Chemical modification studies on Ricinus communis (Castor Bean) agglutinin

Ricinus communis agglutinin was subjected to various chemical treatments and the effect on its hemagglutinating and saccharide-binding properties was studied. Acetylation, succinylation and citraconylation led to a complete loss in the activity of the agglutinin, whereas reductive methylation had no effect on the activity, showing that charged amino groups were involved in the hemagglutinating and saccharide-binding activity of Ricinus agglutinin. Modification of tryptophyl, arginyl and carboxyl-group-containing residues did not lead to any loss in the activity of the agglutinin. Acetylation of tyrosyl groups with N-acetylimidazole strongly reduced the hemagglutinating and saccharide-binding property of Ricinus agglutinin. The loss in activity was restored on deacetylation of the tyrosyl groups. Modification of tyrosyl residues also led to a change in the immunological properties of the agglutinin. The initial rate of modification of tyrosyl and amino groups and the concomitant loss of activity was reduced in the presence of lactose.     

Accumulation and Distribution of Nutrients in Fruits of Castor Bean (Ricinus communis L.)

The nutrition of developing fruits of Ricinus communis was studiednear Perth, Western Australia, where the species grows as aweed on poor sandy soil. Fruits required 60 days to mature anddehydration of the capsule began 20 days before the seeds ripened.Mature seeds accumulated 49 per cent of the fruit dry matterand over 80 per cent of its P, Zn and Cu, 50–80 per centof its Mg, N, Fe and Mn, 41–46 per cent of its S and Caand 11–21 per cent of its K and Na. Losses of nutrientsfrom capsules during fruit ripening were: Zn, 73 per cent, P,42 per cent, Cu, 23 per cent and Mn, 8 per cent. Dry matter,N, K, S, Ca, Mg, Na and Fe were not withdrawn from capsules.Apparent retranslocation from capsules could have provided from6–28 per cent of the Zn, Mn, P and Cu in mature seeds.Seeds from plants on poor sandy soil were small but had adequatelevels of nutrients when compared with those from plants growingon a fertile loam. Concentrations of all nutrients except P were higher in youngcapsules than in young seeds, but levels of N, P, Mg, Fe, Znand Cu were higher in mature seeds than in mature capsules.The intake of most nutrients by fruits was out of phase withdry matter accumulation, especially in capsules, and the elementsappeared to accumulate in fruit parts independently of eachother. Glutamine accounted for over 85 per cent of the amino-Nin phloem sap destined for fruits. Potassium made up over 90per cent of the inorganic cations in phloem exudate. Of theminor elements in the exudate, Fe was present at highest concentrationand Cu at the lowest. The results showed that retranslocation from the capsule madea very small contribution to the nutrition of seeds. It is suggestedthat R. communis would require a sustained supply of soil nutrientsto ensure maximum seed yield, partly due to the restricted retranslocationof most nutrients from capsules. Ricinus communis L., castor bean, mineral nutrition, translocation, retranslocation     

Identification and Characterization of GATA Gene Family in Castor Bean (Ricinus communis)

GATA proteins are considered to be broadly involved in yield associated biological process, such as photoresponse, chlorophyll biosynthesis, and carbon and nitrogen metabolism. Based on castor bean genome database, a total of 19 GATA genes were identified and classified into 4 subfamilies according to gene structure, protein structure and their phylogenetic relationships. Results exhibited that GATA factors were hydrophilic proteins. Analysis of gene structure and protein structure revealed the conserved structural features of GATA factors between castor bean and Arabidopsis thaliana. The high throughput RNA seq data were used to define the expressional profiles of GATA genes among tissues. The results showed that most of the castor GATA genes preferentially expressed in leaf and root in contrast to their expression in developing seeds. In particular, the expression of GATA genes responding to darkness treatment in leaves was detected using semi quantitative RT PCR. It was shown that expression of three genes was down regulated under darkness treatment, which suggests a role for GATA genes of castor bean in light mediated regulation. These results provide important theoretical basis to the functions identification of castor GATA genes and increase castor yields.     

Translocation and Metabolism of Ricinine in the Castor Bean Plant, Ricinus communis L

Ricinine-3,5-¹⁴C (N-methyl-3-cyano-4-methoxy-2-pyridone) administered to senescent leaves of Ricinus communis L. was translocated to all other tissues of the plant. Developing fruit and especially seeds were found to be labeled the most rapidly. Young growing leaves and other developing tissues of the plant imported ricinine from the senescent leaves much more quickly than mature leaves. Relative intensities of the radioactive ricinine imported and deposited in various tissues indicate a possible functional role of ricinine in the castor bean plant. Data on N-demethyl ricinine presented here may stimulate interest in the possible physiological role of the ricinine to N-demethyl ricinine interconversion.     

农杆菌介导的蓖麻转化体系优化

针对影响农杆菌侵染效率的主要因素进行条件优化,确立了以OD600为0.8的菌液侵染、预培养5 d后的外植体为最佳侵染条件;侵染外植体经过5 d的共培养并除菌后,转到含有250 mg/L Kan的培养基中进行再生诱导,获得了多株具有Kan抗性的再生植株;通过在共培培养基中添加20 mg/L AS,124 mg/L Na2S2O3和152.4 mg/L DTT,有效地抑制了侵染后外植体的褐化现象,提高了筛选阶段抗性芽的成活率;对具有Kan抗性的再生植株进行PCR和Southern blot验证,共获得18株包含外源基因的阳性转化株。     

Ionic Interactions of Petiole and Lamina During the Life of a Leaf of Castor Bean (Ricinus communis L.) Under Moderately Saline Conditions

Ion (K⁺, Na⁺, Mg²⁺, Ca²⁺ and Cl) flows and partitioning in thepetiole and lamina of leaf 6 of castor bean {Ricinus communisL.) plants growing in the presence of a mean of 71 mol m^–3NaCl were described by an empirical modelling technique. Thiscombined data on changes in ion contents of petiole and lamina,ion: carbon molar ratios of phloem bleeding sap and pressure-inducedxylem exudates of the leaf with previously described informationon the economies of C and N in identical leaf material. Datawere expressed as daily exchanges of ions in xylem and phloem,or depicted as models of ion balance and transport activityof petiole and lamina during four consecutive phases of leaflife. The early import phase was characterized by high intakeof K and Mg through phloem, and of Ca mainly through xylem,but only limited intake of Na and Cl. The next phase up to fullleaf expansion showed similar relative differences in xylemintake between ions and the onset of rapid phloem export fromthe lamina of K and Mg, some export of Na and Cl but scarcelyany of Ca. The next mature phase, marked by maximal photosynthesisand transpiration by the leaf, showed high xylem intake of allions in xylem. This was more than matched by phloem export ofMg and K, but by only fractional re-export of Na and Cl andagain very limited cycling through the leaf of Ca. The finalpre-senescence phase exhibited similar behaviour, but with generallygreater contribution to phloem transport from mobilization ofion reserves of the lamina. The petiole retained particularlylarge amounts of Na and Cl in its early growth, thereby protectingthe lamina from excessive entry of salt, but these petiolarpools, together with those or other nutrient ions, were laterpartially mobilized to the lamina via the xylem stream. Datawere discussed in relation to the relatively high salt toleranceexhibited by the species. Key words: Ricinus communis, xylem and phloem transport, ion balance, K+ economy, Na+ exclusion, NaCl-stress, salt tolerance, leaf development     

Temporal Patterns of Uptake, Flow and Utilization of Nitrate, Reduced Nitrogen and Carbon in a Leaf of Salt-Treated Castor Bean (Ricinus communis L.)

Changes in net photosynthesis, respiration, transpiration andcontents of total C, NO₃-N and reduced N were followed throughoutthe life of leaf 6 of nitrate-dependent plants of castor beanexposed to moderate salinity stress (71 mol m^–3 NaCl).Salt treatment was applied for measuring mineral flows in aparallel study (Jeschke and Pate, 1991b). Concurrent measurementswere made of solute composition and C: N molar ratios and concentrationsof reduced N and collected NO₃-N in phloem sap bleeding fromshallow incisions in the top and at the base of petioles andin xylem exudates from flaps of proximal leaf midribs followingpressurization of the root system. The resulting data were usedto construct empirical models of the respective economies ofC, total N, NO₃ and reduced N for a sequence of defined phasesof leaf life. Water use efficiency increased 3-fold from emergenceto a maximum of 1·5 mmol CO₂ mol^–1 H₂O before decliningto 0·5 mmol CO₂ mol^–1 H₂O at senescence. Xylemmolar ratios of C:N varied from 1·2–2·8,with nitrate always a smaller component than reduced N. Phloemsap C:N increased from 10–40 with leaf expansion and wasthen maintained in the range of 40–50 until falling steeplyto 20 at leaf senescence. Nitrate comprised less than 1% oftotal N in all phloem sap samples. The models of C uptake, flow,and utilization showed a major role of phloem import and thenincreasingly of laminar photosynthesis in providing C for leafgrowth. The carbon budget was thereafter characterized by ratesof phloem export closely matched to net rates of CO₂ fixationby the lamina. Corresponding data for total N depicted an earlymajor role of both xylem and phloem import, but the eventualdominance of xylem import as the N source for leaf growth. Cyclingof N by xylem to phloem exchange commenced before the leaf hadachieved maximum N content, and was the major contributor tophloem export until leaf senescence when mobilized N providedmost exported N. The nitrate economy of the leaf was characterizedby early establishment of tissue pools of the ion in the petioleand to a lesser extent in the lamina, continued high rates ofnitrate reduction in the lamina but negligible assimilationin the petiole, and a release through xylem of previously accumulatedNO₃ from petiole to lamina. Related data for reduced N illustratedthe much greater importance of this form of N than nitrate intransport, storage and cycling of N at all stages of leaf andpetiole life. Xylem to phloem interchanges of reduced N in petiolewere minimal in comparison with cycling through the lamina.The ratio of CO₂ reduction to NO₃ reduction in the lamina wasat first low (57 mol mol^–1) increasing to a peak valueof 294 during mature leaf functioning before declining to 190during the presenescence phase of leaf development. This patternreflected age-related effects on water use efficiency, changesin NO₃ levels in the xylem stream entering the lamina, and therelatively low photosynthetic performances of very young andsenescent laminae. Key words: Ricinus communis, leaf development, phloem transport, xylem transport, carbon, nitrogen, nitrate, reduced nitrogen, nitrate reduction, partitioning     

Polygalacturonase from Rhizopus stolonifer, an Elicitor of Casbene Synthetase Activity in Castor Bean (Ricinus communis L.) Seedlings

Apparently homogeneous polygalacturonase-elicitor purified from the filtrates of Rhizopus stolonifer cultures stimulates germinating castor bean seedlings to produce greatly increased levels of casbene synthetase activity. The purification procedure involved gel-filtration chromatography on Sephadex G-25 and G-75 columns followed by cation-exchange chromatography on a Sephadex CM C-50 column. Homogeneity of the purified preparation was indicated by the results of cationic polyacrylamide disc gel electrophoresis and isoelectric focusing (pI = 8.0). The identity of the casbene elicitor activity and polygalacturonase were indicated by the coincidence of the two activities at all stages of purification, the coincidence of both activities with the single protein-staining band detected on a cationic polyacrylamide disc gel and an isoelectric focusing gel, and the identical behavior of both activities on an agarose gel affinity column. The purified polygalacturonase-elicitor is a glycoprotein with approximately 20% carbohydrate content and an estimated molecular weight of 32,000 by polyacrylamide disc gel electrophoresis.     

Paclobutrazol Is Phloem Mobile in Castor Oil Plant (Ricinus communis L.)

It is commonly believed that the synthetic triazole growth regulator paclobutrazol (PAC) is exclusively xylem mobile within plants. By contrast, the triazole amitrole and many natural growth regulators are phloem mobile. This raises some doubt as to whether PAC must necessarily be exclusively xylem mobile. PAC was introduced into castor oil plants (Ricinus communis L.) through their hollow petioles. PAC was detected in xylem and phloem sap collected above the point of introduction but not in xylem sap below this point. This finding shows that PAC is not exclusively xylem mobile as believed previously. These results also raise the possibility of introducing PAC into plants in a different way so that it is carried by both the xylem and phloem and thus optimizing its effectiveness. Received February 25, 1997; accepted July 18, 1997     

Responses of Soybean Leaf Angle, Photosynthesis and Stomatal Conductance to Leaf and Soil Water Potential

The hypothesis that soil water potential (_s) is better correlatedto heliotropic leaf orientation, photosaturated photosyntheticCO₂ assimilation and stomatal conductance during periods oflimited water availability than is bulk leaf water potential(₁) was examined in greenhouse-grown soybean (Glycine max) plants,submitted to a progressive drought. Paired plants were exposedto either 1000 or 100 µmol m^–2 s^–1 photonflux densities (PFD) for 45–60 mins. The higher irradianceinduced short-term decreases in ₁, due to increased transpiration,while _l in the plant exposed to low PFD did not decrease. Thesechanges in ₁ occurred independently of changes in soil waterstatus. Concurrent to the light treatments, a single attachedleaf from each of the two plants was isolated from the restof the plant by shading, and the pulvinus of its terminal leafletwas exposed to a perpendicular PFD of 500 µmol m–²S^–1. Leaf movement of this leaflet was recorded in responseto this light, until a stable leaflet angle was achieved. Valuesof _s and _l (before and after light treatment), and photosaturatedrates of photosynthesis and stomatal conductance, were thenmeasured on these leaves. Leaflet angle and gas exchange werebetter correlated with _s (r² = 0.50, 0.50 and 0.57 for angle,photosynthesis and conductance, respectively) than with _l especiallywhen _l was the result of short-term, high-light induced changesin leaf water status (r² = 0.36, 0.32 and 0.49, for the sameparameters). Leaflet angle was also correlated with stomatalconductance (r² = 0.61) and photosynthetic rate (r² = 0.60),suggesting a close association between leaf orientation, leafmetabolism and soil water availability. Glycine max (L.) Merr. cv. Essex, soybean, heliotropism, water potential, photosynthesis, stomatal conductance, solar tracking     

Properties of Rhizopus stolonifer Polygalacturonase, an Elicitor of Casbene Synthetase Activity in Castor Bean (Ricinus communis L.) Seedlings

Some properties of the polygalacturonase-elicitor from the filtrates of Rhizopus stolonifer cultures have been examined in an attempt to understand its mode of action as an elicitor of casbene synthetase activity in castor bean seedlings. Both the polygalacturonase activity and the elicitor activity are heat-labile with similar heat-sensitivity profiles. Also, the catalytic activity of the enzyme is lost on treatment with sodium periodate, as had been shown previously for the elicitor activity. The pH optimum of the enzyme activity with polygalacturonic acid as the substrate is 4.9. Exposures of germinating castor bean seedlings to the elicitor for short-term periods of 1 to 10 minutes followed by washing and incubation in sterile, distilled water are partially effective in elicitation in comparison with the continuous exposure of the seedlings over 11 hours to the same amount of the elicitor. The initial rate of reaction catalyzed by the enzyme is about 3 times faster with polygalacturonic acid as a substrate than with partially (50%) methylated polygalacturonic acid (pectin). The K_m value of the enzyme for polygalacturonic acid is about 4.2 millimolar in terms of monomeric units and about 0.07 millimolar in terms of polymer concentration. Examination of the types of products formed by the action of the enzyme suggests that it is an endo-hydrolase. The amino acid composition of this enzyme is similar to those of other extracellular fungal proteins reported. The carbohydrate moiety of the glycoprotein polygalacturonase-elicitor is composed of 92% mannose and 8% glucosamine by gas chromatography-mass spectrometry analysis. The linkage group analysis of the carbohydrate moiety showed that mannosyl residues which are 1,2-linked comprise about 70% of the total glycosyl residues and demonstrated the presence of some 1,3,6- and 1,2,6-linked branching mannosyl residues.     

Photosynthesis Decrease and Stomatal Control of Gas Exchange in Abies alba Mill. in Response to Vapor Pressure Difference

The responses of steady state CO₂ assimilation rate (A), transpiration rate (E), and stomatal conductance (g_s) to changes in leaf-to-air vapor pressure difference (ΔW) were examined on different dates in shoots from Abies alba trees growing outside. In Ecouves, a provenance representative of wet oceanic conditions in Northern France, both A and g_s decreased when ΔW was increased from 4.6 to 14.5 Pa KPa⁻¹. In Nebias, which represented the dry end of the natural range of A. alba in southern France, A and g_s decreased only after reaching peak levels at 9.0 and 7.0 Pa KPa⁻¹, respectively. The representation of the data in assimilation rate (A) versus intercellular CO₂ partial pressure (C_i) graphs allowed us to determine how stomata and mesophyll photosynthesis interacted when ΔW was increased. Changes in A were primarily due to alterations in mesophyll photosynthesis. At high ΔW, and especially in Ecouves when soil water deficit prevailed, A declined, while C_i remained approximately constant, which may be interpreted as an adjustment of g_s to changes in mesophyll photosynthesis. Such a stomatal control of gas exchange appeared as an alternative to the classical feedforward interpretation of E versus ΔW responses with a peak rate of E. The gas exchange response to ΔW was also characterized by considerable deviations from the optimization theory of IR Cowan and GD Farquhar (1977 Symp Soc Exp Biol 31: 471-505).     

The Evolution of Mechanisms Driving the Stomatal Response to Vapor Pressure Deficit

Stomatal responses to vapor pressure deficit (VPD) are a principal means by which vascular land plants regulate daytime transpiration. While much work has focused on characterizing and modeling this response, there remains no consensus as to the mechanism that drives it. Explanations range from passive regulation by leaf hydration to biochemical regulation by the phytohormone abscisic acid (ABA). We monitored ABA levels, leaf gas exchange, and water status in a diversity of vascular land plants exposed to a symmetrical, mild transition in VPD. The stomata in basal lineages of vascular plants, including gymnosperms, appeared to respond passively to changes in leaf water status induced by VPD perturbation, with minimal changes in foliar ABA levels and no hysteresis in stomatal action. In contrast, foliar ABA appeared to drive the stomatal response to VPD in our angiosperm samples. Increased foliar ABA level at high VPD in angiosperm species resulted in hysteresis in the recovery of stomatal conductance; this was most pronounced in herbaceous species. Increased levels of ABA in the leaf epidermis were found to originate from sites of synthesis in other parts of the leaf rather than from the guard cells themselves. The transition from a passive regulation to ABA regulation of the stomatal response to VPD in the earliest angiosperms is likely to have had critical implications for the ecological success of this lineage.Plants continuously regulate transpiration by controlling the aperture of the stomatal pores on the surface of the leaf. The principal atmospheric determinant of stomatal aperture is the humidity of the air, which can be expressed as the vapor pressure difference between the leaf and the atmosphere. Stomatal responses to atmospheric vapor pressure deficit (VPD) have been well characterized across the diversity of vascular plant species (Darwin, 1898; Lange et al., 1971; Turner et al., 1984; Franks and Farquhar, 1999; Oren et al., 1999; Brodribb and McAdam, 2011; Mott and Peak, 2013), with stomata typically closing at high VPD and opening at low VPD. This comprehensive characterization has allowed for the development of highly effective empirical and mechanistic models of leaf gas exchange that provide robust predictions of the responses of transpiration to changes in VPD (Buckley et al., 2003; Katul et al., 2009; Damour et al., 2010; Medlyn et al., 2011). Despite the success of this modeling, the mechanism for the stomatal response to VPD remains poorly understood (Damour et al., 2010). Different hypotheses range from one extreme, whereby stomata respond passively through changes in leaf water content induced by the VPD or humidity perturbation (Lange et al., 1971; Mott and Peak, 2013), to the other extreme, whereby stomata close uniquely in response to the phytohormone abscisic acid (ABA; Xie et al., 2006; Bauer et al., 2013).From the earliest recognition that stomata open and close by changes in guard cell turgor (Heath, 1938), there have been many attempts to link the passive changes in water status that occur during VPD or humidity transitions with stomatal responses to VPD or humidity (Lange et al., 1971; Mott and Peak, 2013). Studies have suggested that changes in atmospheric water content passively drive stomatal responses by changing bulk leaf water status, which in turn changes guard cell turgor (Oren et al., 1999), or alternatively by changing guard cell turgor directly (Mott and Peak, 2013). Models based on these entirely passive processes are highly effective in predicting steady-state stomatal conductance (g_s) in response to changes in VPD or humidity in angiosperms (Mott and Peak, 2013).While hydraulic models provide robust predictions of steady-state g_s, they are less effective at predicting the dynamic responses of stomata to short-term perturbations, particularly with respect to the wrong-way responses that typically occur as transients (Buckley, 2005), as well as feed-forward behavior (Farquhar, 1978; Bunce, 1997; Franks et al., 1997; Tardieu and Simonneau, 1998; Ocheltree et al., 2014; compare with Mott and Peak, 2013). Although some of these models provide a pathway for incorporating the effect of ABA (Buckley, 2005), a lack of knowledge of ABA dynamics or action makes it difficult to integrate the influence of this active regulator of guard cell aperture into models. The stomatal behavior of single gene mutants (most notably the ABA synthesis and signaling mutants of Arabidopsis) strongly supports a role for ABA in mediating standard stomatal responses to changes in VPD. The stomata of these mutants are known to have less pronounced responses to a reduction in relative humidity compared with wild-type plants (Xie et al., 2006). Recently, molecular work has shown that guard cells express many of the genes required to synthesize ABA (Okamoto et al., 2009; Bauer et al., 2013), with molecular proxies for ABA level also indicating that the biochemical activity of ABA in the guard cell may increase following short-term exposure of leaves to a reduction in relative humidity (Waadt et al., 2014). These findings suggest a role for ABA in regulating stomatal responses to VPD and have led some to the conclusion that ABA synthesized autonomously by the guard cells is the predominant mechanism for stomatal responses to increased VPD (Bauer et al., 2013).Although the experimental evidence from molecular studies presents an argument for the role of ABA in the responses of stomata to changes in VPD, very few studies have quantified changes in ABA level in response to VPD. It is well established that ABA levels in leaves and guard cells can increase following the imposition of turgor loss or water stress (Pierce and Raschke, 1980; Harris et al., 1988; Harris and Outlaw, 1991). However, only a few studies have reported increases in foliar ABA level in response to high VPD (Bauerle et al., 2004; Giday et al., 2013), and none have investigated whether these observed dynamic changes or differences in ABA level were functionally relevant for stomatal control. In addition, no study has quantified the levels of ABA in guard cells during a transition in VPD.Here, we investigate the relative importance of ABA for the stomatal response to VPD in whole plants, sampled from across the vascular land plant lineage. We provide, to our knowledge, the first functional assessment of changes in ABA levels driving stomatal responses to VPD as well as critically investigate the recent suggestion that stomatal responses to VPD are driven by an autonomous guard cell synthesis of ABA.     

Evaluation of larvicidal efficacy of Ricinus communis (Castor) and synthesized green silver nanoparticles against Aedes aegypti L.

Aedes mosquitoes are the most important group of vectors that transmit pathogens, including arboviruses, and cause human diseases such as dengue fever, yellow fever, Zika virus, and Chikungunya. Biosynthesis and the use of green silver nanoparticles (AgNPs) is a vital step to identify reliable and eco-friendly controls for these vectors. In this study, Aedes (Ae.) aegypti larvae (2nd and 3rd instar) were exposed to leaf extracts of Ricinus communis (Castor) and AgNPs synthesized from the extract to evaluate their larvicidal potential. Synthesized AgNPs were characterized by UV–Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), and energy-dispersive X-ray spectroscopy (XRD). Ae. aegypti larvae were treated with different concentrations (50–250 ppm) of the leaf extract and synthesized AgNPs. There were five replicates per treatment, in addition to a positive (temephos) and negative control (dechlorinated water). Mortality was recorded after 12, 24, 36, and 48 h and the data were subjected to Probit analysis. The nanoparticles were more toxic (LC₅₀ = 46.22 ppm and LC₉₀ = 85.30 ppm) than the plant extract (106.24 and 175.73 ppm, respectively). The leaf extracts of Ricinus communis were subjected to HPLC analysis to identify their chemical constituents. This study suggests that plant extracts and synthesized nanoparticles are excellent alternatives to hazardous chemical pesticides used to control vector mosquitoes. This is a potentially useful technique that can reduce aquatic toxicity from insecticide use.     

Modelling of the Partitioning, Assimilation and Storage of Nitrate within Root and Shoot Organs of Castor Bean (Ricinus communis L.)

An experimentally-based modelling technique was developed todescribe quantitatively the uptake, flow, storage and utilizationof NO₃-N over a 9 d period in mid-vegetative growth of sandcultured castor bean (Ricinus communis L.) fed 12 mol m^–3nitrate and exposed to a mean salinity stress of 128 mol m^–3NaCl. Model construction used information on increments or lossesof NO₃-N or total reduced N in plant parts over the study periodand concentration data for NO₃-N and reduced (amino acid) Nin phloem sap and pressure-induced xylem exudates obtained fromstem, petiole and leaf lamina tissue at various levels up ashoot. The resulting models indicated that the bulk (87%) of incomingnitrate was reduced, 51% of this in the root, the remainderprincipally in the laminae of leaves. The shoot was 60% autotrophicfor N through its own nitrate assimilation, but was oversuppliedwith surplus reduced N generated by the root and fed to theshoot through the xylem. The equivalent of over half (53%) ofthis N returned to the root as phloem translocate and, mostly,then cycled back to the shoot via xylem. Nitrate comprised almosthalf of the N of most xylem samples, but less than 1% of phloemsap N. Laminae of leaves of different age varied greatly inN balance. The fully grown lower three leaves generated a surplusof reduced N by nitrate assimilation and this, accompanied byreduced N cycling by xylem to phloem exchange, was exportedfrom the leaf. Leaf 4 was gauged to be just self-sufficientin terms of nitrate reduction, while also cycling reduced N.The three upper leaves (5–7) met their N balance to varyingextents by xylem import, phloem import (leaves 6 and 7 only)and assimilation of nitrate. Petioles and stem tissue generallyshowed low reductase activities, but obtained most of theirN by abstraction from xylem and phloem streams. The models predictedthat nodal tissue of lower parts of the stem abstracted reducedN from the departing leaf traces and transferred this, but notnitrate, to xylem streams passing further up the shoot. As aresult, xylem sap was predicted to become more concentratedin N as it passed up the shoot, and to decrease the ratio ofNO₃-N to reduced N from 0·45 to 0·21 from thebase to the top of the shoot. These changes were reflected inthe measured N values for pressure-induced xylem exudates fromdifferent sites on the shoot. Transfer cells, observed in thexylem of leaf traces exiting from nodal tissue, were suggestedto be involved in the abstraction process. Key words: Ricinus communis, nitrogen, nitrate, nitrate reduction, partitioning, phloem, xylem, flow models     

Functional characterization of four sesquiterpene synthases from Ricinus communis (Castor bean)

Genome sequence analysis of Ricinus communis has indicated the presence of at least 22 putative terpene synthase (TPS) genes, 13 of which appear to encode sesquiterpene synthases (SeTPSs); however, no SeTPS genes have been isolated from this plant to date. cDNAs were recovered for six SeTPS candidates, and these were subjected to characterization in vivo and in vitro. The RcSeTPS candidates were expressed in either Escherichia coli or Saccharomyces cerevisiae strains with engineered sesquiterpene biosynthetic pathways, but only two (RcSeTPS1 and RcSeTPS7) produced detectable levels of product. In order to check whether the engineered microbial hosts were adequately engineered for sesquiterpene production, a selection of SeTPS genes was chosen from other plant species and demonstrated consistently high sesquiterpene titers. Activity could be demonstrated in vitro for two of the RcSeTPS candidates (RcSeTPS5 and RcSeTPS10) that were not observed to be functional in our microbial hosts. RcSeTPS1 produced two products, (−)-α-copaene and (+)-δ-cadinene, while RcSeTPS7 produced a single product, (E, E)-α-farnesene. Both RcSeTPS5 and RcSeTPS10 produced multiple sesquiterpenes.