Phytochrome Controlled Adhesion of Mung Bean Root Tips to Glass: A Detailed characterization of the Phenomenon

Various parameters of the Tanada effect (Proc. Natl. Acad. Sci. U.S. 59: 376–380. 1968) have been defined. This phenomenon, in which root tips of Phaseolus aureus L. adhere to a negatively charged glass surface when they are irradiated with 660 nm (red) light and release under 730 nm (far-red) light, has been characterized as follows. Secondary roots, whether etiolated or light grown exhibit photoreversible adhesion. Primary roots do not. Tips from 6–8 mm secondary roots exhibit the best response to red light, whereas tips from 3 mm roots respond best to far-red light. Red light saturetes the adhesion system at about 50 μ W/cm²xnm and far-red light, release system at about 150 ü W/cm² xnm. The adhesion effect begins to show escape from far-red reversibility within 60–90 seconds, an observation quite different from other “typical” long term de- etiolation effects. In addition, root tips irradiated with red light begin to release spontaneously in the dark after 10 min, and have nearly completed release after 50 min. Tips irradiated with continuous red light show gradual release after 15 minutes of exposure. Whether these data indicate an extremely rapid dark reversion of P_fr to P_r or decay of P_fr under continuous red light is not known at this time. In order to study tip adhesion and release, the glass beaker surface may be negatively charged with thiocyanate (SCN^-), nitrate (NO₃^-), sulfate (SO₄^2-), chloride (Cl^-), phosphate (PO₄^3-), citrate (C₆H₅O₇^3-), oxalate (C₂O₄^2-) or glutamine (C₅H₈NO₄^-). Benzoate (C₇H₅O₂^-) and acetate (CH₃COO^-) were found to be relatively ineffective for red light adhesion, however when citrate and oxalate were used release was inhibited. This was apparently due to a chelation of Ca²⁺since release began immediately as excess Ca⁺² was added to the bathing solution. Substitution of GTP, ITP, UTP, or CTP for ATP resulted in only 20 to 40% adhesion and release for GTP, ITP and UTP, CTP showed normal adhesion kinetics under red light but very slow release kinetics under far-red light. The effects of red and far-red light in the numbers of secondary roots are that red light inhibits root initiation while far-red light partially reverses the red light effect.     

Influence of red light and acetylcholine on 45Ca2+ uptake by oat coleoptile cells

Influence of red light and acetylcholine on ⁴⁵Ca²⁺ uptake by oat coleoptile cells was examined. It was found that the uptake is passive in darkness, while short, 10–15 min. exposure of coleoptile sections to red light or treatment with acetylcholine solution increases the rate of ⁴⁵Ca²⁺ uptake from the medium. Calcium channel blockers, La³⁺ and Verapamil, hinder ⁴⁵Ca²⁺ uptake in darkness and neutralize the stimulative influence of red light and acetylcholine.     

Rapid phytochrome-mediated changes in the uptake by bean roots of sodium acetate [1-14C] and their modification by cholinergic drugs

Summary 4 min of red light increases the uptake of sodium acetate[1-¹⁴C] by excised, etiolated secondary roots of Phaseolus aureus Roxb. 4 min of far-red light reveres this effect. AMO-1618, which inhibits acetylcholinesterase activity, enhances the red-light effect, while d-tubocurarine, which blocks the animal acetylcholine receptor, inhibits it. Red light also increases basipetal translocation of the label. When the metabolic fate of the label was determined in dark-held roots, 36% of the label remained as acetate, 48% evolved as [¹⁴C]CO₂, 3% partitioned with acetylcholine, and 3% effluxed from the roots. The rest of the label was associated with the coarse residue left after extraction. The major effect of red light was to increase the uptake of the label in the acetate fraction.We interpret these observations to mean that the phytochrome mechanism immediately causes an increase in uptake of the label during brief irradiation with red light. Because of our previous demonstration that both red light and acetylcholine increase respiration, it is probable that the increased absorption of the label is a process requiring respiratory energy. These data support the concept of phytochrome as a membrane-bound functional system that in bean roots is mediated by the acetylcholine mechanism.Abbreviations ACh Acetylcholine - AChE acetylcholinesterase - ATP adenosine triphosphate - AMO-1618 2-isopropyl-4-dimethylamino-5-methylphenyl-1-piperidine carboxylate methyl chloride - TPB tetraphenyl boron - D darkness - FR far-red - R red     

Redox Processes in the Blue Light Response of Guard Cell Protoplasts of Commelina communis L

Guard cell protoplasts from Commelina communis L. illuminated with red light responded to a blue light pulse by an H⁺ extrusion which lasted for about 10 minutes. This proton extrusion was accompanied by an O₂ uptake with a 4H⁺ to O₂ ratio. The response to blue light was nil in darkness without a preillumination period of red light and increased with the duration of the red light illumination until about 40 minutes. However, acidification in response to a pulse of blue light was obtained in darkness when external NADH (1 millimolar) was added to the incubation medium, suggesting that redox equivalents necessary for the expression of the response to blue light in darkness may be supplied via red light. In accordance with this hypothesis, the photosystem II inhibitor 3-(3,4-dichlorophenyl)-1, 1-dimethylurea (10 micromolar) decreased the acidification in response to blue light more efficiently when it was added before red light illumination than before the blue light pulse. In the presence of hexacyanoferrate, the acidification in response to a blue light pulse was partly inhibited (53% of control), suggesting a competition for reducing power between ferricyanide reduction and the response to blue light.     

CHLORIDE UPTAKE BY ANACYSTIS NIDULANS (CYANOPHYCEAE)1

Anacystis nidulans (Richt.) Drouet & Daily (UTEX 625), grown in batch culture with 0.5% CO₂ in air, was supplied with chloride labelled with ³⁶Cl in light and dark. Uptake in light was stimulated relative to uptake in darkness. A single transport system for Cl^? with an apparent K_m for Cl^? of 0.14 mM was identified. Chloride in the cells reached a maximum value after 30–50 min at 25 C. At this point the internal Cl^? concentration was calculated to be 60-fold the external (0.1 mM) in light and 37-fold in darkness. DCMU (3-[3,4-dichlorophenyl]–1, 1-dime-thylurea), at concentrations which abolished photosynthetic O₂ evolution did not inhibit Cl^? uptake in light. Carbonyl cyanide m-chlorophenyl hydrazone (CCCP), at uncoupling concentrations for photosynthesis and dark respiration, strongly inhibited Cl^? uptake in light and darkness. N,N'-dicyclohexyl carbodiimide (DCCD), an energy transfer inhibitor, inhibited light Cl^? uptake more slowly than photosynthesis but had no effect on dark Cl^? uptake. It is concluded that Cl^? uptake in A. nidulans was active in light and darkness, and that ATP was the probable energy source for transport.     

Characterization and Effect of Light on the Plasma Membrane H+-ATPase of Bean Leaves

Proton excretion from bean (Phaseolus vulgaris L.) leaf cells is increased by bright white light. To test whether this could be due, at least in part, to an increase in plasma membrane (PM) ATPase activity, PM vesicles were isolated from primary leaves by phase partitioning and used to characterize PM ATPase activity and changes in response to light. ATPase activity was characterized as magnesium ion dependent, vanadate sensitive, and slightly stimulated by potassium chloride. The pH optimum was 6.5, the K_m was approximately 0.30 millimolar ATP, and the activity was about 60% latent. PM vesicles were prepared from leaves of plants grown for 11 days in dim red light (growing slowly) or grown for 10 days in dim red light and then transferred to bright white-light for 1 day (growing rapidly). For both light treatments, ATPase specific activity was approximately 600 to 700 nanomoles per milligram protein per minute, and the latency, K_m, and sensitivity to potassium chloride were also similar. PM vesicles from plants grown in complete darkness, however, exhibited a twofold greater specific activity. We conclude that the promotion of leaf growth and proton excretion by bright white light is not due to an increase in ATPase specific activity. Light does influence ATPase activity, however; both dim red light and bright white light decreased the ATPase specific activity by nearly 50% as compared with dark-grown leaves.     

THE INVOLVEMENT OF A PLASMA MEMBRANE H+‐ATPase IN THE BLUE‐LIGHT ENHANCEMENT OF PHOTOSYNTHESIS IN LAMINARIA DIGITATA (PHAEOPHYTA)1

Many brown algae, including the kelp Laminaria digitata (Huds.) Lamour., exhibit enhanced photosynthesis when they are given a small amount of blue‐light in addition to a background of saturating red light. This blue light effect is correlated with an increased uptake of carbon. In the present study, we tested the hypothesis that blue light acts by increasing the activity of a plasma membrane H ⁺ ‐ATPase, thereby promoting an active carbon uptake across the plasma membrane. Photosynthetic carbon uptake was studied in pH‐drift experiments under illumination with red and blue light and using different inhibitors. Vanadate, an inhibitor of plasma membrane H ⁺ ‐ATPases, had a minor inhibitory effect on carbon uptake rates under saturating red light conditions, but inhibited the blue‐light enhancement by approximately 60%. An inhibitor of external carbonic anhydrase, acetazolamide, decreased the carbon uptake in both red light and in red plus blue light by 48% and 68%, respectively. These results suggest that photosynthetic carbon uptake depends on an external carbonic anhydrase under both red and red plus blue light conditions, and that blue light induces an increased activity of a P‐type H ⁺ ‐ATPase in the plasma membrane. The proton buffer Tris, which has a buffering capacity similar to vanadate in seawater, had no inhibitory effect on carbon uptake rates neither in red light nor in red plus blue light, showing that the inhibitory effect of vanadate is not caused by its effect as a buffer. The blue‐light enhancement was also abolished by a protein kinase inhibitor (H‐7), suggesting that the transduction of the blue‐light signal involves a protein kinase, which activates the plasma membrane H ⁺ ‐ATPase by phosphorylation.     

Relationship between Respiration and Photosynthesis in Guard Cell and Mesophyll Cell Protoplasts of Commelina communis L

A mass spectrometric method combining ¹⁶O/¹⁸O and ¹²C/¹³C isotopes was used to quantify the unidirectional fluxes of O₂ and CO₂ during a dark to light transition for guard cell protoplasts and mesophyll cell protoplasts of Commelina communis L. In darkness, O₂ uptake and CO₂ evolution were similar on a protein basis. Under light, guard cell protoplasts evolved O₂ (61 micromoles of O₂ per milligram of chlorophyll per hour) almost at the same rate as mesophyll cell protoplasts (73 micromoles of O₂ per milligram of chlorophyll per hour). However, carbon assimilation was totally different. In contrast with mesophyll cell protoplasts, guard cell protoplasts were able to fix CO₂ in darkness at a rate of 27 micromoles of CO₂ per milligram of chlorophyll per hour, which was increased by 50% in light. At the onset of light, a delay observed for guard cell protoplasts between O₂ evolution and CO₂ fixation and a time lag before the rate of saturation suggested a carbon metabolism based on phosphoenolpyruvate carboxylase activity. Under light, CO₂ evolution by guard cell protoplasts was sharply decreased (37%), while O₂ uptake was slowly inhibited (14%). A control of mitochondrial activity by guard cell chloroplasts under light via redox equivalents and ATP transfer in the cytosol is discussed. From this study on protoplasts, we conclude that the energy produced at the chloroplast level under light is not totally used for CO₂ assimilation and may be dissipated for other purposes such as ion uptake.     

Control of Bean Bud ATP Levels by Regulatory Molecules and Phytochrome

This study assessed the involvement of exogenously supplied acetylcholine, dibutyryl cyclic AMP, and various inhibitors of acetylcholine and cyclic AMP metabolism on the rapid phytochrome-mediated alteration in the ATP content of etiolated bean buds (Phaseolus vulgaris L. cv. Red Kidney). ATP was extracted in boiling water and measured by the firefly luciferin-luciferase assay. The depression of ATP content by low levels of either acetylcholine or dibutyryl cyclic AMP was independent of irradiation. Atropine, AMO-1618, and theophylline all altered ATP content, and the effects differed in red light and in darkness. In contrast to other reports, no straightforward model of phytochrome action through either acetylcholine or cyclic AMP could be constructed. Also, the time course of ATP content during the standard 5 min red-irradiation period was determined, and effects of light are observed within 1 min.     

Oxidative phosphorylation in pea cotyledon submitochondrial particles

Mitochondria and submitochondrial particles (SMP) from pea cotyledons were shown to catalyze oxidative phosphorylation as measured by ³²Pi uptake into phosphate esters. ATP synthesis was sensitive to the electron transport inhibitor KCN, the uncoupler carbonyl cyanide m-chlorophenylhydrazone, and the coupling factor inhibitor oligomycin. Experiments with the adenine nucleotide translocator inhibitor atractyloside indicated the SMP were inside-out. Mersalyl completely inhibited ATP synthesis by SMP, and a separate experiment indicated that mersalyl has a direct effect on the ATPase complex. The kinetics of ATP synthesis indicated a high affinity for phosphate (K_m = 0.18 millimolar). ADP kinetics gave a biphasic curve with K_m values of about 4.8 and 160 micromolar. O₂ uptake and ATP synthesis had a pH maximum of 7.6 while the ratio of micromoles phosphate esterified to microatoms O₂ taken up was highest at pH 7.2. Sodium chloride inhibited both ATP synthesis and O₂ uptake but stimulated the ATPase reaction. The SMP also catalyzed a slow ATP-phosphate exchange reaction.     

Changes in dormancy of Sisymbrium officinaleseeds do not depend on changes in respiratory activity

Effects of dark incubation at different temperatures were studied on dormancy and respiratory activity of seeds of Sisymbrium officinale (L.) Scop. Because germination of this species absolutely depends on the simultaneous action of light and nitrate, changes in dormancy could be studied in darkness without the interference of early germination events. Upon the start of incubation rates of O₂ uptake and CO₂ release rose. This was followed by a gradual decrease until stable levels of O₂ uptake and CO₂ release were achieved. Seeds kept for prolonged periods at 24^°C, showed neither a change in germination capacity nor in rates of O₂ uptake and CO₂ release. Respiratory quotients were 0.55–0.7. The initial rise in O₂ uptake correlated with the rate of water uptake and with breaking of primary dormancy. However, the subsequent decline in O₂ uptake was not generally linked to induction of secondary dormancy. An increased O₂ uptake was not required during breaking of secondary dormancy. It is concluded that changes in dormancy are not generally related to changes in respiratory activity. However, germination strongly depends on respiration. The increase in O₂ uptake started well before radicle protrusion. A far red irradiation only reversed this increase when it was given before germination escaped from its red light antagonising action. The contribution of different respiratory pathways was followed during prolonged incubation at 24^°C in darkness. KCN at 1.5 mM was needed to inhibit the cytochrome pathway (CP) and benzohydroxamic acid (BHAM) at 30 mM to inhibit the alternative pathway (AP). These concentrations did not exert any side effects. Electron flow was predominantly via the CP, maximally 10% was via the AP. Flow through the CP declined during the first 6 days and residual respiration remained constant. Therefore, the contribution of residual respiration became relatively more important with prolonged incubation. KCN at concentrations that almost completely inhibited flow through the CP, did not dramatically reduce germination. BHAM already inhibited germination at concentrations that do not inhibit oxygen uptake.     

Phytochrome modulation of ATPase activity in a membrane fraction from Phaseolus

Membrane-bound phytochrome and ATPase (ATP phosphohydrolase EC 3.6.1.3.) activity extracted from hypocotyl hooks of etiolated Phaseolus aureus Roxb. were both separated from solute proteins by gel filtration on Sepharose C1-2B. The amount of phytochrome detected in the membrane fraction was very small and was not significantly increased by red irradiation (in vivo or in vitro). Membrane-bound ATPase activity was modulated in vitro by the phytochrome in the membrane fraction, being lower after red light than after far-red light. This effect was potentiated by a preliminary light reaction which occurred only in vivo and, in continuous red light, required 60 to 90 s at 25°C. Thus a two minute, in vivo, red irradiation reduced membrane-bound ATPase activity to about half that of the etiolated state. Subsequently bound-ATPase activity was determined by the form of phytochrome (P_r or P_fr) irrespective of whether established in vivo or in vitro. These results indicate that binding or release (of enzyme, cofactors or inhibitors) is not involved in phytochrome modulation of enzyme activity in the membrane fraction.Abbreviations R red light - F far red light - P_r inactive form of phytochrome (_max=660 nm) - P_fr active form of phytochrome (_max=730 nm) - MOPS N-morpholino-3-propansulphonic acid     

Stimulation of growth and ion uptake in bean leaves by red and blue light

Red and blue light both stimulate growth and ion accumulation in bean (Phaseolus vulgaris L.) leaves, and previous studies showed that the growth response is mediated by phytochrome and a blue-light receptor. Results of this study confirm that there is an additional photosynthetic contribution from the growing cells that supports ion uptake and growth. Disc expansion in the light was enhanced by exogenous K⁺ and Rb⁺, but was not specific for anions. Light increased K⁺ accumulation and the rate of ⁸⁶Rb⁺ uptake by discs, over darkness, with no effect of light quality. The photosynthetic inhibitor, 3-(3,4-dichlorophenyl)-1,1-dimethylurea, inhibited light-driven ⁸⁶Rb⁺ uptake by 75%. Light quality caused differences in short-term kinetics of growth and acidification of the leaf surface. At comparable fluence rates (50 μmol m⁻² s⁻¹), continuous exposure to blue light increased the growth rate 3-fold after a 2-min lag, whereas red light caused a smaller growth response after a lag of 12 min. In contrast, the acidification of the leaf surface normally associated with growth was stimulated 3-fold by red light but only slightly (1.3-fold) by blue light. This result shows that, in addition to acidification caused by red light, a second mechanism specifically stimulated by blue light is normally functioning in light-driven leaf growth.     

Relationship between ATP Level and Activity of Fusicoccin-stimulated H/K-Exchange System in Plant Tissues

The treatment with fusicoccin causes a slight but significant decrease (about 15%) in the ATP level in pea-internode and maize-coleoptile segments. This decrease is detectable within 15 minutes and is accompanied by a parallel increase in O₂ uptake. Sodium azide inhibits O₂ uptake and completely blocks the stimulation of O₂ uptake by fusicoccin in both pea and coleoptile segments. Benzohydroxamic acid does not affect either basal or fusicoccin-induced O₂ uptake in maize-coleoptile sections. The drop of ATP level induced by various treatments (sodium arsenate, 2-deoxyglucose, limiting O₂, and anaerobiosis) is accompanied by a parallel inhibition of K⁺ uptake in maize coleoptiles treated with or without fusicoccin. These results are consistent with the hypothesis that ATP is the energy source for the fusicoccin-activated H⁺/K⁺-exchange system.     

Evidence for A Ca2+ gradient across the plasma membrane of wheat protoplasts

Fluxes of Ca²⁺ across the plasma membrane of isolated wheat protoplasts have been measured both as net accumulation and as uptake under steady-state conditions. The ATPase inhibitors, orthovanadate and diethylstibesterol, and the divalent cation ionophore, A23187, were all found to enhance net Ca²⁺ accumulation by protoplasts. The uptake of Ca²⁺ under steady-state conditions was also stimulated by A23187 but relatively unaffected by a range of plant hormones or by red or far red light. Light treatments were compared to dark controls with protoplasts isolated from etiolated wheat.The results suggest that plant cells maintain a Ca²⁺ gradient across their plasma membrane but it appears not to be under phytochrome control.     

ATP synthesis catalyzed by the ATPase complex from Rhodospirillum rubrum reconstituted into phospholipid vesicles together with bacteriorhodopsin

The coupling factor ATPase complex extracted by Triton X-100 from the photosynthetic bacterium Rhodospirillum rubrum could be incorporated into phospholipid vesicles after removal of the Triton. Vesicles reconstituted with this F₀ · F₁-type ATPase together with bacteriorhodopsin were found to catalyze, in the light, net ATP synthesis which was inhibited by the energy transfer inhibitors oligomycin and N,N-dicyclohexylcarbodiimide as well as by uncouplers. In vesicles reconstituted with the crude ATPase up to 50% of the observed rate of phosphorylation was independent on light and bacteriorhodopsin and insensitive to the above-listed inhibitors. This dark activity was, however, completely blocked by the adenylate kinase inhibitor, p¹,p⁵-di(adenosine-5′)pentaphosphate, which did not affect at all the net light-dependent phosphorylation nor the ATP-³²P_i exchange reaction. Vesicles reconstituted with the purified ATPase catalyzed only the light- and bacteriorhodopsin-dependent diadenosine pentaphosphate-insensitive phosphorylation. The rate of this photophosphorylation was found to be proportional to the amount of ATPase and bacteriorhodopsin, and linear for at least 20 min of illumination. These results indicate that the purified ATPase contains the complete assembly of subunits required to transduce electrochemical gradient energy into chemical energy.     

Active Uptake of Ca++ and Ca++-Activated Mg++ ATPase in Red Cell Membrane Fragments

Isolated human red blood cell membrane fragments (RBCMF) were found to take up Ca⁺⁺ in the presence of ATP.¹ This ATP-dependent Ca⁺⁺ uptake by RBCMF appears to be the manifestation of an active Ca⁺⁺ transport mechanism in the red cell membrane reported previously (Schatzmann, 1966; Lee and Shin, 1969). The influences of altering experimental conditions on Ca⁺⁺-stimulated Mg⁺⁺ ATPase (Ca⁺⁺ ATPase) and Ca⁺⁺ uptake of RBCMF were studied. It was found that pretreatment of RBCMF at 50°C abolished both Ca⁺⁺ ATPase and Ca⁺⁺ uptake. Pretreatment of RBCMF with phospholipases A and C decreased both Ca⁺⁺ ATPase and Ca⁺⁺ uptake, whereas pretreatment with phospholipase D did not significantly alter either Ca⁺⁺ ATPase or Ca⁺⁺ uptake. Both Ca⁺⁺ ATPase and Ca⁺⁺ uptake had ATP specificity, similar optimum pH's, and optimum incubation temperatures. From these results, it was concluded that Ca⁺⁺ uptake is intimately linked to Ca⁺⁺ ATPase.     

Promotion of sink activity of developing rose shoots by light

Holding young rose shoots (Rosa hybrida cv. Marimba) in darkness while the rest of the plant was in light reduced the amount of ¹⁴C assimilates recovered from the darkened shoot by half. Relative specific activity of the shoot tip grown in light was 13.5 times greater than that of the darkened one. The flower bud at the shoot tip degenerated in darkness and died. Shoots 2 to 3 centimeters long, after flower initiation, were most sensitive to the dark treatment. The degeneration is a gradual and reversible process in the first 8 days of darkness, followed by irreversible damage and atrophy. Darkening enhanced the ability of the young leaves to compete for the available assimilates over that of the darkened shoot tip. The enhancement of the mobilizing ability of the shoot tip by light is independent of photosynthesis since spraying with 3-(3,4-dichlorophenyl)-1,1-dimethylurea or holding shoots in a CO₂-free atmosphere did not diminish the promoting effect of light on flower bud development or assimilate import. The possibility that light exerts its effect by photoproduction of ATP was also excluded inasmuch as no differences were found in ATP levels of shoot tips held in darkness and those held in light.