{"title":"一种新型非开花辐射突变体 Platanus × acerifolia Willd.","authors":"","doi":"10.1007/s11627-023-10409-6","DOIUrl":null,"url":null,"abstract":"<h3>Abstract</h3> <p>An efficient <em>in vitro</em> micropropagation system for <em>Platanus</em> × <em>acerifolia</em> ‘F03’, a radiation mutant that has not flowered for 19 yr, has been established. Axillary buds were used as explants. After sprouting on Murashige and Skoog medium (MS) supplemented with 0.3 mg·L<sup>−1</sup> 6-benzylaminopurine (6-BA) together with 0.05 mg·L<sup>−1</sup> α-naphthaleneacetic acid (NAA), the best medium for multiplication and elongation was MS basal medium supplemented with 0.1 mg·L<sup>−1</sup> 6-benzylaminopurine and with a multiplication rate of 3.43 ± 0.57. Plantlets over 1.5 cm could root on McCown Woody Plant Medium (WPM) supplemented with 0.01 mg·L<sup>−1</sup> α-naphthaleneacetic acid and 7.0 g·L<sup>−1</sup> agar with an ideal rooting rate and transplanting survival rate of 100 ± 0%. The optimum survival rate was possible when trays were covered with a thin plastic lid for more than 14 d. After transplanting, air humidity and temperature were crucial for young plant survival. The system established here could serve as a pathway for commercial production of the line and provide sterile leaf explants for regeneration and further genetic improvement of the species.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In vitro micropropagation of a novel non-flowering radiation mutant of Platanus × acerifolia Willd.\",\"authors\":\"\",\"doi\":\"10.1007/s11627-023-10409-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<h3>Abstract</h3> <p>An efficient <em>in vitro</em> micropropagation system for <em>Platanus</em> × <em>acerifolia</em> ‘F03’, a radiation mutant that has not flowered for 19 yr, has been established. Axillary buds were used as explants. After sprouting on Murashige and Skoog medium (MS) supplemented with 0.3 mg·L<sup>−1</sup> 6-benzylaminopurine (6-BA) together with 0.05 mg·L<sup>−1</sup> α-naphthaleneacetic acid (NAA), the best medium for multiplication and elongation was MS basal medium supplemented with 0.1 mg·L<sup>−1</sup> 6-benzylaminopurine and with a multiplication rate of 3.43 ± 0.57. Plantlets over 1.5 cm could root on McCown Woody Plant Medium (WPM) supplemented with 0.01 mg·L<sup>−1</sup> α-naphthaleneacetic acid and 7.0 g·L<sup>−1</sup> agar with an ideal rooting rate and transplanting survival rate of 100 ± 0%. The optimum survival rate was possible when trays were covered with a thin plastic lid for more than 14 d. After transplanting, air humidity and temperature were crucial for young plant survival. The system established here could serve as a pathway for commercial production of the line and provide sterile leaf explants for regeneration and further genetic improvement of the species.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-02-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s11627-023-10409-6\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s11627-023-10409-6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
In vitro micropropagation of a novel non-flowering radiation mutant of Platanus × acerifolia Willd.
Abstract
An efficient in vitro micropropagation system for Platanus × acerifolia ‘F03’, a radiation mutant that has not flowered for 19 yr, has been established. Axillary buds were used as explants. After sprouting on Murashige and Skoog medium (MS) supplemented with 0.3 mg·L−1 6-benzylaminopurine (6-BA) together with 0.05 mg·L−1 α-naphthaleneacetic acid (NAA), the best medium for multiplication and elongation was MS basal medium supplemented with 0.1 mg·L−1 6-benzylaminopurine and with a multiplication rate of 3.43 ± 0.57. Plantlets over 1.5 cm could root on McCown Woody Plant Medium (WPM) supplemented with 0.01 mg·L−1 α-naphthaleneacetic acid and 7.0 g·L−1 agar with an ideal rooting rate and transplanting survival rate of 100 ± 0%. The optimum survival rate was possible when trays were covered with a thin plastic lid for more than 14 d. After transplanting, air humidity and temperature were crucial for young plant survival. The system established here could serve as a pathway for commercial production of the line and provide sterile leaf explants for regeneration and further genetic improvement of the species.