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

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
José Manuel Salvador López, Lea Vidal, Michelle Patricia Adiutama, Filip Van Nieuwerburgh, Dieter Deforce, Jean-Marc Nicaud, Inge Noëlle Adrienne Van Bogaert
{"title":"How do engineered Yarrowia lipolytica strains secrete free fatty acids: hints from comparative transcriptomics.","authors":"José Manuel Salvador López,&nbsp;Lea Vidal,&nbsp;Michelle Patricia Adiutama,&nbsp;Filip Van Nieuwerburgh,&nbsp;Dieter Deforce,&nbsp;Jean-Marc Nicaud,&nbsp;Inge Noëlle Adrienne Van Bogaert","doi":"10.1093/femsyr/foad027","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2023-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/femsyr/foad027","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

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.

工程多脂耶氏菌菌株如何分泌游离脂肪酸:来自比较转录组学的提示。
脂溶耶氏菌被认为是微生物生产脂肪酸及其衍生产品最有前途的平台之一。编码酰基辅酶a合成酶的faa1基因的缺失导致游离脂肪酸(FFAs)积聚和分泌到细胞外空间。产物的分泌有利于微生物细胞工厂的发展,避免细胞内抑制作用,降低下游加工成本。然而,脂肪酸分泌背后的机制尚不清楚。作为起点,我们比较了这种显示FFA分泌的突变体的转录组和不显示这种表型的野生型样菌株。通过创建缺失和过表达突变体来评估12个上调最多的基因参与FFA分泌,其中包括MCH2, YMOH,三个细胞壁蛋白CWP3, CWP4和CWP11, M12B,以及三个功能未知的蛋白YUP1, YUP2和YUP3。这些蛋白中没有一个在FFA输出中起明确或孤立的作用。由于转录组学数据显示细胞壁相关蛋白的过度代表性,因此对其中一些蛋白进行了进一步的理论和实验研究。令人惊讶的是,在野生型遗传背景下,Ygpi的过表达导致了FFAs的产生。最后,一些被评估的基因显示参与对FFA毒性的抗性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信