Creating bacterial strains from genomes that have been cloned and engineered in yeast.

نویسندگان

  • Carole Lartigue
  • Sanjay Vashee
  • Mikkel A Algire
  • Ray-Yuan Chuang
  • Gwynedd A Benders
  • Li Ma
  • Vladimir N Noskov
  • Evgeniya A Denisova
  • Daniel G Gibson
  • Nacyra Assad-Garcia
  • Nina Alperovich
  • David W Thomas
  • Chuck Merryman
  • Clyde A Hutchison
  • Hamilton O Smith
  • J Craig Venter
  • John I Glass
چکیده

We recently reported the chemical synthesis, assembly, and cloning of a bacterial genome in yeast. To produce a synthetic cell, the genome must be transferred from yeast to a receptive cytoplasm. Here we describe methods to accomplish this. We cloned a Mycoplasma mycoides genome as a yeast centromeric plasmid and then transplanted it into Mycoplasma capricolum to produce a viable M. mycoides cell. While in yeast, the genome was altered by using yeast genetic systems and then transplanted to produce a new strain of M. mycoides. These methods allow the construction of strains that could not be produced with genetic tools available for this bacterium.

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عنوان ژورنال:
  • Science

دوره 325 5948  شماره 

صفحات  -

تاریخ انتشار 2009