7WOI
Structure of the shaft pilin Spa2 from Corynebacterium glutamicum
Summary for 7WOI
Entry DOI | 10.2210/pdb7woi/pdb |
Descriptor | Spa2, 1,2-ETHANEDIOL, GLYCEROL, ... (4 entities in total) |
Functional Keywords | bacterial pilus, adhesion, self-assembly, sortase catelyzed pilus, cell adhesion |
Biological source | Corynebacterium glutamicum ATCC 14067 |
Total number of polymer chains | 2 |
Total formula weight | 106448.57 |
Authors | Wu, Y.F.,Wang, L.T.,Huang, Y.Y.,Zhong, C.,Zhou, J. (deposition date: 2022-01-21, release date: 2023-01-25, Last modification date: 2024-11-06) |
Primary citation | Huang, Y.,Wu, Y.,Hu, H.,Tong, B.,Wang, J.,Zhang, S.,Wang, Y.,Zhang, J.,Yin, Y.,Dai, S.,Zhao, W.,An, B.,Pu, J.,Wang, Y.,Peng, C.,Li, N.,Zhou, J.,Tan, Y.,Zhong, C. Accelerating the design of pili-enabled living materials using an integrative technological workflow. Nat.Chem.Biol., 2023 Cited by PubMed Abstract: Bacteria can be programmed to create engineered living materials (ELMs) with self-healing and evolvable functionalities. However, further development of ELMs is greatly hampered by the lack of engineerable nonpathogenic chassis and corresponding programmable endogenous biopolymers. Here, we describe a technological workflow for facilitating ELMs design by rationally integrating bioinformatics, structural biology and synthetic biology technologies. We first develop bioinformatics software, termed Bacteria Biopolymer Sniffer (BBSniffer), that allows fast mining of biopolymers and biopolymer-producing bacteria of interest. As a proof-of-principle study, using existing pathogenic pilus as input, we identify the covalently linked pili (CLP) biosynthetic gene cluster in the industrial workhorse Corynebacterium glutamicum. Genetic manipulation and structural characterization reveal the molecular mechanism of the CLP assembly, ultimately enabling a type of programmable pili for ELM design. Finally, engineering of the CLP-enabled living materials transforms cellulosic biomass into lycopene by coupling the extracellular and intracellular bioconversion ability. PubMed: 38012344DOI: 10.1038/s41589-023-01489-x PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.73 Å) |
Structure validation
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