Integrating cell-free biosyntheses of heme prosthetic group and apoenzyme for the synthesis of functional P450 monooxygenase

Harnessing the isolated protein synthesis machinery, cell‐free protein synthesis reproduces the cellular process of decoding genetic information in artificially controlled environments. More often than not, however, generation of functional proteins requires more than simple translation of genetic s...

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Veröffentlicht in:Biotechnology and bioengineering 2013-04, Vol.110 (4), p.1193-1200
Hauptverfasser: Kwon, Yong-Chan, Oh, In-Seok, Lee, Nahum, Lee, Kyung-Ho, Yoon, Yeo Joon, Lee, Eun Yeol, Kim, Byung-Gee, Kim, Dong-Myung
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Sprache:eng
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Zusammenfassung:Harnessing the isolated protein synthesis machinery, cell‐free protein synthesis reproduces the cellular process of decoding genetic information in artificially controlled environments. More often than not, however, generation of functional proteins requires more than simple translation of genetic sequences. For instance, many of the industrially important enzymes require non‐protein prosthetic groups for biological activity. Herein, we report the complete cell‐free biogenesis of a heme prosthetic group and its integration with concurrent apoenzyme synthesis for the production of functional P450 monooxygenase. Step reactions required for the syntheses of apoenzyme and the prosthetic group have been designed so that these two separate pathways take place in the same reaction mixture, being insulated from each other. Combined pathways for the synthesis of functional P450 monooxygenase were then further integrated with in situ assay reactions to enable real‐time measurement of enzymatic activity during its synthesis. Biotechnol. Bioeng. 2013; 110: 1193–1200. © 2012 Wiley Periodicals, Inc. Functional holoenzyme of P450 monooxygenase was produced in a cell‐free synthesis system. Step reactions required for the syntheses of apoenzyme and prosthetic group have been designed and implemented into a cell‐free synthesis system so that these two separate pathways take place in the same reaction mixture, while being insulated from each other. Combined pathways for the synthesis of functional P450 monooxygenase were then further integrated with in situ assay reactions to enable real‐time measurement of enzymatic activity during its synthesis.
ISSN:0006-3592
1097-0290
DOI:10.1002/bit.24785