第七章园艺植物生物技术.pptxVIP

  1. 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. 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. 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. 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. 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. 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. 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
第七章园艺植物生物技术演示文稿;(优选)第七章园艺植物生物技术;Genetic Engineering also called genetic modification, the direct manipulation of an organisms genome using biotechnology. New DNA may be inserted in the host genome by first isolating and copying the genetic material of interest usi molecular cloning methods to generate a DNA sequence, or by synthesizing the DNA, and then inserting this construct into the host organism. Genes may be removed, or knocked out, using a nuclease. Gene targeting is a different technique that use homologous recombination to change an endogenous gene, and can be used to delete a gene, remove exons, add a gene, or introduce point mutations.; An organism that is generated through genetic engineering is considered to be a genetically modified organism (GMO). The first GMOs were bacteria in 1973. Genetically modified crops (GMCs, GM crops).The first genetically modified plant wa produced in 1982, using an antibiotic-resistan tobacco plant. The first genetically modified crop approved for sale in the U.S., in 1994, was the FlavrSavr tomato, which had a longer shelf life.;7.1 Instrumental Enzyme of Gene Engineering;7.1.1 Restriction Endonuclease;TypeⅡendonuclease;Isoschizomers(同裂酶):指来源不同,但识别相同靶序列的核酸内切酶。 如:HpaⅡ和MspⅠ是一对同裂酶(CCGG) Isocaudarner(同尾酶):指来源不同、识别靶序列不同但产生相同的粘性末端的核酸内切酶。 BamHⅠ BclⅠ G GATC C T GATC A C CTAG G A CTAG T;7.1.2 DNA ligase (DNA连接酶);7.1.3 DNA polymerase;Other DNA-modifying enzymes;7.2 Vectors(载体);7.2.1 Plasmids(质粒);(4363bp);pUC Vectors;现在是16页\一共有98页\编辑于星期四;7.2.2 λ phage(噬菌体) vector;Vector carry LacZ gene: 在诱导物IPTG和X-gal存在时;7.2.3 Cosmid(柯斯质粒) vectors;COSmid pHC79 is 4.3kb DNA fragment and made of pBR322 and cos site of λ phage.;7.2.4 Artificial chromosome vector;Structure of a bacterial artificial chromosome (BAC), used for cloning larg fragments of donor DNA. CMR is a selectable marker for chloramphenicol resistance. oriS, repE, parA, and parB ar F genes for replication an regulation of copy number. cosN is the cos site from l phage. HindIII and BamH

文档评论(0)

150****8199 + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档