Correlation between sensitivity of barley to Pyrenophora teres toxins and susceptibility to the fungus

Detached leaves of 25 barleys, ranging from highly susceptible to highly resistant to Pyrenophora teres f. teres and Pyrenophora teres f. maculata, were tested for their reaction to three phytotoxins isolated from cultures of the fungus: toxin A [ L, L - N -(2-amino-2-carboxyethyl)aspartic acid], toxin C (aspergillomarasmine A) and toxin B (anhydroaspergillomarasmine A). 0.75 m M toxin A caused mainly dark yellow chlorotic symptoms but little necrosis, whereas leaves treated with 0.25 m M toxin C developed distinct necrotic symptoms and zones of light yellow chlorosis. Toxin B is only weakly toxic, and toxin B and control solutions containing aspartic acid in the concentration of 0.75 m M did not cause any symptoms. The best differentiation between the barleys was obtained by scoring chlorosis after 120 h, and the optimal toxin concentrations for this differentiation were 0.75 m M toxin A and 0.25 m M toxin C, respectively. Results with different toxin concentrations inducing distinct variation in symptom expression indicate that the two toxins have different potencies as phytotoxins. The reaction of the barleys to toxins A and C correlated well with their reaction to infection by P. teres f. teres and P. teres f. maculata, suggesting that toxins A and C may be used to select resistant barley lines in the early stages of a breeding programme.     

Optimization of in vitro growth conditions of Pyrenophora teres for production of the phytotoxin aspergillomarasmine A

In liquid cultures of Pyrenophora teres, three phytotoxins may be found: L, L - N -(2-amino-2-carboxyethyl) aspartic acid (toxin A), anhydroaspergillomarasmine A (toxin B) and aspergillomarasmine A (toxin C). In particular, toxins A and C cause chlorotic and necrotic symptoms in detached barley leaves, toxin C being the most damaging, whereas toxin B is only weakly phytotoxic. When P. teres is grown in liquid modified Fries medium, toxin B is the main toxin accumulated, possibly due to a ring closure of toxin C at the low pH value of the medium. The amount of toxin B produced by 11 isolates of P. teres was compared in modified Fries medium. Generally, the most virulent isolates of P. teres produced higher amounts of toxin B than the less virulent isolates. During growth, the pH of the media decreased from 6.7 to about 3.0–3.5, followed by a slight increase to about 3.5–4.0. All isolates, except one, produced toxin B, whereas only two isolates produced toxin C and toxin A. Maintaining the pH at about 6.5 by sterile titration with 1 M NaOH resulted in a shift in toxin accumulation from toxin B to toxin C. The addition of tris or phosphate buffer to the media resulted in higher pH during the growth period, an increase in the total amount of toxins produced, and a shift in toxin accumulation from toxin B to toxin C. The higher pH value probably prevented the conversion of toxin C into toxin B. No toxins were produced in two routinely used media, potato glucose broth and grass broth. Toxin B and toxin C were purified by ion exchange chromatography and precipitation with HCl.     

N-1,3,4- 口 恶 二唑基-N''-对溴苯氧乙酰基硫脲的合成及其抑菌活性

从对溴苯氧乙酸出发,先合成中间体酰基异硫氰酸酯,该中间体与2-氨基-5-芳基-1,3,4- 口 恶 二唑反应合成了10个新的苯氧乙酰基硫脲类化合物,其结构经元素分析、红外光谱、核磁共振氢谱和质谱确认。初步生物活性测试结果表明,在50 mg/L浓度下,所有目标化合物对水稻纹枯病菌Rhizatonia solani和黄瓜灰霉病菌Botrytis cinereapers的抑制率均达85％以上,部分化合物对黄瓜灰霉病菌的抑制率达100%。     

Growth-regulating activity of some thiazole-and thiazoline-acetic acids

The growth-regulating activity of a number of 2-susbstituted thiazole-and thiazoline-acetic acids is reported. 2-ChIorothiazole-4-acetic acid showed appreciable activity in the wheat and pea tests, whilst activity was also observed with the 2-amino-, 2-methylamino-and 2-methyl-analogues. 2-Substituted thiazoline-acetic acids were inactive. The activity of these compounds, N-(carboxymethyl)-rhodanine and other acids is discussed in relation to the usual structural requirements of growth regulators.     

Genetic variation of single nucleotide polymorphisms identified at the mating type locus correlates with form-specific disease phenotype in the barley net blotch fungus Pyrenophora teres

Mating-type (MAT) locus-specific single nucleotide polymorphisms (SNPs) have been shown to be sufficient for conventional PCR-based differentiation of Pyrenophora teres f. teres (Ptt) and P. teres f. maculata (Ptm), the cause of the net and spot form, respectively, of barley net blotch. Here, we report the cloning and characterization of the MAT locus from 10 California isolates that cause atypical blotch symptoms on barley. Analysis of the full-length nucleotide sequences of one MAT1-1 (1,993?bp) and nine MAT1-2 (2,149 or 2,161?bp) idiomorphs revealed high (98?C99?%) similarity to those of Ptt isolates. However, distinct SNP patterns were identified in the newly cloned MAT idiomorphs. Two new MAT1-2-specific SNPs were found to be conserved in one Australia and eight California isolates that all cause similar atypical blotch symptoms. Phylogenetic analysis indicated that all 10 California isolates form a separate branch (or clade) within the Ptt group, except for one that appears to be ancestral to both Ptt and Ptm. PCR primers designed based on the identified SNP patterns were used successfully to differentiate each atypical isolate from highly virulent forms. This study extends our previous work and, taken together, the results demonstrate that the genetic variation at the MAT locus correlates with variation in the form-specific disease phenotype, and that MAT-specific SNPs can serve as reliable and convenient markers for subspecies level differentiation in P. teres, an economically important plant-pathogenic ascomycete (http://en.wikipedia.org/wiki/Single_nucleotide_polymorphism).     

Proteinaceous Metabolites from Pyrenophora teres Contribute to Symptom Development of Barley Net Blotch

ABSTRACT Pyrenophora teres, the causal agent of net blotch of barley (Hordeum vulgare L.), induces a combination of necrosis and extensive chlorosis in susceptible barley cultivars. Cell-free filtrates from both net and spot forms of P. teres; P. teres f. sp. teres, and P. teres f. sp. maculata were found to contain phytotoxic low molecular weight compounds (LMWCs) and proteinaceous metabolites which appear to be responsible for different components of the symptoms induced by the two forms of the pathogen in a susceptible cultivar of barley (cv. Sloop). Proteins induced only brown necrotic spots or lesions similar to those induced by the pathogens 72 h after inoculation. In contrast, LMWCs induced general chlorosis seen 240 h after inoculation but not the localized necrosis. Neither hydrolyzed or heat- or protease-treated proteinaceous metabolites induced the symptoms. This is the first report of the involvement of proteins produced by P. teres in symptom development during net blotch disease of barley.     

Alternate pathways of metribuzin metabolism in soybean: Formation of N-glucoside and homoglutathione conjugates

Metribuzin [4-amino-6-tert-butyl-3(methylthio)-1,2,4-triazin-5(4H)-one] metabolism was studied in soybean [Glycine max (L.) Merr. Tracy]. Pulse treatment studies with seedlings and excised mature leaves showed that [5-¹⁴C]metribuzin was absorbed rapidly and translocated acropetally. In seedlings, >97% of the root-absorbed ¹⁴C was present in foliar tissues after 24 hr. In excised leaves, 50–60% of the absorbed ¹⁴C remained as metribuzin 48 hr after pulse treatment, 12–20% was present as polar metabolites, and 20–30% was present as an insoluble residue. Metabolites were isolated by solvent partitioning, and were purified by adsorption, ion-exchange, thin-layer, and high-performance liquid chromatography. The major metabolite (I) was identified as a homoglutathione conjugate, 4-amino-6-tert-butyl-3-S-(γ-glutamyl-cysteinyl-β-alanine)-1,2,4-triazin-5(4H)-one. Metabolite identification was confirmed by qualitative analysis of amino acid hydrolysis products, fast atom bombardment (FAB), and chemical ionization (CI) mass spectrometry, and by comparison with a reference glutathione conjugate synthesized in vitro with a hepatic microsomal oxidase system from rat. Minor metabolites were identified as an intermediate N-glucoside conjugate (II), a malonyl N-glucoside conjugate (III), and 4-malonylamido-6-tert-butyl-1,2,4-triazin-3,5(2H,4H)-dione (N-malonyl DK, IV) by CI and FAB mass spectrometry. Alternative pathways of metribuzin metabolism are proposed.     

Metolachlor (2-chloro-N-[2-ethyl-6-methylphenyl]-N-[2-methoxy-l-methylethyl] acetamide) and the metolachlor safener CGA 43089 [α-(cyanomethoximino)-benzacetonitrile] in sorghum seedlings: Correlations between morphological effects and ethylene formation

Treatment of germinating sorghum [Sorghum bicolor (L.) Moench] seeds with the grass herbicide, metolachlor (2-chloro-N-[2-ethyl-6-methylphenyl]-N-[2-methoxy-1-methylethyl] acetamide), causes growth retardation, promoted by thickening of the first leaf and thus inhibition of unfolding of secondary leaves, and increased ethylene production. Sorghum seeds pretreated with the safener CGA 43089 [α-(cyanomethoximino)-benzacetonitrile] exhibit neither morphological deformations nor ethylene production upon metolachlor treatment. Aminoethoxyvinylglycine [l-2-amino-4-(2-aminoethoxy)-trans-3-butenoic acid], a specific inhibitor of ethylene formation in higher plants, decreases ethylene formation by metolachlor-treated sorghum seedlings; the observed deformations, however, remain unchanged. Sorghum control seedlings which grow against a covering plate build up ethylene concentrations as after herbicide treatment, but without induction of the morphological symptoms. These observations suggest that the plant hormone ethylene is a symptom and not the inducer of the morphological effects visible after metolachlor treatment of sorghum seedlings.     

S-cysteinyl-hydroxychlorpropham: Formation of the S-cysteinyl conjugate of isopropyl-3′-chloro-4′-hydroxycarbanilate in oat (Avena sativa L.)

Isopropyl-3′-chlorocarbanilate (chlorpropham) forms phenolic metabolites, isopropyl-3′-chloro-4′-hydroxycarbanilate (I), and isopropyl-5′-chloro-2′-hydroxycarbanilate (II), in several plant species. In oat, which is a chlorpropham-susceptible plant, I was converted to an S-cysteinyl-conjugate (III). The reaction in vitro was catalyzed by a partially purified, soluble enzyme. The formation of III by the enzyme preparation and by oat shoot sections was compared. Mass spectral data indicated the presence of an aryl-thioether bond, and chloro-, hydroxy-, and isopropylcarbanilate groups in III. The results of this investigation indicate that III was isopropyl-[(2-amino-2-carboxyethyl)thio]-chloro-hydroxycarbanilate (S-cysteinyl-hydroxychlorpropham).     

Microbial metabolism of dinitramine

The microbial metabolism of N³,N³-diethyl 2,4-dinitro-6-trifluoromethyl-m-phenylenediamine (dinitramine), N-sec-butyl-4-tert-butyl-2,6-dinitroaniline (A-820), N-n-propyl-N-cyclopropylmethyl-4-trifluoromethyl-2,6-dinitroaniline (CGA-10832), and α,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine (trifluralin) by Aspergillus fumigatus Fres., Fusarium oxysporum Schlecht and Paecilomyces sp. was investigated. The dinitrodiamine and dinitroanilines were most readily metabolized by Paecilomyces sp. The metabolism of dinitramine was examined in detail, and four metabolites were isolated: N³-ethyl 2,4-dinitro-6-trifluoromethyl-m-phenylenediamine; 2,4-dinitro-6-tri-fluoromethyl-m-phenylenediamine; 6-amino-1-ethyl-2-methyl-7-nitro-5-trifluoromethylbenzimidazole and 6-amino-2-methyl-7-nitro-5-trifluoromethylbenzimidazole. The presence of a dinitramine-degrading enzyme system in A. fumigatus was demonstrated. The enzyme dealkylates dinitramine and requires NADPH and Fe²⁺ as cofactors.     

Morphological and molecular analysis of <Emphasis Type="Italic">Paratrichodorus teres</Emphasis> (Hooper 1962) (Nematoda: Trichodoridae): a groundwork for discussion on the phylogeny and pathogenicity of <Emphasis Type="Italic">Paratrichodorus</Emphasis> species

Due to its ability to transmit plant viruses, Paratrichodorus teres (Hooper in Nematologica, 7, 273–280, 1962) is recognized as an economically important trichodorid species. Morphological and molecular analyses (18S and 28S rDNA) were performed, and 10 new plant hosts are reported for Polish P. teres populations. Major morphological features and the measurements obtained for the investigated specimens were within the wide ranges indicated for this species. However, a more detailed comparative analysis of Polish and Iranian P. teres showed significant morphological differences, particularly, in the shape and the structure of the walls of pars proximalis vaginae and the shape of the rectum.Phylogenetic study based on the 18S rDNA data suggests positioning of the Polish P. teres sequences within a cluster of sequences originating from the Netherlands. A comparison of the 28S rDNA fragment from Polish populations with the only P. teres 28S rDNA sequence available (from Iran) in GenBank revealed a sequence variability of 9.3%. The variation across these two representatives was higher than in the case of many other pairs of Trichodoridae species. The results obtained on the Polish P. teres specimens are discussed in the framework of the species taxonomy and phylogenetic relationships.     

Synthesis,structure and herbicidal activity of pyrazol-4-yl alkyl ketone derivatives

Novel 5-amino-1-phenylpyrazol-4-yl alkyl ketones were synthesised and their herbicidal properties evaluated. Active compounds in the series induced accumulation of protoporphyrin IX in etiolated cucumber cotyledons and caused light-dependent herbicidal effects in 21-day-old cucumber plants. Structural features of the pyrazoles that contributed to herbicidal potency were found to be a high degree of halogen substitution in the 1-phenyl ring, no substitution in the pyrazole 3-position, and an ethyl group as the alkyl component of the ketone. The structure of 1-[5-amino-1-(2,4,6-trichlorophenyl)pyrazol-4-yl]-2-methylpropan-1-one was determined by X-ray crystallography.     

Synthesis and structure–activity relationships for anticipated molluscicidal activity of some 2-amino-5-substituted pyridine derivatives

A series of 2-amino-5-substituted pyridine derivatives was synthesized and their molluscicidal activity against white garden, Theba pisana (Müller), and brown garden, Helix aspersa (Müller), snails was investigated by two methods of application. Some of these compounds showed strong activity under laboratory conditions against the two types of snail. T pisana was more sensitive to the tested compounds than H aspersa. The most effective compounds were 2-amino-5-(benzotriazole-1-ylmethyl)-3-methylpyridine, 2-amino-5-[1-(benzotriazole-1-yl)nonyl]-3-methylpyridine and 2-[(1,2,4-triazole-1-ylmethyl)amino]-3-methylpyridine which exhibited high molluscicidal activity. The toxicity results are discussed in relation to the chemical structures. © 1999 Society of Chemical Industry     

新型腙类衍生物的合成及其生物活性

利用3-(N-甲基-N-甲氧基氨基)-1-芳基-1-丙酮腙与酰氯反应,合成了14个新型N-酰基-3-(N-甲基-N-甲氧基氨基)-1-芳基-1-丙酮腙化合物,其化学结构经1H核磁共振和元素分析确证。初步的生物活性测试结果表明,部分化合物在50 mg/L时对淡色库蚊Culex pipiens pallens的致死率为95%~100%;化合物 c7 在1 000 mg/L时对粘虫Leucania separata Walke 的致死率达100%。     

Allelopathy and the active metabolites of the endophytic fungus,Alternaria J46, from Platycladus orientalis

The endophytic fungus, Alternaria J46, was isolated from the stem of the medicinal plant, Platycladus orientalis. A suspension of Alternaria J46 mycelial segments and the culture filtrates of the fungi exhibited marked seed germination inhibition against the monocot wheat, large crabgrass, bromegrass, rice and barnyardgrass and weak inhibition against the dicot redroot pigweed and morning glory, but it was safe for use on soybean, rape, cucumber, tomato, lettuce and radish crops. It is possible to use J46 culture filtrates in order to prevent monocot weeds in dicot cropland. Three active metabolites were isolated from an extract of the fungus cultures and elucidated as 3‐acetyl‐5‐sec‐butyltetramic acid (1, tenuazonic acid), 3‐acetyl‐5‐iso‐butyltetramic acid (2, vivotoxin II) and cyclo‐(L‐leucyl‐L‐proline) (3). Among these three compounds, compounds 1 and 2 showed significant phytotoxic effects on the seed germination of large crabgrass, while compound 3 exhibited weak activity, and all were safe for lettuce at 100 μg mL^?1. Accordingly, compounds 1 and 2 were the main active metabolites that were responsible for endophytic fungus Alternaria J46's strong seed germination inhibition against monocotyledons.     

Differential effects of phenoxy herbicides on light-dependent 14CO2 fixation in isolated cells of C3 and C4 plants

Cells were isolated from the developing leaves of Ipomoea aquatica and Digitaria sanguinalis. The effects of phenoxy alkanoic acid herbicides on light-dependent ¹⁴CO₂ fixation and oxygen evolution in these leaf cells were studied. (2,4-Dichlorophenoxy)acetic acid and (2,4,5-trichlorophenoxy) acetic acid (2,4,5-T and 2,4-D) caused a 20% stimulation of ¹⁴CO₂ fixation at 0.8 × 10^?5M and an inhibition at 1 × 10^?4M in I. aquatica leaf cells. Temperature seemed to have a marked influence on such action. No effect or very little effect was observed in the leaf cells of D. sanguinalis. The nonactive (2,4,6-Trichlorophenoxy)acetic acid (2,4,6-T) caused a similar stimulation of CO₂ fixation as 2,4-D and 2,4,5-T at low concentrations in I. aquatica leaf cells, but no inhibition was observed at high concentration. Increase of hight intensity increased the rate of CO₂ fixation in both control and 2,4,6-T-treated cells; however, the percentage of stimulation remained the same. At stimulatory concentration, all three compounds did not cause any stimulation in either photosystem I and II or photosystem II-mediated oxygen evolution. At higher concentrations, the differential effects of 2,4-D and 2,4,5-T on the light-induced CO₂ fixation and photosystem II-mediated oxygen evolution in the I. aquatica leaf cells and D. sanguinalis mesophyll (ms) cells may be attributed in part to their selective action against dicotyledonous plants.     

氟虫腈硫代磷酸酯衍生物的合成及生物活性

以5-氨基-1-(2,6-二氯-4-三氟甲基苯基)-3-氰基吡唑-4-二硫化物( 1 )为起始原料,经过还原和磷酸酯化反应合成了9个新型氟虫腈硫代磷酸酯衍生物,其结构经红外、核磁共振氢谱和质谱确证。初步的生物活性测定结果表明:在50 mg/L浓度下,所有新化合物对孑孓Culex pipiens pallens 24 h的致死率均为100%。     

Diphenamid removal from water and metabolism by aquatic plants

Several aquatic plants and algae were effective for removal of N, N-dimethyl-2,2-diphenylacetamide ([¹⁴C]diphenamid) from water and degradation to various metabolites. Parrotfeather (Myriophyllum brasilience L.) and water hyacinth (Eichornis crossiper L.) removed large quantities of diphenamid from water while algae (Ulothrix sp., Oedogonium sp., Gloeocystis sp., and Scenedesmus sp. mixed culture) and waterthread pondweed (Potamogeton diversifolius Raf.) were less effective in reducing diphenamid concentration in the water. A somewhat stable metabolite in algae, water hyacinth, and parrotfeather was N-methyl-2,2-diphenylacetamide. Algae and water hyacinth degraded diphenamid further to unknown products. One of these compounds moved more slowly than N-methyl-2,2-diphenylacetamide on thin-layer chromatography using benzene, n-heptane saturated with water and methanol solvent. While most solvents did not resolve 2,2-diphenylacetic acid from the base, petroleum ether, ethyl ether, and formic acid (50:50:2, v/v/v) was found to move 2,2-diphenylacetic acid further than diphenamid or N-methyl-2,2-diphenylacetamide on thin-layer chromatography.     

Effect of DDT on photosynthesis of Selanastrum capricormutum

The effect of DDT (2,2-bis-(p-chlorophenyl)-1,1,1-trichloroethane) on carbon assimilation of a green alga, Selanastrum capricormutum was studied. DDT at concentrations between 3.6 and 36 ppb was inhibitory to the photosynthetic CO₂ fixation (ethanol-soluble and/or ethanol-insoluble) and the longer the exposure to DDT, the greater the inhibition. Kinetic studies of photosynthetic CO₂ fixation indicated that DDT stimulated the incorporation of carbon-14 into glycolic acid, a major compound of photorespiration and caused the concomittant suppression of flow of carbon-14 into aspartic acid, a major component of the C₄-dicarboxylic acid pathway. The shift from an efficient pathway into a nonefficient pathway by DDT was interpreted to be through interruption of cyclic photophosphorylation.