High-Force Generation Is a Conserved Property of Type IV Pilus Systems

被引:104
作者
Clausen, Martin [1 ]
Jakovljevic, Vladimir [2 ]
Sogaard-Andersen, Lotte [2 ]
Maier, Berenike [1 ]
机构
[1] Univ Munster, Dept Biol, D-48149 Munster, Germany
[2] Max Planck Inst Terr Microbiol, Dept Ecophysiol, D-35043 Marburg, Germany
关键词
SOCIAL GLIDING MOTILITY; ENTEROPATHOGENIC ESCHERICHIA-COLI; MYXOCOCCUS-XANTHUS; PSEUDOMONAS-AERUGINOSA; TWITCHING MOTILITY; NEISSERIA-GONORRHOEAE; ASSEMBLY COMPLEX; ATPASE ACTIVITY; RETRACTION; PROTEIN;
D O I
10.1128/JB.00396-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The type IV pilus (T4P) system of Neisseria gonorrhoeae is the strongest linear molecular motor reported to date, but it is unclear whether high-force generation is conserved between bacterial species. Using laser tweezers, we found that the average stalling force of single-pilus retraction in Myxococcus xanthus of 149 +/- 14 pN exceeds the force generated by N. gonorrhoeae. Retraction velocities including a bimodal distribution were similar between M. xanthus and N. gonorrhoeae, but force-dependent directional switching was not. Force generation by pilus retraction is energized by the ATPase PilT. Surprisingly, an M. xanthus mutant lacking PilT apparently still retracted T4P, although at a reduced frequency. The retraction velocity was comparable to the high-velocity mode in the wild type at low forces but decreased drastically when the force increased, with an average stalling force of 70 +/- 10 pN. Thus, M. xanthus harbors at least two different retraction motors. Our results demonstrate that the major physical properties are conserved between bacteria that are phylogenetically distant and pursue very different lifestyles.
引用
收藏
页码:4633 / 4638
页数:6
相关论文
共 39 条
[1]   Bacterial translocation motors investigated by single molecule techniques [J].
Allemand, Jean-Francois ;
Maier, Berenike .
FEMS MICROBIOLOGY REVIEWS, 2009, 33 (03) :593-610
[2]   Interactions between the lipoprotein PilP and the secretin PilQ in Neisseria meningitidis [J].
Balasingham, Seetha V. ;
Collins, Richard F. ;
Assalkhou, Reza ;
Homberset, Havard ;
Frye, Stephan A. ;
Derrick, Jeremy P. ;
Tonjum, Tone .
JOURNAL OF BACTERIOLOGY, 2007, 189 (15) :5716-5727
[3]   Weapons of mass retraction [J].
Burrows, LL .
MOLECULAR MICROBIOLOGY, 2005, 57 (04) :878-888
[4]   TreeDyn:: towards dynamic graphics and annotations for analyses of trees [J].
Chevenet, Francois ;
Brun, Christine ;
Banuls, Anne-Laure ;
Jacq, Bernard ;
Christen, Richard .
BMC BIOINFORMATICS, 2006, 7 (1)
[5]   Functional role of conserved residues in the characteristic secretion NTPase motifs of the Pseudomonas aeruginosa type IV pilus motor proteins PilB, PilT and PilU [J].
Chiang, Poney ;
Sampaleanu, Liliana M. ;
Ayers, Melissa ;
Pahuta, Markian ;
Howel, P. Lynne ;
Burrows, Lori L. .
MICROBIOLOGY-SGM, 2008, 154 :114-126
[6]   Dynamics of Type IV Pili Is Controlled by Switching Between Multiple States [J].
Clausen, Martin ;
Koomey, Michael ;
Maier, Berenike .
BIOPHYSICAL JOURNAL, 2009, 96 (03) :1169-1177
[7]   Type IV pilli: paradoxes in form and function [J].
Craig, Lisa ;
Li, Juliana .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2008, 18 (02) :267-277
[8]   Type IV pilus structure by cryo-electron microscopy and crystallography: Implications for pilus assembly and functions [J].
Craig, Lisa ;
Volkmann, Niels ;
Arvai, Andrew S. ;
Pique, Michael E. ;
Yeager, Mark ;
Egelman, Edward H. ;
Tainer, John A. .
MOLECULAR CELL, 2006, 23 (05) :651-662
[9]   RETRACTED: The ATPase activity of BfpD is greatly enhanced by zinc and allosteric interactions with other Bfp proteins (Retracted Article. See vol 284, pg 21100, 2009) [J].
Crowther, LJ ;
Yamagata, A ;
Craig, L ;
Tainer, JA ;
Donnenberg, MS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (26) :24839-24848
[10]   The inner membrane subassembly of the enteropathogenic Escherichia coli bundle-forming pilus machine [J].
Crowther, LJ ;
Anantha, RP ;
Donnenberg, MS .
MOLECULAR MICROBIOLOGY, 2004, 52 (01) :67-79