Literature DB >> 34837493

Enhancing β-alanine production from glucose in genetically modified Corynebacterium glutamicum by metabolic pathway engineering.

Jin-Yu Wang1, Zhi-Ming Rao1,2, Jian-Zhong Xu3, Wei-Guo Zhang4.   

Abstract

To directly produce β-alanine from glucose by microbial fermentation, a recombinant Corynebacterium glutamicum strain with high efficiency of β-alanine production was constructed in this study. To do this, the biosynthetic pathway of β-alanine in an L-lysine-producing strain XQ-5 was modified by enhancing carbon flux in biosynthetic pathway and limiting carbon flux in competitive pathway. This study showed that replacement of L-aspartate kinase (AK) with wild-type AK and disruption of lactate dehydrogenase and alanine/valine aminotransferases increase β-alanine production because of decreasing the by-products accumulation. Moreover, L-aspartate-α-decarboxylase (ADC) from Bacillus subtilis was designed as the best enzyme for increasing β-alanine production, and its variant (BsADCE56S/I88M) showed the highest activity for catalyzing L-aspartate to generate β-alanine. To further increase β-alanine production, expression level of BsADCE56S/I88M was controlled by optimizing promoter and RBS, indicating that Pgro plus ThirRBS is the best combination for BsADCE56S/I88M expression and β-alanine production. The resultant strain XQ-5.5 produced 30.7 ± 2.3 g/L of β-alanine with a low accumulation of lactate (from 5.2 ± 0.14 to 0.2 ± 0.09 g/L) and L-alanine (from 7.6 ± 0.22 to 3.8 ± 0. 32 g/L) in shake-flask fermentation and produced 56.5 ± 3.2 g/L of β-alanine with a productivity of 0.79 g/(L·h) and the glucose conversion efficiency (α) of 39.5% in feed-batch fermentation. This is the first report of genetically modifying the biosynthetic pathway of β-alanine that improves the efficiency of β-alanine production in an L-lysine-producing strain, and these results give us a new insight for constructing the other valuable biochemical. KEY POINTS: • Optimization and overexpression of the key enzyme BsADC increased the accumulation of β-alanine. • The AK was replaced with wild-type AK to increase the conversion of aspartic acid to β-alanine. • A 56.5-g/L β-alanine production in fed-batch fermentation was achieved.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Corynebacterium glutamicum; L-Aspartate-α-decarboxylase; Metabolic engineering; Microbial fermentation; β-Alanine production

Mesh:

Substances:

Year:  2021        PMID: 34837493     DOI: 10.1007/s00253-021-11696-y

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  18 in total

1.  A novel methodology employing Corynebacterium glutamicum genome information to generate a new L-lysine-producing mutant.

Authors:  J Ohnishi; S Mitsuhashi; M Hayashi; S Ando; H Yokoi; K Ochiai; M Ikeda
Journal:  Appl Microbiol Biotechnol       Date:  2002-02       Impact factor: 4.813

Review 2.  Biotechnological production of amino acids and derivatives: current status and prospects.

Authors:  Wolfgang Leuchtenberger; Klaus Huthmacher; Karlheinz Drauz
Journal:  Appl Microbiol Biotechnol       Date:  2005-10-20       Impact factor: 4.813

3.  Metabolic function of Corynebacterium glutamicum aminotransferases AlaT and AvtA and impact on L-valine production.

Authors:  Jan Marienhagen; Lothar Eggeling
Journal:  Appl Environ Microbiol       Date:  2008-10-17       Impact factor: 4.792

4.  Characterization of 582 natural and synthetic terminators and quantification of their design constraints.

Authors:  Ying-Ja Chen; Peng Liu; Alec A K Nielsen; Jennifer A N Brophy; Kevin Clancy; Todd Peterson; Christopher A Voigt
Journal:  Nat Methods       Date:  2013-06-02       Impact factor: 28.547

5.  Fine-Tuning Multi-Gene Clusters via Well-Characterized Gene Expression Regulatory Elements: Case Study of the Arginine Synthesis Pathway in C. glutamicum.

Authors:  Yanting Duan; Weiji Zhai; Weijia Liu; Xiaomei Zhang; Jin-Song Shi; Xiaojuan Zhang; Zhenghong Xu
Journal:  ACS Synth Biol       Date:  2020-12-31       Impact factor: 5.110

6.  (L)-Valine production with minimization of by-products' synthesis in Corynebacterium glutamicum and Brevibacterium flavum.

Authors:  Xiaohu Hou; Xinde Chen; Yue Zhang; He Qian; Weiguo Zhang
Journal:  Amino Acids       Date:  2012-05-03       Impact factor: 3.520

7.  Expression of the Corynebacterium glutamicum panD gene encoding L-aspartate-alpha-decarboxylase leads to pantothenate overproduction in Escherichia coli.

Authors:  N Dusch; A Pühler; J Kalinowski
Journal:  Appl Environ Microbiol       Date:  1999-04       Impact factor: 4.792

8.  Selective production of L-aspartic acid and L-phenylalanine by coupling reactions of aspartase and aminotransferase in Escherichia coli.

Authors: 
Journal:  Enzyme Microb Technol       Date:  2000-07-01       Impact factor: 3.493

9.  Conversion of feedback regulation in aspartate kinase by domain exchange.

Authors:  Chiaki Kato; Takeshi Kurihara; Nobuyuki Kobashi; Hisakazu Yamane; Makoto Nishiyama
Journal:  Biochem Biophys Res Commun       Date:  2004-04-09       Impact factor: 3.575

10.  The Effect of Promoter and RBS Combination on the Growth and Glycogen Productivity of Sodium-Dependent Bicarbonate Transporter (SbtA) Overexpressing Synechococcus sp. PCC 7002 Cells.

Authors:  Jai Kumar Gupta; Shireesh Srivastava
Journal:  Front Microbiol       Date:  2021-04-13       Impact factor: 5.640

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