Peroxidases and ethylene formation in olive tree leaves

The loss of intercellular peroxidases from olive tree leaf sections subjected to isoelectric focusing correlates well with the capacity of the referred sections to convert 1-aminocyclopropane-1-carboxylic acid (ACC) into ethylene. Both activities are compared in leaves of different ages (according to their position on the branch) and it is found that they follow a parallel course. The inhibition of the capacity to convert ACC into ethylene in homogenized olive tree leaves is due to inhibitors release. The results, in relation to other authors' reports, are discussed.     

Composting of olive leaves and pomace from a three-phase olive mill plant

The composting of olive leaves and olive pomace from a three-phase olive mill was tested as a method for solid waste reuse. The process was carried out using a compost windrow and mixing olive leaves and pomace at a ratio of 1:2. Compost was retained in the windrow for 60 days during which thermophilic temperatures developed for the first 40 days. The compost was then placed into a closed area to mature for another 60 days. The final product proved to be high quality amendment with C/N 27.1 and high nutrient concentrations (N, 1.79%; P, 0.17%; K, 4.97%; Na, 2.8%). Mature compost presented the highest germination index (198%) reported to date, as the germination index in the majority of previous studies is under 80%. Furthermore, tests revealed that addition of 31.5 tons of compost per ha, could increase lettuce yield by 145%.     

Metabolism of 2'-carboxyarabinitol in leaves

Results presented here indicate that 2′-carboxyarabinitol (CA) is the in vivo precursor and product of 2′-carboxyarabinitol 1-phosphate (CA1P) metabolism in leaves. When [2-¹⁴C]CA was fed in the light to leaves of five species known to be highly active in CA1P metabolism (Phaseolus vulgaris, Lycopersicon esculentum, Helianthus annuus, Petunia hybrida, and Beta vulgaris), [¹⁴C]CA1P was formed in the dark. Reillumination of a Phaseolus leaf caused this [¹⁴C]CA1P to be rapidly metabolized to [¹⁴C]CA (t_½ = 1 min). The epimer 2′-carboxyribitol could not substitute for CA in the dark synthesis of CA1P, and CA in the anionic form was a better substrate than CA in the lactone form. In leaves of Phaseolus vulgaris, the active CA pool size used in the dark synthesis of CA1P is between about 70 and 110 nanomoles per milligram of chlorophyll. The photosynthetic electron transport inhibitor diuron did not affect the dark synthesis of [¹⁴C]CA1P, but did greatly reduce the rate of its subsequent light degradation (t_½ = approximately 10 min). Dark synthesis of [¹⁴C]CA1P was inhibited by dithiothreitol and NaF. From the present data, we suggest that CA1P and CA participate in a metabolic substrate cycle in vivo.     

Stomatal control of water use in olive tree leaves

Little is known about the strategies used by olive trees to overcome the long dry periods typical of the areas where they are cropped. This makes it difficult to optimize the water supply in orchards. To study the control of water consumption by olive trees, measurements of leaf water potential () and stomatal conductance to H₂O (g) were made on 26-year-old t Manzanillo olive trees under three irrigation treatments. The first treatment provided enough water to cover the crop water demand, the next treatment supplied one third of that rate, and the final treatment was no irrigation at all, typical of dry-farming conditions. Under conditions of high vapour pressure deficit of the air (D_a), the olive trees prevented excessive water loss by closing their stomata. Leaves of the current year showed better stomatal control than did the 1-year-old leaves. The upper-bound functional relationships between t g and t D_a and photon flux density (I_P) were obtained by boundary-line analysis, based on a technique of non-linear least squares. Maximum values of t g were observed at relatively low levels of t I_P, from about 500 mol m^-2 s^-1, and a proportional decrease in t g with increasing t D_a was also found, at least for values of up to approximately 3.5 kPa. Higher values of t g were observed in the morning than in the afternoon, for similar levels of t I_P and t D_a. Unirrigated olive trees recovered quickly after the dry season, showing values of and t g similar to those of irrigated trees after just two days.     

油橄榄叶中橄榄苦苷的分离纯化

考察了6种不同大孔树脂对橄榄苦苷的吸附,筛选出吸附选择性好的D101大孔吸附树脂为实验材料.得到的D101大孔树脂的最佳吸附条件:试样上样质量浓度41.06[J].,流速5 mL/min,50％乙醇溶液洗脱,洗脱液用量260mL,树脂可以反复使用.经大孔树脂富集后,橄榄苦苷的纯度可达55％以上,再经葡聚糖凝胶精纯化后,可达76％以上.     

Cytokinin-induced ethylene biosynthesis in nonsenescing cotton leaves

The influence of cytokinins on ethylene production was examined using cotton leaf tissues. Treatment of intact cotton (Gossypium hirsutum L. cv LG 102) seedlings with both natural and synthetic cytokinins resulted in an increase in ethylene production by excised leaves. The effectiveness of the cytokinins tested was as follows: thidiazuron BA isopentyladenine ≥ zeatin kinetin. Using 100 micromolar thidiazuron (TDZ), an initial increase in ethylene production was observed 7 to 8 hours post-treatment, reached a maximum by 24 hours and then declined. Inhibitors of 1-aminocyclopropane-1-carboxylic acid (ACC) synthesis and its oxidation to ethylene reduced ethylene production 24 hours post-treatment; however, by 48 hours only inhibitors of ACC oxidation were effective. The increase in ethylene production was accompanied by a massive accumulation of ACC and its acid-labile conjugate. TDZ treatment resulted in a significant increase in the capacity of tissues to oxidize ACC to ethylene. Endogenous levels of methionine remained constant following TDZ treatment. It was concluded that the stimulation of ethylene production in cotton leaves following cytokinin treatment was the result of an increase in both the formation and oxidation of ACC.     

Role of ethylene in senescence of watercress leaves

Detached watercress leaves showed a rapid senescence rate as compared with other herbs. It was therefore of interest to investigate the role of ethylene in the rapid senescence of watercress leaves, and So estimate the efficacy of various inhibitors of elhylene synthesis (aminoethoxyvinylglycine, AVG) and action (CO₂, Ag⁺) in retarding senescence processes. The progress of senescence in watercress bunches (leaves attached to cut stems) and in detached leaves was estimated by measuring the rate of chlorophyll (Chl) loss, proteolysis and lipid oxidation. Evidence is presented showing that application of 11% CO₂ to watercress bunches in a flow-through system had a long-lasting effect on senescence, exhibited by highly efficient retardation of all the senescence processes tested. On the other hand, application of AVG (O.1 m M ) or Ag-(30 μ M ) to detached leaves affected Chl loss much more than prciteolysis. These results suggest that the senescence-retarding activity of CO₂ cannot be attributed solely to its action as an anli-ethylene agent and that not all senescence-associated processes are regulated by ethylene.     

Lipid biosynthesis by chloroplasts from olive tree leaves

In vitro incubation of isolated chloroplasts from young olive tree leaves ( Olea europaea L. cv. Marteño) in acetate-1-¹⁴C showed a high labelling of saturated fatty acids (palmitic + stearic) and, above all, of the monounsatured ones (oleic); the low biosynthetic rate of α-linolenic acid being noteworthy. These fatty acids are mainly found as free ones, or incorporated in mono-and diglyceride molecules. Phosphoand galactolipids, the most abundant acyl-lipid components of chloroplast lamellae, showed low incorporation rates. The fatty acid synthesis by isolated chloroplasts depends on exogenous CoA, ATP, NADPH and, especially, on added ACP (acyl carrier protein) preparation from Escherichia coli , whereas it was strongly inhibited by Triton X-100.
In vivo experiments with acetate-1-¹⁴C infiltration into young excised leaves showed a high labelling of chloroplast phospholipids, but a low ¹⁴C incorporation into galactolipids, a remarkable feature because these latter are main components of chloroplast lamellae. The high biosynthetic rate of α-linolenic acid is noteworthy and appears mainly linked to monogalactosyldiglycerides. Also the low incorporation of saturated fatty acids to neutral lipids is remarkable. The low in vitro synthesis of α-linolenic acid in comparison with that of the in vivo conditions, suggests the existence of a cooperation between chloroplasts and other parts of the cell to carry out the synthesis of this compound.     

Metabolism of radiolabelled galactolipids in senescent barley leaves

The metabolism of galactolipids in senescent primary leaves of barley was followed upon the incorporation of [1-¹⁴C]oleic acid during greening of etiolated shoots. In presenscent leaves the bulk of the label was present in apolar compounds of which 36% were galactolipids and 57% phospholipids. In segments induced to senesce in continouos darkness the loss of the predominant 18:3/18:3 molecular species of galactolipids was accompanied by the temporary accumulation of 18:3/18:3 phosphatidylcholine, a species which was almost absent in the presenescent leaves. A large proportion of radiocactivity lost in the galactolipids was eventually released as CO₂. Label was also transferred to sugars and other polar compounds. A pathway of galactolipid breakdown featuring the conversion of the diacylglycerol cores to phosphatidylcholine followed by the release of free fatty acids in glyoxisome-like microbodies and gluconeogenesis via β-oxidation and the glyoxylic acid cycle is proposed.     

Metabolism of cytidine and uridine in bean leaves

The metabolism of cytidine-2-¹⁴C and uridine-2-¹⁴C was studied in discs cut from leaflets of bean plants (Phaseolus vulgaris L.). Cytidine was degraded to carbon dioxide and incorporated into RNA at about the same rates as was uridine. Both nucleosides were converted into the same soluble nucleotides, principally uridine diphosphate glucose, suggesting that cytidine was rapidly deaminated to uridine and then metabolized along the same pathways. However, cytidine was converted to cytidine diphosphate and cytidine triphosphate more effectively than was uridine. Cytidine also was converted into cytidylic acid of RNA much more extensively and into RNA uridylic acid less extensively than was uridine. Azaserine, an antagonist of reactions involving glutamine (including the conversion of uridine triphosphate to cytidine triphosphate), inhibited the conversion of cytidine into RNA uridylic acid with less effect on its incorporation into cytidylic acid. On the other hand, it inhibited the conversion of orotic acid into RNA cytidylic acid much more than into uridylic acid. The results suggest that cytidine is in part metabolized by direct conversion to uridine and in part by conversion to cytidine triphosphate through reactions not involving uridine nucleotides.     

Characteristics of ethylene biosynthesis-inducing xylanase movement in tobacco leaves

¹²⁵I-Labeled ethylene biosynthesis-inducing xylanase (EIX) was used to study the movement of this protein in tobacco (Nicotiana tabacum) tissues. A biologically active ¹²⁵I-labeled EIX was obtained using chloramine-T as the oxidizing agent. Labeled EIX was detected in the far most edges of the leaf 5 min after it was applied to the petiole of a detached leaf. EIX was distributed uniformly throughout the leaf, including the mesophyll area within 5 to 15 min, after which there was only little change in the distribution of radioactivity in the leaf. ¹²⁵I-Labeled EIX was extracted from treated leaves, and EIX translocation in the leaf was blocked by preincubation of labeled EIX with anti-EIX antibodies, indicating that the intact peptide moves in the leaf. Injection of anti-EIX antibodies into the intercellular spaces of the leaf mesophyll prevented induction of necrosis by EIX, suggesting the mesophyll as the site of EIX action. EIX was translocated both to upper and lower parts of the plant when applied to a whole plant through the petiole of a cut leaf. Radioactivity was found in all leaves and in the stem, although some leaves accumulated much more EIX than others; EIX was not found in the roots. There was no difference between the accumulation pattern of EIX in fresh and ethylene-treated leaves or between sensitive (Xanthi) and insensitive (Hicks) tobacco cultivars. These data support the hypothesis that intact EIX protein is translocated to the leaf mesophyll, where it directly elicits plant defense responses.     

Changes in Nucleic-Acid Metabolism in Regreening leaves of Perilla

Regreening of senescent leaves of Perilla occurs after removalof all aerial parts of the plant except for one pair of leaves.After 3 weeks' regreening, chlorophyll had increased twofoldand RNA fourfold, compared with amounts present in the matureleaf. Polyacrylamide-gel electrophoresis of the rRNAs showedthat although at the time of decapitation chloroplast-rRNA synthesishad ceased, this was resumed by 12 h following decapitation.The results are discussed in relation to current knowledge ofthe control of ribosome metabolism.     

Metabolism of molecular species of sulpholipid in barley leaves

Molecular species of sulpholipid (diacylsulphoquinovosylglycerol) were separated and analysed after incubation of developing barley (Hordeum vulgare) leaves with either (1-¹⁴C]-acetate or [³⁵S]-sulphate. The major endogenous molecular species were the trienoic (42%) and the hexaenoic (39%). However, the combined anenoic, monoenoic and dienoic species, which only accounted for 5% of the mass, represented 80% of the labelled species with either precursor. In one experiment, 90% of this radioactivity was found in the dienoic species. The effect of light on the labelling of the molecular species was examined. Acetate is incorporated primarily into the fatty acids of sulpholipid. Transacylation appears to be important in the interconversion of the molecular species of sulpholipid.     

The role of ethylene in the senescence of oat leaves

The evolution of ethylene, both from the endogenous source and from added 1-aminocyclopropane-1-carboxylic acid (ACC), has been followed in close relationship with the senescent loss of chlorophyll from seedling oat leaves. In white light, where chlorophyll loss is slow, the ethylene evolution increases slowly at first, but when the loss of chlorophyll becomes more rapid, ethylene evolution accelerates. CoCl₂ inhibits this increase and correspondingly maintains the chlorophyll content, with an optimum concentration of 10 micromolar. The rapid rate of chlorophyll loss in the dark is slightly decreased by 3-aminoethoxyvinyl glycine (AVG), by cobalt, and slightly stimulated by ACC. The slower chlorophyll loss in white light, however, is almost completely inhibited by silver ions, greatly decreased by cobalt and by AVG, and strongly increased by ACC. Since the chlorophyll loss is accompanied by proteolysis, it represents true senescence. Chlorophyll loss in light is also strongly antagonized by CO₂, 1% CO₂ giving almost 50% chlorophyll maintenance in controls, while in the presence of added ACC or ethylene gas, the chlorophyll loss is 50% reversed by about 3% CO₂. The ethylene system in leaves is thus more sensitive to CO₂ than that in fruits. Indoleacetic acid also clearly decreases the effect of ACC. It is shown that kinetin, CO₂, Ag⁺, and indoleacetic acid, all of which oppose the effect of ethylene, nevertheless increase the evolution of ethylene by the leaves, and it is suggested that ethylene evolution may, in many instances, mean that its hormonal metabolism is being prevented.     

Iron toxicity and stress-induced ethylene production in rice leaves

The relationship among iron toxicity, bronzing symptom, and stress-induced ethylene production (SEP) was investigated in detached rice (Oryza sativa L.) leaves during the vegetative-ripening stage and in whole plants during the vegetative stage. When Fe²⁺ (200 mg L^-1) was applied to the detached leaf through a transpiration stream, SEP was higher in the first leaf than in the second and third leaves from the top and maximal around the panicle primordia initiation stage. The genotype difference in SEP was more pronounced in the second and third leaves than in the first leaf. Bronzing intensity increased as SEP increased; iron concentration increase during treatment in the tissue did not correlate with bronzing intensity or with SEP among the 16 genotypes tested. When the roots of an intact plant were exposed to 300 mg L^-1 of Fe²⁺ in culture solution little stress-induced ethylene was produced. By partially or totally derooting the plant, however, stress-induced ethylene was evoked, indicating that roots reduced the Fe²⁺ uptake so that little stress ethylene is produced in the intact plant. Leaf tissue tolerance for Fe²⁺ may contribute to genotype differences in iron toxicity tolerance of rice plants when roots are injured during transplanting or exposed to toxic substances in the soil.