A Broad-Host-Range Promoter-Probe Vector, pKU20, and Its Use in Promoter Cloning and Expression of Bacillus thuringiensis Crystal Protein Gene in Pseudomonas putida

  • SHIN, BYUNG SIK (Genetic Engineering Research Institute, Korea Institute of Science and Technology) ;
  • BON TAG KOO (Genetic Engineering Research Institute, Korea Institute of Science and Technology) ;
  • SEUNG HWAN PARK (Genetic Engineering Research Institute, Korea Institute of Science and Technology) ;
  • HO YONG PARK (Genetic Engineering Research Institute, Korea Institute of Science and Technology) ;
  • JEONG IL KIM (Genetic Engineering Research Institute, Korea Institute of Science and Technology)
  • Published : 1991.12.01

Abstract

We have constructed a promoter-probe vector pKU20 using pKT230, a derivative of broad-host-range plsmid RSF1010, as a base. The pKU20 contains structural gene for aminoglycoside phos-photransferase (aph), without promoter, and a multiple cloning site upstream the aph. Using this vector, a 412base pairs (bp) PstI fragment showing strong promoter activity both in Escherichia coli LE392 and Pseudomonas putida KCTC1644 has been cloned from Pseudomonas fluorescens chromosomal DNA on the basis of streptomycin resistance. The nucleotide sequence of the 412 bp fragment has been determined and the putative - 35 and -10 region was observed. Insecticidal protein gene of Bacillus thuringiensis subsp. kurstaki HD-73 inserted on downstream of the promoterlike DNA fragment was efficiently expressed in E. coli and P. putida. The toxin protein was efficiently synthesized in an insoluble form in both strains.

Keywords