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工程化解脂耶氏酵母菌株如何分泌游离脂肪酸:比较转录组学的启示。

How do engineered Yarrowia lipolytica strains secrete free fatty acids: hints from comparative transcriptomics.

机构信息

Centre for Synthetic Biology, Ghent University,Coupure Links 653, 9000 Gent, Belgium.

Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Domaine de Vilvert, 78350 Jouy-en-Josas, France.

出版信息

FEMS Yeast Res. 2023 Jan 4;23. doi: 10.1093/femsyr/foad027.

Abstract

Yarrowia lipolytica has been considered one of the most promising platforms for the microbial production of fatty acids and derived products. The deletion of the faa1 gene coding for an acyl-CoA synthetase leads to the accumulation and secretion of free fatty acids (FFAs) into the extracellular space. The secretion of products is beneficial for the development of microbial cell factories to avoid intracellular inhibitory effects and reduce downstream processing costs. However, the mechanism behind the secretion of fatty acids is not well known. As a starting point, we compared the transcriptome of this mutant showing FFA secretion to a wildtype-like strain not showing this phenotype. The 12 most upregulated genes were evaluated for involvement in FFA secretion by the creation of deletion and overexpression mutants, among them MCH2, YMOH, three cell wall proteins CWP3, CWP4, and CWP11, M12B, and three proteins with unknown functions YUP1, YUP2, and YUP3. None of these proteins take a clear or isolated role in FFA export. As the transcriptomic data revealed an overrepresentation of cell wall-related proteins, some of them were further examined on a theoretical and experimental way. Surprisingly, overexpression of Ygpi led to the production of FFAs in the wildtype-like genetic background. Finally, some of the evaluated genes showed involvement in resistance to FFA toxicity.

摘要

解脂耶氏酵母被认为是微生物生产脂肪酸和衍生产品最有前途的平台之一。删除编码酰基辅酶 A 合成酶的 faa1 基因导致游离脂肪酸 (FFA) 在细胞外空间积累和分泌。产物的分泌有利于微生物细胞工厂的发展,可以避免细胞内抑制作用并降低下游加工成本。然而,脂肪酸分泌的机制尚不清楚。作为一个起点,我们比较了显示 FFA 分泌的突变体的转录组与不表现这种表型的野生型样菌株。通过创建缺失和过表达突变体,评估了 12 个上调最多的基因是否参与 FFA 分泌,其中包括 MCH2、YMOH、三个细胞壁蛋白 CWP3、CWP4 和 CWP11、M12B 以及三个具有未知功能的蛋白 YUP1、YUP2 和 YUP3。这些蛋白在 FFA 输出中没有明确或孤立的作用。由于转录组数据显示细胞壁相关蛋白的表达过度,其中一些蛋白从理论和实验两个方面进行了进一步研究。令人惊讶的是,Ygpi 的过表达导致在野生型样遗传背景下产生 FFAs。最后,一些评估的基因显示参与了对 FFA 毒性的抗性。

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