Various mechanisms of flagella helicity formation in haloarchaea

Microbiology (Russian Federation)

Volumn 81, Issue 5, 2012, Pages 573-581

  Syutkin, A S ^a   Pyatibratov, M G ^a   Beznosov, S N ^a   Fedorov, O V ^a  

^a INSTITUTE OF PROTEIN RESEARCH   (Russian Federation)

Author keywords

archaeal flagella; biological motility; filament; flagellin; Haloarcula marismortui; Halorubrum lacusprofundi

Indexed keywords

ARCHAEA; HALOARCULA MARISMORTUI; HALOBACTERIA; HALOBACTERIALES; HALOBACTERIUM SALINARUM; HALORUBRUM LACUSPROFUNDI;

EID: 84867017494     PISSN: 00262617     EISSN: None     Source Type: Journal    
DOI: 10.1134/S0026261712050153     Document Type: Article

References (26)

1. Calladine, C. R., Construction of Bacterial Flagellar Filaments, and Aspects of Their Conversion to Different Helical Forms, Symp. Soc. Exp. Biol., 1982, vol. 35, pp. 33-51.
2. Maki-Yonekura, S., Yonekura, K., and Namba, K., Conformational Change of Flagellin for Polymorphic Supercoiling of the Flagellar Filament, Nat. Struct. Mol. Biol., 2010, vol. 17, pp. 417-422.
3. Ng, S. Y. M., Chaban, B., and Jarrell, K. F., Archaeal Flagella, Bacterial Flagella and Type IV Pili: A Comparison of Genes and Posttranslational Modifications, J. Mol. Microbiol. Biotechnol., 2006, vol. 11, pp. 167-191.
4. Tarasov, V. Y., Pyatibratov, M. G., Tang, S.-L., Dyall-Smith, M., and Fedorov, O. V., Role of Flagellins from A and B Loci in Flagella Formation of Halobacterium salinarum, Mol. Microbiol., 2000, vol. 35, pp. 69-78.
5. Tarasov, V. Y., Pyatibratov, M. G., Beznosov, S. N., and Fedorov, O. V., On the Supramolecular Organization of the Flagellar Filament in Archaea, Doklady Biochem. Biophys., 2004, vol. 396, pp. 203-205.
6. Gerl, L. and Sumper, M., Halobacterial Flagellins Are Encoded by a Multigene Family. Identification of Five Flagellin Genes, J. Biol. Chem., 1988, vol. 263, pp. 13246-13251.
7. Baliga, N. S., Bonneau, R., Facciotti, M. T., Pan, M., Glusman, G., Deutsch, E. W., Shannon, P., Chiu, Y., Weng, R. S., Gan, R. R., Hung, P., Date, S. V., Marcotte, E., Hood, L., and Ng, W. V., Genome Sequence of Haloarcula marismortui: A Halophilic Archaeon from the Dead Sea, Genome Res., 2004, vol. 14, pp. 2221-2234.
8. Pyatibratov, M. G., Beznosov, S. N., Rachel, R., Tiktopulo, E. I., Surin, A. K., Syutkin, A. S., and Fedorov, O. V., Alternative Flagellar Filament Types in the Haloarchaeon Haloarcula marismortui, Can. J. Microbiol., 2008, vol. 54, pp. 835-844.
9. Roh, S. W., Nam, Y. D., Chang, H. W., Sung, Y., Kim, K. H., Oh, H. M., and Bae, J. W., Halalkalicoccus jeotgali sp. nov., a Halophilic Archaeon from Shrimp Jeotgal, a Traditional Korean Fermented Seafood, Int. J. Syst. Evol. Microbiol., 2007, vol. 57, pp. 2296-2298.
10. Antunes, A., Taborda, M., Huber, R., Moissl, C., Nobre, M. F., and Da Costa, M. S., Halorhabdus tiamatea sp. nov., a Non-Pigmented, Extremely Halophilic Archaeon from a Deep-Sea Hypersaline Anoxic Basin of the Red Sea, and Emended Description of the Genus Halorhabdus, Int. J. Syst. Evol. Microbiol., 2008, vol. 58, pp. 215-220.
11. Franzmann, P. D., Stackebrandt, E., Sanderson, K., Volkman, J. K., Cameron, D. E., Stevenson, P. L., McMeekin, T. A., and Burton, H. R., Halobacterium lacusprofundi, sp. nov., a Halophilic Bacterium Isolated from Deep Lake, Antarctica, Syst. Appl. Microbiol., 1988, vol. 11, pp. 20-27.
12. DasSarma, S. (Ed.), Halorubrum lacusprofundi Genome Database, 2002-2011. http://halo4. umbi. umd. edu/cgi-bin/haloweb/hla. pl.
13. Doerner, K. C. and White, B. A., Detection of Glycoproteins Separated by Nondenaturing Polyacrylamide Gel Electrophoresis Using the Periodic Acid-Schiff Stain, Anal. Biochem., 1990, vol. 187, pp. 147-150.
14. Southam, G., Kalmokoff, M. L., Jarrell, K. F., Koval, S. F., and Beveridge, T. J., Isolation, Characterization and Cellular Insertion of the Flagella from Two Strains of the Archaebacterium Methanospirillum hungatei, J. Bacteriol., 1990, vol. 172, pp. 3221-3228.
15. Tu, D., Blaha, G., Moore, P. B., and Steitz, T. A., Gene Replacement in Haloarcula marismortui: Construction of a Strain with Two of Its Three Chromosomal rRNA Operons Deleted, Extremophiles, 2005, vol. 9, pp. 427-435.
16. Cline, S. W., Lam, W. L., Charlebois, R. L., Schalkwyk, L. C., and Doolittle, W. F., Transformation Methods for Halophilic Archaebacteria, Can. J. Microbiol., 1989, vol. 35, pp. 148-152.
17. McGenity, T. J. and Grant, W. D., Transfer of Halobacterium saccharovorum, Halobacterium sodomense, Halobacterium trapanicum NRC 34021 and Halobacterium lacusprofundi to the Genus Halorubrum gen. nov., as Halorubrum saccharovorum comb. nov., Halorubrum sodomense comb. nov., Halorubrum trapanicum comb. nov., and Halorubrum lacusprofundi comb. nov., Syst. Appl. Microbiol., 1995, vol. 18, pp. 237-243.
18. Fedorov, O. V., Pyatibratov, M. G., Kostyukova, A. S., Osina, N. K., and Tarasov, V. Y., Protofilament as a Structural Element of Flagella of Haloalkalophilic Archaebacteria, Can. J. Microbiol., 1994, vol. 40, pp. 45-53.
19. Berg, H. C., The Rotary Motor of Bacterial Flagella, Annu. Rev. Biochem., 2003, vol. 72, pp. 19-54.
20. Chaban, B., Voisin, S., Kelly, J., Logan, S. M., and Jarrell, K. F., Identification of Genes Involved in the Biosynthesis and Attachment of Methanococcus voltae N-Linked Glycans: Insight into N-Linked Glycosylation Pathways in Archaea, Mol. Microbiol., 2006, vol. 61, pp. 259-268.
21. Zeitler, R., Hochmuth, E., Deutzmann, R., and Sumper, M., Exchange of Ser-4 for Val, Leu or Asn in the Sequon Asn-Ala-Ser Does Not Prevent N-Glycosylation of the Cell Surface Glycoprotein from Halobacterium halobium, Glycobiology, 1998, vol. 8, pp. 1157-1164.
22. Bardy, S. L., Mori, T., Komoriya, K., Aizawa, S.-I., and Jarrell, K. F., Identification and Localization of Flagellins FlaA and FlaB3 within the Flagella of Methanococcus voltae, J. Bacteriol., 2002, vol. 184, pp. 5223-5233.
23. Chaban, B., Ng, S. Y. M., Kanbe, M., Saltzman, I., Nimmo, G., Aizawa, S.-I., and Jarrell, K. F., Systematic Deletion Analyses of the fla Genes in the Flagella Operon Identify Several Genes Essential for Proper Assembly and Function of Flagella in the Archaeon, Methanococcus maripaludis, Mol. Microbiol., 2007, vol. 66, pp. 596-609.
24. Szabó, Z., Sani, M., Groeneveld, M., Zolghadr, B., Schelert, J., Albers, S. V., Blum, P., Boekema, E. J., and Driessen, A. J., Flagellar Motility and Structure in the Hyperthermoacidophilic Archaeon Sulfolobus solfataricus, J. Bacteriol., 2007, vol. 189, pp. 4305-4309.
25. Faguy, D. M., Bayley, D. P., Kostyukova, A. S., Thomas, N. A., and Jarrell, K. F., Isolation and Characterization of Flagella and Flagellin Proteins from the Thermoacidophilic Archaea Thermoplasma volcanium and Sulfolobus shibatae, J. Bacteriol., 1996, vol. 178, pp. 902-905.
26. Taguchi, F., Shibata, S., Suzuki, T., Ogawa, Y., Aizawa, S., Takeuchi, K., and Ichinose, Y., Effects of Glycosylation on Swimming Ability and Flagellar Polymorphic Transformation in Pseudomonas syringae pv. tabaci, 6605, J. Bacteriol., 2008, vol. 190, pp. 764-768.