Gene profiling of the red light signalling pathways in roots

Red light, acting through the phytochromes, controls numerousaspects of plant development. Many of the signal transductionelements downstream of the phytochromes have been identifiedin the aerial portions of the plant; however, very few elementsin red-light signalling have been identified specifically forroots. Gene profiling studies using microarrays and quantitativeReal-Time PCR were performed to characterize gene expressionchanges in roots of Arabidopsis seedlings exposed to 1 h ofred light. Several factors acting downstream of phytochromesin red-light signalling in roots were identified. Some of thegenes found to be differentially expressed in this study havealready been characterized in the red-light-signalling pathwayfor whole plants. For example, PHYTOCHROME KINASE 1 (PKS1),LONG HYPOCOTYL 5 (HY5), EARLY FLOWERING 4 (ELF4), and GIGANTEA(GI) were all significantly up-regulated in roots of seedlingsexposed to 1 h of red light. The up-regulation of SUPPRESSOROF PHYTOCHROME A RESPONSES 1 (SPA1) and CONSTITUTIVE PHOTOMORPHOGENIC1-like (COP1-like) genes suggests that the PHYA-mediated pathwaywas attenuated by red light. In addition, genes involved inlateral root and root hair formation, root plastid development,phenylpropanoid metabolism, and hormone signalling were alsoregulated by exposure to red light. Interestingly, members ofthe RPT2/NPH3 (ROOT PHOTOTROPIC 2/NON PHOTOTROPIC HYPOCOTYL3) family, which have been shown to mediate blue-light-inducedphototropism, were also differentially regulated in roots inred light. Therefore, these results suggest that red and bluelight pathways interact in roots of seedlings and that manyelements involved in red-light-signalling found in the aerialportions of the plant are differentially expressed in rootswithin 1 h of red light exposure. Key words: Arabidopsis, gene profiling, microarray, photomorphogenesis, red light, roots     

Expression of Genes for Photosynthesis and the Relationship to Salt Tolerance of Alfalfa (Medicago sativa) Cells

The basis for the salt tolerant phenotype of a line of Medicagosativa (alfalfa) cells (HG2-N1) derived by selection from asalt sensitive line (HG2) was studied. The salt tolerant HG2-N1cell line shows eleven fold elevated chlorophyll content overthat of the parent salt sensitive HG2 cell line, with an additionaltwo fold increase in chlorophyll levels when the cells are grownin 1% NaCl. In this study, we demonstrate that the chlorophyllaccumulation and response to salt was associated with largeincreases in the two photosynthesis related mRNAs, rbcL (ribulose-l,5-bis-phosphatecarboxylase [Rubisco] large subunit) and rbcS (Rubisco smallsubunit) and a substantial increase in the activity of the holoenzyme.The salinity-induced increase in catalytically competent Rubiscoprotein in the salt tolerant cell line was highly responsiveto light and correlated with the salt tolerant phenotype. Inaddition, NaCl stimulated rbcL and rbcS mRNA and Rubisco accumulationin dark grown salt tolerant cells, indicating that salt couldsubstitute to some degree for light in stimulating increasesin specific mRNA and protein concentrations. Increased photosyntheticcompetence associated with these increased protein levels wasapparently important in contributing to the salt tolerant phenotypeof HG2-N1, since PS II electron transport inhibitors (DCMU,cyanazine) were found to significantly reduce the growth ofthis cell line in the presence of salt, but not in the absenceof salt. These results suggest that the salt-induced increasein mRNA and protein accumulation involved in photosynthesismay play a significant role in the salt tolerant capabilityof HG2-N1 alfalfa cells. (Received April 2, 1990; Accepted September 10, 1990)     

Impedance analysis of renal vascular smooth muscle cells

Impedance of renal vascular smooth muscle cells (VSMCs) cultured on microelectrodes was measured by electric cell-substrate impedance sensing. Changes in measured impedance as a function of frequency were compared with the calculated values obtained from an extended cell-electrode model to estimate the junctional resistance, distance between the ventral cell surface and the substratum, and apical and basolateral membrane capacitances of renal VSMCs. This cell-electrode model was derived to accommodate the slender and rectangular shape of VSMCs. The calculated changes in impedance (Z_cal) based on the model agreed well with the experimental measurement (Z_exp), and the percentage error defined as |(Z_cal – Z_exp)/Z_exp| was 1.0%. To test the sensitivity of the new model for capturing changes in cell-cell and cell-substrate interactions induced by changes in cellular environment, we then applied this model to analyze timpedance changes induced by an integrin binding peptide in renal VSMCs. Our result demonstrates that integrin binding peptide decreases junctional resistance between cells, increases the distance between the basolateral cell surface and substratum, and increases the apical membrane capacitance, whereas the basolateral membrane capacitance stays relatively stable. This model provides a generic approach for impedance analysis of cell layers composed of slender, rectangular cells. electric cell-substrate impedance sensing; cell attachment; cell adhesion; extracellular matrix; integrin     

Studies on Fat Accumulation in Nitzschia palea Kutz

Fat accumulation in Nitzschia palea Kütz. starts perceptiblyat the end of the exponential phase of growth and reaches amaximum during the stationary phase of growth when the wholecell is filled with fat. Filtrates from old cultures enhancedfat synthesis probably by the production of an autotoxin whichinhibits cell growth but at the same time favours fat synthesis.The presence of an inhibitory autotoxin has not been provedbut indirect evidence suggests its presence. The nitrogen content of the culture medium also influences theamount of fat formed, more fat being accumulated in nitrogen-deficientmedia than in media provided with adequate nitrate supply. Theoptimum temperature for the growth of N. palea was found tobe about 30 °C while that for fat synthesis was around 35°C. Below 15 °C and above 40 °C, fat synthesis wasdrastically reduced. Blue and red light independently favoured fat synthesis whereasa combination of both did not. This is probably due to the selectiveinfluence of these wavelengths on the production of fat precursorsor intermediates.     

Effects of Natural and Artificial Light in Arctic Latitudes on Long- and Short-day Plants as Revealed by Growth Analysis

The effects on growth and flowering of two short-day and twolong-day plants when grown under different conditions of illuminationare described. The plants fully investigated were Kalanchoeblossfeldiana and Xanthium pennsylvanicum and the annual varietiesof Hyoscyamus niger and Beta vulgaris. Wintex barley, Iberisumbellata, and tomato were also grown in some selected treatments.The conditions investigated comprised continuous full daylight(24 hours), full daylight for the whole of the daily photoperiodand full daylight for half the photoperiods, the other halfconsisting of either daylight reduced by shading or light fromincandescent lamps or fluorescent tubes (daylight-matching type),all of the same low intensity. Two lengths of photoperiod wereused for each species, one nearly optimal for flowering, theother closer to the critical day-length; and the order of thelow and high light treatments was varied. These factors werecombined factorially. Data were collected (or derived) for the following characteristics,though not always for all the species grown: dry weights, leafareas, heights, water contents, epidermal cell sizes, net assimilationrates, times to flowering, leaf-number increments until flowering,numbers of inflorescences, stomatal apertures, and leaf postures. Among other effects, the data revealed that in all four speciesinvestigated the adverse effects on over-all growth to be expectedfrom reduction of the daily photoperiod or of the intensityof illumination are in fact minimized. This compensation waseffected mainly by large increases in leaf areas, even thoughin all cases half the daily photoperiod consisted of full daylight.There are indications that increased efficiencies (net assimilationrates) may also have been involved. The leaf-area increasesappear to have been due to increased cell size rather than cellnumber and a close positive correlation with water content wasfound. The most striking among the effects on flowering was the failureof sugar-beet to bolt when half of its photoperiod (totals of20 and 14 hours) consisted of light from fluorescent lamps.The flowering of barley and Hyoscyamus was also delayed considerablyunder these conditions. The deficiency of red in the spectrumof the fluorescent light is believed to have been the cause.By contrast, the flowering of Iberis, a crucifer, was not affected.     

Haustoria of Cuscuta japonica, a Holoparasitic Flowering Plant, Are Induced by the Cooperative Effects of Far-Red Light and Tactile Stimuli

When seedlings of Cuscuta japonica were grown with Vigna radiata(the host plant) in a flower pot for 6 d under white light andthen irradiated with far-red or blue light (ca. 6 µmolphotons m^–2 s^–1), the seedlings parasitized V. radiata.However, no parasitism of the seedlings was observed under redor white light or in darkness. The parasitic behavior of seedlingsof C. japonica was observed even if an acrylic rod was usedas a substitute for the host plant. Upon incubation under far-redlight, the seedling twined tightly around the rod and developedhaustoria towards it. Haustoria also developed when apical andsubapical regions of seedlings were held between two glass platesthat were about 0.7 mm apart and were irradiated with far-redlight. However, no haustoria were induced by either the holdor irradiation alone. These results indicate that parasitismof Cuscuta japonica is controlled by the cooperative effectsof two physical signals, far-red light and appropriate tactilepressure. Our findings suggest that parasitism by the genusCuscuta involves a novel strategy. (Received April 10, 1996; Accepted August 21, 1996)     

Plant Growth Promoting Rhizobacteria and Soybean [ Glycine max (L.) Merr.] Nodulation and Nitrogen Fixation at Suboptimal Root Zone Temperatures

Co-inoculation of plant growth promoting rhizobacteria (PGPR)withBradyrhizobium has been shown to increase legume nodulationand nitrogen fixation at optimal soil temperatures. Nine rhizobacteriaco-inoculated withBradyrhizobium japonicum532C were tested fortheir ability to reduce the negative effects of low root zonetemperature (RZT) on soybean [Glycine max(L.) Merr.] nodulationand nitrogen fixation. Three RZTs were tested: 25 (optimal),17.5 (somewhat inhibitory), and 15°C (very inhibitory).At each temperature some PGPR strains increased the number ofnodules formed and the amount of fixed nitrogen when co-inoculatedwithB. japonicum,but the stimulatory strains varied with temperatures.The strains that were most stimulatory varied among temperaturesand were as follows: 15°C,Serratia proteamaculans 1-102;17.5°C,S. proteamaculans 1-102andAeromonas hydrophilaP73;25°C,Serratia liquefaciens2-68. Bradyrhizobium japonicum ; Glycine max; plant growth promoting rhizobacteria; suboptimal root zone temperatures     

An Evaluation of the Effects of Ethylene on Carbon Assimilation in Lycopersicon esculentum Mill

Leaf and whole plant gas exchange rates of Lycopersicon esculentumMill, were studied during several days of continuous exposureto ethylene. Steady-state photosynthesis and transpiration ratesof control and ethylene-treated individual leaves were equivalent.However, the photosynthesis and transpiration rates of treatedleaves required at least five times longer to reach 50% of thesteady-state rate. This induction lag was attributed to ethylene—inducedleaf epinasty and temporary acclimation to lower incident lightlevels immediately prior to measurement of gas exchange. Thewhole plant net carbon exchange rate (NCER) of a representativetreated plant was also reduced by 51% after 24 h exposure toethylene relative to both its pre-treatment rate and that ofthe control. Ethylene exposure reduced the growth rate of thetreated plant by 50% when expressed as carbon (C) gain. Theinhibition of NCER and growth rate associated with epinastywas completely reversed when the epinastic leaves were returnedto their original positions and light interception was re-established.The results demonstrate that the inhibition of whole plant CO₂assimilation is indirect and due to reduced light interceptionby epinastic leaves. Morphological changes caused by environmentalethylene are thus shown to reduce plant C accumulation withoutinhibiting leaf photosynthesis processes per se. Key words: Ethylene, carbon assimilation, growth     

Interaction of vernalization, photoperiod and high temperature in flowering of Arabidopsis thaliana (L.) HEYNH.

Flowering of Arabidopsis thaliana (L.) HEYNH., var. "Stockholm",plants, raised from vernalized seeds, may be modified by thephotoperiodic conditions or a short (1 week) exposure to hightemperature (32°C) following vernalization, depending onthe duration of the cold treatment. When vernalization is partial(1 to 4 weeks at 4°C), both short days (8hr light) and hightemperature have a devernalizing effect, but when the cold requirementhas been fully satisfied, after 5 to 6 weeks at 4°C, devernalizationis no longer possible. There is no interaction between photoperiodand high temperature. Fully vernalized plant flower in bothlong and short days, although flowering is delayed in shortdays. This delay is not a photoperiodic effect, however, butmay be ascribed to the decreased radiant energy available inan 8-hr photoperiod. Thus, fully vernalized Arabidopsis plantsare day-neutral. (Received November 5, 1969; )     

Electrical Impedance Analysis in Plant Tissues8

Electrical impedance spectra (100 Hz–800 kHz) were measuredin leaves of Peperomia obtusifolia L. (a succulent) and Brassicaoleracea L. (cabbage). By measuring impedances at three or moreinter-electrode distances in a single leaf, electrode impedanceand specific tissue impedance were separated. Analysis of impedance data from B. oleracea leaves in relationto an equivalent circuit model showed that leaf developmentwas accompanied by increases in extracellular resistance, cytoplasmicresistance and vacuole interior resistance, together with decreasesin plasma membrane capacitance and tonoplast capacitance. AfterB. oleracea leaves were subjected to a –6 °C freeze-thawstress, extracellular resistance, cytoplasmic resistance andvacuole interior resistance decreased, but plasma membrane capacitanceand tonoplast capacitance did not change. These results indicatethat useful measurements of leaf parameters can be obtainedby this technique. Examination of the electrode impedance spectrum showed thatelectrode insertion produced a damaged collar, 0·4–0·5mm wide, around the electrode. This was confirmed by visualobservation of the damage in P. obtusifolia leaf. Key words: Peperomia obtusifolia L., Brassica oleracea L. (cabbage), electrical impedance, equivalent circuit, electrode polarization     

The Distribution and Identity of Assimilates in Tomato with Special Reference to Stem Reserves

Much of the work on the distribution of ¹⁴C-labelled assimilatesin tomato has been done in winter under low light intensities,and consequently the reported distribution patterns of ¹⁴C maynot be representative of plants growing in high light. Further,there are several somewhat conflicting reports on patterns ofdistribution of ¹⁴C-assimilates in young tomato plants. We soughtto clarify the situation by studying the distribution of ¹⁴C-assimilatesin tomato plants of various ages grown in summer when the lightintensity was high. In addition, the role of the stem as a storageorgan for carbon was assessed by (a) identifying the chemicalfractions in the stem internode below a fed leaf and monitoring¹⁴ C activity in these fractions over a period of 49 d, and(b) measuring concentrations of unlabelled carbohydrates inthe stem over the life of the plant. The patterns of distribution of ¹⁴C-assimilates we found fortomato grown under high light intensity confirmed some of thosedescribed for plants grown under low light, but export of ¹⁴Cby fed leaves was generally higher than reported for much ofthe earlier work. Lower leaves of young plants exported over50% of the ¹⁴C they fixed, although export fell sharply as theplants aged. Initially, the roots and apical tuft were strongsinks for assimilates, but they had declined in importance bythe time plants reached the nine-leaf stage. On the other hand,the stem became progressively more important as a sink for ¹⁴C-assimilates.Older, lower leaves exported more of their ¹⁴C-assimilates tothe upper part of the plant than to the roots, whereas youngleaves near the top of the plant exported more of their assimilatesto the roots. The stem internode immediately below a fed leafhad about twice the ¹⁴C activity of the internode above theleaf. Mature leaves above and below a fed leaf rarely importedmuch ¹⁴C, even when in the correct phyllotactic relationshipto the fed leaf. In the first 3 d after feeding leaf 5 of nine-leaf plants, theorganic and amino acid pools and the neutral fraction of theinternode below the fed leaf had most of the ¹⁴C activity, butby 49 d after feeding, the ethanolic-insoluble, starch and lipidfractions had most of the ¹⁴C activity. Glucose, fructose andsucrose were the main sugars in the stem. Although concentrationsof these sugars and starch declined in the stem as the plantsmatured, there was little evidence to indicate their use infruit production. Stems of plants defoliated at the 44-leafstage had lower concentrations of sugars and starch at maturity,and produced less fruit than the controls. It was concludedthat tomato is sink rather than source limited with respectto carbon assimilates, and that the storage of carbon in thestem for a long period is possibly a residual perennial traitin tomato.Copyright 1994, 1999 Academic Press Lycopersicon esculentum, tomato, assimilate distribution, ¹⁴C, internode storage, sink-source relationships, starch, stem reserves, sugars     

Post-transcriptional regulation of protein synthesis during alfalfa embryogenesis: proteins associated with the cytoplasmic polysomal and non-polysomal mRNAs (messenger ribonucleoprotein complex)

Cytoplasmic polysomal and non-polysomal mRNA-associated proteincomplexes were isolated from, and characterized in, developingsomatic and zygotic embryos of alfalfa (Medicago sativa L.).³⁵S-methionine-labelled intact embryos were irradiated withultraviolet light (UV) in situ to cross-link mRNA and proteinsoccurring within one bond length, and the polysomal and non-polysomalfractions were extracted. Then the mRNA-protein complexes wereisolated from the fractions and separated using two cycles ofaffinity chromatography on an oligo(dT)-cellulose column. Followingdigestion with RNase A and T1 and micrococcal nuclease, mRNA-associatedproteins were separated by SDS-PAGE. Several polypeptides of 15–150 kDa were associated withthe polysomal and non-polysomal (ribonucleoprotein, mRNP) fractionsof alfalfa embryos after UV-cross-linking. Many of the polypeptidesassociated with the polysomal and non-polysomal mRNAs were qualitativelysimilar, although their concentration in the two fractions wasdifferent. However, some developmentally stage-specific polypeptideswere found to be associated with the non-polysomal mRNA fractionduring the early stages of embryogenesis (precotyledonary) ofsomatic embryos. Thus the presence of mRNPs during embryogenesishas been demonstrated, and proteins intimately associated withthe mRNAs identified. Key words: Embryogenesis, translational control, protein synthesis, messenger ribonucleoproteins, alfalfa (Medicago sativa L.)     

Requirement of sodium chloride for the action of gibberellic acid in stimulating hypocotyl elongation of a halophyte, Salicornia herbacea L.

NaCl stimulated hypocotyl elongation of the halophyte Salicorniaherbacea L. grown either in light or dark. Its optimal concentrationwas around 0.1–0.2 M and its promoting effect was muchmore prominent in the dark. Gibberellic acid at 10^–5 Mstimulated hypocotyl elongation in light but not in the dark.Indole-3-acetic acid and kinetin were ineffective in promotinghypocotyl elongation. In light, gibberellic acid and NaCl synergisticallyenhanced hypocotyl elongation when both were given simultaneously.The action of NaCl could be replaced by KCl, but not by mannitol.Osmotic pressure of the epidermis of the Salicornia hypocotylincreased in response to gibberellic acid and/or NaCl treatment.Na⁺ content in the hypocotyl increased with NaCl application.Gibberellic acid and NaCl when given alone increased the extensibilityof the hypocotyl cell wall. Synergistic interaction in increasingthe extensibility was observed between gibberellic acid andNaCl. Stress-relaxation analysis of mechanical properties ofthe hypocotyl wall revealed that gibberellic acid and NaCl actedsynergistically in decreasing minimum relaxation time. Basedon these results, a possible mechanism by which gibberellicacid and NaCl regulate hypocotyl elongation of Salicornia herbaceaL., a typical halophilic plant, is discussed. ¹ Present address: Laboratory of Biology, Tezukayama College,Gakuen Minami, Nara 631, Japan. (Received June 13, 1978; )     

Development of the Fifth Leaf is Indicative for Whole Plant Performance at Low Temperature in Tomato

In the search for early-detectable selection criteria for growthat low temperature conditions in tomato, first the initiationand growth of individual leaves was analysed. Scanning electronmicroscopy revealed that the first four primordia had alreadydeveloped during the germination period at 25°C. The primordiumof the fifth leaf, however, was initiated after the transferof seedlings to the experimental conditions. The increase inlength of the first three leaves, and to a lesser extent ofthe fourth leaf, was considerably smaller in comparison withthat of later formed leaves. Moreover, the morphology of thefirst three to four leaves was deviant, whereas the others showedthe normal compound leaf architecture. All these results indicatedthat the fifth leaf was the earliest formed leaf with growthcharacteristics that might reflect the growth potential of thewhole plant. Development of the fifth leaf was tested as a marker for wholeplant growth. At three temperature, 18, 15 and 12°C, growthresponses of the fifth leaf were similar to that of whole plantsin four tomato genotypes: Line A, Line B, Premier and MXXIV-13.Significant differences in relative growth rate of dry weightof whole plants and fifth leaves (RGR_W)and of leaf area of thefifth leaves (RGR_LA between two fast growing and two slow growinggenotypes were found. No genotype by temperature interactionfor RGR_W and RGR_LA was found, indicating that the effect oftemperature decrease was similar for the four genotypes. The structure of the mature fifth leaf of one fast and one slowgrowing genotype, Line A and MXXIV-13, was analysed. For bothgenotypes, leaves were small and thick at low temperature, 12°C.The total number of epidermis and palisade parenchyma cellsper leaf was smaller but the size of the cells developed at12°C was larger than at 18°C. Consequently, the slowgrowth at 12°C was due to a low rate of cell division. Atboth temperatures, the fifth leaf to MXXIV-13 was smaller comparedto that of line A. Since the size of the cells were similar,the smaller leaf size was due to lower number of leaf cells. The results confirm the suitability of the growth, especiallyexpressed as RGR_LA , of the fifth leaf as a nondestructive marketfor vegetative development of tomato at low temperature. Growthdifferences between genotypes were mainly reflected by differencesin cell number of leaves, which might be correlated with geneticallydetermined differences in cell number of leaf primordia.Copyright1993, 1999 Academic Press Lycopersicon esculentum Mill. genotypes, plant growth, selection criteria, low temperature, leaf initiation, leaf development, RGR, leaf structure, cell expansion     

Arbuscular mycorrhizal fungi and water availability affect biomass and C:N:P ecological stoichiometry in alfalfa (<Emphasis Type="Italic">Medicago sativa</Emphasis> L.) during regrowth

Ecological stoichiometry has been widely studied in terrestrial ecosystems, but these studies have been limited in terms of symbiotic association between alfalfa and arbuscular mycorrhizal fungi (AMF), especially during regrowth. To evaluate the effect of AMF on the regrowth and C:N:P stoichiometry of alfalfa (Medicago sativa L.) under well-watered and drought conditions, alfalfa plants inoculated with AMF (Rhizophagus irregularis, M), nitrogen-fixing bacteria (Sinorhizobium, R), both nitrogen-fixing bacteria and AMF or no inoculations (CK) were evaluated in a pot experiment under controlled conditions. The biomass and organic carbon (C), nitrogen (N) and phosphorus (P) nutritional status of plant leaves and roots were measured under two water treatments during regrowth. Water deficit reduced the accumulation of dry matter and the concentrations of C and N in leaves and P in roots but increased the concentrations of P in leaves and C and N in roots of alfalfa during regrowth. Compared to CK plants, inoculation significantly improved the regrowth biomass and the concentrations of C, N and P in the leaves and roots and especially increased P levels when the plant were inoculated with AMF. However, this effect of microbes on alfalfa regrowth was dependent on the soil water status. Drought reduced the C:N and C:P in the leaves and the C:N in roots, while N:P and C:P increased in the roots. Inoculation of AMF decreased the C:P and N:P in the leaves and the C:N and C:P in the roots, whereas it increased the C:N under water stress. These results indicate that AMF play a significant role in regrowth and C:N:P ecological stoichiometry after defoliation by influencing C assimilation, N and P uptake and that the responses in the leaves and the roots are opposite.     

Environmental factors controlling the time of flower-opening in Pharbitis nil

Pharbitis nil, strain Violet, subjected to various photoperiods(24-hr cycle at 24?C) bloomed about 10 hr after light-off whenthe light period was 10 hr or longer, and about 20 hr afterlight-on when the light period was shorter. The higher the temperature(20–30?C) during the dark period, the later the time offlower-opening, with the temperature during the last half ofthe dark period having a stronger effect than that during thefirst half. In continuous dark or light, flower buds of Pharbitis openedabout every 24 hr at all temperatures tested between 20 and28?C, which suggests the participation of a circadian rhythmin determining the time of flower-opening. A light pulse given6–12 or 28–36 hr after the onset of the dark periodgreatly advanced the phase of this rhythm (8–10 hr). Phasedelay of this rhythm could not be obtained by light pulses givenat any time. (Received September 29, 1979; )     

Involvement of Endomannanase in the Control of Tomato Seed Germination under Low Temperature Conditions

The cause of differences in germination rates in a cold-toleranttomato line (PI341988), a control line (UC82B), and six progenylines stemming from crosses and backcrosses between the twoparent lines was investigated. Pursuant to earlier work showingthat differences in germination ability at 12°C are dueto the barrier imposed by the endosperm layer, we analysed theactivity of cell-wall-hydrolysing enzymes extracted from theselines. A significant increase in endomannanase activity wasfound in plant line PI341988 prior to germination at 12°C.Extracts of PI341988 seeds that had imbibed at either 12 or25°C exhibited higher endomannanase activity than theircounterparts from plant line UC82B. Moreover, a positive relationshipwas found between germination ability at low temperature andendomannanase activity in the six progeny lines. Analysis ofendomannanase activity in sub-regions of the seed indicatedthat the increase in activity prior to germination was higherin the micropylar endosperm cap than in the rest of the seed.Exogenous application of mannanase originating from soil-bornebacteria increased germination rates under both moderate andlow temperature conditions. Cellulase (endo-1,4-ß-glucanase)activity was also found to be higher in plant line PI341988.However, the activity of this enzyme probably increases aftergermination and it is therefore not considered as a key enzymecontrolling germination at low temperatures.Copyright 1995,1999 Academic Press Lycopersicon esculentum, tomato, seed germination, cell wall     

Effect of High-intensity Light Given Prior to Low-temperature Treatment on the Long-day Flowering of Pharbitis nil

Pharbitis nil, strain Violet which had been exposed to high-intensitylight (18,000 lux at 23?C) for 7 days followed by a low-temperaturetreatment (13–14?C) for 7 days initiated flower buds evenunder continuous light, but plants given these treatments inreverse order failed to bud. Three days of high-intensity lightat 23?C was most effective in promoting the flower-inducingeffect of the subsequent low-temperature period. Six days oflow temperature following the 3-day high-intensity light periodinduced near-maximum flowering response. DCMU (5?10^–6M) given during the high-intensity light period inhibited flowering,but when given during or after the low-temperature period itwas ineffective. DCMU at the same concentration given before,during or after an inductive 16-hr dark period at 26?C did notinhibit flowering. Sucrose, ATP, NADPH and some other reducingagents tested did not nullify the DCMU effect nor substitutefor the effect of high-intensity light. But, the high-intensitylight effect could be substituted, at least partly, by 5-chlorosalicylicacid, 3,4-dichlorobenzoic acid and some other benzoic acid derivatives,which are highly effective in inducing long-day flowering inthe short-day plant, Lemna paucicostata. (Received October 20, 1981; Accepted February 3, 1982)     

Effect of Temperature on the Activity of Carboxylases in Tropical and Temperate Gramineae

Temperate Gramineae show maximal net photosynthesis at 20–5°C, whereas tropical Gramineae have maxima between 30 and35 °C. Moreover, it has been suggested that different carboxylationreactions are involved in the two groups. The present studyof the temperature dependance of in vitro ribulose-1,5- diphosphate(RuDP), and phosphopyruvate (PEP) carboxylases indicates thatthe two enzymes have clearly marked differences in temperaturesensitivity. RuDP carboxylase, present in the temperate andtropical species studied, showed maximal activity around 20–5°C except in Zea. By contrast, PEP carboxylase activityin all species was maximal between 30 and 35 °C. The dataimply that activity and temperature sensitivity of the relevantcarboxylase enzymes may well be a significant limiting factorin leaf photosynthesis, even at light saturation.