Cloning of Oxetanocin A Biosynthetic and Resistance Genes that Reside on a Plasmid ofBacillus megateriumStrain NK84-0128
Author(s) -
Makoto Morita,
Katsuhisa Tomita,
Masaru ISHIZAWA,
Kenkichi Takagi,
Fujio Kawamura,
Hideo Takahashi,
Tomio Morino
Publication year - 1999
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1271/bbb.63.563
Subject(s) - bacillus megaterium , plasmid , strain (injury) , cloning (programming) , bglii , microbiology and biotechnology , biology , gene , bacteria , genetics , ecori , anatomy , computer science , programming language
Bacillus megaterium strain NK84-0218 produces a potent antiviral antibiotic, oxetanocin A, which has an oxetanosyl-N-glycoside linkage to an adenine moiety. However, the oxetanocin A productivity of the original strain was unstable and low. In this study, oxetanocin A productivity and resistance was shown to be lost simultaneously when a 51.5-kb plasmid, pOXT1, was cured during cultivation. The deficiency of oxetanocin A productivity and resistance was restored by re-introduction of the pOXT1 plasmid into the cured strain. By a cloning experiment it was shown that a 6.8-kb BglI-D fragment of the pOXT1 plasmid was responsible for oxetanocin A productivity and resistance.
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