good pectinase production. Attempts have been done to clone pectinolytic genes, aiming to obtain pectinase-overproducing strains for industrial purposes. Here, two genes coding for pectin lyase were isolated from the P. griseoroseum genome. The plg1 gene has an open reading frame of 1341 bp coding for a putative protein of 374 amino acids with a calculated molecular mass of 40.1 kDa. The plg2 gene is characterized by an open reading frame of 1400 nucleotides and codes for a polypeptide of 383 amino acids. The plg1 gene 5'-flanking region contains putative binding sites for the transcription factors involved in regulation by ambient pH and catabolite repression. The primary structure of Plg1 and Plg2 proteins showed a relatively high homology (varying between 32.4% and 74.8%) to fungal pectin lyases characterized to date. Southern blotting analysis revealed that both genes are present as single copies in the fungus genome. Expression studies revealed a differing pattern of gene expression of plg1 and plg2 when mycelium was cultivated on medium containing different pectic components. Citric pectin followed by apple pectin were the carbon sources that best induced plg1 expression, and transcripts were detected from 24 to 76 h. The expression of the plg2 gene was monitored by reverse transcriptase - polymerase chain reaction, since Northern analysis failed to detect hybridization signals. The differential expression of these genes may provide means for the fungus to adapt to various growth conditions.
机译:由于青霉青霉的果胶酶生产良好,因此我们对其进行了研究。已经尝试克隆果胶分解基因,目的是为了工业目的获得过量生产果胶酶的菌株。在这里,从果糖假单胞菌基因组中分离出两个编码果胶裂解酶的基因。 plg1基因有一个1341 bp的开放阅读框,编码一个374个氨基酸的推定蛋白质,计算分子量为40.1 kDa。 plg2基因的特征是具有1400个核苷酸的开放阅读框,并编码383个氨基酸的多肽。 plg1基因的5'侧翼区域包含与环境pH和分解代谢物阻遏作用有关的转录因子的假定结合位点。 Plg1和Plg2蛋白的一级结构与迄今已表征的真菌果胶裂解酶显示出较高的同源性(在32.4%和74.8%之间变化)。 Southern印迹分析表明,两个基因在真菌基因组中均以单拷贝形式存在。表达研究表明,在含有不同果胶成分的培养基上培养菌丝体时,plg1和plg2的基因表达模式不同。柠檬果胶紧随其后的是苹果果胶,是最能诱导plg1表达的碳源,并且在24至76小时内检测到转录本。由于Northern分析未能检测到杂交信号,因此通过逆转录酶-聚合酶链反应监测了plg2基因的表达。这些基因的差异表达可以为真菌提供适应各种生长条件的手段。

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