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前体蛋白加工蛋白酶基因的缺失导致深层培养过程中pH值依赖性形态转变并增加细胞壁几丁质含量。

Deletion of the Pro-Protein Processing Protease Gene Results in a pH-Dependent Morphological Transition during Submerged Cultivations and Increases Cell Wall Chitin Content.

作者信息

van Leeuwe Tim M, Arentshorst Mark, Forn-Cuní Gabriel, Geoffrion Nicholas, Tsang Adrian, Delvigne Frank, Meijer Annemarie H, Ram Arthur F J, Punt Peter J

机构信息

Institute of Biology Leiden, Microbial Sciences, Leiden University, Sylviusweg 72, 2333 BE Leiden, The Netherlands.

Institute of Biology Leiden, Animal Sciences, Leiden University, Einsteinweg 55, 2333 CC Leiden, The Netherlands.

出版信息

Microorganisms. 2020 Dec 2;8(12):1918. doi: 10.3390/microorganisms8121918.

Abstract

There is a growing interest in the use of post-fermentation mycelial waste to obtain cell wall chitin as an added-value product. In the pursuit to identify suitable production strains that can be used for post-fermentation cell wall harvesting, we turned to an strain in which the gene was deleted. Previous work has shown that the deletion of causes hyper-branching and thicker cell walls, traits that may be beneficial for the reduction in fermentation viscosity and lysis. Hyper-branching of was previously found to be pH-dependent on solid medium at pH 6.0, but was absent at pH 5.0. This phenotype was reported to be less pronounced during submerged growth. Here, we show a series of controlled batch cultivations at a pH range of 5, 5.5, and 6 to examine the pellet phenotype of in liquid medium. Morphological analysis showed that formed wild type-like pellets at pH 5.0, whereas the hyper-branching phenotype was found at pH 6.0. The transition of phenotypic plasticity was found in cultivations at pH 5.5, seen as an intermediate phenotype. Analyzing the cell walls of from these controlled pH-conditions showed an increase in chitin content compared to the wild type across all three pH values. Surprisingly, the increase in chitin content was found to be irrespective of the hyper-branching morphology. Evidence for alterations in cell wall make-up are corroborated by transcriptional analysis that showed a significant cell wall stress response in addition to the upregulation of genes encoding other unrelated cell wall biosynthetic genes.

摘要

利用发酵后的菌丝体废料获取作为增值产品的细胞壁几丁质的兴趣与日俱增。为了寻找可用于发酵后细胞壁收获的合适生产菌株,我们转向了一种基因被敲除的菌株。先前的研究表明,该基因的缺失会导致超分支和更厚的细胞壁,这些特性可能有利于降低发酵粘度和细胞裂解。先前发现,在pH 6.0的固体培养基上,该菌株的超分支呈pH依赖性,但在pH 5.0时不存在。据报道,这种表型在深层培养过程中不太明显。在这里,我们展示了在pH值为5、5.5和6的一系列控制分批培养,以研究该菌株在液体培养基中的颗粒表型。形态学分析表明,该菌株在pH 5.0时形成野生型样颗粒,而在pH 6.0时发现超分支表型。在pH 5.5的培养中发现了表型可塑性的转变,表现为中间表型。分析这些控制pH条件下该菌株的细胞壁发现,与野生型相比,在所有三个pH值下几丁质含量均增加。令人惊讶的是,几丁质含量的增加与超分支形态无关。转录分析证实了细胞壁组成的改变,该分析显示除了编码其他不相关细胞壁生物合成基因的基因上调外,还存在显著的细胞壁应激反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b75/7761569/481a2ead38f9/microorganisms-08-01918-g001.jpg

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