Low temperature breakdown in apples

Low temperature breakdown in apples was increased by geraniol and a number of inhibitors of isoprenoid biosynthesis which were injected into the fruit after harvest. The addition of gibberellic acid reduced breakdown.     

梨果各部分(皮、肉、核)钙运转动态的研究初报

以梨品种“黄花”为试材,研究了不同时期于果实的不同部位引入45Ca后各个部位放射性比活及钙分配比率变化。结果表明:(1)在幼果期,引入果肉的钙可快速向果皮与果核扩散,且向果皮扩散的速率较果核快;引入果核的钙也能向果肉中迅速运转。(2)在膨大期,引入果肉的钙可以向果皮、果核和种子扩散,但速率较幼果期慢;引入果核的钙基本上不向果皮和果肉运转。(3)在成熟期,引入果肉中的钙可以迅速向果皮与果核中积累,引入果核的钙向皮肉的运转微弱。     

Abscisic acid and the development of storage breakdown in apples

(±)-ABA injected into the calyx of mature fruit increased the incidence of storage breakdown in Jonathan apples. The increase in disorder was greater when ABA was added early in the storage period and was proportional to the amount of ABA added. Most of the added ABA was converted into ‘bound’ ADA which remained at high concentrations throughout storage; however, the amount of ‘free’ ABA was also always higher than that in a control fruit. GA₃ decreased and geraniol increased the amount of ‘free’ ABA in the fruit on injection into the calyx. This could explain the ability of these compounds to respectively decrease and increase the incidence of breakdown.     

Sucrose mobilization in relation to essential oil biogenesis during palmarosa (<Emphasis Type="Italic">Cymbopogon martinii</Emphasis> Roxb. Wats. var.<Emphasis Type="Italic">motia</Emphasis>) inflorescence development

Palmarosa inflorescence with partially opened spikelets is biogenetically active to incorporate [U-¹⁴C]sucrose into essential oil. The percent distribution of¹⁴C-radioactivity incorporated into geranyl acetate was relatively higher as compared to that in geraniol, the major essential oil constituent of palmarosa. At the partially opened spikelet stage, more of the geraniol synthesized was acetylated to form geranyl acetate, suggesting that majority of the newly synthesized geraniol undergoes acetylation, thus producing more geranyl acetate.In vitro development of palmarosa inflorescence, fed with [U-¹⁴C]sucrose, resulted in a substantial reduction in percent label from geranyl acetate with a corresponding increase in free geraniol, thereby suggesting the role of an esterase in the production of geraniol from geranyl acetate. At time course measurement of¹⁴CO₂ incorporation into geraniol and geranyl acetate substantiated this observation. Soluble acid invertase was the major enzyme involved in the sucrose breakdown throughout the inflorescence development. The activities of cell wall bound acid invertase, alkaline invertase and sucrose synthase were relatively lower as compared to the soluble acid invertase. Sucrose to reducing sugars ratio decreased till fully opened spikelets stage, concomitant with increased acid invertase activity and higher metabolic activity. The phenomenon of essential oil biosynthesis has been discussed in relation to changes in these physiological parameters.     

Metabolism of added gibberellic acid in Malus pumilla in relation to cool storage breakdown

Gibberellic acid (GA₃) that was injected into the core of apples to reduce internal breakdown, was found to accumulate in the cortical tissue during cool storage only to a limited extent and never exceeded 0.5 % of the added dose. Limitations on the commercial use of GA₃ would appear to be associated with the low level of incorporation into susceptible tissue.     

Air volume measurement of 'Braeburn' apple fruit

The radial disposition of air in the flesh of fruit of Malus domestica Borkh., cv 'Braeburn' was investigated using a gravimetric technique based on Archimedes' principle. Intercellular air volume was measured by weighing a small tissue sample under water before and after vacuum infiltration to remove the air. In a separate procedure, the volume of the same sample was measured by recording the buoyant upthrust experienced by it when fully immersed in water. The method underestimates tissue air volume due to a slight invasion of the intercellular air spaces around the edges of the sample when it is immersed in water. To correct for this error, an adjustment factor was made based upon an analysis of a series of measurements of air volume in samples of different dimensions. In 'Braeburn' there is a gradient of declining air content from just beneath the skin to the centre of the fruit with a sharp discontinuity at the core line. Cell shape and cell packing were observed in the surface layers of freshly excised and stained flesh samples using a dissecting microscope coupled to a video camera and a PC running proprietary software. Tissue organization changed with distance below the skin. It is speculated that reduced internal gas movement, due to the tightly packed tissue of 'Braeburn' and to the potential diffusion barrier at the core line between the cortex and the pith, may increase susceptibility of the flesh to disorders associated with tissue browning and breakdown.     

Production of linalol and geraniol by hydrolytic breakdown of bound forms in disrupted tea shoots

Linalol and geraniol were produced in tea shoots, disrupted by mechanical means, by hydrolytic breakdown of non-volatile compounds. The formation of li     

The response of apples cv. Cox's Orange Pippin to different concentrations of oxygen in the storage atmosphere

The response of apples cv. Cox's Orange Pippin to storage in flowing streams of air and nitrogen mixed to generate atmospheres ranging from 0.5% to 2% oxygen was examined in two seasons. The benefits of reducing store oxygen concentrations below 1.25% were small but storage in 0.75% may be advantageous for Cox's Orange Pippin apples in seasons when flesh firmness is low at harvest. Ethanol-induced flesh breakdown was recorded in samples stored in 0.5% O₂ in one season and the risk of low temperature breakdown was increased in oxygen levels below 1.25%. Ethylene production was reduced by lowering the oxygen concentration.     

Metabolism of intracerebrally injected mevalonate in brain of suckling and young adult rats

We have investigated the in vivo metabolism via sterol and nonsterol pathways of intracerebrally injected mevalonate (MVA) in brains from suckling (10-day-old) and young adult (60-day-old) rats. Results of our study indicated that increasing the amounts of MVA injected increased MVA incorporation into all the lipid fractions examined. The incorporation of MVA into nonsaponiable lipids (NSF) and digitonin precipitable sterols (DPS) was similar in brains from adult and suckling rats. In brain tissue from both suckling and young adult rats the synthesis of dolichol from MVA varied with the amounts of MVA injected. Significant amounts of MVA were recovered in phosphorylated and free polyprenols (farnesol and geraniol) in brain tissue from rats of both ages. Also in both groups of animals, the amounts of MVA incorporated in phosphorylated and free farnesol were higher than the amounts recovered in either, phosphorylated or free geraniol. The amounts of MVA incorporated into the prenoic/fatty acid fraction by brain tissue from both suckling and young adult rats were less than 1% of the total MVA incorporated (nonsaponifiable and saponifiable lipids). Incorporation of MVA into the prenoic/fatty acid fraction by brain tissue was higher in suckling than in young adult rats. These data indicate that the brain tissue from suckling and young adult rats do not differ in their capacity to metabolize MVA into squalene and sterols and that in brain, metabolism of MVA by a shunt pathway is minimal. This suggests that in vivo regulation of cholesterol synthesis during brain development must occur at a step(s) in the sterol synthetic pathway prior to mevalonate, and that metabolism of mevalonate by shunt pathway did not play a role in the developmental regulation of brain sterol synthesis. The data also suggest that in both groups of animals the synthesis of squalene by synthetase may in part control brain sterol synthesis and the synthesis of dolichol is regulated by MVA concentration in the tissue.     

H-ras(val12) induces cytoplasmic but not nuclear events of the cell cycle in small Xenopus oocytes.

Microinjection of H-ras(val12) protein into fully grown Xenopus oocytes has been shown to induce meiotic maturation. In the present study, mRNA encoding the mutant ras protein was injected into both fully grown (stage 6) and growing (stage 4) oocytes. The mRNA induced nuclear breakdown in stage 6 oocytes, as expected. However, the mRNA induced neither nuclear breakdown nor maturation promoting factor when injected into stage 4 oocytes. Instead, the response in stage 4 oocytes included an activation pulse of calcium, cortical granule breakdown, elevation of the vitelline envelope, and abortive cleavage furrows, all of which are characteristics of the activation response in mature eggs. In addition, the injected mRNA led to increased rates of endogenous protein synthesis and the migration of subcortical organelles into the oocyte interior. These observations are discussed relative to the suggestion that oncogenic ras protein leads to an increase in both diacylglycerol and inositol trisphosphate, which then regulate the various cytoplasmic events described.     

Studies on l-glutamate in insect haemolymph.

ABSTRACT. l -Glutamate when injected into the haemolymph of Lucilia sericata larvae and adult male Locusta migratoria was rapidly removed by uptake mechanisms to other tissues in the insect. Data from Lucilia larvae indicate that following uptake glutamate is metabolized and the metabolites are secreted back into the haemolymph. l -Aspartate injected into the haemolymph of Lucilia larvae was also rapidly removed. When both l -aspartate and l -glutamate were injected simultaneously, the rate of glutamate removal was significantly reduced. It is concluded that glutamate and aspartate share the same uptake mechanisms. l -Leucine injected into Lucilia larvae and Locusta was removed at a significantly slower rate than glutamate or aspartate.     

The influence of harvest maturity, calcium concentration and storage conditions on the keeping quality of Spartan apples grown in England

Spartan apples from several commercial orchards were stored in three successive years. The principal physiological disorders that developed were scald and core rowning. These disorders were minimised by picking at the end of September and storing in either 2% O₂ or 2% CO₂+ 2% O₂ at 1.5°C. Fruit calcium concentrations were usually high enough to avoid flesh breakdown but could be increased without risk of skin damage by dipping in a 2% solution of calcium chloride. It was concluded that storage of Spartan for up to 9 months is possible provided that fruit calcium concentrations are adequate and that picking date and storage conditions are optimised.     

Metabolic regulation during early frog development: glycogenic flux in Xenopus oocytes, eggs, and embryos

32P-labeled glucose 6-phosphate and phosphoenolpyruvate were injected into oocytes, fertilized eggs, and early embryos of Xenopus laevis, and the 32P label was followed into glycolytic enzymes and acid-soluble metabolites. The kinetics of labeling of phosphoglucomutase and phosphoglyceromutase and the formation of specific metabolites were used to measure carbon flux through glycolytic intermediates in these cells. In full-grown stage VI oocytes, fertilized eggs, and cells of cleaving embryos, carbon metabolism is in the glycogenic direction. Glycolytic intermediates injected into these cells were metabolized into UDP-glucose and then presumably into glycogen. Carbon flow between phosphoenolpyruvate and glucose 6-phosphate does not utilize fructose 1,6-bisphosphatase; rather, it may depend largely on enzymes of the pentose phosphate pathway. Maturation and fertilization of the oocyte did not result in a change in the qualitative pattern of metabolites formed. Pyruvate kinase, although abundant in oocytes and embryos, is essentially inactive in these cells. Pyruvate kinase also appears to be inactive in small previtellogenic stage II oocytes; however, in these cells injected glycolytic intermediates were not metabolized to UDP-glucose.     

Seasonal Variations in Absorption and Metabolism of Carbon-14 Labelled Arginine in Intact Apple Stem Tissue

At intervals through the year a study was made of the absorption and metabolism of arginine-C 14(U) which had been perfused into the wood of apple stem internodes. Absorption was greater during the period May to September than at any other time of the year. The metabolic breakdown of arginine took place only after absorption but the products found varied widely with season. From the analyses it is concluded that arginine is metabolized by the Krebs-Henseleit cycle at all times of the year, in addition to which during the period from May to August there are other pathways in operation that result in a more extensive breakdown so that all the N in arginine becomes available for new growth.     

Relationships between ligninolytic activities of Lentinula spp. and biotransformation of pentachlorophenol in sterile soil

Ligninolytic activities in strains of Lentinula edodes were related to pentachlorophenol biotransformation in sterile soil and activities in L. lepideus. Strains of L. edodes secreting laccase and manganese peroxidase activities also metabolized pentachlorophenol (PCP) significantly ( P < 0.05). Strains of L. lepideus showed neither enzymic activities nor xenobiotic breakdown. Lentinula edodes strains inhibited by PCP at 5 mg 1^-1 in agar, tolerated 200 mg kg^-1 in soil. Strain LE2 metabolized more PCP in nitrogen-sufficient than nitrogen-limited culture: the reverse was observed with Phanerochaete chrysosporium BKM 1767. Relationships between ligninolytic activities and pentachlorophenol breakdown in L. edodes indicated a suitability for soil bioremediation treatments.     

Analysis of Light Transport Features in Stone Fruits Using Monte Carlo Simulation

The propagation of light in stone fruit tissue was modeled using the Monte Carlo (MC) method. Peaches were used as the representative model of stone fruits. The effects of the fruit core and the skin on light transport features in the peaches were assessed. It is suggested that the skin, flesh and core should be separately considered with different parameters to accurately simulate light propagation in intact stone fruit. The detection efficiency was evaluated by the percentage of effective photons and the detection sensitivity of the flesh tissue. The fruit skin decreases the detection efficiency, especially in the region close to the incident point. The choices of the source-detector distance, detection angle and source intensity were discussed. Accurate MC simulations may result in better insight into light propagation in stone fruit and aid in achieving the optimal fruit quality inspection without extensive experimental measurements.     

An esterase is involved in geraniol production during palmarosa inflorescence development

Total incorporation of exogenously administered [2-14C]acetate into essential oil of palmarosa (Cymbopogon martinii) was found to be relatively higher than that of either [U-14C]sucrose or [U-14C]glucose during inflorescence development. Among the major essential oil constituents, biogenesis of geranyl acetate was much higher than that of geraniol. Alkaline hydrolysis of [14C]labeled geranyl acetate revealed that the majority of the label incorporated into geranyl acetate was present in the geraniol moiety, indicating that only newly synthesized geraniol gets acetylated to form geranyl acetate. Geranyl acetate cleaving esterase (GAE) activity followed a similar pattern during both in vivo and in vitro inflorescence development, with maximum activity at immature inflorescence stages, suggesting the involvement of GAE in geraniol production during inflorescence development. Five esterase isozymes (Est-A to E) were detected in the enzymic fraction of palmarosa inflorescence and all showed GAE activity, with Est-B being significantly increased during inflorescence development. The role of GAE in geraniol production and improving the palmarosa oil quality is discussed.     

Biotransformation of C13-norisoprenoids and monoterpenes by a cell suspension culture of cv. Gamay (Vitis vinifera)

A cell suspension culture of cv. Gamay was studied for its ability to metabolize two different C₁₃-norisoprenoidic volatiles, β-ionone and dehydrovomifoliol, together with monoterpenes, geraniol and linalool, biogenetically common pathways sharing compounds. β-Ionone was totally metabolized leading to fourteen norisoprenoidic volatiles oxygenated mainly at carbons 3 or 4 of the cyclohexane ring or reduced at side chain. The biotransformation of dehydrovomifoliol was at a lesser extent, giving rise to oxygenated and reduced derivatives. The norisoprenoidic metabolites were present both under free and glycosylated forms. Geraniol and linalool were also metabolized, leading to several free and glycosylated compounds. S. Mathieu, J. Wirth contributed equally to the work and should be considered joint first authors. A short part of this paper was published at the proceedings of the 10th Weurman Flavour Research Symposium, Flavour Research at the Dawn of the Twenty-first Century, J.-L.Le Quere, P.-X.Etievant, Editors; Lavoisier,2003/Intercept Ltd, 2003.     

Monoterpene metabolism in cultures of Rosa species

Callus and suspension cultures of Rosa damascena maintained under ranges of conditions that were predicted on the basis of current hypotheses to favour secondary metabolism accumulated negligible amounts of monoterpenes. However, enzymes that converted mevalonate and isopentenyl pyrophosphate into geraniol and nerol could be extracted from the apparently inactive callus with activities up to 100-fold greater than those from the parent plant, and these activities were optimum in cultures that were slow growing or were in the stationary phase. Callus and suspension cultures both rapidly metabolized exogenously supplied monoterpenes via oxidative pathways. Thus nonaccumulation may be due to degradation of nascent products formed endogenously. Similar results were obtained from less detailed studies on R. gallica, R. canina and R. cv. Paul's Scarlet.     

Speciation and metabolism of selenium injected with 82Se-enriched selenite and selenate in rats

Selenate and selenite injected intravenously into rats were speciated by the HPLC–ICP MS method with use of an enriched stable isotope as the tracer. In dose–relation experiments, ⁸²Se-enriched selenate or selenite was injected intravenously into male Wistar rats of 8 weeks of age (three rats/group) at single doses of 10, 25, 50, 100 and 200 μg/kg body weight for the selenate group, and 2, 5, 10, 25 and 50 μg/kg body weight for the selenite group. The animals were sacrificed 1 or 24 h later, and the concentrations and distributions of ⁸²Se in the liver, kidneys, serum, and urine remaining in the bladder or 24-h urine were determined. In time-course experiments, ⁸²Se-enriched selenate and selenite were injected at doses of 50 and 10 μg/kg body weight, respectively, and the animals were sacrificed 5, 15, 30, 60 and 180 min later. It was suggested that selenate is directly taken up by the liver with an efficiency of approximately 1/2 compared with selenite, the latter being taken up by the liver after being metabolized to selenide in red blood cells. Although selenate and selenite were metabolized differently in the bloodstream, and also a part of only selenate was excreted directly into the urine, the ⁸²Se taken up by the liver was shown to be metabolized in a manner indistinguishable between selenate and selenite. ⁸²Se of selenite origin but not of selenate origin was suggested to undergo redox reaction in the bloodstream. These results suggest that although parenteral selenate is utilized less efficiently by the body, it is utilized in the liver in a similar manner to selenite much more safely.