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Optimizing microbial networks through metabolic bypasses

期刊

BIOTECHNOLOGY ADVANCES
卷 60, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biotechadv.2022.108035

关键词

Cell factories; Metabolic networks; Bypass; Bottlenecks; Metabolic nodes; Evolution; Growth -coupled selection

资金

  1. Novo Nordisk Foundation [NNF20CC0035580, NNF18OC0034818, VI.Veni.192.156, 8021-00039B]
  2. German Ministry of Education and Research (BMBF) [033RC023G]
  3. Dutch Science Organization (NWO) [NNF21OC0067996]
  4. Danish Council for Independent Research (SWEET , DFF-Research Project) [814418]
  5. European Union's Horizon 2020 Research and Innovation Programme [031B0825B]
  6. BMBF [031B1028]
  7. [NNF21OC0070572]

向作者/读者索取更多资源

Recent studies have challenged the traditional view of metabolism and discovered the plasticity of metabolic networks, which can be harnessed for bioproduction by establishing unnatural connections between metabolic nodes.
Metabolism has long been considered as a relatively stiff set of biochemical reactions. This somewhat outdated and dogmatic view has been challenged over the last years, as multiple studies exposed unprecedented plasticity of metabolism by exploring rational and evolutionary modifications within the metabolic network of cell factories. Of particular importance is the emergence of metabolic bypasses, which consist of enzymatic reaction(s) that support unnatural connections between metabolic nodes. Such novel topologies can be generated through the introduction of heterologous enzymes or by upregulating native enzymes (sometimes relying on promiscuous activities thereof). Altogether, the adoption of bypasses resulted in an expansion in the capacity of the host's metabolic network, which can be harnessed for bioproduction. In this review, we discuss modifications to the canonical architecture of central carbon metabolism derived from such bypasses towards six optimization pur-poses: stoichiometric gain, overcoming kinetic limitations, solving thermodynamic barriers, circumventing toxic intermediates, uncoupling product synthesis from biomass formation, and altering redox cofactor specificity. The metabolic costs associated with bypass-implementation are likewise discussed, including tailoring their design towards improving bioproduction.

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