4.7 Article

In vitro metabolic engineering for the salvage synthesis of NAD+

Journal

METABOLIC ENGINEERING
Volume 35, Issue -, Pages 114-120

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymben.2016.02.005

Keywords

NAD(+); Thermophilic enzyme; In vitro metabolic pathway

Funding

  1. Japan Science and Technology Agency (JST), PRESTO program
  2. Japan Science and Technology Agency (JST), CREST program
  3. Japan Society for the Promotion of Science (JSPS), KAKENHI Grant [26450088]
  4. Grants-in-Aid for Scientific Research [26450088] Funding Source: KAKEN

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Excellent thermal and operational stabilities of thermophilic enzymes can greatly increase the applicability of biocatalysis in various industrial fields. However, thermophilic enzymes are generally incompatible with thermo-labile substrates, products, and cofactors, since they show the maximal activities at high temperatures. Despite their pivotal roles in a wide range of enzymatic redox reactions, NAD(P)(+) and NAD(P)H exhibit relatively low stabilities at high temperatures, tending to be a major obstacle in the long-term operation of biocatalytic chemical manufacturing with thermophilic enzymes. In this study, we constructed an in vitro artificial metabolic pathway for the salvage synthesis of NAD(+) from its degradation products by the combination of eight thermophilic enzymes. The enzymes were heterologously produced in recombinant Escherichia coli and the heat -treated crude extracts of the recombinant cells were directly used as enzyme solutions. When incubated with experimentally optimized concentrations of the enzymes at 60 degrees C, the NAD(+) concentration could be kept almost constant for 15 h. (C) 2016 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.

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