FliG and FliM distribution in the Salmonella typhimurium cell and flagellar basal bodies

Rongbao Zhao, Charles D. Amsler, Philip Matsumura, Shahid Khan

Research output: Contribution to journalArticlepeer-review

56 Scopus citations

Abstract

Salmonella typhimurium FliG and FliM are two of three proteins known to be necessary for flagellar morphogenesis as well as energization and switching of flagellar rotation. We have determined FliG and FliM levels in cellular fractions and in extended flagellar basal bodies, using antibodies raised against the purified proteins. Both proteins were found predominantly in the detergent-solubilized particulate fraction containing flagellar structures. Basal flagellar fragments could be separated from partially constructed basal bodies by gel filtration chromatography. FliG and FliM were present in an approximately equimolar ratio in all gel-filtered fractions. FliG and FliM copy numbers, estimated relative to that of the hook protein from the early fractions containing long, basal, flagellar fragments, were (means ± standard errors) 41 ± 10 and 37 ± 13 per flagellum, respectively. Extended structures were present in the earliest identifiable basal bodies. Immunolectron microscopy and immunoblot gel analysis suggested that the FliG and, to a less certain degree, the FliM contents of these structures were the same as those for the complete basal bodies. These facts are consistent with the postulate that FliG and FliM affect flagellar morphogenesis as part of the extended basal structure, formation of which is necessary for assembly of more-distal components of the flagellum. The determined stoichiometries will provide important constraints to modelling energization and switching of flagellar rotation.

Original languageEnglish (US)
Pages (from-to)258-265
Number of pages8
JournalJournal of Bacteriology
Volume178
Issue number1
DOIs
StatePublished - Jan 1996

ASJC Scopus subject areas

  • Microbiology
  • Molecular Biology

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