Efficient callus-mediated system for commercial production of sugarcane (Saccharum spp.) planting material in Ghana

E. Azu, W. Elegba, Abigail Tweneboah Asare, Kwame Kumi Asare, C. Akama, Patience Asare, C. Annor, Samuel Azure, K. Danso
{"title":"Efficient callus-mediated system for commercial production of sugarcane (Saccharum spp.) planting material in Ghana","authors":"E. Azu, W. Elegba, Abigail Tweneboah Asare, Kwame Kumi Asare, C. Akama, Patience Asare, C. Annor, Samuel Azure, K. Danso","doi":"10.5897/ajb2021.17440","DOIUrl":null,"url":null,"abstract":"An efficient callus-mediated regeneration system was developed for high-frequency production of planting material of sugarcane genotypes LSC and B36464. Spindle leaf segments cultured on MS basal medium supplemented with 2,4-D or picloram at 1, 2, 3 or 4 mg/L resulted in callus induction. Callus induction was higher on 2,4-D amended medium compared to picloram. Nevertheless, for both auxins, callus induction improved significantly (p ≤ 0.05) with increasing concentration; the highest (82 and 82.5% for B36464 and LSC respectively) was achieved at 4 mg/L. For shoot induction, calli were transferred to MS medium supplemented with BAP (0.1, 0.5, 1.0 or 1.5 mg/L). The highest number of shoots (18.13 and 16.75 for B36464 and LSC respectively) was achieved at 1.5 mg/L. Serial subculture at four-week intervals on a higher concentration of BAP (2.5 mg/L), in combination with NAA (0.5 mg/L) and GA3 (0.5 mg/L), resulted in a four-fold increase in shoot number within 16 weeks. On this medium, 40% of shoot clusters of B36464 formed well-defined shoots. On MS medium containing solely NAA (3 mg/L), 88 and 72% (B36464 and LSC respectively) formed roots. Post-flask acclimatisation of the plantlets led to 85 and 91% survival rates in LSC and B36464 respectively after which plantlets were successfully transferred to field conditions. The callus-mediated regeneration system reported in this study has the potential to sustainably provide sugarcane planting material for the emerging sugar industry in Ghana.","PeriodicalId":7414,"journal":{"name":"African Journal of Biotechnology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"African Journal of Biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5897/ajb2021.17440","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

An efficient callus-mediated regeneration system was developed for high-frequency production of planting material of sugarcane genotypes LSC and B36464. Spindle leaf segments cultured on MS basal medium supplemented with 2,4-D or picloram at 1, 2, 3 or 4 mg/L resulted in callus induction. Callus induction was higher on 2,4-D amended medium compared to picloram. Nevertheless, for both auxins, callus induction improved significantly (p ≤ 0.05) with increasing concentration; the highest (82 and 82.5% for B36464 and LSC respectively) was achieved at 4 mg/L. For shoot induction, calli were transferred to MS medium supplemented with BAP (0.1, 0.5, 1.0 or 1.5 mg/L). The highest number of shoots (18.13 and 16.75 for B36464 and LSC respectively) was achieved at 1.5 mg/L. Serial subculture at four-week intervals on a higher concentration of BAP (2.5 mg/L), in combination with NAA (0.5 mg/L) and GA3 (0.5 mg/L), resulted in a four-fold increase in shoot number within 16 weeks. On this medium, 40% of shoot clusters of B36464 formed well-defined shoots. On MS medium containing solely NAA (3 mg/L), 88 and 72% (B36464 and LSC respectively) formed roots. Post-flask acclimatisation of the plantlets led to 85 and 91% survival rates in LSC and B36464 respectively after which plantlets were successfully transferred to field conditions. The callus-mediated regeneration system reported in this study has the potential to sustainably provide sugarcane planting material for the emerging sugar industry in Ghana.
加纳甘蔗种植材料商业化生产的高效愈伤组织介导系统
开发了一种高效的愈伤组织介导再生系统,用于高频生产甘蔗基因型LSC和B36464的种植材料。在添加2,4-D或苦草胺的MS基础培养基上以1、2、3或4mg/L培养纺锤叶片段,可诱导愈伤组织。在2,4-D改良培养基上,愈伤组织的诱导率高于苦草胺。然而,对于两种生长素,随着浓度的增加,愈伤组织诱导显著改善(p≤0.05);B36464和LSC在4mg/L时达到最高(分别为82%和82.5%)。为了诱导芽,将愈伤组织转移到添加BAP(0.1、0.5、1.0或1.5mg/L)的MS培养基中。在1.5mg/L时,芽数最高(B36464和LSC分别为18.13和16.75)。在较高浓度的BAP(2.5 mg/L)、NAA(0.5 mg/L)和GA3(0.5 mg/L。在该培养基上,B36464 40%的芽簇形成了清晰的芽。在仅含NAA(3mg/L)的MS培养基上,88%和72%(分别为B36464和LSC)生根。试管苗的瓶后驯化在LSC和B36464中分别获得85%和91%的存活率,之后将试管苗成功地转移到田间条件下。本研究中报道的愈伤组织介导的再生系统有可能为加纳新兴的糖业可持续地提供甘蔗种植材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
African Journal of Biotechnology
African Journal of Biotechnology 工程技术-生物工程与应用微生物
自引率
0.00%
发文量
15
审稿时长
4.7 months
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信