4.5 Article

Metabolic engineering of methylotrophic Pichia pastoris for the production of β-alanine

期刊

BIORESOURCES AND BIOPROCESSING
卷 8, 期 1, 页码 -

出版社

SPRINGER HEIDELBERG
DOI: 10.1186/s40643-021-00444-9

关键词

Pichia pastoris (Komagataella phaffii); beta-Alanine (3-aminopropionic acid); Methanol; Aspartate decarboxylation; Aspartate dehydrogenase

资金

  1. National Key R&D Program of China [2018YFA0901400]
  2. Tianjin Synthetic Biotechnology Innovation Capacity Improvement Project [TSBICIP-KJGG-006-19]
  3. National Natural Science Foundation of China [31970039]

向作者/读者索取更多资源

The study demonstrated the feasibility of producing beta-alanine from methanol using Pichia pastoris, achieving a high yield of 5.6g/L through optimizing enzyme activity and carbon source supply. This is the highest metabolite production titer reached in P. pastoris using methanol as the substrate.
beta-Alanine (3-aminopropionic acid) is the only naturally occurring beta-amino acid and an important precursor for the synthesis of a variety of nitrogen-containing chemicals. Fermentative production of beta-alanine from renewable feedstocks such as glucose has attracted significant interest in recent years. Methanol has become an emerging and promising renewable feedstock for biomanufacturing as an alternative to glucose. In this work, we demonstrated the feasibility of beta-alanine production from methanol using Pichia pastoris (Komagataella phaffii) as a methylotrophic cell factory. L-Aspartate-alpha-decarboxylases (ADCs) from different sources were screened and expressed in P. pastoris, followed by the optimization of aspartate decarboxylation by increasing the ADC copy number and C4 precursor supply via the overexpression of aspartate dehydrogenase. The production potential of the best strain was further evaluated in a 1-L fermenter, and a beta-alanine titer of 5.6 g/L was obtained. To our best knowledge, this is the highest metabolite production titer ever reached in P. pastoris using methanol as the substrate.

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

4.5
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