| Literature DB >> 27908688 |
Hemanshu Mundhada1, Jose M Seoane1, Konstantin Schneider1, Anna Koza1, Hanne B Christensen1, Tobias Klein1, Patrick V Phaneuf2, Markus Herrgard1, Adam M Feist3, Alex T Nielsen4.
Abstract
L-serine is a promising building block biochemical with a high theoretical production yield from glucose. Toxicity of L-serine is however prohibitive for high-titer production in E. coli. Here, E. coli lacking L-serine degradation pathways was evolved for improved tolerance by gradually increasing L-serine concentration from 3 to 100g/L using adaptive laboratory evolution (ALE). Genome sequencing of isolated clones revealed multiplication of genetic regions, as well as mutations in thrA, thereby showing a potential mechanism of serine inhibition. Additional mutations were evaluated by MAGE combined with amplicon sequencing, revealing role of rho, lrp, pykF, eno, and rpoB on tolerance and fitness in minimal medium. Production using the tolerant strains resulted in 37g/L of L-serine with a 24% mass yield. The resulting titer is similar to the highest production reported for any organism thereby highlighting the potential of ALE for industrial biotechnology.Entities:
Keywords: Adaptive laboratory evolution (ALE); E. coli; Fermentation; Serine production; Serine tolerance
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Year: 2016 PMID: 27908688 DOI: 10.1016/j.ymben.2016.11.008
Source DB: PubMed Journal: Metab Eng ISSN: 1096-7176 Impact factor: 9.783