Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish
Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ develo...
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| Autor*in: |
Sarhang, Mahtab [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2023 |
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| Anmerkung: |
© The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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| Übergeordnetes Werk: |
Enthalten in: Plant cell, tissue and organ culture - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1981, 154(2023), 1 vom: 03. Mai, Seite 29-41 |
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| Übergeordnetes Werk: |
volume:154 ; year:2023 ; number:1 ; day:03 ; month:05 ; pages:29-41 |
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| DOI / URN: |
10.1007/s11240-023-02507-5 |
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| 520 | |a Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. | ||
| 520 | |a Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. | ||
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10.1007/s11240-023-02507-5 doi (DE-627)SPR051908875 (SPR)s11240-023-02507-5-e DE-627 ger DE-627 rakwb eng Sarhang, Mahtab verfasserin (orcid)0000-0001-7519-3351 aut Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. Biostimulant (dpeaa)DE-He213 Hypocotyl (dpeaa)DE-He213 Plant growth regulators (dpeaa)DE-He213 Tuberization (dpeaa)DE-He213 Acemi, Arda (orcid)0000-0003-0270-8507 aut Türker-Kaya, Sevgi (orcid)0000-0002-5393-0207 aut Enthalten in Plant cell, tissue and organ culture Dordrecht [u.a.] : Springer Science + Business Media B.V, 1981 154(2023), 1 vom: 03. Mai, Seite 29-41 (DE-627)27093278X (DE-600)1478391-5 1573-5044 nnns volume:154 year:2023 number:1 day:03 month:05 pages:29-41 https://dx.doi.org/10.1007/s11240-023-02507-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 154 2023 1 03 05 29-41 |
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10.1007/s11240-023-02507-5 doi (DE-627)SPR051908875 (SPR)s11240-023-02507-5-e DE-627 ger DE-627 rakwb eng Sarhang, Mahtab verfasserin (orcid)0000-0001-7519-3351 aut Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. Biostimulant (dpeaa)DE-He213 Hypocotyl (dpeaa)DE-He213 Plant growth regulators (dpeaa)DE-He213 Tuberization (dpeaa)DE-He213 Acemi, Arda (orcid)0000-0003-0270-8507 aut Türker-Kaya, Sevgi (orcid)0000-0002-5393-0207 aut Enthalten in Plant cell, tissue and organ culture Dordrecht [u.a.] : Springer Science + Business Media B.V, 1981 154(2023), 1 vom: 03. Mai, Seite 29-41 (DE-627)27093278X (DE-600)1478391-5 1573-5044 nnns volume:154 year:2023 number:1 day:03 month:05 pages:29-41 https://dx.doi.org/10.1007/s11240-023-02507-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 154 2023 1 03 05 29-41 |
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10.1007/s11240-023-02507-5 doi (DE-627)SPR051908875 (SPR)s11240-023-02507-5-e DE-627 ger DE-627 rakwb eng Sarhang, Mahtab verfasserin (orcid)0000-0001-7519-3351 aut Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. Biostimulant (dpeaa)DE-He213 Hypocotyl (dpeaa)DE-He213 Plant growth regulators (dpeaa)DE-He213 Tuberization (dpeaa)DE-He213 Acemi, Arda (orcid)0000-0003-0270-8507 aut Türker-Kaya, Sevgi (orcid)0000-0002-5393-0207 aut Enthalten in Plant cell, tissue and organ culture Dordrecht [u.a.] : Springer Science + Business Media B.V, 1981 154(2023), 1 vom: 03. Mai, Seite 29-41 (DE-627)27093278X (DE-600)1478391-5 1573-5044 nnns volume:154 year:2023 number:1 day:03 month:05 pages:29-41 https://dx.doi.org/10.1007/s11240-023-02507-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 154 2023 1 03 05 29-41 |
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10.1007/s11240-023-02507-5 doi (DE-627)SPR051908875 (SPR)s11240-023-02507-5-e DE-627 ger DE-627 rakwb eng Sarhang, Mahtab verfasserin (orcid)0000-0001-7519-3351 aut Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. Biostimulant (dpeaa)DE-He213 Hypocotyl (dpeaa)DE-He213 Plant growth regulators (dpeaa)DE-He213 Tuberization (dpeaa)DE-He213 Acemi, Arda (orcid)0000-0003-0270-8507 aut Türker-Kaya, Sevgi (orcid)0000-0002-5393-0207 aut Enthalten in Plant cell, tissue and organ culture Dordrecht [u.a.] : Springer Science + Business Media B.V, 1981 154(2023), 1 vom: 03. Mai, Seite 29-41 (DE-627)27093278X (DE-600)1478391-5 1573-5044 nnns volume:154 year:2023 number:1 day:03 month:05 pages:29-41 https://dx.doi.org/10.1007/s11240-023-02507-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 154 2023 1 03 05 29-41 |
| allfieldsSound |
10.1007/s11240-023-02507-5 doi (DE-627)SPR051908875 (SPR)s11240-023-02507-5-e DE-627 ger DE-627 rakwb eng Sarhang, Mahtab verfasserin (orcid)0000-0001-7519-3351 aut Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. Biostimulant (dpeaa)DE-He213 Hypocotyl (dpeaa)DE-He213 Plant growth regulators (dpeaa)DE-He213 Tuberization (dpeaa)DE-He213 Acemi, Arda (orcid)0000-0003-0270-8507 aut Türker-Kaya, Sevgi (orcid)0000-0002-5393-0207 aut Enthalten in Plant cell, tissue and organ culture Dordrecht [u.a.] : Springer Science + Business Media B.V, 1981 154(2023), 1 vom: 03. Mai, Seite 29-41 (DE-627)27093278X (DE-600)1478391-5 1573-5044 nnns volume:154 year:2023 number:1 day:03 month:05 pages:29-41 https://dx.doi.org/10.1007/s11240-023-02507-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 154 2023 1 03 05 29-41 |
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Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Biostimulant</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Hypocotyl</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Plant growth regulators</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Tuberization</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Acemi, Arda</subfield><subfield code="0">(orcid)0000-0003-0270-8507</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Türker-Kaya, Sevgi</subfield><subfield code="0">(orcid)0000-0002-5393-0207</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Plant cell, tissue and organ culture</subfield><subfield code="d">Dordrecht [u.a.] : Springer Science + Business Media B.V, 1981</subfield><subfield code="g">154(2023), 1 vom: 03. 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Sarhang, Mahtab |
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Sarhang, Mahtab misc Biostimulant misc Hypocotyl misc Plant growth regulators misc Tuberization Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish |
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Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish Biostimulant (dpeaa)DE-He213 Hypocotyl (dpeaa)DE-He213 Plant growth regulators (dpeaa)DE-He213 Tuberization (dpeaa)DE-He213 |
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Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish |
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Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish |
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Sarhang, Mahtab |
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Plant cell, tissue and organ culture |
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comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish |
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Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish |
| abstract |
Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. © The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
| abstractGer |
Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. © The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
| abstract_unstemmed |
Abstract Comparative determination of the effects of plant growth regulators and chitosan on several plants suggested a cytokinin-like effect of chitosan in in vitro plant propagation. Therefore, we evaluated the impact of several cytokinins and chitosan on in vitro seed germination and organ development in Raphanus sativus ‘Cherry Belle’. The effects of 6-Benzylaminopurine (BAP), kinetin (KIN), zeatin (ZTN), thidiazuron (TDZ), N6-(2-Isopentenyl)adenosine (2IP), and chitosan (CHT) were tested on plants. All the treatments enhanced seed germination. Hypocotyl elongation remarkably increased after CHT treatments, whereas cytokinins reduced the parameter. Low concentration of KIN (0.25 mg $ L^{− 1} $), high concentration of 2IP (2.0 mg $ L^{− 1} $), and CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) led to a limited increase in leaf production. All cytokinin treatments reduced root elongation, whereas CHT treatments (2.5, 5.0, and 10.0 mg $ L^{− 1} $) induced statistically significant increases in the parameter. The highest concentration of 2IP elevated tuberization frequency, while all cytokinin treatments led to an early tuberization. However, CHT treatments did not induce tuberization, which was persistent even during an extended incubation period. The 2IP treatments at 0.5 and 1.0 mg $ L^{− 1} $ stimulated the development of tubers with similar thermotropic properties to the roots produced in the presence of CHT in culture medium. The CHT treatments led to partially similar germination and organ development patterns only with low concentrations of KIN (0.25 and 0.50 mg $ L^{−1} $). These findings suggest that CHT may have a variety of distinct roles than cytokinins tested on the organ development in radish, with significant effects on hypocotyl and root development. Therefore, future studies into the comparative impacts of CHT and auxins on radish cultivation would also be useful. Key Message Chitosan may play different roles than cytokinins on organ development in radish, with its considerable impacts on hypocotyl and root elongation. © The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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Comparison of the effects of cytokinins and chitosan on in vitro seed germination and organ development in radish |
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Acemi, Arda Türker-Kaya, Sevgi |
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| score |
7.4017096 |