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Cell Surface of Lactococcus lactis Is Covered by a Protective Polysaccharide Pellicle

Bibliographic reference Chapot-Chartier, Marie-Pierre ; Vinogradov, Evgeny ; Sadovskaya, Irina ; André, Guillaume ; Mistou, Michel-Yves ; et. al. Cell Surface of Lactococcus lactis Is Covered by a Protective Polysaccharide Pellicle. In: Journal of Biological Chemistry, Vol. 285, no. 14, p. 10464-10471 (2010)
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  1. Veiga Patrick, Piquet Sandra, Maisons Aurélie, Furlan Sylviane, Courtin Pascal, Chapot-Chartier Marie-Pierre, Kulakauskas Saulius, Identification of an essential gene responsible for d-Asp incorporation in the Lactococcus lactis peptidoglycan crossbridge, 10.1111/j.1365-2958.2006.05474.x
  2. Cerning Jutta, Exocellular polysaccharides produced by lactic acid bacteria, 10.1111/j.1574-6968.1990.tb04883.x
  3. Dufrêne Yves F, Atomic force microscopy and chemical force microscopy of microbial cells, 10.1038/nprot.2008.101
  4. Fedtke Iris, Mader Diana, Kohler Thomas, Moll Hermann, Nicholson Graeme, Biswas Raja, Henseler Katja, Götz Friedrich, Zähringer Ulrich, Peschel Andreas, A Staphylococcus aureus ypfP mutant with strongly reduced lipoteichoic acid (LTA) content: LTA governs bacterial surface properties and autolysin activity, 10.1111/j.1365-2958.2007.05854.x
  5. Sadovskaya Irina, Vinogradov Evgueny, Li Jianjun, Jabbouri Saı̈d, Structural elucidation of the extracellular and cell-wall teichoic acids of Staphylococcus epidermidis RP62A, a reference biofilm-positive strain, 10.1016/j.carres.2004.03.017
  6. DuBois Michel., Gilles K. A., Hamilton J. K., Rebers P. A., Smith Fred., Colorimetric Method for Determination of Sugars and Related Substances, 10.1021/ac60111a017
  7. Enghofer Erich, Kress Horst, An evaluation of the Morgan-Elson assay for 2-amino-2-deoxy sugars, 10.1016/0008-6215(79)80022-1
  8. Chen P. S., Toribara T. Y., Warner Huber., Microdetermination of Phosphorus, 10.1021/ac60119a033
  9. Mercier Carine, Domakova Elena, Tremblay Josselyne, Kulakauskas Saulius, Effects of a muramidase on a mixed bacterial community, 10.1111/j.1574-6968.2000.tb09135.x
  10. Mercier Carine, Durrieu Christele, Briandet Romain, Domakova Elena, Tremblay Josselyne, Buist Girbe, Kulakauskas Saulius, Positive role of peptidoglycan breaks in lactococcal biofilm formation : Role of peptidoglycan breaks in biofilm formation, 10.1046/j.1365-2958.2002.03160.x
  11. Buist G, Kok J, Leenhouts K J, Dabrowska M, Venema G, Haandrikman A J, Molecular cloning and nucleotide sequence of the gene encoding the major peptidoglycan hydrolase of Lactococcus lactis, a muramidase needed for cell separation., 10.1128/jb.177.6.1554-1563.1995
  12. Meyrand M., Boughammoura A., Courtin P., Mezange C., Guillot A., Chapot-Chartier M.-P., Peptidoglycan N-acetylglucosamine deacetylation decreases autolysis in Lactococcus lactis, 10.1099/mic.0.2007/005835-0
  13. Delcour Jean, Ferain Thierry, Deghorain Marie, Palumbo Emmanuelle, Hols Pascal, 10.1023/a:1002089722581
  14. Veiga Patrick, Bulbarela-Sampieri Carmen, Furlan Sylviane, Maisons Aurélie, Chapot-Chartier Marie-Pierre, Erkelenz Michael, Mervelet Peggy, Noirot Philippe, Frees Dorte, Kuipers Oscar P., Kok Jan, Gruss Alexandra, Buist Girbe, Kulakauskas Saulius, SpxB RegulatesO-Acetylation-dependent Resistance ofLactococcus lactisPeptidoglycan to Hydrolysis, 10.1074/jbc.m611308200
  15. Chandry P. Scott, Moore Sean C., Boyce John D., Davidson Barrie E., Hillier Alan J., Analysis of the DNA sequence, gene expression, origin of replication and modular structure of theLactococcus lactislytic bacteriophage sk1, 10.1046/j.1365-2958.1997.5491926.x
  16. Bolotin A., Wincker P., Mauger S., Jaillon O., Malarme K., Weissenbach J., Ehrlich S. D., Sorokin A., The Complete Genome Sequence of the Lactic Acid Bacterium Lactococcus lactis ssp. lactis IL1403, 10.1101/
  17. Dufrêne Yves F., Towards nanomicrobiology using atomic force microscopy, 10.1038/nrmicro1948
  18. Francius Grégory, Lebeer Sarah, Alsteens David, Wildling Linda, Gruber Hermann J., Hols Pascal, Keersmaecker Sigrid De, Vanderleyden Jos, Dufrêne Yves F., Detection, Localization, and Conformational Analysis of Single Polysaccharide Molecules on Live Bacteria, 10.1021/nn800341b
  19. Stukalov O., Korenevsky A., Beveridge T. J., Dutcher J. R., Use of Atomic Force Microscopy and Transmission Electron Microscopy for Correlative Studies of Bacterial Capsules, 10.1128/aem.02075-07
  20. Morlot Cécile, Zapun André, Dideberg Otto, Vernet Thierry, Growth and division of Streptococcus pneumoniae: localization of the high molecular weight penicillin-binding proteins during the cell cycle : Localization of the HMW PBPs in S. pneumoniae, 10.1046/j.1365-2958.2003.03767.x
  21. Areschoug Thomas , Gordon Siamon , Pattern Recognition Receptors and Their Role in Innate Immunity: Focus on Microbial Protein Ligands, Contributions to Microbiology (2008) ISBN:9783805585484 p.45-60, 10.1159/000135685
  22. Chen Pei-Min, Chen Heng-Chang, Ho Chun-Ta, Jung Chiau-Jing, Lien Huei-Ting, Chen Jen-Yang, Chia Jean-San, The two-component system ScnRK of Streptococcus mutans affects hydrogen peroxide resistance and murine macrophage killing, 10.1016/j.micinf.2007.12.006
  24. Segura M., Gottschalk M., Olivier M., Encapsulated Streptococcus suis Inhibits Activation of Signaling Pathways Involved in Phagocytosis, 10.1128/iai.72.9.5322-5330.2004
  25. Chapot-Chartier M.-P., Deniel C., Rousseau M., Vassal L., Gripon J.-C., Autolysis of two strains of Lactococcus lactis during cheese ripening, 10.1016/0958-6946(94)90016-7
  26. Dabour N., Kheadr E., Benhamou N., Fliss I., LaPointe G., Improvement of Texture and Structure of Reduced-Fat Cheddar Cheese by Exopolysaccharide-Producing Lactococci, 10.3168/jds.s0022-0302(06)72073-2
  27. Mifune J., Grage K., Rehm B. H. A., Production of Functionalized Biopolyester Granules by Recombinant Lactococcus lactis, 10.1128/aem.00487-09
  28. Pooley, J. Bacteriol., 109, 423 (1972)
  29. Le Gouellec A., Roux L., Fadda D., Massidda O., Vernet T., Zapun A., Roles of Pneumococcal DivIB in Cell Division, 10.1128/jb.00376-08
  30. Chia J.-S., Chang L. Y., Shun C.-T., Chang Y.-Y., Chen J.-Y., A 60-Kilodalton Immunodominant Glycoprotein Is Essential for Cell Wall Integrity and the Maintenance of Cell Shape in Streptococcus mutans, 10.1128/iai.69.11.6987-6998.2001
  31. Toukach P., Joshi H. J, Ranzinger R., Knirel Y., von der Lieth C.-W., Sharing of worldwide distributed carbohydrate-related digital resources: online connection of the Bacterial Carbohydrate Structure DataBase and, 10.1093/nar/gkl883
  32. Stenutz Roland, Weintraub Andrej, Widmalm Göran, The structures ofEscherichia coliO-polysaccharide antigens, 10.1111/j.1574-6976.2006.00016.x
  33. Neuhaus F. C., Baddiley J., A Continuum of Anionic Charge: Structures and Functions of D-Alanyl-Teichoic Acids in Gram-Positive Bacteria, 10.1128/mmbr.67.4.686-723.2003
  34. Sutcliffe I. C., Black G. W., Harrington D. J., Bioinformatic insights into the biosynthesis of the Group B carbohydrate in Streptococcus agalactiae, 10.1099/mic.0.2007/014522-0
  35. Comstock Laurie E., Kasper Dennis L., Bacterial Glycans: Key Mediators of Diverse Host Immune Responses, 10.1016/j.cell.2006.08.021
  36. Naumova, Biochemistry, 62, 809 (1997)
  37. Schaffer C., The structure of secondary cell wall polymers: how Gram-positive bacteria stick their cell walls together, 10.1099/mic.0.27749-0
  38. Glaser Philippe, Rusniok Christophe, Buchrieser Carmen, Chevalier Fabien, Frangeul Lionel, Msadek Tarek, Zouine Mohamed, Couvé Elisabeth, Lalioui Lila, Poyart Claire, Trieu-Cuot Patrick, Kunst Frank, Genome sequence of Streptococcus agalactiae, a pathogen causing invasive neonatal disease : Genome sequence of Streptococcus agalactiae, 10.1046/j.1365-2958.2002.03126.x
  39. van Hylckama Vlieg Johan ET, Rademaker Jan LW, Bachmann Herwig, Molenaar Douwe, Kelly William J, Siezen Roland J, Natural diversity and adaptive responses of Lactococcus lactis, 10.1016/j.copbio.2006.02.007
  40. Corthésy, J. Nutr., 137, 781S (2007)
  41. Zechini Barbara, Cipriani Paola, Papadopoulou Styliani, Di Nucci Giandomenico, Petrucca Andrea, Teggi Antonella, Endocarditis caused by Lactococcus lactis subsp. lactis in a patient with atrial myxoma: a case report, 10.1016/j.diagmicrobio.2006.04.011
  42. Wells Jerry M., Mercenier Annick, Mucosal delivery of therapeutic and prophylactic molecules using lactic acid bacteria, 10.1038/nrmicro1840
  43. Gasson, J. Bacteriol., 154, 1 (1983)
  44. de Ruyter P G, Kuipers O P, Beerthuyzen M M, van Alen-Boerrigter I, de Vos W M, Functional analysis of promoters in the nisin gene cluster of Lactococcus lactis., 10.1128/jb.178.12.3434-3439.1996
  45. Dupont K., Janzen T., Vogensen F. K., Josephsen J., Stuer-Lauridsen B., Identification of Lactococcus lactis Genes Required for Bacteriophage Adsorption, 10.1128/aem.70.10.5825-5832.2004
  46. van Kranenburg, J. Bacteriol., 181, 6347 (1999)
  47. Kranenburg Richard van, Marugg Joey D., van Swam Iris I., Willem Norwin J., de Vos Willem M., Molecular characterization of the plasmid-encoded eps gene cluster essential for exopolysaccharide biosynthesis in Lactococcus lactis, 10.1046/j.1365-2958.1997.3521720.x
  48. Dabour N., LaPointe G., Identification and Molecular Characterization of the Chromosomal Exopolysaccharide Biosynthesis Gene Cluster from Lactococcus lactis subsp. cremoris SMQ-461, 10.1128/aem.71.11.7414-7425.2005
  49. Wegmann U., O'Connell-Motherway M., Zomer A., Buist G., Shearman C., Canchaya C., Ventura M., Goesmann A., Gasson M. J., Kuipers O. P., van Sinderen D., Kok J., Complete Genome Sequence of the Prototype Lactic Acid Bacterium Lactococcus lactis subsp. cremoris MG1363, 10.1128/jb.01768-06