Reprogramming bacterial protein organelles as a nanoreactor for hydrogen production

Li, Tianpei and Jiang, Qiuyao and Huang, Jiafeng and Aitchison, Catherine M. and Huang, Fang and Yang, Mengru and Dykes, Gregory F. and He, Hai Lun and Wang, Qiang and Sprick, Reiner Sebastian and Cooper, Andrew I. and Liu, Lu Ning (2020) Reprogramming bacterial protein organelles as a nanoreactor for hydrogen production. Nature Communications, 11 (1). 5448. ISSN 2041-1723 (https://doi.org/10.1038/s41467-020-19280-0)

[thumbnail of Li-etal-NC-2020-Reprogramming-bacterial-protein-organelles-as-a-nanoreactor-for-hydrogen]
Preview
 Text. Filename: Li_etal_NC_2020_Reprogramming_bacterial_protein_organelles_as_a_nanoreactor_for_hydrogen.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo
Download (2MB)| Preview

Abstract

Compartmentalization is a ubiquitous building principle in cells, which permits segregation of biological elements and reactions. The carboxysome is a specialized bacterial organelle that encapsulates enzymes into a virus-like protein shell and plays essential roles in photosynthetic carbon fixation. The naturally designed architecture, semi-permeability, and catalytic improvement of carboxysomes have inspired rational design and engineering of new nanomaterials to incorporate desired enzymes into the protein shell for enhanced catalytic performance. Here, we build large, intact carboxysome shells (over 90 nm in diameter) in the industrial microorganism Escherichia coli by expressing a set of carboxysome protein-encoding genes. We develop strategies for enzyme activation, shell self-assembly, and cargo encapsulation to construct a robust nanoreactor that incorporates catalytically active [FeFe]-hydrogenases and functional partners within the empty shell for the production of hydrogen. We show that shell encapsulation and the internal microenvironment of the new catalyst facilitate hydrogen production of the encapsulated oxygen-sensitive hydrogenases. The study provides insights into the assembly and formation of carboxysomes and paves the way for engineering carboxysome shell-based nanoreactors to recruit specific enzymes for diverse catalytic reactions.

CORE (COnnecting REpositories)