Changes in the Carbonic Anhydrase Activity and the Rate of Photosynthetic O2 Evolution during the Cell Cycle of Chlorella ellipsoidea C-27

Rhythmical changes in carbonic anhydrase activity(CA) and inphotosynthesis were observed during the cell cycle of Chlorellaellipsoidea C-27 synchronized at various concentrations of dissolvedCO₂ (dCO₂ with a regime of 16 h of light and 8 h of darkness.At a constant low concentration of dCO₂ (11 {diaeresis}M), intracellularCA activity showed obvious fluctuations with a peak at 8 h afterthe initiation of illumination, while extracellular CA activity,located on the cell surface, showed only minor fluctuationsalthough the activity was as high as the maximum activity ofintracellular CA. In contrast, obvious changes in the activitiesof intra- and extracellular CA activities were not observedat a high concentration of dCO₂ (520 {diaeresis}M). The ratioof photosynthetic activity at limiting versus saturating concentrationsof dCO₂, which is indicative of the affinity of cells for CO₂,showed clear rhythmical changes during the cell cycle and theratio was higher in low-CO₂ cells than in high-CO₂ cells. Thechanges in the ratio seemed to reflect the changes in CA activity. When the cells that had been synchronized under high CO₂ conditionswere transferred to low CO₂ conditions at any given stage inthe cell cycle, CA activity was induced in every case but thecapacity for induction of CA was greater in young cells thanin mature cells. This result suggests that the capacity of cellsto induce CA over the course of the cell cycle is closely relatedto endogenous aging of the cell. (Received August 29, 1988; Accepted December 28, 1988)     

Age-Dependent Changes in Levels of Ascorbic Acid and Chlorogenic Acid, and Activities of Peroxidase and Superoxide Dismutase in the Apoplast of Tobacco leaves: Mechanism of the Oxidation of Chlorogenic Acid in the Apoplast

In order to understand browning in tobacco plants during aging,age-dependent changes in the levels of ascorbic acid (AA) andchlorogenic acid (CGA) and its isomers were investigated inthe apoplast and the symplast of the leaves. Also activitiesof peroxidase (POX) and superoxide dismutase (SOD) were determined.AA decreased during aging until it was no longer detectablein the apoplast, while symplastic AA remained although the leveldecreased on aging. In contrast, levels of CGA and its isomersand activity of POX in the apoplast increased on aging, whilethose in the symplast remained nearly constant in mature andold leaves. The activity of SOD in the apoplast increased duringaging, while that in the symplast decreased. Oxidation of CGAby the apoplastic solution was observed in the absence of externallyadded H₂O₂ and the oxidation was inhibited by SOD and catalase.Brown components, which contained caffeic acid moieties, accumulatedin the apoplast on aging and the components produced O–₂and H₂O₂ by autooxidation. From these results, we conclude (i)that brown components are formed in the apoplast by the CGA/POXsystem, (ii) that the H₂O₂ required for the reaction can beprovided by the CGA/POX system itself and by autooxidation ofthe brown components, and (iii) that apoplastic SOD functionsto generate H₂O₂ from apoplastically formed O–₂. (Received February 8, 1999; Accepted May 7, 1999)     

Long-term effects of CO2 enrichment and temperature increase on the carbon balance of a temperate grass sward

Perennial ryegrass swards were grown in large containers ona soil, at two N fertilizer supplies and were exposed duringtwo years in highly ventilated plastic tunnels to elevated (700µl l^–1 [CO₂) or ambient atmospheric CO₂ concentrationat outdoor temperature and to a 3C increase in air temperaturein elevated CO₂. The irrigation was adjusted to obtain a soilwater deficit during summer. The daily net C assimilation wasincreased in elevated CO₂ by 29 and 36% at the low and highN supplies, respectively. Canopies grown in elevated CO₂ for14 to 27 months photosynthetized significantly less rapidly,in both elevated and normal CO₂ concentrations, than their counterpartsdeveloped in ambient CO₂ but the magnitude of this effect wassmall (–8% to –13%). Elevated CO₂ resulted in alarge increase in the fructan concentration in the pseudostemsand laminae (+46% and +189%, respectively). In elevated CO₂,the hexose and sucrose pool increased by 28% in the laminae,whereas it did not vary significantly in the pseudo-stems. A3C temperature increase in elevated CO₂ did not affect significantlythe average WSC concentrations in the pseudostems and laminae.The elevated CO₂ effects on the net C assimilation and on thenocturnal shoot respiration were greater in summer than in spring.On average, a 35% increase in the below-ground respiration wasmeasured in elevated CO₂. At the high N supply, a 3C increasein air temperature led to a decline in the below-ground respirationdue to a low soil moisture. The below-ground carbon storagewas increased by 32% and 96% in elevated CO₂ at the low andhigh N supplies, respectively, with no significant increasedtemperature effect. The role for the below-ground carbon storageof CO₂-induced changes in the root fraction of the grass andof temperature-induced changes in the moisture content of thesoil are discussed. Key words: Climate change, grassland, gas exchange, carbohydrates, carbon cycle     

Composition, Properties and Localisation of Pectins in Young and Mature Cells of the Mung Bean Hypocotyl

Two pectic fractions were extracted along the growth gradientof the mung bean hypocotyl. The first one (PF₁) contained pectinssoluble in boiling water and characterized by low uronic acids/cationsratio, high esterification degree and high neutral sugars/acidicsugars ratio. The second one (PF₂) contained pectins insolublein boiling water characterized by high uronic acids/cationsratio, low esterification degree, very low neutral sugar contentand a high selectivity for calcium. Water soluble pectins werepresent in all the wall area whereas the other ones were detectedmainly in the middle lamella. The PF₁/PF₂ ratio was high infast growing tissues but low in mature, slowly growing tissues.The development of the cell wall exchange properties along thegrowth gradient was related to the changes observed in the PF₁/PF₂balance. (Received July 31, 1985; Accepted January 20, 1986)     

Quantifying the uncontrolled CO2 dynamics of growth chambers

Inside growth chambers, experimenters and plant material canmodify the concentration of CO₂ by physiologically significantamounts. Mathematical equations are derived to account for chamberleak rate, net CO₂ exchange by plants, and respiration by experimenters.These equations can be used to predict the duration and intensityof expected changes in CO₂ concentration inside the growth chambers.Illustrations for two cases are given. Key words: Controlled environment, leak rate, CO₂     

Effects of Elevated Carbon Dioxide on Plant Biomass Production and Competition in a Simulated Neutral Grassland Community

Using open-top chambers, four prominent species (Lolium perenne,Cynosurus cristatus, Holcus lanatusandAgrostis capillaris) ofIrish neutral grasslands were grown at ambient and elevated(700 µmol mol^-1) atmospheric CO₂for a period of 8 months.The effects of interspecific competition on plant responsesto CO₂enrichment were investigated by growing the species ina four-species mixture. The results indicate that the speciesdiffer in their ability to respond to elevated CO₂. CO₂-enrichmenthad the largest effect on the biomass production ofH. lanatus,but substantial stimulations in biomass production were alsofound for the other three species. The CO₂-stimulation of biomassproduction forH. lanatuswas accompanied by increased tillering.In addition, reductions in specific leaf area were found forall species. Exposure to elevated CO₂increased the communitybiomass of the four-species mixture. This increase can be mainlyattributed to a significant increase in the biomass ofH. lanatusatelevated CO₂. No statistically-significant changes in speciescomposition of community biomass were found. However,H. lanatusdidincrease its share of community biomass at each of the harvests,with the other three species, mainlyL. perenne, suffering lossesin their shares at elevated CO₂. The results show that: (1)the species varied in their response to elevated CO₂; and (2)species composition in natural plant communities is likely tochange at elevated CO₂, but these changes may occur rather slowly.Much longer periods of exposure to elevated atmospheric CO₂maybe required to permit detection of significant changes in speciescomposition.Copyright 1998 Annals of Botany Company Carbon dioxide (CO₂) enrichment, competition, Lolium perenne,Cynosurus cristatus, Holcus lanatus, Agrostis capillaris, biomass, specific leaf area, tillering.     

Studies of Interaction between Chloroplast Coupling Factor 1 and Nucleotides by Circular Dichroism and Ultra-Violet Spectroscopies

When ADP, CDP, GDP, IDP or UDP was mixed with chloroplast couplingfactor 1 (CF₁) in the presence of MgCl₂, changes were inducedin the ultraviolet absorption spectrum as well as the circulardichroism spectrum. These changes were about 70% complete inone minute. Also, these two changes were similar in the concentrationcurves of nucleotides, the competition between ADP with CDP,the inhibition by PP₁, and the requirement for divalent cations.A minor difference was also noted in the requirement for divalentcations by some of the nucleotides. The order of the affinitiesof these nucleotides for CF₁ was: ADP>CDP>UDP>IDP>GDP.The UV spectral changes induced by these nucleotides are interpretedas shifts of the absorption spectra of bound nucleotides bysome 10 nm to longer wavelengths accompanied by decrease inabsorbance. In difference CD spectra, negative peaks were foundat about the same wavelengths of the absorption peaks of therespective nucleotides. Ca²⁺ was as effective as Mg²⁺ to these changes induced by ADPor GDP, but less effective than Mg²⁺ for those induced by CDP,UDP or IDP. In the presence of EDTA, the changes induced byADP were somewhat lower and those induced by CDP, UDP or IDPbecame almost zero. However, the UV absorbance change inducedby GDP was larger in the presence of EDTA than in the presenceof Mg²⁺ or Ca²⁺. (Received October 27, 1980; Accepted February 27, 1981)     

Relationships between the effect of O2 on energy metabolism and RNA synthesis in Rhodotorula gracilis

In the aerobic yeast Rhodotorula gracilis, a decrease in O₂availability, from saturating conditions (pO₂ = 100 mm Hg) topO₂ = 1 mm Hg, causes a decrease in the growth rate accompaniedby a fall in the accumulation rate of RNA and, to a lesser extent,of proteins. At pO₂ = 1, no relevant changes in the levels oftriphosphate nucleotides (ATP, GTP, CTP and UTP) are observedwith respect to the controls, while the ADP and AMP levels markedlyincrease. The uptake of labelled precursors and qualitative analysis ofRNA suggest that the decrease in the RNA accumulation rate atpO₂ = 1 is due to a decreased RNA synthesis rate. This paper examines the mechanism by which low availabilityof O₂ causes a decrease in the RNA synthesis rate even thoughtotal triphosphate nucleotide levels remain high. (Received December 28, 1977; )     

Quantity and Kinetic Properties of Ribulose 1,5-Bisphosphate Carboxylase in C3, C4, and C3-C4 Intermediate Species of Flaveria (Asteraceae)

The kinetic properties of ribulose 1,5-bisphosphate carboxylase(RuBPC) appear to have been modified during evolution of photosynthesisto adjust to changes in substrate availability. C₄ plants areconsidered to have a higher concentration of CO₂ available toRuBPC than C₃plants. In this study, the K_m(CO₂ and catalyticcapacity (k_cat) of RuBPC and the ratio of RuBPC protein to totalsoluble protein from several Flaveria species, including C₃,C₃-C₄ intermediate, and C₄ species, were determined. The C₃and intermediate species had similar K_m(CO₂) values while theC₄ species on average had higher K_m(CO₂) values. The mean ratioof K_cat/K_m for species of each group was similar, supportingthe hypothesis that changes in K_m and K_cat, are linked. Theallocation of total soluble protein to RuBPC was lowest in theC₄ Flaveria species, intermediate in the C₃-C₄ species, andhighest in the C₃ species. The results suggest that during evolutionof C₄ photosynthesis adjustments may occur in the quantity ofRuBPC prior to changes in its kinetic properties. (Received January 4, 1989; Accepted April 11, 1989)     

Stomatal Density and Index of Fossil Plants Track Atmospheric Carbon Dioxide in the Palaeozoic

It has been demonstrated that the leaves of a range of foresttree species have responded to the rising concentration of atmosphericCO₂ over the last 200 years by a decrease in both stomatal densityand stomatal index. This response has also been demonstratedexperimentally by growing plants under elevated CO₂ concentrations.Investigation of Quaternary fossil leaves has shown a correspondingstomatal response to changing CO₂ concentrations through a glacial-interglacialcycle, as revealed by ice core data. Tertiary leaves show asimilar pattern of stomatal density change, using palynologicalevidence of palaeo-temperature as a proxy measure of CO₂ concentration.The present work extends this approach into the Palaeozoic fossilplant record. The stomatal density and index of Early Devonian,Carboniferous and Early Permian plants has been investigated,to test for any relationship that they may show with the changesin atmospheric CO₂ concentration, derived from physical evidence,over that period. Observed changes in the stomatal data givesupport to the suggestion from physical evidence, that atmosphericCO₂ concentrations fell from an Early Devonian high of 10-12times its present value, to one comparable to that of the presentday by the end of the Carboniferous. These results suggest thatstomatal density of fossil leaves has potential value for assessingchanges in atmospheric CO₂ concentration through geologicaltime.Copyright 1995, 1999 Academic Press Aglaophyton major, Sawdonia ornata, Swillingtonia denticulata, Lebachia frondosa, Juncus effusus, Psilotum nudum, Araucaria heterophylla, stomatal density, stomatal index, Palaeozoic CO₂     

Phosphocreatine hydrolysis during submaximal exercise: the effect of FIO2

There isevidence that the concentration of the high-energy phosphatemetabolites may be altered during steady-state submaximal exerciseby the breathing of different fractions of inspiredO₂ (FI_O2). Whereasit has been suggested that these changes may be the result ofdifferences in time taken to achieve steady-state O₂ uptake(O₂) at differentFI_O2 values, we postulated that they are due to a direct effect ofO₂ tension. We used³¹P-magnetic resonancespectroscopy during constant-load, steady-state submaximal exercise todetermine 1) whether changes inhigh-energy phosphates do occur at the sameO₂ with variedFI_O2 and2) that these changes are not due todifferences in O₂onset kinetics. Six male subjects performed steady-state submaximal plantar flexion exercise [7.2 ± 0.6 (SE) W] for 10 minwhile lying supine in a 1.5-T clinical scanner. Magnetic resonancespectroscopy data were collected continuously for 2 min beforeexercise, 10 min during exercise, and 6 min during recovery. Subjectsperformed three different exercise bouts at constant load with theFI_O2 switched after 5 min ofthe 10-min exercise bout. The three exercise treatments were1)FI_O2 of 0.1 switched to0.21, 2)FI_O2 of 0.1 switched to1.00, and 3)FI_O2 of 1.00 switched to0.1. For all three treatments, theFI_O2 switch significantly (P  0.05) altered phosphocreatine:1) 55.5 ± 4.8 to 67.8 ± 4.9% (%rest); 2) 59.0 ± 4.3 to72.3 ± 5.1%; and 3) 72.6 ± 3.1 to 64.2 ± 3.4%, respectively. There were no significantdifferences in intracellular pH for the three treatments. The resultsdemonstrate that the differences in phosphocreatine concentration withvaried FI_O2 are not theresult of different O₂onset kinetics, as this was eliminated by the experimental design.These data also demonstrate that changes in intracellular oxygenation,at the same work intensity, result in significant changes in cell homeostasis and thereby suggest a role for metabolic control by O₂ even during submaximalexercise.

     

Quantification of hormone-induced atrophy of large myotubes from C2C12 and L6 cells: atrophy-inducible and atrophy-resistant C2C12 myotubes

Myofiber atrophy is the final outcome of muscle wasting induced by catabolic factors such as glucocorticoids and thyroid hormones. We set up an in vitro system to define the catabolic reaction based on myotube atrophy. Both mouse C₂C₁₂ and rat L6 cells were used. C₂C₁₂ myotube formation was improved by replacing horse serum with the serum substitute Ultroser G. A new method was developed to quantify size changes of large (0.5–1 mm) myotubes only, excluding remaining myoblasts and small myotubes. Dexamethasone reduced myotube size by 30% in L6 but not in C₂C₁₂ myotubes. Expression of the glucocorticoid receptor was twofold higher in L6 myotubes than in C₂C₁₂ myotubes. In both cell lines, 3,3',5-triiodo-L-thyronine (T₃) did not induce a significant size reduction. Expression of the major T₃ receptor (T₃R1) was higher in L6 myotubes. We investigated whether the changes in myotube size are related to changes in atrogin-1 expression, as this enzyme is thought to be a key factor in the initiation of muscle atrophy. Dexamethasone induced a twofold increase of atrogin-1 mRNA; again, only L6 myotubes were susceptible. Interestingly, atrogin-1 expression in Ultroser G-fused C₂C₁₂ myotubes was lower than that in horse serum-fused myotubes. Furthermore, dexamethasone treatment increased atrogin-1 expression only in horse serum-fused myotubes but not in Ultroser G-fused myotubes. Ultroser G-induced fusion may result in atrophy-resistant C₂C₁₂ myotubes. Therefore, C₂C₁₂ myotubes offer an ideal system in which to study skeletal muscle atrophy because, depending on differentiation conditions, C₂C₁₂ cells produce atrophy-inducible and atrophy-resistant myotubes. glucocorticoids; nuclear receptors; atrogin     

Effects of Temperature and CO2 Concentration on Induction of Carbonic Anhydrase and Changes in Efficiency of Photosynthesis in Chlorella vulgaris 11h

The increase in carbonic anhydrase (CA) activity and the decreasein apparent K_m(CO₂) for photosynthesis induced by reducing CO₂concentration during the growth of Chlorella vulgaris 11h cellswere followed under different temperatures. Both changes wereaccelerated by raising the temperature and reached an optimumat 32–37?C. When the CO₂ concentration was lowered from3 to 0.04%, the rate of photosynthetic O₂ evolution at limitingCO₂ concentrations increased and reached a stationary levelafter 3 h. Under such conditions, the concentration of CO₂ dissolvedin the algal suspension decreased logarithmically (t_1/2=10 min)and reached a concentration in equilibrium with 0.04% CO₂ inair after ca. 2 h. When high-CO₂ cells grown with 3% CO₂ in air were transferredto various lower CO₂ concentrations, CA activity and apparentK_m(CO₂) for photosynthesis changed depending on the CO₂ concentration.The CO₂ concentration which gives one-half the maximum valuefor K_m(CO₂) and one-half minimum value foi CA activities wasabout 0.5%. The inverse relationship observed for the changesin CA activity and the affinity for CO₂ in photosynthesis supportsthe theory that CA loweres the apparent K_m(CO₂) for photosynthesisin Chlorella vulgaris 11h. (Received August 27, 1984; Accepted February 8, 1985)     

Sperm extract and inositol 1,4,5-triphosphate induce cytosolic calcium rise in the central cell of Torenia fournieri

Microinjection of soluble sperm extract and Calcium Green-1 10 kDa-dextran conjugate (CG-1) into the mature central cell of Torenia fournieri induced a significant rise in cytosolic free calcium concentration ([Ca²⁺]_i). The rise reached a maximum at 20 min after injection and then steadily declined. Nevertheless, a relatively high level of [Ca²⁺]_i was maintained even 40 min after injection. Microinjection of sperm extract of maize into Torenia central cells, however, did not trigger any increase in [Ca²⁺]_i, suggesting the possibility of distinct triggers in different species. We also injected caged inositol 1,4,5-triphosphate (InsP₃) and caged cyclic ADP-ribose (cADPR) into Torenia central cells to compare the pattern of Ca²⁺ rise induced by the sperm extract. The results showed that [Ca²⁺]_i elevation triggered by the release of InsP₃ after photolysis appears much faster than that induced by sperm extract. The increase in [Ca²⁺]_i reached a maximum at 70-80 s and dropped to the resting level within 300 s after photolysis. Microinjection of cADPR, however, did not induce any changes in [Ca²⁺]_i. The results indicate that sperm extract might contain factors triggering the release of Ca²⁺ in the central cell.     

The effects of endothelin-1 on the cardiorespiratory physiology of the freshwater trout (Oncorhynchus mykiss) and the marine dogfish (Squalus acanthias)

The aim of the present study was to evaluate the effects of endothelin-1-elicited cardiovascular events on respiratory gas transfer in the freshwater rainbow trout (Oncorhynchus mykiss) and the marine dogfish (Squalus acanthias). In both species, endothelin-1 (666 pmol kg^-1) caused a rapid (within 4 min) reduction (ca. 30-50 mmHg) in arterial blood partial pressure of O₂. The effects of endothelin-1 on arterial blood partial pressure of CO₂ were not synchronised with the changes in O₂ partial pressure and the responses were markedly different in trout and dogfish. In trout, arterial CO₂ partial pressure was increased transiently by ~1.0 mmHg but the onset of the response was delayed and occurred 12 min after endothelin-1 injection. In contrast, CO₂ partial pressure remained more-or-less constant in dogfish after injection of endothelin-1 and was increased only slightly (~0.1 mmHg) after 60 min. Pre-treatment of trout with bovine carbonic anhydrase (5 mg ml^-1) eliminated the increase in CO₂ partial pressure that was normally observed after endothelin-1 injection. In both species, endothelin-1 injection caused a decrease in arterial blood pH that mirrored the changes in CO₂ partial pressure. Endothelin-1 injection was associated with transient (trout) or persistent (dogfish) hyperventilation as indicated by pronounced increases in breathing frequency and amplitude. In trout, arterial blood pressure remained constant or was decreased slightly and was accompanied by a transient increase in systemic resistance, and a temporary reduction in cardiac output. The decrease in cardiac output was caused solely by a reduction in cardiac frequency; cardiac stroke volume was unaffected. In dogfish, arterial blood pressure was lowered by ~10 mmHg at 6-10 min after endothelin-1 injection but then was rapidly restored to pre-injection levels. The decrease in arterial blood pressure reflected an increase in branchial vascular resistance (as determined using in situ perfused gill preparations) that was accompanied by simultaneous decreases in systemic resistance and cardiac output. Cardiac frequency and stroke volume were reduced by endothelin-1 injection and thus both variables contributed to the changes in cardiac output. We conclude that the net consequences of endothelin-1 on arterial blood gases result from the opposing effects of reduced gill functional surface area (caused by vasoconstriction) and an increase in blood residence time within the gill (caused by decreased cardiac output.     

Quenching Analysis of Chlorophyll Fluorescence by the Saturation Pulse Method: Particular Aspects Relating to the Study of Eukaryotic Algae and Cyanobacteria

The principles of chlorophyll fluorescence quenching analysisby the saturation pulse method are outlined with emphasis onparticular aspects encountered in the study of eukaryotic algaeand cyanobacteria. Major differences of these photosyntheticorganisms with respect to higher plant leaves, for which quenchinganalysis originally was developed, are very rapid inductionof O₂-dependent electron flow, close interaction between photosyntheticand respiratory metabolism, dark reduction of the plastoquinonepool and pronounced state transitions of energy distributionbetween the two photosystems. It is shown that the use of 25–50ms pulses of saturating light for determination of maximal fluorescenceyield is advantageous, in contrast to the 0.5–2 s pulsescommonly used with higher plants. The shorter pulses are lessinvasive with respect to the induction of energising electronflow which can induce non-photochemical quenching and statechanges. In particular, short saturation pulses are essentialto study true dark changes of fluorescence yield. As an example,the induction of pronounced quenching of maximal fluorescencein Chlamydomonas by dark-anaerobic incubation is demonstrated.Analysis of the rapid rise kinetics upon onset of saturatinglight reveals two major phases, O-I₁ and I₁-I₂, with distinctlydifferent properties. Arguments are put forward that an assessmentof maximal fluorescence yield with single turnover saturatingflashes is problematic, as there is a type of photochemicalquenching, the elimination of which during the I₁-I₂ phase requiresmultiple turnovers at photosystem II. Furthermore, the variablefluorescence represented by the two phases is affected differentlyby non-photochemical quenching. It is shown that dark-anaerobicquenching in Chlamydomonas as well as state 2 quenching in Synechocystisare correlated with a preferential suppression of the I₁-I₂phase. Experiments with Synechocystis are presented which demonstratethe potential of saturation pulse quenching analysis for thestudy of reversible state changes. The mutant M55 of Synechocystis6803 appears to be "locked" in state 1. ¹Present address: Lehrstuhl Botanik I, Mittlerer Dallenbergweg64, D-97082 Würzburg, Germany     

The Optimal Oxygen Equilibrium Curve: A Comparison Between Environmental Hypoxia and Anemia

SYNOPSIS. Internal hypoxia in vertebrates occurs during anemia,when blood oxygen (0₂) carrying capacity is reduced, or duringexposure to environmental hypoxia. In non-altitude adapted vertebrates,exposure to environmental hypoxia results in a change in bloodO₂ affinity which, in some cases is beneficial to tissue O₂delivery. In contrast, the elevation in blood O₂ carrying capacityobserved in almost all vertebrates is always beneficial to tissueO₂ delivery (assuming no large changes in blood viscosity) andmay be more important than changes in blood O₂ affinity in maintainingtissue O₂ delivery. Experimental anemia in vertebrates results in a decrease inblood O₂ affinity which is always beneficial to tissue O₂ delivery.The reduction in affinity is brought about by an increase inthe organic phosphate to hemoglobin ratio (NTP:Hb) within thered cell. In fish NTP:Hb decreases during environmental hypoxiabut increases during anemia indicating that NTP regulation isquite different between these treatments despite the similarityof these treatments at the tissue level.     

Salt-induced alterations of the fluorescence yield and of emission spectra in Chlorella pyrenoidosa

1. The addition of salts to the suspending medium induces a decreasein the yield of chlorophyll a fluorescence in normal and DCMU-poisonedintact algal cells of Chlorella pyrenoidosa. Potassium and sodiumacetate cause a pronounced lowering of the fluorescence at relativelylow concentrations (0.01–0.1 M). MgCl₂ and KCl cause asimilar lowering of fluorescence but at much higher concentrations(0.1–0.4 M). In contrast to sodium acetate, ammonium acetatedoes not cause any significant change in the fluorescence transient.
2. Unlike the case in isolated chloroplasts, MgCl₂ decreasestheratio of short wavelength (mainly system 2) to long wavelength(mainly system 1) emission bands in both DCMU poisoned and normalcells. Since these salt-induced changes do not appear to berelated to the redox reactions of photosynthesis, the saltsmight have caused a decrease in the mutual distance betweenthe two photosystems by changing the microstructure of the chloroplastsin vivo thereby facilitating the spillover of excitation energyfrom strongly fluorescent system 2 to weakly fluorescent system1.
3. The light induced turbidity changes in intact algal cells,asmeasured by the increase in optical density at 540 nm, isreducedin the presence of these salts. However, MgCl₂ producesthegreatest reduction while Na acetate the least, even thoughbothof these salts (at the concentrations used) cause largesuppressionof the fluorescence transient. Moreover, the lightinduced turbiditychanges were, essentially irreversible.
4. Ashigh concentrations of salts increase the osmotic potentialof the bathing medium, it seems that the osmotic changes aswell as the ionic changes in the intact algal cells are responsiblefor the fluorescence quenching and changes in the mode of excitationtransfer observed in this study. In the case of low concentrationsof salts (e.g., 0.1 M Na or K acetate) the effects are predominantlyionic, and in the case of very high concentrations of MgCl₂(0.4 M), the osmotic effects play a much larger role.

(Received July 30, 1973; )     

Factors Controlling Induction of Carbonic Anhydrase and Efficiency of Photosynthesis in Chlorella vulgaris llh Cells

When Chlorella vulgaris llh cells which had been grown in airenriched with 2–4% CO₂ (high-CO₂ cells) were bubbled withair containing ca. 400 ppm CO₂, illumination at an intensityas low as the light compensation point (350 lux) was sufficientto increase the photosynthetic rate under limiting CO₂ concentrations.The same treatment induced carbonic anhydrase (CA) activity.The induction of CA activity and increase in photosyntheticrate at limiting CO₂ concentrations were observed in the presenceof 10 µM DCMU which completely inhibits photosynthesis.These results indicate that photosynthetic electron transportis not involved in CA induction in Chlorella vulgaris llh cells.The parallelism between the changes in CA activity and the rateof photosynthesis under limiting CO₂ concentrations agree withthe previous conclusion that the transport of CO₂ from outsideto the site of CO₂ fixation is facilitated by CA and hence lowersthe apparent K_m(CO₂) for photosynthesis. (Received December 24, 1982; Accepted May 10, 1983)     

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)