PMID:8943245: Difference between revisions
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''' | '''Fan, F and Macnab, RM''' (1996) Enzymatic characterization of FliI. An ATPase involved in flagellar assembly in Salmonella typhimurium. ''J. Biol. Chem.'' '''271''':31981-8 | ||
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!align=left |Abstract | !align=left |Abstract | ||
Latest revision as of 04:56, 15 September 2013
| Citation |
Fan, F and Macnab, RM (1996) Enzymatic characterization of FliI. An ATPase involved in flagellar assembly in Salmonella typhimurium. J. Biol. Chem. 271:31981-8 |
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| Abstract |
FliI is a protein needed for flagellar assembly in Salmonella typhimurium. It shows sequence similarity to the catalytic beta subunit of the F0F1-ATPase and is even more closely related to putative ATPases in Type III bacterial secretory pathways. A His-tagged version of FliI, which was fully functional in complementation tests, was purified to homogeneity. It had an ATPase activity of 0.16 s-1 at 25 degrees C and pH 7, and a Km for ATP of 0.3 mM; Mg2+ was required. The activity was not affected by inhibitors of the F-, V- or P-type ATPases, or inhibitors of the Type I or Type II bacterial secretory pathways. Mutations K188I and Y363S decreased the ATPase activity about 100-fold, increased the Km about 10-fold, blocked flagellar assembly, and were dominant. Other FliI mutations that disrupted flagellar protein export were found near the N terminus; they permitted essentially wild-type ATPase activity, were not dominant, and showed a dosage-dependent phenotype. We propose that FliI has a C-terminal ATPase domain and an N-terminal domain that interacts with other components in the flagellum-specific export apparatus. |
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| Keywords |
Adenosine Diphosphate/metabolism; Adenosine Triphosphatases/metabolism; Bacterial Proteins; Chromatography, High Pressure Liquid; Electrophoresis, Polyacrylamide Gel; Genetic Complementation Test; Mutagenesis, Site-Directed; Proteins/chemistry; Proton-Translocating ATPases; Rosaniline Dyes; Salmonella typhimurium; Temperature |
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