4.5 Review

Recent advances in the metabolic pathways and microbial production of coenzyme Q

出版社

SPRINGER
DOI: 10.1007/s11274-022-03242-3

关键词

Coenzyme Q(10) (CoQ(10)); Corynebacterium glutamicum; Escherichia coli; Metabolic engineering; Q complex; Ubi super complex; Yeast

资金

  1. Projekt DEAL
  2. state of North Rhine Westphalia (NRW)
  3. European Regional Development Fund (EFRE), Project Cluster Industrial Biotechnology (CLIB) Kompetenzzentrum Biotechnologie (CKB) [34.EFRE0300095/1703FI04]
  4. German-Korean MOBKOR program - National Research Foundation of Korea [NRF-2016K1A3A1A04940618]
  5. German Federal Ministry of Education and Research
  6. Basic Science Research Program through the National Research Foundation of Korea [NRF-2018R1D1A1B07047207]
  7. ANR [ANR-19-CE44-0014]
  8. Universite Grenoble Alpes (UGA)
  9. French Centre National de la Recherche Scientifique (CNRS)
  10. National Research Foundation of Korea [2016K1A3A1A04940618] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  11. Agence Nationale de la Recherche (ANR) [ANR-19-CE44-0014] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

This article reviews the discovery and regulation of the CoQ biosynthesis pathway and summarizes the metabolic engineering strategies for the overproduction of CoQ by microorganisms. Studies have revealed the details of CoQ biosynthesis and the existence of multiprotein complexes composed of several enzymes in different species. Currently, only microorganisms that naturally synthesize CoQ have been used for biotechnological production, but with the exploration of new strategies, microbial CoQ production is expected to improve.
Coenzyme Q (CoQ) serves as an electron carrier in aerobic respiration and has become an interesting target for biotechnological production due to its antioxidative effect and benefits in supplementation to patients with various diseases. Here, we review discovery of the pathway with a particular focus on its superstructuration and regulation, and we summarize the metabolic engineering strategies for overproduction of CoQ by microorganisms. Studies in model microorganisms elucidated the details of CoQ biosynthesis and revealed the existence of multiprotein complexes composed of several enzymes that catalyze consecutive reactions in the CoQ pathways of Saccharomyces cerevisiae and Escherichia coli. Recent findings indicate that the identity and the total number of proteins involved in CoQ biosynthesis vary between species, which raises interesting questions about the evolution of the pathway and could provide opportunities for easier engineering of CoQ production. For the biotechnological production, so far only microorganisms have been used that naturally synthesize CoQ(10) or a related CoQ species. CoQ biosynthesis requires the aromatic precursor 4-hydroxybenzoic acid and the prenyl side chain that defines the CoQ species. Up to now, metabolic engineering strategies concentrated on the overproduction of the prenyl side chain as well as fine-tuning the expression of ubi genes from the ubiquinone modification pathway, resulting in high CoQ yields. With expanding knowledge about CoQ biosynthesis and exploration of new strategies for strain engineering, microbial CoQ production is expected to improve.

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