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Isolation of a plasmid responsible for caseinase activity in Clostridium perfringens ATCC 3626B
Author(s) -
Hans P. Blaschek,
Myron Solberg
Publication year - 1981
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.147.1.262-266.1981
Subject(s) - clostridium perfringens , acriflavine , biology , plasmid , microbiology and biotechnology , clostridiaceae , strain (injury) , clostridium , centrifugation , enterobacteriaceae , streptococcaceae , escherichia coli , bacteria , biochemistry , antibiotics , dna , toxin , genetics , anatomy , gene
Clostridium perfringens strain ATCC 3626B was cured of caseinase activity at a high frequency after treatment with acriflavine dye (2.5%) or elevated temperature growth (9.1%). Caseinase-negative isolates retained the larger (9.4 megadaltons) pHB102 cryptic plasmid, but were missing the smaller (2.1 megadaltons) pHB101 plasmid present in the caseinase-positive wild-type strain. Dye-buoyant density-gradient centrifugation at 4 or 15 degrees C revealed that the pHB101 and pHB102 plasmids are temperature labile and easily converted into the nicked non-supercoiled or linear state.

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