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里氏木霉中纤维素酶转录因子XYR1、ACE2和ACE1在高产和低产纤维素酶菌株中的差异调控

Differential regulation of the cellulase transcription factors XYR1, ACE2, and ACE1 in Trichoderma reesei strains producing high and low levels of cellulase.

作者信息

Portnoy Thomas, Margeot Antoine, Seidl-Seiboth Verena, Le Crom Stéphane, Ben Chaabane Fadhel, Linke Rita, Seiboth Bernhard, Kubicek Christian P

机构信息

IFP Energies nouvelles, Département Biotechnologie, 1-4 Avenue de Bois-Préau, 92852 Rueil-Malmaison Cedex, France.

出版信息

Eukaryot Cell. 2011 Feb;10(2):262-71. doi: 10.1128/EC.00208-10. Epub 2010 Dec 17.

Abstract

Due to its capacity to produce large amounts of cellulases, Trichoderma reesei is increasingly being investigated for second-generation biofuel production from lignocellulosic biomass. The induction mechanisms of T. reesei cellulases have been described recently, but the regulation of the genes involved in their transcription has not been studied thoroughly. Here we report the regulation of expression of the two activator genes xyr1 and ace2, and the corepressor gene ace1, during the induction of cellulase biosynthesis by the inducer lactose in T. reesei QM 9414, a strain producing low levels of cellulase (low producer). We show that all three genes are induced by lactose. xyr1 was also induced by d-galactose, but this induction was independent of d-galactose metabolism. Moreover, ace1 was carbon catabolite repressed, whereas full induction of xyr1 and ace2 in fact required CRE1. Significant differences in these regulatory patterns were observed in the high-producer strain RUT C30 and the hyperproducer strain T. reesei CL847. These observations suggest that a strongly elevated basal transcription level of xyr1 and reduced upregulation of ace1 by lactose may have been important for generating the hyperproducer strain and that thus, these genes are major control elements of cellulase production.

摘要

由于里氏木霉具有产生大量纤维素酶的能力,它越来越多地被用于研究从木质纤维素生物质生产第二代生物燃料。里氏木霉纤维素酶的诱导机制最近已有描述,但参与其转录的基因调控尚未得到充分研究。在此,我们报告了在里氏木霉QM 9414(一种纤维素酶产量低的菌株,即低产菌株)中,诱导剂乳糖诱导纤维素酶生物合成过程中,两个激活基因xyr1和ace2以及共抑制基因ace1的表达调控情况。我们发现这三个基因均受乳糖诱导。xyr1也受d -半乳糖诱导,但这种诱导与d -半乳糖代谢无关。此外,ace1受到碳代谢物阻遏,而xyr1和ace2的完全诱导实际上需要CRE1。在高产菌株RUT C30和超产菌株里氏木霉CL847中观察到这些调控模式存在显著差异。这些观察结果表明,xyr1的基础转录水平大幅升高以及乳糖对ace1上调作用的降低可能对产生超产菌株很重要,因此,这些基因是纤维素酶产生的主要控制元件。

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