Glycosylation Regulates Specific Induction of Rice Immune Responses by Acidovorax avenae Flagellin

التفاصيل البيبلوغرافية
العنوان: Glycosylation Regulates Specific Induction of Rice Immune Responses by Acidovorax avenae Flagellin
المؤلفون: Seiji Takayama, Masaru Nakai, Machiko Kondo, Ryota Takai, Megumi Iwano, Akira Isogai, Hiroyuki Hirai, Fang-Sik Che
المصدر: Journal of Biological Chemistry. 286:25519-25530
بيانات النشر: Elsevier BV, 2011.
سنة النشر: 2011
مصطلحات موضوعية: Glycosylation, Molecular Sequence Data, Mutant, Plant Biology, Flagellum, medicine.disease_cause, Biochemistry, Epitope, Microbiology, Comamonadaceae, Epitopes, chemistry.chemical_compound, Immune system, Polysaccharides, Escherichia coli, medicine, Amino Acid Sequence, Molecular Biology, Cells, Cultured, Sequence Deletion, Binding Sites, biology, Acidovorax, food and beverages, Oryza, Cell Biology, biology.organism_classification, Recombinant Proteins, chemistry, biology.protein, bacteria, Flagellin
الوصف: Plants have a sensitive system that detects various pathogen-derived molecules to protect against infection. Flagellin, a main component of the bacterial flagellum, from the rice avirulent N1141 strain of the Gram-negative phytopathogenic bacterium Acidovorax avenae induces plant immune responses including H2O2 generation, whereas flagellin from the rice virulent K1 strain of A. avenae does not induce these immune responses. To clarify the molecular mechanism that leads to these differing responses between the K1 and N1141 flagellins, recombinant K1 and N1141 flagellins were generated using an Escherichia coli expression system. When cultured rice cells were treated with recombinant K1 or N1141 flagellin, both flagellins equally induced H2O2 generation, suggesting that post-translational modifications of the flagellins are involved in the specific induction of immune responses. Mass spectrometry analyses using glycosyltransferase-deficient mutants showed that 1,600- and 2,150-Da glycans were present on the flagellins from N1141 and K1, respectively. A deglycosylated K1 flagellin induced immune responses in the same manner as N1141 flagellin. Site-directed mutagenesis revealed that glycans were attached to four amino acid residues (Ser178, Ser183, Ser212, and Thr351) in K1 flagellin. Among mutant K1 flagellins in which each glycan-attached amino acid residue was changed to alanine, S178A and S183A, K1 flagellin induced a strong immune response in cultured rice cells, indicating that the glycans at Ser178 and Ser183 in K1 flagellin prevent epitope recognition in rice.
تدمد: 0021-9258
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8388fd5672d51f174dfe10d8c04de29
https://doi.org/10.1074/jbc.m111.254029
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....c8388fd5672d51f174dfe10d8c04de29
قاعدة البيانات: OpenAIRE