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Andreas Leclerque Polina V. Mitkovets Ana-Cristina Fatu Christina Schuster Regina G. Kleespies 《Journal of pest science》2013,86(1):107-113
Wireworms, the polyphagous larvae of click beetles belonging to the genus Agriotes (Coleoptera: Elateridae), are severe and widespread agricultural pests affecting numerous crops. Biological control agents and methods for this general pest are highly solicited. In a screening for microbial Agriotes pathogens, an intracellular bacterium and a mitosporic fungus were isolated. Phylogenetic analysis based on ribosomal RNA operon sequences of both micro-organisms corroborated their previous morphology-based taxonomic classification. The bacterial pathogen has been assigned to the taxonomic genus Rickettsiella (Gammaproteobacteria) wherein it represents a new pathotype, ‘Rickettsiella agriotidis’, that appears most closely related to subjective synonyms of the nomenclatural type species, Rickettsiella popillae. The fungal pathogen has been shown to belong to the form-species Beauveria bassiana, i.e., an obligate anamorph related to the genus Cordyceps (Ascomycota: Hypocreales). Furthermore, the B. bassiana strain from Agriotes has been shown to be potentially susceptible to identification by gIi-diagnosis, i.e., a diagnostic method making use of the strain-specific presence of self-splicing group-I introns within the ribosomal RNA operons of certain hyphomycetous fungi. 相似文献
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The objectives of our study were to quantify the impact of endogeic earthworms Aporrectodea caliginosa (Savigny) on iron (Fe), manganese (Mn) and zinc (Zn) mobility and availability in soil. Dried rye straw (Cecale cereale L.), clover aboveground parts (Trifolium pratense L.) or calcium carbonate were added to determine the effects on soil micronutrient mobility. To test the importance of soil–water saturation mediated by earthworms, soil samples were modified to 60% (control) and 100% (as in casts) water holding capacity (WHC). To assess availability of micronutrients, a cucumber plant (Cucumis sativus L.) bioassay were used. Earthworm casts had generally higher amounts of water-soluble micronutrients compared with bulk soils regardless of their moisture contents. The increased micronutrient mobility was more pronounced in casts from soil samples amended with plant residues (especially with straw) and was significantly higher than mobility in control soil for at least 1 week after the casts were deposited. Pre-incubation of soils amended with clover or straw with living earthworms for 4 weeks produced an increase in both shoot biomass and translocation rate of micronutrients (Mn, Zn) into xylem sap of cucumber compared to soils not worked by earthworms. The earthworm-mediated plant performances were determined 4 weeks after the earthworms were removed. The results demonstrated that earthworms can significantly impact the formation of mobile and available micronutrients in a soil. The relationship between micronutrient availability to cucumber plants and earthworm contribution to nitrogen (N) mineralization and micronutrient mobility are discussed. 相似文献
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Blagojević P Radulović N Palić R Stojanović G 《Journal of agricultural and food chemistry》2006,54(13):4780-4789
The chemical composition of the aerial and root essential oils, hydrodistilled from Artemisia absinthium L. and Artemisia vulgaris L. (wild-growing populations from Serbia), were studied by gas chromatography, gas chromatography-mass spectrometry, and 13C nuclear magnetic resonance. During the storage of plant material under controlled conditions, a significant decrease of essential oil yields (isolated directly after drying and after 1 year of storage) and significant differences in their chemical compositions were observed. A possible mechanism for the observed oil component interconversion has been discussed. The noticeable differences in the chemical composition of the oils isolated from roots and aerial parts of A. absinthium and A. vulgaris were also correlated with the diverging biosynthetic pathways of volatiles in the respective plant organs. The antimicrobial activities against the common human pathogens of all of the isolated oils were tested according to National Committee on Clinical Laboratory Standards. The oils showed a broad spectrum of antimicrobial activity against the tested strains. Therefore, these oils can be used as flavor and fragrance ingredients. 相似文献
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M. Wysoki G. Forer E. Dunkelblum Miriam Harel Polina Fraistat Devora Gordon L. Anshelevich M. Kehat M. Kehat L. Anshelevich Devora Gordon Miriam Harel E. Dunkelblum L. Zilberg A. Rubin A. Shani Ada Rafaeli Miriam Altstein Oma Ben-Aziz Irit Schafler I. Seltzer C. Gilon A. Hefetz Tamar Katzav Victoria Soroker Ali R. Harari 《Phytoparasitica》1998,26(2):175-181
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Sergey A. Dyshlovoy Moritz Kaune Jessica Hauschild Malte Kriegs Konstantin Hoffer Tobias Busenbender Polina A. Smirnova Maxim E. Zhidkov Ekaterina V. Poverennaya Su Jung Oh-Hohenhorst Pavel V. Spirin Vladimir S. Prassolov Derya Tilki Carsten Bokemeyer Markus Graefen Gunhild von Amsberg 《Marine drugs》2020,18(12)
Efficacy and mechanism of action of marine alkaloid 3,10-dibromofascaplysin (DBF) were investigated in human prostate cancer (PCa) cells harboring different levels of drug resistance. Anticancer activity was observed across all cell lines examined without signs of cross-resistance to androgen receptor targeting agents (ARTA) or taxane based chemotherapy. Kinome analysis followed by functional investigation identified JNK1/2 to be one of the molecular targets of DBF in 22Rv1 cells. In contrast, no activation of p38 and ERK1/2 MAPKs was observed. Inhibition of the drug-induced JNK1/2 activation or of the basal p38 activity resulted in increased cytotoxicity of DBF, whereas an active ERK1/2 was identified to be important for anticancer activity of the alkaloid. Synergistic effects of DBF were observed in combination with PARP-inhibitor olaparib most likely due to the induction of ROS production by the marine alkaloid. In addition, DBF intensified effects of platinum-based drugs cisplatin and carboplatin, and taxane derivatives docetaxel and cabazitaxel. Finally, DBF inhibited AR-signaling and resensitized AR-V7-positive 22Rv1 prostate cancer cells to enzalutamide, presumably due to AR-V7 down-regulation. These findings propose DBF to be a promising novel drug candidate for the treatment of human PCa regardless of resistance to standard therapy. 相似文献
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Maxim E. Zhidkov Moritz Kaune Alexey V. Kantemirov Polina A. Smirnova Pavel V. Spirin Maria A. Sidorova Sergey A. Stadnik Elena Y. Shyrokova Dmitry N. Kaluzhny Oleg A. Tryapkin Tobias Busenbender Jessica Hauschild Tina Rohlfing Vladimir S. Prassolov Carsten Bokemeyer Markus Graefen Gunhild von Amsberg Sergey A. Dyshlovoy 《Marine drugs》2022,20(3)
Marine alkaloid fascaplysin and its derivatives are known to exhibit promising anticancer properties in vitro and in vivo. However, toxicity of these molecules to non-cancer cells was identified as a main limitation for their clinical use. Here, for the very first time, we synthesized a library of fascaplysin derivatives covering all possible substituent introduction sites, i.e., cycles A, C and E of the 12H-pyrido[1-2-a:3,4-b’]diindole system. Their selectivity towards human prostate cancer versus non-cancer cells, as well as the effects on cellular metabolism, membrane integrity, cell cycle progression, apoptosis induction and their ability to intercalate into DNA were investigated. A pronounced selectivity for cancer cells was observed for the family of di- and trisubstituted halogen derivatives (modification of cycles A and E), while a modification of cycle C resulted in a stronger activity in therapy-resistant PC-3 cells. Among others, 3,10-dibromofascaplysin exhibited the highest selectivity, presumably due to the cytostatic effects executed via the targeting of cellular metabolism. Moreover, an introduction of radical substituents at C-9, C-10 or C-10 plus C-3 resulted in a notable reduction in DNA intercalating activity and improved selectivity. Taken together, our research contributes to understanding the structure–activity relationships of fascaplysin alkaloids and defines further directions of the structural optimization. 相似文献
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Piyush A. Patel Tanja Bruun Polina Ilina Heidi Mkkyl Antti Lempinen Jari Yli-Kauhaluoma Pivi Tammela Paula S. Kiuru 《Marine drugs》2021,19(7)
Marine-originated spirocyclic bromotyrosines are considered as promising scaffolds for new anticancer drugs. In a continuation of our research to develop potent and more selective anticancer compounds, we synthesized a library of 32 spirocyclic clavatadine analogs by replacing the agmatine, i.e., 4-(aminobutyl)guanidine, side chain with different substituents. These compounds were tested for cytotoxicity against skin cancer using the human melanoma cell line (A-375) and normal human skin fibroblast cell line (Hs27). The highest cytotoxicity against the A-375 cell line was observed for dichloro compound 18 (CC50 0.4 ± 0.3 µM, selectivity index (SI) 2). The variation of selectivity ranged from SI 0.4 to reach 2.4 for the pyridin-2-yl derivative 29 and hydrazide analog of 2-picoline 37. The structure–activity relationships of the compounds in respect to cytotoxicity and selectivity toward cancer cell lines are discussed. 相似文献
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Nadezhda E. Ustyuzhanina Polina A. Fomitskaya Alexey G. Gerbst Andrey S. Dmitrenok Nikolay E. Nifantiev 《Marine drugs》2015,13(2):770-787
Natural anionic polysaccharides fucosylated chondroitin sulfates (FCS) from sea cucumbers attract great attention nowadays due to their ability to influence various biological processes, such as blood coagulation, thrombosis, angiogenesis, inflammation, bacterial and viral adhesion. To determine pharmacophore fragments in FCS we have started systematic synthesis of oligosaccharides with well-defined structure related to various fragments of these polysaccharides. In this communication, the synthesis of non-sulfated and selectively O-sulfated di- and trisaccharides structurally related to branching sites of FCS is described. The target compounds are built up of propyl β-d-glucuronic acid residue bearing at O-3 α-l-fucosyl or α-l-fucosyl-(1→3)-α-l-fucosyl substituents. O-Sulfation pattern in the fucose units of the synthetic targets was selected according to the known to date holothurian FCS structures. Stereospecific α-glycoside bond formation was achieved using 2-O-benzyl-3,4-di-O-chloroacetyl-α-l-fucosyl trichloroacetimidate as a donor. Stereochemical outcome of the glycosylation was explained by the remote participation of the chloroacetyl groups with the formation of the stabilized glycosyl cations, which could be attacked by the glycosyl acceptor only from the α-side. The experimental results were in good agreement with the SCF/MP2 calculated energies of such participation. The synthesized oligosaccharides are regarded as model compounds for the determination of a structure-activity relationship in FCS. 相似文献