A rapid bioassay for the detection of photosynthesis inhibitors in water

A modified leaf disc buoyancy procedure for the detection of photosynthesis-inhibiting residues in water is described. The modifications proposed, mainly the presence of sodium hydrogen carbonate in the infiltration solution, increased the sensitivity of the method and reduced the time required. The substituted urea and 1,3,5-triazine herbicides diuron, linuron, monuron, atrazine, ametryn and atraton were detected below 0.7 mg litre^?1 using cucumber (Cucumis sativus L., cv. ‘Dalia’) leaf discs. A concentration as low as 0.09 mg diuron litre^?1 could be detected. Although bean (Phaseolus vulgaris L., cv. ‘Bulgarian’) leaf tissue was less sensitive in this bioassay than cucumber, 0.3 mg diuron litre^?1 could still be detected. The test, being very rapid (less than 30 min per determination) and relatively sensitive, could be used for the detection of photosynthesis inhibitors in recycled water used for irrigation.     

荧光蛋白mNeonGreen、mKOk作为FRET传能对在研究植物蛋白质互作中的应用分析

蛋白质相互作用是蛋白质组学研究的重要方向之一,对解析植物病原微生物与寄主植物之间的博弈具有十分重要的意义。荧光共振能量转移(fluorescence resonance energy transfer,FRET)作为一种新技术,能够在活细胞的正常生理条件下进行检测,并具有灵敏度高,假阳性较低,实验周期短的优势,在研究蛋白质相互作用过程中得到了广泛的应用。本研究选取了2种新型的荧光蛋白mNeonGreen/mKOk作为FRET传能对,并与传统的传能对CFP/YFP相比较,证实mNeonGreen/mKOk背景干扰较低。通过构建并表达荧光蛋白与目标蛋白的融合蛋白,利用FRET技术成功地在植物细胞中验证了蛋白质间的相互作用。本研究为FRET技术在植物细胞中的应用提供了更多的技术支持和借鉴。     

Water use efficiency and photosynthesis of glyphosate-resistant soybean as affected by glyphosate

Previous studies comparing cultivars of different maturity groups in different soils demonstrated that early maturity group cultivars were more sensitive to glyphosate injury than those of other maturity groups. In this work, we evaluated the effect of increasing rates of glyphosate on water absorption and photosynthetic parameters in early maturity group cultivar BRS 242 GR soybean. Plants were grown in a complete nutrient solution and subjected to a range of glyphosate rates either as a single or sequential leaf application. Net photosynthesis, transpiration rate, stomatal conductance, sub-stomatal CO₂, carboxylation efficiency, fluorescence, maximal fluorescence and chlorophyll content were monitored right before and at different stages after herbicide application; water absorption was measured daily. All photosynthetic parameters were affected by glyphosate. Total water absorbed and biomass production by plants were also decreased as glyphosate rates increased, with the affect being more intense with a single full rate than half the rate applied in two sequential applications. Water use efficiency (WUE) was significantly reduced with increasing rates of glyphosate.     

Aryl N-hydroxy- and N-methoxy-N-methylcarbamates as potent reversible inhibitors of acetylcholinesterase

Several aryl N-hydroxy- and N-methoxy-N-methylcarbamates were examined as inhibitors of bovine erythrocyte acetylcholinesterase (AChE). These carbamate derivatives were generally strong inhibitors of AChE, but, unlike the typical N-methyl- and N,N-dimethylcarbamates which are carbamylating agents, they proved to be reversible, competitive inhibitors of the enzyme. The values for the dissociation constant (K_a) for the enzyme-inhibitor complex to enzyme and inhibitor were in the range of 2 × 10^?5?1 × 10^?7M.     

Development of a cell-free assay from Botrytis cinerea as a biochemical screen for sterol biosynthesis inhibitors

An assay for measuring ergosterol synthesis in cell-free extracts of the filamentous plant pathogen Botrytis cinerea is described. The extracts capable of synthesizing C4-desmethyl sterols from [2- 14 C]mevalonate were derived by mechanical disruption of young conidial germlings in a Bead-Beater apparatus. The C4-desmethyl sterol fraction consisted of three distinct compounds and totalled 39% of the non-saponifiable lipids formed. Ergosterol accounted for 63% of the C4-desmethyl sterols. Only small amounts of C4-monomethyl sterols were synthesized, while C4, 4-dimethyl sterols made up 29% of the non-saponifiable lipids. The latter fraction mainly consisted of lanosterol (54%) and eburicol (28%). The cell-free system had a narrow pH optimum for synthesis of C4-desmethyl sterols of pH 7.3–7.4. Cell-free synthesis of C4-desmethyl sterols was inhibited by the imidazole fungicide imazalil, concomitant with an accumulation of eburicol. The IC₅₀ value (concentration of fungicide which inhibited cell-free synthesis of C4-desmethyl sterols by 50%) was 9.1 × 10 ?9 M. These results are consistent with the hypothesis that imazalil is a potent inhibitor of the cytochrome P450-dependent sterol 14x-demethylase of B. cinerea. The method described may be used to screen compounds biochemically for inhibition of sterol synthesis in an agriculturally important plant pathogen.     

Evaluation of phenylaminopyrimidines as antifungal protein kinase inhibitors

The effects of diverse phenylaminopyrimidines (PAP), namely PAP-pyridines (type A), PAP-pyrazoles (type B) and PAP-thiazoles (type C), on Neurospora crassa Shear & Dodge has been investigated. The results revealed that type A strongly inhibit the in vitro growth of N crassa, whereas types B and C are much less active. A significant correlation was observed between the Neurospora growth inhibition and the intrinsic activity of type A compounds on the cyclin-dependent protein kinase p34(CDC2) of starfish, suggesting that the target of phenylaminopyrimidines in fungi is a cyclin-dependent protein kinase (CDK). The phenylaminopyrimidine-binding CDKs Phoss (major band) and CDC2 (minor band) involved in phosphorus uptake, glycogen synthesis and the cell cycle were identified from N crassa by affinity chromatography on phenylaminopyrimidine-sepharose. Comparative experiments with different protein kinases revealed the importance of the side chain of phenylaminopyrimidines for their target selectivity. A type B compound was found to selectively inhibit the MAP-kinase OS-2 involved in the osmoregulatory pathway of Neurospora.     

Assessment of novel inhibitors of Helicoverpa aminopeptidases as anti-insect agents

Helicoverpa species present problems worldwide as pests on a variety of agricultural crops. In Australia, the costs of controlling H. armigera (Hübn.) and H. punctigera (Wall.) are a major burden on the cotton industry, and novel mechanisms are continually sought to combat these pests. Potential new targets for insecticides are the digestive proteases of the insect, including the aminopeptidases (APs). A variety of compounds, designed to be similar in structure to known AP inhibitors, were synthesized and screened for activity in inhibiting H. armigera larval growth and AP activity. The most effective compounds in both assays proved to be hydroxamic acids and methylphosphonic acids. Compounds that incorporated both of these groups were also found to have significant potential as control agents. The most inhibitory compounds included valine methylphosphonic acid and a leucine methylphosphonic acid/hydroxamic acid derivative. The valine methylphosphonic acid compound was tested further in vitro, with the aim of producing a new active capable of restricting the viability of Helicoverpa populations on commercial crops.     

Substituted thiotrifluoropropanones as potent selective inhibitors of juvenile hormone esterase

A series of 27 substituted thio-1,1,1-trifluoropropanones was synthesized by reacting the corresponding thiol with 1,1,1-trifluoro-3-bromopropanone. The resulting sulfides were screened as inhibitors of hemolymph juvenile hormone esterase and α-naphthyl acetate esterase activity of the cabbage looper, Trichoplusia ni, electric eel acetylcholinesterase, bovine trypsin, and bovine α-chymotrypsin. The presence of the sulfide bond increased the inhibitory potency on all of the enzymes tested when compared with compounds lacking the sulfide. In general, the compounds proved to be poor inhibitors of chymotrypsin and moderate inhibitors of trypsin. By varying the substituent on the sulfide, good inhibitory activity was obtained on α-naphthyl acetate esterase, acetylcholinesterase, while some of the compounds proved to be extremely powerful inhibitors of juvenile hormone esterase. The most powerful inhibitor tested was 3-octylthio-1,1,1-trifluoro-2-propanone, with an I₅₀ of 2.3 × 10^?9M on JH esterase. This compound showed a molar refractivity similar to that of the JH II backbone, was not toxic to T. ni, and was moderately toxic to mice, with a 48-hr LD₅₀ of >750 mg/kg. It effectively delayed pupation when applied to prewandering larvae of T. ni, as expected for a JH esterase inhibitor. Thus, some members of this series are promising for evaluating the role of JH esterase in insect development. The series also indicates that, by varying the substituent on the sulfide moiety, potent “transition-state” inhibitors can be developed for a wide variety of esterases and proteases.     

Variable resistance factors of fungicides acting as sterol demethylation inhibitors

The ED₅₀ values and resistance factors of 20 fungicides that all act as inhibitors of the C-14 demethylation of 24-methylenedihydrolanosterol were determined for one wild-type and four resistant strains of Ustilago avenae. All fungicides were cross-resistant to each other; however, the resistance factors varied considerably, ranging from 50 (triadimenol) to 2·2 (miconazole). A tentative structural requirement for low resistant factors was the presence of two phenyl rings separated from each other by at least three atoms. Labeling of lipids with [¹⁴C]acetate in the absence and presence of the inhibitors and subsequent sterol analysis revealed that the variable resistance factors were not related to the presence of a second target site. In spite of reported second modes of action of fenarimol, tebuconazole or miconazole, accumulation of C-14 sterol precursors in both sensitive and resistant isolates was necessary to accomplish growth inhibition.     

Bioassay-led isolation of Myrothecium verrucaria and verrucarin A as germination inhibitors of Orobanche crenata

A total of 188 fungal isolates was obtained from the rhizosphere of Vicia faba grown in an Egyptian soil heavily infested with Orobanche species. Agar cultures of 58 isolates inhibited the germination of conditioned seed of Orobanche crenata exposed to the germination stimulant, GR24. Filtrates of inhibitory fungi grown in liquid medium for 9–15 days were also assayed and those of five isolates, which were morphologically similar, inhibited germination even when diluted 16-fold. The fungus was identified as Myrothecium verrucaria (Alb. & Schwein.) Ditmar by its morphology and the nucleotide sequence of the ITS1 and ITS2 regions of the ribosomal repeat unit. Purification of the inhibitor to homogeneity was accomplished by solvent partitioning, flash chromatography on silica gel, semi-preparative HPLC on a reversed phase C18 column, solid phase extraction and tlc on silica gel. The inhibitor was identified as verrucarin A by nuclear magnetic resonance spectroscopy and comparison of the spectra with those of an authentic sample of the compound. A preliminary experiment demonstrated that infection of V. faba by O. crenata could be prevented by addition of spores of the fungus to soil infested by the parasite.     

Trifluoromethylketones as possible transition state analog inhibitors of juvenile hormone esterase

A series of compounds containing the trifluoromethylketone group have been synthesized utilizing either a modified Grignard procedure or by reacting selected aliphatic bromides or tosylates with the Collman reagent [Na₂Fe(CO)₄]. When tested in vitro as inhibitors of crude juvenile hormone esterase from the hemolymph of the cabbage looper, Trichoplusia ni (Noctuidae), the most active compounds were trifluoromethylketones possessing either a juvenoid-like structure or a straight aliphatic chain. The logarithm of the inhibitory potency of the aliphatic compounds was proportional to their chain length, up to 1,1,1-trifluorotetradecan-2-one (I₅₀ = 1 × 10^?7M). This powerful inhibition was found to be highly selective for JHE, reversible, competitive by Lineweaver-Burk analysis, and was characterized by high affinity of the inhibitor for the esterase (K_i = 3.2 × 10^?9M, K_m JH III = 2 × 10^?7M). Other trifluoromethylketones were shown to be inhibitors of T. ni α-naphthylacetate esterase and bovine trypsin. By analogy with the mechanism of trypsin action, trifluoromethylketones are probably potent inhibitors due to their resemblance to a tetrahedral transition state on the reaction coordinate to the acylated enzyme.     

Structure-activity relationships of 1,2,3-benzothiadiazole insecticide synergists as inhibitors of microsomal oxidation

The activities of 47 substituted 1,2,3-benzothiadiazoles as inhibitors of microsomal epoxidation and/or hydroxylation in enzyme preparations from rat liver or armyworm (Spodoptera eridania) gut have been evaluated. Many were found to be effective inhibitors of microsomal oxidation, the most active being the 6-butyl and 6-propoxy derivatives with I₅₀ values of 4.9 × 10^?7 and 7.0 × 10^?7M, respectively, for the epoxidation reaction. Regression analyses have established that activity of the 5-, 6-, and 5,6-substituted compounds can be satisfactorily described in equations in terms of π², π, and σ whereas that of the 4-substituted derivatives depends on π and the steric parameter E₈.     

Improved bioassay method for Spodoptera litura chitinase inhibitors using a colloidal chitin powder with a uniform particle size as substrate

A previously reported bioassay method for Spodoptera litura chitinase inhibitors has been improved by use of colloidal chitin powder with a uniform particle size. This improvement made the assay four times more sensitive. Detection of three active supernatants by screening of supernatants and cell extracts from 135 fermentation broths has proved the efficiency of this improved method. © 1999 Society of Chemical Industry     

Comparative properties of N-acetyl derivatives of oxime N-methylcarbamates and aryl N-methylcarbamates as insecticides and acetylcholinesterase inhibitors

N-acylation of aryl N-methylcarbamates is known to reduce their mammalian toxicity considerably without adversely affecting their insecticidal activity. It has now been found that N-acylation of several insecticidal oxime carbamates results in loss of toxicity both to insects and mammals. Kinetic data for base-catalysed solvolysis and inhibition of acetylcholinesterase, together with published work on metabolism, are combined to provide a rationale for this unexpected observation and to account for the selective toxicity of aryl N-acetyl-N-methylcarbamates.     

The effect of some heavy metal ions on photosynthesis in a freshwater alga

The effect of the following metals: copper, cadmium, lead, mercury, methyl mercury, and thallium, and the herbicide 3(3,4-dichlorophenyl)1,1-dimethylurea on (a) the light-induced oxygen evolution, (b) the Hill reaction (water → dichlorophenol-indophenol), and (c) a modified Mehler reaction (dichlorophenol-indophenol → methyl viologen) was studied with the freshwater alga Chlamydomonas reinhardii.The light-induced oxygen evolution of whole cells was found to be very sensitive to the cadmium ion, but this ion was almost without effect on the Hill reaction and the modified Mehler reaction. The light-induced oxygen evolution was also very sensitive to methyl mercury and lead.     

Structure-activity relationship studies of dibromo phenolic derivatives as photosynthetic electron chain inhibitors

A number of 2,6-dibromophenols with different substituents in the 4-position have been synthesised and their effect on the whole electron transport chain and on photosystem II have been determined. A study was made to relate the chemical characteristics of the 4-substituent group and the inhibition of the uncoupled electron transport of isolated chloroplasts from spinach plants. The chemical nature of the 4-substituent group varies greatly in the active compounds and it is therefore suggested that this group does not participate in the inhibitor-receptor interaction. The results indicated that the inhibiting power of these compounds increased with the electron-attracting capacity of the 4-substituent group, decreased with increase in its size and that there was no correlation with its hydrophobic nature.