Characterization of vacuolar and extracellular beta(1,3)-glucanases of tobacco: Evidence for a strictly compartmentalized plant defense system
- PMID: 16594025
- PMCID: PMC286980
- DOI: 10.1073/pnas.86.8.2673
Characterization of vacuolar and extracellular beta(1,3)-glucanases of tobacco: Evidence for a strictly compartmentalized plant defense system
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.
Similar articles
-
Plant 'pathogenesis-related' proteins and their role in defense against pathogens.Biochimie. 1993;75(8):687-706. doi: 10.1016/0300-9084(93)90100-7. Biochimie. 1993. PMID: 8286442 Review.
-
Only Specific Tobacco (Nicotiana tabacum) Chitinases and [beta]-1,3-Glucanases Exhibit Antifungal Activity.Plant Physiol. 1993 Mar;101(3):857-863. doi: 10.1104/pp.101.3.857. Plant Physiol. 1993. PMID: 12231736 Free PMC article.
-
Functional analysis of Arabidopsis WRKY25 transcription factor in plant defense against Pseudomonas syringae.BMC Plant Biol. 2007 Jan 10;7:2. doi: 10.1186/1471-2229-7-2. BMC Plant Biol. 2007. PMID: 17214894 Free PMC article.
-
Differential Regulation of beta-1,3-Glucanase Messenger RNAs in Response to Pathogen Infection.Plant Physiol. 1991 Jun;96(2):390-7. doi: 10.1104/pp.96.2.390. Plant Physiol. 1991. PMID: 16668198 Free PMC article.
-
Differential volatile emissions and salicylic acid levels from tobacco plants in response to different strains of Pseudomonas syringae.Planta. 2003 Sep;217(5):767-75. doi: 10.1007/s00425-003-1039-y. Epub 2003 Apr 24. Planta. 2003. PMID: 12712338
Cited by
-
Two Apoplastic alpha-Amylases Are Induced in Tobacco by Virus Infection.Plant Physiol. 1991 Oct;97(2):651-6. doi: 10.1104/pp.97.2.651. Plant Physiol. 1991. PMID: 16668448 Free PMC article.
-
Triticum aestivum puroindolines, two basic cystine-rich seed proteins: cDNA sequence analysis and developmental gene expression.Plant Mol Biol. 1994 Apr;25(1):43-57. doi: 10.1007/BF00024197. Plant Mol Biol. 1994. PMID: 7516201
-
Chitinase, beta-1,3-glucanase, osmotin, and extensin are expressed in tobacco explants during flower formation.Plant Cell. 1990 Jul;2(7):673-84. doi: 10.1105/tpc.2.7.673. Plant Cell. 1990. PMID: 2152343 Free PMC article.
-
An induced hypersensitive-like response limits expression of foreign peptides via a recombinant TMV-based vector in a susceptible tobacco.PLoS One. 2010 Nov 29;5(11):e15087. doi: 10.1371/journal.pone.0015087. PLoS One. 2010. PMID: 21124743 Free PMC article.
-
Cloning and characterization of Tag 1, a tobacco anther beta-1,3-glucanase expressed during tetrad dissolution.Plant Mol Biol. 1994 Mar;24(6):903-14. doi: 10.1007/BF00014444. Plant Mol Biol. 1994. PMID: 8204827
References
LinkOut - more resources
Full Text Sources
Other Literature Sources