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A synthetic cell-free 36-enzyme reaction system for vitamin B<sub>12</sub> production

Chemistry

A synthetic cell-free 36-enzyme reaction system for vitamin B<sub>12</sub> production

Q. Kang, H. Fang, et al.

Discover a groundbreaking method for synthesizing adenosylcobalamin (AdoCbl), a vital form of vitamin B12, using a cell-free reaction system. This innovative approach, developed by Qian Kang, Huan Fang, Mengjie Xiang, Kaixing Xiao, Pingtao Jiang, Chun You, Sang Yup Lee, and Dawei Zhang, promises to revolutionize the production of complex natural compounds by utilizing inexpensive 5-aminolevulinic acid.

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Abstract
Adenosylcobalamin (AdoCbl), a biologically active form of vitamin B12 (coenzyme B12), is one of the most complex metal-containing natural compounds and an essential vitamin for animals. However, AdoCbl can only be de novo synthesized by prokaryotes, and its industrial manufacturing to date was limited to bacterial fermentation. Here, we report a method for the synthesis of AdoCbl based on a cell-free reaction system performing a cascade of catalytic reactions from 5-aminolevulinic acid (5-ALA), an inexpensive compound. More than 30 biocatalytic reactions are integrated and optimized to achieve the complete cell-free synthesis of AdoCbl, after overcoming feedback inhibition, the complicated detection, instability of intermediate products, as well as imbalance and competition of cofactors. In the end, this cell-free system produces 417.41 µg/L and 5.78 mg/L of AdoCbl using 5-ALA and the purified intermediate product hydrogenobyrate as substrates, respectively. The strategies of coordinating synthetic modules of complex cell-free system describe here will be generally useful for developing cell-free platforms to produce complex natural compounds with long and complicated biosynthetic pathways.
Publisher
Nature Communications
Published On
Aug 24, 2023
Authors
Qian Kang, Huan Fang, Mengjie Xiang, Kaixing Xiao, Pingtao Jiang, Chun You, Sang Yup Lee, Dawei Zhang
Tags
adenosylcobalamin
vitamin B12
biocatalytic reactions
cell-free synthesis
5-aminolevulinic acid
natural compounds
industrial biotechnology
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