[1]Nash ZM, Cotter PA. Bordetella Filamentous Hemagglutinin, a model for the two-partner secretion pathway[J]. Microbiol Spectr, 2019,7:1-9. [2]Fan E, Fiedler S, Jacob-Dubuisson F, et al. Two-partner secretion of gram-negative bacteria: a single beta-barrel protein enables transport across the outer membrane[J]. Biol Chem,2012,287:2591-2599. [3]Guedin S, Willery E, Locht C, et al. Evidence that a globular conformation is not compatible with FhaC-mediated secretion of the Bordetella pertussis filamentous haemagglutinin[J]. Mol Microbiol, 1998,29:763-774. [4]Mas G, Thoma J, Hiller S. The periplasmic chaperones Skp and SurA[J]. Subcell Biochem,2019,92:169-186. [5]Hodak H, Wohlkonig A, Smet-Nocca C, et al. The peptidyl-prolyl isomerase and chaperone Par27 of Bordetella pertussis as the prototype for a new group of parvulins[J]. Mol Biol,2008,376:414-426. [6]Furst M, Zhou Y, Merfort J, et al. Involvement of PpiD in Sec-dependent protein translocation[J]. Biochim Biophys Acta Mol Cell Res, 2018,1865:273-280. [7]Schafer U, Beck K, Muller M. Skp, a molecular chaperone of gram-negative bacteria, is required for the formation of soluble periplasmic intermediates of outer membrane proteins[J]. Biol Chem,1999,274:24567-24574. [8]Spiess C, Beil A, Ehrmann M. A temperature-dependent switch from chaperone to protease in a widely conserved heat shock protein[J]. Cell,1999,97:339-347. [9]Gotzke H, Palombo I, Muheim C, et al. YfgM is an ancillary subunit of the SecYEG translocon in Escherichia coli[J]. Biol Chem, 2014,289:19089-19097. [10]Norell D, Heuck A, Tran-Thi TA, et al. Versatile in vitro system to study translocation and functional integration of bacterial outer membrane proteins[J]. Nat Commun,2014,5:5396-5404. [11]Christensen LFB, Schafer N, Wolf-Perez A, et al. Bacterial amyloids: biogenesis and biomaterials[J]. Adv Exp Med Biol,2019,1174:113-159. [12]Konovalova A, Kahne DE, Silhavy TJ. Outer Membrane Biogenesis[J]. Annu Rev Microbiol,2017,71:539-556. [13]Hagan CL, Silhavy TJ, Kahne D. beta-Barrel membrane protein assembly by the Bam complex[J]. Annu Rev Biochem,2011,80:189-210. [14]Mas G, Hiller S.Conformational plasticity of molecular chaperones involved in periplasmic and outer membrane protein folding[J]. FEMS Microbiol Lett,2018,13:1-9. |