help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Originally published as Biophys J. BioFAST on April 13, 2007.
doi:10.1529/biophysj.106.103143
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
biophysj.106.103143v1
93/1/54    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kan, W.
Right arrow Articles by Wolgemuth, C. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kan, W.
Right arrow Articles by Wolgemuth, C. W.
Biophysical Journal 93:54-61 (2007)
© 2007 The Biophysical Society

The Shape and Dynamics of the Leptospiraceae

Wanxi Kan and Charles W. Wolgemuth

University of Connecticut Health Center, Department of Cell Biology, Farmington, Connecticut

Correspondence: Address reprint requests to C. W. Wolgemuth, Tel.: 860-679-1655; E-mail: cwolgemuth{at}uchc.edu.

Most swimming bacteria produce thrust by rotating helical filaments called flagella. Typically, the flagella stick out into the external fluid environment; however, in the spirochetes, a unique group that includes some highly pathogenic species of bacteria, the flagella are internalized, being incased in the periplasmic space; i.e., between the outer membrane and the cell wall. This coupling between the periplasmic flagella and the cell wall allows the flagella to serve a skeletal, as well as a motile, function. In this article, we propose a mathematical model for spirochete morphology based on the elastic interaction between the cell body and the periplasmic flagella. This model describes the mechanics of the composite structure of the cell cylinder and periplasmic flagella and accounts for the morphology of Leptospiraceae. This model predicts that the cell cylinder should be roughly seven times stiffer than the flagellum. In addition, we explore how rotation of the periplasmic flagellum deforms the cell cylinder during motility. We show that the transition between hook-shaped and spiral-shaped ends is purely a consequence of the change in direction of the flagellar motor and does not require flagellar polymorphism.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the Biophysical Society.