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인간의 삶과 역사 속의 미생물

인간의 삶과 역사 속의 미생물. 강의자료 ppt-8. 2011-1 학기. 미생물 은 어떤 존재인가?. 유전공학 (genetic engineering) 을 가능하게 한 미생물. Genetic engineering ( 유전공학 ).

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인간의 삶과 역사 속의 미생물

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  1. 인간의 삶과 역사 속의 미생물 강의자료ppt-8 2011-1학기

  2. 미생물은어떤 존재인가?

  3. 유전공학(genetic engineering)을 가능하게 한 미생물

  4. Genetic engineering (유전공학) The useof in vitro techniques in the isolation, manipulation, alteration, and expression of DNA (or RNA) and in the development of genetically modified organism (GMO) * = Recombinant DNA technology (재조합 DNA 기술) * Biotechnology (생명공학, 생물공학) • use of organisms to form useful products (inindustrial, medical, or agricultural applications)

  5. Restrictionand modification enzymes • Basic techniques include: - Restriction enzymes (restriction endonuclease, 제한 효소) - Cloning vectors (클로닝매개체) - Molecular cloning (분자클로닝)

  6. Restrictionand modification enzymes • Restriction enzymes: • Protect prokaryotes from hostile foreign DNA (e.g., viral genomes) • Widespread among prokaryotes • Rare in eukaryotes • Recognize specific DNA sequences and cut DNA at those sites • Essential for in vitro DNA manipulation

  7. Restriction enzymes and their recognition sequences

  8. Restrictionand modification of DNA • Modification enzymes: protect cell’s DNA for restriction enzymes • Chemically modify nucleotides in restriction recognition sequence • Modification generally consists of methylation(additionof methyl group) of DNA

  9. Restrictionand modification of DNA Target site is modified Target site is not modified

  10. Essentials of molecular cloning • Molecular cloning - Isolation and incorporation of a piece of DNA into a vector so it can be replicated and manipulated • Three main steps of gene cloning • Isolation and fragmentation of source DNA • Inserting DNA fragment into cloning vector • Introduction of cloned DNA into host organism

  11. Essentials of molecular cloning 1) Isolation and fragmentation of source DNA • Source DNA can be genomic DNA, RNA, or PCR amplified fragments • Genomic DNA must first be restriction digested

  12. Essentials of molecular cloning 2) Inserting DNA fragment into cloning vector • Most vectors are derived from plasmids or viruses • DNA is generally inserted in vitro • DNA ligase: enzyme that joins two DNA molecules • Works with sticky or blunt ends

  13. Essentials of molecular cloning

  14. Recombinant plasmid construction

  15. Essentials of molecular cloning 3) Introduction of cloned DNA into host organism • Transformation is often used to get recombinant DNA into host • Some cells will contain desired cloned gene, while other cells will have other cloned genes • Gene library: mixture of cells containing a variety of genes (= genomic library) • Shotgun cloning: gene libraries made by cloning random genome fragments

  16. Plasmids as cloning vectors • Plasmids are natural vectors and have useful properties as cloning vectors • Vector transfer carried out by chemical transformation or electroporation(電氣穿孔法)

  17. Hosts for molecular cloning (microorganisms)

  18. Steps for cloning a gene

  19. Genomic library construction and screening by phenotyphic rescue

  20. Applications of genetic engineering • In medicine • many useful proteins • gene therapy • In agriculture • use of genetic engineers allows for the direct transfer of desirable traits to agriculturally important animals and plants

  21. Social impact of genetic engineering • There is scientific and philosophical concern about • the use of embryonic stem cells in gene therapy. This is currently a major controversial issue • the production of genetically engineered food • the possibility of the production of genetically engineered organisms by bioterrorists • other issues

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