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用 RNA 干扰技术解除康宁木霉中的碳源分解代谢物阻遏作用以提高纤维素酶产量。

RNA interference with carbon catabolite repression in Trichoderma koningii for enhancing cellulase production.

机构信息

School of Life Sciences, Northeast Normal University, Changchun 130024, China.

出版信息

Enzyme Microb Technol. 2013 Jul 10;53(2):104-9. doi: 10.1016/j.enzmictec.2013.04.007. Epub 2013 Apr 30.

DOI:10.1016/j.enzmictec.2013.04.007
PMID:23769310
Abstract

The cellulase and xylanase genes of filamentous Trichoderma fungi exist under carbon catabolite repression mediated by the regulator carbon catabolite repressor (CREI). Our objective was to find the role of CREI in a cellulase-hyperproducing mutant of Trichoderma koningii, and address whether enzyme production can be further improved by silencing the cre1 gene. cre1 partially silenced strains were constructed to improve enzyme production in T. koningii YC01, a cellulase-hyperproducing mutant. Silencing of cre1 resulted in derepression of cellulase gene expression in glucose-based cultivation. The cre1 interference strain C313 produced 2.1-, 1.4-, 0.8-, and 0.8-fold higher amounts of filter paper activity, β-1,4-exoglucanase activity (ρ-nitrophenyl-β-D-cellobioside as substrate), β-1,4-endoglucanase activity (sodium carboxymethyl cellulose as substrate), and xylanase activity, respectively, than the control strain, suggesting that silencing of cre1 resulted in enhanced enzyme production capability. In addition, downregulation of cre1 resulted in elevated expression of another regulator of xylanase and cellulase expression, xyr1, indicating that CREI also acted as a repressor of xyr1 transcription in T. koningii under inducing conditions. These results show that RNAi is a feasible method for analyzing the regulatory mechanisms of gene expression and improving xylanase and cellulase productivity in T. koningii.

摘要

丝状木霉纤维素酶和木聚糖酶基因的表达受到碳分解代谢物阻遏调控,该调控由碳分解代谢物阻遏物(CREI)调节。我们的目的是研究 CREI 在里氏木霉高产纤维素酶突变株中的作用,以及通过沉默 cre1 基因是否可以进一步提高酶的产量。为了提高纤维素酶高产突变株里氏木霉 YC01 的酶产量,我们构建了 cre1 部分沉默的菌株。在以葡萄糖为基础的培养中,cre1 的沉默导致纤维素酶基因表达的去阻遏。cre1 干扰菌株 C313 产生的滤纸活性、β-1,4-外切葡聚糖酶活性(以 ρ-硝基苯-β-D-纤维二糖苷为底物)、β-1,4-内切葡聚糖酶活性(以羧甲基纤维素钠为底物)和木聚糖酶活性分别比对照菌株高出 2.1 倍、1.4 倍、0.8 倍和 0.8 倍,这表明 cre1 的沉默导致了酶产量的提高。此外,cre1 的下调导致另一个木聚糖酶和纤维素酶表达调控因子 xyr1 的表达升高,表明在诱导条件下,CREI 也是里氏木霉中 xyr1 转录的阻遏物。这些结果表明,RNAi 是分析基因表达调控机制和提高里氏木霉木聚糖酶和纤维素酶产量的一种可行方法。

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