T A Kritskaya, A S Kashin, V A Spivak, V E Firstov
{"title":"[石竹科(Silene白垩纪)无性系离体培养繁殖特征]。","authors":"T A Kritskaya, A S Kashin, V A Spivak, V E Firstov","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The features of the formation of microshoots in in vitro culture of Silene cretacea—endangered species\nwith narrow ecological amplitude, which is a promising source of medicinal raw materials—were studied.\nIt was demonstrated that, at the micropropagation step, basic Woody Plant Medium containing vitamins\naccording to Murashige and Skoog and supplemented with 0.2 mg/L 6-benzylaminopurine, 1.0 mg/L kinetin,\n1.0 mg/L gibberellic acid, and 0.5 mg/L indole-3-acetic acid is the most effective. The combination and\nconcentration of these growth regulators, selected using mathematical combinatorial analysis, activated axillary\nbuds and provided a high multiplication factor (9.3 ± 1.3 microshoots per explant). Morpho-histological\nanalysis revealed the main stages of the formation of microshoots and proved the absence of callus formation\nduring the whole time of the cultivation of explants. The features of the dynamics of the culture during the\nyear of continuous cultivation are presented.</p>","PeriodicalId":19673,"journal":{"name":"Ontogenez","volume":"47 6","pages":"386-94"},"PeriodicalIF":0.0000,"publicationDate":"2016-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Features of Clonal Micropropagation of Silene cretacea (Caryophyllaceae) in in vitro Culture].\",\"authors\":\"T A Kritskaya, A S Kashin, V A Spivak, V E Firstov\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The features of the formation of microshoots in in vitro culture of Silene cretacea—endangered species\\nwith narrow ecological amplitude, which is a promising source of medicinal raw materials—were studied.\\nIt was demonstrated that, at the micropropagation step, basic Woody Plant Medium containing vitamins\\naccording to Murashige and Skoog and supplemented with 0.2 mg/L 6-benzylaminopurine, 1.0 mg/L kinetin,\\n1.0 mg/L gibberellic acid, and 0.5 mg/L indole-3-acetic acid is the most effective. The combination and\\nconcentration of these growth regulators, selected using mathematical combinatorial analysis, activated axillary\\nbuds and provided a high multiplication factor (9.3 ± 1.3 microshoots per explant). Morpho-histological\\nanalysis revealed the main stages of the formation of microshoots and proved the absence of callus formation\\nduring the whole time of the cultivation of explants. The features of the dynamics of the culture during the\\nyear of continuous cultivation are presented.</p>\",\"PeriodicalId\":19673,\"journal\":{\"name\":\"Ontogenez\",\"volume\":\"47 6\",\"pages\":\"386-94\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ontogenez\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ontogenez","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Features of Clonal Micropropagation of Silene cretacea (Caryophyllaceae) in in vitro Culture].
The features of the formation of microshoots in in vitro culture of Silene cretacea—endangered species
with narrow ecological amplitude, which is a promising source of medicinal raw materials—were studied.
It was demonstrated that, at the micropropagation step, basic Woody Plant Medium containing vitamins
according to Murashige and Skoog and supplemented with 0.2 mg/L 6-benzylaminopurine, 1.0 mg/L kinetin,
1.0 mg/L gibberellic acid, and 0.5 mg/L indole-3-acetic acid is the most effective. The combination and
concentration of these growth regulators, selected using mathematical combinatorial analysis, activated axillary
buds and provided a high multiplication factor (9.3 ± 1.3 microshoots per explant). Morpho-histological
analysis revealed the main stages of the formation of microshoots and proved the absence of callus formation
during the whole time of the cultivation of explants. The features of the dynamics of the culture during the
year of continuous cultivation are presented.