Photosynthetic Electron Transport During Senescence of the Primary Leaves of Phaseolus vulgaris L.: I. NON-CYCLIC ELECTRON TRANSPORT

Coupled, non-cyclic electron transport was measured for chloroplastsisolated from the primary leaves of Phaseolus vulgaris. Preparationsfrom young, fully expanded leaves gave good rates of electrontransport, but the rates obtained decreased by approximately80% during leaf senescence. Higher rates of electron transportwere recorded for chloroplasts isolated from primary leaveswhich had regreened following removal of the remainder of theshoot. With preparations from leaves of all ages, photophosphorylationwas coupled to electron transport with a mean P/2e ratio ofapproximately 1.3. No evidence was obtained for inactivationof chloroplasts from older leaves during isolation or assay,and it is suggested that the decrease in rate of electron transportover the period of senescence, and its increase during regreening,were consequences of changes in the composition and physicalproperties of the thylakoid membrane which occur in vivo. Thedecrease in rate of non-cyclic electron transport may be importantin limiting the rate of photosynthesis in the senescing leaves.     

Physiological Changes in Phaseolus vulgaris in Response to Long-term Ozone Exposure

The effects of ozone on Phaseolus vulgaris cv. Lit were investigatedusing open-top chambers (OTCs) ventilated with charcoal andPurafil filtered air (CF treatments), ambient air (NF treatments)and ambient air to which low, medium or high concentrationsof ozone were added (NFL, NFM and NFH). Ozone additions of 8,16 and 23 nl l^–1 were made during phase 1 of the experiment(0–44 d after emergence, DAE), and additions of 15, 30and 47 nl l^–1 were made during phase 2 (45–99 DAE).Ozone was added to the chambers between 1100 and 1800 h GMT,for 3 or 4 consecutive days each week. The seasonal 7-h meanozone concentrations were 8, 21, 27, 33 and 38 nl l^–1in the CF, NF, NFL, NFM and NFH treatments, respectively. No visible symptoms of ozone injury or significant physiologicalchanges were detected in P. vulgaris during phase I of the experiment.In phase 2, the photosynthesis (Pn) and stomatal conductance(gs) of NFH-plants were inhibited by 73% and 86%, respectively,during ozone exposure, and recovered to pre-exposure valueson the following day. These observations were made prior tothe appearance, 60 DAE, of bronze lesions on the leaves of NFH-plants.The photosynthetic capacity and gs of NFH-leaves decreased asthe severity of ozone injury increased. Rates of weight lossfrom excised leaves also increased with increasing ozone injury.Microscopic investigations of the bronzed regions revealed extensivecellular breakdown, including tonoplast and chloroplast enveloperupture, and the aggregation of the cytoplasmic contents towardsone end of the cell. Severely damaged leaves abscised from the plants, resultingin premature canopy senescence in the NFM and NFH treatments.This, coupled with the lower photosynthetic capacity of existingleaves led to 25 % lower yield in the NFH than the NF treatment(P < 0.05). Phaseolus vulgaris, green bean, ozone, symptom development, photosynthesis, cell ultrastructure     

Purification and Characterization of an Aminopeptidase, the Enzyme-Hydrolyzing Alanine-p-nitroanilide (APAase), from Euonymus Leaves

An aminopeptidase, the enzyme-hydrolyzing alanine-p-nitroanilide(APAase), from leaves of Euonymus alatus f. ciliato-dentatuswas purified about 1,400-fold by a combination of ion-exchangeand gel filtration column chromatographies. Polyacrylamide gelelectrophoresis showed the purified APAase to be homogenous.The molecular weight of this APAase was estimated to be about100,000, and the optimum pH for its hydrolytic activity againstalanine-p-nitroanilide (APA) was 8.6–9.0. APAase hydrolyzedalanine-ß-naphthylamide (alanine-NA), glycine-NA,lysine-NA and arginine-NA. It was inhibited slightly by p-chloromercuribenzoate(PCMB) and iodoacetic acid and was not activated by thiol reagents.Therefore, a sulfhydryl group could not be present at the activesite of APAase. APAase was inhibited strongly by 1,10-phenanthroline,but was unaffected by EDTA. Of the metal ions tested, Hg²⁺,Zn²⁺ and Mn²⁺ strongly inhibited its activity, and Ca²⁺ stimulatedit to some extent. (Received November 15, 1984; Accepted March 12, 1985)     

Purification and Characterization of an Aminopeptidase, LPAase 2, from Euonymus Leaves

An aminopeptidase, LPAase 2, from the leaves of Euonymus alatusf. ciliato-dentatus was purified about 240-fold by a combinationof DEAE-cellulose and Sephadex G-100 column chromatographies.The molecular weight of LPAase 2 was estimated to be about 62,000,and the optimum pH for the hydrolytic activity against leucinep-nitroanilide(LPA) was 7.6. LPAase 2 hydrolyzed LPA, leucine-rß-naphthylamide(leucine-NA), phenylalanine-NA and tyrosine-NA. It was inhibitedstrongly by p-chloromercuribenzoate (PCMB), iodoacetic acidand heavy metal ions, but was not affected by thiol compoundsand metal-chelating reagents. Therefore, a sulfhydryl groupcould be involved in the active site of LPAase 2. None of themetal ions tested promoted LPAase 2 activity. The propertiesof LPAase 2 were compared with those of aminopeptidases reportedfor other plants. (Received November 24, 1983; Accepted April 16, 1984)     

Purification and Characterization of Thiol Proteinase as a Nitrate Reductase-Inactivating Factor from Leaves of Hordeum distichum L.

A thiol proteinase was purified 6,400-fold from leaves of Hordeumdistichum L. by a sequence of ammonium sulfate fractionation,gel filtration, ion exchange chromatography, hydrophobic chromatographyand chromatofocusing. This enzyme also had nitrate reductase(NR)-inactivating activity, which was associated with proteolyticactivity in almost constant proportions during the purificationprocedures. Its molecular weight was estimated as 74,000 bygel filtration, and it had an isoelectric point of 4.05 andan apparent K_m of 0.83 mg ml^–1 for azocasein. The respectiveoptimum pH for proteolytic and NR-inactivating activities were6.0 and 7.0. On electrophoresis, the proteinase gave a majorband that coincided with both activities; it also produced afaint band associated with no activity. Our purified thiol proteinase inactivated FMNH₂-NR and MVH-NRas well as NADH-NR, but it had only a slight effect on NADHcytochrome c reductase activity. This enzyme also inactivatedglutamine synthetase. (Received September 16, 1983; Accepted January 26, 1984)     

Action of Thiol Proteinase on Nitrate Reductase in Leaves of Hordeum distichum L.

Nitrate reductase (NR) from the leaves of Hordeum distichumwas very susceptible to inactivation by barley leaf thiol proteinase,trypsin, and papain. A cytochrome c reductase species with amolecular weight of about 40,000 was derived from the NR complexby the proteolytic actions. The barley proteinase seemed toattack the Mo⁺-containing component of NR, just like trypsinand papain. It showed a preference for the alanine and tryptophanesters among the carbobenzoxyamino acid-nitrophenylesters tested. In vivo NR activity in the presence of leupeptin was fairlyhigher than that in its absence. Leupeptin also protected NRfrom its cleavage to small cytochrome c reductase species, suggestingthat the barley proteinase may play a role in the in vivo changein NR activity. (Received May 21, 1984; Accepted September 10, 1984)     

Inverse Correlation of Thiol Proteinase with Nitrate Reductase Activities in Barley Leaves

Experiments conducted to determine the effects of leupeptin,a specific inhibitor of thiol proteinase, on extractable nitratereductase (NR) activity in leaves of Hordeum distichum duringdarkness revealed that leupeptin (0.01 mg.ml^–1) appliedto detached leaves significantly reduced the loss of NR activity.At the same time it also reduced the formation of small cytochromec reductase species, which is a degradation product of NR complex,Upon nitrate induction, extractable NR activity increased butthe content of thiol proteinase decreased. This inverse correlationwas also observed upon transfer of nitrate-grown barley seedlingsto nitrate-free nutrient solution. Furthermore, cycloheximide(0.1 mg.ml^–1) treatment of barley seedlings reduced thecontent of thiol proteinase and retarded the loss of NR activityunder noninducing conditions. These results suggest that invivo changes in NR content in leaves of Hordeum distichum arethe result of proteolysis by an endogenous thiol proteinase. (Received May 16, 1985; Accepted July 22, 1985)     

Observations on the Senescence of a Mutant Non-yellowing Genotype of Phaseolus vulgaris L.

A non-yellowing mutant of Phaseolus vulgaris L. was used toinvestigate factors involved in chlorophyll breakdown duringfoliar senescence. The mutant showed physiological changes similarto those of the normal yellowing type during senescence exceptthat leaf chlorophyll did not decline. Transmission electronmicroscope studies did not reveal appreciable differences inchloroplast ultrastructure between the two genotypes, suggestingthat chloroplast membrane integrity was not the factor preventingchlorophyll degradation in the mutant. However, the lack ofplastoglobuli in senescent mutant chloroplasts suggested thatthe lipid environment may be different from that of senescentnormal chloroplasts. Banding patterns of total soluble protein,resolved by sodium dodecyl sulphate-poly aery lamide gel electrophoresisshowed few, if any, differences between mature non-senescentnormal and mutant leaves; however, bands at 14 kD and 58 kDdiminished in senescent normal leaves, but remained in senescentmutant non-yellowing leaves. Key words: Non-yellowing mutant, Phaseolus vulgaris, senescence, chlorophyll degradation     

Hormone Interaction in Apical Dominance in Phaseolus vulgaris L.

Gibberellic acid (GA₃), kinetin, and indole-3yl-acetic acid(IAA) were applied to roots of Phaseolus vulgaris under twodifferent light intensities and when either young or old leaveswere removed In all cases GA₃, promoted stem and lateral growth,especially when light intensity was reduced. Promotion by GA₃,of stem growth under reduced light was reduced if IAA and kinetinwere present; promotion of lateral growth under reduced lightwas reduced if IAA was added and eliminated if kinetin or kinetinplus IAA were added to GA₃. Removal of young and mature leavesreduced main stem growth; removal of young leaves promoted,and of mature leaves reduced, lateral shoot growth. We suggestthat shoot growth and apical dominance are governed by the balanceof hormones present in elongating internodes. There may be twoways of modifying this balance; firstly by altering light, temperature,or nutrients, or by applying hormones generally to the plant.Secondly, local modifications can be made by removing apicesor young leaves, or applying hormones in lanolin to specificareas. Knowledge of both the general and local conditions maybe necessary for a complete understanding of apical dominance.     

Diurnal Geotropic responses of the Primary Leaves of Phaseolus vulgaris

When seedlings of Phaseolus vulgaris with leaves in the daytimeposition (almost horizontal to the ground) were turned upside-downduring the light period, their leaves moved upward away fromthe ground after about 20 min and ceased moving after about1.5 h. But when seedlings with leaves in the night time position(directed downward) were turned upside-down, their leaves moveddownward toward the ground after about 30 min and stopped movingabout 2 h later. Thus, Phaseolus primary leaves showed positiveor negative geotropic responses that correspohded to the darkor light period. This geotropic response of primary leaves was accompanied bythe redistribution of K⁺, Cl^– and NO₃- in the laminarpulvinus. These facts suggest that the circadian endogenousclock that is assumed to exist in Phaseolus vulgaris has atleast two regulation echanisms; one which measures time andanother which determines leaf postition in relation to gravityby changing the ion distribution in the pulvinus (Received February 12, 1983; Accepted May 17, 1983)     

Cytokinin Effects on Leaf Architecture in Phaseolus vulgaris L.

Treatment of expanding primary leaves of bean plants (Phaseolnsvulgaris L. cv. Limburgse vroege) with benzyladenine (BA) orkinetin at 0.5 mM for five consecutive days resulted in thickerleaves showing a significant decrease in intercellular air spacevolume. Compared with control plants, exposed mesophyll cellsurface area was lower per unit tissue volume, but unchangedwhen expressed per unit leaf surface area. Stomata of treatedplants were not fully closed in the dark and they did not openas wide as controls in the middle of the light period, suggestingthat the treatment resulted in impaired stomatal action. Allthe effects mentioned were more pronounced after treatment withBA, compared to kinetin. In spite of their magnitude, the observedchanges in leaf structure and function did not seem to havean important effect on total leaf diffusion resistance to carbondioxide during the course of the light period. Key words: Cytokinins, Leaf architecture     

Phenylpropanoid defence responses in transgenic Lotus corniculatus: II. Modelling plant defence responses in transgenic root cultures using thiol and carbohydrate elicitors

Transformed root cultures of Lotus corniculatus L. cv. Leo weretreated with a range of thiol and carbohydrate elicitors. Boththiol reagents and fungal carbohydrate preparations resultedin an increase in the activity of phenylalanine ammonia lyase(PAL) in a concentration-dependent manner. One representativethiol elicitor, glutathione (GSH), and one fungal elicitor,derived from Rhynchosporium orthosporum autoclaved cell walls(Ro), were analysed in more detail. Both elicitors induced thetransient accumulation of vestitol, an isoflavan phytoalexin,in tissue and in culture medium. Treatment of Lotus root cultureswith the Ro elicitor resulted in a more rapid initial accumulationof this end product when compared with GSH, however, sativan(the 2–methoxy ester of vestitol) previously reportedto co-accumulate in Lotus leaves was only detected followingelicitation with high concentrations of GSH. Ro and GSH elicitorsalso induced the accumulation of a number of other phenylpropanoidcompounds putatively identified as chalcones. The addition ofthiol and carbohydrate elicitors to Lotus root cultures alsoresulted in characteristic changes in root morphology. Glutathione,in particular, resulted in the inhibition of root growth dueto differential damage of meristem cells. Key words: Lotus corniculatus, hairy roots, elicitors, phytoalexins.     

Stomatal responses to changing irradiance in Phaseolus vulgaris L.

The effects of air temperature (T_o), leaf-air vapour pressuredifferences [VPD) and water deficit on stomatal responses tochanging irradiance were studied in Phaseolus vulgaris L. Responseswere approximately sigmoidal, with rates of closure being fasterthan the rates of opening. The mean half-time for closure was5.4 min and for the opening 9.2 min. Under water deficit, bothstomatal opening and closing were faster than in well-wateredconditions. Stomata were more sensitive to VPD and water stressthan to T_o. The higher the VPD or T_o the more rapid was thestomatal response, except in stressed plants where there wasno significant effect of T_o. Under water stress, stomata weremore sensitive to water potential (     

Structural and Functional Properties of Trichomes of Xeromorphic Leaves

Trichomes of xeromorphic leaves of 12 different species (Banksiaspeciosa, Corokia buddleioides, Correa backhousiana, Lavandulaofficinalis, Leucospermum grandiflorum, Metrosideros excelsa,Olea europaea, Olearia rotundifolia, Pittosporum crassifolium,Pittosporum sp., Rosmarinus officinalis, Senecio cineraria)and trichomes of mesomorphic leaves of five species (Achimenesgrandiflora, Geum urbanum, Gynura aurantiaca, Populus alba,and Styrax officinalis) were stained with Sudan IV and Sudanblack. In the trichomes of all xeromorphic leaves the wallsof the basal or stalk cells stained with these reagents. However,none of the cell walls of the trichomes of the mesomorphic leaveswere stained by the Sudan reagents. Portions of leaves of three of the xeromorphic species (Corokia,Correa, Olea) and leaves of three of the mesomorphic species(Achimenes, Geum, Gynura) were floated on 0.1 per cent Calcofluorwhite solution. Examination of cross-sections of these leafportions in the fluorescence microscope indicated that evenafter 4 days of floating the Calcofluor, which is an apoplastictracer, did not enter the trichome walls of the xeromorphicleaves. However, the Calcofluor brightener could already bedetected in the trichome walls of the mesomorphic leaves afterone day. The adapted properties of the trichomes of the xeromorphic leavesare discussed. Endodermal cell, mesomorphic leaves, trichomes, xeromorphic leaves, water diffusion boundary layer     

Senescence in Leaves of Acer pseudoplatanus L. and Parthenocissus tricuspidata Planch: 1. Changes in Some Leaf Constituents during Maturity and Senescence

Data are recorded of the changes in chlorophylls, carotene,sugar, shikimic acid, and anthocyanin in leaves of sycamore(Acer pseudoplatanus L.) and Virginia creeper (Parthenocissustricuspidata Planch.) during leaf maturity and senescence. InParthenocissus the losses of chlorophylls, carotene, sugar,and shikimic acid during senescence were closely correlated,and were inversely related to the accumulation of anthocyanin.The losses of chlorophylls, carotene, and sugar by Acer leaveswere also closely correlated. No evidence was found to supportthe suggestion that anthocyanin formation was caused by accumulationof sugar during senescence, but marked differences in shikimicacid content were found between leaves of Acer, which did notform anthocyanin, and Parthenocissus. which did. It is suggestedthat autumn senescence of these leaves involves the rapid senescenceof an increasing proportion of the leaf tissue during a periodof 80 days, and that measurements of the content of constituentsgive an estimate of the proportion of the leaf tissue whichhas senesced.     

Abscisic Acid Content and Effects During Dehydration of Detached Leaves of Desiccation Tolerant Plants

Borya nitida is an angiospcrm whose detached leaves developcomplete tolerance to dehydration when they are equilibratedto air of 96% r.h. This treatment causes leaves to yellow aschlorophyll is destroyed, and abscisic acid contents increaseseveral-fold. Exogenous ABA (at 0.038–0.38 mol m^–3)promoted desiccation tolerance (a) in leaves undergoing toleranceinduction at 96% r.h., (b) only slightly during rapid dryingat rates which are normally injurious, and (c) considerablyin turgid tissue treated with ABA 48 h before rapid drying. ABA content also increased with intense water stress in Myrothamnusflabellifolia, a desiccation tolerant angiosperm which, unlikeBorya, retains most of its chlorophyll when dehydrated. Preliminaryincubation in ABA of detached leaves of this ‘resurrectionplant’ also promoted survival during rapid drying. Theability of ABA to substitute for the normal induction periodsuggests that this hormone participates in the development ofdesiccation tolerance. Key words: Abscisic acid, ABA, Drought tolerance, Resurrection plant     

A simple porometer for precise recording of leaf resistance

A porometer, which can be easily constructed with a common photometricunit and yet records the air flow through a leaf blade accuratelyand sensitively, was developed and used to record the flow changesthrough Brassica chinensis leaves under several light, air andwater conditions. (Received May 17, 1973; )     

Acclimation of Respiratory Properties of Leaves of Spinacia oleracea L., a Sun Species, and of Alocasia macrorrhiza (L.) G. Don., a Shade Species, to Changes in Growth Irradiance

To clarify the way in which the light available for growth affectsrespiration in leaves of sun and shade plants, we examined therespiratory properties of mature leaves of Spinacia oleraceaL., a sun species, and of Alocasia macrorrhiza (L.) G. Don.,a shade species, that had been grown at various irradiances.In leaves of S. oleracea, the respiratory rates, on a dry massbasis, decreased with time during the night, and the higherwas the growth irradiance during the day, the higher was therespiratory rate. The marked decreases in the respiratory rateduring the night were accompanied by decreases in the concentrationof carbohydrates in the leaves. By contrast, the respiratoryrates of leaves of A. macrorrhiza were virtually constant throughoutthe night and the absolute rates were lower than those of S.oleracea even though the absolute value of the concentrationof carbohydrates and its decrease at night resembled to thosein S. oleracea. The maximum activities of respiratory enzymeswere also similar to those in S. oleracea. However, the leavesof A. macrorrhiza contained less soluble protein than thoseof S. oleracea. These results suggest that, in S. oleracea,the concentration of carbohydrates might determine the respiratoryrate while such is not the case in A. macrorrhiza. The lowerrespiratory rates in A. macrorrhiza might be due to a lowerdemand for ATP. (Received November 29, 1995; Accepted February 15, 1996)     

Changes in Tissue Freezing in Senecio vulgaris infected by Rust (Puccinia lagenophorae)

Freezing of healthy and rust (Puccinia lagenophorae) infectedleaves of Senecio vulgaris was compared calorimetrically bythermal analysis. In fully expanded leaves the threshold freezingtemperature was in the range –6.8 to –8.4 °Cin controls but –3.0 to –5.1 °C in leaves withsporulating rust sori. Comparable values in expanding leaveswere –5.0 to –8.9 °C and –3.9 to –6.7°C for healthy and rusted tissues, respectively. The bulktissue freezing point was between –1.0 and –4.0°C in both fully expanded and expanding healthy leaves,and was increased by infection by between +0.2 and 2.5 °C.Whereas healthy leaves supercooled by 3.1–5.8 °C,rusted leaves supercooled by only 1.8–4.9 °C Supercoolingof control leaves was reduced by dusting with aeciospores, particularlywhen leaves were wounded to simulate the rupture of the surfacecaused by sporulation, but wounding alone had no significanteffect. Supercooling of distilled water was also significantlyreduced by aeciospores, suspended at a concentration of 10⁵spores ml^–1. It is concluded that rust-induced changes in leaf freezing inS. vulgaris grown in controlled environments were due to anincrease in the number of sites for ice nucleation, caused bythe presence of the aeciospores, and increased penetration ofice into internal tissues, resulting from damage to the cuticleand epidermis. Although data for frost resistance obtained inthe growth-room are similar to previous field observations,the role of the above mechanisms under field conditions remainsunproven. Senecio vulgaris (groundsel), Puccinia lagenophorae (rust), low temperature, freezing resistance     

Comparison of Palaeobotanical Observations with Experimental Data on the Leaf Anatomy of Durmast Oak [Quercus petraea(Fagaceae)] in Response to Environmental Change

To test whether stomatal density measurements on oak leaf remainsare reliable tools for assessing palaeoatmospheric carbon dioxideconcentration [CO₂], under changing Late Miocene palaeoenvironmentalconditions, young seedings of oak (Quercus petraea,Liebl.) weregrown at elevatedvs.ambient atmospheric [CO₂] and at high humiditycombined with an increased air temperature. The leaf anatomyof the young oaks was compared with that of fossil leaves ofthe same species. In the experiments, stomatal density and stomatalindex were significantly decreased at elevated [CO₂] in comparisonto ambient [CO₂]. Elevated [CO₂] induced leaf cell expansionand reduced the intercellular air space by 35%. Leaf cell sizeor length were also stimulated at high air humidity and temperature.Regardless of a temperate or subtropical palaeoclimate, leafcell size in fossil oak was not enhanced, since neither epidermalcell density nor length of the stomatal apparatus changed. Theabsence of these effects may be attributed to the phenologicalresponse of trees to climatic changes that balanced temporalchanges in environmental variables to maintain leaf growth underoptimal and stable conditions.Quercus petraea,which evolvedunder recurring depletions in the palaeoatmospheric [CO₂], maypossess sufficient phenotypic plasticity to alter stomatal frequencyin hypostomatous leaves allowing high maximum stomatal conductanceand high assimilation rates during these phases of low [CO₂].Copyright1998 Annals of Botany Company Atmospheric CO₂, high humidity, elevated temperature,Quercus petraea,durmast oak, Late Miocene, palaeoclimates, leaf anatomy, stomatal density, stomatal index