全国最大最全的茶文化书店
联系我们 关闭音乐 加为收藏

首页>产品信息>茶书网:《茶树抗寒研究进展:英文版(Advances in Cold-tolerance Research on Camellia sinensis L.)》的商品信息

茶书网:《茶树抗寒研究进展:英文版(Advances in Cold-tolerance Research on Camellia sinensis L.)》

查看大图

书  名:茶书网:《茶树抗寒研究进展:英文版(Advances in Cold-tolerance Research on Camellia sinensis L.)》
产品状态:上架
版  别:科学出版社
作  者:丁兆堂 王玉编著
书  号:ISBN 9787030462329
定  价:120元  会员价:120元  VIP价:120
出版日期:201501
评  分:评论等级  共有11504位网友参与打分
游览次数:49899
所属类别:茶文化书刊>N.外文类
立即购买

茶书网:《茶树抗寒研究进展:英文版(Advances in Cold-tolerance Research on Camellia sinensis L.)》 的简介:

    编号:GDZPS6191
    《ADVANCES in COLD-TOLERANCE RESEARCH on Camellia sinensisO.Kuntze》由Zhaotang Ding、Yu Wang编著,讲述了:Tea [Camellia sinensis, (L.)] is a chilling-sensitive plant, and the research on its cold- resistant mechanism is one of the most important directions in tea science discipline in recent years. The book is the team's long time research advances in tea plant's cold-resistant mechanism, which mainly includes the deep study on the mechanism of the cold-resistant molecular by means of omics, such as transcriptome, proteome and metabolome, the cloning, verifying as well as the relevant bioinformatics analysis of the function of the important genes expressed under the cold stress condition. It is of higher theory and application values. This book is suitable for scientific researchers, technicians, teachers and postgraduates in the field of molecular biology, biotechnology, tea science and life science.
目录
Preface
Chapter 1 Integrated RNA-Seq and sRNA-Seq analysis identifies chilling and freezing responsive key molecular players and pathways in tea plant [Camellia sinensis (L.)]
  1.1 Introduction
  1.2 Materials and methods
  1.3 Results
  1.4 Discussion
  References
Chapter 2 Metabolite profiling of tea [Camellia sinensis (L.)] leaves in winter
  2.1 Introduction
  2.2 Materials and methods
  2.3 Results
  2.4 Discussion
  References
Chapter 3 Differential proteomic analysis of chilling stress responses in tea plant [Camellia sinensis (L.)]
  3.1 Introduction
  3.2 Materials and methods
  3.3 Results
  3.4 Discussion
  References
Chapter 4 Chloroplast changes in two tea varieties under natural cold conditions..,
  4.1 Introduction
  4.2 Materials and methods
  4.3 Results
  4.4 Discussion
  References
Chaper 5 Isolation and expression of CsFAD7 and CsFAD8, two genes encoding ω-3 fatty acid desaturase from Camellia sinensis (L.)
  5.1 Introduction
  5.2 Materials and methods
  5.3 Results
  5.4 Discussion
  References
Chapter 6 Analysis of codon use features of stearoyl-acyl carrier protein desaturase gene in Camellia sinensis (L.)
  6.1 Introduction
  6.2 Materials and methods
  6.3 Results
  6.4 Discussion
  References
Chapter 7 Analysis of synonymous codon usage in FAD7 genes from 10 species..
  7.1 Introduction
  7.2 Material and methods
  7.3 Results
  7.4 Discussion
  References
Chapter 8 Codon bias of the gene for chloroplast glycerol-3-phosphate acyltransferase in Camellia sinensis (L.)
  8.1 Introduction
  8.2 Materials and methods
  8.3 Results
  8.4 Discussion
  References
Chapter 9 Codon usage bias analysis for the spermidine synthase gene from Camellia sinensis (L.)
  9.1 Introduction
  9.2 Materials and methods
  9.3 Results
  9.4 Discussion
 References
Chapter 10 Pattern of CslCE1 expression under cold or drought treatment and functional verification through analysis of transgenic Arabidopsis
  10.1 Introduction
  10.2 Materials and methods
  10.3 Results
  10.4 Discussion
 References
Chapter 11 Response of a tea plant CBF/DREB 1 gene (CsCBF1) to abiotic stresses and abscisic acid
  11.1 Introduction
  11.2 Materials and methods
  11.3 Results
  11.4 Discussion
 References
Chapter 12 CsSAD: A fatty acid desaturase gene involved in abiotic resistance in Camellia sinensis (L.)
  12.1 Introduction
  12.2 Materials and methods
  12.3 Results
  12.4 Discussion
  References
    丁兆堂,1964年生,山东省日照市人,青岛农业大学园林园艺学院教授,青岛市农业专家顾问团成员,胶南市政府茶学首席专家,泰山茶叶协会副会长,北方茶产业技术创新战略联盟专家委员会副主任。青岛市即墨瑞草园茶业研究院院长。

网友评论 欢迎您对商品进行评论,表明您对此商品的感觉。

发表您的评论:

姓  名:
标  题:
评  级:
正  文:
 
欢迎光临茶书网!!
扫描二维码加入茶书网官方微信平台扫描图片加入官方微信