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Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production

机译:Trichoderma Reesei Rut-C30菌株在纤维素酶生产平台的工业相关平台中的理性工程

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The path for the development of hypersecreting strains of Trichoderma reesei capable of producing industrially relevant enzyme titers remains elusive despite over 70?years of research and industrial utilization. Herein, we describe the rational engineering of the publicly available T. reesei RUT-C30 strain and a customized process for cellulase production based on agroindustrial by-products. A CRISPR/Cas9 system was used to introduce six genetic modifications in RUT-C30. Implemented changes included the constitutive expression of a mutated allele of the cellulase master regulator XYR1, the expression of two heterologous enzymes, the β-glucosidase CEL3A from Talaromyces emersonii and the invertase SUC1 from Aspergillus niger, and the deletion of genes encoding the cellulase repressor ACE1 and the extracellular proteases SLP1 and PEP1. These alterations resulted in a remarkable increase of protein secretion rates by RUT-C30 and amended its well described β-glucosidase deficiency while enabling the utilization of sucrose and eliminating the requirement of inducing sugars for enzyme production. With a developed sugarcane molasses-based bioprocess, the engineered strain reached an extracellular protein titer of 80.6?g?L?1 (0.24?g?L?1?h?1), which is the highest experimentally supported titer so far reported for T. reesei. The produced enzyme cocktail displayed increased levels of cellulase and hemicellulase activities, with particularly large increments being observed for the specific activities of β-glucosidase (72-fold) and xylanase (42-fold). Notably, it also exhibited a saccharification efficiency similar to that of a commercially available cellulase preparation in the deconstruction of industrially pretreated sugarcane straw. This work demonstrates the rational steps for the development of a cellulase hyperproducing strain from a well-characterized genetic background available in the public domain, the RUT-C30, associated with an industrially relevant bioprocess, paving new perspectives for Trichoderma research on cellulase production.
机译:尽管70多年的研究和工业利用,但能够产生工业相关的酶滴度的richoderma Reesei的高度分泌菌株的道路仍然是难以捉摸的。在此,我们描述了基于农业工业副产物的公共可用T.Reesei Rut-C30菌株的合理工程和用于纤维素酶生产的定制方法。 CRISPR / CAS9系统用于引入RUT-C30中的六种遗传修饰。实施的改变包括纤维素酶主调节剂XYR1的突变等位基因的组成型表达,两种异源酶的表达,来自塔罗粒酵母的甲状腺酵母和来自Aspergillus尼日尔的逆变酶Suc1的β-葡糖苷酶Cel3a,以及编码纤维素酶压抑ACE1的基因缺失和细胞外蛋白酶SLP1和PEP1。这些改变导致RUT-C30的蛋白质分泌率显着增加,并修改其良好描述的β-葡糖苷酶缺乏,同时能够利用蔗糖,并消除诱导酶生产糖的要求。通过培养的甘蔗糖蜜生物处理,工程菌株达到了80.6Ω·G?L≤1(0.24≤1≤1≤1Ω1)的细胞外蛋白质滴度,这是迄今为止所报告的最高实验支持的滴度T. Reesei。所产生的酶鸡尾酒显示纤维素酶和半纤维素酶活性水平增加,特别是对于β-葡糖苷酶(72倍)和木聚糖酶(42倍)的特定活性观察到特别大的增量。值得注意的是,它还表现出类似于商业预处理甘蔗秸秆解构中的市售纤维素酶制剂的糖化效率。这项工作证明了从公共领域的良好特征的遗传背景,RUT-C30的纤维化背景下,与工业相关的生物处理相关的合理步骤,铺平了对纤维素酶生产的Trichoderma研究的新观点。

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