Search

The hemibiotrophic oomycetes are significant threats to a wide range of Cucurbitaceae species, causing substantial losses of plant productions. Particularly, Phytophthora melonis Katsura evokes severe symptoms, thus dramatically limiting the yield in cucumber. However, the information about cucumber–P. melonis interaction is still limited. This study explored the changes in the activities of phenylalanine ammonia-lyase (PAL), peroxidase (POX), catalase (CAT), superoxide dismutase (SOD) and polyphenol oxidase (PPO) in cucumber roots of two resistant genotypes (Soheil and Ramezz), one moderately resistant genotype (Baby) and three highly susceptible genotypes (Extrem, Mini 6–23 and Yalda), over the time courses of 7, 14 and 21 days after inoculation (DAI). The results indicated that the activities of defense-related enzymes differed between the resistant and highly susceptible genotypes. Although the defense-related enzymatic activities were elevated sharply in the resistant and moderately resistant genotypes after inoculation, no significant correlations were present between the activity trends of PPO, SOD and CAT and resistance characteristics. Moreover, no significant changes in enzyme activities were found in the control plants, non-inoculated plants of the six genotypes during the testing period. Altogether, the resistance of cucumber to P. melonis is related to POX and PAL activities, but does not show relationship with PPO, SOD and CAT activities. Studying the physiological metabolic pathways of POX and PAL appears to be an important direction in research to elucidate the resistance to P. melonis in cucumber genotypes.

Cucumber (Cucumis sativus L.) damping-off disease caused by Phytophthora melonis is a limiting factor affecting cucurbit production. This study assessed a collection of 38 domestic and exotic commercial cucumber genotypes for damping-off resistance at transplanting and 50% flowering. Plants were classified using a four-score scale, the average damping-off percentage ranging from 7.92% (resistant) to 88.01% [highly susceptible (HS)]. Most of the genotypes were susceptible and HS to P. melonis. These genotypes were analyzed with 15 inter-simple sequence repeat (ISSR) markers. A total of 317 bands were produced, of which 297 bands (93.69%) were polymorphic. The primer ISSR29 possessed the highest resolving power, polymorphic information content and marker index value, which could be the most informative primer for distinguishing cucumber genotypes. Cluster analysis and principal component analysis were carried out and there was a probable connection between cucumber genotypes and resistance level against P. melonis, indicating possible application for ISSR in studying disease resistance of cucumber and producing cultivars that resist damping-off. The expression of three candidate genes probably involved in the defence against P. melonis was quantified by quantitative real-time polymerase chain reaction in five cucumber genotypes showing different susceptibility to the pathogen. CsWRKY20, CsLecRK6.1 and LOX1 genes were differentially expressed depending on genotype in early stages of infection. LOX1 was the most expressed gene across experiments and the one that best discriminated between susceptible and resistant genotypes. These results are a valuable resource for future functional genomics studies to unravel the molecular mechanisms of C. sativus/P. melonis interaction.

Phytophthora melonis is the causal agent of damping-off or crown rot, one of the most destructive cucumber diseases that causes severe economic losses in Iran and some other parts of the world. Despite intense research efforts made in the past years, no permanent cure currently exists for this disease. With the aim to understand the molecular mechanisms of defense against P. melonis, root collars and leaves of four cucumber genotypes consisting of resistant Ramezz; moderately resistant Baby and very susceptible Mini 6-23 and Extrem, were monitored for quantitative gene expression analysis of five antifungal and/or anti-oomycete genes (CsWRKY20, CsLecRK6.1, PR3, PR1-1a and LOX1) at three points after inoculation with P. melonis. The gene expression analysis indicated that P. melonis strongly enhanced the expression of these genes after inoculation in both leaves and root collars. Further, not only the transcript levels of these genes were significantly higher in the resistant and moderately resistance genotypes, but also the time point of the highest relative expression ratio for the five genes was different in the four cucumber genotypes. CsWRKY20 and PR3 showed the maximum expression in Ramezz at 48 hours post inoculation (hpi) while CsLecRK6.1, and LOX1 showed the highest expression at 72 hpi. In addition, PR1-1a showed the maximum expression in the Baby at 72 hpi. Root collars responded faster than leaves and some responses were more strongly up-regulated in root collars than in leaves. The genes found to be involved in disease resistance in two different organs of cucumber after pathogen infection. The results suggest that increased expression of these genes led to activation of defense pathways and could be responsible for a reduced P. melonis colonization capacity in Ramezz and Baby. Overall, this work represents a valuable resource for future functional genomics studies to unravel the molecular mechanisms of C. sativus- P. melonis interaction.

New 2D lead(II) coordination polymers, Pb(4-bpdh)(CH3COO)(NO3)]n (1) and [Pb(4-bpdh)(ClO4)(NO3)]n (2), 4-bpdh ​= ​2,5-bis(4-pyridyl)-3,4-diaza-2,4-hexadiene, were prepared and characterized by single-crystal X-ray diffraction. Compound 3 with formula [Pb(4-bpdh)(NO3)2(H2O)]n (3) was obtained by solid state mechanochemical reaction of the compounds 1 and 2 via anion-exchange process. These conversions are reversible and the grinding of compound 3 with CH3COO¯ and ClO4¯ ions led to the formation of the compounds 1 and 2, respectively. Thermal decomposition of the compounds 1–3 results in the formation of different metallic composites. The composites were characterized by X-ray powder diffraction (XRD) and size and morphology of them were investigated by scanning electron microscopy (SEM).

Nanostructures of three Zinc(II) coordination polymers, [Zn(NNO)2(H2O)4]n (1), [Zn(PNNO)2(H2O)2]n (2) and [Zn(H2O)6]·(INNO)2 (3) {NNO: Nicotinic acid N-oxide, PNNO: Picolinic acid N-oxide and INNO: Isonicotinic acid N-oxide}, have been synthesized by a sonochemical process and reaction of ligands with Zn(CH3COO)2. The Zinc(II) oxide nano-particles have been synthesized from thermolysis of [Zn(NNO)2(H2O)4]n (1), [Zn(PNNO)2(H2O)2]n (2) and [Zn(H2O)6]·(INNO)2 (3) at two different methods (with surfactant and without surfactant) and two temperatures (200 and 600°C). The ZnO nanoparticles were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Comparison of the SEM images of ZnO nano-particles at two different methods and temperatures shows that higher temperature results in an increasing of agglomeration and thus small and spherical ZnO particles with good separation were produced by thermolysis of compounds at 200°C and by use of surfactant.

Nanostructures of the three-dimensional coordination polymers with the ligand 2,5-bis(4-pyridyl)-3,4-diaza-2,4-hexadiene (4-bpdh), [Pb(4-bpdh)(NO3)(μ-NCS)]n (1) and [Pb(4-bpdh)(μ-NCS)2]n (2), have been synthesized by a sonochemical process at different concentrations and characterized by scanning electron microscopy, X-ray powder diffraction, IR spectroscopy and elemental analyses. The solid state structural transformations of nano-compounds 1, 2 by anion-replacement processes under mechanochemical reaction, have been verified by IR and PXRD measurements. The SEM images showed that morphology change occurs on nanostructures during solid state anion-replacements.

A three-dimensional porous coordination polymer, [Pb(4-bpdh)(NO 3 )(H 2 O)] n ( TMU-1 ), has been synthesized with reaction of lead(II) nitrate and 2,5-bis(4-pyridyl)-3,4-diaza-2,4-hexadiene (4-bpdh). When solid TMU-1 was immersed in the ethanol solution of AgNO 3 for 5, 15 or 60 min and 20 h at room temperature, solid including Ag nanoparticles is formed ( Ag@TMU-1 ), as evidenced by HRTEM images and EDX spectrum. The visible fluorescence study of Ag@TMU-1 is another evidence for loading of silver nanoparticles on TMU-1 . Silver oxide and silver nanoparticles supported on nanocrystalline PbO were synthesized by heating of Ag@TMU -1 in air and Ar at 600 °C, respectively. The visible fluorescence study of Ag@TMU-1 is another evidence for loading of silver nanoparticles on TMU-1 .

A reversible anion-exchange of 2D lead(II) coordination polymers with the ligand 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene (4-bpdb), from 2D [Pb(4-bpdb)Br2]n (1) to 2D [Pb(4-bpdb)Cl2]n (2) coordination polymer by solid state anion-replacement processes under mechanochemical reactions, has been studied. The reversible solid state structural transformations of compound 1 to compound 2 by anion-replacement have been verified by PXRD and IR spectroscopy. PbBr2 and PbCl2 nanoparticles were obtained by thermal decomposition of compounds 1 and 2 in oleic acid as surfactant at 180 °C under an air atmosphere. These nanoparticles were characterized by powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM).

Reversible crystal-to-crystal transformations of 3D lead(II) coordination polymers with the ligand 2,5-bis(4-pyridyl)-3,4-diaza-2,4-hexadiene (4-bpdh), from nitrate analoge [Pb(4-bpdh)(NO3)2(H2O)]n (1) to [Pb(4-bpdh)(NO3)(Br)]n (2), [Pb(4-bpdh)(Br)2]n (3), [Pb(4-bpdh)(NO3)(Cl)]n (4) and [Pb(4-bpdh)(Cl)2]n (5) by solid state anion-replacement processes under mechanochemical reactions, have been studied. The reversible solid state structural transformations of compounds 1-5, by anion-replacement processes under mechanochemical reaction, have been verified by PXRD measurements. Nanoparticles of compounds were synthesized by sonochemical process and characterized by scanning electron microscopy (SEM), powder X-ray diffraction, IR spectroscopy and elemental analyses. The SEM images showed that morphology change occurs during solid state anion-replacements of nanocrystals.