Literature DB >> 27832296

Lysine Fermentation: History and Genome Breeding.

Masato Ikeda1.   

Abstract

Lysine fermentation by Corynebacterium glutamicum was developed in 1958 by Kyowa Hakko Kogyo Co. Ltd. (current Kyowa Hakko Bio Co. Ltd.) and is the second oldest amino acid fermentation process after glutamate fermentation. The fundamental mechanism of lysine production, discovered in the early stages of the process's history, gave birth to the concept known as "metabolic regulatory fermentation," which is now widely applied to metabolite production. After the development of rational metabolic engineering, research on lysine production first highlighted the need for engineering of the central metabolism from the viewpoints of precursor supply and NADPH regeneration. Furthermore, the existence of active export systems for amino acids was first demonstrated for lysine in C. glutamicum, and this discovery has resulted in the current recognition of such exporters as an important consideration in metabolite production. Lysine fermentation is also notable as the first process to which genomics was successfully applied to improve amino acid production. The first global "genome breeding" strategy was developed using a lysine producer as a model; this has since led to new lysine producers that are more efficient than classical industrial producers. These advances in strain development technology, combined with recent systems-level approaches, have almost achieved the optimization of entire cellular systems as cell factories for lysine production. In parallel, the continuous improvement of the process has resulted not only in fermentation processes with reduced load on downstream processing but also in commercialization of various product forms according to their intended uses. Nowadays lysine fermentation underpins a giant lysine demand of more than 2 million metric tons per year.

Entities:  

Keywords:  Corynebacterium glutamicum; Downstream processing; Escherichia coli; Genome breeding; Lysine market; Lysine production technology; Lysine-producing strains; Product forms; Systems metabolic engineering

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Year:  2017        PMID: 27832296     DOI: 10.1007/10_2016_27

Source DB:  PubMed          Journal:  Adv Biochem Eng Biotechnol        ISSN: 0724-6145            Impact factor:   2.635


  4 in total

1.  An economically and environmentally acceptable synthesis of chiral drug intermediate L-pipecolic acid from biomass-derived lysine via artificially engineered microbes.

Authors:  Jie Cheng; Yuding Huang; Le Mi; Wujiu Chen; Dan Wang; Qinhong Wang
Journal:  J Ind Microbiol Biotechnol       Date:  2018-05-10       Impact factor: 3.346

2.  Identification and Molecular Characterization of the Operon Required for L-Asparagine Utilization in Corynebacterium glutamicum.

Authors:  Koichi Toyoda; Riki Sugaya; Akihiro Domon; Masako Suda; Kazumi Hiraga; Masayuki Inui
Journal:  Microorganisms       Date:  2022-05-10

3.  Transcriptome profiles of high-lysine adaptation reveal insights into osmotic stress response in Corynebacterium glutamicum.

Authors:  Jian Wang; Jian Yang; Guoxin Shi; Weidong Li; Yun Ju; Liang Wei; Jun Liu; Ning Xu
Journal:  Front Bioeng Biotechnol       Date:  2022-08-09

4.  Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium.

Authors:  Eugen Pfeifer; Cornelia Gätgens; Tino Polen; Julia Frunzke
Journal:  Sci Rep       Date:  2017-12-01       Impact factor: 4.379

  4 in total

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