Efficient and Cost-Effective Synthesis of <i>N</i>-Acetyllactosamine by Sequential Modular Enzymatic Cascade Reactions Involving NTP Regeneration
Human milk oligosaccharides (HMOs) play important roles in the development of infants, which are the third most abundant component in human milk. <i>N</i>-Acetyllactosamine (LacNAc) is an important intermediate for the biosynthesis of other HMOs and antigens. Since currently appropriate synthetic methods for large-scale production of LacNAc are not available, it is urgently needed to develop an efficient and cost-effective synthetic pathway for LacNAc preparation. In this study, a cost-effective pathway of LacNAc synthesis involving regeneration of adenosine triphosphate (ATP) and uridine 5'-triphosphate (UTP) was established. After optimizing the reaction conditions, LacNAc was synthesized at a yield of >90% via a sequential one-pot multienzyme (OPME) method with crude enzymes at 100 mM substrates. Finally, LacNAc was produced efficiently and cost-effectively at a 5 L scale. This strategy would possibly meet the requirements of potential industrial production of LacNAc and would provide guidance for the production of other structurally complex HMOs or functional oligosaccharides in the future.
Authors
- Bowen Jiang (ORCID: https://orcid.org/0000-0002-6751-9275)
- Ran You
- Meirong Hu (ORCID: https://orcid.org/0000-0003-0774-5737)
- Runmiao Jiao (ORCID: https://orcid.org/0000-0002-2779-4846)
- Caixia Pei
- Eika Weihua QIAN (ORCID: https://orcid.org/0000-0002-2424-5673)
- Jianjun Li (ORCID: https://orcid.org/0000-0002-2842-5663)
- Liming Zhang (ORCID: https://orcid.org/0000-0003-1497-1556)
- Yuguang Du (ORCID: https://orcid.org/0000-0002-4809-0717)
- Xinlv Peng
Institutions
- Chinese Academy of Sciences (CN)
- Institute of Process Engineering (CN)
- Institute of Microbiology (CN)
- University of Chinese Academy of Sciences (CN)
- Jiangxi Agricultural University (CN)
- Tokyo University of Agriculture and Technology (JP)
Publication Details
- Journal
- Journal of Agricultural and Food Chemistry
- Published
- 2024-12-03
- DOI
- https://doi.org/10.1021/acs.jafc.4c08638
- Citations
- 7
- Primary Topic
- Enzyme Catalysis and Immobilization
- Type
- article
- Field-Weighted Citation Impact
- 1.64
Funders
- National Natural Science Foundation of China