journal article·2020-01-13

Improving the System Performance of the Asymmetric Biosynthesis of d-Pantoic Acid by Using Artificially Self-Assembled Enzymes in Escherichia coli

Tao Li, Ruifeng Li, Tong Zhu, Xuexian Cui, Chuijian Li, Yinglu Cui, Bian Wu

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Abstract

d-Pantoic acid (d-PA) is an important chiral precursor of a broad range of biologically active compounds. The asymmetric synthesis of d-PA through reductase coupling with NADPH regeneration systems is highly promising, but the process is restricted by expensive cofactor consumption and low cofactor recycling frequency. Here, an effective construction of self-assembled ketopantoic acid reductase and glucose dehydrogenase via protein-peptide interaction of PDZ domain and PDZ ligand was established. The self-assembled enzymes exhibited highly ordered two-dimensional threadlike macromolecular structures with improved cofactor regeneration. Furthermore, the bioconversion with whole-cell catalysis showed that the robustness and efficiency of the system with self-assembled enzymes were significantly higher than those of the unassembled enzymes. This study provides a strategy for the effective asymmetric biosynthesis of d-PA with a trace amount of cofactor and shows potential for industrial applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Chemical Synthesis and Analysis · Peptidase Inhibition and Analysis · RNA and protein synthesis mechanisms

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, PR China

University of Chinese Academy of Sciences, Beijing 100101, PR China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Chinese Academy of Sciences

References (31)

Show source-provided references
1. 10.1021/jf060794m10.1021/jf060794m ↗
2. 10.1016/S0003-2670(00)01203-410.1016/S0003-2670(00)01203-4 ↗
3. 10.1007/s11055-018-0705-210.1007/s11055-018-0705-2 ↗
4. 10.1128/ecosalplus.3.6.3.410.1128/ecosalplus.3.6.3.4 ↗
5. 10.1016/j.jbiotec.2005.03.01510.1016/j.jbiotec.2005.03.015 ↗
6. 10.1016/0141-0229(87)90136-010.1016/0141-0229(87)90136-0 ↗
7. 10.1016/0141-0229(95)00250-210.1016/0141-0229(95)00250-2 ↗
8. 10.1007/s00253-011-3664-x10.1007/s00253-011-3664-x ↗
9. 10.1007/s10295-018-2002-z10.1007/s10295-018-2002-z ↗
10. 10.1016/j.molcatb.2016.09.01610.1016/j.molcatb.2016.09.016 ↗
11. 10.1038/nchem.245910.1038/nchem.2459 ↗
12. 10.1021/acs.chemrev.6b0022810.1021/acs.chemrev.6b00228 ↗
13. 10.1002/cbic.20180039410.1002/cbic.201800394 ↗
14. 10.1016/j.sbi.2013.06.00210.1016/j.sbi.2013.06.002 ↗
15. 10.1039/C6CS00004E10.1039/C6CS00004E ↗
16. 10.1002/anie.20140501610.1002/anie.201405016 ↗
17. 10.1016/j.biotechadv.2014.11.00510.1016/j.biotechadv.2014.11.005 ↗
18. 10.1002/bit.2608110.1002/bit.26081 ↗
19. 10.1021/acssynbio.8b0008610.1021/acssynbio.8b00086 ↗
20. 10.1021/acsbiomaterials.8b0027910.1021/acsbiomaterials.8b00279 ↗
21. 10.1038/nbt.155710.1038/nbt.1557 ↗
22. 10.1186/s40643-015-0046-810.1186/s40643-015-0046-8 ↗
23. 10.1093/protein/15.11.87110.1093/protein/15.11.871 ↗
24. 10.1093/nar/gky42710.1093/nar/gky427 ↗
25. 10.1111/j.1742-4658.2012.08713.x10.1111/j.1742-4658.2012.08713.x ↗
26. 10.1074/jbc.M60788320010.1074/jbc.M607883200 ↗
27. 10.1021/bi027061p10.1021/bi027061p ↗
28. 10.1039/c3cc40454d10.1039/c3cc40454d ↗
29. 10.1016/j.pep.2005.12.00210.1016/j.pep.2005.12.002 ↗
30. 10.1016/j.ymben.2015.03.00110.1016/j.ymben.2015.03.001 ↗
31. 10.1007/s11244-013-0185-010.1007/s11244-013-0185-0 ↗