Uptake and translocation of root-fed32P in response to foliar and root applications of CCC and phosfon inPisum sativum

The uptake and translocation of³²P applied to nutrient solutions, as influenced by (2-chloroethyl) trimethylammonium chloride (CCC) and 2, 4-dichlorobenzyltributylphosphonium chloride (Phosfon), were investigated in growth chambers. Specific effects depended on the “Retardin”, the method of application, and the concentration. Foliar applications of CCC had no significant effect on³²P uptake 5 h after feeding. At 20 and 80h after feeding, CCC at 100 and at 1 000 mg l^?1 decreased P uptake. With root applications of CCC the same concentrations decreased P uptake as early as 5h after feeding, while the 1 mg l^?1 concentration enhanced P uptake by 40% after 20h. Both the foliar and the root applications of Phosfon influenced P uptake 5h after feeding. With foliar applications the low Phosfon concentration of 0.01 mg l^?1 increased P uptake throughout the experimental period of 80h, but the magnitudes of enhancement declined from 109% at 5h to 63% at 80h. Similarly, the enhancement of P uptake due to the 0.1 mg l^?1 foliar treatment declined from 132% at 5h to 80% at 80h. 100 mg l^?1 CCC enhanced P translocation to the shoot in 5h, with magnitudes of 29% (foliar application) and 64% (root application). At 20 and 80h the stimulations were nullified. The highest concentrations (100 mg l^?1 CCC; 10 mg l^?1 Phosfon) enhanced P translocation 80h after feeding. There were thus general enhancements of P uptake at low concentrations and suppressions at high concentrations, but these effects diminished with time, indicating transitory influences.     

Interaction of Growth Retardants and Temperature in Growth, Flowering, Regeneration, and Auxin Activity of Begonia × cheimantha Everett

Soil application of CCC reduced stem and leaf growth in Begonia plants. This effect was evident with all concentrations tested at 18°C, whereas at 21 and 24°C no growth–retarding effect was observed with 2 × 10^?2 M CCC, and with 5 × 10^?3 M growth was even stimulated. Flowering was promoted by CCC in long day and neur–critical temperature, particularly under low light intensity in the winter. The formation of adventitious buds in leaves of plants grown at 21 and 24°C was stimulated when the plants received 5 × 10^?2 and 2 × 10^?2 M CCC, while 8 7times; 10^?2 M was inhibitory. In plants grown at 18°C bud formation was inhibited by all CCC concentrations. Root formation in the the leaves was usually stimulated by high CCC concentrations, while root elongation was reduced. The level of ether–extractable. acidic auxin (presumably IAA) in the leaves was lowered by CCC treatment of the plants, hut this required higher CCC concentrations at higt than at low temperature. When applied to detached leaves CCC stimulated bud formation at concentrations ranging from 10^?4 to 10^?2 M in leaves planted at 18 and 21°C. At 24°C budding was inhibited by 10^?2 M CCC, the lower concentrations being stimulatory also at this temperature. Root formation and growth were not much affected by CCC treatment of the leaves, but increased with the temperature. Soil application of Phosfon (4 × 10^?4 M) had no effect on growth and flowering, nov did it affect the subsequent regeneration of buds and roots in the leaves. In detached leaves Phosfon stimulated bud formation with au optimum at 10^?6 M. Root formation was stimulated by Phosfon at all temperatures, the optimal concentration being 10^?5 M, whereas root length was conversely affected. Foliar application of B-995 to intact plants and treatment of detached leaves greatly inhibited the formation of buds and had little effect on root formation. B-99D reduced the growth and delayed flowering in the plants.     

Vegetative Growth Responses of Pea Plants to CCC and Phosfon in Relation to Phosphorus Nutrition

The effects of 2-chloroethyltrimethylammonium chloride (CCC)and 2,4-dichlorobenzyl-tributylphosphonium chloride (Phosfon)on the growth of pea plants in sand culture at two rates ofapplied phosphorus (P), were studied in controlled-environmentgrowth chambers. CCC at 1 and 10 mg/1, and to a lesser degreePhosfon at 0.1 mg/1, stimulated growth. CCC at 1000 mg/1 andPhosfon at 100 mg/1 retarded growth, due mainly to shortenedstems. The magnitude of such effects depended on the level ofapplied P. Reductions in plant height by the 1000 mg/1 CCC treatmentwere 13 and 50 per cent respectively at the high (160 mg/1)and low (8 mg/1) rates of applied P. Similar decreases due to100 mg/1 Phosfon were 30 and 57 per cent respectively. At thehigh P rate, both CCC and Phosfon had no significant effecton total uptake of P, or on relative distribution in the leaf,stem, and root. At the low P rate, the root, relative to leafand stem, retained more P, at a CCC concentration of 1000 mg/1.With Phosfon at 100 mg/1 relative leaf P content increased whilethat of the stem and root decreased. Phosfon was more activethan CCC in terms of the concentration required to cause a givenmagnitude of growth effect.     

Effect of biotic and abiotic elicitors on production of betulin and betulinic acid in the hairy root culture of Betula pendula Roth

Abstract

Betulin (B) and betulinic acid (BA) are two triterpenoids with a wide range of biological and medicinal activities in different organs of Betula pendula. This research aimed to increase the accumulation of B and BA in the hairy root culture of B. pendula by seven biotic and abiotic elicitors. Hairy root was induced in the stem’s inner bark of B. pendula using the C58C1 strain in the WPM (Woody Plant Medium). The effects of different concentrations of elicitors and different time of root harvest in hairy root culture of B. pendula showed that highest level of growth index (GI), B, and BA was acquired in treated hairy roots with chitosan (CTS), chlorocholine chloride (CCC) and chitosan nano-fiber (CTS NF). Highest GI of B. pendula hairy roots was 13 that was obtained in the roots treated with CTS 150?mg l^?1 on the 8th day. The highest content of BA was 1.3?mg g^?1 DW after treatment with 1?mg l^?1CCC on the 4th and 6th days and 200?mg l^?1CTS NF on the 10th day. The highest B content (0.94?mg g^?1DW) was obtained in the treated hairy root by 2?mg l^?1 CCC after 4 and 6?days.     

Improved Tolerance of Teak (Tectona grandis L.f.) Seedlings to Low-Temperature Stress by the Combined Effect of Arbuscular Mycorrhiza and Paclobutrazol

Low-temperature damage is a common problem for tropical and subtropical plants during their early-growth stage. In this study, an experiment with a L₁₈ (2¹?×?3⁷) mixed orthogonal array in a greenhouse was conducted to determine whether arbuscular mycorrhizal fungi (AMF) inoculation and paclobutrazol (PBZ) application through foliar spray would enhance the chilling tolerance of teak seedlings. One-month-old seedlings of clones 8301, 7544, and 7552 from a Myanmar provenance propagated by tissue culture techniques were inoculated with Glomus versiforme and cultivated for 6?months. The foliar surface of both mycorrhizal and nonmycorrhizal treated plants was sprayed with PBZ at concentrations of 0, 50, and 100?mg?l^?1 once a week for 3?weeks prior to exposure to low temperatures of 6, 3, and 0°C for 12?h in an artificial climate chamber, followed by 12?h of recovery at 20°C room temperature. AMF colonization significantly promoted height and RCD growth and dry biomass accumulation of shoot and root. Under low-temperature stress, AM symbiosis increased leaf chlorophyll content by 22.8%, soluble protein content by 19.6%, superoxide dismutase (SOD) activity by 10.6%, and peroxidase (POX) activity by 9.5%, whereas malondialdehyde content was decreased by 14.1%. Both AMF colonization and the foliar spray PBZ at 50 and 100?mg?l^?1 were capable of alleviating the damage caused by low-temperature stress on teak seedlings by increasing the photosynthetic pigments, accumulation of osmotic adjustment compounds, and antioxidant enzyme (SOD and POX) activity, and by decreasing membrane lipid peroxidation. AMF colonization and foliar spraying of PBZ at 50?mg?l^?1 produced a positive interaction and appears to be a good way to enhance chilling tolerance of teak seedlings experiencing stress at 6, 3 and 0°C for 12?h.     

Interaction of indoleacetic acid with synthetic and native growth regulators during transfer of32P into epicotyls of etiolated pea seedlings

If both cotyledons are amputated from non-decapitated pea seedlings, the intensity of transport of³²P into intact epicotyls is raised more than twofold. This is apparently connected with the regulatory-inhibitory effect of the cotyledons that can be simulated by a 0·1% paste of indoleacetic acid (IAA). If both amputated cotyledons are replaced by this paste, the intensity of³²P transport is again decreased to the level found in plants with intact cotyledons. When etiolated pea seedlings grown in the dark in 100% relative humidity were decapitated, the³²P transport to the top of the epicotyl stumps covered with 0·5% IAA paste was strikingly decreased if the stumps were covered below with a 10% paste containing chlorocholine chloride (CCC) or with a 0·5% paste containing triiodobenzoic acid (TIBA). On the other hand, the intensity of³²P transport was significantly increased if the IAA paste was put above a 0·5% paste with kinetin which alone does not raise the transport intensity. No such synergism toward³²P transport could be established between IAA and gibberellin.     

In Vitro Regeneration of Achillea millefolium L from Shoot-tips and Root Segments of Seedlings

This report describes, for the first time, an efficient plant regeneration system for Achillea millefolium L (yarrow), a medicinal plant, via shoot multiplication from shoot-tips and adventitious shoot regeneration from root segments. Higher numbers of shoots were obtained when shoot-tips were cultured on MSMO medium supplemented with 3.0 mg l^?1 BA and 0.5 mg l^?1 IAA, or 5.0 mg l^?1 KIN and 1.0 mg l^?1 IBA, producing 17.3 and 17.0 shoots per explant at 100% frequency, respectively. For adventitous shoot regeneration, only root segments developed shoots when cultured on medium containing a combination of 1 mg l^?1 TDZ, 0.5 mg l^?1 IAA and 0.5 mg l^?1 GA3 (18.9 shoots per explant at 100% frequency), while other types of explants (i.e., cotyledons, leaf lamina and petiole segments) or hormonal combinations tested were found ineffective. Regenerated shoots rooted readily on MSMO medium containing different concentrations of IAA, IBA, NAA or 2,4-D, however, NAA at 0.5 mg l^?1, or IBA at 0.5 or 1.0 mg l^?1 were found to be the most productive. Nearly all of the regenerated plants (98%) survived through the hardening process when the rooted plantlets were kept at 55–65% relative humidity for 2 weeks, which were then planted in pots containing potting soil and kept at 25–35% humidity.     

Uptake, Distribution and Translocation of 32P Absorbed through Roots of Cotton Seedlings as Affected with CCC Treatment

The effects of CCC on the ³² P amounts absorbed by cotton seedlings were studied. CCC was applied to the seedlings either as spray or as addition to the nutrient solution in concentrations of 0, 25, 50, 100 and 200 mg/1. ³²P was added to the medium as KH₂³²P O₄ in the concentration of 40 μCi/50 ml. During the experimental period, no morphological changes were observed. The total ³²P uptake was inhibited in CCC treated seedlings. The application of CCC, both as spray and as addition to the medium, led to an accumulation of ³²P in stem, but to a decrease in root. The leaves showed different responses to different methods of application; spraying increased, while an addition of CCC to the medium decerases the ³²P content in the leaves. It is concluded that CCC inhibits ³²P uptake, whereas it ac accelerates the ³²P translocation from root to the aerial parts.     

Relative uptake of32P by cassava,banana, elephant foot yam and groundnut in intercropping systems

Absorption of applied³²P by the treated as well as neighbouring plants in two- and three-crop intercropping systems involving cassava (Manihot esculenta Crantz), banana (Musa (AAB) Mysore), elephant foot yam (Amorphophallus campanulatus Blume) and groundnut (Arachis hypogaea L.) was studied in field trials. Radiophosphorus applied to the root zone of one of the component species in the mixed systems was found to be absorbed not only by the treated plant but also by the neighbouring plants. Banana was the most dominant species in the cassava-banana-elephant foot yam intercropping system and accumulated the major portion of the radioactivity recovered in the whole system. Cassava planted on raised mounds absorbed³²P from the root zones of elephant foot yam and banana growing in the interspaces. Absorption of³²P from cassava mounds by elephant foot yam was negligible.In cassava-groundnut intercropping system, cassava was the dominant component accumulating about 96 to 99 per cent of the total³²P recovery in the system when the radiolabel was applied to cassava and about 48 to 88 per cent when applied to the intercrops depending on whether cassava was planted on paired row-ridge, mound or flat bed. The groundnut was able to absorb only negligible quantity of³²P from cassava root zone. The absorption of³²P by treated groundnut was highest in paired-row ridge method of planting and lowest in flat bed method of planting.     

Effects of 2-Chloroethyl Trimethylammonium Chloride (CCC) and 2-Chloroethylphosphonic Acid (CEPA) on Dry Matter Distribution in the Cowpea (Vigna Unguiculata L.)

Effects of foliar applications of CCC and CEPA on dry matterdistribution in two cowpea cultivars which exhibit differentdegrees of premature abscission of fruits were investigated.At the concentration of 0-1 mg1^–1, CCC increased stemweight in the cultivar Adzuki, but had no effect on the cv.Mala (which exhibits a relatively high degree of premature abscission).While CCC did not significantly influence root weight in Adzuki,the concentrations of 1 and 10 mg 1^–1 increased root weightin Mala. In both cultivars, the 1000 mg1^–1 treatment decreasedseed weight, with a greater decrease in Adzuki. All concentrations of CEPA, up to 1000 mg 1^–1, decreasedstem and root weights in Mala, and leaf weight in Adzuki. The10 mg1^–1 concentration increased seed weight in Mala by100 percent, and leaf weight by 28 percent, without any significanteffect on pod weight, or on the weight of the whole plant. Therewas also no increase in pod number. Overall, Mala was more responsive than Adzuki to the growthregulators, particularly CEPA. In the low concentration responses,CEPA increased seed weight not by increasing gross plant weight,but mainly by causing a change in distribution of dry matter.     

Menthol as an alternative anaesthetic and sedative for rainbow trout,Oncorhynchus mykiss

Menthol is known for its analgesic properties, but relatively little information is available on its potential as an anaesthetic on fish. The purpose of this study was to assess anaesthetic and sedative effectiveness of menthol and its safety in rainbow trout (Oncorhynchus mykiss). Juvenile rainbow trout 180 ± 28 g (mean ± SD) within a range of 152–208 g fish^?1 were individually exposed to menthol concentrations between 10 and 150 mg l^?1 and observed for behavioural responses, induction time to anaesthesia and recovery time. Menthol concentrations of 40–150 mg l^?1 induced anaesthesia with varying exposure times. There was an exponential relationship (p < 0.001) between induction time and menthol concentration. Menthol concentrations of 80–150 mg l^?1 induced anaesthesia within three minutes of exposure and fish recovered within three minutes. Induction and recovery data showed that 80 mg l^?1 was most suitable for anaesthesia in juveniles of this species. Concentrations of 10–20 mg l^?1 had sedative effects. Menthol stock solutions prepared using ethanol and acetone and storage time of stock solutions at room temperature for up to 48 h showed no significant differences in anaesthetic efficiency. When exposure time to menthol was kept constant at three minutes, 22% of fish had temporary cessation of gill ventilation. These fish had longer recovery times than those that did not show that response. Menthol was an effective anaesthetic and could be tested as a sedative for trout.     

Enhanced plumbagin production in <Emphasis Type="Italic">Plumbago indica</Emphasis> root cultures by ʟ-alanine feeding and in situ adsorption

Plumbagin is associated with potent antimicrobial and anticancer properties. However, due to poor supply of the natural product, efforts are being made to improve plumbagin biosynthesis and bioproduction. The aim of this work was to enhance production of plumbagin from root cultures of Plumbago indica L. through precursor feeding using l-alanine followed by in situ adsorption of plumbagin on the nonpolar copolymer adsorbent, styrene–divinylbenzene resin (Diaion^® HP-20). l-alanine fed at a concentration of 5 mM to 14 days old root culture followed by the sequential addition of Diaion^® HP-20 (10 g L^?1) after 36 h of l-alanine-fed significantly increased plumbagin production to 22.4 mg g^?1 dry weight (DW). The level of productivity obtained was 14- and 1.6-fold higher than that achieved using untreated root cultures (1.6 mg g^?1 DW) or l-alanine feeding alone (14.4 mg g^?1 DW) within 16 days of the culture. The results of this work suggest the use of precursor feeding in combination with in situ adsorption as an easy and cost effective tool for the large-scale production of medicinally valued compounds like plumbagin.     

Growth of Stigeoclonium and Oedogonium species in artificial ammonium-N and phosphate-P gradients

Four benthic filamentous Chlorophycean species (three Stigeoclonium species and one Oedogonium species) were obtained from two ditches, influenced, respectively, by the point discharges of pig farm and sewage treatment plant effluents. The ditches showed a gradual change in water chemistry, particularly with regard to ammonium-N and phosphate-P. The growth of the algae was studied in artificial ammonium-N (concentration range of 1–100 mg l^?1) and phosphate-P gradients (concentration range of 0.1–15 mg l^?1), which were based on concentrations of these nutrients in the ditches. Maximum growth in ammonium-N was attained for S. aestivale Hazen Z1 and S helveticum Vischer P4 at 50 mg l^?1, for S. aestivale Z4 and Oedogonium sp. Z4 at 10 mg l^?1, and for S. amoenum Kützing P2 at 5 mg l^?1. Maximum growth in phosphate-P was attained for S. helveticum P4 at 15 mg l^?1, for S. aestivale Z1 and S. amoenum P2 at 1.5 mg l^?1, and for S. aestivale Z4 and Oedogonium sp. Z4 at 1 mg l^?1.It is concluded that the ammonium-N and phosphate-P levels of ditches determined the distribution of the algae along the ditches, and therefore influenced the species composition of the periphyton communities.The study revealed a population differentiation with regard to ammonium-N in two closely adjacent populations of S. aestivale.     

Measurement of microbial biomass phosphorus in rhizosphere soil

³²P-labelled monocalcium phosphate solution was supplied by point injection to the root system of wheat plants grown in soil cores in a controlled environment. There was no detectable incorporation of³²P into organic P fractions in the soil remaining after roots were removed, confirming field observations. The techniques used to measure organic P (including biomass P) could detect an incorporation of³²P into soil microbial biomass equivalent to 0.3 μgP.g^?1 soil, compared to a total soil biomass P content estimated to be ca. 6.5 μgP.g^?1 soil. The limited incorporation of the added P into microbial biomass in the root-free soil may be due partly to a limited diffusion of³²P into the non-rhizosphere soil and partly to the removal of³²P-labelled microbial biomass adhering to or in very close association with the root surface. it is proposed that in studies of soil nutrient status, total soil biomass P (roots + soil flora + microfauna) should be measured, rather than attempting an estimate of microbial P. A sequential extraction procedure using a single soil sample, where a biocide is added to the extracting solution, is proposed as an alternative to the conventional procedure for measuring soil biomass P where two soil samples, one treated with a biocide, are extracted simultaneously.     

Induction of adventitious buds on the cotyledons ofAbies concolor x Abies grandis hybrid seedlings

Possibilities of adventitious buds induction on the cotyledons obtained from sterile seedlings ofAbies concolor xAbies grandis hybrid were investigated. The following variables influencing bud induction and their further development were studied: the effect of expiant age, the effect of different growth regulators and their concentrations and duration of their application. The most suitable expiants proved to be the cotyledons of 7 d old seedlings. The most efficient cytokinin was benzylaminopurine (S mg l^?1) in combination with napthaleneacetic acid (0.01 mg l^?1). The most optimal duration of treatment was 17 to 21 d culture of explants on induction medium. Shoot growth was achieved on basal medium to which 14 mg 1^?1 spermidine was added.     

Effect of Growth Retardants on α-Amylase Production in Germinating Barley Seed

The effect of growth retarding compounds, (2-chloroethyl)trimethylammonium chloride (CCC), 2-isopropyl-4-dimethylamino-5-methylphenyl-1-piperidinecarboxylate methyl chloride (AMU-1618), tributyl-2,4-dichlorobenzylphosphonium chloride (Phosfon D) and N-dimethylamino succinamic acid (B-995) on α-amylase production in germinating barley seed was studied. Seeds were germinated in growth retardants in presence and absence of gibberellic acid (GA₃). CCC, AMO-1618 and Phosfon D inhibitedα-amylase production in germinating seed and the effect was reversed by GA₃ Phosfon D and AMO-1618 were stronger inhibitors of α-amylase production than CCC. CCC was by far the strongest inhibitor of all the other analogs tested. B-995 was comparatively only slightly inhibitory. The results reported here, when viewed in light of the results of other workers, provide good evidence that CCC, AMO-1618 and Phosfon D inhibit α-amylase production by inhibiting the synthesis of gibberellin or gibberellin-like hormone(s) during germination of barley seed. Consistent with other reports, B-995 possibly acts by other mechanism (s).     

Dietary Supplementation of Zinc Nanoparticles and Its Influence on Biology,Physiology and Immune Responses of the Freshwater Prawn,Macrobrachium rosenbergii

The present study was conducted to assess the influence of dietary zinc nanoparticles (size 50 nm) on the growth, biochemical constituents, enzymatic antioxidant levels and the nonspecific immune response of the freshwater prawn, Macrobrachium rosenbergii post larvae (PL). The concentrations of dietary supplement zinc nanoparticles (ZnNPs) were 0, 10, 20, 40, 60 and 80 mg kg^?1 with the basal diet, and the level of Zn in ZnNP-supplemented diets were 0.71, 10.61, 20.73, 40.73, 60.61 and 80.60 mg kg^?1, respectively. ZnNP-incorporated diets were fed to M. rosenbergii PL (initial body weight, 0.18?±?0.02 g) in a triplicate experimental setup for a period of 90 days. ZnNP supplemented feed fed PL up to 60 mg kg^?1 showed significantly (P?<?0.05) improved performance in survival, growth and activities of digestive enzymes (protease, amylase and lipase). The concentrations of biochemical constituents (total protein, total amino acid, total carbohydrate and total lipid), total haemocyte count and differential haemocyte count were elevated in 10–60 mg kg^?1 ZnNP supplemented feed fed PL. However, the PL fed with 80 mg ZnNPs kg^?1 showed negative results. Activities of enzymatic antioxidants [superoxide dismutase (SOD) and catalase (CAT)], metabolic enzymes [glutamate–oxaloacetate transaminase (GOT) and glutamate–pyruvate transaminase (GPT)] and the process of lipid peroxidation (LPO) in the hepatopancreas and muscle showed no significant alterations in 10–60 mg kg^?1 ZnNP supplemented feed fed PL. Whereas, 80 mg ZnNPs kg^?1 supplemented feed fed PL showed significant elevations in SOD, CAT, LPO, GOT and GPT. Therefore, 80 mg ZnNPs kg^?1 was found to be toxic to M. rosenbergii PL. Thus, the study suggests that up to 60 mg ZnNPs kg^?1 can be supplemented for regulating survival, growth and immunity of M. rosenbergii.     

The ability of rufous hummingbirds Selasphorus rufus to dilute and concentrate urine

Most terrestrial animals face the challenge of having to conserve water in a desiccating environment. Not surprisingly, the ability to produce concentrated urine has been relatively well studied in birds. Nectar‐feeding birds are unusual among terrestrial animals in that they often ingest and excrete prodigious water volumes to obtain adequate energy. Thus, they confront the unusual challenge of having to conserve electrolytes. The diluting abilities of birds and the renal mechanisms that may correlate with them have been relatively neglected. To elucidate diluting and concentrating abilities in nectar‐feeding birds, we fed rufous hummingbirds Selasphorus rufus an electrolyte‐free nectar and a nectar containing a range of NaCl concentrations. Hummingbirds had a spectacular (and possibly unique) diluting ability: when fed on electrolyte‐free food they produced excreta containing less than 0.5 mM l^?1 each of sodium and potassium. Hummingbirds also had a poor concentrating ability, retaining sodium and chloride when their food (0.632 M l^?1 sucrose) contained more than 35 mM l^?1 of NaCl. The kidneys of hummingbirds do not appear to be suited for concentrating urine, and possibly contain structural features that give them a unique diluting ability compared with those of birds that do not feed on nectar.     

Integrated bioprocess for the stereospecific production of linalool oxides from linalool with Corynespora cassiicola DSM 62475

Linalool oxides are of interest to the flavour industry because of their lavender notes. Corynespora cassiicola DSM 62475 has been identified recently as a production organism because of high stereoselectivity and promising productivities [Mirata et al. (2008) J Agric Food Chem 56(9):3287–3296]. In this work, the stereochemistry of this biotransformation was further investigated. Predominantly (2R)-configured linalool oxide enantiomers were produced from (R)-(?)-linalool. Comparative investigations with racemic linalool suggest that predominantly (2S)-configured derivatives can be expected by using (S)-(+)-configured substrate. Substrate and product inhibited growth even at low concentrations (200?mg?l^?1). To avoid toxic effects and supply sufficient substrates, a substrate feeding product removal (SFPR) system based on hydrophobic adsorbers was established. Applying SFPR, productivity on the shake flask scale was increased from 80 to 490?mg?l^?1?day^?1. Process optimisation increased productivity to 920?mg?l^?1?day^?1 in a bioreactor with an overall product concentration of 4.600?mg?l^?1 linalool oxides.     

Direct Shoot Bud Formation and Tuberization from Aseptically Cultured Root Tubers of Calla Lily (Zantedeschia aethiopica L)

We describe here the development of a micropropagation protocol for mass multiplication of Zantedeschia aethiopica by using root tubers as explant. The surface sterilized root tubers produced five to six shoot-buds on semi-solid Murashige and Skoog’s (MS) medium with 10.0 mg l^?1 of 6-benzylaminopurine (BAP) and additives (50.0 mg l^?1 of ascorbic acid; 25.0 mg l^?1 each of adenine sulphate, L-arginine and citric acid). The cultures were multiplied by sub-culture of individual shoot bud produced in vitro and clumps of shoot buds generated in vitro in cultures on MS medium containing 3.0 mg l^?1 of BAP and additives. Further multiplication of propagules was achieved through tuber formation along with amplifying shoots on MS medium with 5.0 mg l^?1 of BAP. The micropropagated shoots were rooted both in vitro as well as ex vitro. Cent percent of the cloned shoots rooted in vitro within 15–18 days on hormone-free 1/2 strength MS salts with 200.0 mg l^?1 of activated charcoal. Alternatively 95–100% shoots rooted ex vitro under greenhouse conditions on soilrite after pulse-treatment with 500.0 mg l^?1 of Indole-3-butyric acid (IBA) or β-naphthoxyacetic acid (NOA) for 300 sec. The cloned plants were hardened in the greenhouse. The hardened plants were transplanted to soil for further acclimatization.