- 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
- 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载。
- 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
- 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
- 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们。
- 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
- 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
茶树类黄酮基因功能验证相关体系的筛选论文
Abstract
The enzymes involved in the biosynthetic pathways of tea polyphenols, such as
catechin, flavonoid and proanthocyanidin, have been basically clear, but the functions of
the structural gene and the regulator gene have not been proved effectively. The main
difficulty is to establish a stable transgenic system of tea plant, and the cycle of current
regeneration system is long with low efficiency. Thus, it is still a very urgent task that how
to improve the efficiency of regeneration system and achieve an instantaneous genetic
transformation system. In addition, transgenic system of model plant could be used to
verify the functions of related genes in tea. The main results obtained were as follows:
1. A regeneration system of tea plant
In this paper, the regeneration system of callus in tea including five steps (callus
induction, embryogenic callus proliferation, adventitious bud induction, adventitious
proliferation and rooting in vitro) was established. It consists of two proliferation processes,
callus proliferation and adventitious bud proliferation.
Main steps are as follows: seeds of tea plant (Camellia sinensis) in early September
were picked as explants, then, they were disinfected and cultured in vitro on B5 medium
supplemented with 0.5mg/L 2,4-D and 0.1mg/L KT. The callus was induced in two weeks
and subcultured for four years steadily. The callus was subcultured on MS medium
supplemented with 0.1mg/L IBA and 2.0mg/L 6-BA. The shoot induction rate was 65.71%
after being cultured for four weeks. The shoots were cultured on MS medium
supplemented with 0.1mg/L IBA and 0.01mg/L TDZ. The large number of cluster buds
wa
文档评论(0)