RESUMO
Conifer terpenes mediate a number of ecological roles such as deterring herbivory and allelopathic (plant-plant) communication. These terpenes also effect air quality and climate models and are used in chemotaxonomic studies. Herein we report on variation in both intra- and interspecific spruce terpenes using static headspace gas chromatography mass spectrometry (HS-GC-MS) and principal component analysis (PCA) of 'fingerprint' volatile profiles. Samples of blue spruce (Picea pungens), Norway spruce (P. abies), and cedar of Lebanon (Cedrus libani), an outgroup control, were analyzed by HS-GC-MS using both chiral and achiral GC columns. Headspace sampling parameters, temperature and heating time, were optimized to maximize detected terpenes. PCA of terpene 'fingerprint' profiles showed differences by species, by individual trees, but perhaps surprisingly not by environmental conditions. Analysis of blue and Norway spruce over several months show that volatile emissions remained remarkably constant unlike cedar of Lebanon, which showed a much greater variation in volatile profiles. Branches and buds from both spruces were found to release greater amounts of terpenes than samples of needles. The enantiomeric compositions of seven chiral monoterpenes were found to be largely similar between the three conifers with the exception of (-)-α-pinene, which was the dominant enantiomer released by Norway spruce and cedar of Lebanon, while (+)-α-pinene slightly predominated in blue spruce. While not the primary focus of this work, we believe this constitutes the first report on the enantiomeric composition of terpenes in cedar of Lebanon.
Assuntos
Abies , Picea , Cromatografia Gasosa-Espectrometria de Massas , Noruega , Terpenos/análiseRESUMO
The protein Bax Inhibitor-1 (BI-1) has recently emerged as a negative regulator of plant programmed cell death (PCD), but how it functions at the biochemical level remains unknown. To elucidate its regulation and mode of action, we used suspension cells of Nicotiana tabacum to study the effects of cytokinins (CKs) on the expression level of NtBI-1 via western analysis. We found that the NtBI-1 protein is up-regulated following treatments with CKs at concentrations inducing a stress response (determined by growth reduction and PR1a accumulation), but not at PCD-inducing concentrations. These data point toward a role for NtBI-1 in the stress response to CKs. Application of CKs was also accompanied by a rapid cytosolic Ca(2+) pulse, and inhibition of this pulse with La(3+) or EGTA partially restored viability, indicating a signaling role for Ca(2+) in CK-induced cell death. However, CK-induced NtBI-1 accumulation was not altered by pretreatment with La(3+), nor by treatment with several modulators of intracellular Ca(2+) homeostasis and signaling, suggesting that CK-dependent regulation of NtBI-1 accumulation is not directly mediated by Ca(2+).
Assuntos
Proteínas Reguladoras de Apoptose/metabolismo , Cálcio/metabolismo , Citocininas/farmacologia , Citosol/metabolismo , Proteínas de Membrana/metabolismo , Nicotiana/metabolismo , Proteínas de Plantas/metabolismo , Proteínas Reguladoras de Apoptose/genética , Morte Celular , Células Cultivadas , Relação Dose-Resposta a Droga , Proteínas de Membrana/genética , Proteínas de Plantas/genética , Fatores de Tempo , Regulação para CimaRESUMO
The influx of Ca(2+) into the cytosol has long been suggested to serve as a signaling intermediate in the acquisition of tolerance to hyperosmotic and/or salinity stresses. Here we use aequorin-transformed suspension-cultured tobacco cells to directly assess the role of cytosolic calcium (Ca(2+)(cyt)) signaling in salinity tolerance acquisition. Aequorin luminescence recordings and (45)Ca influx measurements using inhibitors of Ca(2+) influx (Gd(3+) and the Ca(2+)-selective chelator EGTA), and modulators of organellar Ca(2+) release (phospholipase C inhibitors U73122 or neomycin) demonstrate that hyperosmolarity, whether imposed by NaCl or by a non-ionic molecule sorbitol, induces a rapid (returning to baseline levels of Ca(2+) within 10 min) and complex Ca(2+)(cyt) pulse in tobacco cells, deriving both from Gd(3+)-sensitive externally derived Ca(2+) influx and from U73122- and neomycin-sensitive Ca(2+) release from an organelle. To determine whether each of the two components of this brief Ca(2+) signal regulate adaptation to hyperosmotic shock, the Ca(2+) pulse was modified by the addition of Gd(3+), U73122, neomycin, or excess Ca(2+), and then cells were treated with salt or sorbitol. After 10 min the cell culture medias were diluted with additional hyperosmotic media to reduce the toxic affects of the modulators, and the growth of cells was measured after 1 week. Gd(3+) treatment reduced growth in salt relative to control cells but not in sorbitol, and exposure to excess Ca(2+) increased growth in salt but not in sorbitol. In contrast, exposure to inhibitors of IP(3) formation had no effect on growth in salt or sorbitol. Therefore, although hyperosmotic treatment stimulates both Ca(2+) influx and Ca(2+) release from an internal Ca(2+) depot, only Ca(2+) influx has a measurable impact on ionic stress tolerance acquisition in tobacco cell suspensions. In contrast, osmoadaptation in these cells appears to occur independent of Ca(2+) signaling.
Assuntos
Adaptação Fisiológica , Sinalização do Cálcio/fisiologia , Cálcio/metabolismo , Nicotiana/metabolismo , Sinalização do Cálcio/efeitos dos fármacos , Células Cultivadas , Citosol/química , Pressão Osmótica , Cloreto de Sódio/farmacologia , Sorbitol/farmacologia , Nicotiana/efeitos dos fármacos , Nicotiana/fisiologia , Fosfolipases Tipo C/metabolismoRESUMO
Hyperosmotic stress caused by NaCl, LiCl, or sorbitol induces an immediate and short duration ( approximately 1 min) transient cytosolic Ca(2+) ([Ca(2+)](cyt)) increase (Ca(2+)-dependent aequorin luminescence) in Saccharomyces cerevisiae cells. The amplitude of the osmotically induced [Ca(2+)](cyt) transient was attenuated by the addition of chelating agents EGTA or BAPTA, cation channel pore blockers, competitive inhibitors of Ca(2+) transport, or mutations (cch1Delta or mid1Delta) that reduce Ca(2+) influx, indicating that Ca(ext)(2+) is a source for the transient. An osmotic pretreatment (30 min) administered by inoculating cells into media supplemented with either NaCl (0.4 or 0.5 m) or sorbitol (0.8 or 1.0 m) enhanced the subsequent growth of these cells in media containing 1 m NaCl or 2 m sorbitol. Inclusion of EGTA in the osmotic pretreatment media or the cch1Delta mutation reduced cellular capacity for NaCl but not hyperosmotic adaptation. The stress-adaptive effect of hyperosmotic pretreatment was mimicked by exposing cells briefly to 20 mm CaCl(2). Thus, NaCl- or sorbitol-induced hyperosmotic shock causes a [Ca(2+)](cyt) transient that is facilitated by Ca(2+) influx, which enhances ionic but not osmotic stress adaptation. NaCl-induced ENA1 expression was inhibited by EGTA, cch1Delta mutation, and FK506, indicating that the [Ca(2+)](cyt) transient activates calcineurin signaling to mediate ion homeostasis and salt tolerance.