Transport of Oxygen by the Blood of the Land Crab, Gecarcinus lateralis

Parameters relating to transport of oxygen were measured inthe pericardial blood and venous outflow from the first walkingleg of Gecarcinus lateralis. O₂-equilibrium curves of the hemocyaninof G. lateralis were found to be sigmoid and, at 27°C andpH 7.45, to have a half-saturation pressure of about 17 mm Hgoxygen. Average partial pressures of oxygen as measured by O₂-electrodewere 32 mm Hg in pericardial blood and 9 mm Hg in the venoussamples. Analysis of the O₂-content in corresponding samplesby the Van Slyke technique revealed an average of 2.17 volumes% O₂-capacity for whole blood, 1.45 volumes % for pericardialblood, and 0.61 volumes % for venous blood. Estimates basedon the Van Slyke analyses indicated an average pO₂ of 29 and14 mm Hg in pericardial and venous samples, respectively. Thesefigures agree fairly well with those obtained by means of O₂-electrodes.Of the oxygen carried to the tissues, about 94% is carried asoxyhemocyanin and about 6% is carried in physical solution.As the blood passes through the gills, the hemocyanin, on anaverage, becomes 80–85% saturated with oxygen and returnedfrom the tissues 18–45% saturated with oxygen. These resultsindicate that the blood of G. lateralis has a higher O₂-capacitythan the blood of most other decapod crustaceans for which similarinformation is available. In addition, the blood of G. lateralistransports more oxygen to the tissues per unit volume than doother crustacean bloods.     

The influence of dissolved oxygen concentration on phosphofructokinase and the glucose metabolism ofEscherichia coli K-12

The glucose metabolism and the response of phosphofructokinase activity to oxygen were investigated using glucose-limited chemostat cultures ofE. coli K-12. With a dilution rate of 0.2 hr^–1 and a glucose input concentration of 0.83 g/litre, 10 steady states were obtained ranging from 320 to 0 mm HgO₂. Dissolved oxygen reached zero level at a pO₂ of 25.8 mm Hg. The specific phosphofructokinase activity was constant above 28 mm Hg O₂ and increased linearly at lower pO₂ levels until it reached highest activity at 0 mm Hg O₂. Cell dry weight also started to decrease linearly from 28 to 5.9 mm Hg O₂, and fell sharply thereafter. Acid production rate did not start before pO₂ reached 25.6 mm Hg, increased progressively with an additional sharp increase below 5.9 mm Hg O₂. The main endproducts formed were acetic acid and ethanol with lactic acid appearing below 5.9 mm Hg O₂. The results suggest an effect of oxygen on phosphofructokinase synthesis rather than an ATP inhibition of the enzyme.This work was supported by a grant from the Australian Research Grant Commission.     

Thermal Dependence of Air Convection Requirement and Blood Gases in the Snake Coluber constrictor

In this report I discuss ventilatory and circulatory adjustmentsthat prov for increased O₂transport associated with increasedbody temperature in the snake Coluber constrictor. Also includedis the effect of temperature upon acid-base status. Minute ventilationincreases with rising body temperature but does not keep pacewith the increment in resting O₂ consumption. The decrease inair convection requirement (i.e., ventilation ÷ oxygenconsumption) causes lung pO₂ and arterial oxygen contentto falland lung pCO₂ to rise. With the rise in lung pCO₂, systemicarterial pCO₂ and H⁺; concentration increase while plasma bicarbonateconcentration does not change. The effect of temperature uponair convection requirement, arterial pCO₂, and pH are most pronouncedat body temperatures above about 27°C whereColuber behavesapproximately as an alphastat pH regulator. Despite the inverserelationship between temperature and lung pO₂, systemic arterialpO₂ is about 80 torr lower at 15°C than at 35°C. Thisdecline in arterial pO₂ as temperature falls is explained byleft shifting the oxygen dissociation curve in the presenceof aconstant right-to-left intracardiac shunt.     

Time-course of changes involved in the operation of the oxygen diffusion barrier in white lupin nodules

Nodulated white lupins (Lupinus albus L. cv. Multolupa) weresubject to either darkening for 12 h, followed by 24 h recoveryin light, or to 50% O₂ for 30 min. For each treatment, noduleswere harvested at intervals for analysis by light and electronmicroscopy and determination of glycoprotein content using EnzymeLinked Immunosorbent Assays (ELISA). This allowed for an analysisof the sequence of events causing an increase in intercellularspace occlusion within the inner cortex. The temporal sequencein response to darkening appears to be: (1) an initial rapidincrease in the detectable levels of intracellular glycoprotein,due to either a state change or de novo synthesis, (2) a concomitantincrease in the volume of thickened cell walls, causing a reductionof intercellular space volume and (3) after 1–3 h a releaseof glycoprotein into the intercellular space network of theinner cortex, accompanied (and possibly spread) by the continuedconstriction of the spaces due to cell wall and cell contentexpansion. The results for exposure to 50% O₂ showed a similar,but much more rapid, sequence of events, operating within 15–30min. The main difference between the two sequences was the lackof expansion of thickened cell walls with increased pO₂. Also,it was possible to detect glycoprotein within cell walls followingexposure to 50% O₂ but not following darkening. These observationsare discussed in relation to proposed mechanisms for the operationof a variable oxygen diffusion barrier in legume nodules. Key words: Oxygen diffusion resistance, glycoprotein, nodules, Lupinus albus     

活性氧在UV-B诱导的玉米幼苗叶片乙烯产生中的作用

 研究了活性氧在UV-B(280～320 nm)诱导的玉米(Zea mays)幼苗叶片乙烯合成中的作用。结果表明,UV-B促进了玉米幼苗活性氧和乙烯的产生;乙 烯合成抑制剂氨氧乙烯基甘氨酸 (AVG)和氨氧乙酸(AOA)能明显减弱UV-B对玉米幼苗乙烯产生的诱导作用,但对活性氧(ROS)的 产生没有明显影 响;ROS的清除剂不但能抑制UV-B诱导的 ROS的产生,而且还可以抑制UV_B诱导的乙烯的产生,但这种抑制作用可以被外源O₂^.-的供体所逆转。这 说明,乙烯的积累不能作为UV-B胁迫下ROS的诱导的因素,相反,ROS的积累则导致了乙烯的积累;因此,ROS可能参与了UV-B胁迫诱导的乙烯的产生 。质膜NADPH氧化酶的抑制剂二苯碘鎓(DPI)和H₂O₂的特异性清除剂过氧化氢酶（CAT）对UV-B胁迫诱导的乙烯积累 几乎没有影响, 这说明H₂O₂ 可能与UV-B诱导的玉米幼苗叶片乙烯的产生无关, 在UV-B诱导的玉米幼苗叶片乙烯的生物合成过程中O₂^.-起着很重要的作用,相关的O₂^.-不是由 NADPH氧化酶催化产生的。     

A microsensor for direct measurement of O2 partial pressure within plant tissues3

Widespread use of O₂ microsensors to measure O₂ partial pressure(pO₂) in plant tissues has been limited in part because of difficultyof construction and other technical obstacles. By modifyingpublished techniques, an O₂ microsensor was constructed thatcombined the advantages of Clark-type microsensors with lesscomplicated construction techniques. The specifications andsome performance characteristics of the microsensor are: tipdiameter 1–5 µm; sensitivity 7.5–25 pA kPa^–1;negligible stir-induced current; response time 540 ms. The microsensorcan be used in air or solution, and each sensor can be usedfor several experiments. The sensitivity of the microsensorwas unchanged during measurements over the physiological rangeof pO₂ in intact, growing maize (Zea mays L.) primary roots,and was thus unaffected by cellular fluids and turgor pressure.Use of the microsensor to compare pO₂ profiles in vermiculite-and solution-grown roots is described. The O₂ microsensor couldfind application in studies in which information on tissue pO₂is needed, but for which conventional O₂ probes are too large. Key words: Oxygen microsensor, Zea mays L., roots, oxygen partial pressure     

Participation of Peroxidase in the Metabolism of 3,4-Dihydroxyphenylalanine and Hydrogen Peroxide in Vacuoles of Vicia faba L. Mesophyll Cells

When leaves of Vicia faba were treated with H₂O₂ or visiblelight in the presence of methyl viologen (MV), the orange-redcompound dopachrome was formed transiently and melanin was accumulated.With the darkening of leaves, the level of 3,4-dihydroxyphenylalanine(DOPA) decreased and then recovered to the original level uponaddition of 1 mM H₂O₂. However, if leaves were incubated inthe presence of 10 mM H₂O₂, the level of DOPA decreased againafter the increase. The time course of the changes in levelsof DOPA observed during the accumulation of melanin as a resultof illumination in the presence of MV was very similar to thatobserved after the addition of 10 mM H₂O₂. Illumination of leavesin the absence of MV did not result in any accumulation of melanin,but the level of DOPA changed slightly. When isolated mesophyllcells were incubated in the dark, the level of DOPA decreased.Illumination of the cells stimulated this decrease. Tropolone,an inhibitor of phenol oxidase, did not inhibit and actuallystimulated the H₂O₂- and light-induced oxidation of DOPA andaccumulation of melanin in leaves. Tropolone also stimulatedthe decrease in the levels of DOPA both in the dark and in thelight in isolated mesophyll cells. These data suggest that aperoxidase-H₂O₂ system, and not phenol oxidase, participatesin the oxidation of DOPA. When DOPA was oxidized by a basicperoxidase isolated from V.faba leaves, an intermediate, whichwas perhaps dopaquinone and which was reducible by ascorbate,was formed. Based on the data, a discussion is presented ofthe physiological significance of the oxidation of DOPA by peroxidasein vacuoles. (Received March 4, 1991; Accepted May 21, 1991)     

A Mutant of Chlamydomonas reinhardtii with Reduced Rate of Photorespiration

Photorespiration rates under air-equilibrated conditions (0.04%CO₂ and 21% O₂) were measured in Chlamydomonas reinhardtii wild-type2137, a phosphoglycolate-phosphatase-deficient (pgp1) mutantand a suppressor double mutant (7FR2N) derived from the pgp1mutant. In both cells grown under 5% CO₂ and adapted air for24 h in the suppressor double mutant, the maximal rate of photorespiration(phosphoglycolate synthesis) was only about half of that ineither the wild type or the pgp1 mutant (18-7F) cells. In theprogeny, the reduced rate of photorespiration was accompaniedby increased photosynthetic affinity for inorganic carbon andthe capacity for growth under air whether accompanied by thepgp1 background or not. Tetrad analyses suggested that thesethree characteristics all resulted from a nuclear single-genemutation at a site unlinked to the pgp1 mutation. The decreasein photorespiration was, however, not due to an increase inthe CO₂/O₂ relative specificity of ribulose-1,5-bisphosphatecarboxylase/oxygenase of 7FR2N or of any other suppressor doublemutants tested. The relationship between the decrease in therate of photorespiration and the CO₂-concentrating mechanismis discussed. ³ Current address: Institute of Botany, Academy of Sciences,Patamdar Shosse, 40, Baku, 370073, Azerbaijan. ⁴ Current address: Department of Management and InformationScience, Jobu University, 270-1, Shinmachi, Tano, Gunma, 370-1393Japan.     

Sugar Accumulation in Barley and Rice Grown in Solutions with low Concentrations of Oxygen

Barley and rice, at the early tillering stage, were grown inaerated nutrient solutions (> 7 mg O₂ l^–1) and transferredto solutions of low O₂ concentrations (< 0.5 mg l ^–1). For barley, low O₂ concentrations during the first 5 days severelyinhibited growth of seminal roots had less effect on nodal roots,and did not reduce shoot growth. Longer exposure to low O₂ concentrationsreduced shoot as well as root growth. Sugar concentrations inroots and shoots increased within 7 h after transfer of plantsto low O₂ concentrations. After 5 days at low O₂ concentrationssugar concentrations were very high in fast growing nodal rootsand in shoots, as well as in the slower growing seminal roots. In rice, low O₂ concentrations increased sugar levels of rootsduring summer, but not during winter. In summer, the highersugar levels at low O₂ concentrations persisted throughout adiurnal cycle. In root apices, sugar concentrations were increasedby low O₂ concentrations, even though the experiment was donein winter and the bulk of the root system showed no differencein sugar levels. The data indicate that sugar accumulation, at low O₂ concentrations,is caused by reduced growth and also that even apices of rootsgrown at low O₂ concentrations have sufficient substrates forrespiration. Hordeum vulgare L, barley, Oryza sativa L, rice, sugar accumulation, oxygen concentration     

Proliferative activity and tumorigenic conversion: impact on cellular metabolism in 3-D culture

Oxygen consumption, glucose, lactate, andATP concentrations, as well as glucose and lactate turnover rates, havebeen studied in a three-dimensional carcinogenesis model of differentlytransformed rat embryo fibroblasts (spontaneously immortalized Rat1 andmyc-transfected M1, and the ras-transfected,tumorigenic descendants Rat1-T1 and MR1) to determine metabolicalterations that accompany tumorigenic conversion. Variousbioluminescence techniques, thymidine labeling, measurement ofPO₂ distributions withmicroelectrodes, and determination of cellular oxygen uptake rates(c_O2)have been applied. In the ras-transfected, tumorigenic spheroidtypes, the size dependencies of some of the measured parametersexhibited sharp breaks at diameters of ~830 µm for Rat1-T1 and~970 µm for MR1 spheroids, respectively, suggesting that somefundamental change in cell metabolism occurred at these characteristicdiameters (denoted as "metabolic switch").c_O2decreased and lactate concentration increased as functions of sizebelow the characteristic diameters. Concomitantly, glucose and lactateturnover rates decreased in MR1 spheroids and increased inRat1-T1. Spheroids larger than the characteristic diameters (exhibitingcell quiescence and lactate accumulation) showed an enhancement ofc_O2with size. Systematic variations in the ATP and glucose levels in theviable cell rim were observed for Rat1-T1 spheroids only. Proliferativeactivity, c_O2,and ATP levels in small, nontumorigenic Rat1 and M1aggregates did not differ systematically from those recorded in thelargest spheroids of the corresponding ras transfectants.Unexpectedly, respiratory activity was present not only in viable butalso in the morphologically disintegrated core regions of M1aggregates. Our data suggest that myc but not rastransfection exerts major impacts on cell metabolism. Moreover, somekind of switch has been detected that triggers profound readjustment oftumor cell metabolism when proliferative activity begins tostagnate, and that is likely to initiate some other, yetunidentified energy-consuming process.

     

Model for the Relationships betweenCO2-Concentrating Mechanism, CO2 Fixation, and Glycolate Synthesis during Photosynthesis in Chlamydomonas reinhardtii

We constructed a mathematical model for simulating the relationshipsof extracellular concentration of dissolved inorganic carbon(DIC), the rates of photosynthetic CO₂ fixation and glycolatesynthesis, and the concentrations of intrachloroplast CO₂ andO₂ in Chlamydomonas reinhardtii. When we compared the photosyntheticrates of I0W-CO₂ (air)-grown C. reinhardtii measured experimentallyand the rates simulated with the incubation conditions in themodel, the model was found to function well. The calculatedrates for glycolate synthesis also matched the measured ratesbetween 80 to 200 µM extracellular DIC, found in the presenceof 1 mM aminooxyacetate. The conformity of the calculated ratesto the measured ones of the glycolate synthesis encouraged usto estimate the O₂ concentration at the active site of ribulosebisphosphate carboxylase/oxygenase; the results were 0.36 and0.40 mM at 80 and 200 µM extracellular DIC, respectively.These high concentrations of O₂ were due to stimulation of photosyntheticCO₂ fixation and further O₂ evolution by a CO₂- concentratingmechanism in the low-CO₂-grown cells. These cells were calculatedto consume 43% of ATP formed photosynthetically for CO₂ concentrationat 200 µM extracellular DIC. The model modified to simulatethese relationships in high-CO₂ (3 to 5% CO₂)-grown C. reinhardtiipredicted O₂ concentration in chloroplasts to be 0.36 mM ina 1% CO₂ atmosphere. This high concentration of O₂ caused activeglycolate synthesis at the measured rate in the high-CO₂-growncells even in the presence of 1% CO₂. The comparisons of themeasured and simulated rates of photosynthesis in low- and high-CO₂-grownC. reinhardtii indicated that no matter how the CO₂ accumulatedin the chloroplasts, it increased the O₂ concentration in theorganelles, and consequently enhanced glycolate synthesis. ¹This paper is the twenty-first in a series on glycolate metabolismin Euglena gracilis. (Received March 11, 1987; Accepted August 17, 1987)     

Assessing the genetic relatedness of higher ozone sensitivity of modern wheat to its wild and cultivated progenitors/relatives

Modern wheat (Triticum aestivum L.) is one of the most ozone(O₃)-sensitive crops. However, little is known about its geneticbackground of O₃ sensitivity, which is fundamental for breedingO₃-resistant cultivars. Wild and cultivated species of winterwheat including donors of the A, B and D genomes of T. aestivumwere exposed to 100 ppb O₃ or charcoal-filtered air in opentop chambers for 21 d. Responses to O₃ were assessed by visibleO₃ injury, gas exchange, chlorophyll fluorescence, relativegrowth rate, and biomass accumulation. Ozone significantly decreasedlight-saturated net photosynthetic rate (–37%) and instantaneoustranspiration efficiency (–42%), but increased stomatalconductance (+11%) and intercellular CO₂ concentration (+11%).Elevated O₃ depressed ground fluorescence (–8%), maximumfluorescence (–26%), variable fluorescence (–31%),and maximum photochemical efficiency (–7%). Ozone alsodecreased relative growth rate and the allometric coefficient,which finally reduced total biomass accumulation (–54%),but to a greater extent in roots (–77%) than in the shoot(–44%). Winter wheat exhibited significant interspeciesvariation in the impacts of elevated O₃ on photosynthesis andgrowth. Primitive cultivated wheat demonstrated the highestrelative O₃ tolerance followed by modern wheat and wild wheatshowed the lowest. Among the genome donors of modern wheat,Aegilops tauschii (DD) behaved as the most O₃-sensitive followedby T. monococcum (AA) and Triticum turgidum ssp. durum (AABB)appeared to be the most O₃-tolerant. It was concluded that thehigher O₃ sensitivity of modern wheat was attributed to theincreased O₃ sensitivity of Aegilops tauschii (DD), but notto Triticum turgidum ssp. durum (AABB) during speciation. Key words: Biomass, Chl a fluorescence, genome, ozone sensitivity, relative growth rate, stomatal conductance, winter wheat Received 20 September 2007; Revised 30 November 2007 Accepted 16 January 2008     

EFFECTS OF TEMPERATURE ON CHRONIC HYPOXIA TOLERANCE IN THE NON-INDIGENOUS BROWN MUSSEL, PERNA PERNA (BIVALVIA: MYTILIDAE) FROM THE TEXAS GULF OF MEXICO

Effects of temperature (15°, 20° and 25°C), O₂ partialpressure (P_O2=0, 1, 2, 4, and 6 kPa), and individual size(12–79 mm shell length; SL) on survivorship of specimensof the non-indigenous, marine, brown mussel, Perna perna, fromTexas were investigated to assess its potential distributionin North America. Its hypoxia tolerance was temperature-dependent,survivorship being significantly extended at lower temperaturesunder all tested lethal P_O2. Incipient tolerated P_O2 was 4 and6 kPa at 15 and 20°C, respectively, with >50% mortalityoccurring at 25°C at all tested levels of hypoxia. P_O2 hadless of an effect on survival of hypoxia than temperature. At25°C, survivorship was not different over a P_O2 range of0–2 kPa and increased only at 4 and 6 kPa. Survivorshipwas size-dependent. Median survival times increased with increasingSL in anoxia and P_O2=1 kPa, but at 2, 4 and 6 kPa,smaller individuals survived longer than larger individuals.With tolerance levels similar to other estuarine bivalve species,P. perna should withstand hypoxia encountered in estuarine environments.Thus, its restriction to intertidal rocky shores may be dueto other parameters, particularly its relatively low temperaturetolerance. (Received 26 January 2004; accepted 31 March 2005)     

Simultaneous CO2- and 16O2/18O2-gas exchange and fluorescence measurements indicate differences in light energy dissipation between the wild type and the phytochrome-deficient aurea mutant of tomato during water stress

The CO₂-, H₂O- and ¹⁶O₂/¹⁸O₂ isotopic-gas exchange and the fluorescencequenching by attached leaves of the wild-type and of the phytochrome-deficienttomato aurea mutant was compared in relation to water stressand the photon fluence rate. The chlorophyll content of aurealeaves was reduced and the ultra-structure of the chloroplastswas altered. Nevertheless, the maximum rate of net CO₂ uptakein air by the yellow-green leaves of the aurea mutant was similarto that by the dark-green wild-type leaves. However, less O₂was produced by the leaves of the aurea mutant than by leavesof the wild-type. This result indicates a reduced rate of photosyntheticelectron flux in aurea mutant leaves. No difference in bothphotochemical and non-photochemical fluorescence quenching wasfound between wild-type and aurea mutant leaves. Water stresswas correlated with a reversible decrease in the rates of bothnet CO₂ uptake and transpiration by wild-type and aurea mutantleaves. The rate of gross ¹⁶O₂ evolution by both wild-type andaurea mutant leaves was fairly unaffected by water stress. Thisresult shows that in both wild-type and aurea leaves, the photochemicalprocesses are highly resistant to water stress. The rate ofgross ¹⁸O₂ uptake by wild-type leaves increased during waterstress when the photon fluence rate was high. Under the sameconditions, the rate of gross ¹⁸O₂ uptake by ^aurea mutant leavesremained unchanged. The physiological significane of this differencewith respect to the (presumed) importance of oxygen reductionin photoprotection is discussed. Key words: Water stress, gas exchange, fluorescence quenching, Lycopersicon esculentum, mutant (tomato, aurea), energy dissipation     

Changes of anabolic and energetic metabolism in the recovery of Rhodotorula gracilis from nitrogen starvation

We studied the changes occurring in the adenylate system andrelated metabolic parameters during the shift from rest to activegrowth, by feeding ammonium ions to N-starved Rhodotorula graciliscells. The addition of ammonium induces an early, rapid dropin ATP level and in energy charge, decrease in RQ, a gradualincrease in O₂ uptake and a rapid increase in the synthesesof amino acids, protein and RNA. CHI at a protein-synthesisblocking concentration also blocks the early decrease in ATPlevel. The data suggest that growth inhibition, due to N-starvationis not determined by the phosphorylation state of the adenylatesystem and that the observed behavior of the adenylate poolis a consequence of the onset of macromolecular synthesis. (Received June 1, 1977; )     

Endogenous light-on rhythm in respiration of a long-day duckweed, Lemna gibba G3 III. Relationship to frond production

Relationship between the C>2-uptake rhythm and frond productionin a long-day duckweed, Lemna gibba G3, was investigated. The rate of frond production and the amplitude of the rhythmwere dependent on light intensity. Photosynthetic inhibitors,CMU and DCMU, at concentrations effective in stopping frondproduction, abolished the O₂-uptake rhythm after a lag of 1day. In the presence of inhibitors of protein and RNA syntheses,ETH, CH and TU, at concentrations which brought about completeinhibition of frond production, the O₂-uptake rhythm disappeared.FUdR, an inhibitor of DNA synthesis, did not eliminate the rhythmalthough it suppressed frond production. This indicates a ratherindirect correlation between the rhythm and the rate of frondproduction which, in turn, is probably related to photosynthesis.The rhythm may be more directly correlated with the cell expansion. (Received July 27, 1971; )     

H2O2-mediated permeability II: importance of tyrosine phosphatase and kinase activity

We previously reportedthat exposure of endothelial cells to H₂O₂results in a loss of cell-cell apposition and increased endothelialsolute permeability. The purpose of this study was to determine howtyrosine phosphorylation and tyrosine phosphatases contribute tooxidant-mediated disorganization of endothelial cell junctions. Wefound that H₂O₂ caused a rapid decrease in total cellular phosphatase activity that facilitates a compensatory increase in cellular phosphotyrosine residues.H₂O₂ exposure also results in increasedendothelial monolayer permeability, which was attenuated by pp60, aninhibitor of src kinase. Inhibition of protein tyrosinephosphatase activity by phenylarsine oxide (PAO) demonstrated a similarpermeability profile compared with H₂O₂,suggesting that tyrosine phosphatase activity is important inmaintaining a normal endothelial solute barrier. Immunofluorescence shows that H₂O₂ exposure caused a loss ofpan-reactive cadherin and -catenin from cell junctions that was notblocked by the src kinase inhibitor PP1.H₂O₂ also caused -catenin to dissociate fromthe endothelial cytoskeleton, which was not prevented by PP1. Finally,we determined that PP1 did not prevent cadherin internalization. Thesedata suggest that oxidants like H₂O₂ produce biological effects through protein phosphotyrosine modifications bydecreasing total cellular phosphatase activity combined with increasedsrc kinase activity, resulting in increased endothelial solute permeability.

     

Normalizing Development of Cultured Triticum aestivum L. Embryos: I. LOW OXYGEN TENSIONS AND EXOGENOUS ABA

Wheat (Triticum aestivum L.) embryos form in dynamically-regulatedovular environments. Our objectives were to improve developmentof cultured immature wheat embryos by simulating, in vitro,abscisic acid (ABA) levels and O₂ tensions as found in wheatovules during zygotic embryogenesis. We characterized from intactwheat kernels embryo respiration, embryo morphology and embryoand endosperm + ABA levels at 13, 19 and 25 d post-anthesis(DPA). Young (13 DPA) embryos were then excised and culturedin vitro, where they were exposed to 0·2 or 2·Ommol m^–3 ±ABA and 2.·1, 2·5 or 7·4mol m^–3 (6, 7 and 21%, respectively) gaseous O₂. At 6and 12 d in culture, + ABA levels, embryo respiration and embryomorphology were characterized by treatment. Thirteen-day-oldembryos from two different plant populations differed by 17-foldin initial ABA content. However, this difference did not affectprecocious germination in vitro, nor did it affect the amountof exogenous ABA required to reduce precocious germination by40%. In this respect, embryos from both populations were equallysensitive to exogenous ABA. Cavity sap O₂ levels (2·1to 2·5 mol m^–3) were much more effective in preventingprecocious germination of cultured embryos than were cavitysap levels of ABA (0·2 to 2·0 mmol m^–3).The combination of physiological levels of both ABA and O₂ largelynormalized DW accumulation and embryo morphology without alteringendogenous + ABA levels. Residual respiration of cultured embryoswas higher than that of embryos grown in situ, and was not influencedby the exogenous O₂ and ABA treatments Key words: Abscisic acid, embryo development, oxygen tensions, respiration, wheat     

Regeneration of Ribulose 1,5-bisphosphate and Ribulose 1,5-bisphosphate carboxylase/oxygenase Activity Associated with Lack of Oxygen Inhibition of Photosynthesis at Low Temperature

The nature of the lack of oxygen inhibition of C₃-photosynthesisat low temperature was investigated in white clover (Trifoliumrepens L.). Detached leaves were brought to steady-state photosynthesisin air (34 Pa p(CO²), 21 kPa p(O₂), balance N₂) at temperaturesof 20°C and 8°C, respectively. Net photosynthesis, ribulose1,5-bisphosphate (RuBP) and ATP contents, and ribulose 1,5-bisphosphatecarboxylase/oxygenase (RuBPCO) activities were followed beforeand after changing to 2·0 kPa p(O₂). At 20°C, lowering p(O₂) increased net photosynthesis by37%. This increase corresponded closely with the increase expectedfrom the effect on the kinetic properties of RuBPCO. Conversely,at 8°C net photosynthesis rapidly decreased following adecrease in p(O₂) and then increased again reaching a steady-statelevel which was only 7% higher than at 21 kPa p(O₂). The steady-staterates of RuBP and associated ATP consumption were both estimatedto have decreased. ATP and RuBP contents decreased by 18% and33% respectively, immediately after the change in p(O₂) suggestingthat RuBP regeneration was reduced at low p(O₂) due to reducedphotophosphorylation. Subsequently, RuBP content increased again.Steady-state RuBP content at 2·0 kPa p(O₂) was 24% higherthan at 21 kPa p(O₂). RuBPCO activity decreased by 22%, indicatingcontrol of steady-state RuBP consumption by RuBPCO activity. It is suggested that lack of oxygen inhibition of photosynthesisat low temperature is due to decreased photophosphorylationat low temperature and low p(O₂). This may be due to assimilateaccumulation within the chloroplasts. Decreased photophosphorylationseems to decrease RuBP synthesis and RuBPCO activity, possiblydue to an acidification of the chloroplast stroma. Key words: Oxygen inhibition, photosynthesis, ribulose bisphosphate carboxylase/oxygenase     

Role of H2O2 and heme-containing O2 sensors in hypoxic regulation of tyrosine hydroxylase gene expression

In the currentstudy, we investigated links betweenO₂-regulatedH₂O₂formation and the hypoxic induction of mRNA for tyrosine hydroxylase(TH), the rate-limiting enzyme in catecholamine synthesis, inO₂-sensitive PC-12 cells. Duringexposure of PC-12 cells to 5% O₂,H₂O₂concentration decreased by 40% as measured with2',7'-dichlorofluorescein (DCF). Treatment withH₂O₂reduced TH mRNA during normoxia and prevented the induction of TH mRNAduring hypoxia. Treatment with catalase orN-(2-mercaptopropionyl)-glycine, areducing antioxidant agent that decreasesH₂O₂concentration, also induced TH mRNA. Deferoxamine (DF), an ironchelator, failed to affectH₂O₂formation but induced TH mRNA in normoxia and hypoxia.CoCl₂ led to a decrease inH₂O₂at 20 h of treatment but induced TH mRNA during normoxia and hypoxiabefore it affectedH₂O₂.In conclusion, TH gene expression correlates inversely withH₂O₂formation. DF and Co²⁺ seem toaffect TH gene expression in themechanism downstream from theH₂O₂formation rather than by interfering with theH₂O₂-generating activity of the O₂ sensor.