Effetti Morfologici,Anatomici Ed Ultrastrutturali Indotti Dai Ritardanti Di Crescita Su Plantule Di Pisum Sativum L. Var. « Gloria Di Quimper » Cultivate in Soluzione Nutritizia

Abstract

The effect of the growth retardants on the structure of Pea seedlings coltured in nutritive solution. – The addition of CCC (2-Chloro-ethyltrimethyl ammonium chloride) and AMO 1618 (4-Hydroxyl-5-isopropyl-2 methyl-phenyl-trimethylammonium chloride. 1-piperidine carboxylate) to Pea seedlings (Pisum sativum L. var. Gloria di Quimper) promotes the usual modifications induced by growth retardants on higher plants. CCC appears less effective than AMO 1618; CCC inhibits growth only at 10²-M. concentration, on the contrary 5×10-⁵M. AMO 1618 inhibits strongly the growth of the seedlings both in the light and in darkness. CCC and AMO 1618 operate similarly as far as the inhibition of expansion growth, the increase of the stem diameter, and the decrease of the apical dominance are concerned. 10-²M. CCC stimulates both the growth of roots and the secondary roots formation, on the contrary 2,5×10-⁴M. AMO 1618 inhibits strongly the growth of the roots. AMO 1618 affects more strongly than CCC the expantion growth of the leaves. Leaves of the AMO 1618 treated plants are greener than the control plants. Plants treated with CCC and AMO 1618 are smaller because these chemicals inhibit the expantion growth of the cells. The increase of the stem diameter induced by CCC and AMO 1618 is due to the stimulation of the mitotic activity of the cambium. AMO and CCC induce a decrease of the size of the vessels and the sieve tubes. In the sieve tubes of the treated plants and slime plugs appear near to the sieve plates many slime bodies. AMO and CCC did not affect the mitotic activity of the apical meristems; in fact the plants grown in the presence of the growth retardants, show a normal primary body. AMO and CCC delay the lignification process. Chloroplasts of this Pisum sativum variety show prolamellary bodies associated to a good lamellar system. Starch granules are always present. Starch was never found in the chloroplasts of the treated plants. The general picture of the effects induced by growth retardants in Pea seedlings show so many modifications that it is very difficult to believe, like some Authors suggest, that all the effects produced by growth retardants are due to the inhibition of gibberellin biosynthesis.     

Naturalizzazione E Riproduzione Spontanea Di Piante Ornamentali Nella Liguria Occidentale

Abstract

Effects of the growth-retarding compounds «CCC» and «AMAB» on the growth and alkaloidal content of Datura Stramonium L. — Datura Stramonium L. was administered two fortnightly-doses of 200 cc 10 ^-2 M solutions of (2-cloroethyl)-trimethylammonium chloride (CCC) or (allyl)-trimethylammonium bromide (AMAB), poured on the soil of every pot. In the treated plants were noted shorter and thicher stems and petioles and leaves larger in size and darker green than in the controls. Yields of leaves in CCC and AMAB-treated plants were not significantly changed while root fresh and dry weights were decreased. The per-cent concentration of total alkaloids in the leaves and roots of both CCC and AMAB-treated plants was not significantly different in comparison with that of normal plants. Therefore the A. assumes that the growth-retarding chemicals must not interfere with alkaloidal synthesis.     

Effects of CCC on Drought Resistance of Triticum aestivum, L and Zea mays, L.

Application of CCC to wheat and maize reduced transpirationin both soil and solution cultures. This reduction in transpirationwas a result of CCC reducing leaf area and increasing the root/shootratio. CCC-treated plants did not show an increased toleranceto internal water deficits induced by osmotic shocks or desiccation.CCC did increase the drought resistance of young wheat and maizeplants, but only by delaying the onset of severe internal waterdeficits, i.e. by drought avoidance.     

On the interaction of growth retardants with IAA and kinetin

In the pea test a highly positive response to the treatment with IAA reversed to a negative one or became 5 to 6 times weaker when CCC was applied together with IAA. In cultivating pea seedlings, following their decapitation, for two days in a 0.25 per cent CCC solution and then in water, growth of their cotyledonous axillaries (cotylaries) were inhibited. This inhibitive action of CCC could be made ineffective when the seedlings, following two-days’ cultivation in the CCC solution, were grown further in kinetin solutions (0.37–3 mg per 1). Cotylaries of decapitated pea seedlings, when grown in kinetin solutions were inhibited. With kinetin solutions of 6–12 mg/l a strong inhibition also occured in the growth of roots at the apical parts of which spherical swellings were developing. The CCC supplied to the roots of intact etiolated pea seedlings is translocated acropetally into the stem at a rate of about 5 cm per hour. Decapitation of the plant causes retardation of this transport, yet a coat of 0.00001–1% IAA or kinetin paste produces acceleration of the stream. Existence of an antagonism between CCC and IAA, demonstrated earlier, was found holding true also for B-9 (N, N-dimethyl-aminesuccinamic acid) and IAA, as the inhibitive action of B-9, 0.06% solution on the growth of lettuce hypocotyls was reduced to a highly significant degree when the plants were supplied with B-9 together with IAA at a concentration of 10 mg/l.     

Trichoderma harzianum SQR-T037 rapidly degrades allelochemicals in rhizospheres of continuously cropped cucumbers

To alleviate the stress of continuous cropping for cucumber continuous cropping (CCC) system, a beneficial fungus Trichoderma harzianum SQR-T037 (SQR-T037) was isolated and applied to soil to degrade allelochemicals exuded from cucumber plants in a Rhizobox experiment. The following phenolic acids (PAs), classified as allelochemicals, were isolated and identified from cucumber rhizospheres: 4-hydroxybenzoic acid, vanillic acid, ferulic acid, benzoic acid, 3-phenylpropionic acid, and cinnamic acid. Mixed PAs added in potato dextrose broth, each with 0.2 gram per liter, were completely degraded by SQR-T037 after 170 h of incubation. In Rhizobox experiments, inoculation of SQR-T037 in the CCC soil also degraded the PAs exuded from cucumber plant roots. This degradation was 88.8% for 4-hydroxybenzoic acid, 90% for vanillic acid, 95% for benzoic acid, and 100% for ferulic acid, 3-phenylpropionic acid, and cinnamic acid at 45 days after plantation. Simultaneously, a significant (p ≥ 0.05) decrease in the disease index of Fusarium wilt and an increase in dry weights of cucumber plants were obtained in pot experiments by application of SQR-T037. This was mostly attributed to degradation of PAs exuded from cucumber roots in CCC soil by SQR-T037 and alleviation of the allelopathic stress. Application of beneficial microorganisms, such as SQR-T037 that biodegrades allelochemicals, is a highly efficient way to resolve the problems associated with continuous cropping system.     

The antagonism of (2-Chlorethyl) trimethylammonium chloride and indole 3-acetic acid in epicotyl and axillary buds growth in the pea seedlings

The 0·03–0·06% indole-3-acetic acid (IAA) in lanoline paste smeared on the cut surface of decapitated epicotyl of the pea seedling inhibited the growth of the axillary buds of the cotyledons. 0·03–0·06% solution of (2-Chlorethyl) trimethylammonium chloride (CCC) considerably weakened the inhibitory effect of IAA when applied simultaneously to the roots. In a similar way CCC diminishes even the growth inhibition of intact pea epicotyls caused by 0·06% IAA lanoline paste. 0·03% solution of CCC administered to the roots of the decapitated pea seedlings significantly increased growth of the axillary buds. This effect may play a role in the demonstrated antagonism between the low concentration of CCC and IAA.     

Chromium Phytoaccumulation from Solution by Selected Hydrophytes

There is increasing interest in the role of wetland plants in the aquatic phytoremediation of toxic metals. In this experiment, we evaluate the Cr removal capacity of four hydrophyte species (Nasturtium officinale L., Veronica beccabunga L., Mentha longifolia L., R.Br., Cardamine uliginosa L.) under varying nutritional conditions (full-strength and half-strength solution cultures), and over a range of Cr concentration (0, 2, 4, 6, and 8 mg L^-1). The results indicate that Cr accumulation is affected by both initial Cr concentration and strength of the nutrient solution. Phytoaccumulation increased with initial Cr concentration and plants grown in the full-strength solution accumulated more Cr at the higher initial solution concentration. Cr was predominantly accumulated in the roots, with minimal shoot translocation, which limits the hazard of Cr entering the food chain through ingestion by animals. Accumulation was large and reached up to 6700 mg Cr Kg^-1 in the roots of Veronica beccabunga.     

The plant growth retardant CCC as inhibitor of gibberellin biosynthesis inFusarium moniliforme

Summary Gibberellin (GA) production inFusarium moniliforme (Gibberella fujikuroi) is suppresed by adding the plant growth retardant CCC [(2-chloroethyl)trimethylammonium chloride] to the culture medium. A concentration of 0.1 mg/l of CCC causes 50% inhibition whereas 10 mg/l and higher concentrations fully suppress GA production. Dry weight of the mycelium is not, or only slightly reduced in the presence of CCC.Thin-layer chromatography of acidic fractions of CCC-free cultures reveals fluorescent spots at 4 differentR _f values. No fluorescent spots can be detected on chromatograms of acidic fractions obtained from CCC cultures, thus demonstrating that production of all GA's is inhibited by CCC.If CCC is added to the medium 2 or 3 days after inoculation, further GA production is blocked, but the level of GA present at the time of CCC application is maintained. CCC does not enhance inactivation of GA₃ in sterile culture medium, nor in the presence of the fungus. It is therefore concluded that CCC inhibits the biosynthesis of GA in the fungus.Transfer of thoroughly washed mycelium from medium with CCC to fresh medium does not result in GA production because sufficient CCC is carried over in the mycelium to block GA biosynthesis completely.     

Re-sorption of organic compounds by roots of Zea mays L. and its consequences in the rhizosphere

The exudation of soluble carbon compounds from Zea mays roots was investigated over a 10 day growth period under sterile and non-sterile solution culture conditions. The results showed that plants grown in sterile static solution culture, where C was allowed to accumulate, released 8 times less C than plants grown under culture conditions in which the solutions were replaced daily. The increased C loss from plant cultures in which exudates were removed daily was attributable to, (a) the reduced potential for root re-sorption of previously lost C, and (b), increasing diffusion gradients between the root and the surrounding bathing solution increasing passive leakage of exudates from the roots. In treatments where C was removed daily from the root-bathing solution, 86% of the total C lost was of a soluble low molecular weight nature, whereas, in sterile and non-sterile static cultures, allowing the accumulation of C over 10 days, this was reduced to 67.5 and 48% respectively. The main C fluxes operating in a solution culture system (efflux and influx of C by both roots and microorganisms) were examined using a computer simulation model to describe movement of soluble sugar-C in both sterile and non-sterile conditions. In sterile static cultures where C was allowed to accumulate in solution over a 10 day growth period, 98% of the C exuded was re-absorbed by the plant. Where C was removed daily from the root-bathing solution this was reduced to 86%. The predicted patterns of C accumulation were similar to those found in the experiments. Simulations showed that the pattern of accumulation and final equilibrium concentrations were dependent on the rate of exudation, the spatial characteristics of exudation, solution volume, root growth rate and the presence of a microbial population. Simulations under non-sterile conditions showed that roots can compete with microorganisms for exudates in solution indicating the possible importance of re-sorption in a soil environment. The results clearly indicate that roots are capable of regulating the net amount of C released into a solution culture with the amount of C collected being highly dependent on the experimental conditions employed. The possible implications of soluble C influx on processes operating within the rhizosphere and in experimental systems is discussed.     

Partial Reversal by Cytokinin and (2-Chloroethyl)-Trimethylammonium Chloride of Near-Ultraviolet Inhibited Growth and Morphogenesis in Callus Cultures

Callus cultures of Haplopappus gracilis, Nicotiana tabacum and Allium cepa var. proliferum were in varying degrees inhibited by blue to near-UV light obtained from fluorescent tubes. The inhibition was considerably reduced for Haplopappus cultures by 6-(3-methyl-2-buten-1-ylamino)-purine (2 iP) and (2-chloro-ethyl)-trimethylammonium chloride (CCC) in combination. Even separately these compounds stimulated growth in blue but not in white light. A high concentration of 2 iP reduced the inhibiting effects of near-UV on tobacco tissue cultures, and a synergism was observed between 2 iP and CCC in respect to shoot formation in blue light. Allium callus was not significantly affected by CCC. It was also observed that the concentration of indol-3-acetic acid (IAA) was more important for the growth of tobacco cultures in blue than in white light. It is believed that the light-inhibition of growth is partly due to a photoinactivation of IAA and that 2 iP and CCC might be active through processes controlling the levels of IAA and other growth hormones.     

Transmission of Pepino mosaic virus by the Fungal Vector Olpidium virulentus

Transmission of Pepino mosaic virus (PepMV) by the fungal vector Olpidium virulentus was studied in two experiments. Two characterized cultures of the fungus were used as stock cultures for the assay: culture A was from lettuce roots collected in Castellón (Spain), and culture B was from tomato roots collected in Murcia (Spain). These fungal cultures were maintained in their original host and irrigated with sterile water. The drainage water collected from irrigating these stock cultures was used for watering PepMV‐infected and non‐infected tomato plants to constitute the acquisition–source plants of the assay, which were divided into six different plots: plants containing fungal culture A (non‐infected and PepMV‐infected); plants containing fungal culture B (non‐infected and PepMV‐infected); PepMV‐infected plants without the fungus; and plants non‐infected either with PepMV and the fungus. Thirty‐six healthy plants grouped into six plots, which constituted the virus acquisition–transmission plants of the assay, were irrigated with different drainage waters obtained by watering the different plots of the acquisition–source plants. PepMV was only transmitted to plants irrigated with the drainage water collected from PepMV‐infected plants whose roots contained the fungal culture B from tomato with a transmission rate of 8%. No infection was detected in plants irrigated with the drainage water collected from plots with only a fungus or virus infection. Both the virus and fungus were detected in water samples collected from the drainage water of the acquisition–source plants of the assay. These transmission assays demonstrated the possibility of PepMV transmission by O. virulentus collected from tomato crops.     

Hairy Root Culture for Mass-Production of High-Value Secondary Metabolites

ABSTRACT

Plant cell cultivations are being considered as an alternative to agricultural processes for producing valuable phytochemicals. Since many of these products (secondary metabolites) are obtained by direct extraction from plants grown in natural habitat, several factors can alter their yield. The use of plant cell cultures has overcome several inconveniences for the production of these secondary metabolites. Organized cultures, and especially root cultures, can make a significant contribution in the production of secondary metabolites. Most of the research efforts that use differentiated cultures instead of cell suspension cultures have focused on transformed (hairy) roots. Agrobacterium rhizogenes causes hairy root disease in plants. The neoplastic (cancerous) roots produced by A. rhizogenes infection are characterized by high growth rate, genetic stability and growth in hormone free media. These genetically transformed root cultures can produce levels of secondary metabolites comparable to that of intact plants. Hairy root cultures offer promise for high production and productivity of valuable secondary metabolites (used as pharmaceuticals, pigments and flavors) in many plants. The main constraint for commercial exploitation of hairy root cultivations is the development and scaling up of appropriate reactor vessels (bioreactors) that permit the growth of interconnected tissues normally unevenly distributed throughout the vessel. Emphasis has focused on designing appropriate bioreactors suitable to culture the delicate and sensitive plant hairy roots. Recent reactors used for mass production of hairy roots can roughly be divided as liquid-phase, gas-phase, or hybrid reactors. The present review highlights the nature, applications, perspectives and scale up of hairy root cultures for the production of valuable secondary metabolites.     

Some morphological and biochemical peculiarities of Datura innoxia callus- and regenerated cultures

Five nutrient media were tested for expression of morphological pathway in Datura innoxia callus cultures. Regenerants-rooted plants and non-rooted shoots obtained from three subsequent subcultures of callus cultures were assayed for tropane alkaloid content and composition. Although no wide variation of bio-chemical traits of regenerants was observed. For a given number of plants decrease of hyoscyamine in their roots was detected. Alkaloid content and composition of upper parts of plants having roots and shoots or lacking roots was studied-receiving an idea about biosynthesis of these organs.     

Modification of growth habit of Majestic potato by growth regulators applied at different times

The effect of gibberellic acid, CCC (2-chloroethyltrimethylammonium chloride) and B 9 (N-dimethylaminosuccinamic acid) was studied on growth of potato plants in pots. Growth was analysed on four occasions and changes in habit defined in terms of internode lengths, leaf areas and growth of lateral branches. Soaking seed pieces for 1 hr. in GA solution caused six internodes to elongate greatly, an effect not prevented by CCC applied when the shoot emerged from the soil. The effects on internode extension were determined by the length of the interval between GA treatment and CCC treatment. Treatment at emergence with CCC shortened all internodes and more CCC applied 4 weeks later had no effect. Late application of CCC or B9 shortened the top two lateral branches, usually very long in untreated plants. The regulators affected leaf growth differently from internode growth: usually growth regulators had less effect on leaf growth. Effects on growth depended on when the regulators were applied. Treatment with GA alone inhibited bud development at higher nodes than in untreated plants; when followed by late treatment with CCC, lateral growth at higher nodes was also less. CCC retarded development of lateral branches especially when applied early. B9 had a similar effect to CCC applied late. When regulators retarded growth of lower laterals, upper laterals often grew more than in untreated plants. Treatments did not affect the number of leaves on the main stem at first but later GA hastened senescence. GA increased the number of leaves on lateral stems, and the effect was enhanced by CCC. CCC alone increased the number of first- and second-order lateral leaves. GA lengthened and CCC shortened stolons. The effect of CCC persisted throughout the life of the plant. CCC or B 9 shortened stolons whenever applied. CCC hastened tuber initiation but slowed tuber growth. CCC at first retarded formation of lateral tubers but had no effect on the ultimate numbers of lateral and terminal tubers. The value of E (net assimilation rate) did not alter with time. CCC applied at emergence increased E, probably because it hastened tuber initiation and temporarily increased sink capacity. Although tubers formed earlier with CCC, their growth was slower and their demand for carbohydrate was also less. The increase in second-order laterals in CCC-treated plants indicates that they utilize carbohydrate that would normally go to tubers. This experiment also demonstrates that crowding leaves by shortening stems did not diminish E, possibly because another over-riding process (bigger sinks) offsets the effect of shading.     

Some effects of chromium toxicity on bush bean plants grown in soil

Summary Chromium applied to a noncalcareous soil at 50 ppm did not decrease yields of bush beans (Phaseolus vulgaris L. var Improved Tendergreen), but when EDTA (ethylenediamine tetraacetic acid) was added with it, it did. Very little Cr was present in leaves. In solution culture 10^-5 M Cr and higher were toxic. With solution culture the highest level of Cr in leaves was about 30 ppm and in general there was a decreasing gradient in Cr from roots to stems to leaves. EDTA had less effect in solution cultures on Cr toxicity because the Cr was already in solution. Chromium toxicity decreased cation levels in plants.     

Traits of transgenic Atropa belladonna doubly transformed with different Agrobacterium rhizogenes strains

Hairy root cultures of Atropa belladonna L. were established by infection either with Agrobacterium rhizogenes ATCC 15834 or MAFF 03-01724, and transgenic plants were obtained from both hairy root cultures. Doubly transformed roots were induced by re-infection of the leaf segments of transgenic Atropa belladonna plants (A. rhizogenes 15834) with MAFF 03-01724. Shoots and viviparous leaves were regenerated from the doubly transformed roots. The genetic transformation was determined by the opine assay (agropine, mannopine and/or mikimopine) and polymerase chain reaction. Physiological changes and tropane alkaloid biosynthesis in the hairy roots (singly and doubly transformed) were investigated. The alkaloid content in the doubly transformed root strain was intermediate as compared to the root strains which were singly transformed. On the other hand endogenous IAA levels in doubly transformed roots were significantly decreased compared to both singly transformed roots.Abbreviations BA benzyladenine - IAA indoleacetic acid - NAA naphthaleneacetic acid - PCR polymerase chain reaction - t-ZR trans-zeatin     

A New Tomato Mutant Inefficient in the Transport of Iron

An Fe-inefficient tomato mutant, T3238fe (Lycopersicon esculentum) was identified by growing the plants in solution cultures containing different concentrations of FeHEDTA. Approach grafts of T3238Fe (Fe-efficient) top on T3238fe rootstock and vice versa, located the cause of Fe inefficiency in T3238fe roots. The T3238Fe tomato takes up more Fe than T3238fe and it responds favorably to Fe-stress by releasing hydrogen ions from its roots, increasing reduction of Fe³⁺ to Fe²⁺ at its roots, and increasing the citrate concentration in its roots. T3238fe showed very little response to Fe stress; it was unable to absorb and transport adequate Fe from PeEDDHA to support growth.     

Genetic transformation of cauliflower (Brassica oleracea L. var. Botrytis) by Agrobacterium rhizogenes

Cauliflower plantlets were inoculated with different Agrobacterium rhizogenes strains. Numerous hairy roots were induced on cauliflower hypocotyls by agropine-type strains. Fewer roots were obtained with mannopine-type strains. In vitro cultures were established both from normal and hairy roots. Plant regeneration occured spontaneously from normal and transformed roots. Regenerated plants contained the same opines (if present) as root cultures. Some mannopine-positive regenerants displayed a modified phenotype. Relationships between phenotype, opine content, T-DNA content and/or expression are discussed.     

Rhizosphere mycoflora of wheat after foliar application of chlorocholine chloride,urea and 4-chloro-2-methylphenoxyacetic acid

A single-step spraying of wheat during shooting under field conditions with solutions of CCC (chlorocholine chloride), CCC and urea, CCC and Aminex (ammonium salt of 4-chloro-2-methylphenoxyacetic acid), or CCC, urea and Aminex caused changes both in numbers and composition of the rhizosphere mycoflora. The numbers both in the rhizosphere of differently treated plants and in the free soil decreased during vegetation. A more pronounced effect in the number of fungi was demonstrated in plants treated only with CCC. The difference was more considerable during first 10 days after the spray. As far as the relative occurrence of individual genera in the rhizosphere soil is concerned, fungi of the generaPenicillium Link ex Fr.,Fusarium Link ex Fr.,Verticillium Nees andTrichoderma Pers were most influenced after the treatment with the used agents.     

In Vitro Haustorium Development in Roots and Root Cultures of the Hemiparasitic Plant Triphysaria Versicolor

Parasitic plants in the Orobanchaceae invade host plant roots through root organs called haustoria. Parasite roots initiate haustorium development when exposed to specific secondary metabolites that are released into the rhizosphere by host plant roots. While molecular approaches are increasingly being taken to understand the genetic mechanism underlying these events, a limitation has been the lack of a transformation system for parasitic plants. Since the haustorium development occurs in roots of Orobanchaceae, root cultures may be suitable material for transient or stable transformation experiments. To this end, root cultures were obtained from explants, and subsequently calluses, from the hemiparasitic plant Triphysaria versicolor. The cultured roots retained their competence to form haustoria when exposed to host roots, host root exudates, or purified haustorium-inducing factors. The root culture haustoria invaded host roots and initiated a vascular continuity between the parasite and host roots. The ontogeny of haustoria development on root cultures was indistinguishable from that on seedlings roots. Root cultures should provide useful material for molecular studies of haustorium development.