{"title":"利用 Kappaphycus alvarezii 硫酸多糖提取物和植物生长调节剂体外再生具有可控酚类分泌的棉花(Gossypium hirsutum L.)栽培品种 KC3","authors":"Packiaraj Gurusaravanan, Sathasivam Vinoth, Rajkumar Vasanthkumar, Muthukrishnan Arun, Muthukrishnan Saradhadevi, Subiramani Sivakumar, Narayanasamy Jayabalan","doi":"10.1007/s11627-024-10444-x","DOIUrl":null,"url":null,"abstract":"<p>An efficient and reproducible <i>in vitro</i> regeneration protocol was developed for elite cotton cultivar KC3 by using plant growth regulators (PGRs) in combination with seaweed polysaccharide (SP) extracts. The existence of polysaccharide in seaweed extract was confirmed by Fourier transform infrared spectroscopy (FT-IR) and carbon-13 (<sup>13</sup>C) nuclear magnetic resonance (NMR) spectroscopy analysis. The extracted SP extract efficacy was tested for <i>in vitro</i> plant regeneration. The maximum callus frequency (89.4%) was obtained from hypocotyl explant in the Murashige and Skoog (MS) medium supplemented with 4.0% glucose, 1.5 mg L<sup>−1</sup> thidiazuron (TDZ), 0.6 mg L<sup>−1</sup> 2,4-dichlorophenoxyacetic acid (2,4-D), and 30.0 mg L<sup>−1</sup> SP. Remarkably, PGR- and SP-fortified medium inhibits the phenolic excretion from the explants. The well-developed yellow green friable texture of callus was transferred to shoot initiation medium. MS medium fortified with 4.0% glucose, 2.0 mg L<sup>−1</sup> 6-(γ,γ-dimethylallylamino) purine (2iP), 1.0 mg L<sup>−1</sup> kinetin (KIN), 1.0 mg L<sup>−1</sup> 6-benzylaminopurine (BA), and 40.0 mg L<sup>−1</sup> SP has shown maximum response (85.2%), and it produced 9.5 shoots per callus. The elongated shoots were cultured on root induction medium which consists of Murashige and Skoog (MS) salts with indole-3-acetic acid (IAA), indole-3-butyric acid (IBA), 1-naphthaleneacetic acid (NAA), and SP. The results revealed that the maximum number of roots (12.9 per shoot) with 8.6 cm in length was achieved on MS medium supplemented with 0.6 mg L<sup>−1</sup> IBA, combined with 30.0 mg L<sup>−1</sup> SP. Therefore, modified MS medium with natural bio-stimulant has more potential and is more reliable for <i>in vitro</i> regeneration of plants by neutralizing the effects of phenolic compounds secreted by the explants.</p>","PeriodicalId":13293,"journal":{"name":"In Vitro Cellular & Developmental Biology - Plant","volume":"43 1","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2024-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In vitro regeneration of cotton (Gossypium hirsutum L.) cultivar KC3 with controlled phenolic secretion by using Kappaphycus alvarezii sulfated polysaccharide extract and plant growth regulators\",\"authors\":\"Packiaraj Gurusaravanan, Sathasivam Vinoth, Rajkumar Vasanthkumar, Muthukrishnan Arun, Muthukrishnan Saradhadevi, Subiramani Sivakumar, Narayanasamy Jayabalan\",\"doi\":\"10.1007/s11627-024-10444-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>An efficient and reproducible <i>in vitro</i> regeneration protocol was developed for elite cotton cultivar KC3 by using plant growth regulators (PGRs) in combination with seaweed polysaccharide (SP) extracts. The existence of polysaccharide in seaweed extract was confirmed by Fourier transform infrared spectroscopy (FT-IR) and carbon-13 (<sup>13</sup>C) nuclear magnetic resonance (NMR) spectroscopy analysis. The extracted SP extract efficacy was tested for <i>in vitro</i> plant regeneration. The maximum callus frequency (89.4%) was obtained from hypocotyl explant in the Murashige and Skoog (MS) medium supplemented with 4.0% glucose, 1.5 mg L<sup>−1</sup> thidiazuron (TDZ), 0.6 mg L<sup>−1</sup> 2,4-dichlorophenoxyacetic acid (2,4-D), and 30.0 mg L<sup>−1</sup> SP. Remarkably, PGR- and SP-fortified medium inhibits the phenolic excretion from the explants. The well-developed yellow green friable texture of callus was transferred to shoot initiation medium. MS medium fortified with 4.0% glucose, 2.0 mg L<sup>−1</sup> 6-(γ,γ-dimethylallylamino) purine (2iP), 1.0 mg L<sup>−1</sup> kinetin (KIN), 1.0 mg L<sup>−1</sup> 6-benzylaminopurine (BA), and 40.0 mg L<sup>−1</sup> SP has shown maximum response (85.2%), and it produced 9.5 shoots per callus. The elongated shoots were cultured on root induction medium which consists of Murashige and Skoog (MS) salts with indole-3-acetic acid (IAA), indole-3-butyric acid (IBA), 1-naphthaleneacetic acid (NAA), and SP. The results revealed that the maximum number of roots (12.9 per shoot) with 8.6 cm in length was achieved on MS medium supplemented with 0.6 mg L<sup>−1</sup> IBA, combined with 30.0 mg L<sup>−1</sup> SP. Therefore, modified MS medium with natural bio-stimulant has more potential and is more reliable for <i>in vitro</i> regeneration of plants by neutralizing the effects of phenolic compounds secreted by the explants.</p>\",\"PeriodicalId\":13293,\"journal\":{\"name\":\"In Vitro Cellular & Developmental Biology - Plant\",\"volume\":\"43 1\",\"pages\":\"\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-07-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"In Vitro Cellular & Developmental Biology - Plant\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s11627-024-10444-x\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"In Vitro Cellular & Developmental Biology - Plant","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s11627-024-10444-x","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
In vitro regeneration of cotton (Gossypium hirsutum L.) cultivar KC3 with controlled phenolic secretion by using Kappaphycus alvarezii sulfated polysaccharide extract and plant growth regulators
An efficient and reproducible in vitro regeneration protocol was developed for elite cotton cultivar KC3 by using plant growth regulators (PGRs) in combination with seaweed polysaccharide (SP) extracts. The existence of polysaccharide in seaweed extract was confirmed by Fourier transform infrared spectroscopy (FT-IR) and carbon-13 (13C) nuclear magnetic resonance (NMR) spectroscopy analysis. The extracted SP extract efficacy was tested for in vitro plant regeneration. The maximum callus frequency (89.4%) was obtained from hypocotyl explant in the Murashige and Skoog (MS) medium supplemented with 4.0% glucose, 1.5 mg L−1 thidiazuron (TDZ), 0.6 mg L−1 2,4-dichlorophenoxyacetic acid (2,4-D), and 30.0 mg L−1 SP. Remarkably, PGR- and SP-fortified medium inhibits the phenolic excretion from the explants. The well-developed yellow green friable texture of callus was transferred to shoot initiation medium. MS medium fortified with 4.0% glucose, 2.0 mg L−1 6-(γ,γ-dimethylallylamino) purine (2iP), 1.0 mg L−1 kinetin (KIN), 1.0 mg L−1 6-benzylaminopurine (BA), and 40.0 mg L−1 SP has shown maximum response (85.2%), and it produced 9.5 shoots per callus. The elongated shoots were cultured on root induction medium which consists of Murashige and Skoog (MS) salts with indole-3-acetic acid (IAA), indole-3-butyric acid (IBA), 1-naphthaleneacetic acid (NAA), and SP. The results revealed that the maximum number of roots (12.9 per shoot) with 8.6 cm in length was achieved on MS medium supplemented with 0.6 mg L−1 IBA, combined with 30.0 mg L−1 SP. Therefore, modified MS medium with natural bio-stimulant has more potential and is more reliable for in vitro regeneration of plants by neutralizing the effects of phenolic compounds secreted by the explants.
期刊介绍:
Founded in 1965, In Vitro Cellular & Developmental Biology - Plant is the only journal devoted solely to worldwide coverage of in vitro biology in plants. Its high-caliber original research and reviews make it required reading for anyone who needs comprehensive coverage of the latest developments and state-of-the-art research in plant cell and tissue culture and biotechnology from around the world.