Leiden University, Institute of Biology Leiden, Molecular Microbiology and Biotechnology, Sylviusweg 72, 2333 BE Leiden, the Netherlands.
Leiden University, Institute of Biology Leiden, Molecular Microbiology and Biotechnology, Sylviusweg 72, 2333 BE Leiden, the Netherlands; Dutch DNA Biotech, Hugo R Kruytgebouw 4-Noord, Padualaan 8, 3584 CH Utrecht, the Netherlands.
Gene. 2020 Dec;763S:100028. doi: 10.1016/j.gene.2020.100028. Epub 2020 Jan 28.
Post-fermentation fungal biomass waste provides a viable source for chitin. Cell wall chitin of filamentous fungi, and in particular its de-N-acetylated derivative chitosan, has a wide range of commercial applications. Although the cell wall of filamentous fungi comprises 10-30% chitin, these yields are too low for cost-effective production. Therefore, we aimed to identify the genes involved in increased chitin deposition by screening a collection of UV-derived cell wall mutants in Aspergillus niger. This screen revealed a mutant strain (RD15.4#55) that showed a 30-40% increase in cell wall chitin compared to the wild type. In addition to the cell wall chitin phenotype, this strain also exhibited sensitivity to SDS and produces an unknown yellow pigment. Genome sequencing combined with classical genetic linkage analysis identified two mutated genes on chromosome VII that were linked with the mutant phenotype. Single gene knockouts and subsequent complementation analysis revealed that an 8 bp deletion in NRRL3_09595 is solely responsible for the associated phenotypes of RD15.4#55. The mutated gene, which was named cwcA (cell wall chitin A), encodes an orthologue of Saccharomyces cerevisiae Bypass of ESS1 (BYE1), a negative regulator of transcription elongation. We propose that this conserved fungal protein is involved in preventing cell wall integrity signaling under non-inducing conditions, where loss of function results in constitutive activation of the cell wall stress response pathway, and consequently leads to increased chitin content in the mutant cell wall.
发酵后真菌生物质废物为甲壳素提供了可行的来源。丝状真菌的细胞壁甲壳素,特别是其去 N-乙酰化衍生物壳聚糖,具有广泛的商业应用。尽管丝状真菌的细胞壁包含 10-30%的甲壳素,但这些产量对于具有成本效益的生产来说太低了。因此,我们旨在通过筛选黑曲霉中紫外线衍生的细胞壁突变体文库来鉴定参与增加甲壳素沉积的基因。该筛选揭示了一种突变株(RD15.4#55),与野生型相比,其细胞壁甲壳素增加了 30-40%。除了细胞壁甲壳素表型外,该菌株还对 SDS 敏感,并产生一种未知的黄色色素。基因组测序结合经典遗传连锁分析确定了第 VII 号染色体上与突变表型相关的两个突变基因。单基因突变体敲除和随后的互补分析表明,NRRL3_09595 中的 8bp 缺失是 RD15.4#55 相关表型的唯一原因。突变基因命名为 cwcA(细胞壁甲壳素 A),编码酿酒酵母绕过 ESS1 的同源物(BYE1),这是转录延伸的负调节剂。我们提出,这种保守的真菌蛋白参与在非诱导条件下防止细胞壁完整性信号,在这种条件下,功能丧失导致细胞壁应激反应途径的组成激活,从而导致突变细胞壁中甲壳素含量增加。