Biotechnology Letters

, Volume 9, Issue 3, pp 163–168

Construction of a shuttle vector betweenEscherichiacoli andZymomonasanaerobia

  • Ki Hong Yoon
  • M. Y. Pack

DOI: 10.1007/BF01024557

Cite this article as:
Yoon, K.H. & Pack, M.Y. Biotechnol Lett (1987) 9: 163. doi:10.1007/BF01024557


A 1.7-kb cryptic plasmid was isolated fromZymomonasanaerobia and used to construct a shuttle vector inserting useful parts of pUC9, pBR322, and pRK2501.Escherichiacoli was employed to clone the new plasmid designated pSR12. The 7.7-kb plasmid pSR12 reisolated from the host cells could transform competent cells ofZ.anaerobia at 2×10−7 frequency. This shuttle vector contains two antibiotic resistance markers, Kanr and Tetr, as well as restriction sites such as EcoRI, PstI, and XhoI, suitable for DNA recombinations.

Copyright information

© Kluwer Academic Publishers 1987

Authors and Affiliations

  • Ki Hong Yoon
    • 1
  • M. Y. Pack
    • 1
  1. 1.Department of Biological Science and EngineeringKorea Advanced Institute of Science and TechnologySeoulKorea

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