钙对烟草叶片热激忍耐和活性氧代谢的影响

热胁迫导致烟草叶片细胞膜系统显著受损,表现为SOD活性降低和MDA含量明显升高,叶片叶绿素含量下降,活性氧增加。10mmol/LcaCl2溶液处理烟草幼苗后,能有效降低热胁迫下叶片细胞膜透性,维持较高的SOD和CAT等抗氧化酶活性,减缓O2^-形成和膜脂过氧化反应。研究结果表明,CaCl2处理提高了烟草叶片膜稳定性和膜保护酶活性,有利于保护细胞膜结构,降低高温对烟草幼苗的伤害。钙离子螯合剂EGTA能在一定程度上降低烟草叶片的抗热性。     

钙对烟草叶片热激忍耐和活性氧代谢的影响

热胁迫导致烟草叶片细胞膜系统显著受损,表现为SOD活性降低和MDA含量明显升高,叶片叶绿素含量下降,活性氧增加。10 mmol/L CaCl2溶液处理烟草幼苗后,能有效降低热胁迫下叶片细胞膜透性,维持较高的SOD和CAT等抗氧化酶活性,减缓 O-·2 形成和膜脂过氧化反应。研究结果表明,CaCl2处理提高了烟草叶片膜稳定性和膜保护酶活性,有利于保护细胞膜结构,降低高温对烟草幼苗的伤害。钙离子螯合剂EGTA能在一定程度上降低烟草叶片的抗热性。     

Nitrogen Metabolism in Senescing Leaves

Leaf senescence is a highly organized process and not a passive decay. Photosynthesizing mesophyll cells lose their functions in an early phase, while the epidermal layer with the stomates and the phloem remains functional throughout senescence. The subcellular compartmentation is maintained and allows the cooperation of different organelles in the remobilization of constituents. Nitrogen metabolism changes at the onset of senescence from assimilation to remobilization. Enzymes involved in nitrate reduction are lost, while some enzymes of intermediary nitrogen metabolism are maintained longer, and some catabolic enzymes reach highest activities during senescence. Chloroplasts are dismantled early, but mitochondria remain active and may fuel remobilization processes. Chloroplast proteins are degraded, and this nitrogen fraction can be translocated via the phloem from senescing leaves to sinks within the same plant. In contrast, chlorophyll is degraded, fragments produced reach the vacuole, and catabolites accumulate there. Nuclear DNA is maintained until a very late phase. The export of nitrogen from senescing plant parts is important for the economic use of this macronutrient. The regulation of senescence at the whole plant level as well as at the molecular level is only rudimentarily known, although interesting new aspects have been presented recently.     

Starch Metabolism in Shoot-forming Tobacco Callus

Starch, free sugars and protein contents, and the specific activitiesof enzymes of starch metabolism were determined in tobacco calluscultured under shoot-forming and non-shoot-forming conditions.Shoot-forming cultures contained higher levels of starch, freesugars and protein. Shoot-forming cultures had higher specificactivities for starch-synthesising enzymes throughout culture.On the other hand, higher levels of activity for starch-degradingenzymes in shoot-forming tissues were only observed during organizeddevelopment. The role of phosphorylase in the cultured tissuewas not clear.     

The Metabolism of Carbon-14 Specifically Labelled Glucose in Leaves Showing Tobacco Mosaic Virus Induced Local Necrotic Lesions

Glucose metabolism of healthy and tobacco mosaic virus-infected leaf-discs of Nicotiana tabocum L. var. Xanthi showing local-necrotic lesions was investigated using glucose-¹⁴C. Local lesion formation following inoculation with tobacco mosaic virus resulted in enhanced glucose metabolism reflected by an increased rate of release of ¹⁴CO₂ from glucose-U-¹⁴C and greater incorporation of ¹⁴C into all cell fractions. When specifically labelled glucose was fed to healthy and tobacco mosaic virus infected leaves, the C₆/C₁ ratio (rate of release of ¹⁴CO₂ from glucose-6-¹⁴C/rate of release of ¹⁴CO₂ from glucose-l-¹⁴C) was similar for healthy and virus-infected leaves. The C₆/C₁ ratios recorded from 0.30 to 0.50 indicate that both the glycolytic and pentose phosphate pathways participate in glucose catobolism in healthy and virus-infected leaves. Although the C₆/C₁ ratio was the same as that of the healthy leaf the rate of release of ¹⁴CO₂ from glucose-6-¹⁴C and glucose-1-¹⁴C was greatly increased in the virus-infected leaf. The increased glucose catabolism occurs by both glycolytic and pentose phosphate pathways in the virus-infected leaf.     

Synthesis of Stress Proteins in Tobacco Leaves

Pathogenesis-related proteins (PR proteins), which are knownto be induced in tobacco leaves in response to infection withtobacco mosaic virus (TMV), were isolated by a simple procedureinvolving ammonium sulfate fractionation and preparative gelelectrophoresis. A rabbit antibody to one of the purified PRproteins, designated as PR1a, also reacted with two other PRproteins, designated as PR1b and PR1c in double immunodiffusiontests. Quantitative analysis of these proteins using rocketimmunoelectrophoresis with the antibody showed that they wereinduced not only by infection with TMV but also by mechanicalinjury and osmotic stress at 20?C, although not at 30?C. Basedon these findings, we propose that these proteins be called"stress proteins" rather than "pathogenesis-related proteins." (Received October 23, 1984; Accepted January 18, 1985)     

Abscisic Acid Metabolism in Water-stressed Bean Leaves

Phaseic acid (PA) and dihydrophaseic acid (DPA) are the major metabolites observed when (S)-2-¹⁴C-abscisic acid (ABA) is fed to 14-day excised primary bean leaves (Phaseolus vulgaris L. cv. Red Kidney). The distribution of ¹⁴C in leaves which were wilted after feeding ABA appears to be the same as that observed in unwilted leaves. A reduction in the relative specific radioactivities of the two metabolites after wilting, compared with the specific radioactivities measured in unwilted plants, indicated that these metabolites continue to be formed endogenously after wilting. Estimates of the endogenous ABA levels showed that they rose from 0.04 μg to approximately 0.5 μg/g fresh weight within 4 hours after the beginning of a 10% wilt and remained at that level during a subsequent 20 hours of wilt. In unwilted leaves, the levels of PA and DPA were 5 times and 20 times higher than that of ABA, respectively. Both PA and DPA levels rose throughout the wilt period. PA rose from 0.20 μg to 1.0 μg and DPA from 0.8 μg to over 3 μg/g fresh weight. From these data, we calculated the rate of ABA synthesis to be at least 0.15 μg/hr.g fresh weight during this period. We have interpreted these results to mean that in wilted leaves an elevated level of ABA is maintained because the rate of synthesis and metabolism are both elevated and approximately equal.     

Metabolism of Adenine in Healthy and Blighted Potato Leaves

Analysis of the distribution of ¹⁴C in extracts prepared fromleaf tissue which had been exposed to labelled adenine by petiolaruptake revealed that this purine is extensively metabolizedin both healthy and Phytophthora-infected potato leaves. Incorporationof labelled adenine into the major ribonucleic acid speciesof the leaf was also extensive as determined by radioactiveassays performed on individual fractions which were separatedon columns of methylated albumin kieselguhr. Examination ofindividual nucleotides released by alkaline hydrolysis showedthat both the adenylic and guanylic acid moieties were labelled.Although the labelling patterns were similar for RNA from healthyand infected leaf tissue, the specific activity of the latterwas consistently higher than the former. When partially purified leaf extracts were assayed for phosphoribosyltransferase,they exhibited relatively high levels of activity with adenineas substrate, but were virtually devoid of activity with hypoxanthineand guanine. However, direct petiolar uptake of labelled hypoxanthineresulted in highly labelled RNA. A comparison of adenine phosphoribosyltransferase activity inextracts from healthy and blighted leaves failed to reveal measurabledifferences. Therefore, it was concluded that the differentialincorporation of labelled adenine into the RNA of healthy andinfected leaves was due neither to increased activity of thisenzyme in response to infection nor to its differential activation. Apart from its role in the recovery of preformed purines fornucleic acid synthesis, adenine phosphoribosyltransferase mayfunction as part of a mechanism for regulating levels of adeninein the potato leaf.     

Induction of Resistance in Tobacco Leaves to Tobacco Mosaic Virus by Dodecylbenzenesulfonate

Application of dodecylbenzenesulfonate (DBS) to half leaves of Nicotiana tabacum cv. Xanthi nc. before TMV inoculation resulted in a marked decrease in lesion number and size as well as in virus content of the lesions in the untreated half leaves. Systemic induction of resistance in untreated leaves of the plants was not detected.     

Studies on Nitrogen Metabolism in Tobacco Plants

Δ¹-Pyrroline-5-carboxylate reductase has been considerably purified from tobacco leaves. This enzyme uses NADPH or NADH for the formation of proline, although the former is better used. This enzyme was found in washed chloroplast extract as well as in cytoplasmic fluid and utilized NADPH, formed by the photosynthetic NADP reduction, for the sythesis of proline in the light.     

Moisture Diffusion within Shredded Tobacco Leaves

The mechanism of moisture transfer into shredded tobacco was investigated in connection with moistening process control in cigarette manufacturing. For shredded tobaccos of less than about 1.0 mm shred width, the moisture was sorbed mainly through the cut faces rather than through the leaf epidermis, indicating that the moisture diffusion within the leaf was the rate limiting step of moisture transfer. The moisture diffusion coefficient values within the cured tobacco leaf ranged from 8.80 × 10^?7 to 64.2 × 10^?7cm²-s^?1 depending on the type of tobacco, the shred width of tobacco and the temperature at sorption. But these values were not affected by the relative humidity at sorption. The entire moisture transfer into the shredded tobacco leaves was predictable with the diffusion theory.