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1.
J Chem Ecol ; 46(11-12): 1131-1143, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33180277

RESUMO

Erysimum cheiranthoides L (Brassicaceae; wormseed wallflower) accumulates not only glucosinolates, which are characteristic of the Brassicaceae, but also abundant and diverse cardenolides. These steroid toxins, primarily glycosylated forms of digitoxigenin, cannogenol, and strophanthidin, inhibit the function of essential Na+/K+-ATPases in animal cells. We screened a population of 659 ethylmethanesulfonate-mutagenized E. cheiranthoides plants to identify isolates with altered cardenolide profiles. One mutant line exhibited 66% lower cardenolide content, resulting from greatly decreased cannogenol and strophanthidin glycosides, partially compensated for by increases in digitoxigenin glycosides. This phenotype was likely caused by a single-locus recessive mutation, as evidenced by a wildtype phenotype of F1 plants from a backcross, a 3:1 wildtype:mutant segregation in the F2 generation, and genetic mapping of the altered cardenolide phenotype to one position in the genome. The mutation created a more even cardenolide distribution, decreased the average cardenolide polarity, but did not impact most glucosinolates. Growth of generalist herbivores from two feeding guilds, Myzus persicae Sulzer (Hemiptera: Aphididae; green peach aphid) and Trichoplusia ni Hübner (Lepidoptera: Noctuidae; cabbage looper), was decreased on the mutant line compared to wildtype. Both herbivores accumulated cardenolides in proportion to the plant content, with T. ni accumulating higher total concentrations than M. persicae. Helveticoside, a relatively abundant cardenolide in E. cheiranthoides, was not detected in M. persicae feeding on these plants. Our results support the hypothesis that increased digitoxigenin glycosides provide improved protection against M. persicae and T. ni, despite an overall decrease in cardenolide content of the mutant line.


Assuntos
Cardenolídeos/metabolismo , Erysimum/genética , Erysimum/metabolismo , Herbivoria/efeitos dos fármacos , Repelentes de Insetos/metabolismo , Animais , Afídeos/fisiologia , Brassica/metabolismo , Cardenolídeos/química , Digitoxigenina/química , Digitoxigenina/metabolismo , Expressão Gênica , Glucosinolatos/química , Glucosinolatos/metabolismo , Repelentes de Insetos/química , Mariposas/metabolismo , Mutação , ATPase Trocadora de Sódio-Potássio/metabolismo , Estrofantidina/química , Estrofantidina/metabolismo
2.
Zootaxa ; 3599: 519-34, 2013 Jan 10.
Artigo em Inglês | MEDLINE | ID: mdl-24614027

RESUMO

During a survey of soil nematodes in Iran, three species of predatory nematodes, including a new species of the genus Mylonchulus Cobb, 1916 were recovered. Mylonchulus kermaniensis sp. n. is characterised by its body length (1.2-1.4 mm), six rows of rasp-like denticles, the sixth line consisting of four denticles, female tail slightly sigmoid, sharply bent ventrad with digitate posterior portion slightly but clearly bent dorsad, (37-49 µm long, c=27.9-38.9, c'=1.2-1.7) with a terminal opening of spinneret. Two advulval papillae present, one is pre-vulval and the other one is located posterior to vulva. Furthermore, two other mononchid species namely M. cf. hawaiiensis (Cassidy, 1931) Goodey, 1951 and Mononchus truncatus Bastian, 1865 were also recovered from soil in the province of Kerman, Iran, the former representing a new geographical record for Iran. Measurements and illustration are provided for these three species. Molecular study of 18S rDNA region of M. cf. hawaiiensis demonstrated that the Iranian population compared with the nearest populations identified as M. hawaiiensis from Japan, shows 5 to 8 nucleotide differences. In addition, phylogeny of Mylonchulus is discussed and a checklist of the species of Mononchida from Iran is provided.


Assuntos
Adenofórios/anatomia & histologia , Adenofórios/classificação , Adenofórios/genética , Animais , Feminino , Irã (Geográfico) , Dados de Sequência Molecular , Filogenia , Reação em Cadeia da Polimerase , RNA Ribossômico 18S/genética , Análise de Sequência de DNA
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