TY - JOUR
T1 - In vivo cloning of arylsulfatase-tyramine oxidase genes in rec strains of klebsiella aerogenes
AU - Murooka, Yoshikatsu
AU - Oka, Masahide
AU - Yamashita, Mitsuo
AU - Sugiyama, Masanori
AU - Harada, Tokuya
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1983/8
Y1 - 1983/8
N2 - A general, genetic technique for in vivo cloning of bacterial genes is presented. We previously introduced the Mu phage into various genera of bacteria including Klebsiella aerogenes with RP4:: Mu. Using these strains carrying RP4:: Mu cts and thermo-inducible Mu prophage in the chromosome, we cloned in vivo the arylsulfatase (ats) and tyramine oxidase (tyn) genes by partial thermo-induction. The donor strains carrying the recombinant plasmids were conjugated with K. aerogenes rec strains, which were isolated as UV-sensitive mutants. The resultant recombinant plasmids, pATl and pAT2, were purified and used for the transformation of mutant strains deficient in the ats and tyn genes. The ats-tyn genes seemed to be transposed into the RP4::Mu cts plasmid together with other chromosomal DNA fragments. This in vivo cloning method is applicable to a wide variety of gram-negative bacteria.
AB - A general, genetic technique for in vivo cloning of bacterial genes is presented. We previously introduced the Mu phage into various genera of bacteria including Klebsiella aerogenes with RP4:: Mu. Using these strains carrying RP4:: Mu cts and thermo-inducible Mu prophage in the chromosome, we cloned in vivo the arylsulfatase (ats) and tyramine oxidase (tyn) genes by partial thermo-induction. The donor strains carrying the recombinant plasmids were conjugated with K. aerogenes rec strains, which were isolated as UV-sensitive mutants. The resultant recombinant plasmids, pATl and pAT2, were purified and used for the transformation of mutant strains deficient in the ats and tyn genes. The ats-tyn genes seemed to be transposed into the RP4::Mu cts plasmid together with other chromosomal DNA fragments. This in vivo cloning method is applicable to a wide variety of gram-negative bacteria.
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U2 - 10.1080/00021369.1983.10865874
DO - 10.1080/00021369.1983.10865874
M3 - Article
AN - SCOPUS:0021067315
SN - 0916-8451
VL - 47
SP - 1807
EP - 1815
JO - Bioscience, Biotechnology and Biochemistry
JF - Bioscience, Biotechnology and Biochemistry
IS - 8
ER -