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7WOI

Structure of the shaft pilin Spa2 from Corynebacterium glutamicum

Summary for 7WOI
Entry DOI10.2210/pdb7woi/pdb
DescriptorSpa2, 1,2-ETHANEDIOL, GLYCEROL, ... (4 entities in total)
Functional Keywordsbacterial pilus, adhesion, self-assembly, sortase catelyzed pilus, cell adhesion
Biological sourceCorynebacterium glutamicum ATCC 14067
Total number of polymer chains2
Total formula weight106448.57
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 citationHuang, 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: 38012344
DOI: 10.1038/s41589-023-01489-x
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.73 Å)
Structure validation

227111

數據於2024-11-06公開中

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