Q1 Agricultural and Biological Sciences
John Connell, Helen J Bates, Ivey Geoghegan, Fiona Wilson, Richard J Harrison, R Jordan Price
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引用次数: 0

摘要

背景:昆恩霉菌蛋白是一种富含蛋白质的肉类替代品,是通过大规模发酵文氏镰刀菌生产的。然而,文氏镰刀菌发酵过程中的一个主要挑战是不断出现被称为菌落变异体(C-变异体)的突变体。这些 C 型变体具有高度分枝的形态,最终导致最终产品不理想,发酵过程提前结束。本研究旨在确定造成 C 型变体形态的基因突变:结果:我们首先从商业发酵样品中分离出了 C 变异菌株和野生型菌株,并对其在固体培养基上的径向生长率进行了鉴定。通过全基因组测序,我们在 12 株 C 型变异株中的 11 株中发现了名为 jg4843 的基因突变,而野生型变异株中没有发现这种突变。jg4843 基因被鉴定为 LRG1 的直向同源物,LRG1 是一种 Rho-GTPase 激活蛋白,可调节影响真菌生长的 Rho1 信号通路。值得注意的是,jg4843 基因的突变主要位于负责 LRG1 活性的 RhoGAP 结构域。为了证实这些突变的作用,我们使用 CRISPR/Cas9 介导的同源定向重组将 C 变体突变导入野生型分离物中,成功地再现了特征性的 C 变体形态:本研究确定了 LRG1 同源物 jg4843 的突变是商业发酵 F. venenatum 分离物出现 C 型变异形态的遗传原因。了解这一遗传基础为制定防止 C 型变异体出现的策略铺平了道路,从而有可能实现更高效、更可持续的昆虫菌体蛋白生产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mutation of the LRG1 Rho-GAP gene is responsible for the hyper branching C-variant phenotype in the quorn mycoprotein fungus Fusarium venenatum A3/5.

Background: Quorn mycoprotein, a protein-rich meat alternative, is produced through large-scale fermentation of the fungus Fusarium venenatum. However, a major challenge during F. venenatum fermentation is the consistent appearance of mutants called colonial variants (C-variants). These C-variants have a highly branched morphology, which ultimately lead to a less desirable final product and early termination of the fermentation process. This study aimed to identify the genetic mutations responsible for C-variant morphology.

Results: We first isolated both C-variant and wild-type strains from commercial fermentation samples and characterised radial growth rates on solid media. Whole genome sequencing facilitated the identification of mutations in a gene called jg4843 in 11 out of 12 C-variant isolates, which were not observed in the wild-type isolates. The jg4843 gene was identified as the ortholog of LRG1, a Rho-GTPase activating protein that regulates the Rho1 signalling pathway affecting fungal growth. Notably, the mutations in jg4843 were primarily located in the RhoGAP domain responsible for LRG1 activity. To confirm the role of these mutations, we used CRISPR/Cas9-mediated homology-directed recombination to introduce the C-variant mutations into the wild-type isolate, which successfully recapitulated the characteristic C-variant morphology.

Conclusions: This study identified mutations in the LRG1 ortholog jg4843 as the genetic cause of C-variant morphology in commercial fermentation F. venenatum isolates. Understanding this genetic basis paves the way for developing strategies to prevent C-variants arising, potentially leading to more efficient and sustainable production of Quorn mycoprotein.

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来源期刊
Fungal Biology and Biotechnology
Fungal Biology and Biotechnology Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
10.20
自引率
0.00%
发文量
17
审稿时长
9 weeks
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