Mach-Aigner Astrid R, Pucher Marion E, Steiger Matthias G, Bauer Gudrun E, Preis Sonja J, Mach Robert L
Gene Technology, Department of Gene Technology and Applied Biochemistry, Institute of Chemical Engineering, Technische Universität Wien, Vienna, Austria.
Appl Environ Microbiol. 2008 Nov;74(21):6554-62. doi: 10.1128/AEM.01143-08. Epub 2008 Sep 12.
In Hypocrea jecorina, Xyr1 (xylanase regulator 1) is the main transcription activator of hydrolase-encoding genes, such as xyn1, xyn2, bxl1, cbh1, cbh2, egl1, and bgl1. Even though Xyr1 mediates the induction signal for all these genes derived from various inducing carbon sources and compounds, xyr1 transcription itself is not inducible by any of these substances. However, cultivation on glucose as the carbon source provokes carbon catabolite repression of xyr1 transcription mediated by Cre1. In addition, xyr1 transcription is repressed by the specific transcription factor Ace1. Moreover, Xyr1 is permanently available in the cell, and no de novo synthesis of this factor is needed for a first induction of xyn1 transcription. The constitutive expression of xyr1 leads to a significant elevation/deregulation of the xyn1, xyn2, and bxl1 transcription compared to what is seen for the parental strain. Overall, the corresponding xylanolytic enzyme activities are clearly elevated in a constitutively xyr1-expressing strain, emphasizing this factor as an auspicious target for genetically engineered strain improvement.
在瑞氏木霉中,Xyr1(木聚糖酶调节因子1)是水解酶编码基因(如xyn1、xyn2、bxl1、cbh1、cbh2、egl1和bgl1)的主要转录激活因子。尽管Xyr1介导了所有这些基因来自各种诱导性碳源和化合物的诱导信号,但xyr1转录本身不受这些物质中的任何一种诱导。然而,以葡萄糖作为碳源进行培养会引发由Cre1介导的xyr1转录的碳分解代谢物阻遏。此外,xyr1转录受到特异性转录因子Ace1的抑制。而且,Xyr1在细胞中是永久存在的,xyn1转录的首次诱导不需要该因子的从头合成。与亲本菌株相比,xyr1的组成型表达导致xyn1、xyn2和bxl1转录显著升高/失调。总体而言,在组成型表达xyr1的菌株中,相应的木聚糖分解酶活性明显升高,强调该因子是基因工程菌株改良的一个理想靶点。