Phasmids as effective and simple tools for construction and analysis of gene libraries

• Published in: Gene Vol. 81; no. 2; p. 203
• Main Authors: Yankovsky, N K, Fonstein MYu, Lashina SYu, Bukanov, N O, Yakubovich, N V, Ermakova, L M, Rebentish, B A, Janulaitis, A A, Debabov, V G
• Format: Journal Article
• Language: English
• Published: Netherlands 30-09-1989
• Subjects: Bacteriophage lambda - genetics; Cloning, Molecular; DNA, Recombinant; Escherichia coli - genetics; Gene Library; Genetic Vectors - genetics; Plasmids - genetics; Restriction Mapping
• ISSN: 0378-1119
• DOI: 10.1016/0378-1119(89)90180-7

Phasmid lambda pMYF131, a hybrid of phage lambda vectors and plasmid pUC19, was constructed. The phasmid and its derivatives were shown to be efficient vectors for construction and analysis of gene libraries in Escherichia coli cells. The lambda pMYF131 DNA molecule contains all the genes and regions essential for phage lytic development. The plasmid cannot be packaged either in the monomeric or the oligomeric form due to its specific length. Elongation of the DNA molecule by ligation with fragments of foreign DNA can make it packageable and this is easily detected by plaque formation. Hence, the procedures used to construct genomic libraries can be simplified by selection of only recombinant DNA molecules just at the time and on the basis of their packaging in vitro. The output of recombinant clones per vector molecule was several times higher for vector lambda pMYF131, compared to phage vector lambda L47.1AB, and attained 3 x 10(6) clones per micrograms DNA. Vector and recombinant phasmids can be obtained in large quantities in plasmid form. lambda pMYF131 contains nine unique restriction sites which allow the cloning of DNA fragments with blunt ends and of fragments with various types of cohesive ends, obtained by digestion with 14 prototype restriction enzymes. The maximal size of the cloned DNA fragments is approx. 20 kb for lambda pMYF131. Phasmid vectors were used to construct libraries of bovine, pig and quail genomes, and genomic libraries of 17 species of bacteria. Application of suitable methods allowed the identification 13 individual genes within these libraries.