会议专题

Expression of an engineered tandem-repeat starch-binding domain in sweetpotato plant

In this study,an artificial tandem repeat of a family 20 starch binding domain(SBD2) was engineered by two copies of the SBD derived from Bacillus circulans cyclodextrin glycosyltransferase via the Pro-thr-rich linker peptide from Xyn10A from Cellulomonas fimi.SBD2 was introduced into the sweetpotato Xu 55-2,using appropriate signal sequence.The presence of the SBD2 gene in the genomic DNA of transgenic sweetpotato plants was verified by PCR amplification as well as by Southern blot analysis.The accumulation of SBD2 into transgenic starch granules was confirmed by Western dot bolt analysis.Most striking were the observations that SBD2 expression could affect granule morphology without altering the primary structure of the constituent starch molecules.

Sweetpotato(Ipomoea batatas) Agrobacterium tumefaciens-mediated transformation Tandem starch-binding domain Starch affinity

Yujun Xing Qin Ji Qing Yang Yuming Luo Qiang Li Xin Wang

Department of Biology,Huaiyin Teachers College,Huaian,China;College of Life Sciences,Nanjing Agricul Department of Biology,Huaiyin Teachers College,Huaian,China College of Life Sciences,Nanjing Agricultural University,Nanjing 210095,China Sweetpotato Research Institute,Chinese Academy of Agricultural Science,Xuzhou 221121,China

国际会议

3rd China-Japan-Korea Workshop on Sweetpotato(第三届中日韩甘薯学术研讨会)

北京

英文

317-325

2008-10-12(万方平台首次上网日期,不代表论文的发表时间)