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bioRxiv · 10.1101/2021.07.26.453782

Correlational networking guides the discovery of cryptic proteases for lanthipeptide maturation

Abstract

Bacterial natural product biosynthetic genes, canonically clustered, have been increasingly found to rely on cryptic enzymes encoded elsewhere in the genome for completion of biosynthesis. The study and application of lanthipeptides are frequently hindered by cryptic proteases required for final maturation. Here, we establish a global correlation network bridging the gap between lanthipeptide precursors and cryptic proteases. Applying our analysis to 161,954 bacterial genomes, we establish 5,209 correlations between precursors and cryptic proteases, with 91 prioritized. We use network predictions and co-expression analysis to reveal a previously missing protease for the maturation of class I lanthipeptide paenilan. We further discover widely distributed bacterial M16B metallopeptidases of previously unclear biological function as a new family of lanthipeptide proteases. We show the involvement of a pair of bifunctional M16B proteases in the production of novel class III lanthipeptides with high substrate specificity. Together, these results demonstrate the strength of our correlational networking approach to the discovery of cryptic lanthipeptide proteases and potentially other missing enzymes for natural products biosynthesis. Graphical abstract O_FIG_DISPLAY_L [Figure 1] M_FIG_DISPLAY C_FIG_DISPLAY

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BibTeXRIS

Xue, D., Older, E. A., Zhong, Z., Shang, Z., Chen, N., Walla, M. D., Dong, S.-H., Tang, X., Nagarkatti, P., Nagarkatti, M., Li, Y.-X., Li, J.. 2021-07-26. Correlational networking guides the discovery of cryptic proteases for lanthipeptide maturation. https://doi.org/10.1101/2021.07.26.453782

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