Werner M, Mehner-Breitfeld D, Bruser T
Sci Rep. 2024; 14(1):13754.
PMID: 38877109
PMC: 11178869.
DOI: 10.1038/s41598-024-64547-x.
Sharma A, Chowdhury R, Musser S
Commun Biol. 2022; 5(1):988.
PMID: 36123532
PMC: 9485244.
DOI: 10.1038/s42003-022-03952-2.
Frain K, Robinson C, van Dijl J
Protein J. 2019; 38(4):377-388.
PMID: 31401776
PMC: 6708511.
DOI: 10.1007/s10930-019-09859-y.
Frain K, van Dijl J, Robinson C
EcoSal Plus. 2019; 8(2).
PMID: 31215506
PMC: 11573298.
DOI: 10.1128/ecosalplus.ESP-0040-2018.
Hamsanathan S, Musser S
FEMS Microbiol Lett. 2018; 365(12).
PMID: 29897510
PMC: 5995166.
DOI: 10.1093/femsle/fny123.
Signal peptides for recombinant protein secretion in bacterial expression systems.
Freudl R
Microb Cell Fact. 2018; 17(1):52.
PMID: 29598818
PMC: 5875014.
DOI: 10.1186/s12934-018-0901-3.
A TatABC-type Tat translocase is required for unimpaired aerobic growth of Corynebacterium glutamicum ATCC13032.
Oertel D, Schmitz S, Freudl R
PLoS One. 2015; 10(4):e0123413.
PMID: 25837592
PMC: 4383559.
DOI: 10.1371/journal.pone.0123413.
TatBC-independent TatA/Tat substrate interactions contribute to transport efficiency.
Taubert J, Hou B, Risselada H, Mehner D, Lunsdorf H, Grubmuller H
PLoS One. 2015; 10(3):e0119761.
PMID: 25774531
PMC: 4361764.
DOI: 10.1371/journal.pone.0119761.
Co-factor insertion and disulfide bond requirements for twin-arginine translocase-dependent export of the Bacillus subtilis Rieske protein QcrA.
Goosens V, Monteferrante C, van Dijl J
J Biol Chem. 2014; 289(19):13124-31.
PMID: 24652282
PMC: 4036324.
DOI: 10.1074/jbc.M113.529677.
The canonical twin-arginine translocase components are not required for secretion of folded green fluorescent protein from the ancestral strain of Bacillus subtilis.
Snyder A, Mukherjee S, Glass J, Kearns D, Mukhopadhyay S
Appl Environ Microbiol. 2014; 80(10):3219-32.
PMID: 24632256
PMC: 4018911.
DOI: 10.1128/AEM.00335-14.
Ultrastructural characterisation of Bacillus subtilis TatA complexes suggests they are too small to form homooligomeric translocation pores.
Beck D, Vasisht N, Baglieri J, Monteferrante C, van Dijl J, Robinson C
Biochim Biophys Acta. 2013; 1833(8):1811-9.
PMID: 23567937
PMC: 3988878.
DOI: 10.1016/j.bbamcr.2013.03.028.
Bacillus subtilis: from soil bacterium to super-secreting cell factory.
van Dijl J, Hecker M
Microb Cell Fact. 2013; 12:3.
PMID: 23311580
PMC: 3564730.
DOI: 10.1186/1475-2859-12-3.
Transmembrane insertion of twin-arginine signal peptides is driven by TatC and regulated by TatB.
Frobel J, Rose P, Lausberg F, Blummel A, Freudl R, Muller M
Nat Commun. 2012; 3:1311.
PMID: 23250441
PMC: 3538955.
DOI: 10.1038/ncomms2308.
Dynamic localization of Tat protein transport machinery components in Streptomyces coelicolor.
Willemse J, Ruban-Osmialowska B, Widdick D, Celler K, Hutchings M, van Wezel G
J Bacteriol. 2012; 194(22):6272-81.
PMID: 23002216
PMC: 3486365.
DOI: 10.1128/JB.01425-12.
High-salinity growth conditions promote Tat-independent secretion of Tat substrates in Bacillus subtilis.
van der Ploeg R, Monteferrante C, Piersma S, Barnett J, Kouwen T, Robinson C
Appl Environ Microbiol. 2012; 78(21):7733-44.
PMID: 22923407
PMC: 3485715.
DOI: 10.1128/AEM.02093-12.
Degradation of the twin-arginine translocation substrate YwbN by extracytoplasmic proteases of Bacillus subtilis.
Krishnappa L, Monteferrante C, van Dijl J
Appl Environ Microbiol. 2012; 78(21):7801-4.
PMID: 22923395
PMC: 3485718.
DOI: 10.1128/AEM.02023-12.
Requirement of signal peptidase ComC and thiol-disulfide oxidoreductase DsbA for optimal cell surface display of pseudopilin ComGC in Staphylococcus aureus.
van der Kooi-Pol M, Reilman E, Sibbald M, Veenstra-Kyuchukova Y, Kouwen T, Buist G
Appl Environ Microbiol. 2012; 78(19):7124-7.
PMID: 22820325
PMC: 3457507.
DOI: 10.1128/AEM.01565-12.
Specific targeting of the metallophosphoesterase YkuE to the bacillus cell wall requires the twin-arginine translocation system.
Monteferrante C, Miethke M, van der Ploeg R, Glasner C, van Dijl J
J Biol Chem. 2012; 287(35):29789-800.
PMID: 22767609
PMC: 3436186.
DOI: 10.1074/jbc.M112.378190.
Molecular dissection of TatC defines critical regions essential for protein transport and a TatB-TatC contact site.
Kneuper H, Maldonado B, Jager F, Krehenbrink M, Buchanan G, Keller R
Mol Microbiol. 2012; 85(5):945-61.
PMID: 22742417
PMC: 3712464.
DOI: 10.1111/j.1365-2958.2012.08151.x.
Processing by rhomboid protease is required for Providencia stuartii TatA to interact with TatC and to form functional homo-oligomeric complexes.
Fritsch M, Krehenbrink M, Tarry M, Berks B, Palmer T
Mol Microbiol. 2012; 84(6):1108-23.
PMID: 22591141
PMC: 3712462.
DOI: 10.1111/j.1365-2958.2012.08080.x.