3.9 Article

Metabolic engineering of an acid-tolerant yeast strain Pichia kudriavzevii for itaconic acid production

期刊

出版社

ELSEVIER
DOI: 10.1016/j.mec.2020.e00124

关键词

Pichia kudriavzevii; Issatchenkia orientalis; Non-conventional microorganisms; Itaconic acid; Biopolymers; Acid tolerance

资金

  1. National Science Foundation [MCB 1716837]
  2. U.S. Department of Energy, Office of Science, Biological and Environmental Research through Ames Laboratory
  3. U.S. Department of Energy by Iowa State University [DE-AC02-07CH11358]
  4. Fundacao para a Ciencia e a Tecnologia [UID/BIO/04565/2019, ERA-IB-2-6/0003/2014, AVS-PD/BD/114151/2015]
  5. EraNet in Industrial Biotechnology (6th edition) through the TTRAFFIC (Toxicity and Transport for Fungal production of Industrial Compounds) project
  6. Programa Operacional Regional de Lisboa [007317]

向作者/读者索取更多资源

Itaconic acid (IA), or 2-methylenesuccinic acid, has a broad spectrum of applications in the biopolymer industry owing to the presence of one vinyl bond and two acid groups in the structure. Its polymerization can follow a similar mechanism as acrylic acid but additional functionality can be incorporated into the extra beta acid group. Currently, the bio-based production of IA in industry relies on the fermentation of the filamentous fungus Aspergillus terreus. However, the difficulties associated with the fermentation undertaken by filamentous fungi together with the pathogenic potential of A. terreus pose a serious challenge for industrial-scale production. In recent years, there has been increasing interest in developing alternative production hosts for fermentation processes that are more homogenous in the production of organic acids. Pichia kudriavzevii is a non-conventional yeast with high acid tolerance to organic acids at low pH, which is a highly desirable trait by easing downstream processing. We introduced cis-aconitic acid decarboxylase gene (cad) from A. terreus (designated At_cad) into this yeast and established the initial titer of IA at 135 +/- 5 mg/L. Subsequent overexpression of a native mitochondrial tricarboxylate transporter (herein designated Pk_mttA) presumably delivered cis-aconitate efficiently to the cytosol and doubled the IA production. By introducing the newly invented CRISPR-Cas9 system into P. kudriavzevii, we successfully knocked out both copies of the gene encoding isocitrate dehydrogenase (ICD), aiming to increase the availability of cis-aconitate. The resulting P. kudriavzevii strain, devoid of ICD and overexpressing Pk_mttA and At_cad on its genome produced IA at 505 +/- 17.7 mg/L in shake flasks, and 1232 +/- 64 mg/L in fed-batch fermentation. Because the usage of an acid-tolerant species does not require pH adjustment during fermentation, this work demonstrates the great potential of engineering P. kudriavzevii as an industrial chassis for the production of organic acid.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.9
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据