Effects of Temporary Droughts on Photosynthesis of Alfalfa Plants

The effect of temporary droughts on photosynthesis, total conductanceto water vapour, intercellular CO² concentration, CO² compensationpoint, light-response curves, photorespiration, dark respiration,chlorophyll content, and ribulose 1,5-bisphosphate (RuBP) carboxylase(EC 4.1.1.39 [EC] ) activity has been examined in nodulated alfalfaplants (Medicago saliva cv. Aragón). Plants were subjectedto moderate (S1/RS1) or severe (S2/RS2) cycles of drought (drought/recovery).Photosynthetic light-response curves showed decreased light-saturatedphotosynthetic capacity and decreased apparent quantum yield.Upon rewatering, photosynthesis did not recover whereas conductancedid in moderately stressed plants. Calculated electron transportrate also declined in drought-stressed plants, but upon rewatering,moderately stressed plants exhibited a total recovery. Comparison of photosynthetic intercellular CO² response curvesin well-watered and stressed leaves led to the assertion thateffects in chloroplast metabolism contribute significantly tophotosynthetic inhibition. Although the validity of this entireline of research has been questioned by some recent studiesbecause the occurrence of heterogeneous stomatal closure wouldaffect these curves, in our case, the effect of water stresswas investigated in experimental systems where stomata had beenremoved. Measurements of in vitro RuBP carboxylase activityand protein content showed a strong decline during drought treatmentsand upon rewatering no recovery was observed. Therefore, ourresults suggest the major implication of non-stomatal factorsin the decline of photosynthesis in alfalfa plants under cyclicdrought conditions. Key words: Alfalfa, water deficits, photosynthesis, ribulose, 1,5-bisphosphate carboxylase activity, stomatal limitation     

Correlation of Activity and Amount of Ribulose 1,5-bisphosphate Carboxylase with Chloroplast Stroma Crystals in Water-Stressed Willow Leaves

Changes in the activity and amount of ribulose 1,5-bisphosphate(RuBP)carboxylase (E.C. 4.1.1.39 [EC] ) were studied in well-watered plantsof Salix ‘aquatica gigantea’ and in similar plantsduring three different water stress treatments and after rewatering.The chloroplast ultrastructure of these plants was examinedby electron microscopy. The amounts of crystallized proteinin the chloroplast stroma were assessed according to the areaof crystal structure seen in the thin sections. RuBP carboxylase activity decreased with decreasing leaf waterpotentials but recovered upon rewatering, except when leaveshad been exposed to severe water stress. The percentage of totalchloroplast area made up of crystal inclusions decreased withdecreasing leaf water potentials. After rewatering, the crystalseither disappeared or the amount decreased markedly. Both RuBPcarboxylase activity and the area of crystal inclusions increasedinitially with increased extractable RuBP carboxylase proteinbut decreased with further increases above 6700–7000 µgRuBP carboxylase protein mg^–1 chlorophyll. In well-wateredand water-stressed plants the activity of RuBP carboxylase,based on amount of chlorophyll, increased with an increasingamount of crystal inclusions in the chloroplast stroma. In rewateredplants no such correlation was observed, and the low percentageof crystal inclusions in the chloroplast area was independentof RuBP carboxylase activity. Key words: Chloroplast stroma crystals, ribulose 1,5-bisphosphate carboxylase, Salix, water stress     

The effects of irradiance and CO2 on the activity and activation of ribulose-1, 5-bisphosphate carboxylase/ oxygenase in the aquatic plant Spirodela polyrhiza

The activation of ribulose–1, 5-bisphosphate carb-oxylase/oxygenase(Rubisco, EC 4.1.1.39 [EC] ) from the floating angiosperm Spirodelapolyrhiza (L.) Schleid. (giant duckweed) grown at a photon irradianceof 200 or 400 mol photons m^–2 s^–1 was consistentlylow, in the range of 56–62%. Similarly low values wereobserved with four other emergent aquatic species growing underfull sun irradiance. Transference of Spirodela plants for short(minutes) or long (days) periods to the higher or lower irradianceincreased or decreased, respectively, the activation by onlyabout 15%. Activation was not greatly altered by exposure ofthe plants to full sun irradiance of >2000 mol photons m^–2s^–1 or CO₂ concentrations in air of 0 and 1170 mol mor^–1but darkness caused a slow decline to 20% activation. Transientoscillations were observed following a change in irradianceor CO₂ concentration indicating that Rubisco was responsiveto environmental perturbations. The low Rubisco activation wasnot due to the tight binding of inhibitors such as carboxyarabinitol-1-phosphate.It is concluded that a substantial proportion of the Rubiscoprotein in these naturally-occurring species may not be usedfor CO₂-fixation at any given moment. Key words: Rubisco     

The Large Subunit of Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase is Fragmented into 37-kDa and 16-kDa Polypeptides by Active Oxygen in the Lysates of Chloroplasts from Primary Leaves of Wheat

Lysates of chloroplasts isolated from wheat (Triticum aestivumL. cv. Aoba) leaves were incubated on ice (pH 5.7) for 0 to60 min in light (15 µmol quanta m^–2 s^–1),and degradation of the large subunit (LSU) of ribulose-l,5-bis-phosphatecarboxylase/oxygenase (Rubisco: EC 4.1.1.39 [EC] ) was analyzed byapplying immunoblotting with site-specific antibodies againstthe N-terminal, internal, and C-terminal amino acid sequencesof the LSU of wheat Rubisco. The most dominant product of thebreakdown of the LSU and that which was first to appear wasan apparent molecular mass of 37-kDa fragment containing theN-terminal region of the LSU. A 16-kDa fragment containing theC-terminal region of the LSU was concomitantly seen. This fragmentationof the LSU was inhibited in the presence of EDTA or 1,10-phenanthroline.The addition of active oxygen scavengers, catalase (for H₂O₂)and n-propyl gallate (for hydroxyl radical) to the lysates alsoinhibited the fragmentation. When the purified Rubisco fromwheat leaves was exposed to a hydroxyl radical-generating systemcomprising H₂O₂, FeSO₄ and ascorbic acid, the LSU was degradedin the same manner as observed in the chloroplast lysates. Theresults suggest that the large subunit of Rubisco was directlydegraded to the 37-kDa fragment containing the N-terminal regionand the 16-kDa fragment containing the C-terminal region ofthe LSU by active oxygen, probably the hydroxyl radical, generatedin the lysates of chloroplasts. (Received October 28, 1996; Accepted February 7, 1997)     

Carbon Partitioning in Mature Leaves of Pepper: Effects of Daylength

Grange, R. 1. 1985. Carbon partitioning in mature leaves ofpepper: effects of daylength.—J. exp. Bot. 36: 1749–1759. The partitioning of recently fixed carbon has been examinedin mature pepper leaves grown in 6, 10 or 14 h photoperiodsat different irradiances chosen to give similar radiation integralsand in a 6 h photoperiod at the lowest of these irradiances.The partitioning of carbon into export, starch, sugars and respirationwas followed over the photopenod and the subsequent night ina mature leaf. The maximum export rate during the day (approximately 18 µgC cm^–2 leaf h^–1) was not significantly differentamong the treatments. Net photosynthesis rate was directly relatedto irradiance; the proportion of net photosynthesis exportedduring the day was 33% in 6-h days and 57% in 14-h days. Leafstarch accumulation (as a proportion of net photosynthesis rate)increased slightly when plants were grown in 6-h days. The remobilization of starch and sugars at night allowed exportrates to remain similar over 24 h when plants were grown in10-h or 14-h photoperiods. Leaves grown in 6-h days showed nosignificant changes in export rate during the first few hoursof night but exhausted their starch reserves during the nightand export rates declined. Sucrose and hexose levels decreased at the onset of darkness,but did not fall below 40 µg cm^–2 in plants grownin 10-h or 14-h photoperiods; when this level was reached after3–4 h of darkness, starch breakdown began. In leaves grownin both 6-h treatments, sucrose levels fell below 40 µgcm^–2 when starch reserves were depleted during the nightand the export rate decreased concurrently. The results are discussed in relation to the control of exportand starch metabolism in the leaf. Key words: Pepper, partitioning, daylength     

Reactions of birch leaves to changes in light during early ontogeny: comparison between in vivo and in vitro techniques to measure carbon uptake

Trends in several photosynthetic parameters and their responseto changed growth light were followed for 15 d in leaves ofyoung birch saplings using a rapid-response gas exchange measuringequipment. These in vivo measurements were compared to biochemicalassays that were made from the same leaves after the gas exchangestudies. The measurements were made on leaves that were selectedprior to the study and were at that time of similar age. Forthe first 7 d the photosynthetic parameters were followed fromthe growth conditions of moderate light (200 µmol m^–2s^–1; referred to as controls later in the text). On day7 some of the saplings were transferred to grow either underhigh (450 µmol m^–2 s^–1; referred to as highlight plants) or low (75 µmol m^–2 s^–1; referredto as low light plants) light and the capability of the preselectedleaves for acclimation was followed for 6 d. For comparison,at the end of the experiment the measurements were made on bothcontrols and on young leaves that had developed under high andlow light. Generally the in vivo measured rate of CO₂ uptake (gross photosynthesis)both at 310 ppm CO₂ and 2000 ppm CO₂ corresponded very wellto the biochemically determined CO₂ fixation capacity in vitroafter rapid extraction (measured as the initial and total activityof Rubisco, respectively). However, if the flux of CO₂ intothe chloroplasts was limited by the closure of the stomata,as was the case of the high light plants, then the in vitromeasured Rubisco activity was greater than the in vivo measuredCO₂ uptake. V_max, calculated from the mesophyll conductanceat 1% O₂, exceeded the initial activity of Rubisco (assayedat saturating RuBP and CO₂) constantly by 60%. The catalyticactivity of Rubisco in birch leaves was overall very low, evenwhen calculated from the total activity of Rubisco (K_cat 0.63–1.18 s^–1), when compared to herbaceous C₃ species. Signs of light acclimation were not observed in most of thephotosynthetic parameters and in chloroplast structure whenmature birch leaves were subjected to changes in growth lightfor 6 d. However, the change of the growth light either to highor low light caused day-to-day fluctuations in most of the measuredphotosynthetic parameters and in the case of the high lightplants signs of photoinhibition and photodestruction were alsoobserved (decrease in the amount of chlorophyll and increasein chlorophyll a/b ratio). As a result of these fluctuationsthese plants achieved a new and lower steady-state conditionbetween the light and dark reactions, as judged from the molarratio of RuBP to Rubisco binding site. Key words: Acclimation, photosynthesis, light, Rubisco, birch     

Inhibition of photosynthesis in olive trees (Olea europaea L.) during water stress and rewatering

The effect of high levels of natural light on leaf photosynthesisin olive trees (Olea europaea L. var. Coratina), grown in potsoutdoors in the summer and subjected to water, stress, was studied.Net photosynthetic rates reached maximum values early in themorning in both control and stressed plants and subsequentlydeclined gradually. This inactivation of photosynthetic activitywas accompanied by changes in the fluorescence characteristicsof the upper intact leaf surface. The maximum fluorescence yield(Fp) and the ratio Fv/Fp decreased at midday especially in water-stressedplants, but the initial fluorescence (Fo) rose to a maximumvalue at midday and declined again in the afternoon. In controlplants the values of maximum fluorescence Fp and the ratio Fv/Fpincreased again in the afternoon and had recovered almost completelyby 8 p.m. as the leaf water potential recovered. In stressedplants this diurnal recovery was not complete, so that the photosyntheticrates and the ratio Fv/Fp declined gradually during the developmentof water stress. These results indicate that in olive treessubjected to severe water stress the non-stomatal componentof photosynthesis was affected and perhaps a light-dependentinactivation of the primary photochemistry associated with photosystemII (PSII) occurred. Four to five days after rewatering severelystressed plants, the predawn leaf water potential, net photosyntheticrates and chlorophyll fluorescence indices recovered only partially. Key words: Olea europaea, photosynthesis, water stress, chlorophyll a fluorescence, inhibition of photosynthesis     

Inactivation of Photosynthetic Oxygen Evolution and Concomitant Release of Three Polypeptides in the Photosystem II Particles of Spinach Chloroplasts

Photosystem II particles having an oxygen evolution activityas high as 300 µmol mg^–1 chlorophyll hr ^–1were prepared from spinach chloroplasts using Triton X-100.The oxygen evolution system in these particles was stable; 70%of the original activity remained after storage of the particlesat 0?C for 7 days. When the particles were treated at pH 9.3,the oxygen evolution was specifically inactivated and threepolypeptides having apparent molecular weights of 32,000. 24,000and 15,000 were simultaneously released. This observation suggeststhat these polypeptides are associated with the oxygen evolutionsystem of photosynthesis. ¹ Present address: Department of Chemistry, Faculty of Science,Toho University, Miyama 2-2-1, Funabashi, Chiba 274, Japan. (Received January 4, 1982; Accepted February 19, 1982)     

Decline of activity and quantity of ribulose bisphosphate carboxylase/oxygenase and net photosynthesis in ozone-treated potato foliage

The effect of ozone (O₃) on ribulose bisphosphate carboxylase/oxygenase (Rubisco) activity and quantity and net photosynthesis in greenhouse-grown Solanum tuberosum L. cv `Norland' foliage was studied in relation to oxidant-induced premature senescence. Plants, 26 days old, were exposed to 0.06 to 0.08 microliters per liter O₃ from 1000 to 1600 hours for 4 days in a controlled environment chamber. On day 5, plants were exposed to a 6-hour simulated inversion in which O₃ peaked at 0.12 microliters per liter. Net photosynthesis declined in response to O₃ but recovered to near control levels 3 days after the exposure ended. Rubisco activity and quantity in control potato foliage increased and then decreased during the 12-day interval of the study. In some experiments foliage studied was physiologically mature and Rubisco activity had peaked when O₃ exposure commenced. In those cases, O₃ accelerated the decline in Rubisco activity. When less mature foliage was treated with O₃, the leaves never achieved the maximal level of Rubisco activity observed in control foliage and also exhibited more rapid decline in initial and total activity. Percent activation of Rubisco (initial/total activity) was not affected significantly by treatment. Quantity of Rubisco decreased in concert with activity. The decrease in activities is most likely due to a decrease in available protein rather than a decrease in the percentage of Rubisco activated in vivo. The reduction in the quantity of Rubisco, an important foliar storage protein, could contribute to premature senescence associated with toxicity of this air pollutant.     

COMPARATIVE STUDIES OF PHOTOSYNTHETIC PROCESSES IN ORDINARY AND FULLY DEUTERATED ALGAE

The light-saturated growth rate of fully deuterated algae hasbeen found less than that of ordinary algae by a factor of threeto four. However, as compared to the net rate of photosynthesis,the Hill reaction rate indicates an unimpaired light reactionsystem. Analysis of cell extracts for amino acid content and¹⁴C-uptake studies indicate a decreased utilization of the productsof photosynthesis by deuterated algae, probably because of agenerally lowered protein metabolism. We conclude that in algaeD₂O does not have a pronounced effect on the light reactionin photosynthesis. ¹ Based on work performed under the auspices of the U. S. AtomicEnergy Commission. ² Resident Research Associate, 1962–64. ³Present address: University of Illinois, Department of Pharmacy,Chicago, Illinois.     

Control of Photosynthesis in Wheat by CO2, O2 and Light Intensity

The regulation of photosynthesis in wheat leaves under varyingO₂, CO₂, and light was studied by analyzing certain metabolitepools and enzyme activities. Under high light when the rateof photosynthesis was limited by low intercellular levels ofCO₂ (C₁) there was a high level of ribulose-1,5-bisphosphate(RuBP) (about 100 nmols per mg chlorophyll). As C, increased,there was a parallel decrease in the ratios of RuBP/3-phosphoglycerate(PGA) (from 0.18 to 0.08 under 21% O₂) and triose-phosphate/PGA(from 0.16 to 0.07 under 21% O₂). The results suggest carboxylationis limited at low C_i, and that there is high carboxylation andlimited assimilatory power at high C_i. As photosynthesis increasedwith increasing Jight intensity under atmospheric levels ofCO₂ the ratios of RuBP/PGA and triosephosphate/PGA remainednearly constant (near 0.12 to 0.13) suggesting there may bea coordinate regulation by light of the different phases ofthe cycle. There was increasing activation of ribulose 1,5-bisphosphatecarboxylase oxygenase (Rubisco) and fructose 1,6-bisphosphatase(FBPase) with increasing light intensity. The ways in whichthe light activation of the enzymes Rubisco and FBPase may regulatecarbon metabolism in the cycle are discussed. ¹ Current address: Biological Sciences Center, Desert ResearchInstitute, PO Box 60220, Reno, Nevada 89506, U.S.A. (Received March 24, 1987; Accepted June 23, 1987)     

Nodule Activity and Allocation of Photosynthate of Soybean during Recovery from Water Stress

Nodulated soybean plants (Glycine max [L.] Merr. cv Ransom) in a growth-chamber study were subjected to a leaf water potential (Ψ_w) of −2.0 megapascal during vegetative growth. Changes in nonstructural carbohydrate contents of leaves, stems, roots, and nodules, allocation of dry matter among plant parts, in situ specific nodule activity, and in situ canopy apparent photosynthetic rate were measured in stressed and nonstressed plants during a 7-day period following rewatering. Leaf and nodule Ψ_w also were determined. At the time of maximum stress, concentration of nonstructural carbohydrates had declined in leaves of stressed, relative to nonstressed, plants, and the concentration of nonstructural carbohydrates had increased in stems, roots, and nodules. Sucrose concentrations in roots and nodules of stressed plants were 1.5 and 3 times greater, respectively, than those of nonstressed plants. Within 12 hours after rewatering, leaf and nodule Ψ_w of stressed plants had returned to values of nonstressed plants. Canopy apparent photosynthesis and specific nodule activity of stressed plants recovered to levels for nonstressed plants within 2 days after rewatering. The elevated sucrose concentrations in roots and nodules of stressed plants also declined rapidly upon rehydration. The increase in sucrose concentration in nodules, as well as the increase of carbohydrates in roots and stems, during water stress and the rapid disappearance upon rewatering indicates that inhibition of carbohydrate utilization within the nodule may be associated with loss of nodule activity. Availability of carbohydrates within the nodules and from photosynthetic activity following rehydration of nodules may mediate the rate of recovery of N₂-fixation activity.     

Changes of photosynthetic activities of maize (<Emphasis Type="Italic">Zea mays</Emphasis> L.) seedlings in response to cadmium stress

Maize (Zea mays L.) seedlings were grown in nutrient solution culture containing 0, 5, and 20 μM cadmium (Cd) and the effects on various aspects of photosynthesis were investigated after 24, 48, 96 and 168 h of Cd treatments. Photosynthetic rate (P _N) decreased after 48 h of 20 μM Cd and 96 h of 5μM Cd addition, respectively. Chl a and total Chl content in leaves declined under 48 h of Cd exposure. Chl b content decreased on extending the period of Cd exposure to 96 h. The maximum quantum efficiency and potential photosynthetic capacity of PSII, indicated by F_v/F_m and F_v/F_o, respectively, were depressed after 96 h onset of Cd exposure. After 48 h of 5μM Cd and 24 h of 20 μM Cd treatments, the activities of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco, EC 4.1.39) and phosphoenolpyruvate carboxylase (PEPC, EC 4.1.1.31) in the leaves started to decrease, respectively. We found that the limitation of photosynthetic capacity in Cd stressed maize leaves was associated with Cd toxicity on the light and the dark stages. However, Cd stress initially reduced the activities of Rubisco and PEPC and subsequently affected the PSII electron transfer, suggesting that the Calvin cycle reactions in maize plants are the primary target of the Cd toxic effect rather than PSII.     

Turgor, Growth and Rheological Gradients of Wheat Roots Following Osmotic Stress

The growth rate of hydroponically grown wheat roots was reducedby mannitol solutions of various osmotic pressures. For example,following 24 h exposure to 0·96 MPa mannitol root elongationwas reduced from 1· mm h^–1 to 0·1 mm h^–1 Mature cell length was reduced from 290 µm in unstressedroots to 100 µm in 0·96 MPa mannitol. This indicatesa reduction in cell production rate from about 4 per h in theunstressed roots to 1 per h in the highest stress treatment. The growing zone extended over the apical 4·5 mm in unstressedroots but became shorter as growth ceased in the proximal regionsat higher levels of osmotic stress. The turgor pressure along the apical 5·0 mm of unstressedroots was between 0·5 and 0·6 MPa but declinedto 0·41 MPa over the next 50 mm. Following 24 h in 0·48(200 mol m^–3) or 0·72 MPa (300 mol m^–) mannitol,turgor along the apical 50 mm was indistinguishable from thatof unstressed roots but turgor declined more steeply in theregion 5·10 mm from the tip. At the highest level ofstress (0·96 MPa or 400 mol m^–3 mannitol) turgordeclined steeply within the apical 20 mm. Key words: Growth, turgor pressure, wall rheology, osmotic stress, osmotic adjustment     

Cardiovascular, ventilatory and total activity responses of brown trout to handling stress

Changes in total activity, heart and ventilation rates were observed in 2-year-old brown trout, following handling stress, using non-contact bioelectronic monitoring equipment. Experiments were carried out in laboratory conditions at water temperatures below 4° C, Transfer between tanks as well as 5 min restraint stress increased the total activity of fish for 24 to 48 h, after which it declined to near the pre-stress level. The transfer and struggle both elevated the heart rate for 3 to 4 days. Ventilation rate was elevated to a maximum of about 30% above the nominal level and recovered within 3 to 4 days. Both heart and ventilation rates were higher in feeding fish relative to fasting fish after stress and rates remained higher throughout a 7 day period of recovery. A diel rhythm of lower rates during the night appeared in both heart and ventilation rates within 3 to 4 days after handling stress.     

Photosynthetic acclimation to elevated CO2 in poplar grown in glasshouse cabinets or in open top chambers depends on duration of exposure

The effects of elevated CO₂ were studied on the photosyntheticgas exchange behaviour and leaf physiology of two contrastingpoplar (Populus) hybrids grown and treated in open top chambers(OTCs in Antwerp, Belgium) and in closed glasshouse cabinets(GHCs in Sussex, UK). The CO₂ concentrations used in the OTCswere ambient and ambient +350 µmol mol^–1 while inthe GHCs they were c. 360 µmol mol^–1 versus 719µmol mol^–1. Measurements of photosynthetic gas exchangewere made for euramerican and interamerican poplar hybrids incombination with measurements of dark respiration rate and Rubiscoactivity. Significant differences in the leaf anatomy and structure(leaf mass per area and chlorophyll content) were observed betweenthe leaves grown in the OTCs and those grown in the GHCs. ElevatedCO₂ stimulated net photosynthesis in the poplar hybrids after1 month in the GHCs and after 4 months in the OTCs, and therewas no evidence of downward acclimation (or down-regulation)of photosynthesis when the plants in the two treatments weremeasured in their growth CO₂ concentration. There was also noevidence of down-regulation of Rubisco activity and there wereeven examples of increases in Rubisco activity. Rubisco exerteda strong control over the light-saturated rate of photosynthesis,which was demonstrated by the close agreement between observednet photosynthetic rates and those that were predicted fromRubisco activities and Michaelis-Menten kinetics. After 17 monthsin elevated CO₂ in the OTCs there was a significant loss ofRubisco activity for one of the hybrid clones, i.e. Beaupr,but not for clone Robusta. The effect of the CO₂ measurementconcentration (i.e. the short-term treatment effect) on netphotosynthesis was always larger than the effect of the growthconcentration in both the OTCs or GHCs (i.e. the longterm growthCO₂ effect), with one exception. For the interamerican hybridBeaupr dark respiration rates in the OTCs were not significantlyaffected by the elevated CO₂ concentrations. The results suggestthat for rapidly growing tree species, such as poplars, thereis little evidence for downward acclimation of photosynthesiswhen plants are exposed to elevated CO₂ for up to 4 months;longer term exposure reveals loss of Rubisco activity. Key words: Elevated CO₂, Populus, Rubisco, photosynthesis, chlorophyll content     

Regulation of Protochlorophyll(ide) Levels in Dark-Grown Non-Dividing Euglena 3. Proplastid Structure during Loss and Regeneration of Protochlorophyll(ide)

Cells of Euglena gracilis Klebs var. bacillaris Cori growingin darkness on a complete medium have small undifferentiatedproplastids. On transfer to an incomplete (resting) medium indarkness, the cells cease division within 72 h. During thistime the proplastid expands and several prothylakoids and prolamellarbodies develop even though phototransformable protochlorophyll(ide)[PT-Pchl(ide)] is decreasing. As PT-Pchl(ide) decreases furtherand reaches a stable plateau after 4–5 more days in darkness,the proplastid structure becomes highly reduced. Forty minutesof light plus a one h dark period, or addition of glutamateor malate for 7 h does not change the proplastid structure significantlyeven though PT-Pchl(ide) returns to the level found in growingcells. Upon prolonged incubation in darkness after light treatment(72 h) an expanded proplastid containing prothylakoids, prolamellarbodies and membrane whorls with mitochondria in close associationis seen; most of the cellular paramylum is lost during thisperiod leaving cavities in the cytoplasm. Without light, prolongedincubation in darkness (72 h) with malate leads to accumulationof cellular paramylum but no change in proplastid structurewhile prolonged treatment with glutamate (72 h) allows the formationof a few prothylakoids but no prolamellar bodies. ¹Supported by Grants GM 14595 from the National Institutes ofHealth. ²Permanent address: Department of Microbiology, Tokyo MedicalCollege, 6-1-1 Shinjuku, Tokyo 160, Japan. ³Abraham and Etta Goodman Professor of Biology. (Received July 23, 1983; Accepted September 22, 1983)     

Regulation of Sulphate Transport in a Tropical Legume, Macroptilium atropurpureum, cv. Siratro

When young plants of Macroptilium atropurpureum, cv. Siratrowere deprived of external sulphate (-S plants) growth of shootsand roots continued at rates comparable to those in plants wellsupplied with sulphate (control) for 3 d and 5 d respectively.Dilution of internal sulphur therefore took place and redistributionof sulphur occurred between inorganic and organic forms andbetween roots and younger leaves. Even when S-deficiency limitedgrowth, plants contained 16% of their total sulphur as sulphate,but most of this was retained in old leaves and redistributedslowly to growing zones. The capacity for sulphate uptake increased in roots of –Splants very soon after they were deprived of external sulphate;within 24 h the absorption from 0.25 mol m^–3 SO₄^2–was more than five times that of control roots. Maximum increasedcapacity was reached after 2–3 d stress when the V_maxof system 1 was 1948 nmol h^–1g^–1root fr. wt. in–S plants and 337 nmol h^–1g^–1root fr. wt.in controls. The K^mfor system 1 did not change significantlywith S-stress being between 5–8 µM in both setsof plants. Absorption of L-cysteine was not stimulated by S-stress. There was a close, positive relationship between plant growthrate and the rate at which sulphate uptake capacity was enhancedby withholding sulphate from culture solutions. When –S plants were replaced in sulphate-containing solutiontheir capacity for SO₄^2– declined to the control levelwithin 24 h. Very marked repression of capacity was also foundwhen –S plants were treated with L-cysteine, but therewas no immediate effect with methionine. Roots of this species appear to have a very active system fordegrading L-cysteine to sulphate, 30% of the label in ³⁵S-cysteineabsorbed by roots was recovered in ³⁵SO₄^2– after 20 minor 2 h incubation. By contrast, roots had a very weak abilityto reduce sulphate. When part of the root system was in solution lacking sulphatethere was enhanced uptake of sulphate by other parts which themselveswere amply supplied with sulphate. This is seen as an exampleof compensatory absorption. The response to S-stress is specific and there were no positiveinteractions between S-stress and the absorption of phosphate,or P-stress and the uptake of sulphate. The results are discussed in relation to the close control ofsulphate uptake by internal sulphate concentration, redistributionof forms of sulphur during stress and mobility of sulphate inthe phloem. Key words: Kinetics, Amino-S, Sulpholipid, Repression;, Deficiency