Promotion and inhibition by ethylene of chlorophyll degradation in orange fruits

The effect of ethylene concentration on chlorophyll destruction in orange (Citrus sinensis cV. Washington Navel) fruits was examined at 15 °C and 25 °C. The reflectance of the fruits at 680 nm was measured, and the results converted to chlorophyll concentrations through an empirically derived formula based on the Kubelka-Munk equation. In all ethylene treatments chlorophyll destruction was faster at 25 °C than at 15 °C and all ethylene concentrations tested increased the rate of loss at 25 °C. At 15 °C the highest rate of chlorophyll destruction was observed at 1 μl litre^-1 ethylene, while chlorophyll loss at 1250 μl litre^-1 was slower than in untreated fruits.     

Post-harvest age-induced seed dormancy of Acer ginnala and its alleviation by growth regulator and low temperature treatments

One-month-old fruits of Acer ginnala with winged pericarp attached gave 44% germination and this was not increased by cold treatment at 4°C for 0, 10, 20, or 30 days, gibberellic acid treatment at 0, 1, 10, 100 or 1000 mg litre^-1, or ethephon treatment at 0, 2, 20, 200 or 2000 mg litre^-1. After 6 months of storage at 20–25 °C, germination of untreated fruits fell to 5% but could be restored to that of 1-month-old fruits by incubation at 4 °C for 30 days. After 9 months storage, no germination occurred in untreated fruits. Cold treatment (30 days at 4 °C partially restored germination (26%). Treatment with either gibberellic acid (1000 mg litre^-1) and 30 days at 4 °C (40%) or ethephon (100 mg litre^-] and 30 days at 4 °C improved germination (69%). The combination of all three treatments, i.e. 100 mg litre^-1 gibberellic acid, 100 mg litre^-1 ethephon and 30 days at 4 °C, optimised germination (86%). Thus, dormancy of A. ginnala developed during storage but could be reversed by a combination of treatment with low temperature and growth regulators. The highest germination (86%) was achieved after low temperature and growth regulator treatment of stored fruit.     

Nitrogen fertilisation and light effects on growth and photosynthesis of lodgepole pine seedlings

Seedlings of Pinus contorta were grown for 16 wk without ectomycorrhizas in the greenhouse at three levels of irradiance (100, 210 and 470 μEm^-2s^-1) and three levels of ammonium nitrate (3, 62 and 248 mg litre^-1 of N). Measurements at 5, 10 and 16 wk of age indicated that plants receiving the highest levels of irradiance and nitrogen had significantly larger biomass, a higher total foliar N and P content and net photosynthesis per unit leaf area than those at lower levels of each factor. Although the root/shoot ratio also increased from low to high irradiance at each harvest, nitrogen application resulted in an increased ratio from 3 to 62 mg litre^-1 N, but decreased ratio at 248 mg litre^-1 N.     

Effects of 1-methylcyclopropene alone and in combination with polyethylene bags on the postharvest life of mango fruit

Experiments were conducted to determine how 1‐methylcyclopropene (1‐MCP) treatments influence ethylene‐stimulated ripening of harvested mango cv. Zihua fruit at 20°C. The ripening response of fungicide (prochloraz) treated fruit was characterised following various 1‐MCP treatments in sealed jars followed by storage in polyethylene bags and/or subsequent ethephon (ethylene) exposure. Exposure of fruit to increasing concentrations of 1‐MCP for 12 h resulted in the reduced softening of produce when subsequently held in air for 7 days after ethephon treatment. Application levels of between 1 and 100 μl litre^?1 1‐MCP had increasing impact, while 200 μl litre^?1 1‐MCP apparently began to approach response saturation. Exposure of fruit to 50 or 100 μl litre^?1 concentrations of 1‐MCP for periods from 1 to 24 h subsequently resulted in reduced softening of produce when held in air for 7 days after ethephon treatment. Increasing periods of exposure from 1 to 12 h had increasing impact, while exposure times greater that 12 h appeared to reach saturation. In the absence of ethephon‐stimulation, the natural ripening of mangoes held in polyethylene bags was delayed by prior exposure to 100 μl litre^?1 1‐MCP for 12 h. Extended holding of 1‐MCP treated and non‐1‐MCP treated control fruit in polyethyene bags encouraged physiological and pathological deterioration. Following exposure to 100 μl litre^?1 1‐MCP for 12 h, mango fruit held for 10 days in polyethylene bags showed a delay in the onset of ripening relative to bagged but non‐1‐MCP treated control fruit. Treatment with 1‐MCP allowed storage of mango fruit in plastic bags at 20°C for 30 days. Observations suggest that 1‐MCP treatments do not adversely influence the quality of the post‐storage ethephon‐ripened fruit. Thus, application of 1‐MCP in combination with the use of polyethylene bags can extend the postharvest life of mango fruit at ambient temperature. Treatments that extend postharvest life are important in developing countries, such as China, where the cold chain infrastructure is often lacking.     

Effects of carbonyl sulfide, methyl iodide, and sulfuryl fluoride on fruit phytotoxicity and insect mortality

Three potential chemical fumigants: carbonyl sulfide (COS), methyl iodide (MI) and sulfuryl fluoride (SF) were tested at selected dosages on lemons against California red scale (Aonidiella aurantii) and MI and COS were tested on nectarines against codling moth (Cydia pomonella). In nectarines, COS was tested at 0, 20, 40, 60 and 80 mg litre^?1, MI at 0, 10, 15, 20 and 25 mg litre^?1. Both fumigants intensified nectarine peel color, delayed fruit softening, but did not alter overall fruit quality. COS at 80 mg litre^?1 resulted in 87% codling moth mortality, but the fumigant dosage was insufficient to reach the desired probits 9 level (99.9968%). MI gave 100% codling moth mortality at 25 mg litre^?1. Lemons were treated with MI at 0,10,20,40,60 mg litre^?1, SF at 0,10,20,40, 80 mg litre^?1 and COS at 0,20,40, 60 and 80 mg litre^?1. MI gave 100% red scale mortality at ≥40 mg litre^?1 but caused significant fruit injury. Conditioning lemons at 15°C for 3 days before MI fumigation lessened lemon phytotoxicity. Forced aeration at 3.5 standard litres per minute of lemons for 24 h following MI fumigation at 20 mg litre^?1 significantly reduced phytotoxicity compared to 2 h postfumigation aeration after MI treatment. SF at ≥40 mg litre^?1 gave 100% red scale mortality but resulted in commodity phytotoxicity. Lemons treated with the highest selected dose of 80 mg litre^?1 COS gave only 87% kill of red scale, but failed to reach the desired probit 9 level.     

Effect of imidacloprid on the sivlerleaf whitefly, Bemisia argentifolii Bellows and Perrring (Homoptera: Aleyrodidae), and whitefly parasitism

Bioassays were conducted under greenhouse conditions to determine the effect of imidacloprid on adult and nymphal stages of the silverleaf whitefly, Bemisia argentifolii Bellows and Perring, and parasitism by Encarsia formosa (Gahan). A flowable formulation (24Oglitre^-1) of imidacloprid at six rates (0.09, 0.04 and 0.02 g a.i. litre^-1 pot volume for experiments 1 and 2; 0.009, 0.004, and 0.002 g a.i. litre^-1 pot volume for experiment 3) was evaluated. After a 48 h exposure to treated plants, high mortality of adult whitefly (>94%) was observed. Adults exposed to poinsettias treated 150 days earlier also had significantly greater mortality (>79%) than the adults on control plants. When exposed to treated plants for only 6 h, >65% of adults were killed. All three rates of imidacloprid caused >97% mortality of immature whiteflies by day 19. When treated plants were continually exposed to adult whiteflies, immature mortality was 100% for the three higher rates of imidacloprid up to and including 88 days after treatment. During the same time, emerging adults were reduced significantly. Immatures reinfested on plants treated 161 days earlier, incurred 80% mortality at the higher rate 0.09 g a.i. litre^-1 pot volume and 38% mortality at 0.02 g a.i. litre^-1 pot volume. At lower treatment rates, results varied. At 0.009 g a.i. litre^-1 of pot volume, mean percentage whitefly mortality (65%) 25 days after treatment was significantly higher than the controls; however, whitefly mortality at 0.004 and 0.002 g a.i. litre^-1 pot volume was not significantly different from controls or plants treated with the higher rate. Parasitoids could develop to the adult stage on whiteflies infesting imidacloprid treated plants. Parasitism occurred at low levels (< 10%), doe to high levels of whitefly mortality on treated plants. No phytotoxicity was observed for any treatment throughout the length of the trials that lasted through flowering.     

Effects of ethylene and acetylene on mango fruit ripening

Mangoes (var. Tommy Atkins) were exposed to ethylene and acetylene over a range of concentrations at high humidity for 24 h at 25°C, then ripened in air alone. Ripeness was assessed after 4 and 8 days by analysis of texture, colour development, soluble solids and acid contents. Ethylene in air at concentrations of 0.01 ml litre^-1 and above or acetylene at 1.0 ml litre^-1 were found to initiate ripening. Treatment with 0.01 ml litre^-1 acetylene resulted in limited softening but had no effect on the other ripening changes analysed. Individual ripening processes responded differently to treatment: texture changes were most rapidly affected, while the rate of acidity losses was often reduced in ethylene treated fruits. Acetylene-treated fruits at concentrations of 0.01 and 0.1 ml litre^-1 showed delayed ripening when compared to those treated with either 1.0 ml litre^-1 acetylene or ethylene. Increased acetylene concentrations of 2.0 ml litre^-1 gave a similar response to 1.0 ml litre^-1, although in some instances there were indications of inhibitory effects.     

Efficacy of alternatives to antibiotic chemicals for the control of fire blight of pears

The efficacy of various chemicals as alternatives to antibiotics for the control of fireblight (Erwinia amylovora) on pear trees was tested. The chemicals were applied in two ways. In 1999 and 2000, preselected pear twigs (80–90% bloom stage) were sprayed once either preventively 1 day before inoculation or curatively one or three days after artificial inoculation with pathogen concentrations of 10⁵ and 10⁷cfu ml^?1. In 2000 and 2001, whole trees were sprayed 2 and 4 days before artificial inoculation of the flowers. From the incidence of diseased flowers it appeared that Bion (50% benzothiadiazole) at 0.2 g litre^?1 H₂O and Aliette (80% fosetyl‐Al) at 2.5 g litre^?1 H₂O showed considerable preventive action by eliciting systemic acquired resistance mostly when they were applied in the whole trees. However the best control was achieved with the antibiotic Agrept (20% streptomycin) at 0.5 g litre^?1 H₂O. This showed both preventive and curative action. Kocide (77% copper hydroxide) at 0.9 g litre^?1 H₂O, Dentamet (citric acid in chelate) at 1.5 ml litre^?1 H₂O, Bactosan (an extract from the plant Pongamia pinnatd) at 3.0 g litre^?1 H₂O and Bion at 0.1 g litre^?1 H₂O, showed preventive action, but only when the inoculum concentration was low.     

The effect of imazalil in the control of decay in yellow yam caused by Penicillium sclerotigenum

A strain of Penicillium sclerotigenum isolated from decaying yellow yams (Dioscorea cayenensis) was found to have developed resistance to benzimidazole fungicides and the use of imazalil was investigated as an alternative agent for controlling it. Two formulations were tested and proved to be equally effective in controlling decay at a concentration of 50 mg imazalil litre^-1 if the yams were dipped in it for 5 s; concentrations down to 10 mg litre^-1 were effective if the immersion time was increased to 5 min or more. These treatments gave good control of decay when applied up to 24 h after inoculation but were less effective when application was 48 h after inoculation, although at 500 mg litre^-1 there was some indication that levels of decay were decreased when compared with untreated tubers. Fungal penetration was unaffected or increased by increasing delays in the time of the fungicide application depending on the concentration applied. In trial shipments of yams from Jamaica to Britain imazalil alone was less effective in controlling overall decay because of the presence of a Rhizopus species. This could be controlled by the addition of dichloran to the dip. Imazalil residues were highest in the peel; levels in the peeled tuber varied and tended to decrease during storage but were generally in the range of 0·5 - 0·8 mg kg^-1 which is higher than the maximum levels accepted for other produce. A simple cooking test showed that residues in treated yam slices declined by about one third after boiling the slices in water for 45 min.     

Phytotoxic Effects and Phytochemical Fingerprinting of Hydrodistilled Oil,Enriched Fractions,and Isolated Compounds Obtained from Cryptocarya massoy (Oken) Kosterm. Bark

The hydrodistilled oil of Cryptocarya massoy bark was characterized by GC‐FID and GC/MS analyses, allowing the identification of unusual C₁₀ massoia lactone ( 3 , 56.2%), C₁₂ massoia lactone ( 4 , 16.5%), benzyl benzoate ( 1 , 12.7%), C₈ massoia lactone (3.4%), δ‐decalactone ( 5 , 1.5%), and benzyl salicylate ( 2 , 1.8%) as main constituents. The phytotoxic activities of the oil, three enriched fractions (lactone‐rich, ester‐rich, and sesquiterpene‐rich), and four constituents (compounds 1, 2, 5 , and δ‐dodecalactone ( 6 )) against Lycopersicon esculentum and Cucumis sativus seeds and seedlings were screened. At a concentration of 1000 μl/l, the essential oil and the massoia lactone‐rich fraction caused a complete inhibition of the germination of both seeds, and, when applied on tomato plantlets, they induced an 85 and 100% dieback, respectively. These performances exceeded those of the well‐known phytotoxic essential oils of Syzygium aromaticum and Cymbopogon citratus, already used in commercial products for the weed and pest management. The same substances were also evaluated against four phytopathogenic bacteria and ten phytopathogenic fungi, providing EC₅₀ values against the most susceptible strains in the 100–500 μl/l range for the essential oil and in the 10–50 μl/l range for compound 6 and the lactone‐rich fraction. The phytotoxic behavior was related mainly to massoia lactones and benzyl esters, while a greater amount of 6 may infer a good activity against some phytopathogenic fungi. Further investigations of these secondary metabolites are warranted, to evaluate their use as natural herbicides.     

Propagation of lettuce (Lactuca sativa) breeding material by tissue culture

A tissue culture method using Murashige and Skoog's (MS) medium was devised to propagate healthy plants from field grown lettuce plants selected for seed production. Explants (2–3 mm long) from axillary buds were successfully grown on MS + 1.0 or 2.0 mg litre^-1 kinetin and 6.4 mg litre^-1 IAA to promote shoot growth. Concentrations of 0.5 and 4.0 mg litre^-1 kinetin gave poor shoot growth. The cultures were successfully rooted after 3–4 wk on MS + 6.4 mg litres^-1 IAA after transfer from MS + 1.0 mg litre^-1 kinetin and on MS + 4.8 mg litre^-1 IAA after transfer from MS + 2.0 mg litre^-1 kinetin. Concentrations of 3.2 and 8.0 mg litre^-1 IAA gave poor root initiation. Root initiation was more successful when cultures were grown at 40 Wm^-2 than in cultures grown at 5 Wm^-2. Rooted cultures were established in compost with a 90–95% success rate and the regenerated plants flowered c. 18 wk after the cultures were initiated.     

Effects of three modern insecticides, pyriproxyfen, spinosad and tebufenozide, on survival and reproduction of Chrysoperla carnea adults

Three novel insecticides, pyriproxyfen, spinosad and tebufenozide, were evaluated for their effect on survival and reproduction of Chrysoperla carnea adults using two methods of exposure: direct contact and ingestion. Pyriproxyfen and tebufenozide proved to be harmless to adult survival, whereas spinosad 72 h after treatment reduced the number of adults by 39.8% and 87.2% in topical and ingestion treatment at the maximum concentration recommended (800 mg a.i. litre^?1). Fecundity was not affected irrespective of the insecticide or time of application (before or after the onset of oviposition). Concerning fertility, only pyriproxyfen exerted a negative effect on hatching when the eggs were deposited by females treated by ingestion in the post‐oviposition period at the highest concentration tested (150 mg a.i. litre^?1).     

Effects of atmospheric CO2 enrichment and root restriction on leaf gas exchange and growth of banana (Musa)

The effects of atmospheric CO₂ enrichment and root restriction on photosynthetic characteristics and growth of banana (Musa sp. AAA cv. Gros Michel) plants were investigated. Plants were grown aeroponically in root chambers in controlled environment glasshouse rooms at CO₂ concentrations of 350 or 1 000 μmol CO₂ mol^-1. At each CO₂ concentration, plants were grown in large (2001) root chambers that did not restrict root growth or in small (20 1) root chambers that restricted root growth. Plants grown at 350 μmol CO₂ mol^-1 generally had a higher carboxylation efficiency than plants grown at 1 000 μmol CO₂ mol^-1 although actual net CO₂ assimilation (A) was higher at the higher ambient CO₂ concentration due to increased intercellular CO₂ concentrations (C_i resulting from CO₂ enrichment. Thus, plants grown at 1 000 μmol CO₂ mol^-1 accumulated more leaf area and dry weight than plants grown at 350 μmol CO₂ mol^-1. Plants grown in the large root chambers were more photosynthetically efficient than plants grown in the small root chambers. At 350 μmol CO₂ mol^-1, leaf area and dry weights of plant organs were generally greater for plants in the large root chambers compared to those in the small root chambers. Atmospheric CO₂ enrichment may have compensated for the effects of root restriction on plant growth since at 1 000 μmol CO₂ mol^-1 there was generally no effect of root chamber size on plant dry weight.     

m-Hydroxyphenylacetic and m-Methoxyphenylacetic Acids of Rhizoctonia solani: Their Effect on Specific Root-Nodule Activity and Histopathology in Soybean

m-Methoxyphenylacetic acid (m-OMePAA), a derivative of m-hydroxyphenylacetic acid (m-OHPAA), having the same chemical composition as that phytotoxic compound produced in culture by Rhizoctonia solani, a fungal pathogen of soybean, reduced growth and symbiotic N₂-fixation activity of ‘Tracy’ soybeans in soil: perlite at 1.5 × 10^-4 M, the lowest concentration used. At twice this concentration m-OMePAA was strongly teratogenic and caused root hypertrophy and root fasciation. At 1.2 × 10^-3 M, m-OMePAA nearly suppressed seed germination. m-OMePAA at the minimum concentration used and equivalent concentrations of the culture filtrate fraction (m-OHPAA and m-OMePAA) caused cytopathological and histopathological disturbances in the nodule central tissue, extrusion of the nucleoli, and abnormal nuclci. The data indicate that these phytotoxic compounds of R. solani are involved in nodule impairment and reduced N₂-fixation in soybean.     

Properties of RNA fractions from nuclei of brain cells which stimulate incorporation of amino acids by brain ribosomes

Abstract— The properties of RNA fractions from nuclei of brain cells which were capable of stimulating amino acid incorporation into proteins of an homologous ribosomal system were investigated. RNA was routinely prepared from crude nuclear preparations of rat brain by a method which involved treatment with sodium dodecyl sulphate and phenol at 65°. The capacity of this preparation to stimulate incorporation of radioactivity from a mixture of 15 l -[¹⁴C]amino acids was greatly enhanced by preliminary incubation of the ribosomal system from brain for 5–20 min. The response was markedly dependent upon the concentrations of ribosomes and of the pH 5 fraction. The optimal level of Mg²⁺ for basal incorporation of amino acids into protein was 8 mm ; however, incorporation in the presence of nuclear RNA was greater at higher concentrations of Mg²⁺. The response to nuclear RNA was also enhanced as the K⁺ concentration was increased from 25 to 100 mm . The stimulatory effect of nuclear RNA on incorporation of l -[¹²C]eucine was either unaltered or depressed by addition of a mixture of 19 l -[¹²C]amino acids each at concentrations, of 10^?8, 10^?2, or 10^?1 mm . Under appropriate conditions of incubation, basal rates of incorporation and rates of incorporation stimulated by nuclear RNA were linear for 30 min. The response was proportional to the concentration of nuclear RNA between 34 and 136 μg. RNA prepared from ribosomes of rat brain essentially failed to stimulate incorporation of amino acids over this range of concentrations. Fractionation of nuclear RNA by centrifugation in sucrose density gradients revealed that 75 per cent of the stimulatory activity was in the fraction which sedimented below 12 S and contained about 25 per cent of the total RNA. Most of the remaining activity was in the 18 S region. Less than 5 per cent of the RNA in the lightest fraction (< 12 S) exhibited amino acid-acceptor activity, The stimulatory action of nuclear RNA on incorporation of amino acids was readily destroyed by mild treatment with pancreatic ribonuclease, whereas amino acid-acceptor activity was relatively resistant to this treatment. The results suggest that the brain may contain low molecular weight RNA with properties of messenger RNA.     

Effects and mechanisms of ghrelin on cardiac microvascular endothelial cells in rats

Ghrelin is thought to directly exert a protective effect on the cardiovascular system, specifically by promoting vascular endothelial cell function. Our study demonstrates the ability of ghrelin to promote rat CMEC (cardiac microvascular endothelial cell) proliferation, migration and NO (nitric oxide) secretion. CMECs were isolated from left ventricle of adult male Sprague—Dawley rat by enzyme digestion and maintained in endothelial cell medium. Dil‐ac‐LDL (1,1′‐dioctadecyl‐3,3,3′,3′‐ tetramethylindocarbocyanine‐labelled acetylated low‐density lipoprotein) intake assays were used to identify CMECs. Cells were split into five groups and treated with varying concentrations of ghrelin as follows: one control non‐treated group; three ghrelin dosage groups (1×10^?9, 1×10^?8, 1×10^?7 mol/l) and one ghrelin+PI3K inhibitor group (1×10^?7 mol/l ghrelin+20 μmol/l LY294002). After 24 h treatment, cell proliferation capability was measured by MTT [3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyl‐2H‐tetrazolium bromide] assay and Western blot for PCNA (proliferating cell nuclear antigen) protein expression. Migration of CMECs was detected by transwell assays, and NO secretion of CMECs was measured via nitrate reduction. Protein expression of AKT and phosphorylated AKT in CMECs was measured by Western blot after exposure to various concentrations of ghrelin and the PI3K inhibitor LY294002. Our results indicate that ghrelin significantly enhanced cell growth at concentrations of 10^?8 mol/l (0.271±0.041 compared with 0.199±0.021, P=0.03) and 10^?7 mol/l (0.296±0.039 compared with 0.199±0.021, P<0.01). However, addition of the PI3K/AKT inhibitor LY294002 inhibited the ghrelin‐mediated enhancement in cell proliferation (0.227±0.042 compared with 0.199±0.021, P=0.15). At a concentration between 10^?8 and 10^?7 mol/l, ghrelin caused a significant increase in the number of migrated cells compared with the control group (126±9 compared with 98±7, P=0.02; 142±6 compared with 98±7, P<0.01), whereas no such change could be observed in the presence of 20 μmol/l of the PI3K/Akt inhibitor LY294002 (103±7 compared with 98±7, P=0.32). Ghrelin treatment significantly enhanced NO production in a dose‐dependent fashion compared with the untreated control group [(39.93±2.12) μmol/l compared with (30.27±2.71) μmol/l, P=0.02; (56.80±1.98) μmol/l compared with (30.27±2.71) μmol/l, P<0.01]. However, pretreatment with 20 μmol/l LY294002 inhibited the ghrelin‐stimulated increase in NO secretion [(28.97±1.64) μmol/l compared with (30.27±2.71) μmol/l, P=0.37]. In summary, we have found that ghrelin treatment promotes the proliferation, migration and NO secretion of CMECs through activation of PI3K/AKT signalling pathway.     

Characterization of a Ryanodine Receptor in Periplaneta Americana

Abstract

Specific binding sites for the alkaloid ryanodine were characterized in membrane preparations from sarcoplasmatic reticulum of Periplaneta americana skeletal muscle. Binding of [³H]ryanodine was optimal at pH 8 and at CaCl₂ concentration of about 300 μmol l^-1. The Ca-chelating agents EGTA (100 μmol l^-1) and EDTA (100 μmol l^-1) abolished 95 % and 90 % of the [³H]ryanodine binding respectively. Preincubation with Ca²⁺ (100 μmol l^-1) restored the ryanodine binding in presence of up to 300 μmol l^-1 EGTA. Radioligand binding experiments showed one class of high affinity binding sites for ryanodine. Determination of rate constants revealed 7.05 × 10⁶ l mol^-1 min^-1 for associating and 3.77 × 10^-3 min^-1 for the dissociating [³H]ryandine ryanodine receptor complex. Solubility of the ryanodine receptor was examined with different anionic, non-ionic and zwitterionic detergents. Best solubilization results of “calcium release channel” of cockroach muscle membrane preparations were obtained with the detergent CHAPS in a concentration of 5 mg ml^-1.     

Feeding deterrent effect of carvone, a compound from caraway seeds, on the slug Arion lusitanicus

The feeding deterrent effect of carvone on the slug Arion lusitanicus was investigated. Carvone, a natural compound from caraway seeds, was incorporated into mulch to reduce its inherent volatility. In a laboratory choice experiment, boxes were filled on one side with carvone‐treated mulch and on the other side with untreated mulch. At carvone concentrations ranging from 0.03–0.75 ml litre^?1 mulch, slugs ate significantly more lettuce on the untreated side. In a laboratory based no‐choice experiment, carvone concentrations of 0.25 and 0.75 ml litre^?1 mulch significantly reduced slug feeding in comparison with the untreated control. Moreover at the highest concentration of carvone (0.75 ml litre^?1 mulch) 50% mortality was recorded over a period of 5 days, indicating a clear molluscicidal effect. Due to its volatility carvone did not decrease plant defoliation by A. lusitanicus when applied directly onto lettuce. Subsequent field evaluation showed 0.75 ml litre^?1 mulch to partially reduce slug feeding damage. However, this effect was not sufficient to significantly increase lettuce yield. The incorporation of a higher carvone concentration into mulch is still to be tested to confirm whether carvone‐treated mulch can be recommended as an effective alternative approach to chemical slug control.     

Interaction between ethylene and ABA in the regulation of polyamine level in <Emphasis Type="Italic">Arabidopsis thaliana</Emphasis> during UV-B stress

The effects of treatment with ethylene (0.01–100 μl/l) on ABA and polyamine contents and treatment with ABA on ethylene synthesis, polyamines content, and the resistance to UV-B radiation of two-week-old Arabidopsis thaliana (L.) Heynh, Columbia ecotype plants grown u?er sterile conditions were studied. Ethylene stimulated the accumulation of polyamines only at concentrations of 0.1–10 μl/l, which could activate ABA synthesis. Treatment with ABA (50–5000 μM, 1 μl per plant) decreased the UV-B-induced ethylene synthesis and a spermine and spermidine loss, increasing the content of putrescine, the precursor of these polyamines. ABA inhibited fresh weight accumulation in irradiated and nonirradiated plants but prevented them from severe damage and death at the high (18 kJ/m²) and lethal (27 kJ/m²) UV-B dose, respectively. The data obtained demonstrated a mutual regulation of ethylene and ABA syntheses and the participation of these hormones in the control of the polyamine level during adaptation of A. thaliana to UV-B stress.     

A neutral proteinase produced by Bacillus cereus with high sequence homology to thermolysin: Production,isolation and characterization

Summary Extracellular neutral proteinase was produced in 10 l and 240 l batch cultivations of Bacillus isolate X-3, identified as B. cereus and deposited as DSM 3101. The enzyme concentration was about 37–47 mg/l in the fermentation broth. The enzyme was extracted from the medium by adsorption chromatography with Amberlite XAD-7-resin, and further purified by acetone precipitation and affinity chromatography. The mol. wt. is 35 000 Da. The enzyme is thermostabilized by calcium, inhibited by EDTA and o-phenanthrolin and has its pH-optimum at pH 6.8. The specific activity is 4.36·10^-4 kat·mg^-1 at 35°C and the k _cat/K _m on FAGLA (furylacryloyl-glyleu-NH₂) is 2.25·10⁴ M^-1 s^-1 at 30°C, pH 6.8. The proteinase is stable up to 60°C. The N-terminal amino acid sequence exhibits a high sequence homology (63%) to thermolysin and a low homology (18%) to B. subtilis neutral protease A. The enzyme may therefore be suitable for structural comparison with thermolysin in order to study factors affecting thermostability.