在不影响里氏木霉JNTR5纤维素酶生产的情况下,山梨糖酸酯过量生产。

Chengcheng Li, Ruihan Gu, Fengming Lin, Huining Xiao
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引用次数: 1

摘要

背景:微生物生产具有生物活性的次生代谢物具有挑战性,因为大多数编码基因是沉默的;即使它们被激活,生物合成途径通常也是复杂的。具有多功能生物活性的山梨甘素类就是这些问题的例子,如果这些问题得到解决,就可以为制药工业提供更可持续、更简单的这些重要化合物。里氏木霉是纤维素酶的优良生产者,能分泌多种山梨脂质。结果:本实验中,我们从T. reesei RUT-C30过表达Tr69957基因的随机突变中获得了T. reesei突变株JNTR5。JNTR5在不影响纤维素酶产量的情况下,显著增加了山梨甘素的产量。共聚焦激光扫描显微镜(CLSM)结果表明,山梨壳蛋白在JNTR5菌丝和孢子中均有分布,并呈现蓝、绿色荧光。与rt - c30相比,JNTR5表现出不同的细胞形态,生长速率降低,产孢量增加,但生物量积累相似。此外,转录组分析显示,所有属于山梨霉素基因簇的基因都上调,而大多数纤维素酶编码基因下调。JNTR5细胞壁完整性受损,这可能有利于纤维素酶的分泌,损伤的细胞壁可以增强纤维素酶和半纤维素酶的分泌,导致纤维素酶和半纤维素酶的活性几乎不变。结论:我们首次构建了山梨二醇酯高产的T. reesei平台,该平台具有相当的纤维素酶产量。JNTR5的这种优异表现是菌株特异性的,据表型和转录组分析显示,这可能是由于Tr69957基因的过表达导致染色体重塑,进而改变细胞形态、结构和整体基因表达。综上所述,JNTR5在纤维素工业微生物生产山梨甘素方面具有很大的潜力,并可作为研究芦杉黄色素分布和分泌的良好模型。
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Sorbicillinoids hyperproduction without affecting the cellulosic enzyme production in Trichoderma reesei JNTR5.

Background: Microbial production of bioactive secondary metabolites is challenging as most of the encoding genes are silent; and even if they are activated, the biosynthetic pathways are usually complex. Sorbicillinoids with multifunctional bioactivities are examples of these problems, which if solved can result in a more sustainable, simple supply of these important compounds to the pharmaceutical industry. As an excellent producer of cellulosic enzymes, Trichoderma reesei can secrete various sorbicillinoids.

Results: Here, we obtained a T. reesei mutant strain JNTR5 from the random mutation during overexpression of gene Tr69957 in T. reesei RUT-C30. JNTR5 exhibited a significant constitutive increase in sorbicillinoids production without affecting the cellulosic enzyme production. Confocal laser scanning microscope (CLSM) results indicated that sorbicillinoids were distributed in both mycelium and spores of JNTR5 with blue and green fluorescence. Compared with RUT-C30, JNTR5 displayed different cell morphology, reduced growth rate, and increased sporulation, but a similar biomass accumulation. Furthermore, transcriptome analysis revealed that all genes belonging to the sorbicillinoid gene cluster were upregulated, while most cellulase-encoding genes were downregulated. The cell wall integrity of JNTR5 was damaged, which might benefit the cellulase secretion and contribute to the almost unchanged cellulase and hemicellulase activity given that the damaged cell wall can enhance the secretion of the enzymes.

Conclusions: For the first time, we constructed a sorbicillinoids hyperproduction T. reesei platform with comparable cellulosic enzymes production. This outperformance of JNTR5, which is strain-specific, is proposed to be attributed to the overexpression of gene Tr69957, causing the chromosome remodeling and subsequently changing the cell morphology, structure, and the global gene expression as shown by phenotype and the transcriptome analysis of JNTR5. Overall, JNTR5 shows great potential for industrial microbial production of sorbicillinoids from cellulose and serves as an excellent model for investigating the distribution and secretion of yellow pigments in T. reesei.

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