| Literature DB >> 28281198 |
Chang Woo Lee1,2, Sun-Ha Park1, Sung Gu Lee1,2, Seung Chul Shin1, Se Jong Han2,3, Han-Woo Kim1,2, Hyun Ho Park4, Sunghwan Kim5, Hak Jun Kim6, Hyun Park1,2, HaJeung Park7, Jun Hyuck Lee8,9.
Abstract
The two-component phosphorelay system is the most prevalent mechanism for sensing and transducing environmental signals in bacteria. Spore formation, which relies on the two-component phosphorelay system, enables the long-term survival of the glacial bacterium Paenisporosarcina sp. TG-14 in the extreme cold environment. Spo0A is a key response regulator of the phosphorelay system in the early stage of spore formation. The protein is composed of a regulatory N-terminal phospho-receiver domain and a DNA-binding C-terminal activator domain. We solved the three-dimensional structure of the unphosphorylated (inactive) form of the receiver domain of Spo0A (PaSpo0A-R) from Paenisporosarcina sp. TG-14. A structural comparison with phosphorylated (active form) Spo0A from Bacillus stearothermophilus (BsSpo0A) showed minor notable differences. A molecular dynamics study of a model of the active form and the crystal structures revealed significant differences in the α4 helix and the preceding loop region where phosphorylation occurs. Although an oligomerization study of PaSpo0A-R by analytical ultracentrifugation (AUC) has shown that the protein is in a monomeric state in solution, both crosslinking and crystal-packing analyses indicate the possibility of weak dimer formation by a previously undocumented mechanism. Collectively, these observations provide insight into the mechanism of phosphorylation-dependent activation unique to Spo0A.Entities:
Keywords: Paenisporosarcina sp. TG-14; Spo0A; X-ray crystallography; analytical ultracentrifugation; spore formation
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Year: 2017 PMID: 28281198 DOI: 10.1007/s12275-017-6599-9
Source DB: PubMed Journal: J Microbiol ISSN: 1225-8873 Impact factor: 3.422