Characterization of vacuolar and extracellular β(1,3)-glucanases of tobacco: Evidence for a strictly compartmentalized plant defense system
- 1 April 1989
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 86 (8) , 2673-2677
- https://doi.org/10.1073/pnas.86.8.2673
Abstract
Beta(1,3)-Glucanases are a class of hormonally and developmentally regulated plant hydrolytic enzymes, which are also induced upon pathogen infection, suggesting a role of these hydrolases in the defense response to pathogens. We have purified several beta(1,3)-glucanases present in tobacco leaves from control plants and from plants treated with salicylic acid or infected with Pseudomonas syringae and studied in detail the subcellular localization of the different isoforms. Partial protein sequence analysis demonstrated that each of the different isoforms had a unique amino acid sequence and was therefore encoded by a different gene. We have also demonstrated that two of these isoforms, similar to the cytokinin/auxin-regulated isoforms previously isolated from tobacco cell suspensions, are located in the central vacuole. Upon salicylic acid treatment or P. syringae infection, three secreted isoforms are induced, belonging to the so-called pathogenesis-related proteins. These pathogenesis-related beta(1,3)-glucanases are all distinct from each other and also different from the vacuolar isoforms. We demonstrate that the vacuolar isoforms are not secreted to the extracellular spaces of the plant following pathogen infection, suggesting that any function they play in the plant defense response is restricted to an intracellularly coordinated defense process.Keywords
This publication has 17 references indexed in Scilit:
- Protein Translocation Across MembranesScience, 1988
- Identification of peroxisomal targeting signals located at the carboxy terminus of four peroxisomal proteins.The Journal of cell biology, 1988
- Biological function of pathogenesis-related proteins: Four tobacco pathogenesis-related proteins are chitinasesProceedings of the National Academy of Sciences, 1987
- Alterations in the phenotype of plant cells studied by NH 2 -terminal amino acid-sequence analysis of proteins electroblotted from two-dimensional gel-separated total extractsProceedings of the National Academy of Sciences, 1987
- A C-terminal signal prevents secretion of luminal ER proteinsPublished by Elsevier ,1987
- Regulation of a plant pathogenesis-related enzyme: Inhibition of chitinase and chitinase mRNA accumulation in cultured tobacco tissues by auxin and cytokininProceedings of the National Academy of Sciences, 1987
- [12] Determination of total proteinPublished by Elsevier ,1983
- Simple rapid procedures for isolation of tobacco leaf nucleiAnalytical Biochemistry, 1972
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acidBiochemical Journal, 1956