椰芽分生组织胚性愈伤组织悬浮培养的初步研究

U. Bhavyashree, K. Jayaraj, K. S. Muralikrishna, K. K. Sajini, M. K. Rajesh, A. Karun
{"title":"椰芽分生组织胚性愈伤组织悬浮培养的初步研究","authors":"U. Bhavyashree, K. Jayaraj, K. S. Muralikrishna, K. K. Sajini, M. K. Rajesh, A. Karun","doi":"10.19071/JP.2016.V8.2979","DOIUrl":null,"url":null,"abstract":"An attempt was made to establish highly competent embryogenic cell suspension culture in coconut, a species recalcitrant to in vitro culture. Embryogenic calli were initiated from shoot meristem explants of coconut. Y3 medium supplemented with 2.4-D (4.5 μM) and glutamine (34.2 μM) was found to be the best medium to initiate cell suspension. Growth evaluation was done by packed cell volume (PCV) and it was found that maximum growth volume of 9.9% was reached at 200 days of culture initiation. About 52% of viable cells were detected through fluorescent microscopy. Cell aggregation was noticed in Y3 medium supplemented with glutamine (34.2 μM), malt extract (100mg/l), biotin (40.9 μM) and kinetin (9.3 μM), but further progress could not be achieved. It was also observed that embryogenic calli were not of a friable type, but were associated with densely aggregated cells. Because of its hard nature, we were unsuccessful to obtain high quality cell suspension.","PeriodicalId":22829,"journal":{"name":"The Journal of Phytology","volume":"13 1","pages":"13-16"},"PeriodicalIF":0.0000,"publicationDate":"2016-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Initiation of coconut cell suspension culture from shoot meristem derived embryogenic calli: A preliminary study\",\"authors\":\"U. Bhavyashree, K. Jayaraj, K. S. Muralikrishna, K. K. Sajini, M. K. Rajesh, A. Karun\",\"doi\":\"10.19071/JP.2016.V8.2979\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An attempt was made to establish highly competent embryogenic cell suspension culture in coconut, a species recalcitrant to in vitro culture. Embryogenic calli were initiated from shoot meristem explants of coconut. Y3 medium supplemented with 2.4-D (4.5 μM) and glutamine (34.2 μM) was found to be the best medium to initiate cell suspension. Growth evaluation was done by packed cell volume (PCV) and it was found that maximum growth volume of 9.9% was reached at 200 days of culture initiation. About 52% of viable cells were detected through fluorescent microscopy. Cell aggregation was noticed in Y3 medium supplemented with glutamine (34.2 μM), malt extract (100mg/l), biotin (40.9 μM) and kinetin (9.3 μM), but further progress could not be achieved. It was also observed that embryogenic calli were not of a friable type, but were associated with densely aggregated cells. Because of its hard nature, we were unsuccessful to obtain high quality cell suspension.\",\"PeriodicalId\":22829,\"journal\":{\"name\":\"The Journal of Phytology\",\"volume\":\"13 1\",\"pages\":\"13-16\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-02-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Phytology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.19071/JP.2016.V8.2979\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Phytology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19071/JP.2016.V8.2979","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

摘要

在对离体培养有抗性的椰子中,建立了高能力的胚性细胞悬浮培养。以椰子茎部分生组织为外植体,培养出胚性愈伤组织。发现添加2.4-D (4.5 μM)和谷氨酰胺(34.2 μM)的Y3培养基是引发细胞悬浮的最佳培养基。用填充细胞体积法(PCV)对其生长进行评价,发现在培养开始200 d时,其最大生长量达到9.9%。荧光显微镜检测到约52%的活细胞。在添加谷氨酰胺(34.2 μM)、麦芽提取物(100mg/l)、生物素(40.9 μM)和动素(9.3 μM)的Y3培养基中发现细胞聚集,但未见进一步进展。胚性愈伤组织不是易碎型,而是由密集聚集的细胞组成。由于其坚硬的性质,我们未能获得高质量的细胞悬液。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Initiation of coconut cell suspension culture from shoot meristem derived embryogenic calli: A preliminary study
An attempt was made to establish highly competent embryogenic cell suspension culture in coconut, a species recalcitrant to in vitro culture. Embryogenic calli were initiated from shoot meristem explants of coconut. Y3 medium supplemented with 2.4-D (4.5 μM) and glutamine (34.2 μM) was found to be the best medium to initiate cell suspension. Growth evaluation was done by packed cell volume (PCV) and it was found that maximum growth volume of 9.9% was reached at 200 days of culture initiation. About 52% of viable cells were detected through fluorescent microscopy. Cell aggregation was noticed in Y3 medium supplemented with glutamine (34.2 μM), malt extract (100mg/l), biotin (40.9 μM) and kinetin (9.3 μM), but further progress could not be achieved. It was also observed that embryogenic calli were not of a friable type, but were associated with densely aggregated cells. Because of its hard nature, we were unsuccessful to obtain high quality cell suspension.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Some nutritional properties of Taiwan Napier grass leaves (Pennisetum purpureum) harvested at different time Synthesis, physicochemical characterization and biological activity of synthesized Silver and Rajat Bhasma nanoparticles using Clerodendrum inerme Morphological characterization and nutrient assessment of wild pepper, Piper umbellatum L. (Piperaceae) grown in Sarawak, Malaysia Green synthesis of silver nanoparticles using Indigofera cordifolia leaf extract and their pharmacological potential Uraria picta: A comprehensive review on evidences of utilization and strategies of conservation
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1